12-66541639-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66541639
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66541639
    reference: chr 12
allele count: 1
allele frequency: 1.109262340543539e-5
allele num: 90150
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.346+49A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.346+49A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*505+49A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.346+49A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-186+49A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.253+49A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.487+49A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*278+49A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.346+49A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.131+49A>G
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16326
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2051
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2026
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4404
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7359
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11183
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13094
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 665
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1382
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 513
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD

12-66541666-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66541666
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66541666
    reference: chr 12
allele count: 95
allele frequency: 9.9949499200404e-4
allele num: 95048
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.131+22A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.346+22A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.346+22A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.253+22A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.487+22A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-186+22A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.346+22A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*505+22A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*278+22A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.346+22A>G
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26651
  bin: 2.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 12235
  bin: 7.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 1.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6068
  bin: 2.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 7433
  bin: 1.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2240
  bin: 3.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2351
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1589
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29686
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS

12-66541680-C-CGG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66541680
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66541682
    reference: chr 12
allele count: 36
allele frequency: 3.550856150871932e-4
allele num: 101384
alternate allele: CGG
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.346+6_346+7dupCC
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.253+6_253+7dupCC
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-186+6_-186+7dupCC
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*505+6_*505+7dupCC
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.131+6_131+7dupCC
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.346+6_346+7dupCC
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*278+6_*278+7dupCC
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.487+6_487+7dupCC
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.346+6_346+7dupCC
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.346+6_346+7dupCC
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2409
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9333
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3575
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 32777
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 1.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7193
  bin: 2.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
hgvs: c.346+6_346+7dupCC
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: African
population: European (Finnish)
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD

12-66541680-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66541680
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66541680
    reference: chr 12
allele count: 2
allele frequency: 1.972697861595518e-5
allele num: 101384
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*278+8G>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.346+8G>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.346+8G>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.487+8G>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.346+8G>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-186+8G>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.253+8G>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*505+8G>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.346+8G>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.131+8G>A
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7193
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9333
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2409
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32777
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3575
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.346+8G>A
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

12-66541681-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66541681
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66541681
    reference: chr 12
allele count: 19
allele frequency: 1.866734786111493e-4
allele num: 101782
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.346+7C>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.131+7C>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.253+7C>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.346+7C>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.346+7C>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.487+7C>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.346+7C>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*278+7C>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-186+7C>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*505+7C>T
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33050
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7329
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9100
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2409
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3403
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.346+7C>T
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

12-66541682-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66541682
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66541682
    reference: chr 12
allele count: 1
allele frequency: 9.777464898901012e-6
allele num: 102276
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.346+6C>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.346+6C>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-186+6C>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.487+6C>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.253+6C>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.346+6C>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*278+6C>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.346+6C>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.131+6C>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*505+6C>T
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2425
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33207
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7450
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8949
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3303
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.346+6C>T
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

12-66541694-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66541694
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66541694
    reference: chr 12
allele count: 2
allele frequency: 1.905596737618385e-5
allele num: 104954
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.481G>A
  hgvsp: ENSP00000286424.7:p.Val161Ile
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*499G>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-192G>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.340G>A
  hgvsp: ENSP00000350965.3:p.Val114Ile
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.340G>A
  hgvsp: ENSP00000454670.1:p.Val114Ile
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.125G>A
  hgvsp: ENSP00000438957.1:p.Ser42Asn
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.340G>A
  hgvsp: ENSP00000451688.1:p.Val114Ile
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.340G>A
  hgvsp: ENSP00000381114.4:p.Val114Ile
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.247G>A
  hgvsp: ENSP00000441291.1:p.Val83Ile
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*272G>A
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2474
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7684
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2687
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34274
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8390
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 396
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Val114Ile
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD

12-66541697-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66541697
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66541697
    reference: chr 12
allele count: 1
allele frequency: 9.483886876197341e-6
allele num: 105442
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.337G>A
  hgvsp: ENSP00000454670.1:p.Ala113Thr
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.337G>A
  hgvsp: ENSP00000350965.3:p.Ala113Thr
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.478G>A
  hgvsp: ENSP00000286424.7:p.Ala160Thr
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.337G>A
  hgvsp: ENSP00000451688.1:p.Ala113Thr
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.337G>A
  hgvsp: ENSP00000381114.4:p.Ala113Thr
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*496G>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-195G>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.244G>A
  hgvsp: ENSP00000441291.1:p.Ala82Thr
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.122G>A
  hgvsp: ENSP00000438957.1:p.Gly41Asp
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*269G>A
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2637
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7415
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2495
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34414
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8606
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 727
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala113Thr
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

12-66541720-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66541720
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66541720
    reference: chr 12
allele count: 4
allele frequency: 3.836341664588648e-5
allele num: 104266
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.314C>T
  hgvsp: ENSP00000381114.4:p.Thr105Met
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-218C>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.314C>T
  hgvsp: ENSP00000454670.1:p.Thr105Met
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.455C>T
  hgvsp: ENSP00000286424.7:p.Thr152Met
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.221C>T
  hgvsp: ENSP00000441291.1:p.Thr74Met
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.314C>T
  hgvsp: ENSP00000451688.1:p.Thr105Met
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*246C>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.314C>T
  hgvsp: ENSP00000350965.3:p.Thr105Met
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*473C>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.99C>T
  hgvsp: ENST00000545504.1:c.99C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7901
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2547
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9345
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5364
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr105Met
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

12-66541724-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66541724
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66541724
    reference: chr 12
allele count: 1
allele frequency: 9.704780574911201e-6
allele num: 103042
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-219-3T>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.313-3T>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.313-3T>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.313-3T>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.313-3T>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.454-3T>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*245-3T>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.220-3T>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-3T>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*472-3T>A
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9232
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2485
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8427
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7285
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27583
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.313-3T>A
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD

12-66541726-TGAAAA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66541726
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66541721
    reference: chr 12
allele count: 1
allele frequency: 9.705157320600167e-6
allele num: 103038
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.454-10_454-6delTTTTC
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.313-10_313-6delTTTTC
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*472-10_*472-6delTTTTC
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.313-10_313-6delTTTTC
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-10_98-6delTTTTC
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.220-10_220-6delTTTTC
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.313-10_313-6delTTTTC
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.313-10_313-6delTTTTC
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*245-10_*245-6delTTTTC
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-219-10_-219-6delTTTTC
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9250
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7298
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27583
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8428
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2480
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.313-10_313-6delTTTTC
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: TGAAAA
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum

12-66541732-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66541732
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66541732
    reference: chr 12
allele count: 1
allele frequency: 9.854935351624093e-6
allele num: 101472
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.313-11C>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.220-11C>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*245-11C>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.313-11C>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.313-11C>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-219-11C>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-11C>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.454-11C>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*472-11C>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.313-11C>A
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23827
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8814
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9014
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10200
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2477
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1587
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 568
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2041
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

12-66541733-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66541733
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66541733
    reference: chr 12
allele count: 1
allele frequency: 9.871863215463286e-6
allele num: 101298
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.220-12T>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-12T>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.313-12T>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.313-12T>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*472-12T>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.313-12T>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*245-12T>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.454-12T>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-219-12T>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.313-12T>A
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8664
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10799
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2410
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23222
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2345
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 957
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

12-66541743-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66541743
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66541743
    reference: chr 12
allele count: 3
allele frequency: 3.033857853646697e-5
allele num: 98884
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*472-22A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.313-22A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-219-22A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.313-22A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-22A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.454-22A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.313-22A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*245-22A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.220-22A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.313-22A>G
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6836
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15050
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9593
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2328
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17027
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4479
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2403
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 365
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18128
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
reference allele: T
site quality: DP
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

12-66541743-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66541743
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66541743
    reference: chr 12
allele count: 3
allele frequency: 3.033857853646697e-5
allele num: 98884
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-22A>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-219-22A>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.313-22A>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.454-22A>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*472-22A>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.313-22A>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.220-22A>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*245-22A>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.313-22A>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.313-22A>C
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4479
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6836
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15050
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9593
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17027
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2328
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1232
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 423
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum

12-66541761-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66541761
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66541761
    reference: chr 12
allele count: 1
allele frequency: 1.072179096796329e-5
allele num: 93268
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*472-40A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.313-40A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-219-40A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.313-40A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-40A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.313-40A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.220-40A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*245-40A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.454-40A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.313-40A>G
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11895
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18172
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4366
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11436
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1940
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6588
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 728
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5466
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16018
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: African
population: South Asian
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD

12-66541765-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66541765
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66541765
    reference: chr 12
allele count: 2
allele frequency: 2.176515398846447e-5
allele num: 91890
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.313-44T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.313-44T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*245-44T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*472-44T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-44T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.454-44T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.220-44T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-219-44T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.313-44T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.313-44T>C
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17669
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11904
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6844
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12121
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1963
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3948
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2528
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

12-66546009-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66546009
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66546009
    reference: chr 12
allele count: 1
allele frequency: 9.09338910611985e-6
allele num: 109970
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.312+42T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.312+42T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*471+42T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-4288T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.312+42T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.312+42T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-220+42T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.453+42T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*244+42T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.219+42T>C
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22148
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6747
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2530
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11866
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4893
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6848
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1665
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Other
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

12-66546013-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66546013
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66546013
    reference: chr 12
allele count: 1
allele frequency: 9.047317470370035e-6
allele num: 110530
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-4292T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.312+38T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.453+38T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.312+38T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.312+38T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.219+38T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-220+38T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*471+38T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.312+38T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*244+38T>C
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7392
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4742
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25893
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4356
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1158
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9973
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2721
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4837
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25202
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4401
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

12-66546021-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66546021
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66546021
    reference: chr 12
allele count: 5
allele frequency: 4.455772007057943e-5
allele num: 112214
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*471+30A>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.312+30A>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-220+30A>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*244+30A>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.453+30A>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-4300A>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.312+30A>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.312+30A>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.312+30A>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.219+30A>C
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3029
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5497
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8327
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4037
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32687
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2571
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32312
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

12-66546029-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66546029
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66546029
    reference: chr 12
allele count: 2
allele frequency: 1.742190630498789e-5
allele num: 114798
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-220+22A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.219+22A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*244+22A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.312+22A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.453+22A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.312+22A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.312+22A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-4308A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*471+22A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.312+22A>G
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9484
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2876
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2723
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3539
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35679
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1617
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ

12-66546032-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66546032
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66546032
    reference: chr 12
allele count: 2
allele frequency: 1.730014013113506e-5
allele num: 115606
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-220+19T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.312+19T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-4311T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*244+19T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.219+19T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.453+19T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.312+19T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.312+19T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*471+19T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.312+19T>C
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3680
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2185
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36190
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9879
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2483
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1656
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 735
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2612
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: A
site quality: DP
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

12-66546035-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66546035
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66546035
    reference: chr 12
allele count: 1
allele frequency: 8.598156555234557e-6
allele num: 116304
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.453+16T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*244+16T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.312+16T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.312+16T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-220+16T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.312+16T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.312+16T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*471+16T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.219+16T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-4314T>C
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2158
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1729
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3788
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1302
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36737
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10082
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4783
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 677
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

12-66546035-AAGTC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66546035
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66546031
    reference: chr 12
allele count: 95
allele frequency: 8.168248727472829e-4
allele num: 116304
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.312+12_312+15delGACT
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.453+12_453+15delGACT
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.312+12_312+15delGACT
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.312+12_312+15delGACT
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-220+12_-220+15delGACT
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.312+12_312+15delGACT
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*244+12_*244+15delGACT
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*471+12_*471+15delGACT
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-4318_98-4315delGACT
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.219+12_219+15delGACT
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3788
  bin: 3.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 36737
  bin: 2.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 4.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1729
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2158
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10082
  bin: 2.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 4.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1302
  bin: 3.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 307
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1696
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: AAGTC
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

12-66546043-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66546043
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66546043
    reference: chr 12
allele count: 34
allele frequency: 2.886002886002886e-4
allele num: 117810
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.312+8C>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.312+8C>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.312+8C>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*471+8C>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.453+8C>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.312+8C>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*244+8C>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.219+8C>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-4322C>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-220+8C>T
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10758
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1353
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1424
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37346
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4073
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 4.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: c.312+8C>T
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

12-66546077-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66546077
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66546077
    reference: chr 12
allele count: 2
allele frequency: 1.668864004272292e-5
allele num: 119842
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-4356C>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*445C>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.427C>T
  hgvsp: ENSP00000286424.7:p.Leu143Phe
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.286C>T
  hgvsp: ENSP00000350965.3:p.Leu96Phe
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.193C>T
  hgvsp: ENSP00000441291.1:p.Leu65Phe
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.286C>T
  hgvsp: ENSP00000451688.1:p.Leu96Phe
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.286C>T
  hgvsp: ENSP00000381114.4:p.Leu96Phe
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-246C>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.286C>T
  hgvsp: ENSP00000454670.1:p.Leu96Phe
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*218C>T
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37690
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11575
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4603
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Leu96Phe
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

12-66546087-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66546087
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66546088
    reference: chr 12
allele count: 1
allele frequency: 8.338197281747686e-6
allele num: 119930
alternate allele: AT
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.275dupA
  hgvsp: ENSP00000350965.3:p.His92GlnfsTer2
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.275dupA
  hgvsp: ENSP00000451688.1:p.His92GlnfsTer2
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.275dupA
  hgvsp: ENSP00000381114.4:p.His92GlnfsTer2
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.416dupA
  hgvsp: ENSP00000286424.7:p.His139GlnfsTer2
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*434dupA
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-4367dupA
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.275dupA
  hgvsp: ENSP00000454670.1:p.His92GlnfsTer2
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.182dupA
  hgvsp: ENSP00000441291.1:p.His61GlnfsTer2
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*207dupA
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-257dupA
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 11665
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37534
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4652
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.His92GlnfsTer2
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum

12-66546088-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66546088
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66546088
    reference: chr 12
allele count: 1
allele frequency: 8.337641114575865e-6
allele num: 119938
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.275A>G
  hgvsp: ENSP00000454670.1:p.His92Arg
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.275A>G
  hgvsp: ENSP00000381114.4:p.His92Arg
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.182A>G
  hgvsp: ENSP00000441291.1:p.His61Arg
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.275A>G
  hgvsp: ENSP00000350965.3:p.His92Arg
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*207A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-257A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.416A>G
  hgvsp: ENSP00000286424.7:p.His139Arg
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-4367A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.275A>G
  hgvsp: ENSP00000451688.1:p.His92Arg
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*434A>G
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4658
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37537
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11669
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 825
  bin: 8.75e1
  variant carriers: 0
hgvs: p.His92Arg
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

12-66546090-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66546090
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66546090
    reference: chr 12
allele count: 2
allele frequency: 1.667500416875104e-5
allele num: 119940
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*205A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.273A>G
  hgvsp: ENST00000556010.1:c.273A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*432A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.414A>G
  hgvsp: ENST00000286424.7:c.414A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-4369A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.180A>G
  hgvsp: ENST00000542724.1:c.180A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.273A>G
  hgvsp: ENST00000358230.3:c.273A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.273A>G
  hgvsp: ENST00000398033.4:c.273A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-259A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.273A>G
  hgvsp: ENST00000539652.1:c.273A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4667
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11686
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37512
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1464
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg91Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
population: European (Finnish)
reference allele: T
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

12-66546100-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66546100
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66546100
    reference: chr 12
allele count: 53741
allele frequency: 4.471932364737797e-1
allele num: 120174
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.170T>C
  hgvsp: ENSP00000441291.1:p.Ile57Thr
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.263T>C
  hgvsp: ENSP00000454670.1:p.Ile88Thr
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.263T>C
  hgvsp: ENSP00000451688.1:p.Ile88Thr
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.263T>C
  hgvsp: ENSP00000381114.4:p.Ile88Thr
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*422T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.404T>C
  hgvsp: ENSP00000286424.7:p.Ile135Thr
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-4379T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.263T>C
  hgvsp: ENSP00000350965.3:p.Ile88Thr
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*195T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-269T>C
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13217
  bin: 2.25e1
  variant carriers: 587
genotype depth: GenotypeDepth
  all individuals: 3433
  bin: 6.25e1
  variant carriers: 3352
genotype depth: GenotypeDepth
  all individuals: 3401
  bin: 4.25e1
  variant carriers: 3210
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.5e0
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 1.75e1
  variant carriers: 331
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 8.25e1
  variant carriers: 1452
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 1.25e1
  variant carriers: 131
genotype depth: GenotypeDepth
  all individuals: 4160
  bin: 5.25e1
  variant carriers: 4040
genotype depth: GenotypeDepth
  all individuals: 4007
  bin: 4.75e1
  variant carriers: 3842
genotype depth: GenotypeDepth
  all individuals: 5568
  bin: 2.75e1
  variant carriers: 1171
genotype depth: GenotypeDepth
  all individuals: 3933
  bin: 5.75e1
  variant carriers: 3832
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 9.25e1
  variant carriers: 866
genotype depth: GenotypeDepth
  all individuals: 2900
  bin: 3.25e1
  variant carriers: 1872
genotype depth: GenotypeDepth
  all individuals: 1895
  bin: 7.75e1
  variant carriers: 1838
genotype depth: GenotypeDepth
  all individuals: 2317
  bin: 7.25e1
  variant carriers: 2250
genotype depth: GenotypeDepth
  all individuals: 2877
  bin: 6.75e1
  variant carriers: 2809
genotype depth: GenotypeDepth
  all individuals: 2879
  bin: 3.75e1
  variant carriers: 2601
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 8.75e1
  variant carriers: 1108
genotype depth: GenotypeDepth
  all individuals: 5391
  bin: 9.75e1
  variant carriers: 5115
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 4.25e1
  variant carriers: 36
hgvs: p.Ile88Thr
num of homozygotes: 13373
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: African
population: Latino
reference allele: A
site quality: QD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum

12-66546101-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66546101
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66546101
    reference: chr 12
allele count: 1
allele frequency: 8.347106058329577e-6
allele num: 119802
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.262A>G
  hgvsp: ENSP00000350965.3:p.Ile88Val
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.169A>G
  hgvsp: ENSP00000441291.1:p.Ile57Val
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.262A>G
  hgvsp: ENSP00000381114.4:p.Ile88Val
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*421A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.403A>G
  hgvsp: ENSP00000286424.7:p.Ile135Val
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-270A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-4380A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*194A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.262A>G
  hgvsp: ENSP00000451688.1:p.Ile88Val
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.262A>G
  hgvsp: ENSP00000454670.1:p.Ile88Val
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24900
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20771
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8258
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ile88Val
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

12-66546105-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66546105
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66546105
    reference: chr 12
allele count: 6
allele frequency: 5.010438413361169e-5
allele num: 119750
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-274G>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.258G>A
  hgvsp: ENST00000556010.1:c.258G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.258G>A
  hgvsp: ENST00000398033.4:c.258G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-4384G>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*417G>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*190G>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.165G>A
  hgvsp: ENST00000542724.1:c.165G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.258G>A
  hgvsp: ENST00000358230.3:c.258G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.399G>A
  hgvsp: ENST00000286424.7:c.399G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.258G>A
  hgvsp: ENST00000539652.1:c.258G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8240
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24865
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20794
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 706
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ala86Ala
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: East Asian
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD

12-66546106-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66546106
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66546106
    reference: chr 12
allele count: 3
allele frequency: 2.506056302731601e-5
allele num: 119710
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.257C>T
  hgvsp: ENSP00000454670.1:p.Ala86Val
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*416C>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-275C>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.257C>T
  hgvsp: ENSP00000381114.4:p.Ala86Val
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.164C>T
  hgvsp: ENSP00000441291.1:p.Ala55Val
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.398C>T
  hgvsp: ENSP00000286424.7:p.Ala133Val
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.257C>T
  hgvsp: ENSP00000451688.1:p.Ala86Val
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.257C>T
  hgvsp: ENSP00000350965.3:p.Ala86Val
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-4385C>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*189C>T
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8235
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24849
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20806
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1520
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala86Val
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

12-66546128-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66546128
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66546128
    reference: chr 12
allele count: 2
allele frequency: 1.682340472064736e-5
allele num: 118882
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*167G>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.235G>A
  hgvsp: ENSP00000454670.1:p.Gly79Arg
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.235G>A
  hgvsp: ENSP00000451688.1:p.Gly79Arg
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.235G>A
  hgvsp: ENSP00000381114.4:p.Gly79Arg
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.142G>A
  hgvsp: ENSP00000441291.1:p.Gly48Arg
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-4407G>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.235G>A
  hgvsp: ENSP00000350965.3:p.Gly79Arg
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-297G>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.376G>A
  hgvsp: ENSP00000286424.7:p.Gly126Arg
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*394G>A
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20585
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8011
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24451
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gly79Arg
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum

12-66546129-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66546129
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66546129
    reference: chr 12
allele count: 11
allele frequency: 9.253962378436585e-5
allele num: 118868
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.234C>T
  hgvsp: ENST00000398033.4:c.234C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.375C>T
  hgvsp: ENST00000286424.7:c.375C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.234C>T
  hgvsp: ENST00000358230.3:c.234C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.141C>T
  hgvsp: ENST00000542724.1:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.234C>T
  hgvsp: ENST00000539652.1:c.234C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.234C>T
  hgvsp: ENST00000556010.1:c.234C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*393C>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-298C>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-4408C>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*166C>T
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24465
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1465
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20627
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7978
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Leu78Leu
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Other
population: East Asian
reference allele: G
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ

12-66546131-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66546131
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66546131
    reference: chr 12
allele count: 1
allele frequency: 8.420059950826851e-6
allele num: 118764
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.373C>G
  hgvsp: ENSP00000286424.7:p.Leu125Val
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*391C>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-4410C>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-300C>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.232C>G
  hgvsp: ENSP00000350965.3:p.Leu78Val
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.232C>G
  hgvsp: ENSP00000381114.4:p.Leu78Val
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.139C>G
  hgvsp: ENSP00000441291.1:p.Leu47Val
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.232C>G
  hgvsp: ENSP00000451688.1:p.Leu78Val
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*164C>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.232C>G
  hgvsp: ENSP00000454670.1:p.Leu78Val
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20637
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7928
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24418
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 667
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Leu78Val
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP

12-66546153-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66546153
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66546153
    reference: chr 12
allele count: 1
allele frequency: 8.653663095588363e-6
allele num: 115558
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.117T>C
  hgvsp: ENST00000542724.1:c.117T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.351T>C
  hgvsp: ENST00000286424.7:c.351T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.210T>C
  hgvsp: ENST00000398033.4:c.210T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.210T>C
  hgvsp: ENST00000358230.3:c.210T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.210T>C
  hgvsp: ENST00000539652.1:c.210T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*369T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-322T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.210T>C
  hgvsp: ENST00000556010.1:c.210T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*142T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-4432T>C
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19091
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1349
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2534
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7288
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22829
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2938
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 558
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Pro70Pro
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

12-66546165-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66546165
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66546165
    reference: chr 12
allele count: 1
allele frequency: 8.935751943526047e-6
allele num: 111910
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.207-9G>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.207-9G>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*139-9G>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.114-9G>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.207-9G>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*366-9G>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-325-9G>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.348-9G>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-4444G>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.207-9G>A
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17159
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6592
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4187
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20177
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6218
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 942
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP

12-66546172-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66546172
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66546172
    reference: chr 12
allele count: 4
allele frequency: 3.659518407377589e-5
allele num: 109304
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-325-16A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.207-16A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-4451A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.348-16A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.207-16A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.114-16A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.207-16A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*366-16A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*139-16A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.207-16A>G
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5278
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11191
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17157
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5334
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1826
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14591
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1738
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14168
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 861
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: African
population: South Asian
population: Latino
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

12-66546191-G-GA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66546191
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66546192
    reference: chr 12
allele count: 1
allele frequency: 9.734633880419757e-6
allele num: 102726
alternate allele: GA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.114-36dupT
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.348-36dupT
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-4471dupT
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.207-36dupT
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*139-36dupT
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*366-36dupT
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.207-36dupT
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-325-36dupT
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.207-36dupT
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.207-36dupT
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7369
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22732
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7028
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6382
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8567
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2587
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 574
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4800
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 582
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

12-66546196-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66546196
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66546196
    reference: chr 12
allele count: 0
allele frequency: 0.0e0
allele num: 100494
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*366-40T>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.114-40T>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-4475T>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-325-40T>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.348-40T>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*139-40T>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.207-40T>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.207-40T>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.207-40T>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.207-40T>A
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: intron
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 1620
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12645
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4061
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22274
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8011
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2225
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5160
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 938
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/12-66546196-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66546196
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66546196
    reference: chr 12
allele count: 1
allele frequency: 9.950842836388241e-6
allele num: 100494
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.207-40T>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.114-40T>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.348-40T>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.207-40T>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.207-40T>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-325-40T>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-4475T>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*366-40T>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.207-40T>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*139-40T>G
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8011
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12645
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1620
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5160
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22274
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2225
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4061
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8842
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3907
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1069
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: Other
population: South Asian
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQ

12-66546204-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66546204
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66546204
    reference: chr 12
allele count: 1
allele frequency: 1.107370659107016e-5
allele num: 90304
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*139-48C>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-325-48C>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*366-48C>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.114-48C>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.348-48C>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.207-48C>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.207-48C>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.207-48C>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-4483C>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.207-48C>G
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13012
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5839
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11675
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2801
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19509
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1705
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1459
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2908
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3380
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: African
population: European (Finnish)
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

12-66547069-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66547069
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66547069
    reference: chr 12
allele count: 2
allele frequency: 1.701982809973619e-5
allele num: 117510
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-5348A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.206+51A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.206+51A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.206+51A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.113+51A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.206+51A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*365+51A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.347+51A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-326+51A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*138+51A>G
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4682
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18649
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8694
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14136
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7140
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2064
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1831
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 718
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2101
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS

12-66547071-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66547071
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66547071
    reference: chr 12
allele count: 6
allele frequency: 5.117096218465895e-5
allele num: 117254
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.206+49C>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*365+49C>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-326+49C>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-5350C>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.206+49C>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.113+49C>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.206+49C>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.347+49C>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*138+49C>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.206+49C>A
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4659
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18702
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7174
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7781
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14996
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2059
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 730
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1381
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

12-66547083-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66547083
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66547083
    reference: chr 12
allele count: 1
allele frequency: 8.486514927779759e-6
allele num: 117834
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.206+37A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.113+37A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-5362A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-326+37A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.206+37A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*365+37A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.347+37A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.206+37A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.206+37A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*138+37A>G
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3424
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2046
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7295
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20973
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19657
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 401
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 691
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: Other
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff

12-66547094-TATTC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66547094
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66547090
    reference: chr 12
allele count: 1
allele frequency: 8.437252155717926e-6
allele num: 118522
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-326+22_-326+25delGAAT
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-5377_98-5374delGAAT
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*365+22_*365+25delGAAT
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.206+22_206+25delGAAT
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.206+22_206+25delGAAT
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.347+22_347+25delGAAT
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.113+22_113+25delGAAT
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*138+22_*138+25delGAAT
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.206+22_206+25delGAAT
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.206+22_206+25delGAAT
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20400
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2047
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23464
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7425
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6208
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1616
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: TATTC
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS

http://identifiers.org/exac.variant/12-66547099-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66547099
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66547099
    reference: chr 12
allele count: 1
allele frequency: 8.405762991106703e-6
allele num: 118966
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.206+21T>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.206+21T>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*365+21T>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.206+21T>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-326+21T>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-5378T>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*138+21T>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.113+21T>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.206+21T>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.347+21T>G
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20670
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24180
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7471
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2043
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/12-66547104-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66547104
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66547104
    reference: chr 12
allele count: 1
allele frequency: 8.373666493610892e-6
allele num: 119422
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.206+16G>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*365+16G>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.206+16G>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-326+16G>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-5383G>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.113+16G>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.206+16G>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.206+16G>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.347+16G>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*138+16G>T
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7540
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2051
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20918
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24708
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

12-66547114-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66547114
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66547114
    reference: chr 12
allele count: 1
allele frequency: 8.33625102119075e-6
allele num: 119958
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-5393G>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.206+6G>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.206+6G>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-326+6G>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*138+6G>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.206+6G>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.347+6G>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.113+6G>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.206+6G>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*365+6G>A
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21166
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25244
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2049
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7569
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.206+6G>A
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/12-66547118-AC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66547118
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66547117
    reference: chr 12
allele count: 1
allele frequency: 8.326533331112925e-6
allele num: 120098
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-326+1delG
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*365+1delG
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.206+1delG
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.113+1delG
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-5398delG
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.206+1delG
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*138+1delG
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.206+1delG
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.347+1delG
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.206+1delG
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: splice donor
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2048
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21256
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25322
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7586
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6359
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1842
  bin: 7.75e1
  variant carriers: 0
hgvs: c.206+1delG
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
reference allele: AC
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ

12-66547126-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66547126
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66547126
    reference: chr 12
allele count: 1
allele frequency: 8.314901967305805e-6
allele num: 120266
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.200A>G
  hgvsp: ENSP00000451688.1:p.His67Arg
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.200A>G
  hgvsp: ENSP00000350965.3:p.His67Arg
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.200A>G
  hgvsp: ENSP00000381114.4:p.His67Arg
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-5405A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*132A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-332A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.107A>G
  hgvsp: ENSP00000441291.1:p.His36Arg
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.200A>G
  hgvsp: ENSP00000454670.1:p.His67Arg
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.341A>G
  hgvsp: ENSP00000286424.7:p.His114Arg
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*359A>G
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25373
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21350
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7613
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2048
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
hgvs: p.His67Arg
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD

12-66547130-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66547130
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66547130
    reference: chr 12
allele count: 1
allele frequency: 8.312137383006666e-6
allele num: 120306
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.196G>A
  hgvsp: ENSP00000451688.1:p.Val66Ile
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-5409G>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*355G>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.196G>A
  hgvsp: ENSP00000350965.3:p.Val66Ile
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.337G>A
  hgvsp: ENSP00000286424.7:p.Val113Ile
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.196G>A
  hgvsp: ENSP00000454670.1:p.Val66Ile
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.103G>A
  hgvsp: ENSP00000441291.1:p.Val35Ile
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.196G>A
  hgvsp: ENSP00000381114.4:p.Val66Ile
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-336G>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*128G>A
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25355
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2048
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21405
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7637
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Val66Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Other
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: FS

12-66547138-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66547138
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66547138
    reference: chr 12
allele count: 1
allele frequency: 8.307027745472669e-6
allele num: 120380
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-5417G>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.188G>A
  hgvsp: ENSP00000381114.4:p.Arg63Gln
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-344G>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.188G>A
  hgvsp: ENSP00000451688.1:p.Arg63Gln
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.95G>A
  hgvsp: ENSP00000441291.1:p.Arg32Gln
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.329G>A
  hgvsp: ENSP00000286424.7:p.Arg110Gln
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*347G>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.188G>A
  hgvsp: ENSP00000350965.3:p.Arg63Gln
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*120G>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.188G>A
  hgvsp: ENSP00000454670.1:p.Arg63Gln
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21476
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7647
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25358
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2051
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg63Gln
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum

12-66547139-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66547139
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66547139
    reference: chr 12
allele count: 2
allele frequency: 1.661295145695584e-5
allele num: 120388
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.94C>T
  hgvsp: ENSP00000441291.1:p.Arg32Trp
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-5418C>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.187C>T
  hgvsp: ENSP00000454670.1:p.Arg63Trp
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.328C>T
  hgvsp: ENSP00000286424.7:p.Arg110Trp
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-345C>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*346C>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.187C>T
  hgvsp: ENSP00000451688.1:p.Arg63Trp
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.187C>T
  hgvsp: ENSP00000350965.3:p.Arg63Trp
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.187C>T
  hgvsp: ENSP00000381114.4:p.Arg63Trp
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*119C>T
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21508
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25338
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2051
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7652
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg63Trp
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: East Asian
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

12-66547142-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66547142
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66547142
    reference: chr 12
allele count: 1
allele frequency: 8.306061763875276e-6
allele num: 120394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.184G>A
  hgvsp: ENSP00000381114.4:p.Val62Ile
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-348G>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*116G>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.184G>A
  hgvsp: ENSP00000451688.1:p.Val62Ile
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.325G>A
  hgvsp: ENSP00000286424.7:p.Val109Ile
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.184G>A
  hgvsp: ENSP00000454670.1:p.Val62Ile
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-5421G>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.184G>A
  hgvsp: ENSP00000350965.3:p.Val62Ile
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.91G>A
  hgvsp: ENSP00000441291.1:p.Val31Ile
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*343G>A
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25343
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21528
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2051
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7654
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1851
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Val62Ile
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

12-66547144-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66547144
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66547144
    reference: chr 12
allele count: 1
allele frequency: 8.304682179812978e-6
allele num: 120414
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*341C>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.182C>T
  hgvsp: ENSP00000350965.3:p.Ser61Phe
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-5423C>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.182C>T
  hgvsp: ENSP00000454670.1:p.Ser61Phe
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.182C>T
  hgvsp: ENSP00000451688.1:p.Ser61Phe
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*114C>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.89C>T
  hgvsp: ENSP00000441291.1:p.Ser30Phe
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.323C>T
  hgvsp: ENSP00000286424.7:p.Ser108Phe
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-350C>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.182C>T
  hgvsp: ENSP00000381114.4:p.Ser61Phe
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7659
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2050
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25339
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21544
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ser61Phe
num of homozygotes: 0
population: African
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/12-66547148-C-CA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66547148
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66547149
    reference: chr 12
allele count: 1
allele frequency: 8.304958059961797e-6
allele num: 120410
alternate allele: CA
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.84dupT
  hgvsp: ENSP00000441291.1:p.Glu29Ter
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-355dupT
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-5428dupT
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*336dupT
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.318dupT
  hgvsp: ENSP00000286424.7:p.Glu107Ter
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.177dupT
  hgvsp: ENSP00000454670.1:p.Glu60Ter
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.177dupT
  hgvsp: ENSP00000381114.4:p.Glu60Ter
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.177dupT
  hgvsp: ENSP00000350965.3:p.Glu60Ter
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.177dupT
  hgvsp: ENSP00000451688.1:p.Glu60Ter
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*109dupT
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21567
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7655
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25330
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2052
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Glu60Ter
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

12-66547153-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66547153
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66547153
    reference: chr 12
allele count: 8
allele frequency: 6.643083719462574e-5
allele num: 120426
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.80A>T
  hgvsp: ENSP00000441291.1:p.Tyr27Phe
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.173A>T
  hgvsp: ENSP00000381114.4:p.Tyr58Phe
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.173A>T
  hgvsp: ENSP00000451688.1:p.Tyr58Phe
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.173A>T
  hgvsp: ENSP00000454670.1:p.Tyr58Phe
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*105A>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-359A>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.314A>T
  hgvsp: ENSP00000286424.7:p.Tyr105Phe
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.173A>T
  hgvsp: ENSP00000350965.3:p.Tyr58Phe
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-5432A>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*332A>T
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7658
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21578
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25330
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2054
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Tyr58Phe
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: VQSLOD

12-66547155-T-TA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66547155
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66547156
    reference: chr 12
allele count: 19
allele frequency: 1.577758586328307e-4
allele num: 120424
alternate allele: TA
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.170dupT
  hgvsp: ENSP00000381114.4:p.Leu57PhefsTer4
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.311dupT
  hgvsp: ENSP00000286424.7:p.Leu104PhefsTer4
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*329dupT
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.77dupT
  hgvsp: ENSP00000441291.1:p.Leu26PhefsTer4
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.170dupT
  hgvsp: ENSP00000350965.3:p.Leu57PhefsTer4
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.170dupT
  hgvsp: ENSP00000454670.1:p.Leu57PhefsTer4
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-5435dupT
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-362dupT
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*102dupT
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.170dupT
  hgvsp: ENSP00000451688.1:p.Leu57PhefsTer4
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25297
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 21590
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7669
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 44487
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Leu57PhefsTer4
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

12-66547156-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66547156
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66547156
    reference: chr 12
allele count: 1
allele frequency: 8.306475728477921e-6
allele num: 120388
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.170T>A
  hgvsp: ENSP00000381114.4:p.Leu57Ter
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.170T>A
  hgvsp: ENSP00000451688.1:p.Leu57Ter
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*102T>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-5435T>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.170T>A
  hgvsp: ENSP00000350965.3:p.Leu57Ter
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.311T>A
  hgvsp: ENSP00000286424.7:p.Leu104Ter
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.170T>A
  hgvsp: ENSP00000454670.1:p.Leu57Ter
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.77T>A
  hgvsp: ENSP00000441291.1:p.Leu26Ter
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*329T>A
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-362T>A
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21592
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7665
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25301
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu57Ter
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: European (Finnish)
reference allele: A
site quality: DP
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff

12-66547159-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66547159
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66547159
    reference: chr 12
allele count: 1
allele frequency: 8.303440945927993e-6
allele num: 120432
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.167T>C
  hgvsp: ENSP00000451688.1:p.Phe56Ser
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*99T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.167T>C
  hgvsp: ENSP00000381114.4:p.Phe56Ser
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-365T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.308T>C
  hgvsp: ENSP00000286424.7:p.Phe103Ser
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.74T>C
  hgvsp: ENSP00000441291.1:p.Phe25Ser
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.167T>C
  hgvsp: ENSP00000454670.1:p.Phe56Ser
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*326T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-5438T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.167T>C
  hgvsp: ENSP00000350965.3:p.Phe56Ser
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25308
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7671
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2054
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21612
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Phe56Ser
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

12-66547182-T-TA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66547182
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66547183
    reference: chr 12
allele count: 2
allele frequency: 1.661654010401954e-5
allele num: 120362
alternate allele: TA
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.284dupT
  hgvsp: ENSP00000286424.7:p.Leu95PhefsTer13
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.143dupT
  hgvsp: ENSP00000454670.1:p.Leu48PhefsTer13
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.50dupT
  hgvsp: ENSP00000441291.1:p.Leu17PhefsTer13
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.143dupT
  hgvsp: ENSP00000350965.3:p.Leu48PhefsTer13
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.143dupT
  hgvsp: ENSP00000381114.4:p.Leu48PhefsTer13
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.143dupT
  hgvsp: ENSP00000451688.1:p.Leu48PhefsTer13
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-389dupT
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*302dupT
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*75dupT
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-5462dupT
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21637
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2053
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7670
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25185
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu48PhefsTer13
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/12-66547189-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66547189
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66547189
    reference: chr 12
allele count: 1
allele frequency: 8.311722853913159e-6
allele num: 120312
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-395T>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.137T>G
  hgvsp: ENSP00000381114.4:p.Val46Gly
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.137T>G
  hgvsp: ENSP00000454670.1:p.Val46Gly
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.44T>G
  hgvsp: ENSP00000441291.1:p.Val15Gly
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*69T>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.137T>G
  hgvsp: ENSP00000350965.3:p.Val46Gly
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.137T>G
  hgvsp: ENSP00000451688.1:p.Val46Gly
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*296T>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.278T>G
  hgvsp: ENSP00000286424.7:p.Val93Gly
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-5468T>G
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25117
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21645
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7669
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2052
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3383
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Val46Gly
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD

12-66547199-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66547199
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66547199
    reference: chr 12
allele count: 2
allele frequency: 1.663838141825563e-5
allele num: 120204
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.127T>C
  hgvsp: ENSP00000451688.1:p.Ser43Pro
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*59T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-5478T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.127T>C
  hgvsp: ENSP00000350965.3:p.Ser43Pro
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-405T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.43-9T>C
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.268T>C
  hgvsp: ENSP00000286424.7:p.Ser90Pro
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.127T>C
  hgvsp: ENSP00000381114.4:p.Ser43Pro
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.127T>C
  hgvsp: ENSP00000454670.1:p.Ser43Pro
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*286T>C
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24986
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7667
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21644
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2051
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ser43Pro
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD

12-66547206-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66547206
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66547206
    reference: chr 12
allele count: 1
allele frequency: 8.328752519447637e-6
allele num: 120066
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-412C>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-5485C>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*279C>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.120C>T
  hgvsp: ENST00000539652.1:c.120C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.120C>T
  hgvsp: ENST00000398033.4:c.120C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.120C>T
  hgvsp: ENST00000556010.1:c.120C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.43-16C>T
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.120C>T
  hgvsp: ENST00000358230.3:c.120C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.261C>T
  hgvsp: ENST00000286424.7:c.261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*52C>T
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24855
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2052
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7673
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21626
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ser40Ser
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: African
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

12-66547210-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66547210
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66547210
    reference: chr 12
allele count: 1
allele frequency: 8.337641114575865e-6
allele num: 119938
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*275A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.116A>G
  hgvsp: ENSP00000451688.1:p.Tyr39Cys
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-416A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.116A>G
  hgvsp: ENSP00000381114.4:p.Tyr39Cys
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.116A>G
  hgvsp: ENSP00000454670.1:p.Tyr39Cys
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.257A>G
  hgvsp: ENSP00000286424.7:p.Tyr86Cys
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.116A>G
  hgvsp: ENSP00000350965.3:p.Tyr39Cys
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-5489A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.43-20A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*48A>G
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21600
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2051
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24745
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7668
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Tyr39Cys
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: QD

12-66547212-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66547212
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66547211
    reference: chr 12
allele count: 2
allele frequency: 1.668001067520683e-5
allele num: 119904
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.254delT
  hgvsp: ENSP00000286424.7:p.Val85AlafsTer11
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-5492delT
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.113delT
  hgvsp: ENSP00000454670.1:p.Val38AlafsTer11
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-419delT
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.113delT
  hgvsp: ENSP00000350965.3:p.Val38AlafsTer11
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.113delT
  hgvsp: ENSP00000381114.4:p.Val38AlafsTer11
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*272delT
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.113delT
  hgvsp: ENSP00000451688.1:p.Val38AlafsTer11
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.43-23delT
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*45delT
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7672
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21596
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24714
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2051
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Val38AlafsTer11
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: GA
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

12-66547215-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 66547215
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 66547215
    reference: chr 12
allele count: 1
allele frequency: 8.347245409015026e-6
allele num: 119800
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000451688
  ensembl transcript: ENST00000556010
  gene symbol: TMBIM4
  hgvsc: ENST00000556010.1:c.111A>G
  hgvsp: ENST00000556010.1:c.111A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000228144
  ensembl protein: ENSP00000454670
  ensembl transcript: ENST00000539652
  gene symbol: TMBIM4
  hgvsc: ENST00000539652.1:c.111A>G
  hgvsp: ENST00000539652.1:c.111A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000381114
  ensembl transcript: ENST00000398033
  gene symbol: TMBIM4
  hgvsc: ENST00000398033.4:c.111A>G
  hgvsp: ENST00000398033.4:c.111A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000286424
  ensembl transcript: ENST00000286424
  gene symbol: TMBIM4
  hgvsc: ENST00000286424.7:c.252A>G
  hgvsp: ENST00000286424.7:c.252A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000440964
  ensembl transcript: ENST00000545407
  gene symbol: TMBIM4
  hgvsc: ENST00000545407.1:c.*270A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000441291
  ensembl transcript: ENST00000542724
  gene symbol: TMBIM4
  hgvsc: ENST00000542724.1:c.43-25A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000350965
  ensembl transcript: ENST00000358230
  gene symbol: TMBIM4
  hgvsc: ENST00000358230.3:c.111A>G
  hgvsp: ENST00000358230.3:c.111A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000444639
  ensembl transcript: ENST00000544599
  gene symbol: TMBIM4
  hgvsc: ENST00000544599.1:c.-421A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000439310
  ensembl transcript: ENST00000534930
  gene symbol: TMBIM4
  hgvsc: ENST00000534930.1:c.*43A>G
  variant of: http://identifiers.org/hgnc/24257
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000155957
  ensembl protein: ENSP00000438957
  ensembl transcript: ENST00000545504
  gene symbol: TMBIM4
  hgvsc: ENST00000545504.1:c.98-5494A>G
  variant of: http://identifiers.org/hgnc/24257
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7679
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21572
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2052
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24585
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Lys37Lys
num of homozygotes: 0
reference allele: T

GenotypeQuality
all individuals: 224
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3104
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2997
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1383
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8224
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3938
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 392
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6288
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6803
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10036
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4640
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3063
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1888
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 301
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2833
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 757
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 925
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7072
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47036
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6722
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.357268981753973e-5
allele num: 13592
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5368
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9634
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 726
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.4e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.127082e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.52e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.14e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.03e0

QD
type: SiteQuality
SIO_000300: 1.502e1

VQSLOD
type: SiteQuality
SIO_000300: 7.199999999999999e-2

GenotypeQuality
all individuals: 3080
bin: 9.75e1
variant carriers: 94

GenotypeQuality
all individuals: 234
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3071
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 402
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 908
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 391
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12749
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 396
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 155
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2443
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 493
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 388
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 641
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 754
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 301
bin: 5.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5546
num of homozygotes: 0

African
type: Population
allele count: 87
allele frequency: 1.161858974358974e-2
allele num: 7488
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7302
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 752
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.000880387370443e-5
allele num: 49978
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 5.009016229212583e-4
allele num: 9982
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.428571428571429e-4
allele num: 14000
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.5e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.8e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.13e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.468e1

DP
type: SiteQuality
SIO_000300: 1.312109e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.84e0

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 41
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3033
bin: 9.75e1
variant carriers: 37

GenotypeQuality
all individuals: 373
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 595
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2599
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1236
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36401
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 507
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 964
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1265
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 817
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 343
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 662
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10160
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 395
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7946
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54064
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 776
num of homozygotes: 0

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

South Asian
type: Population
allele count: 36
allele frequency: 2.480363786688714e-3
allele num: 14514
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7980
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5800
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.405363e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.77e-1

FS
type: SiteQuality
SIO_000300: 1.876e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

QD
type: SiteQuality
SIO_000300: 1.613e1

MQ
type: SiteQuality
SIO_000300: 5.947e1

MQRankSum
type: SiteQuality
SIO_000300: 1.46e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.76e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.2e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.35e0

GenotypeQuality
all individuals: 2599
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3033
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 310
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10160
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 395
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 595
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1236
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 36401
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 817
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 507
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 662
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 373
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 343
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1265
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 964
bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 776
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14514
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7980
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7946
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5800
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.699319325244155e-5
allele num: 54064
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.876e0

MQRankSum
type: SiteQuality
SIO_000300: 1.46e-1

MQ
type: SiteQuality
SIO_000300: 5.947e1

VQSLOD
type: SiteQuality
SIO_000300: 3.35e0

QD
type: SiteQuality
SIO_000300: 1.613e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.2e-2

DP
type: SiteQuality
SIO_000300: 1.405363e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.76e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.77e-1

GenotypeQuality
all individuals: 9965
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1159
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1179
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 666
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 964
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36903
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 821
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 474
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 549
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 397
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3009
bin: 9.75e1
variant carriers: 18

GenotypeQuality
all individuals: 2632
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8018
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54366
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7974
num of homozygotes: 0

South Asian
type: Population
allele count: 19
allele frequency: 1.310344827586207e-3
allele num: 14500
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10330
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5814
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.016e1

MQ
type: SiteQuality
SIO_000300: 5.952e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.9e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.699999999999999e-2

DP
type: SiteQuality
SIO_000300: 1.411648e6

FS
type: SiteQuality
SIO_000300: 5.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.5e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.44e0

VQSLOD
type: SiteQuality
SIO_000300: 1.49e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

GenotypeQuality
all individuals: 91
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1118
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2997
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 485
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 307
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1104
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9833
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 386
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 674
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2675
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 830
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37121
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 977
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 520
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 399
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7994
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5836
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.829290601104892e-5
allele num: 54666
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14596
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.599e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.51e0

VQSLOD
type: SiteQuality
SIO_000300: -2.152e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.67e0

QD
type: SiteQuality
SIO_000300: 5.43e0

DP
type: SiteQuality
SIO_000300: 1.414653e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

GenotypeQuality
all individuals: 38
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8853
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 683
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 675
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 795
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 566
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 522
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2994
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 998
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38835
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 886
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 301
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2850
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8296
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.348799568384138e-4
allele num: 14828
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8216
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5976
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56336
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10504
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 798
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.44e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.7e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.825e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.17e0

FS
type: SiteQuality
SIO_000300: 1.0864e1

DP
type: SiteQuality
SIO_000300: 1.446419e6

QD
type: SiteQuality
SIO_000300: 5.4e0

GenotypeQuality
all individuals: 238
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8677
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 672
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 299
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 617
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 521
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 379
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2992
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 876
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 396
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39351
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 989
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2873
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 800
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8344
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10544
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5990
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8232
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.765038124823496e-5
allele num: 56656
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14876
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.39e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 3.17e-1

DP
type: SiteQuality
SIO_000300: 1.452922e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.41e-1

QD
type: SiteQuality
SIO_000300: 1.132e1

FS
type: SiteQuality
SIO_000300: 1.507e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.683e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.71e-1

GenotypeDepth
all individuals: 30181
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 159
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 450
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 413
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 389
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2721
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1149
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 783
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 910
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 299
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11295
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36165
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 912
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 651
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 405
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2994
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 172
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55922
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8288
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5948
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.917913310318374e-4
allele num: 10428
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.358695652173913e-4
allele num: 14720
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.8e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.31e1

MQRankSum
type: SiteQuality
SIO_000300: -1.03e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.92e0

FS
type: SiteQuality
SIO_000300: 1.076e0

DP
type: SiteQuality
SIO_000300: 1.423925e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.24e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.54e-1

GenotypeQuality
all individuals: 12956
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 390
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 650
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1281
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 560
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 775
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33233
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 891
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 763
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2652
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 388
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 461
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1524
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2990
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 296
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8046
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10376
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14634
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55094
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5900
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 792
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.219512195121951e-4
allele num: 8200
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 7.55e-1

DP
type: SiteQuality
SIO_000300: 1.393312e6

FS
type: SiteQuality
SIO_000300: 7.852e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.19e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.02e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.28e-1

QD
type: SiteQuality
SIO_000300: 1.179e1

VQSLOD
type: SiteQuality
SIO_000300: 5.4e-2

GenotypeQuality
all individuals: 304
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13012
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 766
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1524
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 884
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1273
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 33840
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 387
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 563
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 647
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 163
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 387
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2991
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 107
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2648
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 796
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8048
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5900
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8198
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55092
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.643201542912247e-5
allele num: 10370
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14634
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.15e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.37e0

MQ
type: SiteQuality
SIO_000300: 5.54e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.48e0

MQRankSum
type: SiteQuality
SIO_000300: -1.164e0

DP
type: SiteQuality
SIO_000300: 1.393458e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.185e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.12e-1

GenotypeQuality
all individuals: 387
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2164
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 895
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 296
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29899
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15101
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 423
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 638
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 864
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2347
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 729
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2992
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 201
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8100
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14492
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7898
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.74089226573154e-5
allele num: 10266
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5812
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54114
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.33e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 4.38e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.9e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.736e0

MQRankSum
type: SiteQuality
SIO_000300: -8.100000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.728e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

MQ
type: SiteQuality
SIO_000300: 5.714e1

DP
type: SiteQuality
SIO_000300: 1.348762e6

GenotypeQuality
all individuals: 387
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2226
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 592
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 730
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15494
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29195
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2992
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 864
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 369
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2291
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 638
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7878
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
allele num: 14472
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10250
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54014
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.236399604352127e-4
allele num: 8088
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5806
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -7.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 6.69e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.34e-1

DP
type: SiteQuality
SIO_000300: 1.338846e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 9.34e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.05e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.06e-1

GenotypeQuality
all individuals: 93
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4713
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3933
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1232
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2997
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 420
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 442
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 386
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 539
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 854
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 706
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2060
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 423
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 553
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19206
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 635
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 3
allele frequency: 2.102312543798178e-4
allele num: 14270
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5710
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7670
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10056
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52482
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 786
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7910
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.236586e6

QD
type: SiteQuality
SIO_000300: 1.093e1

MQ
type: SiteQuality
SIO_000300: 5.896e1

MQRankSum
type: SiteQuality
SIO_000300: -4.62e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.16e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.03e-1

FS
type: SiteQuality
SIO_000300: 6.43e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.97e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

VQSLOD
type: SiteQuality
SIO_000300: -4.966e-1

GenotypeQuality
all individuals: 2997
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 442
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 365
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19206
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2403
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2060
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 386
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18128
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 539
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 706
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 553
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 854
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 420
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4713
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3933
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 635
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10056
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52482
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 786
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7910
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5710
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7670
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 2.102312543798178e-4
allele num: 14270
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.03e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.62e-1

FS
type: SiteQuality
SIO_000300: 6.43e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.966e-1

DP
type: SiteQuality
SIO_000300: 1.236586e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.97e0

MQ
type: SiteQuality
SIO_000300: 5.896e1

QD
type: SiteQuality
SIO_000300: 1.093e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.16e-1

GenotypeQuality
all individuals: 340
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7463
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1586
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2126
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 832
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4976
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1726
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1937
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 626
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2003
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7406
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2621
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2992
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 383
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 647
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.050020500205002e-5
allele num: 48780
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9630
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5542
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7254
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 740
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7518
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13804
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.33e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.437e1

MQRankSum
type: SiteQuality
SIO_000300: -7.41e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.6e-3

DP
type: SiteQuality
SIO_000300: 1.129861e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.38e0

VQSLOD
type: SiteQuality
SIO_000300: 3.0e-3

GenotypeQuality
all individuals: 5710
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4968
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 626
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 383
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15304
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2478
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1513
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7487
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2733
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 847
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2172
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 641
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 819
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2049
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6392
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2993
bin: 9.75e1
variant carriers: 2

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13672
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7142
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7434
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5480
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.176934965122593e-5
allele num: 47882
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.74e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.51e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.120838e6

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.342e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.39e0

GenotypeQuality
all individuals: 228
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5356
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21591
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1186
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5055
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4964
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 878
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2383
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2511
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1338
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3942
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 322
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 667
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4572
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 451
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2745
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10936
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60102
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15042
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6390
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.127141568981064e-4
allele num: 8872
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7796
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.904e0

VQSLOD
type: SiteQuality
SIO_000300: -1.217e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.767e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.63e0

DP
type: SiteQuality
SIO_000300: 1.389838e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

MQ
type: SiteQuality
SIO_000300: 5.92e1

QD
type: SiteQuality
SIO_000300: 6.74e0

GenotypeQuality
all individuals: 2312
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1831
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1435
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 489
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1294
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 483
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1611
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 628
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4117
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4588
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 705
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4285
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1632
bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7840
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 834
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6402
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10970
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15132
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.655245472903632e-5
allele num: 60414
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 7.14e-1

QD
type: SiteQuality
SIO_000300: 1.463e1

FS
type: SiteQuality
SIO_000300: 4.064e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.56e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.95e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.14e0

DP
type: SiteQuality
SIO_000300: 1.426936e6

GenotypeQuality
all individuals: 4166
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 539
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4859
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 629
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2026
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1781
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1430
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1598
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 508
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1656
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4614
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 756
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6450
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11058
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15322
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61444
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9076
num of homozygotes: 0

East Asian
type: Population
allele count: 5
allele frequency: 6.240639041437844e-4
allele num: 8012
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.85e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.3e0

MQRankSum
type: SiteQuality
SIO_000300: 2.06e-1

QD
type: SiteQuality
SIO_000300: 1.387e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.9e-1

DP
type: SiteQuality
SIO_000300: 1.502079e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e0

GenotypeQuality
all individuals: 258
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4675
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 863
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1273
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3000
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 337
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2313
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35678
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 349
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 771
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 935
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5445
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 624
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 307
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1801
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8286
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15642
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.175611305176246e-5
allele num: 62980
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11208
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 862
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.7e-3

DP
type: SiteQuality
SIO_000300: 1.563453e6

VQSLOD
type: SiteQuality
SIO_000300: 7.85e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.19e0

MQRankSum
type: SiteQuality
SIO_000300: 5.75e-1

QD
type: SiteQuality
SIO_000300: 1.481e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.4e0

FS
type: SiteQuality
SIO_000300: 1.608e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.2e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 262
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 312
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 456
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1014
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 654
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2388
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36289
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 629
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5576
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1873
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 887
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4688
bin: 9.75e1
variant carriers: 2

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9362
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.150400100812803e-5
allele num: 63484
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15780
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8356
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11238
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6520
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.579709e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.25e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -9.21e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.72e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.25e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.16e-1

QD
type: SiteQuality
SIO_000300: 1.402e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.09e-1

GenotypeQuality
all individuals: 5681
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 307
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1915
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 497
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 778
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2445
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37034
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 192
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 611
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 907
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1696
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2255
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.05999576001696e-4
allele num: 9434
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15876
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6538
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63890
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8412
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11282
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.604e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.78e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.37e-1

QD
type: SiteQuality
SIO_000300: 1.298e1

FS
type: SiteQuality
SIO_000300: 7.19e-1

DP
type: SiteQuality
SIO_000300: 1.593935e6

VQSLOD
type: SiteQuality
SIO_000300: 3.01e0

MQRankSum
type: SiteQuality
SIO_000300: -1.079e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.73e-1

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

GenotypeQuality
all individuals: 2255
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5681
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 4783
bin: 9.75e1
variant carriers: 95

GenotypeQuality
all individuals: 37034
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 611
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1915
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2445
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 907
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 497
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 677
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 778
bin: 3.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6538
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11282
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.17998728005088e-4
allele num: 9434
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8412
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.298815822625347e-5
allele num: 15876
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 91
allele frequency: 1.424323055251213e-3
allele num: 63890
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.37e-1

FS
type: SiteQuality
SIO_000300: 7.19e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.079e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.78e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.73e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.01e0

DP
type: SiteQuality
SIO_000300: 1.593935e6

MQ
type: SiteQuality
SIO_000300: 5.604e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

QD
type: SiteQuality
SIO_000300: 1.298e1

GenotypeQuality
all individuals: 17
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 953
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 374
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2035
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 188
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 478
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 713
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38247
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1503
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1815
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4781
bin: 9.75e1
variant carriers: 34

GenotypeQuality
all individuals: 2595
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5869
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9556
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11358
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 34
allele frequency: 5.2409285692265e-4
allele num: 64874
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16064
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.08e0

VQSLOD
type: SiteQuality
SIO_000300: 3.33e0

DP
type: SiteQuality
SIO_000300: 1.619698e6

MQ
type: SiteQuality
SIO_000300: 5.963e1

MQRankSum
type: SiteQuality
SIO_000300: -2.46e-1

QD
type: SiteQuality
SIO_000300: 1.297e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.63e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.92e-1

GenotypeQuality
all individuals: 2868
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 819
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1050
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 97
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 509
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 5.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 6229
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 39148
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2212
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2010
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4880
bin: 9.75e1
variant carriers: 2

South Asian
type: Population
allele count: 2
allele frequency: 1.218620521569583e-4
allele num: 16412
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9674
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11488
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8590
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66184
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.82e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.284e0

MQRankSum
type: SiteQuality
SIO_000300: -1.77e-1

FS
type: SiteQuality
SIO_000300: 6.830000000000001e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.973e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.735e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.656009e6

GenotypeQuality
all individuals: 131
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2232
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 20
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2877
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4891
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 126
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38992
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2025
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 470
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6246
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1062
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 825
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11494
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16424
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9678
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.509570678099149e-5
allele num: 66244
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 4.24e-1

QD
type: SiteQuality
SIO_000300: 1.562e1

DP
type: SiteQuality
SIO_000300: 1.658174e6

FS
type: SiteQuality
SIO_000300: 5.84e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.93e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.85e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.598e0

MQ
type: SiteQuality
SIO_000300: 6.11e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.301e0

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

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

GenotypeQuality
all individuals: 4892
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 21
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 2028
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 50
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6244
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 461
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 120
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1062
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2233
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2882
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39059
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16426
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9680
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11492
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.509388395822013e-5
allele num: 66252
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.0e-2

QD
type: SiteQuality
SIO_000300: 1.053e1

FS
type: SiteQuality
SIO_000300: 7.42e0

VQSLOD
type: SiteQuality
SIO_000300: 3.54e-1

DP
type: SiteQuality
SIO_000300: 1.658437e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.48e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.3e-2

GenotypeQuality
all individuals: 137
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2238
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 106
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 464
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2034
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39015
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4897
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2882
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 825
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6247
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1062
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.018685664261781e-5
allele num: 66254
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11492
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16424
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9678
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 1.658683e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.37e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.65e0

MQRankSum
type: SiteQuality
SIO_000300: 2.04e-1

FS
type: SiteQuality
SIO_000300: 1.21e0

VQSLOD
type: SiteQuality
SIO_000300: -1.582e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

QD
type: SiteQuality
SIO_000300: 1.702e1

MQ
type: SiteQuality
SIO_000300: 5.855e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.98e-1

GenotypeQuality
all individuals: 260
bin: 2.25e1
variant carriers: 13

GenotypeQuality
all individuals: 35
bin: 2.5e0
variant carriers: 7

GenotypeQuality
all individuals: 178
bin: 8.75e1
variant carriers: 128

GenotypeQuality
all individuals: 108
bin: 4.75e1
variant carriers: 49

GenotypeQuality
all individuals: 29
bin: 1.25e1
variant carriers: 16

GenotypeQuality
all individuals: 322
bin: 7.25e1
variant carriers: 75

GenotypeQuality
all individuals: 72
bin: 3.25e1
variant carriers: 28

GenotypeQuality
all individuals: 89
bin: 3.75e1
variant carriers: 42

GenotypeQuality
all individuals: 1487
bin: 6.75e1
variant carriers: 113

GenotypeQuality
all individuals: 23
bin: 1.75e1
variant carriers: 8

GenotypeQuality
all individuals: 357
bin: 8.25e1
variant carriers: 175

GenotypeQuality
all individuals: 44
bin: 2.75e1
variant carriers: 8

GenotypeQuality
all individuals: 27
bin: 7.5e0
variant carriers: 13

GenotypeQuality
all individuals: 16209
bin: 6.25e1
variant carriers: 84

GenotypeQuality
all individuals: 40112
bin: 9.75e1
variant carriers: 39157

GenotypeQuality
all individuals: 300
bin: 9.25e1
variant carriers: 226

GenotypeQuality
all individuals: 148
bin: 5.25e1
variant carriers: 71

GenotypeQuality
all individuals: 411
bin: 7.75e1
variant carriers: 133

GenotypeQuality
all individuals: 115
bin: 5.75e1
variant carriers: 51

European (Non-Finnish)
type: Population
allele count: 28806
allele frequency: 4.338122345712478e-1
allele num: 66402
num of homozygotes: 6260

South Asian
type: Population
allele count: 8566
allele frequency: 5.202234908295883e-1
allele num: 16466
num of homozygotes: 2311

East Asian
type: Population
allele count: 7393
allele frequency: 8.584533209475151e-1
allele num: 8612
num of homozygotes: 3171

Other
type: Population
allele count: 411
allele frequency: 4.587053571428572e-1
allele num: 896
num of homozygotes: 104

European (Finnish)
type: Population
allele count: 3330
allele frequency: 5.042398546335555e-1
allele num: 6604
num of homozygotes: 843

African
type: Population
allele count: 2797
allele frequency: 2.881722645786112e-1
allele num: 9706
num of homozygotes: 391

Latino
type: Population
allele count: 2438
allele frequency: 2.122214484679666e-1
allele num: 11488
num of homozygotes: 293

QD
type: SiteQuality
SIO_000300: 1.971e1

DP
type: SiteQuality
SIO_000300: 3.267674e6

MQ
type: SiteQuality
SIO_000300: 5.959e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.38e-2

MQRankSum
type: SiteQuality
SIO_000300: 9.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.56e0

VQSLOD
type: SiteQuality
SIO_000300: 4.69e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.98e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.58e-1

GenotypeQuality
all individuals: 2905
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 97
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45235
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 795
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 348
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 657
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 268
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6575
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1432
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1518
bin: 7.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16404
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9648
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11476
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510710940568632e-5
allele num: 66194
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 9.0e-2

VQSLOD
type: SiteQuality
SIO_000300: 8.48e-1

QD
type: SiteQuality
SIO_000300: 1.345e1

DP
type: SiteQuality
SIO_000300: 1.755221e6

FS
type: SiteQuality
SIO_000300: 1.549e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.37e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.5e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.74e-1

MQ
type: SiteQuality
SIO_000300: 5.932e1

GenotypeQuality
all individuals: 24
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6565
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 98
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45263
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 338
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2892
bin: 9.75e1
variant carriers: 6

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

GenotypeQuality
all individuals: 264
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 139
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1423
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 777
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1488
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.046314771146986e-5
allele num: 66156
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11466
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9644
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.0960741282614e-5
allele num: 16404
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.164958061509786e-4
allele num: 8584
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.974e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.0e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.95e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.91e-1

QD
type: SiteQuality
SIO_000300: 1.238e1

DP
type: SiteQuality
SIO_000300: 1.753896e6

FS
type: SiteQuality
SIO_000300: 5.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.13e0

GenotypeQuality
all individuals: 759
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6552
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 707
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1482
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2888
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 45256
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1415
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 9.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.074258452603194e-4
allele num: 9642
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: 11462
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66126
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.096817461285209e-5
allele num: 16402
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.09e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.21e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.47e-1

FS
type: SiteQuality
SIO_000300: 4.45e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.18e-1

QD
type: SiteQuality
SIO_000300: 1.136e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.37e-1

MQ
type: SiteQuality
SIO_000300: 5.925e1

DP
type: SiteQuality
SIO_000300: 1.753446e6

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6378
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2833
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1438
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1333
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44455
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1382
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 691
bin: 8.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9596
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.762705923589205e-5
allele num: 11412
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -8.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.139e0

QD
type: SiteQuality
SIO_000300: 1.776e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.04e-1

FS
type: SiteQuality
SIO_000300: 6.55e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.99e-1

DP
type: SiteQuality
SIO_000300: 1.736502e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.974e1

MQRankSum
type: SiteQuality
SIO_000300: 2.74e-1

GenotypeQuality
all individuals: 235
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 29
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6363
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1442
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 685
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1324
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2823
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 1366
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44647
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11412
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.068669658941712e-4
allele num: 65502
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16322
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 4.168403501458941e-4
allele num: 9596
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.228e0

QD
type: SiteQuality
SIO_000300: 1.255e1

VQSLOD
type: SiteQuality
SIO_000300: 2.66e0

DP
type: SiteQuality
SIO_000300: 1.73577e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.62e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.666e0

MQRankSum
type: SiteQuality
SIO_000300: -1.46e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

GenotypeQuality
all individuals: 2810
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 137
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 228
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 44629
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1541
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1317
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 157
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1354
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6333
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65440
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9590
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8550
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.764241893076249e-5
allele num: 11410
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16304
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.57e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.04e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.2e-2

QD
type: SiteQuality
SIO_000300: 1.667e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.069e0

DP
type: SiteQuality
SIO_000300: 1.732918e6

GenotypeQuality
all individuals: 1127
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 105
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 372
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2769
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4891
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 467
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 400
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5761
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41491
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1151
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9314
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11216
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8344
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6500
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15986
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.578980610118108e-5
allele num: 63332
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.879e1

DP
type: SiteQuality
SIO_000300: 1.670006e6

MQRankSum
type: SiteQuality
SIO_000300: 1.05e0

FS
type: SiteQuality
SIO_000300: 2.17e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.33e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.56e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.664e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

QD
type: SiteQuality
SIO_000300: 1.069e1

GenotypeQuality
all individuals: 235
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36647
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9502
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 866
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 488
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2745
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 456
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 994
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 939
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5000
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 339
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9002
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7992
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.637679735350955e-5
allele num: 61062
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10952
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.16e0

QD
type: SiteQuality
SIO_000300: 1.405e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.266e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

MQRankSum
type: SiteQuality
SIO_000300: -8.86e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.51e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.938e0

DP
type: SiteQuality
SIO_000300: 1.577984e6

GenotypeQuality
all individuals: 50
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1505
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 681
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 458
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30953
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 845
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2745
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 4460
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.719752713100158e-5
allele num: 59526
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7696
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6332
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8770
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15410
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10738
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.09e-1

FS
type: SiteQuality
SIO_000300: 1.908e0

DP
type: SiteQuality
SIO_000300: 1.483417e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.4e0

VQSLOD
type: SiteQuality
SIO_000300: 8.24e-1

MQ
type: SiteQuality
SIO_000300: 5.931e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.59e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

QD
type: SiteQuality
SIO_000300: 1.561e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.9e-1

GenotypeQuality
all individuals: 2025
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 397
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 171
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23090
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5439
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 13248
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2585
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 377
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2732
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2067
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 457
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 423
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55448
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.729475100942126e-5
allele num: 14860
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6974
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10258
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6116
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 786
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.3e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.56e0

DP
type: SiteQuality
SIO_000300: 1.205386e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.32e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.32e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.06e0

QD
type: SiteQuality
SIO_000300: 7.53e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.04e-1

GenotypeQuality
all individuals: 678
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22412
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3021
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1597
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1069
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 142
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8842
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6805
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5370
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3907
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 730
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 542
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 423
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2733
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 388
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14640
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54054
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8074
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6798
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 764
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6060
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.482e1

DP
type: SiteQuality
SIO_000300: 1.152516e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.73e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 6.34e-1

FS
type: SiteQuality
SIO_000300: 2.935e0

VQSLOD
type: SiteQuality
SIO_000300: 5.91e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.42e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.42e-1

GenotypeQuality
all individuals: 22412
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1597
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 938
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6805
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 678
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5370
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 388
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2733
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3021
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 542
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 423
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 730
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.85000185000185e-5
allele num: 54054
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6060
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8074
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 764
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14640
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6798
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.73e0

MQRankSum
type: SiteQuality
SIO_000300: 6.34e-1

FS
type: SiteQuality
SIO_000300: 2.935e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.42e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.42e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.91e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-3

DP
type: SiteQuality
SIO_000300: 1.152516e6

QD
type: SiteQuality
SIO_000300: 1.482e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 2202
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2731
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1094
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7416
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 677
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3569
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 354
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 503
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 716
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 16951
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1779
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5320
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 370
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5208
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4574
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5744
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47832
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.073883161512027e-4
allele num: 9312
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13782
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 722
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7246
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5666
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.93e0

DP
type: SiteQuality
SIO_000300: 1.098433e6

QD
type: SiteQuality
SIO_000300: 1.184e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.6e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.52e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.14e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.6e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.2e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 3659
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1249
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1773
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 51
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6173
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 339
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1280
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 511
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3442
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2463
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 921
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1521
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3294
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27058
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.226692836113837e-4
allele num: 8152
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9576
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11256
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6544
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.146281499692685e-5
allele num: 16270
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64838
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.23e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.196e0

QD
type: SiteQuality
SIO_000300: 1.665e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.44e0

DP
type: SiteQuality
SIO_000300: 1.537365e6

MQRankSum
type: SiteQuality
SIO_000300: 6.19e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.06e0

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 1692
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3066
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3294
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28891
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2468
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1156
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 939
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 265
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1590
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 694
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1893
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1955
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 477
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3420
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 6068
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11230
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9554
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8146
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 3.69321679182568e-4
allele num: 16246
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64662
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6544
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.203e0

MQ
type: SiteQuality
SIO_000300: 5.945e1

QD
type: SiteQuality
SIO_000300: 1.282e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.99e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.89e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.2e0

DP
type: SiteQuality
SIO_000300: 1.5415e6

GenotypeQuality
all individuals: 1868
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1496
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1587
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6124
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 888
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1615
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 467
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1439
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 711
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 744
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37429
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3403
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1102
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.136475208640157e-5
allele num: 16296
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65038
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11282
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9596
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8194
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 2.017e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.37e0

VQSLOD
type: SiteQuality
SIO_000300: 4.0e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.43e0

MQRankSum
type: SiteQuality
SIO_000300: 6.1e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.584795e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.43e0

QD
type: SiteQuality
SIO_000300: 1.314e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

GenotypeQuality
all individuals: 1086
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 812
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 668
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 432
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41027
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 687
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 467
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1109
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1841
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3404
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 147
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.038421599169263e-4
allele num: 9630
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16322
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65474
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11344
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8298
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 3.8e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 5.92e-1

MQ
type: SiteQuality
SIO_000300: 5.581e1

VQSLOD
type: SiteQuality
SIO_000300: 2.59e0

QD
type: SiteQuality
SIO_000300: 1.43e1

DP
type: SiteQuality
SIO_000300: 1.616998e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.93e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.498e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 904
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42173
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 552
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1612
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 422
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1847
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6237
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3403
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 683
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1074
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16344
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.191895113230036e-4
allele num: 8390
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11378
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9658
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65738
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.02e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.2e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.84e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 9.99e0

VQSLOD
type: SiteQuality
SIO_000300: -6.437e-1

DP
type: SiteQuality
SIO_000300: 1.628636e6

GenotypeQuality
all individuals: 135
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1071
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 674
bin: 2.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 42957
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1608
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1840
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3399
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6259
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 684
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 7.5e0
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65996
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8504
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9674
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11408
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.10798924993892e-5
allele num: 16372
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.767e0

DP
type: SiteQuality
SIO_000300: 1.639638e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

QD
type: SiteQuality
SIO_000300: 1.012e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.02e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.799999999999999e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.106e0

MQRankSum
type: SiteQuality
SIO_000300: 1.22e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.79e-1

MQ
type: SiteQuality
SIO_000300: 5.924e1

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

GenotypeQuality
all individuals: 1844
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43892
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3397
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 66
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 410
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1069
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 684
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6338
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1621
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.087168249330411e-5
allele num: 16428
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9718
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66296
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11462
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.54e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.64e-1

DP
type: SiteQuality
SIO_000300: 1.649601e6

FS
type: SiteQuality
SIO_000300: 3.809e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

MQRankSum
type: SiteQuality
SIO_000300: -8.94e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.648e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.5e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.74e-1

GenotypeQuality
all individuals: 29
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1071
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 78
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1630
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44105
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3397
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 39
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 685
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9730
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66366
num of homozygotes: 0

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.6e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.621e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.5e0

DP
type: SiteQuality
SIO_000300: 1.652204e6

MQRankSum
type: SiteQuality
SIO_000300: 2.54e0

VQSLOD
type: SiteQuality
SIO_000300: 9.78e-1

FS
type: SiteQuality
SIO_000300: 9.795999999999999e0

QD
type: SiteQuality
SIO_000300: 1.418e1

MQ
type: SiteQuality
SIO_000300: 6.017e1

GenotypeQuality
all individuals: 464
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 683
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 48
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1637
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 83
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6380
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3398
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 29
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 44230
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1850
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1071
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11498
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9744
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66464
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16468
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.516530178950561e-4
allele num: 6594
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.37e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.46e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -9.75e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.15e0

DP
type: SiteQuality
SIO_000300: 1.654962e6

MQ
type: SiteQuality
SIO_000300: 5.939e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.15e-1

QD
type: SiteQuality
SIO_000300: 1.537e1

GenotypeQuality
all individuals: 29
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 44296
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1069
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6389
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 464
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 683
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1634
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 3.25e1
variant carriers: 0

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

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

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

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

GenotypeQuality
all individuals: 1854
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3397
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 234
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 5.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.071645415907711e-5
allele num: 16470
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9746
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11502
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.2e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.597e0

MQRankSum
type: SiteQuality
SIO_000300: -1.194e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.31e-1

QD
type: SiteQuality
SIO_000300: 1.383e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.89e-1

DP
type: SiteQuality
SIO_000300: 1.656132e6

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 27
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 465
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44398
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1633
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1848
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1071
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 6398
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3397
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 34
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 684
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11518
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16482
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9750
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503352476021528e-5
allele num: 66518
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.07e0

QD
type: SiteQuality
SIO_000300: 1.564e1

MQRankSum
type: SiteQuality
SIO_000300: 2.32e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.77e-1

DP
type: SiteQuality
SIO_000300: 1.657731e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.082e0

FS
type: SiteQuality
SIO_000300: 2.846e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.1e0

GenotypeQuality
all individuals: 43
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 6401
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 27
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1848
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44425
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 464
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1632
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 684
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1071
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3396
bin: 9.75e1
variant carriers: 2

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66526
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9750
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16482
num of homozygotes: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.319647413593134e-4
allele num: 8622
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.051e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.138e0

FS
type: SiteQuality
SIO_000300: 1.1712e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.47e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.141e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.38e0

DP
type: SiteQuality
SIO_000300: 1.658321e6

GenotypeQuality
all individuals: 6413
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1074
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 683
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44448
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 28
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 45
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3395
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 465
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1634
bin: 7.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9754
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503262078710802e-5
allele num: 66522
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.12e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 2.848e0

MQ
type: SiteQuality
SIO_000300: 5.914e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.92e-1

QD
type: SiteQuality
SIO_000300: 9.58e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.24e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.4e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.71e-1

DP
type: SiteQuality
SIO_000300: 1.658463e6

GenotypeQuality
all individuals: 182
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1849
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44463
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1635
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 683
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3395
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 24
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 34
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1075
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 463
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 6414
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9758
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: 11520
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503081316699233e-5
allele num: 66530
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.961e1

MQRankSum
type: SiteQuality
SIO_000300: -1.041e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.61e0

VQSLOD
type: SiteQuality
SIO_000300: 1.89e-1

DP
type: SiteQuality
SIO_000300: 1.658712e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.2e-1

FS
type: SiteQuality
SIO_000300: 5.602e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.23e-1

QD
type: SiteQuality
SIO_000300: 1.342e1

GenotypeQuality
all individuals: 683
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 27
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1850
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 44468
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6415
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 20
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 43
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 463
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1076
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3394
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1634
bin: 7.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9758
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503216884132043e-5
allele num: 66524
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 6.57e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.13e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.27e-1

DP
type: SiteQuality
SIO_000300: 1.658948e6

QD
type: SiteQuality
SIO_000300: 9.09e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.4e0

MQRankSum
type: SiteQuality
SIO_000300: -1.98e-1

MQ
type: SiteQuality
SIO_000300: 5.94e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.1e-1

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

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

GenotypeQuality
all individuals: 20
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1635
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 44519
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3396
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 6419
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1850
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 174
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 683
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1077
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 463
bin: 8.75e1
variant carriers: 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: 11522
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66536
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9758
num of homozygotes: 0

South Asian
type: Population
allele count: 8
allele frequency: 4.851425106124924e-4
allele num: 16490
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.31e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.27e0

MQRankSum
type: SiteQuality
SIO_000300: -3.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.659651e6

QD
type: SiteQuality
SIO_000300: 1.243e1

VQSLOD
type: SiteQuality
SIO_000300: 2.64e0

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

GenotypeQuality
all individuals: 6417
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 18
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1633
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 683
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3404
bin: 9.75e1
variant carriers: 19

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

GenotypeQuality
all individuals: 1852
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1074
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 463
bin: 8.75e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.679048776254123e-5
allele num: 11522
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.024800163968026e-4
allele num: 9758
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 17
allele frequency: 2.555007815318024e-4
allele num: 66536
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.41e0

QD
type: SiteQuality
SIO_000300: 1.081e1

FS
type: SiteQuality
SIO_000300: 5.28e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.4e-2

DP
type: SiteQuality
SIO_000300: 1.660255e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.986e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.39e-1

GenotypeQuality
all individuals: 171
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 683
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6419
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44503
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3385
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 463
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 13
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1854
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1634
bin: 7.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66506
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11520
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9754
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.660586e6

QD
type: SiteQuality
SIO_000300: 1.23e1

MQ
type: SiteQuality
SIO_000300: 5.924e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.61e0

VQSLOD
type: SiteQuality
SIO_000300: 3.21e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.18e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.38e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.590000000000001e-1

FS
type: SiteQuality
SIO_000300: 7.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

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

GenotypeQuality
all individuals: 3385
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 683
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1858
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44510
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6422
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 463
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1638
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 170
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1075
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 5.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9756
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11524
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502810255177181e-5
allele num: 66542
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.03e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.69e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.58e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.044e0

MQ
type: SiteQuality
SIO_000300: 5.922e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.41e0

DP
type: SiteQuality
SIO_000300: 1.659487e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.88e-1

QD
type: SiteQuality
SIO_000300: 9.619999999999999e0

GenotypeQuality
all individuals: 3385
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 260
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1075
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6412
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1856
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 682
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 33
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44442
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1631
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 463
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9746
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.213739531496541e-4
allele num: 16478
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
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: 894
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.000000000000001e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.05e-1

FS
type: SiteQuality
SIO_000300: 1.707e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.78e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.77e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.78e0

MQ
type: SiteQuality
SIO_000300: 6.05e1

QD
type: SiteQuality
SIO_000300: 1.52e1

DP
type: SiteQuality
SIO_000300: 1.65875e6

GenotypeQuality
all individuals: 21
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 463
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 1632
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 682
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1075
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1854
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6410
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 44394
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504347564461293e-5
allele num: 66474
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9738
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.94e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.67e-1

DP
type: SiteQuality
SIO_000300: 1.657914e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.064e0

QD
type: SiteQuality
SIO_000300: 1.376e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.49e0

MQ
type: SiteQuality
SIO_000300: 5.943e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.93e0

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

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

GenotypeQuality
all individuals: 417
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 463
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 44286
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1627
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6397
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3383
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 682
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 45
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1847
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11502
num of homozygotes: 0

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

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

African
type: Population
allele count: 2
allele frequency: 2.058036633052068e-4
allele num: 9718
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16462
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -2.46e-1

FS
type: SiteQuality
SIO_000300: 3.807e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.79e0

QD
type: SiteQuality
SIO_000300: 1.246e1

DP
type: SiteQuality
SIO_000300: 1.656372e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.159999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.914e1

MQRankSum
type: SiteQuality
SIO_000300: 3.92e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.34e0

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

GenotypeQuality
all individuals: 1843
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1072
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 463
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 682
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 528
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 52
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6377
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 24
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3382
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1625
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44155
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.161710037174721e-4
allele num: 8608
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66318
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11484
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9708
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.019e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.429e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.409e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.699e1

MQRankSum
type: SiteQuality
SIO_000300: 5.31e-1

DP
type: SiteQuality
SIO_000300: 1.654672e6

VQSLOD
type: SiteQuality
SIO_000300: -1.096e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.57e-1

GenotypeQuality
all individuals: 1624
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 463
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 619
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44011
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6363
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1841
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1072
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 682
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3382
bin: 9.75e1
variant carriers: 1

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16440
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11478
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9694
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: 894
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.509889778046203e-5
allele num: 66230
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.28e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.23e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.5e-2

MQRankSum
type: SiteQuality
SIO_000300: -2.16e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.93e0

DP
type: SiteQuality
SIO_000300: 1.652866e6

ClippingRankSum
type: SiteQuality
SIO_000300: 7.66e-1

QD
type: SiteQuality
SIO_000300: 1.165e1

GenotypeQuality
all individuals: 6359
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1840
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 463
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3382
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 43995
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 36
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 648
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 38
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1071
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1623
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 682
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66202
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9694
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11476
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 2
allele frequency: 1.216693028348948e-4
allele num: 16438
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.46e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.08e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.0e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.25e0

DP
type: SiteQuality
SIO_000300: 1.652495e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.143e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.83e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQ
type: SiteQuality
SIO_000300: 6.11e1

QD
type: SiteQuality
SIO_000300: 1.605e1