1-67423816-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67423816
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67423816
    reference: chr 1
allele count: 3
allele frequency: 2.489130795526202e-5
allele num: 120524
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.453T>C
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.414T>C
  hgvsp: ENST00000371014.1:c.414T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.306T>C
  hgvsp: ENST00000357692.2:c.306T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.255T>C
  hgvsp: ENST00000355356.3:c.255T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.306T>C
  hgvsp: ENST00000371018.3:c.306T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.306T>C
  hgvsp: ENST00000371016.1:c.306T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.255T>C
  hgvsp: ENST00000401042.3:c.255T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.66T>C
  hgvsp: ENST00000355977.6:c.66T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.414T>C
  hgvsp: ENST00000401041.1:c.414T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3647
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15698
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1960
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8641
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26018
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2982
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Asp138Asp
num of homozygotes: 1
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: African
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP

1-67423816-TGAGGAA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67423816
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67423810
    reference: chr 1
allele count: 2
allele frequency: 1.659420530350801e-5
allele num: 120524
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.75_80delGGAAGA
  hgvsp: ENSP00000348253.6:p.Glu30_Glu31del
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.315_320delGGAAGA
  hgvsp: ENSP00000360055.1:p.Glu110_Glu111del
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.264_269delGGAAGA
  hgvsp: ENSP00000383821.3:p.Glu93_Glu94del
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.315_320delGGAAGA
  hgvsp: ENSP00000350321.2:p.Glu110_Glu111del
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.423_428delGGAAGA
  hgvsp: ENSP00000383820.1:p.Glu146_Glu147del
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.264_269delGGAAGA
  hgvsp: ENSP00000347514.3:p.Glu93_Glu94del
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.315_320delGGAAGA
  hgvsp: ENSP00000360057.3:p.Glu110_Glu111del
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.462_467delGGAAGA
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.423_428delGGAAGA
  hgvsp: ENSP00000360053.1:p.Glu146_Glu147del
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3647
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15698
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26018
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8641
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1960
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4066
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6513
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1699
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Glu146_Glu147del
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: TGAGGAA
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum

1-67423819-GGAAGAGGAA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67423819
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67423810
    reference: chr 1
allele count: 8
allele frequency: 6.635920236238761e-5
allele num: 120556
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.324_332delGGAAGAAGA
  hgvsp: ENSP00000360057.3:p.Glu109_Glu111del
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.273_281delGGAAGAAGA
  hgvsp: ENSP00000347514.3:p.Glu92_Glu94del
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.471_479delGGAAGAAGA
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.273_281delGGAAGAAGA
  hgvsp: ENSP00000383821.3:p.Glu92_Glu94del
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.432_440delGGAAGAAGA
  hgvsp: ENSP00000360053.1:p.Glu145_Glu147del
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.324_332delGGAAGAAGA
  hgvsp: ENSP00000350321.2:p.Glu109_Glu111del
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.84_92delGGAAGAAGA
  hgvsp: ENSP00000348253.6:p.Glu29_Glu31del
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.324_332delGGAAGAAGA
  hgvsp: ENSP00000360055.1:p.Glu109_Glu111del
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.432_440delGGAAGAAGA
  hgvsp: ENSP00000383820.1:p.Glu145_Glu147del
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8678
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15742
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3663
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 25936
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1947
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Glu145_Glu147del
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: GGAAGAGGAA
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

1-67423828-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67423828
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67423828
    reference: chr 1
allele count: 1
allele frequency: 8.2917364554485e-6
allele num: 120602
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.465A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.318A>G
  hgvsp: ENST00000371018.3:c.318A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.318A>G
  hgvsp: ENST00000357692.2:c.318A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.267A>G
  hgvsp: ENST00000401042.3:c.267A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.426A>G
  hgvsp: ENST00000371014.1:c.426A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.78A>G
  hgvsp: ENST00000355977.6:c.78A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.318A>G
  hgvsp: ENST00000371016.1:c.318A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.426A>G
  hgvsp: ENST00000401041.1:c.426A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.267A>G
  hgvsp: ENST00000355356.3:c.267A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8722
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3665
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1945
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25751
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15904
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1704
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Glu142Glu
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

1-67423834-GGAA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67423834
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67423831
    reference: chr 1
allele count: 3
allele frequency: 2.486984779653149e-5
allele num: 120628
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.479_481delAAG
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.281_283delAAG
  hgvsp: ENSP00000383821.3:p.Glu94del
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.332_334delAAG
  hgvsp: ENSP00000360055.1:p.Glu111del
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.281_283delAAG
  hgvsp: ENSP00000347514.3:p.Glu94del
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.92_94delAAG
  hgvsp: ENSP00000348253.6:p.Glu31del
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.440_442delAAG
  hgvsp: ENSP00000360053.1:p.Glu147del
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.332_334delAAG
  hgvsp: ENSP00000350321.2:p.Glu111del
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.440_442delAAG
  hgvsp: ENSP00000383820.1:p.Glu147del
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.332_334delAAG
  hgvsp: ENSP00000360057.3:p.Glu111del
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3674
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1950
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25735
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8738
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15929
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1705
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Glu147del
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: South Asian
reference allele: GGAA
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: MQ

1-67423845-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67423845
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67423845
    reference: chr 1
allele count: 14
allele frequency: 1.160265866635726e-4
allele num: 120662
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.482G>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.284G>A
  hgvsp: ENSP00000347514.3:p.Gly95Asp
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.443G>A
  hgvsp: ENSP00000360053.1:p.Gly148Asp
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.335G>A
  hgvsp: ENSP00000350321.2:p.Gly112Asp
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.335G>A
  hgvsp: ENSP00000360055.1:p.Gly112Asp
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.443G>A
  hgvsp: ENSP00000383820.1:p.Gly148Asp
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.95G>A
  hgvsp: ENSP00000348253.6:p.Gly32Asp
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.284G>A
  hgvsp: ENSP00000383821.3:p.Gly95Asp
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.335G>A
  hgvsp: ENSP00000360057.3:p.Gly112Asp
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3685
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15938
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25735
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8753
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1950
  bin: 4.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2988
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gly148Asp
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

1-67423850-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67423850
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67423850
    reference: chr 1
allele count: 1
allele frequency: 8.286102548805144e-6
allele num: 120684
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.289G>T
  hgvsp: ENSP00000383821.3:p.Asp97Tyr
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.340G>T
  hgvsp: ENSP00000360057.3:p.Asp114Tyr
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.340G>T
  hgvsp: ENSP00000360055.1:p.Asp114Tyr
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.487G>T
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.448G>T
  hgvsp: ENSP00000360053.1:p.Asp150Tyr
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.340G>T
  hgvsp: ENSP00000350321.2:p.Asp114Tyr
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.289G>T
  hgvsp: ENSP00000347514.3:p.Asp97Tyr
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.100G>T
  hgvsp: ENSP00000348253.6:p.Asp34Tyr
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.448G>T
  hgvsp: ENSP00000383820.1:p.Asp150Tyr
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25732
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1945
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15963
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3683
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8754
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Asp150Tyr
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ

1-67423852-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67423852
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67423852
    reference: chr 1
allele count: 1
allele frequency: 8.286926544683108e-6
allele num: 120672
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.342T>A
  hgvsp: ENSP00000350321.2:p.Asp114Glu
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.342T>A
  hgvsp: ENSP00000360057.3:p.Asp114Glu
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.450T>A
  hgvsp: ENSP00000383820.1:p.Asp150Glu
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.291T>A
  hgvsp: ENSP00000347514.3:p.Asp97Glu
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.102T>A
  hgvsp: ENSP00000348253.6:p.Asp34Glu
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.342T>A
  hgvsp: ENSP00000360055.1:p.Asp114Glu
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.450T>A
  hgvsp: ENSP00000360053.1:p.Asp150Glu
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.489T>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.291T>A
  hgvsp: ENSP00000383821.3:p.Asp97Glu
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25729
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15962
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3683
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1947
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8754
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4084
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2990
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Asp150Glu
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: T
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum

1-67423855-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67423855
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67423855
    reference: chr 1
allele count: 1
allele frequency: 8.286377195889957e-6
allele num: 120680
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.294T>G
  hgvsp: ENSP00000383821.3:p.Asp98Glu
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.453T>G
  hgvsp: ENSP00000383820.1:p.Asp151Glu
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.492T>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.345T>G
  hgvsp: ENSP00000350321.2:p.Asp115Glu
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.453T>G
  hgvsp: ENSP00000360053.1:p.Asp151Glu
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.294T>G
  hgvsp: ENSP00000347514.3:p.Asp98Glu
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.345T>G
  hgvsp: ENSP00000360055.1:p.Asp115Glu
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.345T>G
  hgvsp: ENSP00000360057.3:p.Asp115Glu
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.105T>G
  hgvsp: ENSP00000348253.6:p.Asp35Glu
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8754
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1945
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1118
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25724
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3680
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15967
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1711
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Asp151Glu
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/1-67423858-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67423858
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67423858
    reference: chr 1
allele count: 1
allele frequency: 8.286102548805144e-6
allele num: 120684
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.297A>C
  hgvsp: ENSP00000347514.3:p.Glu99Asp
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.456A>C
  hgvsp: ENSP00000383820.1:p.Glu152Asp
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.348A>C
  hgvsp: ENSP00000360057.3:p.Glu116Asp
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.495A>C
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.348A>C
  hgvsp: ENSP00000350321.2:p.Glu116Asp
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.108A>C
  hgvsp: ENSP00000348253.6:p.Glu36Asp
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.348A>C
  hgvsp: ENSP00000360055.1:p.Glu116Asp
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.456A>C
  hgvsp: ENSP00000360053.1:p.Glu152Asp
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.297A>C
  hgvsp: ENSP00000383821.3:p.Glu99Asp
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25715
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1943
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3678
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8758
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15973
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1118
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Glu152Asp
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

1-67423865-GATA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67423865
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67423862
    reference: chr 1
allele count: 1
allele frequency: 8.288300235387727e-6
allele num: 120652
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.505_507delAAT
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.358_360delAAT
  hgvsp: ENSP00000360055.1:p.Asn120del
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.307_309delAAT
  hgvsp: ENSP00000347514.3:p.Asn103del
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.466_468delAAT
  hgvsp: ENSP00000383820.1:p.Asn156del
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.466_468delAAT
  hgvsp: ENSP00000360053.1:p.Asn156del
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.358_360delAAT
  hgvsp: ENSP00000360057.3:p.Asn120del
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.358_360delAAT
  hgvsp: ENSP00000350321.2:p.Asn120del
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.118_120delAAT
  hgvsp: ENSP00000348253.6:p.Asn40del
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.307_309delAAT
  hgvsp: ENSP00000383821.3:p.Asn103del
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25674
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3678
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8768
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1944
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1118
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15975
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6534
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Asn156del
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: GATA
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

http://identifiers.org/exac.variant/1-67423876-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67423876
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67423876
    reference: chr 1
allele count: 4
allele frequency: 3.316474587513473e-5
allele num: 120610
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.366C>A
  hgvsp: ENSP00000360055.1:p.Asp122Glu
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.126C>A
  hgvsp: ENSP00000348253.6:p.Asp42Glu
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.366C>A
  hgvsp: ENSP00000350321.2:p.Asp122Glu
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.366C>A
  hgvsp: ENSP00000360057.3:p.Asp122Glu
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.315C>A
  hgvsp: ENSP00000347514.3:p.Asp105Glu
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.315C>A
  hgvsp: ENSP00000383821.3:p.Asp105Glu
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.474C>A
  hgvsp: ENSP00000360053.1:p.Asp158Glu
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.513C>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.474C>A
  hgvsp: ENSP00000383820.1:p.Asp158Glu
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1950
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3687
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25574
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8768
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15971
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1332
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Asp158Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ

1-67423887-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67423887
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67423887
    reference: chr 1
allele count: 1
allele frequency: 8.313104778372627e-6
allele num: 120292
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.485G>A
  hgvsp: ENSP00000383820.1:p.Cys162Tyr
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.524G>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.377G>A
  hgvsp: ENSP00000360055.1:p.Cys126Tyr
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.377G>A
  hgvsp: ENSP00000360057.3:p.Cys126Tyr
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.137G>A
  hgvsp: ENSP00000348253.6:p.Cys46Tyr
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.485G>A
  hgvsp: ENSP00000360053.1:p.Cys162Tyr
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.326G>A
  hgvsp: ENSP00000383821.3:p.Cys109Tyr
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.326G>A
  hgvsp: ENSP00000347514.3:p.Cys109Tyr
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.377G>A
  hgvsp: ENSP00000350321.2:p.Cys126Tyr
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: missense
filter: VQSRTrancheINDEL99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3678
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15930
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25202
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8742
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4066
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2968
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Cys162Tyr
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum

1-67423888-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67423888
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67423888
    reference: chr 1
allele count: 16
allele frequency: 1.335782267490399e-4
allele num: 119780
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.486T>G
  hgvsp: ENSP00000383820.1:p.Cys162Trp
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.378T>G
  hgvsp: ENSP00000360057.3:p.Cys126Trp
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.378T>G
  hgvsp: ENSP00000360055.1:p.Cys126Trp
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.486T>G
  hgvsp: ENSP00000360053.1:p.Cys162Trp
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.378T>G
  hgvsp: ENSP00000350321.2:p.Cys126Trp
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.327T>G
  hgvsp: ENSP00000347514.3:p.Cys109Trp
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.327T>G
  hgvsp: ENSP00000383821.3:p.Cys109Trp
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.138T>G
  hgvsp: ENSP00000348253.6:p.Cys46Trp
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.525T>G
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8645
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 9.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25049
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3611
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15793
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1914
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4024
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 2.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.25e1
  variant carriers: 1
hgvs: p.Cys162Trp
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: FS

1-67423896-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67423896
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67423896
    reference: chr 1
allele count: 3
allele frequency: 2.509620210808098e-5
allele num: 119540
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.335A>G
  hgvsp: ENSP00000383821.3:p.Glu112Gly
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.533A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.494A>G
  hgvsp: ENSP00000383820.1:p.Glu165Gly
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.146A>G
  hgvsp: ENSP00000348253.6:p.Glu49Gly
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.386A>G
  hgvsp: ENSP00000360055.1:p.Glu129Gly
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.386A>G
  hgvsp: ENSP00000350321.2:p.Glu129Gly
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.335A>G
  hgvsp: ENSP00000347514.3:p.Glu112Gly
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.386A>G
  hgvsp: ENSP00000360057.3:p.Glu129Gly
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.494A>G
  hgvsp: ENSP00000360053.1:p.Glu165Gly
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3645
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8622
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15589
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1124
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1943
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 24356
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2937
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1315
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Glu165Gly
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum

1-67423900-T-TAAATC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67423900
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67423905
    reference: chr 1
allele count: 1
allele frequency: 8.382932349735938e-6
allele num: 119290
alternate allele: TAAATC
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.153_153+1insTCAAA
  hgvsp: ENSP00000348253.6:p.Glu52SerfsTer6
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.393_393+1insTCAAA
  hgvsp: ENSP00000350321.2:p.Glu132SerfsTer6
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.342_342+1insTCAAA
  hgvsp: ENSP00000347514.3:p.Glu115SerfsTer6
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.393_393+1insTCAAA
  hgvsp: ENSP00000360057.3:p.Glu132SerfsTer6
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.540_540+1insTCAAA
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.393_393+1insTCAAA
  hgvsp: ENSP00000360055.1:p.Glu132SerfsTer6
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.501_501+1insTCAAA
  hgvsp: ENSP00000383820.1:p.Glu168SerfsTer6
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.501_501+1insTCAAA
  hgvsp: ENSP00000360053.1:p.Glu168SerfsTer6
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.342_342+1insTCAAA
  hgvsp: ENSP00000383821.3:p.Glu115SerfsTer6
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3644
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8598
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24125
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1124
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15533
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1701
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Glu168SerfsTer6
num of homozygotes: 0
population: African
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: VQSLOD

1-67423900-T-TAAATCAAAATA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67423900
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67423911
    reference: chr 1
allele count: 1
allele frequency: 8.382932349735938e-6
allele num: 119290
alternate allele: TAAATCAAAATA
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsp: ENSP00000348253.6:p.Glu52SerfsTer3
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsp: ENSP00000383821.3:p.Glu115SerfsTer3
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsp: ENSP00000360053.1:p.Glu168SerfsTer3
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsp: ENSP00000383820.1:p.Glu168SerfsTer3
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsp: ENSP00000350321.2:p.Glu132SerfsTer3
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsp: ENSP00000347514.3:p.Glu115SerfsTer3
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsp: ENSP00000360055.1:p.Glu132SerfsTer3
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsp: ENSP00000360057.3:p.Glu132SerfsTer3
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3644
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8598
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1124
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24125
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15533
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1701
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Glu168SerfsTer3
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQ

1-67423903-A-ATCAAAATAAAAG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67423903
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67423915
    reference: chr 1
allele count: 1
allele frequency: 8.406328283932143e-6
allele num: 118958
alternate allele: ATCAAAATAAAAG
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: inframe_insertion
  consequence: splice_region_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: inframe_insertion
  consequence: splice_region_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: stop_gained
  consequence: inframe_insertion
  consequence: splice_region_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: inframe_insertion
  consequence: splice_region_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: inframe_insertion
  consequence: splice_region_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: inframe_insertion
  consequence: splice_region_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: inframe_insertion
  consequence: splice_region_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: inframe_insertion
  consequence: splice_region_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: stop gained
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8578
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3637
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23798
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15401
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1943
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1124
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1939
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Lys167_Glu168insSerLysTerLys
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: A
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ

1-67423904-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67423904
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67423904
    reference: chr 1
allele count: 1
allele frequency: 8.441383036196651e-6
allele num: 118464
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.393+1G>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.342+1G>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.540+1G>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.342+1G>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.501+1G>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.393+1G>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.153+1G>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.501+1G>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.393+1G>A
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: splice donor
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8586
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15384
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3663
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23558
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1949
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
hgvs: c.501+1G>A
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum

1-67423905-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67423905
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67423905
    reference: chr 1
allele count: 1
allele frequency: 8.469408496510604e-6
allele num: 118072
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.501+2T>C
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.342+2T>C
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.393+2T>C
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.342+2T>C
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.393+2T>C
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.153+2T>C
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.540+2T>C
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.393+2T>C
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.501+2T>C
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15280
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8556
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23231
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3664
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1645
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1954
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1700
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7238
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2966
  bin: 8.25e1
  variant carriers: 0
hgvs: c.501+2T>C
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: African
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: DP
site quality: VQSLOD

http://identifiers.org/exac.variant/1-67423910-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67423910
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67423910
    reference: chr 1
allele count: 2
allele frequency: 1.69756230053643e-5
allele num: 117816
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.501+7C>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.153+7C>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.393+7C>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.342+7C>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.501+7C>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.393+7C>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.540+7C>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.393+7C>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.342+7C>A
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3638
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8471
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1949
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15148
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2029
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22946
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1314
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4023
  bin: 7.75e1
  variant carriers: 0
hgvs: c.501+7C>A
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

1-67423912-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67423912
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67423912
    reference: chr 1
allele count: 1
allele frequency: 8.490694199157722e-6
allele num: 117776
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.393+9A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.153+9A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.342+9A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.540+9A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.501+9A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.393+9A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.393+9A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.501+9A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.342+9A>G
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2369
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15007
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3636
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22606
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1124
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8420
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2918
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 467
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1702
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum

1-67423913-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67423913
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67423913
    reference: chr 1
allele count: 0
allele frequency: 0.0e0
allele num: 117544
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.393+10T>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.342+10T>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.540+10T>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.393+10T>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.153+10T>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.342+10T>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.501+10T>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.393+10T>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.501+10T>A
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1943
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14997
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3636
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2380
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8413
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22611
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7157
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6726
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2962
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

1-67423914-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67423914
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67423914
    reference: chr 1
allele count: 2
allele frequency: 1.698138839831544e-5
allele num: 117776
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.540+11A>T
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.393+11A>T
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.393+11A>T
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.153+11A>T
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.342+11A>T
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.342+11A>T
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.501+11A>T
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.501+11A>T
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.393+11A>T
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22603
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8410
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2409
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3629
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14996
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1938
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4022
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6733
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 463
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

1-67423918-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67423918
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67423918
    reference: chr 1
allele count: 4
allele frequency: 3.409303990590321e-5
allele num: 117326
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.540+15A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.342+15A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.393+15A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.501+15A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.342+15A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.393+15A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.393+15A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.153+15A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.501+15A>G
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22245
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3619
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8363
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14805
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2811
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2905
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3582
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7125
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1702
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum

1-67423937-CTTTA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67423937
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67423933
    reference: chr 1
allele count: 2
allele frequency: 1.729445539759953e-5
allele num: 115644
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.342+37_342+40delTATT
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.501+37_501+40delTATT
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.153+37_153+40delTATT
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.393+37_393+40delTATT
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.540+37_540+40delTATT
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.393+37_393+40delTATT
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.501+37_501+40delTATT
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.393+37_393+40delTATT
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.342+37_342+40delTATT
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8200
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13881
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20714
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3610
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1929
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1377
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3816
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1922
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 419
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4216
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 874
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 635
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: CTTTA
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

1-67423944-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67423944
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67423944
    reference: chr 1
allele count: 13
allele frequency: 1.132483099867587e-4
allele num: 114792
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.540+41C>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.501+41C>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.393+41C>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.501+41C>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.393+41C>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.393+41C>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.153+41C>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.342+41C>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.342+41C>G
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8090
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3615
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20073
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13339
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2272
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3593
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1922
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 863
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1024
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 319
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 822
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24588
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: QD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum

1-67423955-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67423955
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67423955
    reference: chr 1
allele count: 1
allele frequency: 8.909479686386316e-6
allele num: 112240
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.342+52T>C
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.393+52T>C
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.393+52T>C
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.342+52T>C
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.501+52T>C
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.153+52T>C
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.501+52T>C
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.393+52T>C
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.540+52T>C
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2902
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2467
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19510
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3080
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8335
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13432
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1921
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3676
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1310
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2742
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1960
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1733
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1700
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: T
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

1-67423955-T-TA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67423955
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67423956
    reference: chr 1
allele count: 1
allele frequency: 8.909479686386316e-6
allele num: 112240
alternate allele: TA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.342+56dupA
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.153+56dupA
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.393+56dupA
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.501+56dupA
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.393+56dupA
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.393+56dupA
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.540+56dupA
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.342+56dupA
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.501+56dupA
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3080
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19510
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1921
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2467
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8335
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3676
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2902
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13432
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2942
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1960
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 968
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2180
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 994
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

1-67424483-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67424483
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67424483
    reference: chr 1
allele count: 1
allele frequency: 8.510058889607517e-6
allele num: 117508
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.541-51C>T
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.502-51C>T
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.343-51C>T
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.394-51C>T
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.394-51C>T
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.394-51C>T
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.154-51C>T
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.502-51C>T
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.343-51C>T
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5795
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6211
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15066
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14330
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12176
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1738
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2543
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1949
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20931
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2348
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1729
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum

http://identifiers.org/exac.variant/1-67424486-CA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67424486
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67424485
    reference: chr 1
allele count: 1
allele frequency: 8.513391564931637e-6
allele num: 117462
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.394-46delA
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.541-46delA
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.502-46delA
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.502-46delA
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.154-46delA
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.343-46delA
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.394-46delA
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.394-46delA
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.343-46delA
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14481
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6170
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5801
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1740
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16620
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10515
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 567
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1725
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1256
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1053
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4451
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2252
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: South Asian
reference allele: CA
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

1-67424488-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67424488
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67424488
    reference: chr 1
allele count: 3668
allele frequency: 3.114968493639282e-2
allele num: 117754
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.541-46A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.343-46A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.343-46A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.154-46A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.502-46A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.394-46A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.394-46A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.394-46A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.502-46A>G
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1777
  bin: 3.75e1
  variant carriers: 205
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 5924
  bin: 3.25e1
  variant carriers: 411
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 9.75e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 5.25e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 7.5e0
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 4.25e1
  variant carriers: 113
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 6040
  bin: 1.25e1
  variant carriers: 366
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 14639
  bin: 2.75e1
  variant carriers: 623
genotype depth: GenotypeDepth
  all individuals: 17763
  bin: 2.25e1
  variant carriers: 839
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 9175
  bin: 1.75e1
  variant carriers: 691
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 4.75e1
  variant carriers: 69
genotype quality: GenotypeQuality
  all individuals: 1133
  bin: 2.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 3148
  bin: 3.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6379
  bin: 9.75e1
  variant carriers: 3472
genotype quality: GenotypeQuality
  all individuals: 3735
  bin: 4.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 2018
  bin: 4.25e1
  variant carriers: 3
num of homozygotes: 81
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
reference allele: A
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

1-67424497-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67424497
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67424497
    reference: chr 1
allele count: 220
allele frequency: 1.865861519150524e-3
allele num: 117908
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.502-37C>T
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.541-37C>T
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.154-37C>T
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.343-37C>T
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.502-37C>T
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.394-37C>T
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.394-37C>T
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.394-37C>T
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.343-37C>T
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 15637
  bin: 2.75e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5320
  bin: 1.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1683
  bin: 3.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 6066
  bin: 3.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 5012
  bin: 1.75e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 4.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 21847
  bin: 2.25e1
  variant carriers: 54
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1090
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2180
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2840
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2145
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: East Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD

http://identifiers.org/exac.variant/1-67424500-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67424500
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67424500
    reference: chr 1
allele count: 1
allele frequency: 8.467400508044031e-6
allele num: 118100
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.343-34A>C
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.394-34A>C
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.502-34A>C
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.394-34A>C
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.394-34A>C
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.343-34A>C
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.154-34A>C
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.541-34A>C
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.502-34A>C
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4888
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15960
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6113
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3886
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23084
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3106
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 992
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6732
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 819
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2039
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum

1-67424501-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67424501
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67424501
    reference: chr 1
allele count: 1
allele frequency: 8.467830711128423e-6
allele num: 118094
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.541-33C>T
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.502-33C>T
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.154-33C>T
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.343-33C>T
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.394-33C>T
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.394-33C>T
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.502-33C>T
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.343-33C>T
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.394-33C>T
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4649
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1176
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1678
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23472
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16156
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6177
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3484
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1507
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 947
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 455
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1533
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

1-67424503-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67424503
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67424503
    reference: chr 1
allele count: 1
allele frequency: 8.455658526686058e-6
allele num: 118264
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.394-31T>C
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.394-31T>C
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.343-31T>C
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.502-31T>C
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.541-31T>C
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.394-31T>C
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.154-31T>C
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.502-31T>C
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.343-31T>C
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4280
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6173
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24365
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16349
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2804
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36561
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3105
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1458
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 458
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1147
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1528
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
population: European (Finnish)
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ

1-67424504-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67424504
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67424504
    reference: chr 1
allele count: 1
allele frequency: 8.456516591685553e-6
allele num: 118252
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.541-30C>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.154-30C>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.394-30C>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.343-30C>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.502-30C>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.343-30C>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.394-30C>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.394-30C>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.502-30C>G
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2503
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4076
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1145
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16466
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6263
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24676
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1038
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 319
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36914
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1429
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

1-67424518-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67424518
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67424518
    reference: chr 1
allele count: 149
allele frequency: 1.252395521635343e-3
allele num: 118972
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.343-16A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.394-16A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.394-16A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.394-16A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.343-16A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.154-16A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.502-16A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.541-16A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.502-16A>G
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 4.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 5.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 6438
  bin: 3.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 5.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 3.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1823
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17564
  bin: 2.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 27713
  bin: 2.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 4.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 9.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 1541
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 471
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 1
population: East Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

1-67424521-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67424521
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67424521
    reference: chr 1
allele count: 6
allele frequency: 5.036430178289628e-5
allele num: 119132
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.343-13T>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.502-13T>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.154-13T>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.502-13T>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.394-13T>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.343-13T>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.541-13T>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.394-13T>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.394-13T>G
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6456
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 28074
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17735
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 449
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1491
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7111
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

1-67424524-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67424524
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67424524
    reference: chr 1
allele count: 1
allele frequency: 8.379279717115517e-6
allele num: 119342
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.154-10T>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.394-10T>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.394-10T>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.502-10T>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.541-10T>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.343-10T>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.394-10T>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.343-10T>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.502-10T>A
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28437
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6494
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17875
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1687
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 423
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3079
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD

1-67424534-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67424534
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67424534
    reference: chr 1
allele count: 15
allele frequency: 1.25e-4
allele num: 120000
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.343G>A
  hgvsp: ENSP00000383821.3:p.Glu115Lys
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.502G>A
  hgvsp: ENSP00000383820.1:p.Glu168Lys
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.154G>A
  hgvsp: ENSP00000348253.6:p.Glu52Lys
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.394G>A
  hgvsp: ENSP00000360057.3:p.Glu132Lys
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.394G>A
  hgvsp: ENSP00000360055.1:p.Glu132Lys
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.394G>A
  hgvsp: ENSP00000350321.2:p.Glu132Lys
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.343G>A
  hgvsp: ENSP00000347514.3:p.Glu115Lys
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.502G>A
  hgvsp: ENSP00000360053.1:p.Glu168Lys
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.541G>A
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28924
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18517
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1704
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6651
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Glu168Lys
num of homozygotes: 1
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

1-67424539-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67424539
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67424539
    reference: chr 1
allele count: 1
allele frequency: 8.324453915823122e-6
allele num: 120128
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.546G>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.159G>A
  hgvsp: ENST00000355977.6:c.159G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.348G>A
  hgvsp: ENST00000401042.3:c.348G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.399G>A
  hgvsp: ENST00000357692.2:c.399G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.348G>A
  hgvsp: ENST00000355356.3:c.348G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.399G>A
  hgvsp: ENST00000371018.3:c.399G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.507G>A
  hgvsp: ENST00000401041.1:c.507G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.399G>A
  hgvsp: ENST00000371016.1:c.399G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.507G>A
  hgvsp: ENST00000371014.1:c.507G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28846
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18712
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6689
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3080
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 382
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Glu169Glu
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: South Asian
reference allele: G
site quality: DP
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

1-67424544-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67424544
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67424544
    reference: chr 1
allele count: 1
allele frequency: 8.318637074501714e-6
allele num: 120212
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.404T>C
  hgvsp: ENSP00000350321.2:p.Ile135Thr
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.353T>C
  hgvsp: ENSP00000347514.3:p.Ile118Thr
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.551T>C
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.164T>C
  hgvsp: ENSP00000348253.6:p.Ile55Thr
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.404T>C
  hgvsp: ENSP00000360057.3:p.Ile135Thr
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.512T>C
  hgvsp: ENSP00000383820.1:p.Ile171Thr
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.404T>C
  hgvsp: ENSP00000360055.1:p.Ile135Thr
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.512T>C
  hgvsp: ENSP00000360053.1:p.Ile171Thr
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.353T>C
  hgvsp: ENSP00000383821.3:p.Ile118Thr
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6708
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18791
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28848
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44044
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ile171Thr
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

1-67424545-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67424545
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67424545
    reference: chr 1
allele count: 1
allele frequency: 8.317530026283395e-6
allele num: 120228
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.354A>G
  hgvsp: ENSP00000347514.3:p.Ile118Met
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.513A>G
  hgvsp: ENSP00000383820.1:p.Ile171Met
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.405A>G
  hgvsp: ENSP00000360057.3:p.Ile135Met
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.405A>G
  hgvsp: ENSP00000350321.2:p.Ile135Met
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.165A>G
  hgvsp: ENSP00000348253.6:p.Ile55Met
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.354A>G
  hgvsp: ENSP00000383821.3:p.Ile118Met
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.405A>G
  hgvsp: ENSP00000360055.1:p.Ile135Met
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.513A>G
  hgvsp: ENSP00000360053.1:p.Ile171Met
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.552A>G
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18810
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28855
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6714
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1700
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1505
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3080
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ile171Met
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

1-67424553-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67424553
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67424553
    reference: chr 1
allele count: 2
allele frequency: 1.662178783950002e-5
allele num: 120324
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.521C>T
  hgvsp: ENSP00000383820.1:p.Ser174Leu
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.413C>T
  hgvsp: ENSP00000350321.2:p.Ser138Leu
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.362C>T
  hgvsp: ENSP00000383821.3:p.Ser121Leu
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.413C>T
  hgvsp: ENSP00000360057.3:p.Ser138Leu
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.413C>T
  hgvsp: ENSP00000360055.1:p.Ser138Leu
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.362C>T
  hgvsp: ENSP00000347514.3:p.Ser121Leu
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.560C>T
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.173C>T
  hgvsp: ENSP00000348253.6:p.Ser58Leu
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.521C>T
  hgvsp: ENSP00000360053.1:p.Ser174Leu
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19015
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6750
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1705
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28740
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1510
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ser174Leu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: DP

1-67424563-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67424563
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67424563
    reference: chr 1
allele count: 1
allele frequency: 8.300821781356355e-6
allele num: 120470
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.570G>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.531G>A
  hgvsp: ENST00000371014.1:c.531G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.423G>A
  hgvsp: ENST00000371018.3:c.423G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.531G>A
  hgvsp: ENST00000401041.1:c.531G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.183G>A
  hgvsp: ENST00000355977.6:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.372G>A
  hgvsp: ENST00000401042.3:c.372G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.372G>A
  hgvsp: ENST00000355356.3:c.372G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.423G>A
  hgvsp: ENST00000357692.2:c.423G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.423G>A
  hgvsp: ENST00000371016.1:c.423G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19294
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6802
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28614
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gln177Gln
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQRankSum

1-67424578-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67424578
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67424578
    reference: chr 1
allele count: 1
allele frequency: 8.293799555452344e-6
allele num: 120572
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.438G>C
  hgvsp: ENSP00000360055.1:p.Gln146His
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.438G>C
  hgvsp: ENSP00000350321.2:p.Gln146His
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.546G>C
  hgvsp: ENSP00000383820.1:p.Gln182His
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.387G>C
  hgvsp: ENSP00000347514.3:p.Gln129His
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.585G>C
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.546G>C
  hgvsp: ENSP00000360053.1:p.Gln182His
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.198G>C
  hgvsp: ENSP00000348253.6:p.Gln66His
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.438G>C
  hgvsp: ENSP00000360057.3:p.Gln146His
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.387G>C
  hgvsp: ENSP00000383821.3:p.Gln129His
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6829
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19513
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28563
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1626
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gln182His
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

1-67424585-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67424585
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67424585
    reference: chr 1
allele count: 1
allele frequency: 8.290911502810618e-6
allele num: 120614
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.445A>G
  hgvsp: ENSP00000350321.2:p.Asn149Asp
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.592A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.553A>G
  hgvsp: ENSP00000383820.1:p.Asn185Asp
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.445A>G
  hgvsp: ENSP00000360057.3:p.Asn149Asp
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.553A>G
  hgvsp: ENSP00000360053.1:p.Asn185Asp
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.394A>G
  hgvsp: ENSP00000383821.3:p.Asn132Asp
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.445A>G
  hgvsp: ENSP00000360055.1:p.Asn149Asp
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.394A>G
  hgvsp: ENSP00000347514.3:p.Asn132Asp
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.205A>G
  hgvsp: ENSP00000348253.6:p.Asn69Asp
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19600
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28507
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6840
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1704
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44711
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1629
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Asn185Asp
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
reference allele: A
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum

1-67424586-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67424586
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67424586
    reference: chr 1
allele count: 5
allele frequency: 4.145387013331564e-5
allele num: 120616
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.554A>G
  hgvsp: ENSP00000383820.1:p.Asn185Ser
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.446A>G
  hgvsp: ENSP00000360055.1:p.Asn149Ser
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.395A>G
  hgvsp: ENSP00000347514.3:p.Asn132Ser
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.554A>G
  hgvsp: ENSP00000360053.1:p.Asn185Ser
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.395A>G
  hgvsp: ENSP00000383821.3:p.Asn132Ser
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.593A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.446A>G
  hgvsp: ENSP00000350321.2:p.Asn149Ser
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.446A>G
  hgvsp: ENSP00000360057.3:p.Asn149Ser
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.206A>G
  hgvsp: ENSP00000348253.6:p.Asn69Ser
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1706
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19604
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28497
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6843
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 865
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Asn185Ser
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: A
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD

1-67424590-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67424590
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67424590
    reference: chr 1
allele count: 1
allele frequency: 8.290636555074699e-6
allele num: 120618
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.450T>C
  hgvsp: ENST00000371016.1:c.450T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.210T>C
  hgvsp: ENST00000355977.6:c.210T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.399T>C
  hgvsp: ENST00000355356.3:c.399T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.399T>C
  hgvsp: ENST00000401042.3:c.399T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.450T>C
  hgvsp: ENST00000371018.3:c.450T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.558T>C
  hgvsp: ENST00000371014.1:c.558T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.558T>C
  hgvsp: ENST00000401041.1:c.558T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.597T>C
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.450T>C
  hgvsp: ENST00000357692.2:c.450T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1699
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6859
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19641
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28466
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asp186Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: T
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD

1-67424593-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67424593
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67424593
    reference: chr 1
allele count: 1
allele frequency: 8.290086714307032e-6
allele num: 120626
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.453T>A
  hgvsp: ENSP00000360055.1:p.Asp151Glu
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.213T>A
  hgvsp: ENSP00000348253.6:p.Asp71Glu
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.402T>A
  hgvsp: ENSP00000347514.3:p.Asp134Glu
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.453T>A
  hgvsp: ENSP00000350321.2:p.Asp151Glu
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.453T>A
  hgvsp: ENSP00000360057.3:p.Asp151Glu
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.561T>A
  hgvsp: ENSP00000360053.1:p.Asp187Glu
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.561T>A
  hgvsp: ENSP00000383820.1:p.Asp187Glu
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.600T>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.402T>A
  hgvsp: ENSP00000383821.3:p.Asp134Glu
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1700
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28423
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6864
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19662
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1620
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Asp187Glu
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

1-67424603-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67424603
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67424603
    reference: chr 1
allele count: 1
allele frequency: 8.289949265510494e-6
allele num: 120628
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.463T>A
  hgvsp: ENSP00000360057.3:p.Ser155Thr
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.463T>A
  hgvsp: ENSP00000350321.2:p.Ser155Thr
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.571T>A
  hgvsp: ENSP00000360053.1:p.Ser191Thr
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.463T>A
  hgvsp: ENSP00000360055.1:p.Ser155Thr
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.610T>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.412T>A
  hgvsp: ENSP00000347514.3:p.Ser138Thr
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.571T>A
  hgvsp: ENSP00000383820.1:p.Ser191Thr
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.223T>A
  hgvsp: ENSP00000348253.6:p.Ser75Thr
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000493357
  gene symbol: MIER1
  hgvsc: ENST00000493357.1:n.10T>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.412T>A
  hgvsp: ENSP00000383821.3:p.Ser138Thr
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6867
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1699
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28381
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19730
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 326
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ser191Thr
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff

1-67424604-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67424604
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67424604
    reference: chr 1
allele count: 1
allele frequency: 8.289674381590291e-6
allele num: 120632
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000493357
  gene symbol: MIER1
  hgvsc: ENST00000493357.1:n.11C>T
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.572C>T
  hgvsp: ENSP00000383820.1:p.Ser191Phe
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.413C>T
  hgvsp: ENSP00000347514.3:p.Ser138Phe
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.611C>T
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.464C>T
  hgvsp: ENSP00000350321.2:p.Ser155Phe
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.464C>T
  hgvsp: ENSP00000360057.3:p.Ser155Phe
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.224C>T
  hgvsp: ENSP00000348253.6:p.Ser75Phe
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.413C>T
  hgvsp: ENSP00000383821.3:p.Ser138Phe
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.572C>T
  hgvsp: ENSP00000360053.1:p.Ser191Phe
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.464C>T
  hgvsp: ENSP00000360055.1:p.Ser155Phe
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6869
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19735
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1700
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28372
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1615
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ser191Phe
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP

1-67424606-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67424606
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67424606
    reference: chr 1
allele count: 1
allele frequency: 8.289674381590291e-6
allele num: 120632
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.415G>A
  hgvsp: ENSP00000347514.3:p.Val139Ile
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.466G>A
  hgvsp: ENSP00000360055.1:p.Val156Ile
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.466G>A
  hgvsp: ENSP00000360057.3:p.Val156Ile
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.574G>A
  hgvsp: ENSP00000383820.1:p.Val192Ile
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.415G>A
  hgvsp: ENSP00000383821.3:p.Val139Ile
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000493357
  gene symbol: MIER1
  hgvsc: ENST00000493357.1:n.13G>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.226G>A
  hgvsp: ENSP00000348253.6:p.Val76Ile
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.574G>A
  hgvsp: ENSP00000360053.1:p.Val192Ile
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.466G>A
  hgvsp: ENSP00000350321.2:p.Val156Ile
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.613G>A
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19747
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6870
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28363
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1700
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1507
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Val192Ile
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP

1-67424606-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67424606
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67424606
    reference: chr 1
allele count: 4
allele frequency: 3.315869752636116e-5
allele num: 120632
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.466G>T
  hgvsp: ENSP00000360055.1:p.Val156Phe
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.415G>T
  hgvsp: ENSP00000347514.3:p.Val139Phe
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000493357
  gene symbol: MIER1
  hgvsc: ENST00000493357.1:n.13G>T
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.574G>T
  hgvsp: ENSP00000360053.1:p.Val192Phe
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.226G>T
  hgvsp: ENSP00000348253.6:p.Val76Phe
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.466G>T
  hgvsp: ENSP00000350321.2:p.Val156Phe
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.574G>T
  hgvsp: ENSP00000383820.1:p.Val192Phe
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.466G>T
  hgvsp: ENSP00000360057.3:p.Val156Phe
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.415G>T
  hgvsp: ENSP00000383821.3:p.Val139Phe
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.613G>T
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19747
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28363
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1700
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6870
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Val192Phe
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

1-67424617-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67424617
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67424617
    reference: chr 1
allele count: 2
allele frequency: 1.657852417977751e-5
allele num: 120638
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.426A>G
  hgvsp: ENST00000355356.3:c.426A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.477A>G
  hgvsp: ENST00000371016.1:c.477A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000493357
  gene symbol: MIER1
  hgvsc: ENST00000493357.1:n.24A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.585A>G
  hgvsp: ENST00000371014.1:c.585A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.477A>G
  hgvsp: ENST00000357692.2:c.477A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.477A>G
  hgvsp: ENST00000371018.3:c.477A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.585A>G
  hgvsp: ENST00000401041.1:c.585A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.426A>G
  hgvsp: ENST00000401042.3:c.426A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.624A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.237A>G
  hgvsp: ENST00000355977.6:c.237A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19788
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28364
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6876
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1700
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1619
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gln195Gln
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

1-67424636-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67424636
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67424636
    reference: chr 1
allele count: 7
allele frequency: 5.806430206708915e-5
allele num: 120556
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.256C>T
  hgvsp: ENSP00000348253.6:p.Arg86Cys
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.496C>T
  hgvsp: ENSP00000360057.3:p.Arg166Cys
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.643C>T
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.604C>T
  hgvsp: ENSP00000383820.1:p.Arg202Cys
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000493357
  gene symbol: MIER1
  hgvsc: ENST00000493357.1:n.43C>T
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.604C>T
  hgvsp: ENSP00000360053.1:p.Arg202Cys
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.496C>T
  hgvsp: ENSP00000360055.1:p.Arg166Cys
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.496C>T
  hgvsp: ENSP00000350321.2:p.Arg166Cys
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.445C>T
  hgvsp: ENSP00000347514.3:p.Arg149Cys
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.445C>T
  hgvsp: ENSP00000383821.3:p.Arg149Cys
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19827
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28191
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6893
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7543
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg202Cys
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum

1-67424637-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67424637
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67424637
    reference: chr 1
allele count: 4
allele frequency: 3.317684919463199e-5
allele num: 120566
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.446G>A
  hgvsp: ENSP00000383821.3:p.Arg149His
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.644G>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.257G>A
  hgvsp: ENSP00000348253.6:p.Arg86His
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000493357
  gene symbol: MIER1
  hgvsc: ENST00000493357.1:n.44G>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.605G>A
  hgvsp: ENSP00000360053.1:p.Arg202His
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.497G>A
  hgvsp: ENSP00000360057.3:p.Arg166His
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.497G>A
  hgvsp: ENSP00000360055.1:p.Arg166His
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.605G>A
  hgvsp: ENSP00000383820.1:p.Arg202His
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.497G>A
  hgvsp: ENSP00000350321.2:p.Arg166His
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.446G>A
  hgvsp: ENSP00000347514.3:p.Arg149His
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1705
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28209
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6880
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19821
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 444
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg202His
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

1-67424642-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67424642
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67424642
    reference: chr 1
allele count: 5
allele frequency: 4.149033275246868e-5
allele num: 120510
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.649C>T
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.451C>T
  hgvsp: ENSP00000347514.3:p.Arg151Cys
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.502C>T
  hgvsp: ENSP00000360057.3:p.Arg168Cys
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.502C>T
  hgvsp: ENSP00000360055.1:p.Arg168Cys
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.610C>T
  hgvsp: ENSP00000383820.1:p.Arg204Cys
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.262C>T
  hgvsp: ENSP00000348253.6:p.Arg88Cys
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000493357
  gene symbol: MIER1
  hgvsc: ENST00000493357.1:n.49C>T
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.502C>T
  hgvsp: ENSP00000350321.2:p.Arg168Cys
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.610C>T
  hgvsp: ENSP00000360053.1:p.Arg204Cys
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.451C>T
  hgvsp: ENSP00000383821.3:p.Arg151Cys
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28158
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19814
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6883
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1706
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 44633
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg204Cys
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD

1-67424643-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67424643
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67424643
    reference: chr 1
allele count: 1
allele frequency: 8.298479718515568e-6
allele num: 120504
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.263G>A
  hgvsp: ENSP00000348253.6:p.Arg88His
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.611G>A
  hgvsp: ENSP00000360053.1:p.Arg204His
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.650G>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.452G>A
  hgvsp: ENSP00000383821.3:p.Arg151His
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.452G>A
  hgvsp: ENSP00000347514.3:p.Arg151His
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.611G>A
  hgvsp: ENSP00000383820.1:p.Arg204His
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.503G>A
  hgvsp: ENSP00000360055.1:p.Arg168His
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000493357
  gene symbol: MIER1
  hgvsc: ENST00000493357.1:n.50G>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.503G>A
  hgvsp: ENSP00000350321.2:p.Arg168His
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.503G>A
  hgvsp: ENSP00000360057.3:p.Arg168His
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28137
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1704
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6879
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19828
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg204His
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/1-67424645-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67424645
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67424645
    reference: chr 1
allele count: 2
allele frequency: 1.659971448491086e-5
allele num: 120484
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.652C>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.505C>A
  hgvsp: ENST00000371016.1:c.505C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000493357
  gene symbol: MIER1
  hgvsc: ENST00000493357.1:n.52C>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.265C>A
  hgvsp: ENST00000355977.6:c.265C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.505C>A
  hgvsp: ENST00000357692.2:c.505C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.613C>A
  hgvsp: ENST00000371014.1:c.613C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.613C>A
  hgvsp: ENST00000401041.1:c.613C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.454C>A
  hgvsp: ENST00000401042.3:c.454C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.505C>A
  hgvsp: ENST00000371018.3:c.505C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.454C>A
  hgvsp: ENST00000355356.3:c.454C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6878
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19820
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28111
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1709
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg205Arg
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

1-67424665-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67424665
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67424665
    reference: chr 1
allele count: 1
allele frequency: 8.332777814812346e-6
allele num: 120008
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.633A>G
  hgvsp: ENST00000371014.1:c.633A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.525A>G
  hgvsp: ENST00000371016.1:c.525A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.633A>G
  hgvsp: ENST00000401041.1:c.633A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.474A>G
  hgvsp: ENST00000401042.3:c.474A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.672A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.525A>G
  hgvsp: ENST00000357692.2:c.525A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.474A>G
  hgvsp: ENST00000355356.3:c.474A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.525A>G
  hgvsp: ENST00000371018.3:c.525A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.285A>G
  hgvsp: ENST00000355977.6:c.285A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000493357
  gene symbol: MIER1
  hgvsc: ENST00000493357.1:n.72A>G
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1706
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19799
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27196
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6858
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.633A>G
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

1-67424670-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67424670
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67424670
    reference: chr 1
allele count: 18
allele frequency: 1.503759398496241e-4
allele num: 119700
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.286+4A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.526+4A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.634+4A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.526+4A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.475+4A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.475+4A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000493357
  gene symbol: MIER1
  hgvsc: ENST00000493357.1:n.73+4A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.526+4A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.634+4A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.673+4A>G
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26641
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19693
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6851
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
hgvs: c.634+4A>G
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: A
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

1-67424700-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67424700
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67424700
    reference: chr 1
allele count: 24
allele frequency: 2.183406113537118e-4
allele num: 109920
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.634+34A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.526+34A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.673+34A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.526+34A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.526+34A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.286+34A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.475+34A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.475+34A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000493357
  gene symbol: MIER1
  hgvsc: ENST00000493357.1:n.73+34A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.634+34A>G
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11906
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 10534
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 13665
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4016
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4222
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10085
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4791
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1576
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 666
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16738
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

1-67424718-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67424718
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67424718
    reference: chr 1
allele count: 1
allele frequency: 9.814120556656918e-6
allele num: 101894
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.526+52A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.475+52A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.475+52A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.673+52A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.634+52A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.526+52A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.286+52A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.526+52A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.634+52A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000493357
  gene symbol: MIER1
  hgvsc: ENST00000493357.1:n.73+52A>G
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2655
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6620
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12502
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11978
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6412
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14208
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1238
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1252
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1788
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 388
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4101
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum

1-67425311-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67425311
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67425311
    reference: chr 1
allele count: 3
allele frequency: 2.505805115183508e-5
allele num: 119722
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.476-51T>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.527-51T>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.476-51T>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000493357
  gene symbol: MIER1
  hgvsc: ENST00000493357.1:n.74-51T>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.635-51T>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.527-51T>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.527-51T>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.674-51T>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.287-51T>A
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.635-51T>A
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3232
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7669
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6258
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8565
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2147
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6785
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8502
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3894
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1640
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1484
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4508
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 606
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 279
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 982
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

1-67425311-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67425311
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67425311
    reference: chr 1
allele count: 94030
allele frequency: 7.854028499356843e-1
allele num: 119722
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.476-51T>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.674-51T>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.476-51T>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.635-51T>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.635-51T>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.527-51T>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.527-51T>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.527-51T>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000493357
  gene symbol: MIER1
  hgvsc: ENST00000493357.1:n.74-51T>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.287-51T>G
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6785
  bin: 2.75e1
  variant carriers: 5914
genotype depth: GenotypeDepth
  all individuals: 4508
  bin: 5.25e1
  variant carriers: 4464
genotype depth: GenotypeDepth
  all individuals: 8502
  bin: 3.75e1
  variant carriers: 8087
genotype depth: GenotypeDepth
  all individuals: 1640
  bin: 9.75e1
  variant carriers: 1608
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 1.25e1
  variant carriers: 621
genotype depth: GenotypeDepth
  all individuals: 7669
  bin: 4.25e1
  variant carriers: 7466
genotype depth: GenotypeDepth
  all individuals: 3232
  bin: 5.75e1
  variant carriers: 3191
genotype depth: GenotypeDepth
  all individuals: 1484
  bin: 6.75e1
  variant carriers: 1459
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 7.25e1
  variant carriers: 947
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 3894
  bin: 2.25e1
  variant carriers: 3570
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.5e0
  variant carriers: 209
genotype depth: GenotypeDepth
  all individuals: 2147
  bin: 6.25e1
  variant carriers: 2119
genotype depth: GenotypeDepth
  all individuals: 8565
  bin: 3.25e1
  variant carriers: 7711
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 7.75e1
  variant carriers: 680
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 8.25e1
  variant carriers: 539
genotype depth: GenotypeDepth
  all individuals: 6258
  bin: 4.75e1
  variant carriers: 6151
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 9.25e1
  variant carriers: 308
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 8.75e1
  variant carriers: 373
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 1.75e1
  variant carriers: 1647
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 1.25e1
  variant carriers: 35
genotype quality: GenotypeQuality
  all individuals: 2240
  bin: 6.25e1
  variant carriers: 743
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 3.25e1
  variant carriers: 162
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 2.5e0
  variant carriers: 14
num of homozygotes: 37235
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP

1-67425312-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67425312
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67425312
    reference: chr 1
allele count: 3
allele frequency: 2.502293769288514e-5
allele num: 119890
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.674-50T>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.527-50T>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.635-50T>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.527-50T>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000493357
  gene symbol: MIER1
  hgvsc: ENST00000493357.1:n.74-50T>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.476-50T>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.476-50T>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.527-50T>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.287-50T>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.635-50T>G
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11263
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13482
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2390
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17298
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5444
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4548
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 530
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2380
  bin: 9.75e1
  variant carriers: 3
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum

1-67425313-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67425313
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67425313
    reference: chr 1
allele count: 1
allele frequency: 8.339448929214757e-6
allele num: 119912
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.527-49A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.287-49A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360053
  ensembl transcript: ENST00000371014
  gene symbol: MIER1
  hgvsc: ENST00000371014.1:c.635-49A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.527-49A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000493357
  gene symbol: MIER1
  hgvsc: ENST00000493357.1:n.74-49A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.674-49A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.635-49A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.527-49A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.476-49A>G
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383821
  ensembl transcript: ENST00000401042
  gene symbol: MIER1
  hgvsc: ENST00000401042.3:c.476-49A>G
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5442
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4605
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1458
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13515
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2394
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11262
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17307
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 306
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2890
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 633
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 277
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ClippingRankSum

1-67425314-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67425314
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 67425314
    reference: chr 1
allele count: 2
allele frequency: 1.66786196774355e-5
allele num: 119914
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360055
  ensembl transcript: ENST00000371016
  gene symbol: MIER1
  hgvsc: ENST00000371016.1:c.527-48G>T
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000347514
  ensembl transcript: ENST00000355356
  gene symbol: MIER1
  hgvsc: ENST00000355356.3:c.476-48G>T
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000360057
  ensembl transcript: ENST00000371018
  gene symbol: MIER1
  hgvsc: ENST00000371018.3:c.527-48G>T
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000350321
  ensembl transcript: ENST00000357692
  gene symbol: MIER1
  hgvsc: ENST00000357692.2:c.527-48G>T
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000383820
  ensembl transcript: ENST00000401041
  gene symbol: MIER1
  hgvsc: ENST00000401041.1:c.635-48G>T
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000479067
  gene symbol: MIER1
  hgvsc: ENST00000479067.1:n.674-48G>T
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl protein: ENSP00000348253
  ensembl transcript: ENST00000355977
  gene symbol: MIER1
  hgvsc: ENST00000355977.6:c.287-48G>T
  variant of: http://identifiers.org/hgnc/29657
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198160
  ensembl transcript: ENST00000493357
  gene symbol: MIER1
  hgvsc: ENST00000493357.1:n.74-48G>T
  variant of: http://identifiers.org/hgnc/29657
canonical: true
consequence: intron
filter: PASS
num of homozygotes: 0
reference allele: G

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

GenotypeQuality
all individuals: 50
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7501
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4066
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 32800
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1699
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6513
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 58
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1329
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2988
bin: 7.25e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 3
allele frequency: 2.610511660285416e-4
allele num: 11492
num of homozygotes: 1

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9782
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.159e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.48e-1

FS
type: SiteQuality
SIO_000300: 1.29e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.25e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.47e-1

QD
type: SiteQuality
SIO_000300: 2.176e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.79e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.07e0

MQ
type: SiteQuality
SIO_000300: 5.591e1

DP
type: SiteQuality
SIO_000300: 1.772197e6

GenotypeQuality
all individuals: 45
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 43
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1329
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 105
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2982
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7501
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2988
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 52
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32800
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.21197430614471e-4
allele num: 16502
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9782
num of homozygotes: 0

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.47e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.25e-2

FS
type: SiteQuality
SIO_000300: 1.29e0

QD
type: SiteQuality
SIO_000300: 2.176e1

VQSLOD
type: SiteQuality
SIO_000300: 2.07e0

DP
type: SiteQuality
SIO_000300: 1.772197e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.48e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.159e0

MQ
type: SiteQuality
SIO_000300: 5.591e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.79e-1

GenotypeQuality
all individuals: 33
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 7526
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1703
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1336
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4068
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2996
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32785
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2984
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6525
bin: 9.75e1
variant carriers: 8

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

Latino
type: Population
allele count: 1
allele frequency: 8.686587908269631e-5
allele num: 11512
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.319109461966605e-4
allele num: 8624
num of homozygotes: 0

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

South Asian
type: Population
allele count: 3
allele frequency: 1.818622696411251e-4
allele num: 16496
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.021659174499387e-4
allele num: 9788
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500690317546071e-5
allele num: 66636
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.418e1

VQSLOD
type: SiteQuality
SIO_000300: -4.903e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.9e-1

FS
type: SiteQuality
SIO_000300: 1.0045e1

DP
type: SiteQuality
SIO_000300: 1.772851e6

MQRankSum
type: SiteQuality
SIO_000300: -2.29e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.91e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.95e-1

QD
type: SiteQuality
SIO_000300: 4.0e0

GenotypeQuality
all individuals: 4076
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6527
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1331
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 28
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2994
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2985
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 32872
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7538
bin: 6.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
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: 9788
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11520
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499925003749813e-5
allele num: 66670
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.46e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.31e0

MQRankSum
type: SiteQuality
SIO_000300: -1.12e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.473e1

VQSLOD
type: SiteQuality
SIO_000300: -1.091e0

FS
type: SiteQuality
SIO_000300: 2.367e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.03e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.48e-1

DP
type: SiteQuality
SIO_000300: 1.773984e6

GenotypeQuality
all individuals: 6529
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2982
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 22
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32953
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 106
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4074
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1335
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2991
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7541
bin: 6.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66678
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.477857639693948e-4
allele num: 8626
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11524
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9790
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.39e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.28e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.41e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.42e-1

FS
type: SiteQuality
SIO_000300: 4.31e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.47e-1

QD
type: SiteQuality
SIO_000300: 1.788e1

DP
type: SiteQuality
SIO_000300: 1.775052e6

MQ
type: SiteQuality
SIO_000300: 5.804e1

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7562
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 33016
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6542
bin: 9.75e1
variant carriers: 14

GenotypeQuality
all individuals: 14
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1711
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1335
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2990
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4087
bin: 7.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9794
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11534
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66700
num of homozygotes: 0

South Asian
type: Population
allele count: 14
allele frequency: 8.484848484848485e-4
allele num: 16500
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.08e-1

FS
type: SiteQuality
SIO_000300: 5.18e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.775959e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.075e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.3e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.26e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.85e-1

MQ
type: SiteQuality
SIO_000300: 5.871e1

QD
type: SiteQuality
SIO_000300: 1.289e1

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

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

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

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2992
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7574
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9796
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499205421126803e-5
allele num: 66702
num of homozygotes: 0

VQSLOD
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QD
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ClippingRankSum
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SIO_000300: 6.929999999999999e-1

DP
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ReadPosRankSum
type: SiteQuality
SIO_000300: -8.090000000000001e-1

MQRankSum
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SIO_000300: 1.11e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.292e0

FS
type: SiteQuality
SIO_000300: 4.226e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

MQ
type: SiteQuality
SIO_000300: 5.773e1

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

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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variant carriers: 1

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9796
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499295331194339e-5
allele num: 66698
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.7e0

ReadPosRankSum
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SIO_000300: 1.09e0

DP
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.746e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.73e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.7e-1

GenotypeQuality
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variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9796
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499205421126803e-5
allele num: 66702
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.76e0

FS
type: SiteQuality
SIO_000300: 1.932e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.775556e6

BaseQRankSum
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MQRankSum
type: SiteQuality
SIO_000300: 1.23e-1

QD
type: SiteQuality
SIO_000300: 1.725e1

VQSLOD
type: SiteQuality
SIO_000300: -3.971e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.17e0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9798
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66702
num of homozygotes: 0

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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.115e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

DP
type: SiteQuality
SIO_000300: 1.77553e6

FS
type: SiteQuality
SIO_000300: 6.104e0

MQ
type: SiteQuality
SIO_000300: 5.733e1

VQSLOD
type: SiteQuality
SIO_000300: -1.724e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.444e0

MQRankSum
type: SiteQuality
SIO_000300: 3.9e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.13e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.399999999999999e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.020616452337212e-4
allele num: 9798
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16482
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66684
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 1.34e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.93e-1

DP
type: SiteQuality
SIO_000300: 1.77537e6

MQ
type: SiteQuality
SIO_000300: 5.692e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.79e-1

FS
type: SiteQuality
SIO_000300: 6.657e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.79e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 6.1e-2

QD
type: SiteQuality
SIO_000300: 1.698e1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 4

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.500585076059888e-5
allele num: 66658
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16464
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 1
allele frequency: 1.020408163265306e-4
allele num: 9800
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.610000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.775056e6

InbreedingCoeff
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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FS
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SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.3e-1

BaseQRankSum
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SIO_000300: -2.161e0

MQ
type: SiteQuality
SIO_000300: 5.666e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

Other
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allele frequency: 0.0e0
allele num: 896
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: 16266
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.656509695290859e-5
allele num: 11552
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9792
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66558
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.22476e2

MQ
type: SiteQuality
SIO_000300: 5.716e1

DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ReadPosRankSum
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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VQSLOD
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ClippingRankSum
type: SiteQuality
SIO_000300: 3.53e0

MQRankSum
type: SiteQuality
SIO_000300: -9.59e-1

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

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

African
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allele count: 3
allele frequency: 3.072511265874642e-4
allele num: 9764
num of homozygotes: 0

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

European (Finnish)
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allele count: 5
allele frequency: 7.735148514851486e-4
allele num: 6464
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.141552511415525e-3
allele num: 876
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.05587064076264e-4
allele num: 66296
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
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ReadPosRankSum
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MQ
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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QD
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FS
type: SiteQuality
SIO_000300: 2.96062e2

GenotypeQuality
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variant carriers: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.507613447911955e-5
allele num: 66330
num of homozygotes: 0

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

Other
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allele count: 1
allele frequency: 1.123595505617978e-3
allele num: 890
num of homozygotes: 0

European (Finnish)
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allele count: 1
allele frequency: 1.513317191283293e-4
allele num: 6608
num of homozygotes: 0

MQ
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SIO_000300: 5.748e1

InbreedingCoeff
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ReadPosRankSum
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QD
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DP
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FS
type: SiteQuality
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ClippingRankSum
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SIO_000300: -5.7e-2

VQSLOD
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SIO_000300: -5.036e2

MQRankSum
type: SiteQuality
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BaseQRankSum
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SIO_000300: -6.206e0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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South Asian
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allele frequency: 6.406149903907751e-5
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num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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MQ
type: SiteQuality
SIO_000300: 4.867e1

QD
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BaseQRankSum
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FS
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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DP
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VQSLOD
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SIO_000300: -3.317e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66260
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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South Asian
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allele frequency: 6.406149903907751e-5
allele num: 15610
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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ReadPosRankSum
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FS
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QD
type: SiteQuality
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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DP
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MQ
type: SiteQuality
SIO_000300: 4.867e1

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

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9768
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15372
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.510756586898719e-5
allele num: 66192
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 1.813e1

QD
type: SiteQuality
SIO_000300: 1.1e-1

InbreedingCoeff
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SIO_000300: -1.0e-4

BaseQRankSum
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ClippingRankSum
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SIO_000300: 1.51e0

ReadPosRankSum
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VQSLOD
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MQRankSum
type: SiteQuality
SIO_000300: -1.124e0

DP
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 3.724e1

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9756
num of homozygotes: 0

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

South Asian
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allele count: 1
allele frequency: 6.648936170212766e-5
allele num: 15040
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66058
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -3.65e-1

VQSLOD
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ReadPosRankSum
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InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
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DP
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MQRankSum
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QD
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MQ
type: SiteQuality
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BaseQRankSum
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SIO_000300: -1.221e0

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

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 65924
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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East Asian
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African
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allele frequency: 1.026272577996716e-4
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South Asian
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InbreedingCoeff
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SIO_000300: -1.2e-3

MQRankSum
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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QD
type: SiteQuality
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FS
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MQ
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DP
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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num of homozygotes: 0

South Asian
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Latino
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European (Non-Finnish)
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allele num: 65878
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East Asian
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European (Finnish)
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Other
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MQRankSum
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MQ
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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FS
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BaseQRankSum
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ClippingRankSum
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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Other
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European (Non-Finnish)
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European (Finnish)
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East Asian
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Latino
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ReadPosRankSum
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BaseQRankSum
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DP
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VQSLOD
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MQ
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InbreedingCoeff
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MQRankSum
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QD
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FS
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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num of homozygotes: 0

East Asian
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South Asian
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Other
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European (Finnish)
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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InbreedingCoeff
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FS
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VQSLOD
type: SiteQuality
SIO_000300: -4.962e0

MQRankSum
type: SiteQuality
SIO_000300: -1.155e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.494e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.02e0

DP
type: SiteQuality
SIO_000300: 1.739045e6

MQ
type: SiteQuality
SIO_000300: 3.713e1

QD
type: SiteQuality
SIO_000300: 1.2e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.733e0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7176
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variant carriers: 0

GenotypeQuality
all individuals: 1700
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9732
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65834
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.688097306689835e-5
allele num: 11510
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.833401667350006e-5
allele num: 14634
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e0

QD
type: SiteQuality
SIO_000300: 1.254e1

MQRankSum
type: SiteQuality
SIO_000300: 2.39e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.12e0

DP
type: SiteQuality
SIO_000300: 1.738388e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.136e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e0

MQ
type: SiteQuality
SIO_000300: 5.852e1

GenotypeQuality
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bin: 9.75e1
variant carriers: 4

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 4
allele frequency: 4.113533525298231e-4
allele num: 9724
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14366
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65698
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -8.487e-1

FS
type: SiteQuality
SIO_000300: 3.006e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

MQ
type: SiteQuality
SIO_000300: 5.831e1

QD
type: SiteQuality
SIO_000300: 1.446e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.75e-1

DP
type: SiteQuality
SIO_000300: 1.729125e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.38e0

MQRankSum
type: SiteQuality
SIO_000300: 3.81e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.43e-1

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 2871
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variant carriers: 0

GenotypeQuality
all individuals: 3994
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9666
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8532
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13296
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.53261402648357e-5
allele num: 65248
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.726003490401397e-5
allele num: 11460
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.81e-1

FS
type: SiteQuality
SIO_000300: 1.206e0

VQSLOD
type: SiteQuality
SIO_000300: 2.43e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.91e-1

MQ
type: SiteQuality
SIO_000300: 5.031e1

MQRankSum
type: SiteQuality
SIO_000300: -1.614e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.03e-1

QD
type: SiteQuality
SIO_000300: 1.382e1

DP
type: SiteQuality
SIO_000300: 1.695162e6

GenotypeQuality
all individuals: 82
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 14

GenotypeQuality
all individuals: 1313
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variant carriers: 0

GenotypeQuality
all individuals: 6799
bin: 6.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11428
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12788
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9636
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8524
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 13
allele frequency: 2.000369298947498e-4
allele num: 64988
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 838
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.541e1

DP
type: SiteQuality
SIO_000300: 1.681193e6

FS
type: SiteQuality
SIO_000300: 9.08e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.7e-2

MQ
type: SiteQuality
SIO_000300: 5.752e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.93e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.269e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.815e0

GenotypeQuality
all individuals: 2942
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9504
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.563037294069836e-5
allele num: 63978
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11346
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8440
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.442e1

VQSLOD
type: SiteQuality
SIO_000300: 1.8e0

FS
type: SiteQuality
SIO_000300: 4.165e0

MQ
type: SiteQuality
SIO_000300: 5.739e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

DP
type: SiteQuality
SIO_000300: 1.680049e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.04e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.6e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.67e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.41e0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8440
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9504
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11346
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.563037294069836e-5
allele num: 63978
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.6e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.04e-1

DP
type: SiteQuality
SIO_000300: 1.680049e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

QD
type: SiteQuality
SIO_000300: 1.442e1

MQ
type: SiteQuality
SIO_000300: 5.739e1

VQSLOD
type: SiteQuality
SIO_000300: 1.8e0

FS
type: SiteQuality
SIO_000300: 4.165e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.41e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.67e0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.543829314231019e-5
allele num: 64774
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16034
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9602
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11318
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8338
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6564
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.69e0

MQRankSum
type: SiteQuality
SIO_000300: 9.5e-2

QD
type: SiteQuality
SIO_000300: 1.259e1

DP
type: SiteQuality
SIO_000300: 1.489709e6

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.35e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.3019e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.847e0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3449
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64768
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9600
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8340
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11318
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6560
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.250781347668459e-5
allele num: 15998
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.5e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -9.51e-1

DP
type: SiteQuality
SIO_000300: 1.497142e6

MQ
type: SiteQuality
SIO_000300: 6.102e1

MQRankSum
type: SiteQuality
SIO_000300: 1.02e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.474e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.14e0

QD
type: SiteQuality
SIO_000300: 1.16e1

GenotypeQuality
all individuals: 472
bin: 9.25e1
variant carriers: 22

GenotypeQuality
all individuals: 345
bin: 8.75e1
variant carriers: 15

GenotypeQuality
all individuals: 2370
bin: 5.25e1
variant carriers: 13

GenotypeQuality
all individuals: 25819
bin: 6.25e1
variant carriers: 13

GenotypeQuality
all individuals: 156
bin: 1.75e1
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GenotypeQuality
all individuals: 95
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 1553
bin: 7.75e1
variant carriers: 10

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

GenotypeQuality
all individuals: 6138
bin: 6.75e1
variant carriers: 9

GenotypeQuality
all individuals: 1647
bin: 2.25e1
variant carriers: 2

GenotypeQuality
all individuals: 488
bin: 5.75e1
variant carriers: 11

GenotypeQuality
all individuals: 2270
bin: 3.25e1
variant carriers: 7

GenotypeQuality
all individuals: 1523
bin: 7.25e1
variant carriers: 13

GenotypeQuality
all individuals: 920
bin: 8.25e1
variant carriers: 17

European (Finnish)
type: Population
allele count: 98
allele frequency: 1.493447119780555e-2
allele num: 6562
num of homozygotes: 1

South Asian
type: Population
allele count: 499
allele frequency: 3.099378881987578e-2
allele num: 16100
num of homozygotes: 10

East Asian
type: Population
allele count: 323
allele frequency: 3.869190225203641e-2
allele num: 8348
num of homozygotes: 4

Other
type: Population
allele count: 29
allele frequency: 3.295454545454545e-2
allele num: 880
num of homozygotes: 2

Latino
type: Population
allele count: 183
allele frequency: 1.614041277121185e-2
allele num: 11338
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 1600
allele frequency: 2.464723642861544e-2
allele num: 64916
num of homozygotes: 19

African
type: Population
allele count: 936
allele frequency: 9.739854318418315e-2
allele num: 9610
num of homozygotes: 44

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.029e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.95e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.19e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.75e0

MQRankSum
type: SiteQuality
SIO_000300: 5.2e-2

DP
type: SiteQuality
SIO_000300: 1.510545e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.97e-1

QD
type: SiteQuality
SIO_000300: 1.525e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.05e-1

GenotypeQuality
all individuals: 1483
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 879
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32318
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 51
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1609
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1541
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 326
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1508
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 654
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3308
bin: 9.75e1
variant carriers: 218

GenotypeQuality
all individuals: 6612
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 457
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1124
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 196
allele frequency: 3.015477399304594e-3
allele num: 64998
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 4.406062742333451e-4
allele num: 11348
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.205783790492739e-5
allele num: 16114
num of homozygotes: 0

African
type: Population
allele count: 9
allele frequency: 9.336099585062241e-4
allele num: 9640
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.126126126126126e-3
allele num: 888
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8358
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 8
allele frequency: 1.21914050594331e-3
allele num: 6562
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.570000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.532305e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.8e-2

QD
type: SiteQuality
SIO_000300: 1.338e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.78e-1

FS
type: SiteQuality
SIO_000300: 8.24e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.18e0

GenotypeQuality
all individuals: 1485
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1203
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 334
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1550
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34503
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 430
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1531
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 886
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1633
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2488
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 456
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6566
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16154
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.037559659680432e-4
allele num: 9638
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11362
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65112
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8380
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.15e0

MQRankSum
type: SiteQuality
SIO_000300: -7.4e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.5e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.543293e6

QD
type: SiteQuality
SIO_000300: 1.746e1

VQSLOD
type: SiteQuality
SIO_000300: 3.68e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.21e-1

GenotypeQuality
all individuals: 1477
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1117
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6717
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35073
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 433
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 329
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1969
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2374
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 769
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3106
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 865
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1516
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.535909565644775e-5
allele num: 65108
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11362
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: 0
allele frequency: 0.0e0
allele num: 16152
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6564
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.549395e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.8e-2

QD
type: SiteQuality
SIO_000300: 1.069e1

VQSLOD
type: SiteQuality
SIO_000300: 4.55e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.48e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.79e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.32e-1

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

GenotypeQuality
all individuals: 1829
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 870
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 562
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2080
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 878
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 877
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6811
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1498
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65218
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8390
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9654
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.182762458266353e-5
allele num: 16174
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.869e1

MQRankSum
type: SiteQuality
SIO_000300: -2.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.04e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.557346e6

VQSLOD
type: SiteQuality
SIO_000300: -9.357e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.68e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.99e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.94e1

GenotypeQuality
all individuals: 454
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 589
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1969
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1800
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1509
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1476
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6771
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3104
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 794
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 877
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 868
bin: 2.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9656
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.5220700152207e-4
allele num: 6570
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16182
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11370
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65192
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8392
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.158e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.28e-1

FS
type: SiteQuality
SIO_000300: 1.664e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.04e-1

MQ
type: SiteQuality
SIO_000300: 5.948e1

MQRankSum
type: SiteQuality
SIO_000300: 7.76e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.19e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.31e-1

DP
type: SiteQuality
SIO_000300: 1.562511e6

GenotypeQuality
all individuals: 275
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 448
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7044
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 854
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 327
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 986
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1470
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 41431
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 682
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3213
bin: 9.75e1
variant carriers: 146

GenotypeQuality
all individuals: 844
bin: 3.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 4
allele frequency: 3.502013657853266e-4
allele num: 11422
num of homozygotes: 0

African
type: Population
allele count: 135
allele frequency: 1.393188854489164e-2
allele num: 9690
num of homozygotes: 1

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

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 1.523554147114388e-4
allele num: 65636
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16292
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.899999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.54e-1

QD
type: SiteQuality
SIO_000300: 1.598e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.18e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.0e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.21e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.75e0

VQSLOD
type: SiteQuality
SIO_000300: 3.98e0

DP
type: SiteQuality
SIO_000300: 1.608324e6

GenotypeQuality
all individuals: 326
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 567
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 417
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 900
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1555
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3082
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 858
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42040
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 713
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65728
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11426
num of homozygotes: 0

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

East Asian
type: Population
allele count: 6
allele frequency: 7.070469007777516e-4
allele num: 8486
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9698
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.15e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.02e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

FS
type: SiteQuality
SIO_000300: 6.27e-1

QD
type: SiteQuality
SIO_000300: 1.353e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.56e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.611189e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.35e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.46e-1

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

GenotypeQuality
all individuals: 136
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42612
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 449
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1562
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 582
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7151
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 802
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 863
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1493
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 325
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9706
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11432
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16348
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: 8512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.518418415378542e-5
allele num: 65858
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.12e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.78e0

DP
type: SiteQuality
SIO_000300: 1.61751e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.95e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.354e0

VQSLOD
type: SiteQuality
SIO_000300: 1.17e-1

FS
type: SiteQuality
SIO_000300: 3.078e0

MQ
type: SiteQuality
SIO_000300: 5.946e1

QD
type: SiteQuality
SIO_000300: 1.415e1

GenotypeQuality
all individuals: 3091
bin: 9.75e1
variant carriers: 14

GenotypeQuality
all individuals: 19
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7314
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 5.75e1
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1499
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 447
bin: 9.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16414
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9748
num of homozygotes: 0

East Asian
type: Population
allele count: 15
allele frequency: 1.746623195156032e-3
allele num: 8588
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66278
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11480
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.45e-2

DP
type: SiteQuality
SIO_000300: 1.636913e6

VQSLOD
type: SiteQuality
SIO_000300: 3.02e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.714e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.843e0

MQRankSum
type: SiteQuality
SIO_000300: 5.4e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.02e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.52e-1

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 43801
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 8.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66346
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: 11490
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9754
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.082725060827251e-5
allele num: 16440
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.639933e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.13e1

MQRankSum
type: SiteQuality
SIO_000300: 7.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.1e-3

VQSLOD
type: SiteQuality
SIO_000300: 6.06e-1

FS
type: SiteQuality
SIO_000300: 1.72e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.095e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.51e-1

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

GenotypeQuality
all individuals: 335
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 83
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variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9760
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66392
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.076810889645114e-5
allele num: 16456
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -6.81e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.84e0

VQSLOD
type: SiteQuality
SIO_000300: 7.13e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.2e-3

QD
type: SiteQuality
SIO_000300: 1.328e1

FS
type: SiteQuality
SIO_000300: 4.561e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.3e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.641838e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 130
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variant carriers: 0

GenotypeQuality
all individuals: 7386
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66402
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: 898
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.024590163934426e-4
allele num: 9760
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16456
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.01e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

FS
type: SiteQuality
SIO_000300: 6.1e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.97e0

MQ
type: SiteQuality
SIO_000300: 5.93e1

QD
type: SiteQuality
SIO_000300: 1.735e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.29e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.205e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.76e-1

DP
type: SiteQuality
SIO_000300: 1.642292e6

GenotypeQuality
all individuals: 84
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 97
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 329
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variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 4.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.076072426783327e-5
allele num: 16458
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11518
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9764
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66472
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.975e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.7e-3

VQSLOD
type: SiteQuality
SIO_000300: -3.92e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.38e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.546e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.91e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.88e0

FS
type: SiteQuality
SIO_000300: 7.28e-1

QD
type: SiteQuality
SIO_000300: 1.158e1

DP
type: SiteQuality
SIO_000300: 1.645717e6

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

GenotypeQuality
all individuals: 44383
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 179
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
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variant carriers: 0

GenotypeQuality
all individuals: 3083
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 1
allele frequency: 1.022076860179886e-4
allele num: 9784
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11520
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66570
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.56e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.012e0

DP
type: SiteQuality
SIO_000300: 1.649779e6

VQSLOD
type: SiteQuality
SIO_000300: 7.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.03e-1

QD
type: SiteQuality
SIO_000300: 1.375e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -5.03e-1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.676036786395974e-5
allele num: 11526
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66636
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: 9788
num of homozygotes: 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: 900
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.23e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.95e0

VQSLOD
type: SiteQuality
SIO_000300: -8.141e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.704e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.45e-1

DP
type: SiteQuality
SIO_000300: 1.653194e6

FS
type: SiteQuality
SIO_000300: 4.231e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.19e-2

QD
type: SiteQuality
SIO_000300: 1.737e1

MQ
type: SiteQuality
SIO_000300: 5.924e1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 445
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11534
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66664
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9792
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.365e1

MQ
type: SiteQuality
SIO_000300: 5.976e1

VQSLOD
type: SiteQuality
SIO_000300: 1.2e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.654436e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.41e-1

FS
type: SiteQuality
SIO_000300: 3.039e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.326e0

MQRankSum
type: SiteQuality
SIO_000300: -9.0e-2

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
all individuals: 1629
bin: 7.25e1
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GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 445
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 5

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 327
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 5.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9792
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.000060000600006e-5
allele num: 66666
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 1.654651e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.43e0

MQ
type: SiteQuality
SIO_000300: 5.961e1

VQSLOD
type: SiteQuality
SIO_000300: 8.81e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 2.71e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.02e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.97e-1

FS
type: SiteQuality
SIO_000300: 5.509e0

QD
type: SiteQuality
SIO_000300: 1.243e1

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

GenotypeQuality
all individuals: 3079
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1625
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500015000150001e-5
allele num: 66666
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9792
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: 11538
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.114e1

FS
type: SiteQuality
SIO_000300: 6.15e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.504e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.875e0

DP
type: SiteQuality
SIO_000300: 1.654815e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.63e0

MQ
type: SiteQuality
SIO_000300: 5.988e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.45e0

VQSLOD
type: SiteQuality
SIO_000300: -9.761e-1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 2.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9792
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66670
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 2.51e0

DP
type: SiteQuality
SIO_000300: 1.654963e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.25e0

MQ
type: SiteQuality
SIO_000300: 5.966e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.900000000000001e-2

FS
type: SiteQuality
SIO_000300: 1.054e0

MQRankSum
type: SiteQuality
SIO_000300: 1.9e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 4.5e-1

QD
type: SiteQuality
SIO_000300: 1.423e1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7522
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 444
bin: 9.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499970000599988e-5
allele num: 66668
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9794
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.65e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.3e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 6.08e-1

QD
type: SiteQuality
SIO_000300: 1.247e1

MQ
type: SiteQuality
SIO_000300: 5.969e1

FS
type: SiteQuality
SIO_000300: 1.16e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.5e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.04e0

DP
type: SiteQuality
SIO_000300: 1.655698e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeQuality
all individuals: 444
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 3079
bin: 9.75e1
variant carriers: 1

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9794
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66668
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.74e-2

MQRankSum
type: SiteQuality
SIO_000300: 6.15e-1

QD
type: SiteQuality
SIO_000300: 1.001e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.32e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.328e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.655737e6

GenotypeQuality
all individuals: 31
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.021033285685113e-4
allele num: 9794
num of homozygotes: 0

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

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

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

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -4.82e-1

MQ
type: SiteQuality
SIO_000300: 5.948e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.308e0

QD
type: SiteQuality
SIO_000300: 1.103e1

VQSLOD
type: SiteQuality
SIO_000300: 3.13e0

MQRankSum
type: SiteQuality
SIO_000300: 2.28e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.17e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.65606e6

GenotypeQuality
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bin: 9.75e1
variant carriers: 4

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 4
allele frequency: 2.425418384671356e-4
allele num: 16492
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9794
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.948e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.65606e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.308e0

QD
type: SiteQuality
SIO_000300: 1.103e1

VQSLOD
type: SiteQuality
SIO_000300: 3.13e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.17e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9792
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.000030000300003e-5
allele num: 66666
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 3.91e-1

FS
type: SiteQuality
SIO_000300: 3.081e0

VQSLOD
type: SiteQuality
SIO_000300: -9.1e-2

BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.11e-1

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.924e1

InbreedingCoeff
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DP
type: SiteQuality
SIO_000300: 1.656307e6

GenotypeQuality
all individuals: 15
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 35
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 3083
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
all individuals: 1608
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 2.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 863
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 325
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1502
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.819505094614265e-4
allele num: 16488
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.002552169343942e-5
allele num: 66610
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9790
num of homozygotes: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.319109461966605e-4
allele num: 8624
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -8.999999999999999e-3

MQ
type: SiteQuality
SIO_000300: 5.982e1

FS
type: SiteQuality
SIO_000300: 6.04e-1

DP
type: SiteQuality
SIO_000300: 1.656026e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.27e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.68e-1

QD
type: SiteQuality
SIO_000300: 1.311e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.31e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.56e-1

GenotypeQuality
all individuals: 13
bin: 4.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 18
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1503
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7545
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 183
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 863
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3080
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 44704
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1608
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 325
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.02124183006536e-4
allele num: 9792
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.064281382656155e-5
allele num: 16490
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.159554730983302e-4
allele num: 8624
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66614
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.966e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.86e0

MQRankSum
type: SiteQuality
SIO_000300: -6.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.392e0

DP
type: SiteQuality
SIO_000300: 1.655762e6

QD
type: SiteQuality
SIO_000300: 1.133e1

FS
type: SiteQuality
SIO_000300: 2.686e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.05e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.47e-1

GenotypeQuality
all individuals: 860
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18
bin: 2.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 7536
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variant carriers: 0

GenotypeQuality
all individuals: 20
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variant carriers: 0

GenotypeQuality
all individuals: 239
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variant carriers: 0

GenotypeQuality
all individuals: 8
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GenotypeQuality
all individuals: 1502
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3080
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 326
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 443
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9792
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.066488716330988e-5
allele num: 16484
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66574
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 4
allele frequency: 6.053268765133172e-4
allele num: 6608
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.71e-1

MQ
type: SiteQuality
SIO_000300: 5.945e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.93e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.66e-1

DP
type: SiteQuality
SIO_000300: 1.655028e6

QD
type: SiteQuality
SIO_000300: 1.347e1

VQSLOD
type: SiteQuality
SIO_000300: 3.42e0

GenotypeQuality
all individuals: 1607
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
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variant carriers: 0

GenotypeQuality
all individuals: 859
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variant carriers: 0

GenotypeQuality
all individuals: 1500
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variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7538
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 44627
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3077
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 325
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 443
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66572
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9792
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.067961165048543e-5
allele num: 16480
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.654623e6

FS
type: SiteQuality
SIO_000300: 3.693e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.070000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.178e1

VQSLOD
type: SiteQuality
SIO_000300: 1.87e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.99e-1

MQ
type: SiteQuality
SIO_000300: 5.96e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.22e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.613e0

GenotypeQuality
all individuals: 20
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 44596
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3078
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 17
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 859
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 5.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 13
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1496
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 443
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7527
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1608
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9790
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502448991856726e-5
allele num: 66558
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.670019074041963e-5
allele num: 11534
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16480
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.835e0

VQSLOD
type: SiteQuality
SIO_000300: 1.57e0

DP
type: SiteQuality
SIO_000300: 1.654421e6

MQ
type: SiteQuality
SIO_000300: 5.972e1

MQRankSum
type: SiteQuality
SIO_000300: -1.53e-1

QD
type: SiteQuality
SIO_000300: 1.292e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.208e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.12e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.27e0

GenotypeDepth
all individuals: 103
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 27
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 117
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variant carriers: 0

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

GenotypeQuality
all individuals: 1464
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variant carriers: 0

GenotypeQuality
all individuals: 102
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 1568
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variant carriers: 0

GenotypeQuality
all individuals: 7496
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variant carriers: 0

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

GenotypeQuality
all individuals: 851
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variant carriers: 0

GenotypeQuality
all individuals: 1029
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 443
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43725
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3075
bin: 9.75e1
variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.509433962264151e-5
allele num: 66250
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9744
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16418
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.128e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.13e0

MQRankSum
type: SiteQuality
SIO_000300: -9.57e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.1e-2

DP
type: SiteQuality
SIO_000300: 1.643681e6

FS
type: SiteQuality
SIO_000300: 1.808e0

VQSLOD
type: SiteQuality
SIO_000300: -2.048e0

MQ
type: SiteQuality
SIO_000300: 5.95e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.15e0

GenotypeQuality
all individuals: 847
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43093
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 442
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GenotypeQuality
all individuals: 320
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 1562
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variant carriers: 0

GenotypeQuality
all individuals: 17
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variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
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variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3085
bin: 9.75e1
variant carriers: 18

GenotypeQuality
all individuals: 1540
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7465
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1462
bin: 7.75e1
variant carriers: 0

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

African
type: Population
allele count: 2
allele frequency: 2.059732234809475e-4
allele num: 9710
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8576
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 16
allele frequency: 2.42270070561158e-4
allele num: 66042
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16390
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11498
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.636733e6

QD
type: SiteQuality
SIO_000300: 1.34e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.46e0

MQ
type: SiteQuality
SIO_000300: 5.96e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.6e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.5e-2

FS
type: SiteQuality
SIO_000300: 5.116e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.98e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.65e-1

GenotypeQuality
all individuals: 439
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6279
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 305
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GenotypeQuality
all individuals: 1423
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3746
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1537
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variant carriers: 0

GenotypeQuality
all individuals: 556
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variant carriers: 0

GenotypeQuality
all individuals: 3466
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variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 2.5e0
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GenotypeQuality
all individuals: 980
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3088
bin: 9.75e1
variant carriers: 24

GenotypeQuality
all individuals: 1102
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10881
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 862
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.592356687898089e-4
allele num: 6280
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 23
allele frequency: 3.817680841881619e-4
allele num: 60246
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11104
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8664
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7482
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15292
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.87e0

FS
type: SiteQuality
SIO_000300: 4.413e0

MQRankSum
type: SiteQuality
SIO_000300: -4.6e-2

QD
type: SiteQuality
SIO_000300: 1.547e1

VQSLOD
type: SiteQuality
SIO_000300: 7.77e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.6e-3

DP
type: SiteQuality
SIO_000300: 1.30632e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.84e-1

GenotypeQuality
all individuals: 797
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3926
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7125
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1033
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1994
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4450
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7085
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3736
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2129
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3065
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5571
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 438
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8064
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55472
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14506
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10622
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5946
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.545595054095827e-4
allele num: 6470
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.43e-1

QD
type: SiteQuality
SIO_000300: 1.333e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.7e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.186e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.031e0

DP
type: SiteQuality
SIO_000300: 1.234247e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.64e0

GenotypeQuality
all individuals: 47148
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 131
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1714
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 715
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
all individuals: 432
bin: 4.75e1
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GenotypeQuality
all individuals: 1915
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GenotypeQuality
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GenotypeQuality
all individuals: 2240
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 3.25e1
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GenotypeQuality
all individuals: 1495
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8544
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9674
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: 888
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.545041359876375e-5
allele num: 66006
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.9e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.609098e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 3.159e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.55e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.68e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.2e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.59e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.73e0

GenotypeQuality
all individuals: 1915
bin: 9.25e1
variant carriers: 1850

GenotypeQuality
all individuals: 1495
bin: 7.75e1
variant carriers: 1351

GenotypeQuality
all individuals: 606
bin: 5.25e1
variant carriers: 521

GenotypeQuality
all individuals: 82
bin: 1.75e1
variant carriers: 62

GenotypeQuality
all individuals: 432
bin: 4.75e1
variant carriers: 361

GenotypeQuality
all individuals: 715
bin: 7.25e1
variant carriers: 589

GenotypeQuality
all individuals: 279
bin: 3.75e1
variant carriers: 231

GenotypeQuality
all individuals: 100
bin: 2.75e1
variant carriers: 65

GenotypeQuality
all individuals: 131
bin: 2.25e1
variant carriers: 96

GenotypeQuality
all individuals: 1468
bin: 6.75e1
variant carriers: 1028

GenotypeQuality
all individuals: 419
bin: 5.75e1
variant carriers: 355

GenotypeQuality
all individuals: 982
bin: 8.75e1
variant carriers: 945

GenotypeQuality
all individuals: 37
bin: 7.5e0
variant carriers: 23

GenotypeQuality
all individuals: 47148
bin: 9.75e1
variant carriers: 46899

GenotypeQuality
all individuals: 1714
bin: 8.25e1
variant carriers: 1595

GenotypeQuality
all individuals: 202
bin: 4.25e1
variant carriers: 170

East Asian
type: Population
allele count: 7463
allele frequency: 8.734784644194756e-1
allele num: 8544
num of homozygotes: 3254

European (Finnish)
type: Population
allele count: 4183
allele frequency: 6.349423193685488e-1
allele num: 6588
num of homozygotes: 1365

African
type: Population
allele count: 8052
allele frequency: 8.323340913789539e-1
allele num: 9674
num of homozygotes: 3351

South Asian
type: Population
allele count: 14272
allele frequency: 8.659143307850989e-1
allele num: 16482
num of homozygotes: 6217

Other
type: Population
allele count: 697
allele frequency: 7.849099099099099e-1
allele num: 888
num of homozygotes: 271

European (Non-Finnish)
type: Population
allele count: 49138
allele frequency: 7.444474744720176e-1
allele num: 66006
num of homozygotes: 18240

Latino
type: Population
allele count: 10225
allele frequency: 8.860485268630849e-1
allele num: 11540
num of homozygotes: 4537

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.68e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.9e0

MQRankSum
type: SiteQuality
SIO_000300: 3.2e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.59e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.73e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.55e-1

QD
type: SiteQuality
SIO_000300: 3.159e1

DP
type: SiteQuality
SIO_000300: 2.609098e6

GenotypeQuality
all individuals: 359
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10149
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 273
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 38
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variant carriers: 0

GenotypeQuality
all individuals: 2471
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variant carriers: 0

GenotypeQuality
all individuals: 146
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variant carriers: 0

GenotypeQuality
all individuals: 12
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GenotypeQuality
all individuals: 882
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variant carriers: 0

GenotypeQuality
all individuals: 74
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variant carriers: 0

GenotypeQuality
all individuals: 637
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variant carriers: 0

GenotypeQuality
all individuals: 815
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2918
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 585
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1721
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35689
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9652
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8574
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 3
allele frequency: 2.597852441981296e-4
allele num: 11548
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66142
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.82e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

QD
type: SiteQuality
SIO_000300: 1.562e1

DP
type: SiteQuality
SIO_000300: 2.058374e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.79e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e0

MQRankSum
type: SiteQuality
SIO_000300: -1.98e-1

GenotypeQuality
all individuals: 2465
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1697
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 296
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variant carriers: 0

GenotypeQuality
all individuals: 31
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variant carriers: 0

GenotypeQuality
all individuals: 10157
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variant carriers: 0

GenotypeQuality
all individuals: 351
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variant carriers: 0

GenotypeQuality
all individuals: 66
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variant carriers: 0

GenotypeQuality
all individuals: 364
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GenotypeQuality
all individuals: 35971
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
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variant carriers: 0

GenotypeQuality
all individuals: 808
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variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
all individuals: 816
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variant carriers: 0

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

GenotypeQuality
all individuals: 2373
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 578
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9656
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66162
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16470
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -9.346e-1

FS
type: SiteQuality
SIO_000300: 2.609e0

MQ
type: SiteQuality
SIO_000300: 5.972e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.42e0

MQRankSum
type: SiteQuality
SIO_000300: 2.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

DP
type: SiteQuality
SIO_000300: 2.058992e6

QD
type: SiteQuality
SIO_000300: 3.442e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.22e-1