11-67234904-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67234904
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67234904
    reference: chr 11
allele count: 12
allele frequency: 9.984856301276397e-5
allele num: 120182
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.385-45C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.279-45C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535813
  gene symbol: TMEM134
  hgvsc: ENST00000535813.1:n.94-45C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.441C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.303-45C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.330-45C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.330-45C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.408C>T
  hgvsp: ENST00000544903.1:c.408C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.330-45C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.314-45C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.341-45C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541059
  gene symbol: TMEM134
  hgvsc: ENST00000541059.1:n.35-45C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.263-45C>T
  variant of: http://identifiers.org/hgnc/26142
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13841
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6517
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1737
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11868
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3462
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Pro136Pro
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: East Asian
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

11-67234905-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67234905
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67234905
    reference: chr 11
allele count: 4
allele frequency: 3.328340822100183e-5
allele num: 120180
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.263-46C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.341-46C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.330-46C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.314-46C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.407C>T
  hgvsp: ENSP00000439609.1:p.Pro136Leu
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541059
  gene symbol: TMEM134
  hgvsc: ENST00000541059.1:n.35-46C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.385-46C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.440C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.330-46C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.279-46C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535813
  gene symbol: TMEM134
  hgvsc: ENST00000535813.1:n.94-46C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.330-46C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.303-46C>T
  variant of: http://identifiers.org/hgnc/26142
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3460
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1213
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6516
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18670
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro136Leu
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ

11-67234905-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67234905
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67234905
    reference: chr 11
allele count: 1
allele frequency: 8.320852055250457e-6
allele num: 120180
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.341-46C>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.440C>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.263-46C>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.279-46C>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.303-46C>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.385-46C>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.407C>A
  hgvsp: ENSP00000439609.1:p.Pro136His
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.330-46C>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535813
  gene symbol: TMEM134
  hgvsc: ENST00000535813.1:n.94-46C>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.314-46C>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541059
  gene symbol: TMEM134
  hgvsc: ENST00000541059.1:n.35-46C>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.330-46C>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.330-46C>A
  variant of: http://identifiers.org/hgnc/26142
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6516
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1213
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3460
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11851
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13843
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1737
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18670
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro136His
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum

11-67234908-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67234908
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67234908
    reference: chr 11
allele count: 1
allele frequency: 8.322237017310253e-6
allele num: 120160
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.385-49C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.263-49C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541059
  gene symbol: TMEM134
  hgvsc: ENST00000541059.1:n.35-49C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.279-49C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.330-49C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.330-49C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.341-49C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.330-49C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.404C>T
  hgvsp: ENSP00000439609.1:p.Thr135Ile
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.437C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535813
  gene symbol: TMEM134
  hgvsc: ENST00000535813.1:n.94-49C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.314-49C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.303-49C>T
  variant of: http://identifiers.org/hgnc/26142
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11793
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3468
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18710
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13830
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr135Ile
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

11-67234910-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67234910
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67234910
    reference: chr 11
allele count: 15
allele frequency: 1.248855216051952e-4
allele num: 120110
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.263-51C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.435C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541059
  gene symbol: TMEM134
  hgvsc: ENST00000541059.1:n.35-51C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.385-51C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535813
  gene symbol: TMEM134
  hgvsc: ENST00000535813.1:n.94-51C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.279-51C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.330-51C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.303-51C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.402C>T
  hgvsp: ENST00000544903.1:c.402C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.330-51C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.314-51C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.341-51C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.330-51C>T
  variant of: http://identifiers.org/hgnc/26142
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6515
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3466
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11675
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13884
  bin: 3.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Cys134Cys
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD

11-67234911-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67234911
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67234911
    reference: chr 11
allele count: 1
allele frequency: 8.339170752860335e-6
allele num: 119916
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.330-52G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.303-52G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.385-52G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.330-52G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.434G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.263-52G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.330-52G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535813
  gene symbol: TMEM134
  hgvsc: ENST00000535813.1:n.94-52G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.401G>A
  hgvsp: ENSP00000439609.1:p.Cys134Tyr
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.341-52G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.314-52G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541059
  gene symbol: TMEM134
  hgvsc: ENST00000541059.1:n.35-52G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.279-52G>A
  variant of: http://identifiers.org/hgnc/26142
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11602
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6531
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18728
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13892
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1751
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3485
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys134Tyr
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: African
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

11-67234913-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67234913
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67234913
    reference: chr 11
allele count: 1
allele frequency: 8.320852055250457e-6
allele num: 120180
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.341-54C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.330-54C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.432C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535813
  gene symbol: TMEM134
  hgvsc: ENST00000535813.1:n.94-54C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.330-54C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.314-54C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.399C>T
  hgvsp: ENST00000544903.1:c.399C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.279-54C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.330-54C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.263-54C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.303-54C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.385-54C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541059
  gene symbol: TMEM134
  hgvsc: ENST00000541059.1:n.35-54C>T
  variant of: http://identifiers.org/hgnc/26142
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18842
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1743
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6513
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3449
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11589
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13943
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser133Ser
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

11-67234916-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67234916
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67234916
    reference: chr 11
allele count: 1
allele frequency: 8.319467554076538e-6
allele num: 120200
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535813
  gene symbol: TMEM134
  hgvsc: ENST00000535813.1:n.93+56C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.262+56C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.329+56C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.329+56C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.278+56C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.429C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.329+56C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.313+56C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.384+56C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.396C>T
  hgvsp: ENST00000544903.1:c.396C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541059
  gene symbol: TMEM134
  hgvsc: ENST00000541059.1:n.34+56C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.340+56C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.302+56C>T
  variant of: http://identifiers.org/hgnc/26142
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11548
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13955
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3435
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18948
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6514
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala132Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
population: African
population: European (Finnish)
reference allele: G
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ

11-67234916-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67234916
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67234916
    reference: chr 11
allele count: 2
allele frequency: 1.663893510815308e-5
allele num: 120200
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535813
  gene symbol: TMEM134
  hgvsc: ENST00000535813.1:n.93+56C>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541059
  gene symbol: TMEM134
  hgvsc: ENST00000541059.1:n.34+56C>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.329+56C>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.262+56C>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.329+56C>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.396C>G
  hgvsp: ENST00000544903.1:c.396C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.278+56C>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.329+56C>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.302+56C>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.429C>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.384+56C>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.340+56C>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.313+56C>G
  variant of: http://identifiers.org/hgnc/26142
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11548
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13955
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6514
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala132Ala
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: G
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP

11-67234919-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67234919
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67234919
    reference: chr 11
allele count: 1
allele frequency: 8.325840077263796e-6
allele num: 120108
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.329+53A>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.262+53A>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.302+53A>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.384+53A>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.426A>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.329+53A>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535813
  gene symbol: TMEM134
  hgvsc: ENST00000535813.1:n.93+53A>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.340+53A>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.393A>G
  hgvsp: ENST00000544903.1:c.393A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.278+53A>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.329+53A>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541059
  gene symbol: TMEM134
  hgvsc: ENST00000541059.1:n.34+53A>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.313+53A>G
  variant of: http://identifiers.org/hgnc/26142
canonical: false
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 18999
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3453
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11558
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6491
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1745
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13982
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr131Thr
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

11-67234922-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67234922
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67234922
    reference: chr 11
allele count: 10
allele frequency: 8.316561600771777e-5
allele num: 120242
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.302+50C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.384+50C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.329+50C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541059
  gene symbol: TMEM134
  hgvsc: ENST00000541059.1:n.34+50C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.329+50C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.329+50C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.390C>T
  hgvsp: ENST00000544903.1:c.390C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.340+50C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535813
  gene symbol: TMEM134
  hgvsc: ENST00000535813.1:n.93+50C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.423C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.262+50C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.278+50C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.313+50C>T
  variant of: http://identifiers.org/hgnc/26142
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1723
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11533
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19131
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6512
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3425
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Pro130Pro
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP

11-67234923-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67234923
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67234923
    reference: chr 11
allele count: 1
allele frequency: 8.317806760713336e-6
allele num: 120224
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535813
  gene symbol: TMEM134
  hgvsc: ENST00000535813.1:n.93+49C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.262+49C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.340+49C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.329+49C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.329+49C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.313+49C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.422C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.389C>T
  hgvsp: ENSP00000439609.1:p.Pro130Leu
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.278+49C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.302+49C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.329+49C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.384+49C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541059
  gene symbol: TMEM134
  hgvsc: ENST00000541059.1:n.34+49C>T
  variant of: http://identifiers.org/hgnc/26142
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11550
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14067
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19156
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3425
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1719
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6507
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro130Leu
num of homozygotes: 0
population: African
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: FS

11-67234925-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67234925
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67234925
    reference: chr 11
allele count: 1
allele frequency: 8.315593400745077e-6
allele num: 120256
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.420C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.387C>T
  hgvsp: ENST00000544903.1:c.387C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541059
  gene symbol: TMEM134
  hgvsc: ENST00000541059.1:n.34+47C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.329+47C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.384+47C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535813
  gene symbol: TMEM134
  hgvsc: ENST00000535813.1:n.93+47C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.313+47C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.278+47C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.329+47C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.302+47C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.262+47C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.340+47C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.329+47C>T
  variant of: http://identifiers.org/hgnc/26142
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19233
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6491
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11574
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1709
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3426
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14075
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Thr129Thr
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD
site quality: DP

11-67234928-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67234928
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67234928
    reference: chr 11
allele count: 4
allele frequency: 3.325020781379884e-5
allele num: 120300
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.302+44C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.329+44C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.384C>T
  hgvsp: ENST00000544903.1:c.384C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.340+44C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.262+44C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.278+44C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535813
  gene symbol: TMEM134
  hgvsc: ENST00000535813.1:n.93+44C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.417C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.329+44C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541059
  gene symbol: TMEM134
  hgvsc: ENST00000541059.1:n.34+44C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.313+44C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.384+44C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.329+44C>T
  variant of: http://identifiers.org/hgnc/26142
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3394
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1695
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11618
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6478
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14092
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19365
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ser128Ser
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD
site quality: DP
site quality: ClippingRankSum

11-67234931-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67234931
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67234931
    reference: chr 11
allele count: 118
allele frequency: 9.80864823527456e-4
allele num: 120302
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535813
  gene symbol: TMEM134
  hgvsc: ENST00000535813.1:n.93+41C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.313+41C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.384+41C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.329+41C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.414C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.381C>T
  hgvsp: ENST00000544903.1:c.381C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.329+41C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.262+41C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.340+41C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.329+41C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.302+41C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541059
  gene symbol: TMEM134
  hgvsc: ENST00000541059.1:n.34+41C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.278+41C>T
  variant of: http://identifiers.org/hgnc/26142
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 11577
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19386
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 5.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 1706
  bin: 4.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3377
  bin: 4.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 6476
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.25e1
  variant carriers: 10
genotype quality: GenotypeQuality
hgvs: p.Gly127Gly
num of homozygotes: 2
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: European (Finnish)
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

11-67234935-GGGCTGCTC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67234935
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67234927
    reference: chr 11
allele count: 1
allele frequency: 8.308408109006315e-6
allele num: 120360
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.402_409delGAGCAGCC
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541059
  gene symbol: TMEM134
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.369_376delGAGCAGCC
  hgvsp: ENSP00000439609.1:p.Ser124TrpfsTer?
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535813
  gene symbol: TMEM134
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  variant of: http://identifiers.org/hgnc/26142
canonical: false
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19611
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14177
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11554
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6479
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3362
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 752
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser124TrpfsTer?
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: GGGCTGCTC
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: DP

11-67234938-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67234938
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67234938
    reference: chr 11
allele count: 10
allele frequency: 8.309374636464859e-5
allele num: 120346
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535813
  gene symbol: TMEM134
  hgvsc: ENST00000535813.1:n.93+34G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.407G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.302+34G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.329+34G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.329+34G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.313+34G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.262+34G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.384+34G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.374G>A
  hgvsp: ENSP00000439609.1:p.Ser125Asn
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.278+34G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541059
  gene symbol: TMEM134
  hgvsc: ENST00000541059.1:n.34+34G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.329+34G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.340+34G>A
  variant of: http://identifiers.org/hgnc/26142
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6468
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14205
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19662
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11538
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ser125Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ClippingRankSum

11-67234943-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67234943
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67234943
    reference: chr 11
allele count: 7
allele frequency: 5.815402508930797e-5
allele num: 120370
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.329+29G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.262+29G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.369G>A
  hgvsp: ENST00000544903.1:c.369G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.384+29G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.402G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541059
  gene symbol: TMEM134
  hgvsc: ENST00000541059.1:n.34+29G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535813
  gene symbol: TMEM134
  hgvsc: ENST00000535813.1:n.93+29G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.329+29G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.329+29G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.313+29G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.340+29G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.278+29G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.302+29G>A
  variant of: http://identifiers.org/hgnc/26142
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11540
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19776
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3343
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14224
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6471
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1678
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro123Pro
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ

11-67234944-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67234944
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67234944
    reference: chr 11
allele count: 8
allele frequency: 6.642752756742394e-5
allele num: 120432
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541059
  gene symbol: TMEM134
  hgvsc: ENST00000541059.1:n.34+28C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.329+28C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.340+28C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.278+28C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.262+28C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535813
  gene symbol: TMEM134
  hgvsc: ENST00000535813.1:n.93+28C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.368C>T
  hgvsp: ENSP00000439609.1:p.Pro123Leu
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.302+28C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.313+28C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.329+28C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.384+28C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.401C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.329+28C>T
  variant of: http://identifiers.org/hgnc/26142
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19836
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14230
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6456
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11592
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3330
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro123Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP

11-67234945-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67234945
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67234945
    reference: chr 11
allele count: 1
allele frequency: 8.302613662781043e-6
allele num: 120444
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.329+27C>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535813
  gene symbol: TMEM134
  hgvsc: ENST00000535813.1:n.93+27C>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.262+27C>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.278+27C>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.313+27C>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.400C>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.329+27C>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.367C>G
  hgvsp: ENSP00000439609.1:p.Pro123Ala
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.384+27C>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.329+27C>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.340+27C>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541059
  gene symbol: TMEM134
  hgvsc: ENST00000541059.1:n.34+27C>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.302+27C>G
  variant of: http://identifiers.org/hgnc/26142
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14237
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6454
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3334
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11618
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro123Ala
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

11-67234959-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67234959
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67234959
    reference: chr 11
allele count: 3
allele frequency: 2.487603442843165e-5
allele num: 120598
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.262+13G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.353G>A
  hgvsp: ENSP00000439609.1:p.Arg118His
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.386G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.313+13G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.384+13G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.278+13G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.329+13G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.340+13G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.302+13G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535813
  gene symbol: TMEM134
  hgvsc: ENST00000535813.1:n.93+13G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.329+13G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000536773
  gene symbol: TMEM134
  hgvsc: ENST00000536773.1:n.393G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541059
  gene symbol: TMEM134
  hgvsc: ENST00000541059.1:n.34+13G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.329+13G>A
  variant of: http://identifiers.org/hgnc/26142
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11737
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14286
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20055
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1664
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg118His
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD

11-67234960-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67234960
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67234960
    reference: chr 11
allele count: 1
allele frequency: 8.289124668435012e-6
allele num: 120640
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.385C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.384+12C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.352C>T
  hgvsp: ENSP00000439609.1:p.Arg118Cys
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.278+12C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541059
  gene symbol: TMEM134
  hgvsc: ENST00000541059.1:n.34+12C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.329+12C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.302+12C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.340+12C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.313+12C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.329+12C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000536773
  gene symbol: TMEM134
  hgvsc: ENST00000536773.1:n.392C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.329+12C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535813
  gene symbol: TMEM134
  hgvsc: ENST00000535813.1:n.93+12C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.262+12C>T
  variant of: http://identifiers.org/hgnc/26142
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1664
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11803
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14283
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6461
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3322
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg118Cys
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff

11-67234965-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67234965
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67234965
    reference: chr 11
allele count: 1
allele frequency: 8.282808203293245e-6
allele num: 120732
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.340+7C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.329+7C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541059
  gene symbol: TMEM134
  hgvsc: ENST00000541059.1:n.34+7C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.347C>T
  hgvsp: ENSP00000439609.1:p.Pro116Leu
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.329+7C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.384+7C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535813
  gene symbol: TMEM134
  hgvsc: ENST00000535813.1:n.93+7C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.278+7C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.302+7C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.262+7C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.313+7C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.380C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000536773
  gene symbol: TMEM134
  hgvsc: ENST00000536773.1:n.387C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.329+7C>T
  variant of: http://identifiers.org/hgnc/26142
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3314
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14294
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20131
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11835
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1663
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Pro116Leu
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP

11-67234969-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67234969
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67234969
    reference: chr 11
allele count: 3
allele frequency: 2.484924789609701e-5
allele num: 120728
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535813
  gene symbol: TMEM134
  hgvsc: ENST00000535813.1:n.93+3G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.384+3G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.329+3G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.340+3G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.343G>A
  hgvsp: ENSP00000439609.1:p.Glu115Lys
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.329+3G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541059
  gene symbol: TMEM134
  hgvsc: ENST00000541059.1:n.34+3G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.262+3G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.278+3G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.329+3G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.302+3G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000536773
  gene symbol: TMEM134
  hgvsc: ENST00000536773.1:n.383G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.376G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.313+3G>A
  variant of: http://identifiers.org/hgnc/26142
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11858
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20156
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6454
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu115Lys
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

11-67234971-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67234971
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67234971
    reference: chr 11
allele count: 1
allele frequency: 8.280476292996373e-6
allele num: 120766
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541059
  gene symbol: TMEM134
  hgvsc: ENST00000541059.1:n.34+1G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.384+1G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.262+1G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000536773
  gene symbol: TMEM134
  hgvsc: ENST00000536773.1:n.381G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.329+1G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.340+1G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535813
  gene symbol: TMEM134
  hgvsc: ENST00000535813.1:n.93+1G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.329+1G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.313+1G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.374G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.278+1G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.329+1G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.302+1G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.341G>A
  hgvsp: ENSP00000439609.1:p.Gly114Asp
  variant of: http://identifiers.org/hgnc/26142
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14311
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3315
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6451
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11862
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.329+1G>A
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

11-67234986-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67234986
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67234986
    reference: chr 11
allele count: 1
allele frequency: 8.274583788435442e-6
allele num: 120852
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.288C>T
  hgvsp: ENST00000452789.2:c.288C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.264C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.299C>T
  hgvsp: ENSP00000440630.1:p.Thr100Ile
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.326C>T
  hgvsp: ENSP00000439609.1:p.Thr109Ile
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.326C>T
  hgvsp: ENSP00000441975.1:p.Thr109Ile
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541059
  gene symbol: TMEM134
  hgvsc: ENST00000541059.1:n.20C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.370C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.315C>T
  hgvsp: ENST00000393877.3:c.315C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000536773
  gene symbol: TMEM134
  hgvsc: ENST00000536773.1:n.366C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.315C>T
  hgvsp: ENST00000545682.1:c.315C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.248C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.359C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535813
  gene symbol: TMEM134
  hgvsc: ENST00000535813.1:n.79C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.315C>T
  hgvsp: ENST00000308022.2:c.315C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26142
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1663
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6455
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12026
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr109Ile
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum

11-67234989-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67234989
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67234989
    reference: chr 11
allele count: 1
allele frequency: 8.274036074797286e-6
allele num: 120860
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.367C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.312C>T
  hgvsp: ENST00000545682.1:c.312C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.323C>T
  hgvsp: ENSP00000439609.1:p.Pro108Leu
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535813
  gene symbol: TMEM134
  hgvsc: ENST00000535813.1:n.76C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.245C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000536773
  gene symbol: TMEM134
  hgvsc: ENST00000536773.1:n.363C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.296C>T
  hgvsp: ENSP00000440630.1:p.Pro99Leu
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.323C>T
  hgvsp: ENSP00000441975.1:p.Pro108Leu
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541059
  gene symbol: TMEM134
  hgvsc: ENST00000541059.1:n.17C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.312C>T
  hgvsp: ENST00000393877.3:c.312C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.261C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.312C>T
  hgvsp: ENST00000308022.2:c.312C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.356C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.285C>T
  hgvsp: ENST00000452789.2:c.285C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26142
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20329
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14317
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6457
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro108Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ

11-67234993-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67234993
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67234993
    reference: chr 11
allele count: 4
allele frequency: 3.30988829127017e-5
allele num: 120850
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.363G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.292G>A
  hgvsp: ENSP00000440630.1:p.Ala98Thr
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.241G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.319G>A
  hgvsp: ENSP00000439609.1:p.Ala107Thr
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.352G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.308G>A
  hgvsp: ENSP00000377455.3:p.Arg103His
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000536773
  gene symbol: TMEM134
  hgvsc: ENST00000536773.1:n.359G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.308G>A
  hgvsp: ENSP00000312615.2:p.Arg103His
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.281G>A
  hgvsp: ENSP00000395482.2:p.Arg94His
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.257G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.319G>A
  hgvsp: ENSP00000441975.1:p.Ala107Thr
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535813
  gene symbol: TMEM134
  hgvsc: ENST00000535813.1:n.72G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.308G>A
  hgvsp: ENSP00000438439.1:p.Arg103His
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541059
  gene symbol: TMEM134
  hgvsc: ENST00000541059.1:n.13G>A
  variant of: http://identifiers.org/hgnc/26142
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14317
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3313
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20348
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11997
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg103His
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

11-67234994-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67234994
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67234994
    reference: chr 11
allele count: 1
allele frequency: 8.274036074797286e-6
allele num: 120860
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000536773
  gene symbol: TMEM134
  hgvsc: ENST00000536773.1:n.358C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.307C>T
  hgvsp: ENSP00000438439.1:p.Arg103Cys
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.280C>T
  hgvsp: ENSP00000395482.2:p.Arg94Cys
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.240C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.307C>T
  hgvsp: ENSP00000312615.2:p.Arg103Cys
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.291C>T
  hgvsp: ENST00000536020.1:c.291C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535813
  gene symbol: TMEM134
  hgvsc: ENST00000535813.1:n.71C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.362C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.351C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.307C>T
  hgvsp: ENSP00000377455.3:p.Arg103Cys
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.318C>T
  hgvsp: ENST00000540133.1:c.318C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.318C>T
  hgvsp: ENST00000544903.1:c.318C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541059
  gene symbol: TMEM134
  hgvsc: ENST00000541059.1:n.12C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.256C>T
  variant of: http://identifiers.org/hgnc/26142
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1662
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14324
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3313
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11983
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6455
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg103Cys
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: European (Finnish)
population: East Asian
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff

11-67234996-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67234996
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67234996
    reference: chr 11
allele count: 1
allele frequency: 8.27348843366317e-6
allele num: 120868
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000536773
  gene symbol: TMEM134
  hgvsc: ENST00000536773.1:n.356A>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.278A>T
  hgvsp: ENSP00000395482.2:p.Gln93Leu
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.305A>T
  hgvsp: ENSP00000312615.2:p.Gln102Leu
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.305A>T
  hgvsp: ENSP00000377455.3:p.Gln102Leu
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.305A>T
  hgvsp: ENSP00000438439.1:p.Gln102Leu
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.360A>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541059
  gene symbol: TMEM134
  hgvsc: ENST00000541059.1:n.10A>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.254A>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.349A>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535813
  gene symbol: TMEM134
  hgvsc: ENST00000535813.1:n.69A>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.238A>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.289A>T
  hgvsp: ENSP00000440630.1:p.Ser97Cys
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.316A>T
  hgvsp: ENSP00000441975.1:p.Ser106Cys
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.316A>T
  hgvsp: ENSP00000439609.1:p.Ser106Cys
  variant of: http://identifiers.org/hgnc/26142
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1662
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11999
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14319
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3314
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20364
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln102Leu
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum

11-67235003-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67235003
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67235003
    reference: chr 11
allele count: 2
allele frequency: 1.655026314918407e-5
allele num: 120844
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.298A>G
  hgvsp: ENSP00000377455.3:p.Ser100Gly
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.309A>G
  hgvsp: ENST00000540133.1:c.309A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541059
  gene symbol: TMEM134
  hgvsc: ENST00000541059.1:n.3A>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.282A>G
  hgvsp: ENST00000536020.1:c.282A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.298A>G
  hgvsp: ENSP00000438439.1:p.Ser100Gly
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.247A>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.309A>G
  hgvsp: ENST00000544903.1:c.309A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.231A>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000536773
  gene symbol: TMEM134
  hgvsc: ENST00000536773.1:n.349A>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.342A>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.353A>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.298A>G
  hgvsp: ENSP00000312615.2:p.Ser100Gly
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.271A>G
  hgvsp: ENSP00000395482.2:p.Ser91Gly
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535813
  gene symbol: TMEM134
  hgvsc: ENST00000535813.1:n.62A>G
  variant of: http://identifiers.org/hgnc/26142
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1663
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14316
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12004
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6453
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20378
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser100Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: African
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

11-67235005-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67235005
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67235005
    reference: chr 11
allele count: 11
allele frequency: 9.102042167278986e-5
allele num: 120852
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.229G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535813
  gene symbol: TMEM134
  hgvsc: ENST00000535813.1:n.60G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.296G>A
  hgvsp: ENSP00000438439.1:p.Ser99Asn
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541059
  gene symbol: TMEM134
  hgvsc: ENST00000541059.1:n.1G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.280G>A
  hgvsp: ENSP00000440630.1:p.Ala94Thr
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.307G>A
  hgvsp: ENSP00000441975.1:p.Ala103Thr
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.296G>A
  hgvsp: ENSP00000312615.2:p.Ser99Asn
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.296G>A
  hgvsp: ENSP00000377455.3:p.Ser99Asn
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.340G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.269G>A
  hgvsp: ENSP00000395482.2:p.Ser90Asn
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000536773
  gene symbol: TMEM134
  hgvsc: ENST00000536773.1:n.347G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.307G>A
  hgvsp: ENSP00000439609.1:p.Ala103Thr
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.351G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.245G>A
  variant of: http://identifiers.org/hgnc/26142
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1662
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20386
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 3311
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser99Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: Latino
population: East Asian
population: European (Finnish)
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

11-67235012-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67235012
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67235012
    reference: chr 11
allele count: 1
allele frequency: 8.274994621253496e-6
allele num: 120846
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.289A>C
  hgvsp: ENSP00000438439.1:p.Ile97Leu
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.300A>C
  hgvsp: ENST00000544903.1:c.300A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.273A>C
  hgvsp: ENST00000536020.1:c.273A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.344A>C
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.300A>C
  hgvsp: ENST00000540133.1:c.300A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.289A>C
  hgvsp: ENSP00000377455.3:p.Ile97Leu
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000536773
  gene symbol: TMEM134
  hgvsc: ENST00000536773.1:n.340A>C
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.262A>C
  hgvsp: ENSP00000395482.2:p.Ile88Leu
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.289A>C
  hgvsp: ENSP00000312615.2:p.Ile97Leu
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.333A>C
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.238A>C
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535813
  gene symbol: TMEM134
  hgvsc: ENST00000535813.1:n.53A>C
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.222A>C
  variant of: http://identifiers.org/hgnc/26142
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6450
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11993
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3310
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20410
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile97Leu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP

11-67235013-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67235013
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67235013
    reference: chr 11
allele count: 1
allele frequency: 8.275405494869249e-6
allele num: 120840
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.332C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.299C>T
  hgvsp: ENSP00000441975.1:p.Pro100Leu
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.288C>T
  hgvsp: ENST00000308022.2:c.288C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.288C>T
  hgvsp: ENST00000393877.3:c.288C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535813
  gene symbol: TMEM134
  hgvsc: ENST00000535813.1:n.52C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.237C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.272C>T
  hgvsp: ENSP00000440630.1:p.Pro91Leu
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000536773
  gene symbol: TMEM134
  hgvsc: ENST00000536773.1:n.339C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.343C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.221C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.299C>T
  hgvsp: ENSP00000439609.1:p.Pro100Leu
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.261C>T
  hgvsp: ENST00000452789.2:c.261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.288C>T
  hgvsp: ENST00000545682.1:c.288C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26142
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1664
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14321
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20407
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro100Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: African
population: Latino
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

11-67235022-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67235022
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67235022
    reference: chr 11
allele count: 1
allele frequency: 8.277323444690924e-6
allele num: 120812
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.263C>T
  hgvsp: ENSP00000440630.1:p.Pro88Leu
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.279C>T
  hgvsp: ENST00000393877.3:c.279C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535813
  gene symbol: TMEM134
  hgvsc: ENST00000535813.1:n.43C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.228C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.279C>T
  hgvsp: ENST00000545682.1:c.279C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.212C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.279C>T
  hgvsp: ENST00000308022.2:c.279C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.290C>T
  hgvsp: ENSP00000441975.1:p.Pro97Leu
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.290C>T
  hgvsp: ENSP00000439609.1:p.Pro97Leu
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.334C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.323C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.252C>T
  hgvsp: ENST00000452789.2:c.252C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000536773
  gene symbol: TMEM134
  hgvsc: ENST00000536773.1:n.330C>T
  variant of: http://identifiers.org/hgnc/26142
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6447
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3310
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11871
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20402
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1663
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro97Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

11-67235023-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67235023
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67235023
    reference: chr 11
allele count: 1
allele frequency: 8.277734549608463e-6
allele num: 120806
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.278C>T
  hgvsp: ENSP00000377455.3:p.Ser93Phe
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.262C>T
  hgvsp: ENSP00000440630.1:p.Pro88Ser
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.227C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.211C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.289C>T
  hgvsp: ENSP00000441975.1:p.Pro97Ser
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.322C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.333C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.278C>T
  hgvsp: ENSP00000438439.1:p.Ser93Phe
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.278C>T
  hgvsp: ENSP00000312615.2:p.Ser93Phe
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.289C>T
  hgvsp: ENSP00000439609.1:p.Pro97Ser
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.251C>T
  hgvsp: ENSP00000395482.2:p.Ser84Phe
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000536773
  gene symbol: TMEM134
  hgvsc: ENST00000536773.1:n.329C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535813
  gene symbol: TMEM134
  hgvsc: ENST00000535813.1:n.42C>T
  variant of: http://identifiers.org/hgnc/26142
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3310
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11872
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6447
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser93Phe
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

11-67235026-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67235026
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67235026
    reference: chr 11
allele count: 2
allele frequency: 1.655738790648387e-5
allele num: 120792
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535813
  gene symbol: TMEM134
  hgvsc: ENST00000535813.1:n.39G>C
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.259G>C
  hgvsp: ENSP00000440630.1:p.Gly87Arg
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.275G>C
  hgvsp: ENSP00000438439.1:p.Trp92Ser
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.330G>C
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.224G>C
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.286G>C
  hgvsp: ENSP00000439609.1:p.Gly96Arg
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.275G>C
  hgvsp: ENSP00000377455.3:p.Trp92Ser
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.208G>C
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.275G>C
  hgvsp: ENSP00000312615.2:p.Trp92Ser
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000536773
  gene symbol: TMEM134
  hgvsc: ENST00000536773.1:n.326G>C
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.248G>C
  hgvsp: ENSP00000395482.2:p.Trp83Ser
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.286G>C
  hgvsp: ENSP00000441975.1:p.Gly96Arg
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.319G>C
  variant of: http://identifiers.org/hgnc/26142
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11833
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6446
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14319
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3312
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1663
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Trp92Ser
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum

11-67235038-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67235038
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67235038
    reference: chr 11
allele count: 1
allele frequency: 8.287338604080686e-6
allele num: 120666
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.196G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.216-4G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.263G>A
  hgvsp: ENSP00000377455.3:p.Arg88His
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.274G>A
  hgvsp: ENSP00000439609.1:p.Ala92Thr
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535813
  gene symbol: TMEM134
  hgvsc: ENST00000535813.1:n.27G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.263G>A
  hgvsp: ENSP00000438439.1:p.Arg88His
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.251-4G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.274G>A
  hgvsp: ENSP00000441975.1:p.Ala92Thr
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.263G>A
  hgvsp: ENSP00000312615.2:p.Arg88His
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000536773
  gene symbol: TMEM134
  hgvsc: ENST00000536773.1:n.314G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.318G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.240-4G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.307G>A
  variant of: http://identifiers.org/hgnc/26142
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1664
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14319
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3310
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg88His
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD

11-67235039-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67235039
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67235039
    reference: chr 11
allele count: 13
allele frequency: 1.077621937066879e-4
allele num: 120636
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535813
  gene symbol: TMEM134
  hgvsc: ENST00000535813.1:n.26C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.262C>T
  hgvsp: ENSP00000438439.1:p.Arg88Cys
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.273C>T
  hgvsp: ENST00000540133.1:c.273C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.251-5C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.216-5C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.262C>T
  hgvsp: ENSP00000377455.3:p.Arg88Cys
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000536773
  gene symbol: TMEM134
  hgvsc: ENST00000536773.1:n.313C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.273C>T
  hgvsp: ENST00000544903.1:c.273C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.306C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.240-5C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.262C>T
  hgvsp: ENSP00000312615.2:p.Arg88Cys
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.195C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.317C>T
  variant of: http://identifiers.org/hgnc/26142
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20289
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14303
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 11657
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6446
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3309
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg88Cys
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: African
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum

11-67235039-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67235039
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67235039
    reference: chr 11
allele count: 1
allele frequency: 8.289399515899069e-6
allele num: 120636
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.216-5C>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000536773
  gene symbol: TMEM134
  hgvsc: ENST00000536773.1:n.313C>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.251-5C>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.262C>G
  hgvsp: ENSP00000312615.2:p.Arg88Gly
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.240-5C>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.317C>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.262C>G
  hgvsp: ENSP00000438439.1:p.Arg88Gly
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535813
  gene symbol: TMEM134
  hgvsc: ENST00000535813.1:n.26C>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.273C>G
  hgvsp: ENST00000540133.1:c.273C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.306C>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.195C>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.262C>G
  hgvsp: ENSP00000377455.3:p.Arg88Gly
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.273C>G
  hgvsp: ENST00000544903.1:c.273C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26142
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3309
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11657
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20289
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6446
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg88Gly
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

11-67235050-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67235050
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67235050
    reference: chr 11
allele count: 1
allele frequency: 8.299995020002988e-6
allele num: 120482
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.184G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.251-16G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000536773
  gene symbol: TMEM134
  hgvsc: ENST00000536773.1:n.302G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.216-16G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.251G>A
  hgvsp: ENSP00000377455.3:p.Arg84Gln
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.251G>A
  hgvsp: ENSP00000438439.1:p.Arg84Gln
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.262G>A
  hgvsp: ENSP00000441975.1:p.Glu88Lys
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.295G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535813
  gene symbol: TMEM134
  hgvsc: ENST00000535813.1:n.15G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.262G>A
  hgvsp: ENSP00000439609.1:p.Glu88Lys
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.240-16G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.251G>A
  hgvsp: ENSP00000312615.2:p.Arg84Gln
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.306G>A
  variant of: http://identifiers.org/hgnc/26142
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3312
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6448
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20109
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11474
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14300
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1666
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg84Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

11-67235051-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67235051
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67235051
    reference: chr 11
allele count: 559
allele frequency: 4.639620198532585e-3
allele num: 120484
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.216-17C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.250C>T
  hgvsp: ENSP00000438439.1:p.Arg84Ter
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.305C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.261C>T
  hgvsp: ENST00000544903.1:c.261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.250C>T
  hgvsp: ENSP00000312615.2:p.Arg84Ter
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.261C>T
  hgvsp: ENST00000540133.1:c.261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.250C>T
  hgvsp: ENSP00000377455.3:p.Arg84Ter
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535813
  gene symbol: TMEM134
  hgvsc: ENST00000535813.1:n.14C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.251-17C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.240-17C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000536773
  gene symbol: TMEM134
  hgvsc: ENST00000536773.1:n.301C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.183C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.294C>T
  variant of: http://identifiers.org/hgnc/26142
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1646
  bin: 4.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 14211
  bin: 3.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 7.25e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 5.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 6.75e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 11420
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6362
  bin: 3.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 8.75e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3247
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 6.25e1
  variant carriers: 25
genotype quality: GenotypeQuality
hgvs: p.Arg84Ter
num of homozygotes: 4
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD

11-67235054-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67235054
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67235054
    reference: chr 11
allele count: 1
allele frequency: 8.303854649328218e-6
allele num: 120426
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.216-20A>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.291A>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.251-20A>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.247A>G
  hgvsp: ENSP00000377455.3:p.Ser83Gly
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.258A>G
  hgvsp: ENST00000540133.1:c.258A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.247A>G
  hgvsp: ENSP00000312615.2:p.Ser83Gly
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.258A>G
  hgvsp: ENST00000544903.1:c.258A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.240-20A>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.302A>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000536773
  gene symbol: TMEM134
  hgvsc: ENST00000536773.1:n.298A>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.247A>G
  hgvsp: ENSP00000438439.1:p.Ser83Gly
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535813
  gene symbol: TMEM134
  hgvsc: ENST00000535813.1:n.11A>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.180A>G
  variant of: http://identifiers.org/hgnc/26142
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6420
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11369
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20073
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14389
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3289
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser83Gly
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: East Asian
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/11-67235060-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67235060
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67235060
    reference: chr 11
allele count: 138
allele frequency: 1.146922424826715e-3
allele num: 120322
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.216-26G>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.296G>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.174G>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000536773
  gene symbol: TMEM134
  hgvsc: ENST00000536773.1:n.292G>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.240-26G>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.241G>T
  hgvsp: ENSP00000438439.1:p.Asp81Tyr
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.241G>T
  hgvsp: ENSP00000377455.3:p.Asp81Tyr
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.252G>T
  hgvsp: ENST00000540133.1:c.252G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.241G>T
  hgvsp: ENSP00000312615.2:p.Asp81Tyr
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.252G>T
  hgvsp: ENST00000544903.1:c.252G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.251-26G>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535813
  gene symbol: TMEM134
  hgvsc: ENST00000535813.1:n.5G>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.285G>T
  variant of: http://identifiers.org/hgnc/26142
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6399
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3273
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 14350
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 5.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 20004
  bin: 2.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
hgvs: p.Asp81Tyr
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: QD

11-67235062-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67235062
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67235062
    reference: chr 11
allele count: 4
allele frequency: 3.325131342688036e-5
allele num: 120296
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.284-1G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.251-1G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.216-28G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.251-1G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.295-1G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.240-1G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.240-28G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.240-1G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000536773
  gene symbol: TMEM134
  hgvsc: ENST00000536773.1:n.291-1G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.240-1G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.251-28G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.173-1G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535813
  gene symbol: TMEM134
  hgvsc: ENST00000535813.1:n.3G>A
  variant of: http://identifiers.org/hgnc/26142
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20005
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11232
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14360
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3281
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6417
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.240-1G>A
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ

11-67235076-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67235076
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67235076
    reference: chr 11
allele count: 50
allele frequency: 4.168959594443611e-4
allele num: 119934
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.240-15C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.251-15C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.240-15C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.251-15C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.216-42C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.251-42C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.240-42C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000536773
  gene symbol: TMEM134
  hgvsc: ENST00000536773.1:n.291-15C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.284-15C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.295-15C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.173-15C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.240-15C>T
  variant of: http://identifiers.org/hgnc/26142
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 19556
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 5.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 3282
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10863
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 14243
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1421
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1648
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6396
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: Other
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS

11-67235076-GC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67235076
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67235075
    reference: chr 11
allele count: 4
allele frequency: 3.335167675554888e-5
allele num: 119934
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.240-16delG
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.240-16delG
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.240-16delG
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000536773
  gene symbol: TMEM134
  hgvsc: ENST00000536773.1:n.291-16delG
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.251-16delG
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.216-43delG
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.251-16delG
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.173-16delG
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.295-16delG
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.251-43delG
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.284-16delG
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.240-43delG
  variant of: http://identifiers.org/hgnc/26142
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19556
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14243
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3282
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10863
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1421
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1648
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: South Asian
reference allele: GC
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: MQ

11-67235080-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67235080
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67235080
    reference: chr 11
allele count: 4
allele frequency: 3.337004037774885e-5
allele num: 119868
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.173-19T>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.251-19T>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.251-19T>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.240-19T>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.295-19T>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.251-46T>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.216-46T>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.240-19T>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.284-19T>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.240-19T>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.240-46T>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000536773
  gene symbol: TMEM134
  hgvsc: ENST00000536773.1:n.291-19T>A
  variant of: http://identifiers.org/hgnc/26142
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14189
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3271
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6394
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1650
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19421
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10653
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum

11-67235092-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67235092
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67235092
    reference: chr 11
allele count: 1
allele frequency: 8.356592515835743e-6
allele num: 119666
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.240-31C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.216-58C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.240-31C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.173-31C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.284-31C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.240-31C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000536773
  gene symbol: TMEM134
  hgvsc: ENST00000536773.1:n.291-31C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.240-58C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.251-31C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.251-58C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.251-31C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.295-31C>T
  variant of: http://identifiers.org/hgnc/26142
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1650
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6333
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9930
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13777
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2484
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18459
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3265
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

http://identifiers.org/exac.variant/11-67235094-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67235094
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67235094
    reference: chr 11
allele count: 1
allele frequency: 8.360225391676559e-6
allele num: 119614
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.251-33T>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.251-60T>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.251-33T>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.216-60T>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.240-33T>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.173-33T>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.240-60T>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.295-33T>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.284-33T>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000536773
  gene symbol: TMEM134
  hgvsc: ENST00000536773.1:n.291-33T>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.240-33T>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.240-33T>G
  variant of: http://identifiers.org/hgnc/26142
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6310
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2702
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17943
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1647
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2824
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3268
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9694
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13598
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD

11-67235097-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67235097
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67235097
    reference: chr 11
allele count: 4
allele frequency: 3.34817691766833e-5
allele num: 119468
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.173-36G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.240-36G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.240-36G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000536773
  gene symbol: TMEM134
  hgvsc: ENST00000536773.1:n.291-36G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.284-36G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.251-36G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.295-36G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.240-63G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.251-63G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.251-36G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.240-36G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.216-63G>A
  variant of: http://identifiers.org/hgnc/26142
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3864
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2851
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13212
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3269
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9473
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6241
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17373
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Other
population: Latino
population: East Asian
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

11-67235103-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67235103
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67235103
    reference: chr 11
allele count: 1
allele frequency: 8.393063971933595e-6
allele num: 119146
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.251-42G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.295-42G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.251-69G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000536773
  gene symbol: TMEM134
  hgvsc: ENST00000536773.1:n.291-42G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.216-69G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.240-42G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.240-69G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.173-42G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.240-42G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.240-42G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.284-42G>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.251-42G>A
  variant of: http://identifiers.org/hgnc/26142
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6055
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12052
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10254
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15415
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2902
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6285
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3246
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

11-67235104-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67235104
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67235104
    reference: chr 11
allele count: 3
allele frequency: 2.519526329050139e-5
allele num: 119070
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.216-70C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.295-43C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.284-43C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.240-43C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.251-70C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.173-43C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.251-43C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000536773
  gene symbol: TMEM134
  hgvsc: ENST00000536773.1:n.291-43C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.251-43C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.240-43C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.240-70C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.240-43C>T
  variant of: http://identifiers.org/hgnc/26142
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15053
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5990
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6288
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1632
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11002
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2902
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3223
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

11-67235106-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67235106
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67235106
    reference: chr 11
allele count: 4472
allele frequency: 3.765704469668901e-2
allele num: 118756
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000536773
  gene symbol: TMEM134
  hgvsc: ENST00000536773.1:n.291-45C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.240-45C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.295-45C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.251-45C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.240-72C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.240-45C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.251-72C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.173-45C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.216-72C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.240-45C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.251-45C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.284-45C>T
  variant of: http://identifiers.org/hgnc/26142
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 2.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2872
  bin: 1.25e1
  variant carriers: 126
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.25e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 7.5e0
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 12981
  bin: 2.25e1
  variant carriers: 481
genotype depth: GenotypeDepth
  all individuals: 5837
  bin: 3.75e1
  variant carriers: 445
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 5.25e1
  variant carriers: 161
genotype depth: GenotypeDepth
  all individuals: 6322
  bin: 1.75e1
  variant carriers: 270
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 10730
  bin: 3.25e1
  variant carriers: 589
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 3248
  bin: 4.25e1
  variant carriers: 354
genotype depth: GenotypeDepth
  all individuals: 1730
  bin: 4.75e1
  variant carriers: 250
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 5.75e1
  variant carriers: 87
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 6.25e1
  variant carriers: 66
genotype depth: GenotypeDepth
  all individuals: 13749
  bin: 2.75e1
  variant carriers: 637
genotype quality: GenotypeQuality
num of homozygotes: 872
population: Latino
population: South Asian
population: Other
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

11-67235110-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67235110
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67235110
    reference: chr 11
allele count: 1
allele frequency: 8.434832484226864e-6
allele num: 118556
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.216-76C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.240-49C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.284-49C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.251-49C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.251-76C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.251-49C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.173-49C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.295-49C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.240-49C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000536773
  gene symbol: TMEM134
  hgvsc: ENST00000536773.1:n.291-49C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.240-49C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.240-76C>T
  variant of: http://identifiers.org/hgnc/26142
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1646
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2949
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10108
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3141
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13629
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5715
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13896
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6481
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

11-67235439-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67235439
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67235439
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 18510
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000538561
  gene symbol: TMEM134
  hgvsc: ENST00000538561.1:n.379C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000536773
  gene symbol: TMEM134
  hgvsc: ENST00000536773.1:n.290+60C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.215+60C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.239+60C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.172+60C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.250+49C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.294+49C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.250+49C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.239+60C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.283+60C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.250+49C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.239+60C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.239+60C>T
  variant of: http://identifiers.org/hgnc/26142
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1505
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2088
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1956
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1782
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4130
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36089
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD

11-67235445-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67235445
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67235445
    reference: chr 11
allele count: 1
allele frequency: 5.407159078620093e-5
allele num: 18494
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.250+43A>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.239+54A>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000538561
  gene symbol: TMEM134
  hgvsc: ENST00000538561.1:n.373A>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000536773
  gene symbol: TMEM134
  hgvsc: ENST00000536773.1:n.290+54A>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.250+43A>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.172+54A>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.215+54A>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.283+54A>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.294+43A>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.250+43A>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.239+54A>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.239+54A>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.239+54A>G
  variant of: http://identifiers.org/hgnc/26142
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1576
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1743
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2518
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36288
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4109
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: African
reference allele: T
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum

11-67235447-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67235447
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67235447
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 18536
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.215+52C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000538561
  gene symbol: TMEM134
  hgvsc: ENST00000538561.1:n.371C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000536773
  gene symbol: TMEM134
  hgvsc: ENST00000536773.1:n.290+52C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.172+52C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.239+52C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.283+52C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.239+52C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.250+41C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.239+52C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.250+41C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.294+41C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.239+52C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.250+41C>T
  variant of: http://identifiers.org/hgnc/26142
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4152
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1610
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36335
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1717
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

11-67235450-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67235450
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67235450
    reference: chr 11
allele count: 1
allele frequency: 5.380393844829442e-5
allele num: 18586
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.250+38T>C
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.250+38T>C
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.239+49T>C
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000536773
  gene symbol: TMEM134
  hgvsc: ENST00000536773.1:n.290+49T>C
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.239+49T>C
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.283+49T>C
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.250+38T>C
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000538561
  gene symbol: TMEM134
  hgvsc: ENST00000538561.1:n.368T>C
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.294+38T>C
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.215+49T>C
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.172+49T>C
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.239+49T>C
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.239+49T>C
  variant of: http://identifiers.org/hgnc/26142
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36439
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2838
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4272
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD

11-67235452-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67235452
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67235452
    reference: chr 11
allele count: 1
allele frequency: 5.382131324004306e-5
allele num: 18580
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.215+47T>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000538561
  gene symbol: TMEM134
  hgvsc: ENST00000538561.1:n.366T>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.239+47T>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.239+47T>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000536773
  gene symbol: TMEM134
  hgvsc: ENST00000536773.1:n.290+47T>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.250+36T>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.294+36T>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.172+47T>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.239+47T>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.239+47T>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.250+36T>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.283+47T>A
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.250+36T>A
  variant of: http://identifiers.org/hgnc/26142
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4396
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36577
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1647
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: Other
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

11-67235462-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67235462
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67235462
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 18778
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.172+37C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.215+37C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.294+26C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.283+37C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000538561
  gene symbol: TMEM134
  hgvsc: ENST00000538561.1:n.356C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.250+26C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.239+37C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.250+26C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.239+37C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.239+37C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.239+37C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000536773
  gene symbol: TMEM134
  hgvsc: ENST00000536773.1:n.290+37C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.250+26C>T
  variant of: http://identifiers.org/hgnc/26142
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3500
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37095
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5268
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1896
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

11-67235467-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67235467
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67235467
    reference: chr 11
allele count: 1
allele frequency: 5.28597103287874e-5
allele num: 18918
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.239+32C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000538561
  gene symbol: TMEM134
  hgvsc: ENST00000538561.1:n.351C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.215+32C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.172+32C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.294+21C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.250+21C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.250+21C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.250+21C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000536773
  gene symbol: TMEM134
  hgvsc: ENST00000536773.1:n.290+32C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.283+32C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.239+32C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.239+32C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.239+32C>T
  variant of: http://identifiers.org/hgnc/26142
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37151
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6085
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2039
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3650
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

11-67235471-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67235471
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67235471
    reference: chr 11
allele count: 2
allele frequency: 1.051082615093546e-4
allele num: 19028
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000538561
  gene symbol: TMEM134
  hgvsc: ENST00000538561.1:n.347G>C
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.283+28G>C
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.215+28G>C
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.250+17G>C
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.239+28G>C
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.239+28G>C
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.239+28G>C
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.294+17G>C
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.172+28G>C
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000536773
  gene symbol: TMEM134
  hgvsc: ENST00000536773.1:n.290+28G>C
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.250+17G>C
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.250+17G>C
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.239+28G>C
  variant of: http://identifiers.org/hgnc/26142
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6864
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3752
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36994
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: DP
site quality: FS
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/11-67235472-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67235472
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67235472
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 19060
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.239+27T>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.294+16T>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.172+27T>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.250+16T>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000538561
  gene symbol: TMEM134
  hgvsc: ENST00000538561.1:n.346T>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000536773
  gene symbol: TMEM134
  hgvsc: ENST00000536773.1:n.290+27T>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.250+16T>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.283+27T>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.239+27T>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.215+27T>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.250+16T>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.239+27T>G
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.239+27T>G
  variant of: http://identifiers.org/hgnc/26142
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36919
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3808
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2167
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7179
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff

11-67235473-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67235473
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67235473
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 19090
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000538561
  gene symbol: TMEM134
  hgvsc: ENST00000538561.1:n.345C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.294+15C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.239+26C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.250+15C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.239+26C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.239+26C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.250+15C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.239+26C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.250+15C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.172+26C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.215+26C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.283+26C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000536773
  gene symbol: TMEM134
  hgvsc: ENST00000536773.1:n.290+26C>T
  variant of: http://identifiers.org/hgnc/26142
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3852
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36870
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7390
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum

11-67235490-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67235490
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 67235490
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 19852
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000395482
  ensembl transcript: ENST00000452789
  gene symbol: TMEM134
  hgvsc: ENST00000452789.2:c.239+9C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000537601
  gene symbol: TMEM134
  hgvsc: ENST00000537601.1:n.172+9C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000501408
  gene symbol: TMEM134
  hgvsc: ENST00000501408.2:n.292C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000438439
  ensembl transcript: ENST00000545682
  gene symbol: TMEM134
  hgvsc: ENST00000545682.1:c.239+9C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000536773
  gene symbol: TMEM134
  hgvsc: ENST00000536773.1:n.290+9C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000441975
  ensembl transcript: ENST00000540133
  gene symbol: TMEM134
  hgvsc: ENST00000540133.1:c.248C>T
  hgvsp: ENSP00000441975.1:p.Pro83Leu
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000439609
  ensembl transcript: ENST00000544903
  gene symbol: TMEM134
  hgvsc: ENST00000544903.1:c.248C>T
  hgvsp: ENSP00000439609.1:p.Pro83Leu
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000541598
  gene symbol: TMEM134
  hgvsc: ENST00000541598.1:n.283+9C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000312615
  ensembl transcript: ENST00000308022
  gene symbol: TMEM134
  hgvsc: ENST00000308022.2:c.239+9C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000535585
  gene symbol: TMEM134
  hgvsc: ENST00000535585.1:n.215+9C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000440630
  ensembl transcript: ENST00000536020
  gene symbol: TMEM134
  hgvsc: ENST00000536020.1:c.248C>T
  hgvsp: ENSP00000440630.1:p.Pro83Leu
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000172663
  ensembl protein: ENSP00000377455
  ensembl transcript: ENST00000393877
  gene symbol: TMEM134
  hgvsc: ENST00000393877.3:c.239+9C>T
  variant of: http://identifiers.org/hgnc/26142
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000172663
  ensembl transcript: ENST00000538561
  gene symbol: TMEM134
  hgvsc: ENST00000538561.1:n.328C>T
  variant of: http://identifiers.org/hgnc/26142
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 12221
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2370
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34240
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4230
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro83Leu
num of homozygotes: 0
reference allele: G

GenotypeDepth
all individuals: 18632
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 43
bin: 7.75e1
variant carriers: 4

GenotypeDepth
all individuals: 894
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 43
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2109
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 489
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3919
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 322
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9386
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 969
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25449
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 368
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 489
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6222
bin: 9.75e1
variant carriers: 12

GenotypeQuality
all individuals: 1572
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3431
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4620
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 521
bin: 3.25e1
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: 11524
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 12
allele frequency: 1.82132774792824e-4
allele num: 65886
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6546
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10200
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.505e1

VQSLOD
type: SiteQuality
SIO_000300: 1.71e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.877e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

DP
type: SiteQuality
SIO_000300: 1.828126e6

MQ
type: SiteQuality
SIO_000300: 5.97e1

MQRankSum
type: SiteQuality
SIO_000300: 3.88e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.015e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.25e-1

GenotypeDepth
all individuals: 1737
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11851
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13843
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 898
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1569
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6211
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 4612
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3424
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9377
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 984
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 487
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 481
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 346
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25626
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2105
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 503
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3916
bin: 7.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16486
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6542
num of homozygotes: 0

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

African
type: Population
allele count: 4
allele frequency: 3.919263178522438e-4
allele num: 10206
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65892
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.39e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.505e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.7e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.63e-1

DP
type: SiteQuality
SIO_000300: 1.828392e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.9e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.794e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

MQ
type: SiteQuality
SIO_000300: 5.945e1

GenotypeDepth
all individuals: 133
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 979
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 79
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 452
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3916
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 346
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9377
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 487
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25626
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6211
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 481
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 984
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3424
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 503
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4612
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2105
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1569
bin: 8.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.517634917744187e-5
allele num: 65892
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16486
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10206
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6542
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.39e0

MQRankSum
type: SiteQuality
SIO_000300: -2.63e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.7e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.945e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.9e-2

QD
type: SiteQuality
SIO_000300: 1.505e1

DP
type: SiteQuality
SIO_000300: 1.828392e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.794e0

GenotypeDepth
all individuals: 987
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1745
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6513
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1571
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 65
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 493
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3408
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6212
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 25696
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 510
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 481
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9367
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3903
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2115
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4577
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 981
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 338
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.067961165048543e-5
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Latino
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East Asian
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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QD
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FS
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DP
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VQSLOD
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ReadPosRankSum
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MQ
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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European (Finnish)
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Latino
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European (Non-Finnish)
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South Asian
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MQ
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ReadPosRankSum
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VQSLOD
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DP
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MQRankSum
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InbreedingCoeff
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FS
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ClippingRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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South Asian
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Latino
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African
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East Asian
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InbreedingCoeff
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FS
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MQRankSum
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QD
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BaseQRankSum
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MQ
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VQSLOD
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DP
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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Other
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Latino
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South Asian
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East Asian
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FS
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DP
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VQSLOD
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ClippingRankSum
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MQ
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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Latino
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Other
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African
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European (Finnish)
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DP
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FS
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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QD
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InbreedingCoeff
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MQRankSum
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MQ
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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East Asian
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European (Non-Finnish)
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European (Finnish)
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African
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MQ
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FS
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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QD
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VQSLOD
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DP
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South Asian
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European (Finnish)
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European (Non-Finnish)
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Latino
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East Asian
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QD
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DP
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VQSLOD
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MQRankSum
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FS
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MQ
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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num of homozygotes: 0

European (Finnish)
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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

European (Non-Finnish)
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allele frequency: 1.516162290011523e-4
allele num: 65956
num of homozygotes: 0

African
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South Asian
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East Asian
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VQSLOD
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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QD
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ReadPosRankSum
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FS
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ClippingRankSum
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MQ
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
allele num: 10210
num of homozygotes: 0

Latino
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Other
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.51666818333485e-5
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num of homozygotes: 0

South Asian
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ReadPosRankSum
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DP
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MQRankSum
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VQSLOD
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QD
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ClippingRankSum
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InbreedingCoeff
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MQ
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BaseQRankSum
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FS
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

Other
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South Asian
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African
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East Asian
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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MQ
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FS
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QD
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DP
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GenotypeDepth
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variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
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African
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allele count: 1
allele frequency: 9.780907668231612e-5
allele num: 10224
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 3
allele frequency: 4.545316808581558e-5
allele num: 66002
num of homozygotes: 0

Other
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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FS
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MQ
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QD
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DP
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ClippingRankSum
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GenotypeDepth
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variant carriers: 7

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 117
allele frequency: 1.357308584686775e-2
allele num: 8620
num of homozygotes: 2

European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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Other
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African
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6532
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Latino
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ClippingRankSum
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FS
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QD
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MQRankSum
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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MQ
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DP
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Non-Finnish)
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African
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European (Finnish)
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East Asian
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South Asian
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FS
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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MQ
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VQSLOD
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QD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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num of homozygotes: 0

European (Finnish)
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African
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South Asian
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Other
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Latino
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East Asian
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DP
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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FS
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InbreedingCoeff
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MQ
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QD
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 4.25e1
variant carriers: 0

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

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

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

African
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allele count: 2
allele frequency: 1.95388823759281e-4
allele num: 10236
num of homozygotes: 0

Other
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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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European (Non-Finnish)
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allele count: 4
allele frequency: 6.05638494382703e-5
allele num: 66046
num of homozygotes: 0

FS
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DP
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ClippingRankSum
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QD
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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variant carriers: 2

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.51336299524804e-5
allele num: 66078
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10250
num of homozygotes: 0

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

South Asian
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Other
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East Asian
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allele frequency: 8.11500115928588e-4
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InbreedingCoeff
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BaseQRankSum
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MQ
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FS
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ClippingRankSum
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VQSLOD
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MQRankSum
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QD
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ReadPosRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6536
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66088
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

FS
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SIO_000300: 3.183e0

ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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DP
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QD
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MQ
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MQRankSum
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InbreedingCoeff
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SIO_000300: -1.0e-4

VQSLOD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 10282
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6536
num of homozygotes: 0

South Asian
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allele count: 2
allele frequency: 1.211827435773146e-4
allele num: 16504
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.510847887834653e-5
allele num: 66188
num of homozygotes: 0

Other
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allele count: 0
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MQRankSum
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DP
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InbreedingCoeff
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VQSLOD
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MQ
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ReadPosRankSum
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BaseQRankSum
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FS
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ClippingRankSum
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SIO_000300: 2.59e-1

QD
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GenotypeDepth
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.510391493475109e-5
allele num: 66208
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Other
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VQSLOD
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MQ
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BaseQRankSum
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FS
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QD
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ReadPosRankSum
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ClippingRankSum
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DP
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MQRankSum
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InbreedingCoeff
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GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.508978421608571e-5
allele num: 66270
num of homozygotes: 0

African
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Other
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South Asian
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Latino
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European (Finnish)
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InbreedingCoeff
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QD
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VQSLOD
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FS
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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MQ
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MQRankSum
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DP
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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num of homozygotes: 0

East Asian
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European (Finnish)
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African
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MQRankSum
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DP
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VQSLOD
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FS
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MQ
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ReadPosRankSum
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InbreedingCoeff
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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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South Asian
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African
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European (Finnish)
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European (Non-Finnish)
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East Asian
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InbreedingCoeff
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DP
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BaseQRankSum
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FS
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MQ
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MQRankSum
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QD
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ReadPosRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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East Asian
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European (Finnish)
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South Asian
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European (Non-Finnish)
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MQRankSum
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FS
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ReadPosRankSum
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QD
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VQSLOD
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DP
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MQ
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ClippingRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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African
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Latino
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Other
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South Asian
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East Asian
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BaseQRankSum
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DP
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FS
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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QD
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MQ
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GenotypeQuality
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European (Finnish)
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European (Non-Finnish)
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African
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MQ
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DP
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QD
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FS
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MQRankSum
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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VQSLOD
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MQRankSum
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MQ
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QD
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DP
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African
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Latino
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South Asian
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East Asian
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European (Non-Finnish)
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DP
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MQ
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FS
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VQSLOD
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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African
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South Asian
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QD
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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Latino
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East Asian
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InbreedingCoeff
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VQSLOD
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DP
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FS
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MQ
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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African
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East Asian
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European (Non-Finnish)
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MQ
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VQSLOD
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MQRankSum
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FS
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DP
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European (Finnish)
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VQSLOD
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DP
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QD
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African
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QD
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ReadPosRankSum
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DP
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European (Non-Finnish)
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VQSLOD
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DP
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MQ
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
all individuals: 28
bin: 4.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.017410458344649e-5
allele num: 66282
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: -9.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.212e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.21e-1

MQ
type: SiteQuality
SIO_000300: 5.966e1

VQSLOD
type: SiteQuality
SIO_000300: 1.84e0

DP
type: SiteQuality
SIO_000300: 1.84633e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.767e0

FS
type: SiteQuality
SIO_000300: 2.822e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.0e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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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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variant carriers: 0

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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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
all individuals: 26
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4583
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6556
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
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: 10324
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66186
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.01e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.563e0

QD
type: SiteQuality
SIO_000300: 1.063e1

FS
type: SiteQuality
SIO_000300: 1.069e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.46e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.27e0

DP
type: SiteQuality
SIO_000300: 1.84302e6

VQSLOD
type: SiteQuality
SIO_000300: 6.63e-1

GenotypeDepth
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bin: 7.75e1
variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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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: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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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bin: 9.75e1
variant carriers: 13

GenotypeQuality
all individuals: 52
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1533
bin: 8.75e1
variant carriers: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 13
allele frequency: 1.964636542239686e-4
allele num: 66170
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: 10316
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.11e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.86e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

QD
type: SiteQuality
SIO_000300: 1.314e1

MQ
type: SiteQuality
SIO_000300: 5.962e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.73e-1

DP
type: SiteQuality
SIO_000300: 1.843372e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.14e-1

GenotypeDepth
all individuals: 14303
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 74
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variant carriers: 0

GenotypeDepth
all individuals: 13
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
all individuals: 935
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 3813
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 9
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.75e1
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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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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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

GenotypeQuality
all individuals: 28354
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511258878645912e-5
allele num: 66170
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
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: 6552
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.73e-1

MQ
type: SiteQuality
SIO_000300: 5.962e1

VQSLOD
type: SiteQuality
SIO_000300: 2.86e0

DP
type: SiteQuality
SIO_000300: 1.843372e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.11e-1

QD
type: SiteQuality
SIO_000300: 1.314e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.14e-1

GenotypeDepth
all individuals: 73
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 36
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 13
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variant carriers: 0

GenotypeDepth
all individuals: 245
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variant carriers: 0

GenotypeQuality
all individuals: 2060
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4581
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variant carriers: 0

GenotypeQuality
all individuals: 76
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variant carriers: 0

GenotypeQuality
all individuals: 47
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 9640
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6140
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.513454611496201e-5
allele num: 66074
num of homozygotes: 0

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

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6532
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 1.491e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

QD
type: SiteQuality
SIO_000300: 2.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.8e-2

MQ
type: SiteQuality
SIO_000300: 5.951e1

MQRankSum
type: SiteQuality
SIO_000300: -7.93e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.381e0

DP
type: SiteQuality
SIO_000300: 1.837812e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.74e-1

GenotypeDepth
all individuals: 51
bin: 8.25e1
variant carriers: 31

GenotypeDepth
all individuals: 431
bin: 5.75e1
variant carriers: 20

GenotypeDepth
all individuals: 20014
bin: 2.75e1
variant carriers: 9

GenotypeDepth
all individuals: 51
bin: 9.25e1
variant carriers: 38

GenotypeDepth
all individuals: 231
bin: 9.75e1
variant carriers: 192

GenotypeQuality
all individuals: 48
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 219
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GenotypeQuality
all individuals: 27834
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 74
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GenotypeQuality
all individuals: 6474
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variant carriers: 556

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3780
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 800
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GenotypeQuality
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GenotypeQuality
all individuals: 1518
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GenotypeQuality
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GenotypeQuality
all individuals: 2020
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variant carriers: 1

GenotypeQuality
all individuals: 9589
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 461
allele frequency: 6.976603408093465e-3
allele num: 66078
num of homozygotes: 3

African
type: Population
allele count: 9
allele frequency: 8.751458576429405e-4
allele num: 10284
num of homozygotes: 0

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

South Asian
type: Population
allele count: 25
allele frequency: 1.514417252241338e-3
allele num: 16508
num of homozygotes: 0

Other
type: Population
allele count: 8
allele frequency: 8.948545861297539e-3
allele num: 894
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 39
allele frequency: 5.968778696051423e-3
allele num: 6534
num of homozygotes: 0

Latino
type: Population
allele count: 17
allele frequency: 1.471606648199446e-3
allele num: 11552
num of homozygotes: 1

MQ
type: SiteQuality
SIO_000300: 5.957e1

VQSLOD
type: SiteQuality
SIO_000300: 6.22e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.900000000000001e-3

BaseQRankSum
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SIO_000300: 5.97e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.61e-1

DP
type: SiteQuality
SIO_000300: 1.863985e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.820000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.348e1

GenotypeDepth
all individuals: 40
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variant carriers: 0

GenotypeDepth
all individuals: 1659
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variant carriers: 0

GenotypeDepth
all individuals: 20
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GenotypeDepth
all individuals: 18
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GenotypeDepth
all individuals: 239
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GenotypeQuality
all individuals: 9
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GenotypeQuality
all individuals: 9673
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 75
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 6014
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 249
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2048
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GenotypeQuality
all individuals: 3347
bin: 8.25e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10286
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.318e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.67e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.590000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.330000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.91e-1

MQ
type: SiteQuality
SIO_000300: 5.95e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.865e0

DP
type: SiteQuality
SIO_000300: 1.834613e6

GenotypeDepth
all individuals: 350
bin: 1.75e1
variant carriers: 3

GenotypeDepth
all individuals: 11240
bin: 2.25e1
variant carriers: 8

GenotypeDepth
all individuals: 423
bin: 5.75e1
variant carriers: 11

GenotypeDepth
all individuals: 82
bin: 7.25e1
variant carriers: 10

GenotypeDepth
all individuals: 1665
bin: 4.75e1
variant carriers: 14

GenotypeDepth
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bin: 9.75e1
variant carriers: 16

GenotypeDepth
all individuals: 30
bin: 8.75e1
variant carriers: 12

GenotypeQuality
all individuals: 4579
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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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bin: 9.75e1
variant carriers: 138

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 9633
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variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.750390015600624e-5
allele num: 10256
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 20
allele frequency: 3.078817733990148e-3
allele num: 6496
num of homozygotes: 0

Latino
type: Population
allele count: 6
allele frequency: 5.193006750908776e-4
allele num: 11554
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 109
allele frequency: 1.651965687611773e-3
allele num: 65982
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.242152466367713e-3
allele num: 892
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.69e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.115e0

MQ
type: SiteQuality
SIO_000300: 5.952e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 4.05e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.72e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.65e-1

FS
type: SiteQuality
SIO_000300: 6.66e-1

DP
type: SiteQuality
SIO_000300: 1.835691e6

QD
type: SiteQuality
SIO_000300: 1.093e1

GenotypeDepth
all individuals: 39
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 19
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 41
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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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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variant carriers: 0

GenotypeQuality
all individuals: 3344
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5981
bin: 9.75e1
variant carriers: 4

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6500
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10254
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.06446526577519e-5
allele num: 65958
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.93e0

QD
type: SiteQuality
SIO_000300: 1.147e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.72e-1

DP
type: SiteQuality
SIO_000300: 1.830557e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.79e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.785e0

FS
type: SiteQuality
SIO_000300: 4.644e0

MQRankSum
type: SiteQuality
SIO_000300: 1.17e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

GenotypeDepth
all individuals: 240
bin: 6.25e1
variant carriers: 5

GenotypeDepth
all individuals: 23
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variant carriers: 3

GenotypeQuality
all individuals: 147
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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
all individuals: 1240
bin: 2.25e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 6007
bin: 9.75e1
variant carriers: 50

GenotypeQuality
all individuals: 288
bin: 3.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 47
allele frequency: 7.151769682583158e-4
allele num: 65718
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.600104004160167e-4
allele num: 11538
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10214
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.309e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.359e0

DP
type: SiteQuality
SIO_000300: 1.819068e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.82e0

MQRankSum
type: SiteQuality
SIO_000300: -2.5e-2

MQ
type: SiteQuality
SIO_000300: 5.964e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.0e-2

FS
type: SiteQuality
SIO_000300: 9.23e-1

GenotypeDepth
all individuals: 6396
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 38
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variant carriers: 0

GenotypeQuality
all individuals: 73
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variant carriers: 0

GenotypeQuality
all individuals: 3754
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variant carriers: 0

GenotypeQuality
all individuals: 147
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variant carriers: 0

GenotypeQuality
all individuals: 110
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variant carriers: 0

GenotypeQuality
all individuals: 186
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variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 26710
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6007
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 2035
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variant carriers: 0

GenotypeQuality
all individuals: 4561
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: 886
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65718
num of homozygotes: 0

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

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

African
type: Population
allele count: 4
allele frequency: 3.916193459956922e-4
allele num: 10214
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.819068e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.359e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e-1

FS
type: SiteQuality
SIO_000300: 9.23e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.0e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.82e0

MQRankSum
type: SiteQuality
SIO_000300: -2.5e-2

QD
type: SiteQuality
SIO_000300: 1.309e1

MQ
type: SiteQuality
SIO_000300: 5.964e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 1515
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 5959
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variant carriers: 4

GenotypeQuality
all individuals: 185
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 4
allele frequency: 3.916960438699569e-4
allele num: 10212
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11530
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: 65678
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6436
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.056e1

InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
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FS
type: SiteQuality
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DP
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ReadPosRankSum
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SIO_000300: 4.62e-1

MQ
type: SiteQuality
SIO_000300: 5.891e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.69e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.03e0

GenotypeDepth
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6416
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11512
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65556
num of homozygotes: 0

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

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

InbreedingCoeff
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SIO_000300: -9.0e-4

ClippingRankSum
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FS
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BaseQRankSum
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MQRankSum
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QD
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DP
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VQSLOD
type: SiteQuality
SIO_000300: 7.73e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.4e-2

MQ
type: SiteQuality
SIO_000300: 5.949e1

GenotypeDepth
all individuals: 20
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 8785
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GenotypeQuality
all individuals: 1951
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variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10198
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65512
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -1.45e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.53e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 9.35e0

DP
type: SiteQuality
SIO_000300: 1.775942e6

ClippingRankSum
type: SiteQuality
SIO_000300: 7.75e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

FS
type: SiteQuality
SIO_000300: 3.729e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.499e0

VQSLOD
type: SiteQuality
SIO_000300: -4.875e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 4

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1591
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65436
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10186
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6396
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

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

East Asian
type: Population
allele count: 4
allele frequency: 4.651162790697675e-4
allele num: 8600
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.86e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.416e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.71e-1

MQ
type: SiteQuality
SIO_000300: 5.925e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.1e-2

MQRankSum
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SIO_000300: 1.05e0

DP
type: SiteQuality
SIO_000300: 1.761073e6

VQSLOD
type: SiteQuality
SIO_000300: 6.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

QD
type: SiteQuality
SIO_000300: 1.287e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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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: 5932
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variant carriers: 1

GenotypeQuality
all individuals: 7724
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10168
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11466
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65200
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6384
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.165501165501166e-4
allele num: 8580
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 9.360000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.8e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.76e-1

QD
type: SiteQuality
SIO_000300: 1.22e1

FS
type: SiteQuality
SIO_000300: 5.961e0

MQRankSum
type: SiteQuality
SIO_000300: 4.2e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.76e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.722585e6

GenotypeDepth
all individuals: 11724
bin: 3.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1662
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variant carriers: 0

GenotypeQuality
all individuals: 3368
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16466
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65158
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11468
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.334812047630166e-4
allele num: 8566
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10162
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6374
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.3e-1

DP
type: SiteQuality
SIO_000300: 1.715001e6

MQRankSum
type: SiteQuality
SIO_000300: -4.5e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.64e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.57e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.9e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

QD
type: SiteQuality
SIO_000300: 1.289e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 161
bin: 6.75e1
variant carriers: 53

GenotypeDepth
all individuals: 29
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variant carriers: 11

GenotypeQuality
all individuals: 2569
bin: 5.25e1
variant carriers: 41

GenotypeQuality
all individuals: 85
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variant carriers: 2

GenotypeQuality
all individuals: 1979
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variant carriers: 13

GenotypeQuality
all individuals: 1384
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variant carriers: 26

GenotypeQuality
all individuals: 2334
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variant carriers: 13

GenotypeQuality
all individuals: 1922
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variant carriers: 59

GenotypeQuality
all individuals: 8563
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variant carriers: 3158

GenotypeQuality
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bin: 2.75e1
variant carriers: 11

GenotypeQuality
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variant carriers: 5

GenotypeQuality
all individuals: 6300
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variant carriers: 53

GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 22

GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 61

GenotypeQuality
all individuals: 3539
bin: 4.75e1
variant carriers: 26

GenotypeQuality
all individuals: 1015
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variant carriers: 19

GenotypeQuality
all individuals: 13940
bin: 6.25e1
variant carriers: 44

GenotypeQuality
all individuals: 1966
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variant carriers: 6

GenotypeQuality
all individuals: 3088
bin: 7.25e1
variant carriers: 37

GenotypeQuality
all individuals: 3096
bin: 8.25e1
variant carriers: 48

Latino
type: Population
allele count: 197
allele frequency: 1.727767058410805e-2
allele num: 11402
num of homozygotes: 4

South Asian
type: Population
allele count: 8
allele frequency: 4.86322188449848e-4
allele num: 16450
num of homozygotes: 1

Other
type: Population
allele count: 15
allele frequency: 1.716247139588101e-2
allele num: 874
num of homozygotes: 0

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

African
type: Population
allele count: 4149
allele frequency: 4.094138543516874e-1
allele num: 10134
num of homozygotes: 867

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6346
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 103
allele frequency: 1.584664143512108e-3
allele num: 64998
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.77e-1

QD
type: SiteQuality
SIO_000300: 2.039e1

FS
type: SiteQuality
SIO_000300: 1.43e0

MQRankSum
type: SiteQuality
SIO_000300: 1.12e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.9e-2

InbreedingCoeff
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SIO_000300: 3.251e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.536e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.51e-1

DP
type: SiteQuality
SIO_000300: 1.709924e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1472
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GenotypeQuality
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GenotypeQuality
all individuals: 2013
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6338
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10116
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16412
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11392
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.149425287356322e-3
allele num: 870
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64894
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8534
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.416e0

FS
type: SiteQuality
SIO_000300: 3.055e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.92e-1

ReadPosRankSum
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SIO_000300: 7.9e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.54e-1

DP
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SIO_000300: 1.68856e6

MQRankSum
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SIO_000300: -7.9e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

QD
type: SiteQuality
SIO_000300: 2.223e1

GenotypeDepth
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7592
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 492
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 7556
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 334
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2316
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.51e-1

InbreedingCoeff
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DP
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VQSLOD
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BaseQRankSum
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MQRankSum
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SIO_000300: 7.51e-1

ClippingRankSum
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SIO_000300: 1.54e0

FS
type: SiteQuality
SIO_000300: 3.979e0

QD
type: SiteQuality
SIO_000300: 1.485e1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
all individuals: 7
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 677
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 557
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 264
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GenotypeQuality
all individuals: 578
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 309
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GenotypeQuality
all individuals: 799
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variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 336
num of homozygotes: 0

European (Non-Finnish)
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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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num of homozygotes: 0

African
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num of homozygotes: 0

InbreedingCoeff
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DP
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ReadPosRankSum
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QD
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ClippingRankSum
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VQSLOD
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FS
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BaseQRankSum
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MQ
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MQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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African
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South Asian
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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European (Non-Finnish)
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MQRankSum
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ReadPosRankSum
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MQ
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DP
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FS
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele frequency: 4.317789291882556e-4
allele num: 2316
num of homozygotes: 0

Latino
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num of homozygotes: 0

South Asian
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num of homozygotes: 0

Other
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European (Non-Finnish)
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East Asian
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European (Finnish)
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VQSLOD
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ReadPosRankSum
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DP
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MQRankSum
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MQ
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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FS
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QD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 4.325259515570934e-4
allele num: 2312
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 7598
num of homozygotes: 0

South Asian
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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

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

East Asian
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Other
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num of homozygotes: 0

MQRankSum
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MQ
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VQSLOD
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BaseQRankSum
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FS
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QD
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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African
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South Asian
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East Asian
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Latino
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European (Non-Finnish)
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MQRankSum
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InbreedingCoeff
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MQ
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BaseQRankSum
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VQSLOD
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DP
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QD
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FS
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ClippingRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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African
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Latino
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East Asian
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Other
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European (Non-Finnish)
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ClippingRankSum
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MQRankSum
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VQSLOD
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InbreedingCoeff
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FS
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QD
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DP
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MQ
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ReadPosRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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Latino
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East Asian
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African
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European (Non-Finnish)
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DP
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FS
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QD
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MQ
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 503
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 321
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 5514
bin: 2.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2382
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 520
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7828
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 346
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 192
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 32
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7760
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

FS
type: SiteQuality
SIO_000300: 3.68e0

QD
type: SiteQuality
SIO_000300: 6.29e0

DP
type: SiteQuality
SIO_000300: 3.83196e5

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.402e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.01e-2

GenotypeDepth
all individuals: 10
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 7.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 2179
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1572
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1031
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5700
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 355
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1077
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2634
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33579
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 870
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 360
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 507
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 435
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 325
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4607
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2384
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 346
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 520
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7774
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7842
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.746e1

DP
type: SiteQuality
SIO_000300: 3.85218e5

VQSLOD
type: SiteQuality
SIO_000300: -1.697e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.72e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.59e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.98e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -5.72e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeDepth
all individuals: 876
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 482
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 29
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 96
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5101
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 31
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1596
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 470
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 520
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10092
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1347
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32246
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 297
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1483
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1100
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 133
bin: 3.75e1
variant carriers: 0