9-130939818-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130939818
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130939818
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 8854
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000471839
  gene symbol: CIZ1
  hgvsc: ENST00000471839.1:n.43+27G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1650+27G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1731+27G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1578+27G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1818+27G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1734+27G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1515+27G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1818+27G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+1834G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1584+27G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1818+27G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1734+27G>A
  variant of: http://identifiers.org/hgnc/16744
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37072
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2897
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

9-130939820-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130939820
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130939820
    reference: chr 9
allele count: 1
allele frequency: 1.125365743866757e-4
allele num: 8886
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1734+25G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1734+25G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1650+25G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1731+25G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000471839
  gene symbol: CIZ1
  hgvsc: ENST00000471839.1:n.43+25G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1818+25G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1584+25G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1578+25G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1515+25G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1818+25G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+1832G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1818+25G>A
  variant of: http://identifiers.org/hgnc/16744
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37718
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ

9-130939825-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130939825
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130939825
    reference: chr 9
allele count: 566
allele frequency: 6.227992957746479e-2
allele num: 9088
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1578+20G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000471839
  gene symbol: CIZ1
  hgvsc: ENST00000471839.1:n.43+20G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1818+20G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1818+20G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1515+20G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1731+20G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+1827G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1584+20G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1650+20G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1734+20G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1734+20G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1818+20G>A
  variant of: http://identifiers.org/hgnc/16744
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 3.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 38611
  bin: 2.5e0
  variant carriers: 172
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 2.25e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 4.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 4.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 2.75e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 4697
  bin: 7.5e0
  variant carriers: 285
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 3.25e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 1.25e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.25e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 1.75e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 28
genotype quality: GenotypeQuality
num of homozygotes: 65
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

9-130939833-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130939833
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130939833
    reference: chr 9
allele count: 1
allele frequency: 1.076194575979337e-4
allele num: 9292
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1818+12G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1584+12G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+1819G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1515+12G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1818+12G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1578+12G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1818+12G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000471839
  gene symbol: CIZ1
  hgvsc: ENST00000471839.1:n.43+12G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1650+12G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1734+12G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1731+12G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1734+12G>A
  variant of: http://identifiers.org/hgnc/16744
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7202
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39926
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum

9-130939842-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130939842
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130939842
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 9740
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1731+3A>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1584+3A>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1578+3A>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+1810A>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000471839
  gene symbol: CIZ1
  hgvsc: ENST00000471839.1:n.43+3A>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1818+3A>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1734+3A>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1650+3A>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1818+3A>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1818+3A>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1734+3A>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1515+3A>T
  variant of: http://identifiers.org/hgnc/16744
canonical: true
consequence: splice region
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1684
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10970
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38700
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1588
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1818+3A>T
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQ

9-130939872-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130939872
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130939872
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 14020
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1707C>T
  hgvsp: ENST00000277465.4:c.1707C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1623C>T
  hgvsp: ENST00000372948.3:c.1623C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1488C>T
  hgvsp: ENST00000541172.1:c.1488C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.812C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1704C>T
  hgvsp: ENST00000325721.8:c.1704C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1791C>T
  hgvsp: ENST00000393608.1:c.1791C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.848C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000471839
  gene symbol: CIZ1
  hgvsc: ENST00000471839.1:n.16C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1791C>T
  hgvsp: ENST00000372938.5:c.1791C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+1780C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1551C>T
  hgvsp: ENST00000372954.1:c.1551C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1557C>T
  hgvsp: ENST00000415526.1:c.1557C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1707C>T
  hgvsp: ENST00000357558.5:c.1707C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1791C>T
  hgvsp: ENST00000538431.1:c.1791C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26437
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25452
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile597Ile
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ

9-130939875-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130939875
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130939875
    reference: chr 9
allele count: 2
allele frequency: 1.38217000691085e-4
allele num: 14470
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1788C>T
  hgvsp: ENST00000538431.1:c.1788C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1704C>T
  hgvsp: ENST00000357558.5:c.1704C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1548C>T
  hgvsp: ENST00000372954.1:c.1548C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1788C>T
  hgvsp: ENST00000372938.5:c.1788C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1788C>T
  hgvsp: ENST00000393608.1:c.1788C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1620C>T
  hgvsp: ENST00000372948.3:c.1620C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1704C>T
  hgvsp: ENST00000277465.4:c.1704C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1554C>T
  hgvsp: ENST00000415526.1:c.1554C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1485C>T
  hgvsp: ENST00000541172.1:c.1485C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.809C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1701C>T
  hgvsp: ENST00000325721.8:c.1701C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000471839
  gene symbol: CIZ1
  hgvsc: ENST00000471839.1:n.13C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.845C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+1777C>T
  variant of: http://identifiers.org/hgnc/16744
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27633
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2045
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24162
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1871
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr596Tyr
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: G
site quality: FS
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum

9-130939918-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130939918
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130939918
    reference: chr 9
allele count: 1
allele frequency: 3.389141191622043e-5
allele num: 29506
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+1734C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1505C>T
  hgvsp: ENSP00000362045.1:p.Ala502Val
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1577C>T
  hgvsp: ENSP00000362039.3:p.Ala526Val
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1658C>T
  hgvsp: ENSP00000320374.8:p.Ala553Val
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1661C>T
  hgvsp: ENSP00000277465.4:p.Ala554Val
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.766C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1745C>T
  hgvsp: ENSP00000362029.5:p.Ala582Val
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1442C>T
  hgvsp: ENSP00000445057.1:p.Ala481Val
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1745C>T
  hgvsp: ENSP00000439244.1:p.Ala582Val
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1745C>T
  hgvsp: ENSP00000377232.1:p.Ala582Val
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1511C>T
  hgvsp: ENSP00000398011.1:p.Ala504Val
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1661C>T
  hgvsp: ENSP00000350169.5:p.Ala554Val
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.802C>T
  variant of: http://identifiers.org/hgnc/16744
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9431
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5355
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5346
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35701
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2252
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala582Val
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ

9-130939921-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130939921
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130939921
    reference: chr 9
allele count: 1
allele frequency: 3.175813008130082e-5
allele num: 31488
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1658C>T
  hgvsp: ENSP00000350169.5:p.Ala553Val
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1658C>T
  hgvsp: ENSP00000277465.4:p.Ala553Val
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1574C>T
  hgvsp: ENSP00000362039.3:p.Ala525Val
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1742C>T
  hgvsp: ENSP00000439244.1:p.Ala581Val
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1439C>T
  hgvsp: ENSP00000445057.1:p.Ala480Val
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1742C>T
  hgvsp: ENSP00000377232.1:p.Ala581Val
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1502C>T
  hgvsp: ENSP00000362045.1:p.Ala501Val
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1742C>T
  hgvsp: ENSP00000362029.5:p.Ala581Val
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1655C>T
  hgvsp: ENSP00000320374.8:p.Ala552Val
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1508C>T
  hgvsp: ENSP00000398011.1:p.Ala503Val
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.763C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.799C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+1731C>T
  variant of: http://identifiers.org/hgnc/16744
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1637
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2374
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8516
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5697
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5890
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala581Val
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: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum

9-130939928-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130939928
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130939928
    reference: chr 9
allele count: 2
allele frequency: 5.600044800358403e-5
allele num: 35714
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1735A>G
  hgvsp: ENSP00000362029.5:p.Thr579Ala
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1501A>G
  hgvsp: ENSP00000398011.1:p.Thr501Ala
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1432A>G
  hgvsp: ENSP00000445057.1:p.Thr478Ala
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.756A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.792A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1648A>G
  hgvsp: ENSP00000320374.8:p.Thr550Ala
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1651A>G
  hgvsp: ENSP00000277465.4:p.Thr551Ala
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1495A>G
  hgvsp: ENSP00000362045.1:p.Thr499Ala
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1567A>G
  hgvsp: ENSP00000362039.3:p.Thr523Ala
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1735A>G
  hgvsp: ENSP00000377232.1:p.Thr579Ala
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1735A>G
  hgvsp: ENSP00000439244.1:p.Thr579Ala
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1651A>G
  hgvsp: ENSP00000350169.5:p.Thr551Ala
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+1724A>G
  variant of: http://identifiers.org/hgnc/16744
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1876
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7273
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34626
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6740
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr579Ala
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

9-130939930-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130939930
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130939930
    reference: chr 9
allele count: 674
allele frequency: 1.754385964912281e-2
allele num: 38418
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1565C>T
  hgvsp: ENSP00000362039.3:p.Ser522Phe
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1499C>T
  hgvsp: ENSP00000398011.1:p.Ser500Phe
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1733C>T
  hgvsp: ENSP00000439244.1:p.Ser578Phe
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1646C>T
  hgvsp: ENSP00000320374.8:p.Ser549Phe
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1733C>T
  hgvsp: ENSP00000377232.1:p.Ser578Phe
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1493C>T
  hgvsp: ENSP00000362045.1:p.Ser498Phe
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1649C>T
  hgvsp: ENSP00000277465.4:p.Ser550Phe
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1430C>T
  hgvsp: ENSP00000445057.1:p.Ser477Phe
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.790C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.754C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1733C>T
  hgvsp: ENSP00000362029.5:p.Ser578Phe
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1649C>T
  hgvsp: ENSP00000350169.5:p.Ser550Phe
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+1722C>T
  variant of: http://identifiers.org/hgnc/16744
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 2024
  bin: 1.75e1
  variant carriers: 144
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 34362
  bin: 7.5e0
  variant carriers: 203
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 3.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 4.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 6463
  bin: 2.5e0
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 7490
  bin: 2.25e1
  variant carriers: 58
genotype depth: GenotypeDepth
  all individuals: 6510
  bin: 1.25e1
  variant carriers: 243
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
hgvs: p.Ser578Phe
num of homozygotes: 24
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQRankSum

9-130939932-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130939932
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130939932
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 39344
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1731C>A
  hgvsp: ENST00000538431.1:c.1731C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1731C>A
  hgvsp: ENST00000372938.5:c.1731C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1497C>A
  hgvsp: ENST00000415526.1:c.1497C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1647C>A
  hgvsp: ENST00000277465.4:c.1647C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1491C>A
  hgvsp: ENST00000372954.1:c.1491C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1731C>A
  hgvsp: ENST00000393608.1:c.1731C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1644C>A
  hgvsp: ENST00000325721.8:c.1644C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1647C>A
  hgvsp: ENST00000357558.5:c.1647C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1563C>A
  hgvsp: ENST00000372948.3:c.1563C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.752C>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1428C>A
  hgvsp: ENST00000541172.1:c.1428C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.788C>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+1720C>A
  variant of: http://identifiers.org/hgnc/16744
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2770
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6201
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6537
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7856
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34268
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser577Ser
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

9-130939933-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130939933
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130939933
    reference: chr 9
allele count: 9
allele frequency: 2.256430827859399e-4
allele num: 39886
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.787C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1646C>T
  hgvsp: ENSP00000277465.4:p.Ser549Phe
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1427C>T
  hgvsp: ENSP00000445057.1:p.Ser476Phe
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1490C>T
  hgvsp: ENSP00000362045.1:p.Ser497Phe
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1730C>T
  hgvsp: ENSP00000377232.1:p.Ser577Phe
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1562C>T
  hgvsp: ENSP00000362039.3:p.Ser521Phe
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1496C>T
  hgvsp: ENSP00000398011.1:p.Ser499Phe
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.751C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1730C>T
  hgvsp: ENSP00000439244.1:p.Ser577Phe
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1643C>T
  hgvsp: ENSP00000320374.8:p.Ser548Phe
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1646C>T
  hgvsp: ENSP00000350169.5:p.Ser549Phe
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+1719C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1730C>T
  hgvsp: ENSP00000362029.5:p.Ser577Phe
  variant of: http://identifiers.org/hgnc/16744
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34168
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1987
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6070
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6563
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser577Phe
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

9-130939937-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130939937
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130939937
    reference: chr 9
allele count: 37
allele frequency: 8.886540493803439e-4
allele num: 41636
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1726G>A
  hgvsp: ENSP00000362029.5:p.Val576Ile
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1423G>A
  hgvsp: ENSP00000445057.1:p.Val475Ile
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.783G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1726G>A
  hgvsp: ENSP00000377232.1:p.Val576Ile
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1639G>A
  hgvsp: ENSP00000320374.8:p.Val547Ile
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.747G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1492G>A
  hgvsp: ENSP00000398011.1:p.Val498Ile
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1642G>A
  hgvsp: ENSP00000277465.4:p.Val548Ile
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1486G>A
  hgvsp: ENSP00000362045.1:p.Val496Ile
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+1715G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1642G>A
  hgvsp: ENSP00000350169.5:p.Val548Ile
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1726G>A
  hgvsp: ENSP00000439244.1:p.Val576Ile
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1558G>A
  hgvsp: ENSP00000362039.3:p.Val520Ile
  variant of: http://identifiers.org/hgnc/16744
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2879
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5440
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8855
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33670
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 1.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 6636
  bin: 1.25e1
  variant carriers: 15
genotype quality: GenotypeQuality
hgvs: p.Val576Ile
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum

9-130939938-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130939938
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130939938
    reference: chr 9
allele count: 2
allele frequency: 4.686035613870666e-5
allele num: 42680
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1641C>T
  hgvsp: ENST00000277465.4:c.1641C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1638C>T
  hgvsp: ENST00000325721.8:c.1638C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1557C>T
  hgvsp: ENST00000372948.3:c.1557C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1641C>T
  hgvsp: ENST00000357558.5:c.1641C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1491C>T
  hgvsp: ENST00000415526.1:c.1491C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.746C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1485C>T
  hgvsp: ENST00000372954.1:c.1485C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1725C>T
  hgvsp: ENST00000538431.1:c.1725C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1725C>T
  hgvsp: ENST00000393608.1:c.1725C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1422C>T
  hgvsp: ENST00000541172.1:c.1422C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.782C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+1714C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1725C>T
  hgvsp: ENST00000372938.5:c.1725C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2155
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9161
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2970
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5160
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33478
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6707
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser575Ser
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD
site quality: BaseQRankSum

9-130939951-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130939951
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130939951
    reference: chr 9
allele count: 3
allele frequency: 5.933544303797468e-5
allele num: 50560
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1628G>A
  hgvsp: ENSP00000350169.5:p.Arg543His
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.769G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1712G>A
  hgvsp: ENSP00000439244.1:p.Arg571His
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.733G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1628G>A
  hgvsp: ENSP00000277465.4:p.Arg543His
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1472G>A
  hgvsp: ENSP00000362045.1:p.Arg491His
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1712G>A
  hgvsp: ENSP00000377232.1:p.Arg571His
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1712G>A
  hgvsp: ENSP00000362029.5:p.Arg571His
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1409G>A
  hgvsp: ENSP00000445057.1:p.Arg470His
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+1701G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1478G>A
  hgvsp: ENSP00000398011.1:p.Arg493His
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1544G>A
  hgvsp: ENSP00000362039.3:p.Arg515His
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1625G>A
  hgvsp: ENSP00000320374.8:p.Arg542His
  variant of: http://identifiers.org/hgnc/16744
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6548
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12903
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2150
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 31059
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3621
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg571His
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

9-130939952-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130939952
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130939952
    reference: chr 9
allele count: 5
allele frequency: 9.653255077612171e-5
allele num: 51796
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1477C>T
  hgvsp: ENSP00000398011.1:p.Arg493Cys
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+1700C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1624C>T
  hgvsp: ENSP00000320374.8:p.Arg542Cys
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1627C>T
  hgvsp: ENSP00000277465.4:p.Arg543Cys
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1711C>T
  hgvsp: ENSP00000362029.5:p.Arg571Cys
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1711C>T
  hgvsp: ENSP00000377232.1:p.Arg571Cys
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.732C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1408C>T
  hgvsp: ENSP00000445057.1:p.Arg470Cys
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1471C>T
  hgvsp: ENSP00000362045.1:p.Arg491Cys
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1627C>T
  hgvsp: ENSP00000350169.5:p.Arg543Cys
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1711C>T
  hgvsp: ENSP00000439244.1:p.Arg571Cys
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.768C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1543C>T
  hgvsp: ENSP00000362039.3:p.Arg515Cys
  variant of: http://identifiers.org/hgnc/16744
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6485
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30709
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3449
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13435
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg571Cys
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

9-130939960-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130939960
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130939960
    reference: chr 9
allele count: 8
allele frequency: 1.36518771331058e-4
allele num: 58600
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1616C>T
  hgvsp: ENSP00000320374.8:p.Pro539Leu
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1703C>T
  hgvsp: ENSP00000377232.1:p.Pro568Leu
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1535C>T
  hgvsp: ENSP00000362039.3:p.Pro512Leu
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1619C>T
  hgvsp: ENSP00000350169.5:p.Pro540Leu
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1619C>T
  hgvsp: ENSP00000277465.4:p.Pro540Leu
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1469C>T
  hgvsp: ENSP00000398011.1:p.Pro490Leu
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1703C>T
  hgvsp: ENSP00000439244.1:p.Pro568Leu
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1400C>T
  hgvsp: ENSP00000445057.1:p.Pro467Leu
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1463C>T
  hgvsp: ENSP00000362045.1:p.Pro488Leu
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.760C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1703C>T
  hgvsp: ENSP00000362029.5:p.Pro568Leu
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.724C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+1692C>T
  variant of: http://identifiers.org/hgnc/16744
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6143
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28431
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1898
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16839
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3732
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro568Leu
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/9-130939986-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130939986
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130939986
    reference: chr 9
allele count: 1
allele frequency: 1.518141794443601e-5
allele num: 65870
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1677G>T
  hgvsp: ENST00000538431.1:c.1677G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1677G>T
  hgvsp: ENST00000393608.1:c.1677G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+1666G>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1374G>T
  hgvsp: ENST00000541172.1:c.1374G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1593G>T
  hgvsp: ENST00000357558.5:c.1593G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1443G>T
  hgvsp: ENST00000415526.1:c.1443G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.734G>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1437G>T
  hgvsp: ENST00000372954.1:c.1437G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1590G>T
  hgvsp: ENST00000325721.8:c.1590G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1677G>T
  hgvsp: ENST00000372938.5:c.1677G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1593G>T
  hgvsp: ENST00000277465.4:c.1593G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.698G>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1509G>T
  hgvsp: ENST00000372948.3:c.1509G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19102
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2040
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25527
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4459
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg559Arg
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

9-130939988-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130939988
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130939988
    reference: chr 9
allele count: 2
allele frequency: 3.035914872946963e-5
allele num: 65878
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1675C>T
  hgvsp: ENSP00000377232.1:p.Arg559Trp
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1675C>T
  hgvsp: ENSP00000362029.5:p.Arg559Trp
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1435C>T
  hgvsp: ENSP00000362045.1:p.Arg479Trp
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1591C>T
  hgvsp: ENSP00000277465.4:p.Arg531Trp
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1507C>T
  hgvsp: ENSP00000362039.3:p.Arg503Trp
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1588C>T
  hgvsp: ENSP00000320374.8:p.Arg530Trp
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1675C>T
  hgvsp: ENSP00000439244.1:p.Arg559Trp
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1372C>T
  hgvsp: ENSP00000445057.1:p.Arg458Trp
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.732C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1441C>T
  hgvsp: ENSP00000398011.1:p.Arg481Trp
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+1664C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1591C>T
  hgvsp: ENSP00000350169.5:p.Arg531Trp
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.696C>T
  variant of: http://identifiers.org/hgnc/16744
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1958
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18910
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2130
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg559Trp
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

9-130939992-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130939992
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130939992
    reference: chr 9
allele count: 1
allele frequency: 1.503985561738607e-5
allele num: 66490
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1587C>G
  hgvsp: ENSP00000277465.4:p.Asp529Glu
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.728C>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1437C>G
  hgvsp: ENSP00000398011.1:p.Asp479Glu
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1503C>G
  hgvsp: ENSP00000362039.3:p.Asp501Glu
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1671C>G
  hgvsp: ENSP00000439244.1:p.Asp557Glu
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1368C>G
  hgvsp: ENSP00000445057.1:p.Asp456Glu
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1671C>G
  hgvsp: ENSP00000377232.1:p.Asp557Glu
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1431C>G
  hgvsp: ENSP00000362045.1:p.Asp477Glu
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1584C>G
  hgvsp: ENSP00000320374.8:p.Asp528Glu
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1671C>G
  hgvsp: ENSP00000362029.5:p.Asp557Glu
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+1660C>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1587C>G
  hgvsp: ENSP00000350169.5:p.Asp529Glu
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.692C>G
  variant of: http://identifiers.org/hgnc/16744
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4542
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25181
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1972
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2009
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Asp557Glu
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP

9-130940010-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130940010
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130940010
    reference: chr 9
allele count: 1
allele frequency: 1.577386585904473e-5
allele num: 63396
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1485C>T
  hgvsp: ENST00000372948.3:c.1485C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.710C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1569C>T
  hgvsp: ENST00000277465.4:c.1569C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1653C>T
  hgvsp: ENST00000372938.5:c.1653C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.674C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1419C>T
  hgvsp: ENST00000415526.1:c.1419C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1413C>T
  hgvsp: ENST00000372954.1:c.1413C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1569C>T
  hgvsp: ENST00000357558.5:c.1569C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1566C>T
  hgvsp: ENST00000325721.8:c.1566C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1653C>T
  hgvsp: ENST00000393608.1:c.1653C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1653C>T
  hgvsp: ENST00000538431.1:c.1653C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1350C>T
  hgvsp: ENST00000541172.1:c.1350C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+1642C>T
  variant of: http://identifiers.org/hgnc/16744
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15213
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2053
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26055
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9435
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2582
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr551Thr
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

9-130940018-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130940018
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130940018
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 60026
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1561A>C
  hgvsp: ENSP00000277465.4:p.Lys521Gln
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1645A>C
  hgvsp: ENSP00000377232.1:p.Lys549Gln
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1342A>C
  hgvsp: ENSP00000445057.1:p.Lys448Gln
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1411A>C
  hgvsp: ENSP00000398011.1:p.Lys471Gln
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1477A>C
  hgvsp: ENSP00000362039.3:p.Lys493Gln
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1405A>C
  hgvsp: ENSP00000362045.1:p.Lys469Gln
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1561A>C
  hgvsp: ENSP00000350169.5:p.Lys521Gln
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1558A>C
  hgvsp: ENSP00000320374.8:p.Lys520Gln
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+1634A>C
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.702A>C
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.666A>C
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1645A>C
  hgvsp: ENSP00000439244.1:p.Lys549Gln
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1645A>C
  hgvsp: ENSP00000362029.5:p.Lys549Gln
  variant of: http://identifiers.org/hgnc/16744
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3204
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27121
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4015
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11183
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys549Gln
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum

9-130940028-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130940028
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130940028
    reference: chr 9
allele count: 3
allele frequency: 5.649291955408256e-5
allele num: 53104
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.656G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.692G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1332G>A
  hgvsp: ENST00000541172.1:c.1332G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1635G>A
  hgvsp: ENST00000538431.1:c.1635G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1467G>A
  hgvsp: ENST00000372948.3:c.1467G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1401G>A
  hgvsp: ENST00000415526.1:c.1401G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1635G>A
  hgvsp: ENST00000393608.1:c.1635G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1548G>A
  hgvsp: ENST00000325721.8:c.1548G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1551G>A
  hgvsp: ENST00000357558.5:c.1551G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+1624G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1395G>A
  hgvsp: ENST00000372954.1:c.1395G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1635G>A
  hgvsp: ENST00000372938.5:c.1635G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1551G>A
  hgvsp: ENST00000277465.4:c.1551G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2785
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13508
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4868
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2548
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7590
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28647
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly545Gly
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: BaseQRankSum

9-130940030-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130940030
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130940030
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 52122
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1330G>A
  hgvsp: ENSP00000445057.1:p.Gly444Arg
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1633G>A
  hgvsp: ENSP00000362029.5:p.Gly545Arg
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1633G>A
  hgvsp: ENSP00000377232.1:p.Gly545Arg
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1465G>A
  hgvsp: ENSP00000362039.3:p.Gly489Arg
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1393G>A
  hgvsp: ENSP00000362045.1:p.Gly465Arg
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1633G>A
  hgvsp: ENSP00000439244.1:p.Gly545Arg
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1546G>A
  hgvsp: ENSP00000320374.8:p.Gly516Arg
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.690G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1549G>A
  hgvsp: ENSP00000277465.4:p.Gly517Arg
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1549G>A
  hgvsp: ENSP00000350169.5:p.Gly517Arg
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+1622G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.654G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1399G>A
  hgvsp: ENSP00000398011.1:p.Gly467Arg
  variant of: http://identifiers.org/hgnc/16744
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2649
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5038
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28703
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2509
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7362
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13671
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly545Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: Latino
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

9-130940033-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130940033
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130940033
    reference: chr 9
allele count: 1
allele frequency: 1.985151069996427e-5
allele num: 50374
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1462G>A
  hgvsp: ENSP00000362039.3:p.Ala488Thr
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.687G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1630G>A
  hgvsp: ENSP00000362029.5:p.Ala544Thr
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+1619G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1630G>A
  hgvsp: ENSP00000377232.1:p.Ala544Thr
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1390G>A
  hgvsp: ENSP00000362045.1:p.Ala464Thr
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1546G>A
  hgvsp: ENSP00000277465.4:p.Ala516Thr
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1396G>A
  hgvsp: ENSP00000398011.1:p.Ala466Thr
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1543G>A
  hgvsp: ENSP00000320374.8:p.Ala515Thr
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1327G>A
  hgvsp: ENSP00000445057.1:p.Ala443Thr
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1546G>A
  hgvsp: ENSP00000350169.5:p.Ala516Thr
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1630G>A
  hgvsp: ENSP00000439244.1:p.Ala544Thr
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.651G>A
  variant of: http://identifiers.org/hgnc/16744
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6513
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29102
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14225
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5685
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2327
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ala544Thr
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD

9-130940035-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130940035
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130940035
    reference: chr 9
allele count: 1
allele frequency: 2.006984305382732e-5
allele num: 49826
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.685G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+1617G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1628G>A
  hgvsp: ENSP00000377232.1:p.Gly543Asp
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1460G>A
  hgvsp: ENSP00000362039.3:p.Gly487Asp
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1394G>A
  hgvsp: ENSP00000398011.1:p.Gly465Asp
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1388G>A
  hgvsp: ENSP00000362045.1:p.Gly463Asp
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1541G>A
  hgvsp: ENSP00000320374.8:p.Gly514Asp
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1544G>A
  hgvsp: ENSP00000277465.4:p.Gly515Asp
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1544G>A
  hgvsp: ENSP00000350169.5:p.Gly515Asp
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1628G>A
  hgvsp: ENSP00000362029.5:p.Gly543Asp
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1325G>A
  hgvsp: ENSP00000445057.1:p.Gly442Asp
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.649G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1628G>A
  hgvsp: ENSP00000439244.1:p.Gly543Asp
  variant of: http://identifiers.org/hgnc/16744
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14396
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5942
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly543Asp
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: VQSLOD

9-130940054-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130940054
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130940054
    reference: chr 9
allele count: 1
allele frequency: 2.484595507851322e-5
allele num: 40248
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1537-12C>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1381-12C>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+1598C>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1534-12C>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1537-12C>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1621-12C>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.678-12C>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1621-12C>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1318-12C>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1453-12C>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.642-12C>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1387-12C>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1621-12C>G
  variant of: http://identifiers.org/hgnc/16744
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1440
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2267
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15295
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11452
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28364
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

9-130940066-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130940066
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130940066
    reference: chr 9
allele count: 486
allele frequency: 1.565217391304348e-2
allele num: 31050
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1621-24G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1387-24G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1453-24G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1537-24G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1534-24G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1381-24G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1537-24G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1621-24G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+1586G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.642-24G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1318-24G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1621-24G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.678-24G>A
  variant of: http://identifiers.org/hgnc/16744
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 3.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12715
  bin: 1.25e1
  variant carriers: 233
genotype depth: GenotypeDepth
  all individuals: 17115
  bin: 2.5e0
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 26634
  bin: 7.5e0
  variant carriers: 314
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 4.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 1.75e1
  variant carriers: 98
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 2.75e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 3.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 2.25e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 15
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum

9-130940081-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130940081
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130940081
    reference: chr 9
allele count: 160
allele frequency: 7.049700387733521e-3
allele num: 22696
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1318-39A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.678-39A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1534-39A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.642-39A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+1571A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1537-39A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1381-39A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1621-39A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1453-39A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1387-39A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1621-39A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1621-39A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1537-39A>G
  variant of: http://identifiers.org/hgnc/16744
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27119
  bin: 7.5e0
  variant carriers: 202
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20749
  bin: 2.5e0
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 8840
  bin: 1.25e1
  variant carriers: 120
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1321
  bin: 1.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 1
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff

9-130940087-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130940087
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130940087
    reference: chr 9
allele count: 1
allele frequency: 5.239442523315519e-5
allele num: 19086
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1381-45A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+1565A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1534-45A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1387-45A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1537-45A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.678-45A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1621-45A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1318-45A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.642-45A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1621-45A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1453-45A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1621-45A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1537-45A>G
  variant of: http://identifiers.org/hgnc/16744
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1328
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7140
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21050
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

9-130940090-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130940090
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130940090
    reference: chr 9
allele count: 6
allele frequency: 3.289473684210526e-4
allele num: 18240
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1621-48A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+1562A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1453-48A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1387-48A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1621-48A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1621-48A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1318-48A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1537-48A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1537-48A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1534-48A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1381-48A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.642-48A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.678-48A>G
  variant of: http://identifiers.org/hgnc/16744
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6801
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28606
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 21064
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1302
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

9-130940094-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130940094
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130940094
    reference: chr 9
allele count: 1
allele frequency: 6.100536847242558e-5
allele num: 16392
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1621-52G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1381-52G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1537-52G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1621-52G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1387-52G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.642-52G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+1558G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1534-52G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1453-52G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1621-52G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1318-52G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1537-52G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.678-52G>A
  variant of: http://identifiers.org/hgnc/16744
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1286
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28885
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6442
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21107
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

9-130940614-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130940614
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130940614
    reference: chr 9
allele count: 12
allele frequency: 1.003999263733873e-4
allele num: 119522
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.641+34C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1533+34C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+1038C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1380+34C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1452+34C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1620+34C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1536+34C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1317+34C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1386+34C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1536+34C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.677+34C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1620+34C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1620+34C>T
  variant of: http://identifiers.org/hgnc/16744
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2129
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4327
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5122
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4269
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1729
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2995
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5574
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5552
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2284
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3133
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5007
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2385
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3674
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

9-130940630-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130940630
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130940630
    reference: chr 9
allele count: 2195
allele frequency: 1.824999584282555e-2
allele num: 120274
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1620+18T>C
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1452+18T>C
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1380+18T>C
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1536+18T>C
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+1022T>C
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1317+18T>C
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1620+18T>C
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.641+18T>C
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1536+18T>C
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.677+18T>C
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1533+18T>C
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1620+18T>C
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1386+18T>C
  variant of: http://identifiers.org/hgnc/16744
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2128
  bin: 4.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 3590
  bin: 8.25e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 3.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 1.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 4971
  bin: 5.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 5463
  bin: 6.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5055
  bin: 7.25e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 4239
  bin: 5.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 8069
  bin: 9.75e1
  variant carriers: 1708
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 3.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 4210
  bin: 7.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 1474
  bin: 2.75e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 1.75e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 2885
  bin: 8.75e1
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 3052
  bin: 2.25e1
  variant carriers: 52
genotype quality: GenotypeQuality
num of homozygotes: 32
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

9-130940654-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130940654
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130940654
    reference: chr 9
allele count: 2
allele frequency: 1.651554938975045e-5
allele num: 121098
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.635G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1614G>A
  hgvsp: ENSP00000362029.5:p.Met538Ile
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1530G>A
  hgvsp: ENSP00000350169.5:p.Met510Ile
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1380G>A
  hgvsp: ENSP00000398011.1:p.Met460Ile
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+998G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1374G>A
  hgvsp: ENSP00000362045.1:p.Met458Ile
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1530G>A
  hgvsp: ENSP00000277465.4:p.Met510Ile
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1311G>A
  hgvsp: ENSP00000445057.1:p.Met437Ile
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1527G>A
  hgvsp: ENSP00000320374.8:p.Met509Ile
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1446G>A
  hgvsp: ENSP00000362039.3:p.Met482Ile
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1614G>A
  hgvsp: ENSP00000377232.1:p.Met538Ile
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1614G>A
  hgvsp: ENSP00000439244.1:p.Met538Ile
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.671G>A
  variant of: http://identifiers.org/hgnc/16744
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4384
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3696
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5724
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1656
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5651
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2294
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3299
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1729
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2236
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5127
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met538Ile
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD

9-130940658-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130940658
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130940658
    reference: chr 9
allele count: 1
allele frequency: 8.253549026081216e-6
allele num: 121160
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1610A>G
  hgvsp: ENSP00000377232.1:p.Glu537Gly
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1307A>G
  hgvsp: ENSP00000445057.1:p.Glu436Gly
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1526A>G
  hgvsp: ENSP00000277465.4:p.Glu509Gly
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.667A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1523A>G
  hgvsp: ENSP00000320374.8:p.Glu508Gly
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1610A>G
  hgvsp: ENSP00000439244.1:p.Glu537Gly
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1370A>G
  hgvsp: ENSP00000362045.1:p.Glu457Gly
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1610A>G
  hgvsp: ENSP00000362029.5:p.Glu537Gly
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1442A>G
  hgvsp: ENSP00000362039.3:p.Glu481Gly
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1376A>G
  hgvsp: ENSP00000398011.1:p.Glu459Gly
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.631A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+994A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1526A>G
  hgvsp: ENSP00000350169.5:p.Glu509Gly
  variant of: http://identifiers.org/hgnc/16744
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2240
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5127
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1753
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5724
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3216
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1657
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5651
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1936
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6643
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3696
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu537Gly
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

9-130940663-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130940663
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130940663
    reference: chr 9
allele count: 1
allele frequency: 8.25082508250825e-6
allele num: 121200
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.662G>C
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.626G>C
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1302G>C
  hgvsp: ENST00000541172.1:c.1302G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+989G>C
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1521G>C
  hgvsp: ENST00000357558.5:c.1521G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1521G>C
  hgvsp: ENST00000277465.4:c.1521G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1605G>C
  hgvsp: ENST00000372938.5:c.1605G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1605G>C
  hgvsp: ENST00000393608.1:c.1605G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1371G>C
  hgvsp: ENST00000415526.1:c.1371G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1518G>C
  hgvsp: ENST00000325721.8:c.1518G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1365G>C
  hgvsp: ENST00000372954.1:c.1365G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1605G>C
  hgvsp: ENST00000538431.1:c.1605G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1437G>C
  hgvsp: ENST00000372948.3:c.1437G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1666
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3695
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5652
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2938
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2294
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3217
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3346
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4347
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala535Ala
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff

9-130940663-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130940663
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130940663
    reference: chr 9
allele count: 2
allele frequency: 1.65016501650165e-5
allele num: 121200
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1371G>A
  hgvsp: ENST00000415526.1:c.1371G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1302G>A
  hgvsp: ENST00000541172.1:c.1302G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1365G>A
  hgvsp: ENST00000372954.1:c.1365G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1605G>A
  hgvsp: ENST00000372938.5:c.1605G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1518G>A
  hgvsp: ENST00000325721.8:c.1518G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1605G>A
  hgvsp: ENST00000393608.1:c.1605G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1437G>A
  hgvsp: ENST00000372948.3:c.1437G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1521G>A
  hgvsp: ENST00000277465.4:c.1521G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.626G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+989G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1605G>A
  hgvsp: ENST00000538431.1:c.1605G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.662G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1521G>A
  hgvsp: ENST00000357558.5:c.1521G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4347
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4385
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1666
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6643
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5127
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5724
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1950
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2938
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5652
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala535Ala
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD

9-130940664-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130940664
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130940664
    reference: chr 9
allele count: 1
allele frequency: 8.250961236984109e-6
allele num: 121198
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1436C>T
  hgvsp: ENSP00000362039.3:p.Ala479Val
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.661C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1364C>T
  hgvsp: ENSP00000362045.1:p.Ala455Val
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.625C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1604C>T
  hgvsp: ENSP00000439244.1:p.Ala535Val
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1517C>T
  hgvsp: ENSP00000320374.8:p.Ala506Val
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1370C>T
  hgvsp: ENSP00000398011.1:p.Ala457Val
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1520C>T
  hgvsp: ENSP00000350169.5:p.Ala507Val
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1301C>T
  hgvsp: ENSP00000445057.1:p.Ala434Val
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1520C>T
  hgvsp: ENSP00000277465.4:p.Ala507Val
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+988C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1604C>T
  hgvsp: ENSP00000362029.5:p.Ala535Val
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1604C>T
  hgvsp: ENSP00000377232.1:p.Ala535Val
  variant of: http://identifiers.org/hgnc/16744
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6641
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4347
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2938
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5724
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4384
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3695
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5192
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3351
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1774
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala535Val
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/9-130940674-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130940674
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130940674
    reference: chr 9
allele count: 1
allele frequency: 8.248375070111188e-6
allele num: 121236
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1360G>T
  hgvsp: ENSP00000398011.1:p.Glu454Ter
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1594G>T
  hgvsp: ENSP00000439244.1:p.Glu532Ter
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1594G>T
  hgvsp: ENSP00000377232.1:p.Glu532Ter
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1291G>T
  hgvsp: ENSP00000445057.1:p.Glu431Ter
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.615G>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1426G>T
  hgvsp: ENSP00000362039.3:p.Glu476Ter
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1510G>T
  hgvsp: ENSP00000277465.4:p.Glu504Ter
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1354G>T
  hgvsp: ENSP00000362045.1:p.Glu452Ter
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.651G>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1507G>T
  hgvsp: ENSP00000320374.8:p.Glu503Ter
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+978G>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1510G>T
  hgvsp: ENSP00000350169.5:p.Glu504Ter
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1594G>T
  hgvsp: ENSP00000362029.5:p.Glu532Ter
  variant of: http://identifiers.org/hgnc/16744
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3219
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3695
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1789
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4384
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2294
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5724
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1678
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5652
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5192
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu532Ter
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

9-130940682-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130940682
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130940682
    reference: chr 9
allele count: 2
allele frequency: 1.649566164098842e-5
allele num: 121244
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1586G>A
  hgvsp: ENSP00000377232.1:p.Gly529Glu
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.643G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1502G>A
  hgvsp: ENSP00000350169.5:p.Gly501Glu
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1283G>A
  hgvsp: ENSP00000445057.1:p.Gly428Glu
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1352G>A
  hgvsp: ENSP00000398011.1:p.Gly451Glu
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1586G>A
  hgvsp: ENSP00000439244.1:p.Gly529Glu
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+970G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1346G>A
  hgvsp: ENSP00000362045.1:p.Gly449Glu
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1502G>A
  hgvsp: ENSP00000277465.4:p.Gly501Glu
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1499G>A
  hgvsp: ENSP00000320374.8:p.Gly500Glu
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1586G>A
  hgvsp: ENSP00000362029.5:p.Gly529Glu
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.607G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1418G>A
  hgvsp: ENSP00000362039.3:p.Gly473Glu
  variant of: http://identifiers.org/hgnc/16744
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4347
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1789
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1966
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5128
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5192
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2254
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5724
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3444
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4385
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly529Glu
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP

9-130940694-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130940694
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130940694
    reference: chr 9
allele count: 5
allele frequency: 4.123235255310727e-5
allele num: 121264
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1574G>C
  hgvsp: ENSP00000439244.1:p.Gly525Ala
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1271G>C
  hgvsp: ENSP00000445057.1:p.Gly424Ala
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1574G>C
  hgvsp: ENSP00000377232.1:p.Gly525Ala
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1490G>C
  hgvsp: ENSP00000350169.5:p.Gly497Ala
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.595G>C
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1334G>C
  hgvsp: ENSP00000362045.1:p.Gly445Ala
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1406G>C
  hgvsp: ENSP00000362039.3:p.Gly469Ala
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1487G>C
  hgvsp: ENSP00000320374.8:p.Gly496Ala
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1490G>C
  hgvsp: ENSP00000277465.4:p.Gly497Ala
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1340G>C
  hgvsp: ENSP00000398011.1:p.Gly447Ala
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+958G>C
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1574G>C
  hgvsp: ENSP00000362029.5:p.Gly525Ala
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.631G>C
  variant of: http://identifiers.org/hgnc/16744
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5193
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4385
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5724
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6641
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3219
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5128
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3493
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2293
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1978
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1791
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly525Ala
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

9-130940702-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130940702
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130940702
    reference: chr 9
allele count: 2
allele frequency: 1.648940555692967e-5
allele num: 121290
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1482G>A
  hgvsp: ENST00000277465.4:c.1482G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1332G>A
  hgvsp: ENST00000415526.1:c.1332G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1566G>A
  hgvsp: ENST00000538431.1:c.1566G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+950G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1263G>A
  hgvsp: ENST00000541172.1:c.1263G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.623G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1398G>A
  hgvsp: ENST00000372948.3:c.1398G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1326G>A
  hgvsp: ENST00000372954.1:c.1326G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1566G>A
  hgvsp: ENST00000393608.1:c.1566G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1479G>A
  hgvsp: ENST00000325721.8:c.1479G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.587G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1482G>A
  hgvsp: ENST00000357558.5:c.1482G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1566G>A
  hgvsp: ENST00000372938.5:c.1566G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1984
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1682
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1794
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4386
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6638
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3694
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5128
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5194
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3219
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3541
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser522Ser
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ

9-130940717-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130940717
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130940717
    reference: chr 9
allele count: 15
allele frequency: 1.236481139541018e-4
allele num: 121312
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1551G>A
  hgvsp: ENST00000538431.1:c.1551G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1383G>A
  hgvsp: ENST00000372948.3:c.1383G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1467G>A
  hgvsp: ENST00000277465.4:c.1467G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1248G>A
  hgvsp: ENST00000541172.1:c.1248G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1551G>A
  hgvsp: ENST00000393608.1:c.1551G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.608G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1464G>A
  hgvsp: ENST00000325721.8:c.1464G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.572G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1317G>A
  hgvsp: ENST00000415526.1:c.1317G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1311G>A
  hgvsp: ENST00000372954.1:c.1311G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1467G>A
  hgvsp: ENST00000357558.5:c.1467G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+935G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1551G>A
  hgvsp: ENST00000372938.5:c.1551G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2254
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4386
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1999
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5654
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3219
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3693
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3589
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1796
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5725
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu517Glu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ

9-130940727-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130940727
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130940727
    reference: chr 9
allele count: 3
allele frequency: 2.472799208704253e-5
allele num: 121320
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1457G>A
  hgvsp: ENSP00000350169.5:p.Ser486Asn
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1541G>A
  hgvsp: ENSP00000377232.1:p.Ser514Asn
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1301G>A
  hgvsp: ENSP00000362045.1:p.Ser434Asn
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1238G>A
  hgvsp: ENSP00000445057.1:p.Ser413Asn
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1457G>A
  hgvsp: ENSP00000277465.4:p.Ser486Asn
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1373G>A
  hgvsp: ENSP00000362039.3:p.Ser458Asn
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1541G>A
  hgvsp: ENSP00000439244.1:p.Ser514Asn
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1454G>A
  hgvsp: ENSP00000320374.8:p.Ser485Asn
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1541G>A
  hgvsp: ENSP00000362029.5:p.Ser514Asn
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+925G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.598G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.562G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1307G>A
  hgvsp: ENSP00000398011.1:p.Ser436Asn
  variant of: http://identifiers.org/hgnc/16744
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2937
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6633
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3611
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5727
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1797
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1682
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5654
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5129
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser514Asn
num of homozygotes: 1
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD

9-130940736-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130940736
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130940736
    reference: chr 9
allele count: 1
allele frequency: 8.241984669908513e-6
allele num: 121330
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.553C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+916C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1532C>T
  hgvsp: ENSP00000439244.1:p.Thr511Ile
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1364C>T
  hgvsp: ENSP00000362039.3:p.Thr455Ile
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.589C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1229C>T
  hgvsp: ENSP00000445057.1:p.Thr410Ile
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1532C>T
  hgvsp: ENSP00000362029.5:p.Thr511Ile
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1448C>T
  hgvsp: ENSP00000277465.4:p.Thr483Ile
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1532C>T
  hgvsp: ENSP00000377232.1:p.Thr511Ile
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1292C>T
  hgvsp: ENSP00000362045.1:p.Thr431Ile
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1448C>T
  hgvsp: ENSP00000350169.5:p.Thr483Ile
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1445C>T
  hgvsp: ENSP00000320374.8:p.Thr482Ile
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1298C>T
  hgvsp: ENSP00000398011.1:p.Thr433Ile
  variant of: http://identifiers.org/hgnc/16744
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3616
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1797
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2937
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5654
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3219
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6631
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2019
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4387
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr511Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: African
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum

9-130940741-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130940741
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130940741
    reference: chr 9
allele count: 1
allele frequency: 8.242256400112095e-6
allele num: 121326
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1527G>A
  hgvsp: ENST00000538431.1:c.1527G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1440G>A
  hgvsp: ENST00000325721.8:c.1440G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1359G>A
  hgvsp: ENST00000372948.3:c.1359G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1443G>A
  hgvsp: ENST00000277465.4:c.1443G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1527G>A
  hgvsp: ENST00000393608.1:c.1527G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1443G>A
  hgvsp: ENST00000357558.5:c.1443G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1224G>A
  hgvsp: ENST00000541172.1:c.1224G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1527G>A
  hgvsp: ENST00000372938.5:c.1527G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1293G>A
  hgvsp: ENST00000415526.1:c.1293G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1287G>A
  hgvsp: ENST00000372954.1:c.1287G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.548G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.584G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+911G>A
  variant of: http://identifiers.org/hgnc/16744
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3696
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4387
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2937
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1683
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5728
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3219
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1795
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2255
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4350
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val509Val
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

9-130940745-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130940745
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130940745
    reference: chr 9
allele count: 1
allele frequency: 8.242120532770671e-6
allele num: 121328
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1436C>T
  hgvsp: ENSP00000320374.8:p.Pro479Leu
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1523C>T
  hgvsp: ENSP00000377232.1:p.Pro508Leu
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1439C>T
  hgvsp: ENSP00000277465.4:p.Pro480Leu
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+907C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1523C>T
  hgvsp: ENSP00000362029.5:p.Pro508Leu
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1283C>T
  hgvsp: ENSP00000362045.1:p.Pro428Leu
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1439C>T
  hgvsp: ENSP00000350169.5:p.Pro480Leu
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1355C>T
  hgvsp: ENSP00000362039.3:p.Pro452Leu
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1220C>T
  hgvsp: ENSP00000445057.1:p.Pro407Leu
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1289C>T
  hgvsp: ENSP00000398011.1:p.Pro430Leu
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.544C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.580C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1523C>T
  hgvsp: ENSP00000439244.1:p.Pro508Leu
  variant of: http://identifiers.org/hgnc/16744
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6629
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2024
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5728
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4350
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1795
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1683
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2255
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3605
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2937
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5130
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro508Leu
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

9-130940757-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130940757
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130940757
    reference: chr 9
allele count: 1
allele frequency: 8.242120532770671e-6
allele num: 121328
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.568C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1343C>T
  hgvsp: ENSP00000362039.3:p.Thr448Ile
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1424C>T
  hgvsp: ENSP00000320374.8:p.Thr475Ile
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1511C>T
  hgvsp: ENSP00000377232.1:p.Thr504Ile
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1208C>T
  hgvsp: ENSP00000445057.1:p.Thr403Ile
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1511C>T
  hgvsp: ENSP00000439244.1:p.Thr504Ile
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1271C>T
  hgvsp: ENSP00000362045.1:p.Thr424Ile
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.532C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1427C>T
  hgvsp: ENSP00000277465.4:p.Thr476Ile
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1511C>T
  hgvsp: ENSP00000362029.5:p.Thr504Ile
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1277C>T
  hgvsp: ENSP00000398011.1:p.Thr426Ile
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+895C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1427C>T
  hgvsp: ENSP00000350169.5:p.Thr476Ile
  variant of: http://identifiers.org/hgnc/16744
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5196
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5728
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4350
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3567
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2030
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2255
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3219
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2937
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1800
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1684
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr504Ile
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD

9-130940757-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130940757
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130940757
    reference: chr 9
allele count: 1
allele frequency: 8.242120532770671e-6
allele num: 121328
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+895C>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1277C>A
  hgvsp: ENSP00000398011.1:p.Thr426Asn
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1427C>A
  hgvsp: ENSP00000350169.5:p.Thr476Asn
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1511C>A
  hgvsp: ENSP00000362029.5:p.Thr504Asn
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1424C>A
  hgvsp: ENSP00000320374.8:p.Thr475Asn
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1427C>A
  hgvsp: ENSP00000277465.4:p.Thr476Asn
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1271C>A
  hgvsp: ENSP00000362045.1:p.Thr424Asn
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1343C>A
  hgvsp: ENSP00000362039.3:p.Thr448Asn
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1511C>A
  hgvsp: ENSP00000439244.1:p.Thr504Asn
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1511C>A
  hgvsp: ENSP00000377232.1:p.Thr504Asn
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1208C>A
  hgvsp: ENSP00000445057.1:p.Thr403Asn
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.568C>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.532C>A
  variant of: http://identifiers.org/hgnc/16744
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4387
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1684
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2937
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4350
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3219
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3567
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2030
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2255
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5654
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5196
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr504Asn
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD

9-130940758-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130940758
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130940758
    reference: chr 9
allele count: 1
allele frequency: 8.242256400112095e-6
allele num: 121326
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+894A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1423A>G
  hgvsp: ENSP00000320374.8:p.Thr475Ala
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1510A>G
  hgvsp: ENSP00000377232.1:p.Thr504Ala
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1270A>G
  hgvsp: ENSP00000362045.1:p.Thr424Ala
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1510A>G
  hgvsp: ENSP00000439244.1:p.Thr504Ala
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1207A>G
  hgvsp: ENSP00000445057.1:p.Thr403Ala
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1342A>G
  hgvsp: ENSP00000362039.3:p.Thr448Ala
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.531A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1426A>G
  hgvsp: ENSP00000350169.5:p.Thr476Ala
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1426A>G
  hgvsp: ENSP00000277465.4:p.Thr476Ala
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1510A>G
  hgvsp: ENSP00000362029.5:p.Thr504Ala
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.567A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1276A>G
  hgvsp: ENSP00000398011.1:p.Thr426Ala
  variant of: http://identifiers.org/hgnc/16744
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4350
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3564
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3697
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5654
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1683
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5729
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2255
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3219
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6628
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Thr504Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum

9-130940766-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130940766
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130940766
    reference: chr 9
allele count: 1
allele frequency: 8.242392271933006e-6
allele num: 121324
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1418T>C
  hgvsp: ENSP00000350169.5:p.Met473Thr
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1262T>C
  hgvsp: ENSP00000362045.1:p.Met421Thr
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1199T>C
  hgvsp: ENSP00000445057.1:p.Met400Thr
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1334T>C
  hgvsp: ENSP00000362039.3:p.Met445Thr
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.523T>C
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1502T>C
  hgvsp: ENSP00000377232.1:p.Met501Thr
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1418T>C
  hgvsp: ENSP00000277465.4:p.Met473Thr
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1415T>C
  hgvsp: ENSP00000320374.8:p.Met472Thr
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1268T>C
  hgvsp: ENSP00000398011.1:p.Met423Thr
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1502T>C
  hgvsp: ENSP00000439244.1:p.Met501Thr
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.559T>C
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+886T>C
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1502T>C
  hgvsp: ENSP00000362029.5:p.Met501Thr
  variant of: http://identifiers.org/hgnc/16744
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5196
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2026
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6628
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4387
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3697
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2255
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5654
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5729
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3220
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met501Thr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff

9-130940786-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130940786
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130940786
    reference: chr 9
allele count: 2
allele frequency: 1.648695881557688e-5
allele num: 121308
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1196-17C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1412-17C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.503C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+866C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1331-17C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1499-17C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1265-17C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1415-17C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.556-17C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1415-17C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1499-17C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1259-17C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1499-17C>T
  variant of: http://identifiers.org/hgnc/16744
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2008
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3220
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4388
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1795
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6626
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3458
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5196
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3697
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2255
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5729
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1678
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5654
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2289
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

9-130940799-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130940799
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130940799
    reference: chr 9
allele count: 1
allele frequency: 8.244838730954422e-6
allele num: 121288
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+853C>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1331-30C>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1265-30C>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1259-30C>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1196-30C>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1415-30C>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1415-30C>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.490C>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1499-30C>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1412-30C>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1499-30C>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1499-30C>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.556-30C>G
  variant of: http://identifiers.org/hgnc/16744
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3219
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3696
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4389
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2255
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4350
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5196
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2289
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1785
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6625
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3381
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5655
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS

9-130940803-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130940803
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130940803
    reference: chr 9
allele count: 1
allele frequency: 8.244838730954422e-6
allele num: 121288
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.486G>C
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1415-34G>C
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1412-34G>C
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+849G>C
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1415-34G>C
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1265-34G>C
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1331-34G>C
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1499-34G>C
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1259-34G>C
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1499-34G>C
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1196-34G>C
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.556-34G>C
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1499-34G>C
  variant of: http://identifiers.org/hgnc/16744
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5131
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4350
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2937
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2289
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5730
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1778
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4388
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3220
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1666
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5655
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1959
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3696
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2257
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

9-130940806-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130940806
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130940806
    reference: chr 9
allele count: 1
allele frequency: 8.245246615326264e-6
allele num: 121282
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1196-37G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+846G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.483G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1265-37G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1415-37G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1331-37G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1259-37G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1415-37G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1499-37G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.556-37G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1499-37G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1499-37G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1412-37G>A
  variant of: http://identifiers.org/hgnc/16744
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5730
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3221
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5131
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2289
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4388
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4351
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3381
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1665
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2255
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6623
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2938
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3696
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum

9-130940809-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130940809
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130940809
    reference: chr 9
allele count: 3
allele frequency: 2.473777953690877e-5
allele num: 121272
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.480C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1499-40C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1196-40C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1499-40C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1259-40C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1412-40C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1331-40C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1415-40C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1499-40C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+843C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.556-40C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1265-40C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1415-40C>T
  variant of: http://identifiers.org/hgnc/16744
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5131
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2254
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1943
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5730
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2289
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3221
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1662
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5655
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4388
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5195
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2938
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4350
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

9-130940810-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130940810
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130940810
    reference: chr 9
allele count: 2
allele frequency: 1.648994937585542e-5
allele num: 121286
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1265-41G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1196-41G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.479G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1412-41G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1331-41G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1499-41G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.556-41G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1415-41G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+842G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1415-41G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1259-41G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1499-41G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1499-41G>A
  variant of: http://identifiers.org/hgnc/16744
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1762
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2937
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5131
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5730
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3371
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2254
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5654
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1662
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4389
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1943
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3220
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5197
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6623
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ

9-130940812-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130940812
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130940812
    reference: chr 9
allele count: 1
allele frequency: 8.245382585751979e-6
allele num: 121280
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1412-43G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1331-43G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1499-43G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1265-43G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1415-43G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+840G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1415-43G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.556-43G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1259-43G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1196-43G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.477G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1499-43G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1499-43G>A
  variant of: http://identifiers.org/hgnc/16744
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3696
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1658
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5196
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5131
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2937
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4389
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3220
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6622
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3391
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2255
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4350
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5731
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

9-130940819-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130940819
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130940819
    reference: chr 9
allele count: 1
allele frequency: 8.245654540057389e-6
allele num: 121276
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+833A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1412-50A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1265-50A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.470A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1196-50A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1499-50A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1415-50A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1499-50A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1415-50A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1259-50A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1331-50A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.556-50A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1499-50A>G
  variant of: http://identifiers.org/hgnc/16744
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2937
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5196
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3466
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2289
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1629
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1973
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4389
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5654
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1687
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2245
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5131
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5731
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4350
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

9-130940821-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130940821
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130940821
    reference: chr 9
allele count: 1
allele frequency: 8.246742536698004e-6
allele num: 121260
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.468G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1265-52G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1415-52G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1499-52G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1415-52G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1499-52G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1196-52G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1412-52G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1259-52G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+831G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1331-52G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1499-52G>A
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.556-52G>A
  variant of: http://identifiers.org/hgnc/16744
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4385
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2009
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5196
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3459
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2289
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2223
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5730
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5654
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2937
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4350
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD

9-130940937-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130940937
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130940937
    reference: chr 9
allele count: 1
allele frequency: 8.483347189467077e-6
allele num: 117878
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1330+51A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1498+51A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+715A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1498+51A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.352A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.555+51A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1258+51A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1264+51A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1411+51A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1195+51A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1414+51A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1498+51A>G
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1414+51A>G
  variant of: http://identifiers.org/hgnc/16744
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1516
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18543
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10326
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4292
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3708
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12272
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1441
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQ

9-130940943-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130940943
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130940943
    reference: chr 9
allele count: 3
allele frequency: 2.54569522936714e-5
allele num: 117846
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1498+45C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1258+45C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1414+45C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+709C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.346C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1264+45C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1330+45C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1498+45C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1411+45C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.555+45C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1414+45C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1195+45C>T
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1498+45C>T
  variant of: http://identifiers.org/hgnc/16744
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4247
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18879
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3693
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1502
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13439
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5618
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

9-130940955-CACCAG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130940955
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130940950
    reference: chr 9
allele count: 3
allele frequency: 2.546819023040223e-5
allele num: 117794
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1264+28_1264+32delCTGGT
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1195+28_1195+32delCTGGT
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1411+28_1411+32delCTGGT
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1258+28_1258+32delCTGGT
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1414+28_1414+32delCTGGT
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1498+28_1498+32delCTGGT
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1414+28_1414+32delCTGGT
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1330+28_1330+32delCTGGT
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+692_733+696delCTGGT
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1498+28_1498+32delCTGGT
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1498+28_1498+32delCTGGT
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.329_333delCTGGT
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.555+28_555+32delCTGGT
  variant of: http://identifiers.org/hgnc/16744
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1514
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10611
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3702
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2877
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3715
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15650
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19667
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: CACCAG
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

9-130940959-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 130940959
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 130940959
    reference: chr 9
allele count: 1
allele frequency: 8.471560969824299e-6
allele num: 118042
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476727
  gene symbol: CIZ1
  hgvsc: ENST00000476727.2:n.733+693T>C
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000377232
  ensembl transcript: ENST00000393608
  gene symbol: CIZ1
  hgvsc: ENST00000393608.1:c.1498+29T>C
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362029
  ensembl transcript: ENST00000372938
  gene symbol: CIZ1
  hgvsc: ENST00000372938.5:c.1498+29T>C
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000476239
  gene symbol: CIZ1
  hgvsc: ENST00000476239.1:n.555+29T>C
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362039
  ensembl transcript: ENST00000372948
  gene symbol: CIZ1
  hgvsc: ENST00000372948.3:c.1330+29T>C
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000398011
  ensembl transcript: ENST00000415526
  gene symbol: CIZ1
  hgvsc: ENST00000415526.1:c.1264+29T>C
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000445057
  ensembl transcript: ENST00000541172
  gene symbol: CIZ1
  hgvsc: ENST00000541172.1:c.1195+29T>C
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148337
  ensembl transcript: ENST00000475471
  gene symbol: CIZ1
  hgvsc: ENST00000475471.1:n.330T>C
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000277465
  ensembl transcript: ENST00000277465
  gene symbol: CIZ1
  hgvsc: ENST00000277465.4:c.1414+29T>C
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000320374
  ensembl transcript: ENST00000325721
  gene symbol: CIZ1
  hgvsc: ENST00000325721.8:c.1411+29T>C
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000350169
  ensembl transcript: ENST00000357558
  gene symbol: CIZ1
  hgvsc: ENST00000357558.5:c.1414+29T>C
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000362045
  ensembl transcript: ENST00000372954
  gene symbol: CIZ1
  hgvsc: ENST00000372954.1:c.1258+29T>C
  variant of: http://identifiers.org/hgnc/16744
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148337
  ensembl protein: ENSP00000439244
  ensembl transcript: ENST00000538431
  gene symbol: CIZ1
  hgvsc: ENST00000538431.1:c.1498+29T>C
  variant of: http://identifiers.org/hgnc/16744
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3704
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15931
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1512
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3497
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2495
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1502
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19959
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: Latino
reference allele: A
site quality: VQSLOD

GenotypeDepth
all individuals: 14
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 61
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31926
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 466
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4687
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1096
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2002
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 519
bin: 6.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 2170
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 248
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5502
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2258
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 378
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 76
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 382
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.649999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.84e0

FS
type: SiteQuality
SIO_000300: 2.632e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.31e-1

QD
type: SiteQuality
SIO_000300: 9.970000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

MQ
type: SiteQuality
SIO_000300: 5.616e1

DP
type: SiteQuality
SIO_000300: 2.22871e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

GenotypeDepth
all individuals: 3217
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 560
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 520
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 340
bin: 9.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 45
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4284
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 32991
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2176
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1049
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 182
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 39
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2258
bin: 2.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2270
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 250
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 382
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 78
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 382
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.813565469713457e-4
allele num: 5514
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.9e-1

DP
type: SiteQuality
SIO_000300: 2.27092e5

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.8e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.763e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.85e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.433e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.550000000000001e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 19
bin: 7.75e1
variant carriers: 15

GenotypeQuality
all individuals: 3532
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 529
bin: 6.75e1
variant carriers: 22

GenotypeQuality
all individuals: 2302
bin: 6.25e1
variant carriers: 26

GenotypeQuality
all individuals: 1014
bin: 1.25e1
variant carriers: 56

GenotypeQuality
all individuals: 45
bin: 8.75e1
variant carriers: 14

GenotypeQuality
all individuals: 35
bin: 4.25e1
variant carriers: 1

GenotypeQuality
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bin: 3.25e1
variant carriers: 34

GenotypeQuality
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bin: 3.75e1
variant carriers: 4

GenotypeQuality
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bin: 7.5e0
variant carriers: 70

GenotypeQuality
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bin: 7.25e1
variant carriers: 13

GenotypeQuality
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bin: 4.75e1
variant carriers: 3

GenotypeQuality
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bin: 1.75e1
variant carriers: 63

GenotypeQuality
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bin: 2.25e1
variant carriers: 39

GenotypeQuality
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bin: 7.75e1
variant carriers: 16

GenotypeQuality
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bin: 2.75e1
variant carriers: 44

GenotypeQuality
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bin: 5.25e1
variant carriers: 7

GenotypeQuality
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bin: 9.75e1
variant carriers: 507

GenotypeQuality
all individuals: 73
bin: 8.25e1
variant carriers: 11

GenotypeQuality
all individuals: 43
bin: 9.25e1
variant carriers: 16

GenotypeQuality
all individuals: 28
bin: 5.75e1
variant carriers: 15

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

Latino
type: Population
allele count: 5
allele frequency: 1.953125e-2
allele num: 256
num of homozygotes: 0

African
type: Population
allele count: 552
allele frequency: 2.340966921119593e-1
allele num: 2358
num of homozygotes: 65

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.430615164520744e-3
allele num: 5592
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 2.525252525252525e-3
allele num: 396
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 78
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.89e-2

FS
type: SiteQuality
SIO_000300: 1.162e0

QD
type: SiteQuality
SIO_000300: 1.978e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.58e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.42e-1

DP
type: SiteQuality
SIO_000300: 2.46012e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.7e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-1

GenotypeDepth
all individuals: 56
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
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variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 18
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 260
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2386
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.336448598130841e-3
allele num: 428
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 78
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 440
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5682
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.262e0

DP
type: SiteQuality
SIO_000300: 2.58732e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.870000000000001e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.48e-1

QD
type: SiteQuality
SIO_000300: 7.7e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.173e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.2e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.43e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.73e0

GenotypeDepth
all individuals: 57
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variant carriers: 0

GenotypeDepth
all individuals: 12
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variant carriers: 0

GenotypeDepth
all individuals: 2
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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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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
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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bin: 1.25e1
variant carriers: 1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 608
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GenotypeQuality
all individuals: 81
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variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 9.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5872
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 272
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 540
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2474
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 478
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 84
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 20
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.35e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.87894e5

QD
type: SiteQuality
SIO_000300: 1.117e1

VQSLOD
type: SiteQuality
SIO_000300: 3.55e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 11
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 42
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 46
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variant carriers: 0

GenotypeDepth
all individuals: 7
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variant carriers: 0

GenotypeDepth
all individuals: 5
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variant carriers: 0

GenotypeDepth
all individuals: 145
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GenotypeDepth
all individuals: 11
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
all individuals: 24612
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variant carriers: 0

GenotypeQuality
all individuals: 24
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variant carriers: 0

GenotypeQuality
all individuals: 1050
bin: 2.5e0
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GenotypeQuality
all individuals: 59
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3605
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 82
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GenotypeQuality
all individuals: 40
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GenotypeQuality
all individuals: 48
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variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 4.75e1
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GenotypeQuality
all individuals: 170
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GenotypeQuality
all individuals: 633
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variant carriers: 1

GenotypeQuality
all individuals: 1298
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 193
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variant carriers: 0

GenotypeQuality
all individuals: 639
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2018
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2830
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 424
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 116
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7664
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 104
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.068e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.76e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.64e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

DP
type: SiteQuality
SIO_000300: 4.07319e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 2288
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 46
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variant carriers: 0

GenotypeDepth
all individuals: 11
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GenotypeDepth
all individuals: 7
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GenotypeDepth
all individuals: 7
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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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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
all individuals: 23400
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 56
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GenotypeQuality
all individuals: 646
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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
all individuals: 40
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7864
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 9.199632014719411e-4
allele num: 2174
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 116
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 436
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 4.17624e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.776e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.56e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.71e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.98e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.31e-1

MQRankSum
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SIO_000300: -1.84e-1

GenotypeDepth
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variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 2.745744096650192e-4
allele num: 3642
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1898
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1210
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 236
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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6424
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 15548
num of homozygotes: 0

QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQRankSum
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
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VQSLOD
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FS
type: SiteQuality
SIO_000300: 2.115e0

DP
type: SiteQuality
SIO_000300: 5.80552e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.12e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

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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bin: 4.75e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 2026
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16606
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6884
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 7.485029940119761e-4
allele num: 1336
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 600
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

MQ
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ReadPosRankSum
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SIO_000300: -2.48e-1

VQSLOD
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FS
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InbreedingCoeff
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ClippingRankSum
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QD
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DP
type: SiteQuality
SIO_000300: 6.01109e5

BaseQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

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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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 292
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2342
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 1.048437827636821e-4
allele num: 19076
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4010
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7626
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

ClippingRankSum
type: SiteQuality
SIO_000300: 5.5e-1

MQ
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SIO_000300: 5.948e1

MQRankSum
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FS
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VQSLOD
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ReadPosRankSum
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QD
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SIO_000300: 1.223e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.67e-2

DP
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SIO_000300: 6.3983e5

BaseQRankSum
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SIO_000300: 0.0e0

GenotypeDepth
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variant carriers: 25

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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variant carriers: 18

GenotypeQuality
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bin: 8.25e1
variant carriers: 17

European (Non-Finnish)
type: Population
allele count: 34
allele frequency: 1.666339933346403e-3
allele num: 20404
num of homozygotes: 0

Other
type: Population
allele count: 4
allele frequency: 1.282051282051282e-2
allele num: 312
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 838
num of homozygotes: 0

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

African
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allele count: 598
allele frequency: 1.306818181818182e-1
allele num: 4576
num of homozygotes: 24

Latino
type: Population
allele count: 37
allele frequency: 1.93717277486911e-2
allele num: 1910
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 1.270971021860702e-4
allele num: 7868
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.53e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.06e-1

BaseQRankSum
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SIO_000300: -1.096e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.11e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

QD
type: SiteQuality
SIO_000300: 1.373e1

DP
type: SiteQuality
SIO_000300: 6.51216e5

MQRankSum
type: SiteQuality
SIO_000300: 2.12e-1

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4548
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 318
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1990
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 20990
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.73e-1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.332e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.44e-2

MQRankSum
type: SiteQuality
SIO_000300: -5.73e-1

BaseQRankSum
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SIO_000300: -2.054e0

DP
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SIO_000300: 6.54891e5

QD
type: SiteQuality
SIO_000300: 1.387e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.48e-1

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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4564
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2052
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 320
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8060
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 4.215851602023609e-4
allele num: 21348
num of homozygotes: 0

VQSLOD
type: SiteQuality
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ClippingRankSum
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FS
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MQRankSum
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InbreedingCoeff
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QD
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DP
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MQ
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SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.54e-1

BaseQRankSum
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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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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: 2

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8320
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 332
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2206
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
type: Population
allele count: 2
allele frequency: 4.301075268817204e-4
allele num: 4650
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European (Non-Finnish)
type: Population
allele count: 35
allele frequency: 1.563058235083959e-3
allele num: 22392
num of homozygotes: 0

InbreedingCoeff
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ClippingRankSum
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DP
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FS
type: SiteQuality
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MQ
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ReadPosRankSum
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QD
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MQRankSum
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VQSLOD
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BaseQRankSum
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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
all individuals: 2080
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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 980
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 4.27715996578272e-4
allele num: 2338
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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Other
type: Population
allele count: 1
allele frequency: 2.941176470588235e-3
allele num: 340
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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MQ
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VQSLOD
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FS
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DP
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QD
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BaseQRankSum
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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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1294
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 9212
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 3548
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 7.151029748283753e-5
allele num: 27968
num of homozygotes: 0

African
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allele frequency: 1.994415636218588e-4
allele num: 5014
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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QD
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ClippingRankSum
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MQRankSum
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FS
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MQ
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InbreedingCoeff
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BaseQRankSum
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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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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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 3262
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.77623542476402e-4
allele num: 3602
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1338
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 400
num of homozygotes: 0

European (Non-Finnish)
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allele count: 4
allele frequency: 1.389564371569513e-4
allele num: 28786
num of homozygotes: 0

South Asian
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num of homozygotes: 0

African
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num of homozygotes: 0

VQSLOD
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SIO_000300: 7.5e-1

ClippingRankSum
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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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SIO_000300: 6.0e1

MQRankSum
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SIO_000300: 2.2e-1

BaseQRankSum
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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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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: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 450
num of homozygotes: 0

Latino
type: Population
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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num of homozygotes: 0

European (Non-Finnish)
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allele count: 5
allele frequency: 1.513408801985592e-4
allele num: 33038
num of homozygotes: 0

African
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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: 3
allele frequency: 1.908396946564885e-3
allele num: 1572
num of homozygotes: 0

South Asian
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allele count: 0
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ClippingRankSum
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SIO_000300: 3.9e-2

InbreedingCoeff
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BaseQRankSum
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QD
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VQSLOD
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MQRankSum
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FS
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MQ
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DP
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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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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

East Asian
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Latino
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allele frequency: 1.926782273603083e-4
allele num: 5190
num of homozygotes: 0

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

South Asian
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European (Finnish)
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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FS
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DP
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ClippingRankSum
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ReadPosRankSum
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MQ
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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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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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South Asian
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num of homozygotes: 0

Other
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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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allele frequency: 5.372300419039433e-5
allele num: 37228
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African
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MQRankSum
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ClippingRankSum
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FS
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DP
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MQ
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QD
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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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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South Asian
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Other
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
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Latino
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European (Finnish)
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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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VQSLOD
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ClippingRankSum
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MQ
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ReadPosRankSum
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BaseQRankSum
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QD
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DP
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GenotypeDepth
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variant carriers: 1

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

African
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South Asian
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European (Finnish)
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Other
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East Asian
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Latino
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MQ
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MQRankSum
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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QD
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FS
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InbreedingCoeff
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BaseQRankSum
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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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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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East Asian
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Latino
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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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MQ
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MQRankSum
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DP
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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FS
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QD
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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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European (Non-Finnish)
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DP
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QD
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MQRankSum
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FS
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VQSLOD
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East Asian
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African
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South Asian
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FS
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BaseQRankSum
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SIO_000300: -1.9e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.772e0

QD
type: SiteQuality
SIO_000300: 1.412e1

DP
type: SiteQuality
SIO_000300: 5.42705e5

MQRankSum
type: SiteQuality
SIO_000300: -5.6e-2

MQ
type: SiteQuality
SIO_000300: 5.873e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.38e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 9.92e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.104e0

GenotypeDepth
all individuals: 3
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
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variant carriers: 1

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27052
bin: 2.25e1
variant carriers: 24

GenotypeQuality
all individuals: 2029
bin: 2.75e1
variant carriers: 20

GenotypeQuality
all individuals: 234
bin: 6.75e1
variant carriers: 21

GenotypeQuality
all individuals: 46
bin: 8.75e1
variant carriers: 22

GenotypeQuality
all individuals: 54
bin: 9.25e1
variant carriers: 36

GenotypeQuality
all individuals: 1135
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1636
bin: 3.25e1
variant carriers: 8

GenotypeQuality
all individuals: 589
bin: 3.75e1
variant carriers: 5

GenotypeQuality
all individuals: 85
bin: 7.75e1
variant carriers: 8

GenotypeQuality
all individuals: 125
bin: 4.25e1
variant carriers: 2

GenotypeQuality
all individuals: 17593
bin: 7.5e0
variant carriers: 7

GenotypeQuality
all individuals: 3558
bin: 1.25e1
variant carriers: 6

GenotypeQuality
all individuals: 91
bin: 4.75e1
variant carriers: 8

GenotypeQuality
all individuals: 3466
bin: 1.75e1
variant carriers: 19

GenotypeQuality
all individuals: 73
bin: 8.25e1
variant carriers: 26

GenotypeQuality
all individuals: 85
bin: 7.25e1
variant carriers: 17

GenotypeQuality
all individuals: 595
bin: 9.75e1
variant carriers: 522

GenotypeQuality
all individuals: 94
bin: 5.25e1
variant carriers: 10

GenotypeQuality
all individuals: 1371
bin: 6.25e1
variant carriers: 33

GenotypeQuality
all individuals: 67
bin: 5.75e1
variant carriers: 15

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

African
type: Population
allele count: 454
allele frequency: 1.34478672985782e-1
allele num: 3376
num of homozygotes: 15

Latino
type: Population
allele count: 15
allele frequency: 7.267441860465116e-3
allele num: 2064
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2078
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 4.424778761061947e-3
allele num: 226
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 6.244796003330558e-4
allele num: 4804
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 13
allele frequency: 7.372958257713249e-4
allele num: 17632
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.231e0

FS
type: SiteQuality
SIO_000300: 1.543e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.03e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.11e0

MQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

DP
type: SiteQuality
SIO_000300: 4.71313e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.96e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.419e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.87e-1

GenotypeDepth
all individuals: 23
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 12

GenotypeQuality
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variant carriers: 14

GenotypeQuality
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variant carriers: 19

GenotypeQuality
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bin: 3.25e1
variant carriers: 3

GenotypeQuality
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variant carriers: 12

GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 23

GenotypeQuality
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variant carriers: 17

GenotypeQuality
all individuals: 1644
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variant carriers: 0

GenotypeQuality
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variant carriers: 10

GenotypeQuality
all individuals: 21861
bin: 7.5e0
variant carriers: 5

GenotypeQuality
all individuals: 76
bin: 7.25e1
variant carriers: 8

GenotypeQuality
all individuals: 807
bin: 6.25e1
variant carriers: 9

GenotypeQuality
all individuals: 168
bin: 4.75e1
variant carriers: 8

GenotypeQuality
all individuals: 271
bin: 9.75e1
variant carriers: 193

GenotypeQuality
all individuals: 65
bin: 8.25e1
variant carriers: 17

GenotypeQuality
all individuals: 1842
bin: 2.75e1
variant carriers: 2

GenotypeQuality
all individuals: 6657
bin: 1.25e1
variant carriers: 10

GenotypeQuality
all individuals: 38
bin: 9.25e1
variant carriers: 19

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1296
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 1.174628034455756e-3
allele num: 2554
num of homozygotes: 0

South Asian
type: Population
allele count: 71
allele frequency: 1.891315929675013e-2
allele num: 3754
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 606
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 5.813953488372093e-3
allele num: 172
num of homozygotes: 0

East Asian
type: Population
allele count: 85
allele frequency: 6.168359941944847e-2
allele num: 1378
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12936
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.21e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.01e-1

QD
type: SiteQuality
SIO_000300: 1.521e1

FS
type: SiteQuality
SIO_000300: 1.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.34e0

DP
type: SiteQuality
SIO_000300: 4.07872e5

BaseQRankSum
type: SiteQuality
SIO_000300: 1.92e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.88e-2

GenotypeDepth
all individuals: 3
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 28330
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variant carriers: 0

GenotypeDepth
all individuals: 0
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 21970
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1755
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2354
bin: 2.5e0
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GenotypeQuality
all individuals: 145
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variant carriers: 0

GenotypeQuality
all individuals: 19
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GenotypeQuality
all individuals: 636
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GenotypeQuality
all individuals: 13888
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 553
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variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10882
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1086
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3118
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1012
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 4.258943781942078e-4
allele num: 2348
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 482
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.463e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 3.90365e5

FS
type: SiteQuality
SIO_000300: 3.005e0

QD
type: SiteQuality
SIO_000300: 1.271e1

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.51e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.22e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.29e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.860000000000001e-1

GenotypeDepth
all individuals: 0
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variant carriers: 0

GenotypeDepth
all individuals: 5
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variant carriers: 0

GenotypeDepth
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 21606
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 27
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GenotypeQuality
all individuals: 84
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variant carriers: 7

GenotypeQuality
all individuals: 621
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GenotypeQuality
all individuals: 12539
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GenotypeQuality
all individuals: 21
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GenotypeQuality
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GenotypeQuality
all individuals: 519
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GenotypeQuality
all individuals: 177
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GenotypeQuality
all individuals: 164
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GenotypeQuality
all individuals: 8104
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GenotypeQuality
all individuals: 8530
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variant carriers: 0

GenotypeQuality
all individuals: 200
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GenotypeQuality
all individuals: 1485
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GenotypeQuality
all individuals: 78
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GenotypeQuality
all individuals: 1738
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GenotypeQuality
all individuals: 258
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variant carriers: 0

GenotypeQuality
all individuals: 49
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GenotypeQuality
all individuals: 24
bin: 8.75e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 150
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 458
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.061571125265393e-3
allele num: 942
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 3.847633705271258e-4
allele num: 10396
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1024
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 4.329004329004329e-4
allele num: 2310
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2960
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.61e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 9.960000000000001e0

VQSLOD
type: SiteQuality
SIO_000300: 3.55e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.447e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

DP
type: SiteQuality
SIO_000300: 3.88113e5

ClippingRankSum
type: SiteQuality
SIO_000300: 2.22e-1

GenotypeDepth
all individuals: 4
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variant carriers: 0

GenotypeDepth
all individuals: 3
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variant carriers: 0

GenotypeDepth
all individuals: 0
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GenotypeQuality
all individuals: 20284
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1703
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GenotypeQuality
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GenotypeQuality
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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: 217
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GenotypeQuality
all individuals: 1508
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GenotypeQuality
all individuals: 23
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GenotypeQuality
all individuals: 9238
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GenotypeQuality
all individuals: 78
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GenotypeQuality
all individuals: 274
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GenotypeQuality
all individuals: 8683
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GenotypeQuality
all individuals: 20
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GenotypeQuality
all individuals: 81
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variant carriers: 0

East Asian
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: 802
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 136
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 4.524886877828054e-4
allele num: 2210
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2600
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 380
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9378
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.648e0

VQSLOD
type: SiteQuality
SIO_000300: 1.01e0

DP
type: SiteQuality
SIO_000300: 3.86533e5

MQRankSum
type: SiteQuality
SIO_000300: 6.7e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -7.18e-1

FS
type: SiteQuality
SIO_000300: 2.222e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.91e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.2e-2

QD
type: SiteQuality
SIO_000300: 1.312e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 1509
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1060
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variant carriers: 3

GenotypeDepth
all individuals: 7276
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1040
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 502
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GenotypeQuality
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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: 1831
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GenotypeQuality
all individuals: 46812
bin: 9.75e1
variant carriers: 13

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10346
num of homozygotes: 0

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

South Asian
type: Population
allele count: 12
allele frequency: 7.836990595611285e-4
allele num: 15312
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66160
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.62e0

MQRankSum
type: SiteQuality
SIO_000300: 8.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

DP
type: SiteQuality
SIO_000300: 3.966767e6

QD
type: SiteQuality
SIO_000300: 1.311e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.05e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.3e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.29e-1

GenotypeDepth
all individuals: 3107
bin: 4.75e1
variant carriers: 10

GenotypeDepth
all individuals: 5519
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variant carriers: 10

GenotypeDepth
all individuals: 2258
bin: 9.25e1
variant carriers: 37

GenotypeQuality
all individuals: 1527
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GenotypeQuality
all individuals: 686
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GenotypeQuality
all individuals: 108
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GenotypeQuality
all individuals: 14
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GenotypeQuality
all individuals: 15
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GenotypeQuality
all individuals: 24
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GenotypeQuality
all individuals: 121
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GenotypeQuality
all individuals: 13
bin: 2.5e0
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GenotypeQuality
all individuals: 1300
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 137
bin: 4.75e1
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GenotypeQuality
all individuals: 369
bin: 3.25e1
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GenotypeQuality
all individuals: 306
bin: 2.75e1
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GenotypeQuality
all individuals: 65
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GenotypeQuality
all individuals: 744
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GenotypeQuality
all individuals: 890
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GenotypeQuality
all individuals: 3793
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GenotypeQuality
all individuals: 1853
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GenotypeQuality
all individuals: 47044
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variant carriers: 2156

GenotypeQuality
all individuals: 264
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GenotypeQuality
all individuals: 1433
bin: 8.25e1
variant carriers: 2

African
type: Population
allele count: 50
allele frequency: 4.831851565519907e-3
allele num: 10348
num of homozygotes: 2

Latino
type: Population
allele count: 157
allele frequency: 1.357661708751297e-2
allele num: 11564
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 93
allele frequency: 1.406533575317604e-2
allele num: 6612
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 1681
allele frequency: 2.532923484916975e-2
allele num: 66366
num of homozygotes: 27

South Asian
type: Population
allele count: 195
allele frequency: 1.230594471790988e-2
allele num: 15846
num of homozygotes: 2

East Asian
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allele frequency: 0.0e0
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Other
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allele frequency: 2.134831460674157e-2
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FS
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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QD
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MQ
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DP
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SIO_000300: 4.077027e6

ReadPosRankSum
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SIO_000300: 3.96e-1

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

European (Finnish)
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allele count: 1
allele frequency: 1.512401693889897e-4
allele num: 6612
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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Other
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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: 1.501726986033939e-5
allele num: 66590
num of homozygotes: 0

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

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

South Asian
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allele frequency: 6.073120369245719e-5
allele num: 16466
num of homozygotes: 0

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

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

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

Latino
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allele count: 1
allele frequency: 8.652015919709292e-5
allele num: 11558
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66632
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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South Asian
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FS
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MQRankSum
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MQ
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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QD
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DP
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BaseQRankSum
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SIO_000300: -8.44e-1

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Latino
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allele num: 11558
num of homozygotes: 0

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

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

European (Finnish)
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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African
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Latino
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allele frequency: 1.730403183941858e-4
allele num: 11558
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Other
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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QD
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BaseQRankSum
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MQRankSum
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FS
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MQ
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VQSLOD
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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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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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East Asian
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allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 1
allele frequency: 1.512401693889897e-4
allele num: 6612
num of homozygotes: 0

African
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allele frequency: 0.0e0
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Latino
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 5.999160117583539e-5
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DP
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InbreedingCoeff
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FS
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VQSLOD
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QD
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MQRankSum
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ClippingRankSum
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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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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

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 frequency: 0.0e0
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East Asian
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African
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European (Non-Finnish)
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allele num: 66690
num of homozygotes: 0

South Asian
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Other
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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DP
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QD
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ReadPosRankSum
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FS
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MQRankSum
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BaseQRankSum
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MQ
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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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

African
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European (Non-Finnish)
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allele num: 66704
num of homozygotes: 0

East Asian
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South Asian
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Other
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QD
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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FS
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MQRankSum
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DP
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MQ
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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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num of homozygotes: 0

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

European (Non-Finnish)
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Latino
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Other
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European (Finnish)
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South Asian
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African
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East Asian
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InbreedingCoeff
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ReadPosRankSum
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DP
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FS
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MQRankSum
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VQSLOD
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ClippingRankSum
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QD
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MQ
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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European (Finnish)
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DP
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African
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African
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East Asian
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European (Non-Finnish)
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VQSLOD
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MQ
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DP
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GenotypeQuality
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European (Finnish)
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East Asian
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European (Non-Finnish)
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African
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MQRankSum
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MQ
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FS
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BaseQRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

Other
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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num of homozygotes: 0

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

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

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

Latino
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Other
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BaseQRankSum
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ClippingRankSum
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MQ
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VQSLOD
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FS
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MQRankSum
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DP
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InbreedingCoeff
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ReadPosRankSum
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QD
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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 frequency: 0.0e0
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num of homozygotes: 0

African
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East Asian
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South Asian
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European (Non-Finnish)
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European (Finnish)
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Other
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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QD
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FS
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MQRankSum
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DP
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ReadPosRankSum
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MQ
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BaseQRankSum
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GenotypeDepth
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variant carriers: 1

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: 3
allele frequency: 1.817520901490367e-4
allele num: 16506
num of homozygotes: 0

Other
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European (Non-Finnish)
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allele num: 66664
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Latino
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num of homozygotes: 0

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

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

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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num of homozygotes: 0

Latino
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South Asian
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East Asian
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European (Finnish)
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European (Non-Finnish)
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Other
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QD
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FS
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DP
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ClippingRankSum
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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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MQ
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GenotypeDepth
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variant carriers: 0

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
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num of homozygotes: 0

European (Non-Finnish)
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num of homozygotes: 0

Other
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European (Finnish)
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Latino
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East Asian
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South Asian
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DP
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ClippingRankSum
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BaseQRankSum
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QD
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FS
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MQ
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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VQSLOD
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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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Other
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Latino
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European (Finnish)
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European (Non-Finnish)
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African
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South Asian
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East Asian
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MQ
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VQSLOD
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BaseQRankSum
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DP
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ClippingRankSum
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MQRankSum
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FS
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QD
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ReadPosRankSum
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InbreedingCoeff
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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: 6.75e1
variant carriers: 0

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

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

African
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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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num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500105007350515e-5
allele num: 66662
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -7.02e-1

QD
type: SiteQuality
SIO_000300: 1.973e1

FS
type: SiteQuality
SIO_000300: 2.698e0

MQ
type: SiteQuality
SIO_000300: 5.893e1

BaseQRankSum
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SIO_000300: -4.678e0

DP
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SIO_000300: 3.963701e6

InbreedingCoeff
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SIO_000300: 2.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.69e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.05e-1

VQSLOD
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SIO_000300: -1.934e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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variant carriers: 0

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

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

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.827802813054759e-5
allele num: 14646
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10170
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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MQRankSum
type: SiteQuality
SIO_000300: 8.01e-1

BaseQRankSum
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SIO_000300: -2.404e0

FS
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SIO_000300: 0.0e0

ClippingRankSum
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SIO_000300: -4.67e-1

VQSLOD
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SIO_000300: -9.182e-1

InbreedingCoeff
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SIO_000300: 3.7e-3

ReadPosRankSum
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SIO_000300: 6.7e-2

QD
type: SiteQuality
SIO_000300: 6.57e0

DP
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SIO_000300: 1.558533e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6540
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65568
num of homozygotes: 0

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

African
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allele num: 10174
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.841817186644773e-5
allele num: 14616
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
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QD
type: SiteQuality
SIO_000300: 1.227e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: 4.7e-3

ClippingRankSum
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SIO_000300: 3.32e-1

VQSLOD
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SIO_000300: 1.75e0

DP
type: SiteQuality
SIO_000300: 1.566785e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.83e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 850
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14530
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.940599882376005e-4
allele num: 10202
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65534
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Other
type: Population
allele count: 0
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DP
type: SiteQuality
SIO_000300: 1.591651e6

BaseQRankSum
type: SiteQuality
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InbreedingCoeff
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QD
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MQ
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SIO_000300: 5.065e1

FS
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SIO_000300: 6.221e0

MQRankSum
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SIO_000300: -2.454e0

VQSLOD
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SIO_000300: 1.84e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.4e-2

GenotypeDepth
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variant carriers: 0

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65642
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
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Latino
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allele count: 1
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allele num: 11482
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VQSLOD
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SIO_000300: -2.327e0