CUTA cutA divalent cation tolerance homolog
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 26 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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28 |
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0 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data | : |
MGeND data only
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Search word | : | |
Filtering | : |
Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | ACHAP |
SYNONYM | C6orf82 |
MIM | 616953 OMIM |
HGNC | HGNC:21101 HGNC |
Ensembl | ENSG00000112514 Ensembl |
AllianceGenome | HGNC:21101 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000607266.5 | hg38 | chr6 | 33,416,550 | 33,417,931 | 1,382 |
ENST00000494751.5 | hg38 | chr6 | 33,416,550 | 33,418,058 | 1,509 |
ENST00000488478.5 | hg38 | chr6 | 33,416,550 | 33,418,086 | 1,537 |
ENST00000440279.7 | hg38 | chr6 | 33,416,552 | 33,417,921 | 1,370 |
ENST00000374500.10 | hg38 | chr6 | 33,416,442 | 33,418,317 | 1,876 |
ENST00000488034.6 | hg38 | chr6 | 33,416,442 | 33,418,107 | 1,666 |
ENST00000374496.3 | hg38 | chr6 | 33,416,619 | 33,418,070 | 1,452 |
ENST00000488034.6 | hg19 | chr6 | 33,384,219 | 33,385,884 | 1,666 |
ENST00000374500.10 | hg19 | chr6 | 33,384,219 | 33,386,094 | 1,876 |
ENST00000607266.5 | hg19 | chr6 | 33,384,327 | 33,385,708 | 1,382 |
ENST00000494751.5 | hg19 | chr6 | 33,384,327 | 33,385,835 | 1,509 |
ENST00000488478.5 | hg19 | chr6 | 33,384,327 | 33,385,863 | 1,537 |
ENST00000440279.7 | hg19 | chr6 | 33,384,329 | 33,385,698 | 1,370 |
ENST00000374496.3 | hg19 | chr6 | 33,384,396 | 33,385,847 | 1,452 |
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