Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs8406
- Species
- Homo sapiens
- Symbol
- rs8406
- Category
- Variant
- Variant type
- SNP
- Overlaps
- CHCHD2
- Location
- 7:56101726
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- 3 prime UTR variant
- HGVS.g name
- (GRCh38)7:56101726C>T
- HGVS.c name
- ENSEMBL:ENST00000395422.4:c.*125G>A
- ENSEMBL:ENST00000716930.1:c.300+2500G>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr7:56094567...56106479 (11.91 kb)
- Assembly version
- Not Available
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