Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs757129608
- Species
- Homo sapiens
- Symbol
- rs757129608
- Category
- Variant
- Variant type
- SNP
- Overlaps
- LRRC73
- Location
- 6:43509698
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)6:43509698C>G
- HGVS.c name
- ENSEMBL:ENST00000372441.2:c.88G>C
- HGVS.p name
- ENSP00000361518:p.Val30Leu
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr6:43506968...43510346 (3.38 kb)
- Assembly version
- Not Available
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