Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs147238760
- Species
- Homo sapiens
- Symbol
- rs147238760
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ANXA3
- Location
- 4:78610057
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant&splice region variant
- HGVS.g name
- NC_000004.12:g.78610057C>T
- HGVS.c name
- ENSEMBL:ENST00000264908.11:c.914C>T
- ENSEMBL:ENST00000503570.6:c.797C>T
- HGVS.p name
- ENSP00000264908:p.Ser305Leu
- ENSP00000421015:p.Ser266Leu
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr4:78551747...78610451 (58.70 kb)
- Assembly version
- Not Available
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