Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs1250695710
- Species
- Homo sapiens
- Symbol
- rs1250695710
- Category
- Variant
- Variant type
- SNP
- Overlaps
- RNF175
- Location
- 4:153710412
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- 3 prime UTR variant
- HGVS.g name
- (GRCh38)4:153710412A>G
- HGVS.c name
- ENSEMBL:ENST00000347063.9:c.944T>C
- RefSeq:NM_173662.4:c.944T>C
- HGVS.p name
- ENSP00000340979:p.Ile315Thr
- NP_775933:p.Ile315Thr
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr4:153710160...153760024 (49.86 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction