Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs782797091
- Species
- Homo sapiens
- Symbol
- rs782797091
- Category
- Variant
- Variant type
- SNP
- Overlaps
- GSPT2
- Location
- X:51744014
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000023.11:g.51744014A>G
- HGVS.c name
- ENSEMBL:ENST00000340438.6:c.388A>G
- RefSeq:NM_018094.5:c.388A>G
- HGVS.p name
- ENSP00000341247:p.Met130Val
- NP_060564:p.Met130Val
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- ChrX:51743442...51746232 (2.79 kb)
- Assembly version
- Not Available
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