Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs774492395
- Species
- Homo sapiens
- Symbol
- rs774492395
- Category
- Variant
- Variant type
- SNP
- Overlaps
- NDFIP1
- Location
- 5:142131892
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)5:142131892G>A
- HGVS.c name
- ENSEMBL:ENST00000253814.6:c.148G>A
- ENSEMBL:ENST00000509436.1:n.335G>A
- HGVS.p name
- ENSP00000253814:p.Ala50Thr
- NP_085048:p.Ala50Thr
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr5:142108779...142154440 (45.66 kb)
- Assembly version
- Not Available
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