Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs767265770
- Species
- Homo sapiens
- Symbol
- rs767265770
- Category
- Variant
- Variant type
- SNP
- Overlaps
- TMEFF1
- Location
- 9:100473555
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCh38)9:100473555C>T
- HGVS.c name
- ENSEMBL:ENST00000374879.5:c.11C>T
- ENSEMBL:ENST00000502978.1:c.80-25210C>T
- HGVS.p name
- ENSP00000364013:p.Ala4Val
- NP_003683:p.Ala4Val
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr9:100473149...100577636 (104.49 kb)
- Assembly version
- Not Available
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