Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs760451724
- Species
- Homo sapiens
- Symbol
- rs760451724
- Category
- Variant
- Variant type
- SNP
- Overlaps
- TMEFF1
- Location
- 9:100473671
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_000009.12:g.100473671C>T
- HGVS.c name
- ENSEMBL:ENST00000374879.5:c.127C>T
- ENSEMBL:ENST00000502978.1:c.80-25094C>T
- HGVS.p name
- ENSP00000364013:p.Pro43Ser
- NP_003683:p.Pro43Ser
- 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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