Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs896478611
- Species
- Homo sapiens
- Symbol
- rs896478611
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ENTREP3
- Location
- 1:155248262
- Nucleotide Change
- G>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)1:155248262G>T
- HGVS.c name
- ENSEMBL:ENST00000350210.6:c.1333C>A
- ENSEMBL:ENST00000361361.7:c.1621C>A
- HGVS.p name
- ENSP00000307128:p.Pro445Thr
- ENSP00000354958:p.Pro541Thr
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:155247205...155255483 (8.28 kb)
- Assembly version
- Not Available
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