Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1376867601
- Species
- Homo sapiens
- Symbol
- rs1376867601
- Category
- Variant
- Variant type
- SNP
- Overlaps
- PFN3
- Location
- 5:177400416
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000005.10:g.177400416G>A
- HGVS.c name
- ENSEMBL:ENST00000358571.3:c.161C>T
- RefSeq:NM_001029886.3:c.161C>T
- HGVS.p name
- ENSP00000351379:p.Pro54Leu
- NP_001025057:p.Pro54Leu
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr5:177400109...177400661 (0.55 kb)
- Assembly version
- Not Available
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