Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs1351643627
- Species
- Homo sapiens
- Symbol
- rs1351643627
- Category
- Variant
- Variant type
- SNP
- Overlaps
- LRRIQ1
- Location
- 12:85057019
- Nucleotide Change
- A>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)12:85057019A>C
- HGVS.c name
- ENSEMBL:ENST00000393217.7:c.2226A>C
- ENSEMBL:ENST00000525971.6:n.2344A>C
- HGVS.p name
- ENSP00000376910:p.Arg742Ser
- NP_001073379:p.Arg742Ser
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr12:85036314...85272805 (236.49 kb)
- Assembly version
- Not Available
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