Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs778415975
- Species
- Homo sapiens
- Symbol
- rs778415975
- Category
- Variant
- Variant type
- SNP
- Overlaps
- LRRIQ1
- Location
- 12:85154058
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)12:85154058C>G
- HGVS.c name
- ENSEMBL:ENST00000393217.7:c.4684C>G
- RefSeq:NM_001079910.2:c.4684C>G
- HGVS.p name
- ENSP00000376910:p.Gln1562Glu
- NP_001073379:p.Gln1562Glu
- 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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