Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs761148661
- Species
- Homo sapiens
- Symbol
- rs761148661
- Category
- Variant
- Variant type
- SNP
- Overlaps
- SDE2
- Location
- 1:225985339
- Nucleotide Change
- G>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)1:225985339G>C
- HGVS.c name
- ENSEMBL:ENST00000272091.8:c.1319C>G
- RefSeq:NM_152608.4:c.1319C>G
- HGVS.p name
- ENSP00000272091:p.Ala440Gly
- NP_689821:p.Ala440Gly
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:225982702...225999343 (16.64 kb)
- Assembly version
- Not Available
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