Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs374702162
- Species
- Homo sapiens
- Symbol
- rs374702162
- Category
- Variant
- Variant type
- SNP
- Overlaps
- GOLT1A
- Location
- 1:204202967
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)1:204202967C>T
- HGVS.c name
- ENSEMBL:ENST00000308302.4:c.46G>A
- HGVS.p name
- ENSP00000308535:p.Gly16Ser
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:204198163...204213988 (15.83 kb)
- Assembly version
- Not Available
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