Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1192155325
- Species
- Homo sapiens
- Symbol
- rs1192155325
- Category
- Variant
- Variant type
- SNP
- Overlaps
- GOLGA8T
- Location
- 15:30145297
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- synonymous variant
- HGVS.g name
- (GRCh38)15:30145297C>T
- HGVS.c name
- ENSEMBL:ENST00000569052.2:c.1710C>T
- RefSeq:NM_001355469.2:c.1710C>T
- HGVS.p name
- ENSP00000455826:p.Asp570=
- NP_001342398:p.Asp570=
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr15:30135051...30148748 (13.70 kb)
- Assembly version
- Not Available
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