Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs1375502403
- Species
- Homo sapiens
- Symbol
- rs1375502403
- Category
- Variant
- Variant type
- SNP
- Overlaps
- GLTPD2
- Location
- 17:4790189
- Nucleotide Change
- G>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000017.11:g.4790189G>C
- HGVS.c name
- ENSEMBL:ENST00000331264.8:c.769G>C
- RefSeq:NM_001014985.3:c.769G>C
- HGVS.p name
- ENSP00000328070:p.Glu257Gln
- NP_001014985:p.Glu257Gln
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr17:4788964...4790589 (1.63 kb)
- Assembly version
- Not Available
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