Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs140907780
- Species
- Homo sapiens
- Symbol
- rs140907780
- Category
- Variant
- Variant type
- SNP
- Overlaps
- CGNL1
- Location
- 15:57545684
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)15:57545684C>G
- HGVS.c name
- ENSEMBL:ENST00000281282.6:c.3593C>G
- RefSeq:XM_017022686.2:c.3593C>G
- HGVS.p name
- ENSP00000281282:p.Thr1198Ser
- XP_016878175:p.Thr1198Ser
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr15:57375967...57550717 (174.75 kb)
- Assembly version
- Not Available
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