Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs138877502
- Species
- Homo sapiens
- Symbol
- rs138877502
- Category
- Variant
- Variant type
- SNP
- Overlaps
- CCDC63
- Location
- 12:110904611
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)12:110904611G>A
- HGVS.c name
- ENSEMBL:ENST00000308208.10:c.1366G>A
- ENSEMBL:ENST00000545036.5:c.1246G>A
- HGVS.p name
- ENSP00000312399:p.Asp456Asn
- ENSP00000445881:p.Asp416Asn
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr12:110844486...110907535 (63.05 kb)
- Assembly version
- Not Available
- Viewer Help
Data currently unavailable; sequence viewer under construction