Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs145983403
- Species
- Homo sapiens
- Symbol
- rs145983403
- Category
- Variant
- Variant type
- SNP
- Overlaps
- MCMDC2
- Location
- 8:66877506
- Nucleotide Change
- G>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)8:66877506G>C
- HGVS.c name
- ENSEMBL:ENST00000313616.5:c.443G>C
- ENSEMBL:ENST00000396592.7:c.443G>C
- HGVS.p name
- ENSP00000317234:p.Arg148Thr
- ENSP00000379837:p.Arg148Thr
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr8:66870749...66926382 (55.63 kb)
- Assembly version
- Not Available
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