Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs532044107
- Species
- Homo sapiens
- Symbol
- rs532044107
- Category
- Variant
- Variant type
- SNP
- Overlaps
- RMDN1
- Location
- 8:86477302
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCh38)8:86477302G>A
- HGVS.c name
- ENSEMBL:ENST00000406452.8:c.752C>T
- ENSEMBL:ENST00000430676.6:c.662C>T
- HGVS.p name
- ENSP00000385927:p.Ala251Val
- ENSP00000409661:p.Ala221Val
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr8:86468257...86514357 (46.10 kb)
- Assembly version
- Not Available
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