Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs200984268
- Species
- Homo sapiens
- Symbol
- rs200984268
- Category
- Variant
- Variant type
- SNP
- Overlaps
- RNF175
- Location
- 4:153712556
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)4:153712556C>T
- HGVS.c name
- ENSEMBL:ENST00000347063.9:c.785G>A
- ENSEMBL:ENST00000513656.5:n.751G>A
- HGVS.p name
- ENSP00000340979:p.Arg262Gln
- XP_005262997:p.Arg181Gln
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr4:153710160...153760024 (49.86 kb)
- Assembly version
- Not Available
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