Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs774905053
- Species
- Homo sapiens
- Symbol
- rs774905053
- Category
- Variant
- Variant type
- SNP
- Overlaps
- LRRCC1
- Location
- 8:85107362
- Nucleotide Change
- T>A
- Most Severe Consequence
- See all consequences
- intron variant&non coding transcript variant
- HGVS.g name
- (GRCh38)8:85107362T>A
- HGVS.c name
- ENSEMBL:ENST00000360375.8:c.67T>A
- ENSEMBL:ENST00000517875.5:n.125T>A
- HGVS.p name
- ENSP00000353538:p.Cys23Ser
- XP_047278325:p.Cys23Ser
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr8:85107215...85146080 (38.87 kb)
- Assembly version
- Not Available
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