Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs771505314
- Species
- Homo sapiens
- Symbol
- rs771505314
- Category
- Variant
- Variant type
- SNP
- Overlaps
- CIBAR2
- Location
- 16:85107856
- Nucleotide Change
- T>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)16:85107856T>G
- HGVS.c name
- ENSEMBL:ENST00000539556.6:c.416A>C
- ENSEMBL:ENST00000618669.3:c.133A>C
- HGVS.p name
- ENSP00000443411:p.Gln139Pro
- ENSP00000478373:p.Ser45Arg
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr16:85098358...85112472 (14.11 kb)
- Assembly version
- Not Available
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