Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs77469895
- Species
- Homo sapiens
- Symbol
- rs77469895
- Category
- Variant
- Variant type
- SNP
- Overlaps
- CARD9
- Location
- 9:136364362
- Nucleotide Change
- C>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)9:136364362C>G
- HGVS.c name
- ENSEMBL:ENST00000371732.10:c.1551G>C
- ENSEMBL:ENST00000371734.7:c.1441+191G>C
- HGVS.p name
- ENSP00000360797:p.Gln517His
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr9:136363956...136373681 (9.73 kb)
- Assembly version
- Not Available
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