Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1217226709
- Species
- Homo sapiens
- Symbol
- rs1217226709
- Category
- Variant
- Variant type
- SNP
- Overlaps
- TXNDC9
- Location
- 2:99327537
- Nucleotide Change
- G>C
- Most Severe Consequence
- See all consequences
- missense variant&splice region variant
- HGVS.g name
- NC_000002.12:g.99327537G>C
- HGVS.c name
- ENSEMBL:ENST00000264255.8:c.306C>G
- ENSEMBL:ENST00000409434.5:c.306C>G
- HGVS.p name
- ENSP00000264255:p.Phe102Leu
- ENSP00000386889:p.Phe102Leu
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:99306184...99340702 (34.52 kb)
- Assembly version
- Not Available
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