Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs1244709098
- Species
- Homo sapiens
- Symbol
- rs1244709098
- Category
- Variant
- Variant type
- SNP
- Overlaps
- B3GALT4
- Location
- 6:33278033
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)6:33278033C>T
- HGVS.c name
- ENSEMBL:ENST00000451237.3:c.614C>T
- RefSeq:NM_003782.4:c.614C>T
- HGVS.p name
- ENSP00000390784:p.Pro205Leu
- NP_003773:p.Pro205Leu
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr6:33277123...33284832 (7.71 kb)
- Assembly version
- Not Available
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