Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1004014848
- Species
- Homo sapiens
- Symbol
- rs1004014848
- Category
- Variant
- Variant type
- SNP
- Overlaps
- TARBP1
- Location
- 1:234478879
- Nucleotide Change
- G>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000001.11:g.234478879G>T
- HGVS.c name
- ENSEMBL:ENST00000040877.2:c.225C>A
- RefSeq:XM_047429061.1:c.225C>A
- HGVS.p name
- ENSP00000040877:p.Ser75Arg
- XP_047285017:p.Ser75Arg
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:234391313...234479179 (87.87 kb)
- Assembly version
- Not Available
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