Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1032979701
- Species
- Homo sapiens
- Symbol
- rs1032979701
- Category
- Variant
- Variant type
- SNP
- Overlaps
- C1orf74
- Location
- 1:209780592
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)1:209780592G>A
- HGVS.c name
- ENSEMBL:ENST00000294811.2:c.*2233C>T
- ENSEMBL:ENST00000367024.5:c.1435G>A
- HGVS.p name
- ENSP00000355991:p.Ala479Thr
- ENSP00000355992:p.Ala479Thr
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:209779208...209784559 (5.35 kb)
- Assembly version
- Not Available
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