Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs762690654
- Species
- Homo sapiens
- Symbol
- rs762690654
- Category
- Variant
- Variant type
- SNP
- Overlaps
- WTAP
- Location
- 6:159755280
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000006.12:g.159755280C>T
- HGVS.c name
- ENSEMBL:ENST00000358372.8:c.860C>T
- ENSEMBL:ENST00000546087.5:c.-336+5757G>A
- HGVS.p name
- ENSP00000351141:p.Thr287Met
- ENSP00000479438:p.Thr287Met
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr6:159725585...159756319 (30.73 kb)
- Assembly version
- Not Available
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