Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs781065961
- Species
- Homo sapiens
- Symbol
- rs781065961
- Category
- Variant
- Variant type
- SNP
- Overlaps
- TSPAN18
- Location
- 11:44926684
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000011.10:g.44926684C>T
- HGVS.c name
- ENSEMBL:ENST00000340160.7:c.626C>T
- ENSEMBL:ENST00000354556.8:n.778+10119G>A
- HGVS.p name
- ENSP00000339820:p.Thr209Met
- ENSP00000429020:p.His212=
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr11:44726310...44932423 (206.11 kb)
- Assembly version
- Not Available
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