Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs765136099
- Species
- Homo sapiens
- Symbol
- rs765136099
- Category
- Variant
- Variant type
- SNP
- Overlaps
- MAP3K15
- Location
- X:19464234
- Nucleotide Change
- T>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000023.11:g.19464234T>G
- HGVS.c name
- ENSEMBL:ENST00000338883.9:c.698A>C
- ENSEMBL:ENST00000518578.5:n.589A>C
- HGVS.p name
- ENSP00000345629:p.Lys233Thr
- XP_047298056:p.Lys244Thr
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- ChrX:19360056...19515508 (155.45 kb)
- Assembly version
- Not Available
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