Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs1258691915
- Species
- Homo sapiens
- Symbol
- rs1258691915
- Category
- Variant
- Variant type
- SNP
- Overlaps
- MAP3K15
- Location
- X:19515045
- Nucleotide Change
- C>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000023.11:g.19515045C>A
- HGVS.c name
- ENSEMBL:ENST00000338883.9:c.217G>T
- RefSeq:NM_001001671.4:c.217G>T
- HGVS.p name
- ENSP00000345629:p.Gly73Cys
- NP_001001671:p.Gly73Cys
- 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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