Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1424056144
- Species
- Homo sapiens
- Symbol
- rs1424056144
- Category
- Variant
- Variant type
- SNP
- Overlaps
- MAP3K15
- Location
- X:19431553
- Nucleotide Change
- G>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)X:19431553G>C
- HGVS.c name
- ENSEMBL:ENST00000338883.9:c.1051C>G
- ENSEMBL:ENST00000359173.7:n.306C>G
- HGVS.p name
- ENSP00000345629:p.Gln351Glu
- XP_047298056:p.Gln362Glu
- 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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