Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs200747400
- Species
- Homo sapiens
- Symbol
- rs200747400
- Category
- Variant
- Variant type
- SNP
- Overlaps
- EVI5
- Location
- 1:92697972
- Nucleotide Change
- T>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)1:92697972T>G
- HGVS.c name
- ENSEMBL:ENST00000370331.5:c.785A>C
- ENSEMBL:ENST00000540033.3:c.785A>C
- HGVS.p name
- ENSP00000359356:p.Glu262Ala
- ENSP00000440826:p.Glu262Ala
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:92508696...92792410 (283.71 kb)
- Assembly version
- Not Available
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