Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs943066714
- Species
- Homo sapiens
- Symbol
- rs943066714
- Category
- Variant
- Variant type
- SNP
- Overlaps
- LHX8
- Location
- 1:75143937
- Nucleotide Change
- G>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)1:75143937G>C
- HGVS.c name
- ENSEMBL:ENST00000294638.9:c.703G>C
- ENSEMBL:ENST00000356261.4:c.673G>C
- HGVS.p name
- ENSP00000294638:p.Asp235His
- ENSP00000348597:p.Asp225His
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:75128434...75199454 (71.02 kb)
- Assembly version
- Not Available
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