Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs142189388
- Species
- Homo sapiens
- Symbol
- rs142189388
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ZNF326
- Location
- 1:90005020
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)1:90005020G>A
- HGVS.c name
- ENSEMBL:ENST00000340281.9:c.79G>A
- ENSEMBL:ENST00000361911.9:c.79G>A
- HGVS.p name
- ENSP00000340796:p.Gly27Ser
- ENSP00000355318:p.Gly27Ser
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:89995110...90035533 (40.42 kb)
- Assembly version
- Not Available
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