Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs2075205929
- Species
- Homo sapiens
- Symbol
- rs2075205929
- Category
- Variant
- Variant type
- SNP
- Overlaps
- RSPRY1
- Location
- 16:57230828
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCh38)16:57230828T>C
- HGVS.c name
- ENSEMBL:ENST00000394420.9:c.1376+15T>C
- ENSEMBL:ENST00000537866.5:c.1376+15T>C
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr16:57186137...57240469 (54.33 kb)
- Assembly version
- Not Available
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