Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1173270890
- Species
- Homo sapiens
- Symbol
- rs1173270890
- Category
- Variant
- Variant type
- SNP
- Overlaps
- CPVL
- Location
- 7:29146646
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- 5 prime UTR variant
- HGVS.g name
- (GRCh38)7:29146646C>T
- HGVS.c name
- ENSEMBL:ENST00000409850.5:c.-10-25575G>A
- ENSEMBL:ENST00000437527.1:c.-10-25575G>A
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr7:28994636...29195451 (200.82 kb)
- Assembly version
- Not Available
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