Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs207473207
- Species
- Homo sapiens
- Symbol
- rs207473207
- Category
- Variant
- Variant type
- SNP
- Overlaps
- LRRIQ1
- Location
- 12:85168364
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_000012.12:g.85168364T>C
- HGVS.c name
- ENSEMBL:ENST00000393217.7:c.4822+7650T>C
- ENSEMBL:ENST00000526363.1:c.84+7650T>C
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr12:85036314...85272805 (236.49 kb)
- Assembly version
- Not Available
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