Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1217969029
- Species
- Homo sapiens
- Symbol
- rs1217969029
- Category
- Variant
- Variant type
- SNP
- Overlaps
- ZC3H10
- Location
- 12:56121092
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- (GRCh38)12:56121092C>T
- HGVS.c name
- ENSEMBL:ENST00000257940.7:c.530C>T
- ENSEMBL:ENST00000551790.5:c.-144+1941C>T
- HGVS.p name
- ENSP00000257940:p.Ser177Leu
- NP_001290054:p.Ser177Leu
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr12:56118260...56127514 (9.25 kb)
- Assembly version
- Not Available
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