Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1441194351
- Species
- Homo sapiens
- Symbol
- rs1441194351
- Category
- Variant
- Variant type
- SNP
- Overlaps
- CDC20B
- Location
- 5:55161154
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)5:55161154T>C
- HGVS.c name
- ENSEMBL:ENST00000296733.5:c.126+11434A>G
- ENSEMBL:ENST00000296734.6:c.204+758T>C
- HGVS.p name
- ENSP00000423822:p.Val122Ala
- ENSP00000427466:p.Val71Ala
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr5:55112971...55173177 (60.21 kb)
- Assembly version
- Not Available
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