Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs201016876
- Species
- Homo sapiens
- Symbol
- rs201016876
- Category
- Variant
- Variant type
- SNP
- Overlaps
- POLD4
- Location
- 11:67352749
- Nucleotide Change
- G>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000011.10:g.67352749G>T
- HGVS.c name
- ENSEMBL:ENST00000312419.8:c.241C>A
- ENSEMBL:ENST00000524743.1:n.268C>A
- HGVS.p name
- ENSP00000311368:p.Pro81Thr
- ENSP00000433408:p.Pro6Thr
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr11:67350765...67356972 (6.21 kb)
- Assembly version
- Not Available
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