Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1558660477
- Species
- Homo sapiens
- Symbol
- rs1558660477
- Category
- Variant
- Variant type
- SNP
- Overlaps
- DYNC2LI1
- Location
- 2:43776899
- Nucleotide Change
- G>C
- Most Severe Consequence
- See all consequences
- missense variant&splice region variant
- HGVS.g name
- NC_000002.12:g.43776899G>C
- HGVS.c name
- ENSEMBL:ENST00000260605.12:c.126G>C
- ENSEMBL:ENST00000378587.3:c.77G>C
- HGVS.p name
- ENSP00000260605:p.Gly42=
- ENSP00000367850:p.Gly26Ala
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr2:43774039...43828347 (54.31 kb)
- Assembly version
- Not Available
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