Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs181029958
- Species
- Homo sapiens
- Symbol
- rs181029958
- Category
- Variant
- Variant type
- SNP
- Overlaps
- MCMDC2
- Location
- 8:66878928
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_000008.11:g.66878928A>G
- HGVS.c name
- ENSEMBL:ENST00000313616.5:c.709+9A>G
- ENSEMBL:ENST00000396592.7:c.709+9A>G
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr8:66870749...66926382 (55.63 kb)
- Assembly version
- Not Available
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