Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs31180149
- Species
- Mus musculus
- Symbol
- rs31180149
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Ncf2
- Location
- 1:152683851
- Nucleotide Change
- G>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000067.7:g.152683851G>T
- HGVS.c name
- ENSEMBL:ENSMUST00000027754.1:c.69G>T
- ENSEMBL:ENSMUST00000186568.1:c.69G>T
- HGVS.p name
- ENSEMBL:ENSMUSP00000027754:p.Lys23Asn
- ENSEMBL:ENSMUSP00000140404:p.Lys23Asn
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:152675945...152712742 (36.80 kb)
- Assembly version
- Not Available
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