Allele/Variant
rs29299042
- Species
- Mus musculus
- Symbol
- rs29299042
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Samt4
- Location
- X:153267199
- Nucleotide Change
- G>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCm39)X:153267199G>T
- HGVS.c name
- ENSEMBL:ENSMUST00000026029.1:c.337G>T
- RefSeq:NM_029199.3:c.337G>T
- HGVS.p name
- ENSEMBL:ENSMUSP00000026029:p.Val113Phe
- RefSeq:NP_083475.1:p.Val113Phe
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- ChrX:153264998...153267678 (2.68 kb)
- Assembly version
- Not Available
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