Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs3323652172
- Species
- Rattus norvegicus
- Symbol
- rs3323652172
- Category
- Variant
- Variant type
- SNP
- Overlaps
- Fbxl17l1
- Location
- X:13917233
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- 5 prime UTR variant
- HGVS.g name
- (mRatBN7.2)X:13917233G>A
- HGVS.c name
- ENSEMBL:ENSRNOT00000049864.3:c.441C>T
- RefSeq:NM_001301646.1:c.-662G>A
- HGVS.p name
- ENSRNOP00000046759:p.Ala147=
- XP_038956498:p.Ala147=
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- ChrX:13915423...13918090 (2.67 kb)
- Assembly version
- Not Available
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