Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs985898074
- Species
- Homo sapiens
- Symbol
- rs985898074
- Category
- Variant
- Variant type
- SNP
- Overlaps
- SAP30
- Location
- 4:173377251
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)4:173377251C>T
- HGVS.c name
- ENSEMBL:ENST00000296504.4:c.587C>T
- RefSeq:NM_003864.4:c.587C>T
- HGVS.p name
- ENSP00000296504:p.Thr196Ile
- NP_003855:p.Thr196Ile
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr4:173369969...173377532 (7.56 kb)
- Assembly version
- Not Available
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