Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs1984070156
- Species
- Homo sapiens
- Symbol
- rs1984070156
- Category
- Variant
- Variant type
- SNP
- Overlaps
- SCRT2
- Location
- 20:664186
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)20:664186C>T
- HGVS.c name
- ENSEMBL:ENST00000246104.7:c.409G>A
- RefSeq:NM_033129.4:c.409G>A
- HGVS.p name
- ENSP00000246104:p.Gly137Ser
- NP_149120:p.Gly137Ser
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr20:661596...675802 (14.21 kb)
- Assembly version
- Not Available
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