Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1002698716
- Species
- Homo sapiens
- Symbol
- rs1002698716
- Category
- Variant
- Variant type
- SNP
- Overlaps
- FOXN4
- Location
- 12:109279835
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)12:109279835C>T
- HGVS.c name
- ENSEMBL:ENST00000299162.10:c.1390G>A
- ENSEMBL:ENST00000355216.5:c.850G>A
- HGVS.p name
- ENSP00000299162:p.Gly464Ser
- ENSP00000347354:p.Gly284Ser
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr12:109277978...109309284 (31.31 kb)
- Assembly version
- Not Available
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