Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs773506129
- Species
- Homo sapiens
- Symbol
- rs773506129
- Category
- Variant
- Variant type
- SNP
- Overlaps
- BMP4
- Location
- 14:53950666
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000014.9:g.53950666C>T
- HGVS.c name
- ENSEMBL:ENST00000245451.9:c.593G>A
- ENSEMBL:ENST00000417573.5:c.593G>A
- HGVS.p name
- ENSP00000245451:p.Arg198Gln
- ENSP00000394165:p.Arg198Gln
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr14:53949736...53958761 (9.03 kb)
- Assembly version
- Not Available
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