Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs556354713
- Species
- Homo sapiens
- Symbol
- rs556354713
- Category
- Variant
- Variant type
- SNP
- Overlaps
- MBOAT7
- Location
- 19:54174234
- Nucleotide Change
- A>G
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000019.10:g.54174234A>G
- HGVS.c name
- ENSEMBL:ENST00000245615.6:c.1229T>C
- ENSEMBL:ENST00000338624.10:c.1010T>C
- HGVS.p name
- ENSP00000245615:p.Met410Thr
- ENSP00000344377:p.Met337Thr
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr19:54173412...54189882 (16.47 kb)
- Assembly version
- Not Available
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