Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
rs1557988401
- Species
- Homo sapiens
- Symbol
- rs1557988401
- Category
- Variant
- Variant type
- SNP
- Overlaps
- TRMT1L
- Location
- 1:185137684
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000001.11:g.185137684C>T
- HGVS.c name
- ENSEMBL:ENST00000367506.10:c.1435G>A
- ENSEMBL:ENST00000458395.1:c.307G>A
- HGVS.p name
- ENSP00000356476:p.Ala479Thr
- ENSP00000414339:p.Ala103Thr
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:185118101...185157537 (39.44 kb)
- Assembly version
- Not Available
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