Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs142906342
- Species
- Homo sapiens
- Symbol
- rs142906342
- Category
- Variant
- Variant type
- SNP
- Overlaps
- TRMT1L
- Location
- 1:185124952
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)1:185124952T>C
- HGVS.c name
- ENSEMBL:ENST00000367506.10:c.1751A>G
- ENSEMBL:ENST00000458395.1:c.623A>G
- HGVS.p name
- ENSP00000356476:p.Asn584Ser
- ENSP00000414339:p.Asn208Ser
- 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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