Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs2045801762
- Species
- Homo sapiens
- Symbol
- rs2045801762
- Category
- Variant
- Variant type
- SNP
- Overlaps
- TRIM37
- Location
- 17:59104367
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000017.11:g.59104367T>C
- HGVS.c name
- ENSEMBL:ENST00000262294.12:c.49A>G
- ENSEMBL:ENST00000393065.6:c.21+2074A>G
- HGVS.p name
- ENSP00000262294:p.Ile17Val
- ENSP00000376785:p.Ile17Val
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr17:58967201...59106921 (139.72 kb)
- Assembly version
- Not Available
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