Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs758955317
- Species
- Homo sapiens
- Symbol
- rs758955317
- Category
- Variant
- Variant type
- SNP
- Overlaps
- IGF2BP1
- Location
- 17:49040021
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)17:49040021C>T
- HGVS.c name
- ENSEMBL:ENST00000290341.8:c.748C>T
- ENSEMBL:ENST00000431824.2:c.402-1357C>T
- HGVS.p name
- ENSP00000290341:p.Pro250Ser
- XP_047291098:p.Pro238Ser
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr17:48996558...49056145 (59.59 kb)
- Assembly version
- Not Available
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