Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs770503468
- Species
- Homo sapiens
- Symbol
- rs770503468
- Category
- Variant
- Variant type
- SNP
- Overlaps
- RORB
- Location
- 9:74642552
- Nucleotide Change
- G>A
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)9:74642552G>A
- HGVS.c name
- ENSEMBL:ENST00000376896.8:c.374G>A
- ENSEMBL:ENST00000396204.2:c.407G>A
- HGVS.p name
- ENSP00000366093:p.Ser125Asn
- ENSP00000379507:p.Ser136Asn
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr9:74497335...74693177 (195.84 kb)
- Assembly version
- Not Available
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