Allele/Variant
rs769067430
- Species
- Homo sapiens
- Symbol
- rs769067430
- Category
- Variant
- Variant type
- SNP
- Overlaps
- DNAJC6
- Location
- 1:65395018
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- (GRCh38)1:65395018C>T
- HGVS.c name
- ENSEMBL:ENST00000263441.11:c.1814C>T
- ENSEMBL:ENST00000371069.5:c.2024C>T
- HGVS.p name
- ENSP00000263441:p.Ser605Leu
- ENSP00000360108:p.Ser675Leu
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:65248219...65415871 (167.65 kb)
- Assembly version
- Not Available
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