Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs149097758
- Species
- Homo sapiens
- Symbol
- rs149097758
- Category
- Variant
- Variant type
- SNP
- Overlaps
- DNAJC6
- Location
- 1:65411312
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000001.11:g.65411312C>T
- HGVS.c name
- ENSEMBL:ENST00000263441.11:c.2487C>T
- ENSEMBL:ENST00000371069.5:c.2697C>T
- HGVS.p name
- ENSP00000263441:p.Thr829=
- ENSP00000360108:p.Thr899=
- 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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