Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1282869756
- Species
- Homo sapiens
- Symbol
- rs1282869756
- Category
- Variant
- Variant type
- SNP
- Overlaps
- PDSS2
- Location
- 6:107459132
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000006.12:g.107459132C>T
- HGVS.c name
- ENSEMBL:ENST00000369031.4:c.154G>A
- ENSEMBL:ENST00000369037.9:c.154G>A
- HGVS.p name
- ENSP00000358027:p.Val52Ile
- ENSP00000358033:p.Val52Ile
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr6:107152562...107459564 (307.00 kb)
- Assembly version
- Not Available
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