Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs182375791
- Species
- Homo sapiens
- Symbol
- rs182375791
- Category
- Variant
- Variant type
- SNP
- Overlaps
- PGAP4
- Location
- 9:101477080
- Nucleotide Change
- T>C
- Most Severe Consequence
- See all consequences
- intron variant&non coding transcript variant
- HGVS.g name
- NC_000009.12:g.101477080T>C
- HGVS.c name
- ENSEMBL:ENST00000374847.5:c.13A>G
- ENSEMBL:ENST00000374848.8:c.13A>G
- HGVS.p name
- ENSP00000363980:p.Thr5Ala
- ENSP00000363981:p.Thr5Ala
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr9:101473170...101533686 (60.52 kb)
- Assembly version
- Not Available
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