Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs142666444
- Species
- Homo sapiens
- Symbol
- rs142666444
- Category
- Variant
- Variant type
- SNP
- Overlaps
- GALNT10
- Location
- 5:154409732
- Nucleotide Change
- C>T
- Most Severe Consequence
- See all consequences
- intron variant&non coding transcript variant
- HGVS.g name
- NC_000005.10:g.154409732C>T
- HGVS.c name
- ENSEMBL:ENST00000297107.11:c.1356C>T
- ENSEMBL:ENST00000377661.2:c.1170C>T
- HGVS.p name
- ENSP00000297107:p.Pro452=
- ENSP00000366889:p.Pro390=
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr5:154190730...154420984 (230.25 kb)
- Assembly version
- Not Available
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