Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs142204172
- Species
- Homo sapiens
- Symbol
- rs142204172
- Category
- Variant
- Variant type
- SNP
- Overlaps
- DGCR6
- Location
- 22:18911655
- Nucleotide Change
- A>T
- Most Severe Consequence
- See all consequences
- missense variant
- HGVS.g name
- NC_000022.11:g.18911655A>T
- HGVS.c name
- ENSEMBL:ENST00000331444.12:c.629A>T
- ENSEMBL:ENST00000413981.5:c.221A>T
- HGVS.p name
- ENSP00000331681:p.Gln210Leu
- ENSP00000402409:p.Gln74Leu
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr22:18906028...18914238 (8.21 kb)
- Assembly version
- Not Available
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