Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs1569140042
- Species
- Homo sapiens
- Symbol
- rs1569140042
- Category
- Variant
- Variant type
- SNP
- Overlaps
- PTCHD1
- Location
- X:23379992
- Nucleotide Change
- T>G
- Most Severe Consequence
- See all consequences
- synonymous variant
- HGVS.g name
- NC_000023.11:g.23379992T>G
- HGVS.c name
- ENSEMBL:ENST00000379361.5:c.753T>G
- ENSEMBL:ENST00000456522.1:c.159-12539T>G
- HGVS.p name
- ENSP00000368666:p.Pro251=
- NP_775766:p.Pro251=
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- ChrX:23334396...23404374 (69.98 kb)
- Assembly version
- Not Available
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