Annotation Detail
Information
- Associated Genes
- MC1R
- Associated Variants
-
MC1R p.Arg163Gln (p.R163Q), ENSG00000198211 p.Arg163Gln (p.R163Q)
(
ENST00000639847.1,
ENST00000555427.1,
ENST00000555147.2 )
MC1R p.Arg163Gln (p.R163Q), ENSG00000198211 p.Arg163Gln (p.R163Q) ( ENST00000555147.2, ENST00000555427.1, ENST00000639847.1 ) - Associated Disease
- Melanoma, cutaneous malignant, susceptibility to, 5 Tyrosinase-positive oculocutaneous albinism Skin/hair/eye pigmentation, variation in, 2 Increased analgesia from kappa-opioid receptor agonist, female-specific
- Source Database
- ClinVar
- Description
- NM_002386.4(MC1R):c.488G>A (p.Arg163Gln) AND multiple conditions
- ClinVar Allele ID
- 256010
- ClinVar RefSeq Alternation Syntax
- NM_002386.4:c.488G>A
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2022-04-14
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV002500893
- ClinVar Disease
- Melanoma, cutaneous malignant, susceptibility to, 5
- ClinVar Disease
- Skin/hair/eye pigmentation, variation in, 2
- ClinVar Disease
- Tyrosinase-positive oculocutaneous albinism
- ClinVar Disease
- Increased analgesia from kappa-opioid receptor agonist, female-specific
- Observed Origin Sample
- unknown
Drugs