RGD:11647787 Rat Genome Database

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Variant: RGD:11647787 -  Homo sapiens

RGD ID: 11647787
RS ID: rs886052510
ClinVar ID: CV344689
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC127885247  MC1R  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 16 89,987,218
GRCh38 16 89,920,810
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_012026.1:g.7932T>C
NC_000016.10:g.89920810T>C
NC_000016.9:g.89987218T>C
NM_002386.4:c.*598T>C
More... 		01/12/2018 3 prime utr variant uncertain significance Cutaneous malignant melanoma 5
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:MC1R
Accession:NM_002386
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000278218 CLINVAR
dbSNP (RS) rs886052510 CLINVAR
MedGen C2751295 CLINVAR
NCBI Gene MC1R CLINVAR
OMIM 155555 CLINVAR
  613099 CLINVAR