RGD:11658774 Rat Genome Database

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Variant: RGD:11658774 -  Homo sapiens

RGD ID: 11658774
RS ID: rs886052496
ClinVar ID: CV326879
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC124903759  LOC127885244  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 16 89,984,661
GRCh38 16 89,918,253
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.5375G>T
NC_000016.10:g.89918253G>T
NC_000016.9:g.89984661G>T
NG_027810.1:g.1245G>T
More... 		01/12/2018 5 prime utr variant uncertain significance Cutaneous malignant melanoma 5
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:LOC124903759
Accession:XM_047435031
Location:INTRON

Gene Symbol:LOC124903759
Accession:XM_047435032
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000351584 CLINVAR
dbSNP (RS) rs886052496 CLINVAR
MedGen C2751295 CLINVAR
NCBI Gene MC1R CLINVAR
OMIM 155555 CLINVAR
  613099 CLINVAR