RGD:14746403 Rat Genome Database

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Variant: RGD:14746403 -  Homo sapiens

RGD ID: 14746403
RS ID: rs10804888
ClinVar ID: CV659897
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MCCC1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 3 182,735,311
GRCh38 3 183,017,523
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001363880.1:c.1651-186G>A
NM_020166.5:c.1978-186G>A
NG_008100.1:g.87055G>A
NC_000003.12:g.183017523C>T
More... 		06/14/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:MCCC1
Accession:XM_011512992
Location:INTRON

Gene Symbol:MCCC1
Accession:XM_047448589
Location:INTRON

Gene Symbol:MCCC1
Accession:NM_020166
Location:INTRON

Gene Symbol:MCCC1
Accession:XM_047448591
Location:INTRON

Gene Symbol:MCCC1
Accession:NM_001293273
Location:INTRON

Gene Symbol:MCCC1
Accession:NM_001363880
Location:INTRON

Gene Symbol:MCCC1
Accession:XM_047448586
Location:INTRON

Gene Symbol:MCCC1
Accession:XM_047448587
Location:INTRON

Gene Symbol:MCCC1
Accession:XM_047448590
Location:INTRON

Gene Symbol:MCCC1
Accession:XM_047448588
Location:INTRON

Gene Symbol:MCCC1
Accession:NR_120640
Location:INTRON;NON-CODING

Gene Symbol:MCCC1
Accession:XR_007095707
Location:INTRON;NON-CODING

Gene Symbol:MCCC1
Accession:NR_120639
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000844414 CLINVAR
dbSNP (RS) rs10804888 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene MCCC1 CLINVAR
OMIM 609010 CLINVAR