RGD:14717217 Rat Genome Database

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Variant: RGD:14717217 -  Homo sapiens

RGD ID: 14717217
RS ID: rs17653354
ClinVar ID: CV663184
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KCNQ3  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 8 133,175,805
GRCh38 8 132,163,558
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_004519.4:c.1236-64C>T
NG_008854.2:g.322200C>T
NC_000008.11:g.132163558G>A
NC_000008.10:g.133175805G>A
More... 		06/19/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:KCNQ3
Accession:XM_047421769
Location:INTRON

Gene Symbol:KCNQ3
Accession:NM_001204824
Location:INTRON

Gene Symbol:KCNQ3
Accession:XM_011517026
Location:INTRON

Gene Symbol:KCNQ3
Accession:XM_017013400
Location:INTRON

Gene Symbol:KCNQ3
Accession:NM_004519
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000829992 CLINVAR
dbSNP (RS) rs17653354 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene KCNQ3 CLINVAR
OMIM 602232 CLINVAR