RGD:34890786 Rat Genome Database

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Variant: RGD:34890786 -  Homo sapiens

RGD ID: 34890786
RS ID: rs377738158
ClinVar ID: CV904396
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KCNAB2  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 1 6,149,119
GRCh38 1 6,089,059
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001199862.2:c.514+8C>T
NC_000001.11:g.6089059C>T
NC_000001.10:g.6149119C>T
NG_047091.1:g.101762C>T
More...
03/01/2020 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:KCNAB2
Accession:NM_001199862
Location:INTRON

Gene Symbol:KCNAB2
Accession:XM_005263514
Location:INTRON

Gene Symbol:KCNAB2
Accession:XM_011542321
Location:INTRON

Gene Symbol:KCNAB2
Accession:XM_047432866
Location:INTRON

Gene Symbol:KCNAB2
Accession:XM_011542322
Location:INTRON

Gene Symbol:KCNAB2
Accession:XM_047432872
Location:INTRON

Gene Symbol:KCNAB2
Accession:XM_047432867
Location:INTRON

Gene Symbol:KCNAB2
Accession:NM_001199863
Location:INTRON

Gene Symbol:KCNAB2
Accession:NM_172130
Location:INTRON

Gene Symbol:KCNAB2
Accession:NM_001199860
Location:INTRON

Gene Symbol:KCNAB2
Accession:XM_017002620
Location:INTRON

Gene Symbol:KCNAB2
Accession:XM_047432878
Location:INTRON

Gene Symbol:KCNAB2
Accession:NM_003636
Location:INTRON

Gene Symbol:KCNAB2
Accession:XM_047432870
Location:INTRON

Gene Symbol:KCNAB2
Accession:NM_001199861
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001171745 CLINVAR
dbSNP (RS) rs377738158 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene KCNAB2 CLINVAR
OMIM 601142 CLINVAR