RGD:152170669 Rat Genome Database

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Variant: RGD:152170669 -  Homo sapiens

RGD ID: 152170669
RS ID: rs774020920
ClinVar ID: CV1592531
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CARD8  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 19 48,722,113
GRCh38 19 48,218,856
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001351788.2:c.1011+2874G>A
NM_001351789.2:c.1011+2874G>A
NM_001184901.1:c.1153+15G>A
NM_001351783.2:c.1153+15G>A
More... 		01/27/2021 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:CARD8
Accession:NM_001184902
Location:INTRON

Gene Symbol:CARD8
Accession:NM_001184901
Location:INTRON

Gene Symbol:CARD8
Accession:NM_001184903
Location:INTRON

Gene Symbol:CARD8
Accession:NM_014959
Location:INTRON

Gene Symbol:CARD8
Accession:NM_001184900
Location:INTRON

Gene Symbol:CARD8
Accession:NM_001184904
Location:INTRON

Gene Symbol:CARD8
Accession:XM_006723097
Location:INTRON

Gene Symbol:CARD8
Accession:XM_006723093
Location:INTRON

Gene Symbol:CARD8
Accession:XM_006723092
Location:INTRON

Gene Symbol:CARD8
Accession:XM_006723096
Location:INTRON

Gene Symbol:CARD8
Accession:XM_006723110
Location:INTRON

Gene Symbol:CARD8
Accession:XM_011526650
Location:INTRON

Gene Symbol:CARD8
Accession:XM_011526643
Location:INTRON

Gene Symbol:CARD8
Accession:XM_011526641
Location:INTRON

Gene Symbol:CARD8
Accession:XM_017026485
Location:INTRON

Gene Symbol:CARD8
Accession:XM_017026482
Location:INTRON

Gene Symbol:CARD8
Accession:XM_017026484
Location:INTRON

Gene Symbol:CARD8
Accession:XM_017026483
Location:INTRON

Gene Symbol:CARD8
Accession:XM_017026487
Location:INTRON

Gene Symbol:CARD8
Accession:NM_001351787
Location:INTRON

Gene Symbol:CARD8
Accession:NM_001351791
Location:INTRON

Gene Symbol:CARD8
Accession:NM_001351788
Location:INTRON

Gene Symbol:CARD8
Accession:NM_001351786
Location:INTRON

Gene Symbol:CARD8
Accession:NM_001351789
Location:INTRON

Gene Symbol:CARD8
Accession:NM_001351792
Location:INTRON

Gene Symbol:CARD8
Accession:NM_001351784
Location:INTRON

Gene Symbol:CARD8
Accession:NM_001351790
Location:INTRON

Gene Symbol:CARD8
Accession:NM_001351782
Location:INTRON

Gene Symbol:CARD8
Accession:NM_001351783
Location:INTRON

Gene Symbol:CARD8
Accession:NM_001365950
Location:INTRON

Gene Symbol:CARD8
Accession:XM_047438455
Location:INTRON

Gene Symbol:CARD8
Accession:XM_047438461
Location:INTRON

Gene Symbol:CARD8
Accession:XM_047438453
Location:INTRON

Gene Symbol:CARD8
Accession:XM_047438454
Location:INTRON

Gene Symbol:CARD8
Accession:XM_047438463
Location:INTRON

Gene Symbol:CARD8
Accession:XM_047438447
Location:INTRON

Gene Symbol:CARD8
Accession:XM_047438437
Location:INTRON

Gene Symbol:CARD8
Accession:XM_047438452
Location:INTRON

Gene Symbol:CARD8
Accession:XM_047438446
Location:INTRON

Gene Symbol:CARD8
Accession:XM_047438439
Location:INTRON

Gene Symbol:CARD8
Accession:XM_047438449
Location:INTRON

Gene Symbol:CARD8
Accession:XM_047438435
Location:INTRON

Gene Symbol:CARD8
Accession:XM_047438445
Location:INTRON

Gene Symbol:CARD8
Accession:XM_047438441
Location:INTRON

Gene Symbol:CARD8
Accession:XM_047438436
Location:INTRON

Gene Symbol:CARD8
Accession:XM_047438451
Location:INTRON

Gene Symbol:CARD8
Accession:XM_047438444
Location:INTRON

Gene Symbol:CARD8
Accession:XM_047438443
Location:INTRON

Gene Symbol:CARD8
Accession:XM_047438459
Location:INTRON

Gene Symbol:CARD8
Accession:XM_047438450
Location:INTRON

Gene Symbol:CARD8
Accession:XM_047438438
Location:INTRON

Gene Symbol:CARD8
Accession:XM_047438448
Location:INTRON

Gene Symbol:CARD8
Accession:XM_047438440
Location:INTRON

Gene Symbol:CARD8
Accession:XM_047438434
Location:INTRON

Gene Symbol:CARD8
Accession:XM_047438442
Location:INTRON

Gene Symbol:CARD8
Accession:XM_047438458
Location:INTRON

Gene Symbol:CARD8
Accession:XM_047438457
Location:INTRON

Gene Symbol:CARD8
Accession:XM_047438456
Location:INTRON

Gene Symbol:CARD8
Accession:XM_047438460
Location:INTRON

Gene Symbol:CARD8
Accession:XM_047438465
Location:INTRON

Gene Symbol:CARD8
Accession:XM_047438462
Location:INTRON

Gene Symbol:CARD8
Accession:XM_047438464
Location:INTRON

Gene Symbol:CARD8
Accession:NR_033680
Location:INTRON;NON-CODING

Gene Symbol:CARD8
Accession:NR_033678
Location:INTRON;NON-CODING

Gene Symbol:CARD8
Accession:NR_033679
Location:INTRON;NON-CODING

Gene Symbol:CARD8
Accession:XR_001753636
Location:INTRON;NON-CODING

Gene Symbol:CARD8
Accession:NR_147707
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002161849 CLINVAR
dbSNP (RS) rs774020920 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CARD8 CLINVAR
OMIM 609051 CLINVAR