RGD:8638223 Rat Genome Database

Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

Variant: RGD:8638223 -  Homo sapiens

RGD ID: 8638223
RS ID: rs76528895
ClinVar ID: CV93448
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: APC  
Reference Nucleotide: A
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 5 112,151,371
GRCh38 5 112,815,674
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_130:g.128154A>C
NG_008481.4:g.128154A>C
NC_000005.10:g.112815674A>C
NC_000005.9:g.112151371A>C
More...
intron|intron variant other
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:APC
Accession:NM_001127511
Location:INTRON

Gene Symbol:APC
Accession:NM_001127510
Location:INTRON

Gene Symbol:APC
Accession:NM_000038
Location:INTRON

Gene Symbol:APC
Accession:NM_001354895
Location:INTRON

Gene Symbol:APC
Accession:NM_001354897
Location:INTRON

Gene Symbol:APC
Accession:NM_001354902
Location:INTRON

Gene Symbol:APC
Accession:NM_001354898
Location:INTRON

Gene Symbol:APC
Accession:NM_001354904
Location:INTRON

Gene Symbol:APC
Accession:NM_001354906
Location:INTRON

Gene Symbol:APC
Accession:NM_001354896
Location:INTRON

Gene Symbol:APC
Accession:NM_001354903
Location:INTRON

Gene Symbol:APC
Accession:NM_001354899
Location:INTRON

Gene Symbol:APC
Accession:NM_001354900
Location:INTRON

Gene Symbol:APC
Accession:NM_001354901
Location:INTRON

Gene Symbol:APC
Accession:NM_001354905
Location:INTRON

Gene Symbol:APC
Accession:NM_001407470
Location:INTRON

Gene Symbol:APC
Accession:NM_001407472
Location:INTRON

Gene Symbol:APC
Accession:NM_001407447
Location:INTRON

Gene Symbol:APC
Accession:NM_001407456
Location:INTRON

Gene Symbol:APC
Accession:NM_001407460
Location:INTRON

Gene Symbol:APC
Accession:NM_001407452
Location:INTRON

Gene Symbol:APC
Accession:NM_001407469
Location:INTRON

Gene Symbol:APC
Accession:NM_001407446
Location:INTRON

Gene Symbol:APC
Accession:NM_001407448
Location:INTRON

Gene Symbol:APC
Accession:NM_001407450
Location:INTRON

Gene Symbol:APC
Accession:NM_001407457
Location:INTRON

Gene Symbol:APC
Accession:NM_001407458
Location:INTRON

Gene Symbol:APC
Accession:NM_001407453
Location:INTRON

Gene Symbol:APC
Accession:NM_001407449
Location:INTRON

Gene Symbol:APC
Accession:NM_001407455
Location:INTRON

Gene Symbol:APC
Accession:NM_001407459
Location:INTRON

Gene Symbol:APC
Accession:NM_001407451
Location:INTRON

Gene Symbol:APC
Accession:NM_001407471
Location:INTRON

Gene Symbol:APC
Accession:NM_001407454
Location:INTRON

Gene Symbol:APC
Accession:NM_001407467
Location:INTRON

Gene Symbol:APC
Accession:NR_176366
Location:INTRON;NON-CODING

Gene Symbol:APC
Accession:NR_176365
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000073546 CLINVAR
dbSNP (RS) rs76528895 CLINVAR
MedGen CN280943 CLINVAR
NCBI Gene APC CLINVAR
OMIM 114500 CLINVAR
  611731 CLINVAR