RGD:8638461 Rat Genome Database

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Variant: RGD:8638461 -  Homo sapiens

RGD ID: 8638461
RS ID: rs28373740
ClinVar ID: CV93686
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: APC  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 5 112,085,611
GRCh38 5 112,749,914
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_130:g.62394T>G
NG_008481.4:g.62394T>G
NC_000005.10:g.112749914T>G
NC_000005.9:g.112085611T>G
More... 		intron|intron variant other
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:APC
Accession:NM_001354901
Location:5UTRS;INTRON

Gene Symbol:APC
Accession:NM_001407459
Location:5UTRS;INTRON

Gene Symbol:APC
Accession:NM_001407450
Location:5UTRS;INTRON

Gene Symbol:APC
Accession:NM_001407457
Location:5UTRS;INTRON

Gene Symbol:APC
Accession:NM_001127510
Location:5UTRS;INTRON

Gene Symbol:APC
Accession:NM_001354903
Location:5UTRS;INTRON

Gene Symbol:APC
Accession:NM_001407470
Location:5UTRS;INTRON

Gene Symbol:APC
Accession:NM_001407447
Location:5UTRS;INTRON

Gene Symbol:APC
Accession:NM_001407452
Location:5UTRS;INTRON

Gene Symbol:APC
Accession:NM_001354906
Location:5UTRS;INTRON

Gene Symbol:APC
Accession:NM_001407458
Location:5UTRS;INTRON

Gene Symbol:APC
Accession:NM_001407455
Location:5UTRS;INTRON

Gene Symbol:APC
Accession:NM_001407454
Location:5UTRS;INTRON

Gene Symbol:APC
Accession:NM_000038
Location:5UTRS;INTRON

Gene Symbol:APC
Accession:NM_001354905
Location:5UTRS;INTRON

Gene Symbol:APC
Accession:NM_001407471
Location:5UTRS;INTRON

Gene Symbol:APC
Accession:NM_001407460
Location:5UTRS;INTRON

Gene Symbol:APC
Accession:NM_001407469
Location:5UTRS;INTRON

Gene Symbol:APC
Accession:NM_001407467
Location:5UTRS;INTRON

Gene Symbol:APC
Accession:NM_001407472
Location:5UTRS;INTRON

Gene Symbol:APC
Accession:NM_001407449
Location:5UTRS;INTRON

Gene Symbol:APC
Accession:NM_001354899
Location:5UTRS;INTRON

Gene Symbol:APC
Accession:NM_001407448
Location:5UTRS;INTRON

Gene Symbol:APC
Accession:NM_001407453
Location:5UTRS;INTRON

Gene Symbol:APC
Accession:NM_001354895
Location:5UTRS;INTRON

Gene Symbol:APC
Accession:NM_001354896
Location:5UTRS;INTRON

Gene Symbol:APC
Accession:NM_001354900
Location:5UTRS;INTRON

Gene Symbol:APC
Accession:NM_001407456
Location:5UTRS;INTRON

Gene Symbol:APC
Accession:NM_001407451
Location:INTRON

Gene Symbol:APC
Accession:NM_001127511
Location:INTRON

Gene Symbol:APC
Accession:NM_001354902
Location:INTRON

Gene Symbol:APC
Accession:NM_001354904
Location:INTRON

Gene Symbol:APC
Accession:NM_001354897
Location:INTRON

Gene Symbol:APC
Accession:NM_001354898
Location:INTRON

Gene Symbol:APC
Accession:NM_001407446
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 RCV000073784 CLINVAR
dbSNP (RS) rs28373740 CLINVAR
MedGen CN280943 CLINVAR
NCBI Gene APC CLINVAR
OMIM 611731 CLINVAR