RGD:150407435 Rat Genome Database

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Variant: RGD:150407435 -  Homo sapiens

RGD ID: 150407435
RS ID: rs28760438
ClinVar ID: CV1182471
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: AXIN2  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 17 63,532,914
GRCh38 17 65,536,796
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_296:g.29827T>C
NG_012142.1:g.29827T>C
NC_000017.11:g.65536796A>G
NC_000017.10:g.63532914A>G
More... 		07/14/2021 intron variant benign none provided; Oligodontia-colorectal cancer syndrome; TOOTH AGENESIS-COLORECTAL CANCER SYNDROME
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:AXIN2
Accession:XM_011525321
Location:INTRON

Gene Symbol:AXIN2
Accession:XM_017025193
Location:INTRON

Gene Symbol:AXIN2
Accession:XM_011525319
Location:INTRON

Gene Symbol:AXIN2
Accession:XM_047436872
Location:INTRON

Gene Symbol:AXIN2
Accession:XM_047436874
Location:INTRON

Gene Symbol:AXIN2
Accession:XM_047436873
Location:INTRON

Gene Symbol:AXIN2
Accession:XM_011525320
Location:INTRON

Gene Symbol:AXIN2
Accession:NM_004655
Location:INTRON

Gene Symbol:AXIN2
Accession:XM_047436871
Location:INTRON

Gene Symbol:AXIN2
Accession:XM_017025192
Location:INTRON

Gene Symbol:AXIN2
Accession:XM_047436870
Location:INTRON

Gene Symbol:AXIN2
Accession:NM_001363813
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001553954 CLINVAR
  RCV001658287 CLINVAR
dbSNP (RS) rs28760438 CLINVAR
MedGen C1837750 CLINVAR
  C3661900 CLINVAR
NCBI Gene AXIN2 CLINVAR
OMIM 604025 CLINVAR
  608615 CLINVAR