RGD:13541897 Rat Genome Database

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Variant: RGD:13541897 -  Homo sapiens

RGD ID: 13541897
RS ID: rs1553302992
ClinVar ID: CV498223
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TGFB2  
Reference Nucleotide: T
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 1 218,607,662
GRCh38 1 218,434,320
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_003238.6:c.644-18T>A
NM_001135599.4:c.728-18T>A
NG_027721.2:g.93987T>A
NC_000001.11:g.218434320T>A
More...
02/11/2019 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:TGFB2
Accession:NM_001135599
Location:INTRON

Gene Symbol:TGFB2
Accession:NM_003238
Location:INTRON

Gene Symbol:TGFB2
Accession:NR_138149
Location:INTRON;NON-CODING

Gene Symbol:TGFB2
Accession:NR_138148
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001718925 CLINVAR
dbSNP (RS) rs1553302992 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene TGFB2 CLINVAR
OMIM 190220 CLINVAR