RGD:9586969 Rat Genome Database

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Variant: RGD:9586969 -  Homo sapiens

RGD ID: 9586969
RS ID: rs587776396
ClinVar ID: CV165744
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TGFB2  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 1 218,609,625
GRCh38 1 218,436,283
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000001.11:g.218436283C>T
NC_000001.10:g.218609625C>T
NG_027721.2:g.95950C>T
NG_027721.1:g.95950C>T
More...
intron variant not provided 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 RCV000144055 CLINVAR
dbSNP (RS) rs587776396 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene TGFB2 CLINVAR
OMIM 190220 CLINVAR