Variant #0000518972 (NC_000003.11:g.30713706_30713711del, NM_003242.5:c.1031_1036del (TGFBR2))

Chromosome 3
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.30713706_30713711del
DNA change (hg38) g.30672214_30672219del
Published as TGFBR2(NM_001024847.2):c.1106_1111delGGGAGG (p.W369_D371delinsY)
ISCN -
DB-ID TGFBR2_000066
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TGFBR2 NM_003242.5 +/. - c.1031_1036del r.(?) p.(Trp344_Asp346delinsTyr)


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