Variant #0000316529 (NC_000009.11:g.101904939G>C, NM_004612.2:c.927G>C (TGFBR1))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.101904939G>C
DNA change (hg38) g.99142657G>C
Published as TGFBR1(NM_004612.3):c.927G>C (p.T309=), TGFBR1(NM_004612.4):c.927G>C (p.T309=)
ISCN -
DB-ID TGFBR1_000021 See all 2 reported entries
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TGFBR1 NM_004612.2 -?/. - c.927G>C r.(?) p.(Thr309=)


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