Variant #0000505425 (NC_000001.10:g.218607532G>C, NM_003238.3:c.619G>C (TGFB2))

Chromosome 1
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.218607532G>C
DNA change (hg38) g.218434190G>C
Published as TGFB2(NM_001135599.2):c.703G>C (p.(Val235Leu)), TGFB2(NM_001135599.3):c.703G>C (p.V235L), TGFB2(NM_001135599.4):c.703G>C (p.V235L), TGFB2(NM_00323...)
ISCN -
DB-ID TGFB2_000039 See all 5 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) 0.0033 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TGFB2 NM_003238.3 -?/. - c.619G>C r.(?) p.(Val207Leu)


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