Variant #0001013283 (NC_000001.10:g.218578712_218578717del, NC_000001.10(NM_003238.3):c.510+38_510+43del (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.218578712_218578717del
DNA change (hg38) -
Published as TGFB2(NM_001135599.3):c.594+38_594+43delGTTGTT, TGFB2(NM_001135599.4):c.594+38_594+43delGTTGTT
ISCN -
DB-ID TGFB2_000013 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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-10-29 20:49:11 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TGFB2 NM_003238.3 -?/. - c.510+38_510+43del r.(=) p.(=)


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