Variant #0000441426 (NC_000014.8:g.76437614A>G, NC_000014.8(NM_003239.2):c.517-16T>C (TGFB3))

Chromosome 14
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Does not affect function
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.76437614A>G
DNA change (hg38) g.75971271A>G
Published as -
ISCN -
DB-ID TGFB3_000008 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs3917176
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.0015 View details
Owner Paul van der Zwaag
Database submission license No license selected
Created by Paul van der Zwaag
Date created 2009-02-25 10:11:50 +01:00 (CET)
Date last edited 2009-06-17 15:07:14 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
TGFB3 NM_003239.2 -/- 2i c.517-16T>C r.(?) p.(=) -


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