Variant #0001037728 (NC_000010.10:g.114711262G>A, NM_030756.4:c.277G>A (TCF7L2))

Chromosome 10
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.114711262G>A
DNA change (hg38) -
Published as TCF7L2(NM_001367943.1):c.277G>A (p.(Gly93Arg)), TCF7L2(NM_030756.5):c.277G>A (p.G93R)
ISCN -
DB-ID TCF7L2_000024 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) 7.0E-5 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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited 2025-07-08 13:22:38 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TCF7L2 NM_030756.4 -?/. - c.277G>A r.(?) p.(Gly93Arg)


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