Variant #0000314476 (NC_000022.10:g.31008882G>A, NM_000355.3:c.280G>A (TCN2))

Chromosome 22
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.31008882G>A
DNA change (hg38) g.30612895G>A
Published as TCN2(NM_000355.3):c.280G>A (p.(Gly94Ser)), TCN2(NM_001184726.1):c.280G>A (p.G94S)
ISCN -
DB-ID TCN2_000001 See all 3 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) 0.00212 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2019-12-04 15:24:38 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TCN2 NM_000355.3 -?/. - c.280G>A r.(?) p.(Gly94Ser)


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