Variant #0000571765 (NC_000022.10:g.31011674T>C, NM_000355.3:c.840T>C (TCN2))

Chromosome 22
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.31011674T>C
DNA change (hg38) g.30615687T>C
Published as TCN2(NM_000355.2):c.840T>C (p.D280=), TCN2(NM_001184726.1):c.759T>C (p.D253=)
ISCN -
DB-ID TCN2_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) 0.00217 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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     
TCN2 NM_000355.3 -/. - c.840T>C r.(?) p.(Asp280=)


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