Variant #0000553196 (NC_000014.8:g.80677805A>T, NM_000793.5:c.11T>A (DIO2))

Chromosome 14
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.80677805A>T
DNA change (hg38) g.80211462A>T
Published as DIO2(NM_000793.6):c.11T>A (p.L4H)
ISCN -
DB-ID DIO2_000007
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) 0.00065 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DIO2 NM_000793.5 -?/. - c.11T>A r.(?) p.?
DIO2-AS1 NR_038355.1 -?/. - n.44A>T r.(?) -


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