Variant #0000883499 (NC_000001.10:g.54360103G>A, NM_000792.5:c.220G>A (DIO1))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.54360103G>A
DNA change (hg38) -
Published as DIO1(NM_000792.7):c.220G>A (p.V74I)
ISCN -
DB-ID DIO1_000005
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) 1.0E-5 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 2022-11-01 13:01:21 +01:00 (CET)
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     
DIO1 NM_000792.5 ?/. - c.220G>A r.(?) p.?
YIPF1 NM_018982.4 ?/. - c.-4987C>T r.(?) p.(=)


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