Variant #0000278140 (NC_000006.11:g.150716696T>C, NM_001164694.1:c.793T>C (IYD))

Chromosome 6
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.150716696T>C
DNA change (hg38) g.150395560T>C
Published as IYD(NM_001164694.2):c.793T>C (p.C265R)
ISCN -
DB-ID IYD_000012 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) 0.87772 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IYD NM_001164694.1 -/. - c.793T>C r.(?) p.(Cys265Arg)
IYD NM_203395.2 -/. - c.687+1305T>C r.(=) p.(=)


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