Variant #0000278131 (NC_000006.11:g.150719380C>T, NM_001164694.1:c.*107C>T (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.150719380C>T
DNA change (hg38) g.150398244C>T
Published as IYD(NM_001164694.2):c.*107C>T
ISCN -
DB-ID IYD_000014
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) 0.1153 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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IYD NM_001164694.1 -/. - c.*107C>T r.(=) p.(=)
IYD NM_203395.2 -/. - c.*7C>T r.(=) p.(=)


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