Variant #0000527437 (NC_000006.11:g.150716651C>T, NM_001164694.1:c.748C>T (IYD))

Chromosome 6
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.150716651C>T
DNA change (hg38) g.150395515C>T
Published as IYD(NM_001164694.2):c.748C>T (p.P250S)
ISCN -
DB-ID IYD_000016
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) 0.00023 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 2020-03-23 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.748C>T r.(?) p.(Pro250Ser)
IYD NM_203395.2 ?/. - c.687+1260C>T r.(=) p.(=)


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