Variant #0000549742 (NC_000013.10:g.110436319_110436321dup, NM_003749.2:c.2102_2104dup (IRS2))

Chromosome 13
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.110436319_110436321dup
DNA change (hg38) g.109783972_109783974dup
Published as IRS2(NM_003749.2):c.2102_2104dupCCG (p.(Ala701dup)), IRS2(NM_003749.2):c.2102_2104dupCCG (p.A701dup), IRS2(NM_003749.3):c.2102_2104dupCCG (p.A701dup)
ISCN -
DB-ID IRS2_000011 See all 3 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) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IRS2 NM_003749.2 -?/. - c.2102_2104dup r.(?) p.(Ala701dup)


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