Variant #0000285354 (NC_000002.11:g.227661416_227661418del, NM_005544.2:c.2057_2059del (IRS1))

Chromosome 2
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.227661416_227661418del
DNA change (hg38) g.226796700_226796702del
Published as IRS1(NM_005544.2):c.2057_2059delGCA (p.S686del), IRS1(NM_005544.3):c.2057_2059delGCA (p.S686del)
ISCN -
DB-ID IRS1_000009 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) 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 2018-01-15 20:58:59 +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     
IRS1 NM_005544.2 -?/. - c.2057_2059del r.(?) p.(Ser686del)


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