Variant #0000525815 (NC_000005.9:g.52385852_52385853insT, NM_002203.3:c.3425_3426insT (ITGA2))

Chromosome 5
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.52385852_52385853insT
DNA change (hg38) g.53090022_53090023insT
Published as ITGA2(NM_002203.3):c.3425_3426insT (p.I1143Nfs*22)
ISCN -
DB-ID ITGA2_000015
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-17 10:13:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ITGA2 NM_002203.3 ?/. - c.3425_3426insT r.(?) p.(Ile1143AsnfsTer22)


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