Variant #0000894262 (NC_000017.10:g.73727943C>T, NM_000213.3:c.1266C>T (ITGB4))

Chromosome 17
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.73727943C>T
DNA change (hg38) -
Published as ITGB4(NM_000213.4):c.1266C>T (p.H422=), ITGB4(NM_000213.5):c.1266C>T (p.H422=)
ISCN -
DB-ID ITGB4_000050 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) 0.00016 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ITGB4 NM_000213.3 -?/. - c.1266C>T r.(?) p.(His422=)


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