Variant #0000658247 (NC_000017.10:g.73753337G>T, NM_000213.3:c.5275G>T (ITGB4))

Chromosome 17
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.73753337G>T
DNA change (hg38) g.75757256G>T
Published as ITGB4(NM_000213.5):c.5275G>T (p.E1759*)
ISCN -
DB-ID ITGB4_000055
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) 1.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GALK1 NM_000154.1 ?/. - c.*800C>A r.(=) p.(=)
ITGB4 NM_000213.3 ?/. - c.5275G>T r.(?) p.(Glu1759Ter)


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