Variant #0000865497 (NC_000017.10:g.73752819A>G, NM_000213.3:c.4932A>G (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.73752819A>G
DNA change (hg38) -
Published as ITGB4(NM_000213.4):c.4932A>G (p.P1644=), ITGB4(NM_000213.5):c.4932A>G (p.P1644=)
ISCN -
DB-ID ITGB4_000048 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) 3.0E-5 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 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GALK1 NM_000154.1 -?/. - c.*1318T>C r.(=) p.(=)
ITGB4 NM_000213.3 -?/. - c.4932A>G r.(?) p.(Pro1644=)


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