Variant #0000692468 (NC_000017.10:g.73758812G>A, NM_000213.3:c.*5176G>A (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.73758812G>A
DNA change (hg38) -
Published as GALK1(NM_000154.1):c.766C>T (p.R256W), GALK1(NM_000154.2):c.766C>T (p.(Arg256Trp))
ISCN -
DB-ID GALK1_000013 See all 3 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) 0.0002 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +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.766C>T r.(?) p.(Arg256Trp)
ITGB4 NM_000213.3 ?/. - c.*5176G>A r.(=) p.(=)


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