Variant #0000288177 (NC_000017.10:g.73758830G>A, NM_000213.3:c.*5194G>A (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.73758830G>A
DNA change (hg38) g.75762749G>A
Published as GALK1(NM_000154.1):c.748C>T (p.L250=)
ISCN -
DB-ID GALK1_000004
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-14 12:57:24 +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.748C>T r.(?) p.(Leu250=)
ITGB4 NM_000213.3 -?/. - c.*5194G>A r.(=) p.(=)


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