Variant #0000802968 (NC_000007.13:g.141352616_141352619del, NM_018238.3:c.1161_1164del (AGK))

Chromosome 7
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.141352616_141352619del
DNA change (hg38) -
Published as AGK(NM_018238.4):c.1161_1164delTGAG (p.S387Rfs*10)
ISCN -
DB-ID AGK_000019
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2021-09-17 14:40:49 +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     
KIAA1147 NM_001080392.1 +/. - c.*9839_*9842del r.(=) p.(=)
AGK NM_018238.3 +/. - c.1161_1164del r.(?) p.(Ser387Argfs*10)


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