Variant #0000516978 (NC_000002.11:g.74691724_74691725del, NM_006302.2:c.480_481del (MOGS))

Chromosome 2
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.74691724_74691725del
DNA change (hg38) g.74464597_74464598del
Published as MOGS(NM_006302.3):c.480_481delCA (p.I161Pfs*10)
ISCN -
DB-ID INO80B_000008
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MOGS NM_006302.2 +/. - c.480_481del r.(?) p.(Ile161ProfsTer10)
WBP1 NM_012477.3 +/. - c.*3916_*3917del r.(=) p.(=)
INO80B NM_031288.3 +/. - c.*6733_*6734del r.(=) p.(=)


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