Variant #0000608133 (NC_000002.11:g.74690045_74690046insCAGG, NM_006302.2:c.870_871insCCTG (MOGS))

Chromosome 2
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.74690045_74690046insCAGG
DNA change (hg38) g.74462918_74462919insCAGG
Published as MOGS(NM_001146158.1):c.552_553insCCTG (p.(Gly185ProfsTer6))
ISCN -
DB-ID INO80B_000015
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-12-04 14:54:23 +01:00 (CET)
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.870_871insCCTG r.(?) p.(Gly291ProfsTer6)
WBP1 NM_012477.3 -?/. - c.*2237_*2238insCAGG r.(=) p.(=)
INO80B NM_031288.3 -?/. - c.*5054_*5055insCAGG r.(=) p.(=)


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