Variant #0000858704 (NC_000002.11:g.74684671C>A, NM_006302.2:c.*3731G>T (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.74684671C>A
DNA change (hg38) -
Published as INO80B(NM_031288.4):c.751C>A (p.R251=)
ISCN -
DB-ID INO80B_000025
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) 4.0E-5 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 2022-05-09 15:51:19 +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     
MOGS NM_006302.2 -?/. - c.*3731G>T r.(=) p.(=)
WBP1 NM_012477.3 -?/. - c.-1059C>A r.(?) p.(=)
INO80B NM_031288.3 -?/. - c.751C>A r.(?) p.(Arg251=)
INO80B-WBP1 NR_037849.1 -?/. - n.845C>A r.(?) -


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