Variant #0000676723 (NC_000002.11:g.74688527G>A, NM_006302.2:c.2389C>T (MOGS))

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.74688527G>A
DNA change (hg38) -
Published as MOGS(NM_006302.3):c.2389C>T (p.R797C)
ISCN -
DB-ID INO80B_000016
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) 5.0E-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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +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.2389C>T r.(?) p.(Arg797Cys)
WBP1 NM_012477.3 ?/. - c.*719G>A r.(=) p.(=)
INO80B NM_031288.3 ?/. - c.*3536G>A r.(=) p.(=)


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