Variant #0000516971 (NC_000002.11:g.74688544A>G, NM_006302.2:c.2372T>C (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.74688544A>G
DNA change (hg38) g.74461417A>G
Published as MOGS(NM_001146158.1):c.2054T>C (p.(Val685Ala))
ISCN -
DB-ID INO80B_000001
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 2019-07-18 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.2372T>C r.(?) p.(Val791Ala)
WBP1 NM_012477.3 -?/. - c.*736A>G r.(=) p.(=)
INO80B NM_031288.3 -?/. - c.*3553A>G r.(=) p.(=)


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