Variant #0000621121 (NC_000002.11:g.74688861A>G, NM_006302.2:c.2055T>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.74688861A>G
DNA change (hg38) g.74461734A>G
Published as MOGS(NM_006302.3):c.2055T>C (p.Y685=)
ISCN -
DB-ID INO80B_000014
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) 0.00095 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 2019-12-06 12:43:26 +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.2055T>C r.(?) p.(Tyr685=)
WBP1 NM_012477.3 -?/. - c.*1053A>G r.(=) p.(=)
INO80B NM_031288.3 -?/. - c.*3870A>G r.(=) p.(=)


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