Variant #0000885409 (NC_000002.11:g.74689719A>G, NM_006302.2:c.1197T>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.74689719A>G
DNA change (hg38) -
Published as MOGS(NM_006302.3):c.1197T>C (p.L399=)
ISCN -
DB-ID INO80B_000026
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) 2.0E-5 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:01:21 +01:00 (CET)
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.1197T>C r.(?) p.(Leu399=)
WBP1 NM_012477.3 -?/. - c.*1911A>G r.(=) p.(=)
INO80B NM_031288.3 -?/. - c.*4728A>G r.(=) p.(=)


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