Variant #0000885408 (NC_000002.11:g.74689671G>C, NM_006302.2:c.1245C>G (MOGS))

Chromosome 2
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.74689671G>C
DNA change (hg38) -
Published as MOGS(NM_006302.3):c.1245C>G (p.I415M)
ISCN -
DB-ID INO80B_000005
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) 0.00346 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.1245C>G r.(?) p.(Ile415Met)
WBP1 NM_012477.3 -/. - c.*1863G>C r.(=) p.(=)
INO80B NM_031288.3 -/. - c.*4680G>C r.(=) p.(=)


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