Variant #0000993036 (NC_000002.11:g.74689667_74689668insA, NM_006302.2:c.1248_1249insT (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.74689667_74689668insA
DNA change (hg38) -
Published as MOGS(NM_006302.2):c.1248_1249insT (p.(Val417fs))
ISCN -
DB-ID INO80B_000032
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 2024-08-28 13:16:32 +02:00 (CEST)
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.1248_1249insT r.(?) p.(Val417Cysfs*5)
WBP1 NM_012477.3 ?/. - c.*1859_*1860insA r.(=) p.(=)
INO80B NM_031288.3 ?/. - c.*4676_*4677insA r.(=) p.(=)


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