Variant #0001057109 (NC_000022.10:g.28194933_28194934insGTTGC, NM_002430.2:c.1598_1599insGCAAC (MN1))

Chromosome 22
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.28194933_28194934insGTTGC
DNA change (hg38) -
Published as MN1(NM_002430.3):c.1598_1599insGCAAC (p.(Gln535Hisfs*25))
ISCN -
DB-ID MN1_000061
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 2025-11-01 13:22:20 +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     
MN1 NM_002430.2 ?/. - c.1598_1599insGCAAC r.(?) p.(Gln535Hisfs*25)


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