Variant #0000984164 (NC_000022.10:g.28194932_28194933insC, NM_002430.2:c.1599_1600insG (MN1))

Chromosome 22
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.28194932_28194933insC
DNA change (hg38) -
Published as MN1(NM_002430.3):c.1599_1600insG (p.(Gln534Alafs*26))
ISCN -
DB-ID MN1_000045
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 2024-04-19 20:27:30 +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     
MN1 NM_002430.2 -?/. - c.1599_1600insG r.(?) p.(Gln534Alafs*26)


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