Variant #0001015921 (NC_000022.10:g.28194960_28194962dup, NM_002430.2:c.1596_1598dup (MN1))

Chromosome 22
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.28194960_28194962dup
DNA change (hg38) -
Published as MN1(NM_002430.2):c.1596_1598dup (p.(Gln550dup)), MN1(NM_002430.3):c.1596_1598dupGCA (p.Q550dup)
ISCN -
DB-ID MN1_000036 See all 2 reported entries
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-10-29 21:08:56 +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.1596_1598dup r.(?) p.(Gln550dup)


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