Variant #0000998193 (NC_000010.10:g.127462732del, NM_147191.1:c.365del (MMP21))

Chromosome 10
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.127462732del
DNA change (hg38) -
Published as MMP21(NM_147191.1):c.365delT (p.(Met122fs)), MMP21(NM_147191.1):c.365delT (p.M122Sfs*55)
ISCN -
DB-ID MMP21_000010 See all 3 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_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     
MMP21 NM_147191.1 ?/. - c.365del r.(?) p.(Met122Serfs*55)


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