Variant #0000001526 (NC_000011.10:g.102799766del, NM_002421.3:c.-1674del (MMP1))

Individual ID 00000321
Chromosome 11
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.102799766del
Published as MMP-1 1607 1G/2G
Reference dbSNP
DB-ID MMP1_000001 See all 2 reported entries
dbSNP ID rs1799750
Frequency 61/133
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Nuur Athirah Binti Mohd Daud
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Nuur Athirah Binti Mohd Daud
Date created 2021-01-05 16:12:19 +08:00 (CST)
Date last edited 2021-09-01 11:43:10 +08:00 (CST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
MMP1 NM_002421.3 +/. - c.-1674del - r.(=) p.(=) - -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000336 DNA PCR MMP1 2 Nuur Athirah Binti Mohd Daud