Variant #0000313113 (NC_000011.9:g.102666316T>C, NM_002421.3:c.648A>G (MMP1))

Chromosome 11
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.102666316T>C
DNA change (hg38) g.102795585T>C
Published as MMP1(NM_002421.4):c.648A>G (p.A216=), WTAPP1(NR_038390.1):n.583+361T>C
ISCN -
DB-ID MMP1_000001
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) 0.92405 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MMP1 NM_002421.3 -/. - c.648A>G r.(?) p.(Ala216=)
MMP3 NM_002422.3 -/. - c.*40541A>G r.(=) p.(=)
WTAPP1 NR_038390.1 -/. - n.583+361T>C r.(?) -


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