Variant #0000612848 (NC_000011.9:g.102665933G>A, NM_002421.3:c.871C>T (MMP1))

Chromosome 11
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.102665933G>A
DNA change (hg38) g.102795202G>A
Published as MMP1(NM_002421.3):c.871C>T (p.R291W)
ISCN -
DB-ID MMP1_000004
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) 5.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-07-01 11:19:05 +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.871C>T r.(?) p.(Arg291Trp)
MMP3 NM_002422.3 ?/. - c.*40924C>T r.(=) p.(=)
WTAPP1 NR_038390.1 ?/. - n.561G>A r.(?) -


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