Variant #0000804670 (NC_000011.9:g.102668051C>T, NM_002421.3:c.286G>A (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.102668051C>T
DNA change (hg38) -
Published as MMP1(NM_002421.3):c.286G>A (p.D96N)
ISCN -
DB-ID MMP1_000008
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) 0.00102 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 2021-09-17 14:40:49 +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     
MMP1 NM_002421.3 ?/. - c.286G>A r.(?) p.(Asp96Asn)
MMP3 NM_002422.3 ?/. - c.*38806G>A r.(=) p.(=)
WTAPP1 NR_038390.1 ?/. - n.584-704C>T r.(?) -


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