Variant #0000539484 (NC_000010.10:g.127456139G>A, NM_147191.1:c.1372C>T (MMP21))

Chromosome 10
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.127456139G>A
DNA change (hg38) g.125767570G>A
Published as MMP21(NM_147191.1):c.1372C>T (p.(Arg458Ter), p.R458*)
ISCN -
DB-ID C10orf137_000002 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) 0.00016 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-29 11:26:56 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C10orf137 NM_015608.2 +?/. - c.*4098G>A r.(=) p.(=)
MMP21 NM_147191.1 +?/. - c.1372C>T r.(?) p.(Arg458Ter)


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