Variant #0000929020 (NC_000005.9:g.138658499A>C, NM_199189.2:c.1991A>C (MATR3))

Chromosome 5
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.138658499A>C
DNA change (hg38) -
Published as MATR3(NM_199189.2):c.1991A>C (p.E664A), MATR3(NM_199189.3):c.1991A>C (p.E664A)
ISCN -
DB-ID MATR3_000006 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) 0.00028 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 2023-07-07 10:10:56 +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     
MATR3 NM_199189.2 -?/. - c.1991A>C r.(?) p.(Glu664Ala)


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