Variant #0001034927 (NC_000005.9:g.138661340A>G, NM_199189.2:c.2360A>G (MATR3))

Chromosome 5
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.138661340A>G
DNA change (hg38) -
Published as MATR3(NM_018834.6):c.2360A>G (p.(Asn787Ser)), MATR3(NM_199189.2):c.2360A>G (p.N787S)
ISCN -
DB-ID MATR3_000007 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) 0.0003 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 2025-05-05 21:14:00 +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.2360A>G r.(?) p.(Asn787Ser)


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