Variant #0000689746 (NC_000006.11:g.49426858G>A, NM_000255.3:c.322C>T (MUT))

Chromosome 6
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.49426858G>A
DNA change (hg38) -
Published as MMUT(NM_000255.3):c.322C>T (p.R108C)
ISCN -
DB-ID MUT_000006 See all 7 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) 0.00011 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 2020-09-15 15:50:26 +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     
MUT NM_000255.3 +/. - c.322C>T r.(?) p.(Arg108Cys)
CENPQ NM_018132.3 +/. - c.-4327G>A r.(?) p.(=)


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