Variant #0000979668 (NC_000011.9:g.58980122T>C, NM_015177.1:c.*7740T>C (DTX4))

Chromosome 11
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.58980122T>C
DNA change (hg38) -
Published as MPEG1(NM_001039396.2):c.217A>G (p.T73A)
ISCN -
DB-ID DTX4_000010
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) 0.00212 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 2024-04-19 20:27:30 +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     
MPEG1 NM_001039396.1 -?/. - c.217A>G r.(?) p.(Thr73Ala)
DTX4 NM_015177.1 -?/. - c.*7740T>C r.(=) p.(=)


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