Variant #0000993197 (NC_000003.11:g.122284891A>G, NM_138287.3:c.373A>G (DTX3L))

Chromosome 3
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.122284891A>G
DNA change (hg38) -
Published as DTX3L(NM_138287.3):c.373A>G (p.(Asn125Asp))
ISCN -
DB-ID DTX3L_000005
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +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     
PARP9 NM_031458.2 -?/. - c.-1695T>C r.(?) p.(=)
DTX3L NM_138287.3 -?/. - c.373A>G r.(?) p.(Asn125Asp)


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