Variant #0000677033 (NC_000003.11:g.49059911A>C, NM_001009996.2:c.-3914T>G (DALRD3))

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.49059911A>C
DNA change (hg38) -
Published as NDUFAF3(NM_199069.1):c.210A>C (p.I70=)
ISCN -
DB-ID IMPDH2_000007
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) 0.0001 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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2024-10-29 21:08:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IMPDH2 NM_000884.2 -?/. - c.*1905T>G r.(=) p.(=)
DALRD3 NM_001009996.2 -?/. - c.-3914T>G r.(?) p.(=)
WDR6 NM_018031.3 -?/. - c.*7190A>C r.(=) p.(=)
NDUFAF3 NM_199069.1 -?/. - c.210A>C r.(?) p.(Ile70=)


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