Variant #0000677031 (NC_000003.11:g.49059789C>G, NM_001009996.2:c.-3792G>C (DALRD3))

Chromosome 3
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.49059789C>G
DNA change (hg38) -
Published as NDUFAF3(NM_199069.1):c.88C>G (p.R30G)
ISCN -
DB-ID IMPDH2_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) 3.0E-5 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.*2027G>C r.(=) p.(=)
DALRD3 NM_001009996.2 ?/. - c.-3792G>C r.(?) p.(=)
WDR6 NM_018031.3 ?/. - c.*7068C>G r.(=) p.(=)
NDUFAF3 NM_199069.1 ?/. - c.88C>G r.(?) p.(Arg30Gly)


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