Variant #0000801285 (NC_000003.11:g.49060125C>G, NM_001009996.2:c.-4128G>C (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.49060125C>G
DNA change (hg38) -
Published as NDUFAF3(NM_199069.1):c.271-10C>G
ISCN -
DB-ID DALRD3_000004
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) 0.00026 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 2021-09-17 14:40:49 +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.*1691G>C r.(=) p.(=)
DALRD3 NM_001009996.2 -?/. - c.-4128G>C r.(?) p.(=)
WDR6 NM_018031.3 -?/. - c.*7404C>G r.(=) p.(=)
NDUFAF3 NM_199069.1 -?/. - c.271-10C>G r.(=) p.(=)


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