Variant #0000677032 (NC_000003.11:g.49059873A>G, NM_001009996.2:c.-3876T>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.49059873A>G
DNA change (hg38) -
Published as NDUFAF3(NM_199073.1):c.1A>G (p.M1?)
ISCN -
DB-ID IMPDH2_000006
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_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)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IMPDH2 NM_000884.2 ?/. - c.*1943T>C r.(=) p.(=)
DALRD3 NM_001009996.2 ?/. - c.-3876T>C r.(?) p.(=)
WDR6 NM_018031.3 ?/. - c.*7152A>G r.(=) p.(=)
NDUFAF3 NM_199069.1 ?/. - c.172A>G r.(?) p.(Met58Val)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.