Variant #0001034031 (NC_000003.11:g.49062387C>T, NM_017730.2:c.*5498G>A (QRICH1))

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.49062387C>T
DNA change (hg38) -
Published as IMPDH2(NM_000884.3):c.1237G>A (p.(Gly413Ser))
ISCN -
DB-ID IMPDH2_000016
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 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +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     
IMPDH2 NM_000884.2 ?/. - c.1237G>A r.(?) p.(Gly413Ser)
DALRD3 NM_001009996.2 ?/. - c.-6390G>A r.(?) p.(=)
QRICH1 NM_017730.2 ?/. - c.*5498G>A r.(=) p.(=)
WDR6 NM_018031.3 ?/. - c.*9666C>T r.(=) p.(=)
NDUFAF3 NM_199069.1 ?/. - c.*1782C>T r.(=) p.(=)


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