Variant #0000911963 (NC_000003.11:g.49065217G>A, NM_017730.2:c.*2668C>T (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.49065217G>A
DNA change (hg38) -
Published as IMPDH2(NM_000884.3):c.457C>T (p.R153C)
ISCN -
DB-ID IMPDH2_000012
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) 0.00014 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-01-11 15:44:22 +01:00 (CET)
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.457C>T r.(?) p.(Arg153Cys)
QRICH1 NM_017730.2 ?/. - c.*2668C>T r.(=) p.(=)
NDUFAF3 NM_199069.1 ?/. - c.*4612G>A r.(=) p.(=)


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