Variant #0001024834 (NC_000003.11:g.49070150A>G, NM_017730.2:c.1952T>C (QRICH1))

Chromosome 3
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.49070150A>G
DNA change (hg38) -
Published as QRICH1(NM_017730.4):c.1952T>C (p.L651S)
ISCN -
DB-ID IMPDH2_000015
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2025-02-07 18:57:27 +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.-3367T>C r.(?) p.(=)
QRICH1 NM_017730.2 +?/. - c.1952T>C r.(?) p.(Leu651Ser)


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