Variant #0001067150 (NC_000019.9:g.18208606G>A, NM_005535.1:c.-10973C>T (IL12RB1))

Chromosome 19
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.18208606G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID chr19_008906
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2026-01-20 18:57:21 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IL12RB1 NM_005535.1 ?/. - c.-10973C>T r.(?) p.(=)
MAST3 NM_015016.1 ?/. - c.4G>A r.(?) p.(Asp2Asn)


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