Variant #0000915166 (NC_000019.9:g.18193068G>A, NM_005535.1:c.131C>T (IL12RB1))

Chromosome 19
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.18193068G>A
DNA change (hg38) -
Published as IL12RB1(NM_005535.1):c.131C>T (p.A44V)
ISCN -
DB-ID IL12RB1_000236
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) 0.00015 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
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     
IL12RB1 NM_005535.1 -?/. - c.131C>T r.(?) p.(Ala44Val)
MAST3 NM_015016.1 -?/. - c.-15535G>A r.(?) p.(=)


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