Variant #0000313596 (NC_000019.9:g.36398148C>T, NM_003332.3:c.248G>A (TYROBP))

Chromosome 19
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.36398148C>T
DNA change (hg38) g.35907246C>T
Published as TYROBP(NM_003332.4):c.248G>A (p.R83H)
ISCN -
DB-ID TYROBP_000008
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) 0.0001 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TYROBP NM_003332.3 -/. - c.248G>A r.(?) p.(Arg83His)
HCST NM_014266.3 -/. - c.*3086C>T r.(=) p.(=)
NFKBID NM_139239.1 -/. - c.-7170G>A r.(?) p.(=)


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