Variant #0000951280 (NC_000019.9:g.36399123C>T, NM_003332.3:c.8G>A (TYROBP))

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.36399123C>T
DNA change (hg38) -
Published as TYROBP(NM_003332.3):c.8G>A (p.(Gly3Glu))
ISCN -
DB-ID TYROBP_000029
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) 1.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2023-11-27 17:35:39 +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     
TYROBP NM_003332.3 -?/. - c.8G>A r.(?) p.(Gly3Glu)
HCST NM_014266.3 -?/. - c.*4061C>T r.(=) p.(=)


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