Variant #0001015786 (NC_000019.9:g.36395386G>A, NM_003332.3:c.*85C>T (TYROBP))

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.36395386G>A
DNA change (hg38) -
Published as TYROBP(NM_001173514.1):c.*85C>T (p.(=))
ISCN -
DB-ID TYROBP_000032
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) 0.00044 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 2024-10-29 21:08:56 +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.*85C>T r.(=) p.(=)
HCST NM_014266.3 ?/. - c.*324G>A r.(=) p.(=)
NFKBID NM_139239.1 ?/. - c.-4408C>T r.(?) p.(=)


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