Variant #0001034246 (NC_000004.11:g.107173063T>C, NM_001163435.1:c.557A>G (TBCK))

Chromosome 4
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.107173063T>C
DNA change (hg38) -
Published as TBCK(NM_001163435.3):c.557A>G (p.(Asp186Gly))
ISCN -
DB-ID AIMP1_000048
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AIMP1 NM_001142415.1 ?/. - c.-63756T>C r.(?) p.(=)
TBCK NM_001163435.1 ?/. - c.557A>G r.(?) p.(Asp186Gly)
AIMP1 NM_004757.3 ?/. - c.-64464T>C r.(?) p.(=)


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