Variant #0000912026 (NC_000004.11:g.107183323G>A, NM_001163435.1:c.313C>T (TBCK))

Chromosome 4
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.107183323G>A
DNA change (hg38) -
Published as TBCK(NM_001163435.1):c.313C>T (p.(Gln105*))
ISCN -
DB-ID AIMP1_000038
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 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     
AIMP1 NM_001142415.1 +?/. - c.-53496G>A r.(?) p.(=)
TBCK NM_001163435.1 +?/. - c.313C>T r.(?) p.(Gln105*)
AIMP1 NM_004757.3 +?/. - c.-54204G>A r.(?) p.(=)


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