Variant #0000976055 (NC_000004.11:g.107229957C>T, NM_001163435.1:c.161G>A (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.107229957C>T
DNA change (hg38) -
Published as TBCK(NM_001163435.3):c.161G>A (p.(Cys54Tyr))
ISCN -
DB-ID AIMP1_000042
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 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 2024-04-19 20:27:30 +02:00 (CEST)
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.-6862C>T r.(?) p.(=)
TBCK NM_001163435.1 ?/. - c.161G>A r.(?) p.(Cys54Tyr)
AIMP1 NM_004757.3 ?/. - c.-7570C>T r.(?) p.(=)


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