Variant #0000689187 (NC_000004.11:g.107157622C>T, NM_001163435.1:c.1275G>A (TBCK))

Chromosome 4
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.107157622C>T
DNA change (hg38) -
Published as TBCK(NM_001290768.2):c.759G>A (p.T253=)
ISCN -
DB-ID AIMP1_000022
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) 0.0009 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AIMP1 NM_001142415.1 -?/. - c.-79197C>T r.(?) p.(=)
TBCK NM_001163435.1 -?/. - c.1275G>A r.(?) p.(Thr425=)
AIMP1 NM_004757.3 -?/. - c.-79905C>T r.(?) p.(=)


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