Variant #0000521122 (NC_000004.11:g.106967749G>A, NM_001163435.1:c.2660C>T (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.106967749G>A
DNA change (hg38) g.106046592G>A
Published as TBCK(NM_001290768.1):c.2144C>T (p.T715I)
ISCN -
DB-ID AIMP1_000008
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) 0.00174 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AIMP1 NM_001142415.1 -?/. - c.-269070G>A r.(?) p.(=)
TBCK NM_001163435.1 -?/. - c.2660C>T r.(?) p.(Thr887Ile)
AIMP1 NM_004757.3 -?/. - c.-269778G>A r.(?) p.(=)


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