Variant #0000719685 (NC_000004.11:g.107165912T>C, NM_001163435.1:c.941A>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.107165912T>C
DNA change (hg38) -
Published as TBCK(NM_001290768.1):c.425A>G (p.N142S)
ISCN -
DB-ID AIMP1_000028
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) 0.0004 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 2021-02-08 18:36:18 +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.-70907T>C r.(?) p.(=)
TBCK NM_001163435.1 ?/. - c.941A>G r.(?) p.(Asn314Ser)
AIMP1 NM_004757.3 ?/. - c.-71615T>C r.(?) p.(=)


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