Variant #0000521127 (NC_000004.11:g.107168423_107168424insTTCA, NM_001163435.1:c.803_804insTGAA (TBCK))

Chromosome 4
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.107168423_107168424insTTCA
DNA change (hg38) g.106247266_106247267insTTCA
Published as -
ISCN -
DB-ID AIMP1_000012
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-16 14:16:59 +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.-68396_-68395insTTCA r.(?) p.(=)
TBCK NM_001163435.1 +/. - c.803_804insTGAA r.(?) p.(Met268IlefsTer9)
AIMP1 NM_004757.3 +/. - c.-69104_-69103insTTCA r.(?) p.(=)


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