Variant #0000521132 (NC_000004.11:g.107249358del, NM_001163435.1:c.-12299del (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.107249358del
DNA change (hg38) g.106328201del
Published as AIMP1(NM_004757.4):c.349delA (p.T117Qfs*25)
ISCN -
DB-ID AIMP1_000016
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +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.349del r.(?) p.(Thr117GlnfsTer25)
TBCK NM_001163435.1 +/. - c.-12299del r.(?) p.(=)
AIMP1 NM_004757.3 +/. - c.349del r.(?) p.(Thr117GlnfsTer25)


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