Variant #0000993998 (NC_000004.11:g.107168423_107168426del, NM_001163435.1:c.803_806del (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_107168426del
DNA change (hg38) -
Published as TBCK(NM_001163435.1):c.803_806delTGAA (p.(Met268fs)), TBCK(NM_001290768.2):c.287_290delTGAA (p.M96Rfs*26)
ISCN -
DB-ID TBCK_000002 See all 4 reported entries
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
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.-68396_-68393del r.(?) p.(=)
TBCK NM_001163435.1 +/. - c.803_806del r.(?) p.(Met268ArgfsTer26)
AIMP1 NM_004757.3 +/. - c.-69104_-69101del r.(?) p.(=)


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