Variant #0001034243 (NC_000004.11:g.107114937G>A, NC_000004.11(NM_001163435.1):c.1898-10C>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.107114937G>A
DNA change (hg38) -
Published as TBCK(NM_001163435.3):c.1898-10C>T, TBCK(NM_001290768.1):c.1382-10C>T
ISCN -
DB-ID TBCK_000014 See all 2 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) 0.00024 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AIMP1 NM_001142415.1 -?/. - c.-121882G>A r.(?) p.(=)
TBCK NM_001163435.1 -?/. - c.1898-10C>T r.(=) p.(=)
AIMP1 NM_004757.3 -?/. - c.-122590G>A r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.