Variant #0000521131 (NC_000004.11:g.107248623T>C, NM_001163435.1:c.-11565A>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.107248623T>C
DNA change (hg38) g.106327466T>C
Published as AIMP1(NM_004757.3):c.125T>C (p.(Leu42Ser))
ISCN -
DB-ID AIMP1_000015
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 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AIMP1 NM_001142415.1 ?/. - c.125T>C r.(?) p.(Leu42Ser)
TBCK NM_001163435.1 ?/. - c.-11565A>G r.(?) p.(=)
AIMP1 NM_004757.3 ?/. - c.125T>C r.(?) p.(Leu42Ser)


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