Variant #0000608965 (NC_000004.11:g.107253029C>T, NM_001163435.1:c.-15971G>A (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.107253029C>T
DNA change (hg38) g.106331872C>T
Published as AIMP1(NM_004757.3):c.592C>T (p.P198S)
ISCN -
DB-ID AIMP1_000021
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) 0.00067 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +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.592C>T r.(?) p.(Pro198Ser)
TBCK NM_001163435.1 ?/. - c.-15971G>A r.(?) p.(=)
AIMP1 NM_004757.3 ?/. - c.592C>T r.(?) p.(Pro198Ser)


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