Variant #0000977797 (NC_000007.13:g.6078213C>A, NM_006303.3:c.*14891C>A (AIMP2))

Chromosome 7
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.6078213C>A
DNA change (hg38) -
Published as EIF2AK1(NM_014413.4):c.1209G>T (p.(Arg403=))
ISCN -
DB-ID AIMP2_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) 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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited 2025-11-01 13:22:20 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ANKRD61 NM_001271700.1 -?/. - c.*2196C>A r.(=) p.(=)
AIMP2 NM_006303.3 -?/. - c.*14891C>A r.(=) p.(=)
EIF2AK1 NM_014413.3 -?/. - c.1209G>T r.(?) p.(=)


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