Variant #0000611170 (NC_000007.13:g.6054965G>T, NM_006303.3:c.324G>T (AIMP2))

Chromosome 7
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.6054965G>T
DNA change (hg38) g.6015334G>T
Published as AIMP2(NM_001326609.1):c.90G>T (p.L30F)
ISCN -
DB-ID AIMP2_000006
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +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     
AIMP2 NM_006303.3 ?/. - c.324G>T r.(?) p.(Leu108Phe)
EIF2AK1 NM_014413.3 ?/. - c.*9339C>A r.(=) p.(=)


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