Variant #0000331419 (NC_000007.13:g.6094254A>T, NM_006303.3:c.*30932A>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.6094254A>T
DNA change (hg38) g.6054623A>T
Published as EIF2AK1(NM_001134335.1):c.200T>A (p.(Leu67His))
ISCN -
DB-ID EIF2AK1_000004
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 2018-01-15 20:58:59 +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     
ANKRD61 NM_001271700.1 ?/. - c.*18237A>T r.(=) p.(=)
AIMP2 NM_006303.3 ?/. - c.*30932A>T r.(=) p.(=)
EIF2AK1 NM_014413.3 ?/. - c.200T>A r.(?) p.(Leu67His)


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