Variant #0000851649 (NC_000007.13:g.6066574C>G, NM_006303.3:c.*3252C>G (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.6066574C>G
DNA change (hg38) -
Published as EIF2AK1(NM_014413.4):c.1549G>C (p.G517R)
ISCN -
DB-ID AIMP2_000016
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) 2.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ANKRD61 NM_001271700.1 ?/. - c.-4433C>G r.(?) p.(=)
AIMP2 NM_006303.3 ?/. - c.*3252C>G r.(=) p.(=)
EIF2AK1 NM_014413.3 ?/. - c.1549G>C r.(?) p.(Gly517Arg)


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