Variant #0000331053 (NC_000006.11:g.44268970G>C, NM_020745.3:c.2716C>G (AARS2))

Chromosome 6
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.44268970G>C
DNA change (hg38) g.44301233G>C
Published as AARS2(NM_020745.3):c.2716C>G (p.(Gln906Glu))
ISCN -
DB-ID AARS2_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) 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 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AARS2 NM_020745.3 -?/. - c.2716C>G r.(?) p.(Gln906Glu)
TCTE1 NM_182539.3 -?/. - c.-3668C>G r.(?) p.(=)


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