Variant #0000519867 (NC_000003.11:g.45542003C>T, NM_015340.3:c.1692C>T (LARS2))

Chromosome 3
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.45542003C>T
DNA change (hg38) g.45500511C>T
Published as LARS2(NM_015340.4):c.1692C>T (p.A564=)
ISCN -
DB-ID LARS2_000018
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) 0.00212 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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     
LARS2 NM_015340.3 -?/. - c.1692C>T r.(?) p.(Ala564=)
LARS2-AS1 NR_048543.1 -?/. - n.261-5011G>A r.(?) -


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