Variant #0000550866 (NC_000013.10:g.48528650G>A, NM_003850.2:c.845C>T (SUCLA2))

Chromosome 13
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.48528650G>A
DNA change (hg38) g.47954515G>A
Published as SUCLA2(NM_003850.2):c.845C>T (p.A282V)
ISCN -
DB-ID SUCLA2_000012
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SUCLA2 NM_003850.2 ?/. - c.845C>T r.(?) p.(Ala282Val)
NUDT15 NM_018283.1 ?/. - c.-83233G>A r.(?) p.(=)


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