Variant #0000550869 (NC_000013.10:g.48562769T>C, NM_003850.2:c.441A>G (SUCLA2))

Chromosome 13
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.48562769T>C
DNA change (hg38) g.47988634T>C
Published as SUCLA2(NM_003850.2):c.441A>G (p.E147=)
ISCN -
DB-ID SUCLA2_000014
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 2020-07-03 16:55:41 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SUCLA2 NM_003850.2 -?/. - c.441A>G r.(?) p.(Glu147=)
NUDT15 NM_018283.1 -?/. - c.-49114T>C r.(?) p.(=)


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