Variant #0000314227 (NC_000013.10:g.48528283C>T, NM_003850.2:c.1099G>A (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.48528283C>T
DNA change (hg38) g.47954148C>T
Published as SUCLA2(NM_003850.2):c.1099G>A (p.D367N)
ISCN -
DB-ID SUCLA2_000007
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) 0.01684 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SUCLA2 NM_003850.2 -?/. - c.1099G>A r.(?) p.(Asp367Asn)
NUDT15 NM_018283.1 -?/. - c.-83600C>T r.(?) p.(=)


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