Variant #0000550870 (NC_000013.10:g.48563008G>A, NC_000013.10(NM_003850.2):c.371+9C>T (SUCLA2))

Chromosome 13
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.48563008G>A
DNA change (hg38) g.47988873G>A
Published as SUCLA2(NM_003850.3):c.371+9C>T
ISCN -
DB-ID SUCLA2_000009 See all 2 reported entries
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) 0.74802 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +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.371+9C>T r.(=) p.(=)
NUDT15 NM_018283.1 -/. - c.-48875G>A r.(?) p.(=)


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