Variant #0000336078 (NC_000023.10:g.153051413T>C, NM_014370.3:c.*438T>C (SRPK3))

Chromosome X
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.153051413T>C
DNA change (hg38) g.153785958T>C
Published as IDH3G(NM_004135.3):c.1096A>G (p.(Ile366Val))
ISCN -
DB-ID IDH3G_000001
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) 2.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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     
IDH3G NM_004135.3 ?/. - c.1096A>G r.(?) p.(Ile366Val)
SRPK3 NM_014370.3 ?/. - c.*438T>C r.(=) p.(=)


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