Variant #0000867175 (NC_000023.10:g.153051877C>T, NM_014370.3:c.*902C>T (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.153051877C>T
DNA change (hg38) -
Published as IDH3G(NM_004135.3):c.952G>A (p.(Ala318Thr))
ISCN -
DB-ID SRPK3_000035
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IDH3G NM_004135.3 ?/. - c.952G>A r.(?) p.(Ala318Thr)
SRPK3 NM_014370.3 ?/. - c.*902C>T r.(=) p.(=)


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