Variant #0000981053 (NC_000014.8:g.91633956C>T, NC_000014.8(NM_024952.6):c.257+234C>T (C14orf159))

Chromosome 14
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.91633956C>T
DNA change (hg38) -
Published as DGLUCY(NM_001286473.2):c.401C>T (p.(Ser134Phe))
ISCN -
DB-ID C14orf159_000003
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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RPS6KA5 NM_004755.2 -?/. - c.-107178G>A r.(?) p.(=)
C14orf159 NM_024952.6 -?/. - c.257+234C>T r.(=) p.(=)


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