Variant #0001014214 (NC_000006.11:g.34385676T>C, NC_000006.11(NM_001203245.2):c.457-352A>G (RPS10))

Chromosome 6
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.34385676T>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID NUDT3_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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2024-10-29 21:08:56 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RPS10-NUDT3 NM_001202470.2 -?/. - c.456+470A>G r.(=) p.(=)
RPS10 NM_001203245.2 -?/. - c.457-352A>G r.(=) p.(=)
NUDT3 NM_006703.3 -?/. - c.-25537A>G r.(?) p.(=)


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