Variant #0000528735 (NC_000006.11:g.34386194G>A, NM_001203245.2:c.408C>T (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.34386194G>A
DNA change (hg38) g.34418417G>A
Published as RPS10(NM_001203245.2):c.408C>T (p.A136=)
ISCN -
DB-ID NUDT3_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) 0.00217 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-19 11:25:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RPS10-NUDT3 NM_001202470.2 -?/. - c.408C>T r.(?) p.(Ala136=)
RPS10 NM_001203245.2 -?/. - c.408C>T r.(?) p.(Ala136=)
NUDT3 NM_006703.3 -?/. - c.-26055C>T r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.