Variant #0000307368 (NC_000006.11:g.34392537C>T, NM_001203245.2:c.231G>A (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.34392537C>T
DNA change (hg38) g.34424760C>T
Published as RPS10(NM_001203245.2):c.231G>A (p.Q77=)
ISCN -
DB-ID RPS10_000014
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) 0.00163 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-19 11:26:02 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RPS10-NUDT3 NM_001202470.2 -?/. - c.231G>A r.(?) p.(Gln77=)
RPS10 NM_001203245.2 -?/. - c.231G>A r.(?) p.(Gln77=)
NUDT3 NM_006703.3 -?/. - c.-32398G>A r.(?) p.(=)


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