Variant #0000608401 (NC_000003.11:g.167422676C>T, NM_007217.3:c.104G>A (PDCD10))

Chromosome 3
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.167422676C>T
DNA change (hg38) g.167704888C>T
Published as PDCD10(NM_007217.3):c.104G>A (p.R35Q, p.(Arg35Gln)), PDCD10(NM_007217.4):c.104G>A (p.R35Q), PDCD10(NM_145860.2):c.104G>A (p.R35Q)
ISCN -
DB-ID PDCD10_000010 See all 4 reported entries
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) 4.0E-5 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2023-11-27 17:27:23 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PDCD10 NM_007217.3 -?/. - c.104G>A r.(?) p.(Arg35Gln)


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