Variant #0000534923 (NC_000008.10:g.48776016T>C, NM_006904.6:c.5694A>G (PRKDC))

Chromosome 8
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.48776016T>C
DNA change (hg38) g.47863455T>C
Published as PRKDC(NM_006904.6):c.5694A>G (p.Q1898=)
ISCN -
DB-ID PRKDC_000049
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) 0.00022 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 2020-06-23 19:43:29 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRKDC NM_001081640.1 -?/. - c.5694A>G r.(?) p.(Gln1898=)
PRKDC NM_006904.6 -?/. - c.5694A>G r.(?) p.(Gln1898=)


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