Variant #0000534932 (NC_000008.10:g.48826575C>G, NM_006904.6:c.2667G>C (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.48826575C>G
DNA change (hg38) g.47914015C>G
Published as PRKDC(NM_001081640.1):c.2667G>C (p.(Glu889Asp)), PRKDC(NM_006904.6):c.2667G>C (p.E889D)
ISCN -
DB-ID PRKDC_000058 See all 2 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) 0.00033 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-23 19:43:37 +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.2667G>C r.(?) p.(Glu889Asp)
PRKDC NM_006904.6 -?/. - c.2667G>C r.(?) p.(Glu889Asp)


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