Variant #0000611636 (NC_000008.10:g.48877154C>T, NM_006904.6:c.-4468G>A (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.48877154C>T
DNA change (hg38) g.47964594C>T
Published as MCM4(NM_005914.4):c.714C>T (p.D238=)
ISCN -
DB-ID MCM4_000018 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) 1.0E-5 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-06-23 19:45:09 +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.-4468G>A r.(?) p.(=)
MCM4 NM_005914.3 -?/. - c.714C>T r.(?) p.(Asp238=)
PRKDC NM_006904.6 -?/. - c.-4468G>A r.(?) p.(=)


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