Variant #0000255095 (NC_000008.10:g.48874162A>G, NM_006904.6:c.-1476T>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.48874162A>G
DNA change (hg38) g.47961602A>G
Published as MCM4(NM_005914.4):c.157A>G (p.T53A)
ISCN -
DB-ID MCM4_000002
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) 0.00015 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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRKDC NM_001081640.1 -?/. - c.-1476T>C r.(?) p.(=)
MCM4 NM_005914.3 -?/. - c.157A>G r.(?) p.(Thr53Ala)
PRKDC NM_006904.6 -?/. - c.-1476T>C r.(?) p.(=)


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