Variant #0000912964 (NC_000008.10:g.48869906T>C, NC_000008.10(NM_006904.6):c.231+9A>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.48869906T>C
DNA change (hg38) -
Published as PRKDC(NM_006904.6):c.231+9A>G
ISCN -
DB-ID MCM4_000044
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) 0.0001 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-01-11 15:44:22 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRKDC NM_001081640.1 -?/. - c.231+9A>G r.(=) p.(=)
MCM4 NM_005914.3 -?/. - c.-3799T>C r.(?) p.(=)
PRKDC NM_006904.6 -?/. - c.231+9A>G r.(=) p.(=)


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