Variant #0000306251 (NC_000017.10:g.74536236C>G, NM_001077620.2:c.13C>G (PRCD))

Chromosome 17
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.74536236C>G
DNA change (hg38) g.76540154C>G
Published as PRCD(NM_001077620.2):c.13C>G (p.L5V)
ISCN -
DB-ID PRCD_000003
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) 0.00012 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     
PRCD NM_001077620.2 ?/. - c.13C>G r.(?) p.(Leu5Val)
CYGB NM_134268.4 ?/. - c.-2612G>C r.(?) p.(=)


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