Variant #0000297297 (NC_000017.10:g.74539092C>T, NC_000017.10(NM_001077620.2):c.*60-19C>T (PRCD))

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.74539092C>T
DNA change (hg38) g.76543010C>T
Published as PRCD(NM_001077620.3):c.*60-19C>T
ISCN -
DB-ID PRCD_000005
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) 0.9949 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRCD NM_001077620.2 -/. - c.*60-19C>T r.(=) p.(=)
CYGB NM_134268.4 -/. - c.-5468G>A r.(?) p.(=)


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