Variant #0000297362 (NC_000019.9:g.11558240T>C, NC_000019.9(NM_001001329.1):c.850-14T>C (PRKCSH))

Chromosome 19
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.11558240T>C
DNA change (hg38) g.11447425T>C
Published as PRKCSH(NM_001289103.1):c.850-14T>C, PRKCSH(NM_002743.3):c.850-14T>C
ISCN -
DB-ID PRKCSH_000002 See all 3 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) 0.99208 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 2019-12-04 15:24:38 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRKCSH NM_001001329.1 -/. - c.850-14T>C r.(=) p.(=)
ELAVL3 NM_001420.3 -/. - c.*7101A>G r.(=) p.(=)


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