Variant #0000249090 (NC_000006.11:g.31085269A>G, NC_000006.11(NM_014068.2):c.-229+2601A>G (PSORS1C1))

Chromosome 6
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.31085269A>G
DNA change (hg38) g.31117492A>G
Published as CDSN(NM_001264.5):c.123T>C (p.P41=), PSORS1C1(NM_014068.3):c.-229+2601A>G
ISCN -
DB-ID CDSN_000019
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) 0.75533 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 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CDSN NM_001264.4 -/. - c.123= r.(=) p.(Pro41=)
PSORS1C1 NM_014068.2 -/. - c.-229+2601A>G r.(=) p.(=)
PSORS1C2 NM_014069.2 -/. - c.*20459T>C r.(=) p.(=)
C6orf15 NM_014070.2 -/. - c.-4937T>C r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.