Variant #0000266645 (NC_000006.11:g.31084964T>C, NC_000006.11(NM_014068.2):c.-229+2296T>C (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.31084964T>C
DNA change (hg38) g.31117187T>C
Published as CDSN(NM_001264.5):c.428A>G (p.N143S), PSORS1C1(NM_014068.3):c.-229+2296T>C
ISCN -
DB-ID CDSN_000017
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) 0.75521 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)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CDSN NM_001264.4 -/. - c.428= r.(=) p.(Ser143=)
PSORS1C1 NM_014068.2 -/. - c.-229+2296T>C r.(=) p.(=)
PSORS1C2 NM_014069.2 -/. - c.*20764A>G r.(=) p.(=)
C6orf15 NM_014070.2 -/. - c.-4632A>G r.(?) p.(=)


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