Variant #0000248830 (NC_000006.11:g.31084163A>G, NC_000006.11(NM_014068.2):c.-229+1495A>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.31084163A>G
DNA change (hg38) g.31116386A>G
Published as CDSN(NM_001264.5):c.1229T>C (p.L410S), PSORS1C1(NM_014068.3):c.-229+1495A>G
ISCN -
DB-ID CDSN_000008
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) 0.5698 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.1229T>C r.(?) p.(Leu410Ser)
PSORS1C1 NM_014068.2 -/. - c.-229+1495A>G r.(=) p.(=)
PSORS1C2 NM_014069.2 -/. - c.*21565T>C r.(=) p.(=)
C6orf15 NM_014070.2 -/. - c.-3831T>C r.(?) p.(=)


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