Variant #0000266638 (NC_000006.11:g.31084090G>T, NC_000006.11(NM_014068.2):c.-229+1422G>T (PSORS1C1))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.31084090G>T
DNA change (hg38) g.31116313G>T
Published as CDSN(NM_001264.4):c.1302C>A (p.S434R), CDSN(NM_001264.5):c.1302C>A (p.S434R)
ISCN -
DB-ID CDSN_000007 See all 2 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) 0.00326 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.1302C>A r.(?) p.(Ser434Arg)
PSORS1C1 NM_014068.2 -?/. - c.-229+1422G>T r.(=) p.(=)
PSORS1C2 NM_014069.2 -?/. - c.*21638C>A r.(=) p.(=)
C6orf15 NM_014070.2 -?/. - c.-3758C>A r.(?) p.(=)


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