Variant #0000929165 (NC_000006.11:g.31084716G>A, NC_000006.11(NM_014068.2):c.-229+2048G>A (PSORS1C1))

Chromosome 6
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.31084716G>A
DNA change (hg38) -
Published as CDSN(NM_001264.5):c.676C>T (p.P226S)
ISCN -
DB-ID C6orf15_000005
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) 0.00017 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 2023-07-07 10:10:56 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CDSN NM_001264.4 ?/. - c.676C>T r.(?) p.(Pro226Ser)
PSORS1C1 NM_014068.2 ?/. - c.-229+2048G>A r.(=) p.(=)
PSORS1C2 NM_014069.2 ?/. - c.*21012C>T r.(=) p.(=)
C6orf15 NM_014070.2 ?/. - c.-4384C>T r.(?) p.(=)


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