Variant #0000275550 (NC_000018.9:g.28681903T>C, NM_004949.3:c.32A>G (DSC2))

Chromosome 18
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.28681903T>C
DNA change (hg38) g.31101940T>C
Published as DSC2(NM_004949.3):c.32A>G (p.(Asn11Ser), p.N11S), DSC2(NM_004949.5):c.32A>G (p.N11S), DSC2(NM_024422.4):c.32A>G (p.N11S)
ISCN -
DB-ID DSC2_000001 See all 7 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) 0.01368 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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     

P-domain     
DSC1 NM_004948.3 -/. - c.*28782A>G r.(=) p.(=) -
DSC2 NM_004949.3 -/. - c.32A>G r.(?) p.(Asn11Ser) -


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