Variant #0000564426 (NC_000018.9:g.28935073G>A, NM_001942.2:c.2914G>A (DSG1))

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.28935073G>A
DNA change (hg38) g.31355110G>A
Published as DSG1(NM_001942.2):c.2914G>A (p.(Gly972Ser)), DSG1(NM_001942.3):c.2914G>A (p.G972S)
ISCN -
DB-ID DSG1_000019 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) 0.00127 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2019-12-04 15:24:38 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DSG1 NM_001942.2 -/. - c.2914G>A r.(?) p.(Gly972Ser)


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