Variant #0000441356 (NC_000006.11:g.7571692A>G, NM_004415.2:c.1778A>G (DSP))

Chromosome 6
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Does not affect function
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.7571692A>G
DNA change (hg38) g.7571459A>G
Published as -
ISCN -
DB-ID DSP_000032 See all 8 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs34239595
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00054 View details
Owner Paul van der Zwaag
Database submission license No license selected
Created by Paul van der Zwaag
Date created 2009-01-27 14:16:08 +01:00 (CET)
Date last edited 2018-12-24 13:09:58 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
DSP NM_004415.2 -/- 14 c.1778A>G r.(?) p.(Asn593Ser) -


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