Variant #0000441340 (NC_000006.11:g.7542274T>C, DSP(NM_004415.2):c.126T>C)

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.7542274T>C
DNA change (hg38) g.7542041T>C
Published as -
ISCN -
DB-ID DSP_000003 See all 6 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs36087964
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.05458 View details
Owner Paul van der Zwaag
Database submission license No license selected
Created by Paul van der Zwaag
Date created 2009-01-26 15:51:42 +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 -/- 1 c.126T>C r.(?) p.(=) PKP1 and JUP interacting domain