Genomic variant #0000085538

Individual ID 00055570
Chromosome 17
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.39727757C>T
DNA change (hg38) g.41571505C>T
Published as -
ISCN -
DB-ID KRT9_000004 See all 10 reported entries
Variant remarks -
Reference PubMed: Yang 2003
ClinVar ID -
dbSNP ID rs57758262
Origin Unknown
Segregation ?
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner Michel van Geel




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     
KRT9 NM_000226.3 +/. 1 c.488G>A - r.(?) p.(Arg163Gln)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000055523 DNA SEQ - - KRT9 1 Michel van Geel