Genomic variant #0000348476

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.44068924G>A
DNA change (hg38) -
Published as MAPT:NM_001123066.2:c.1479G>A (Pro493Pro)
ISCN -
DB-ID MAPT_000024 See all 5 reported entries
Variant remarks VKGL data sharing initiative Nederland; correct HGVS to be checked
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) 0.16254 View details
Owner VKGL-NL_Nijmegen




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

ClassClinical     

RNA change     

Protein     
MAPT NM_001123066.3 -/. - c.1479G>A benign r.(=) p.(=)
MAPT NM_016835.4 -/. - c.1479G>A benign r.(=) p.(=)