Variant #0000243971 (NC_000017.10:g.44039757C>T, NM_001123066.3:c.54C>T (MAPT))

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Effect unknown
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.44039757C>T
DNA change (hg38) g.45962391C>T
Published as -
ISCN -
DB-ID MAPT_000013
Variant remarks Observed in 1 Asian individual of the <a href=\""http://www.cephb.fr/en/hgdp/diversity.php/"""" target=”blank”> Human Genome Diversity Panel</a>. /r/Silent point mutation in coding region""
Reference -
ClinVar ID -
dbSNP ID rs63750811
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 7.0E-5 View details
Owner Marc Cruts
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Julia Lopez
Date created 2013-05-01 13:44:57 +02:00 (CEST)
Date last edited 2020-07-13 16:29:41 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAPT NM_001123066.3 -/? 2 c.54C>T r.(?) p.(=)


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