Variant #0001601592 (NC_000017.10:g.44087787C>G, NC_000017.10(NM_016835.4):c.1866+19C>G (MAPT))

Chromosome 17
DNA change (genomic) (Relative to hg19 / GRCh37) g.44087787C>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID MAPT_000143
Frequency 2/12972
Freq. EA 1/8580
Freq. AA 1/4392
Average frequency (gnomAD v.2.1.1) -
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Ivo F.A.C. Fokkema
Date created 2013-05-03 16:44:12 +02:00 (CEST)
Date last edited 2013-05-05 18:04:55 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
MAPT NM_016835.4 ?/? c.1866+19C>G r.(=) p.(=)


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