Variant #0000291482 (NC_000017.10:g.44101605_44101607del, NM_001377265.1:c.*68_*70del (MAPT))

Chromosome 17
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.44101605_44101607del
DNA change (hg38) g.46024239_46024241del
Published as MAPT(NM_005910.5):c.*68_*70delAAT
ISCN -
DB-ID MAPT_000111
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
STH NM_001007532.2 ?/. - c.*24573_*24575del r.(=) p.(=)
MAPT NM_001377265.1 ?/. - c.*68_*70del r.(?) p.(=)
MAPT NM_016835.4 ?/. - c.*68_*70del r.(=) p.(=)


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