Variant #0000291503 (NC_000017.10:g.44087754C>T, NM_001123066.3:c.1906C>T (MAPT))

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.44087754C>T
DNA change (hg38) g.46010388C>T
Published as MAPT(NM_005910.5):c.901C>T (p.P301S)
ISCN -
DB-ID MAPT_000053 See all 7 reported entries
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.*10722C>T r.(=) p.(=)
MAPT NM_001123066.3 +/. - c.1906C>T r.(?) p.(Pro636Ser)
MAPT NM_016835.4 +/. - c.1852C>T r.(?) p.(Pro618Ser)


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