Variant #0000808051 (NC_000017.10:g.44060605G>C, NM_001377265.1:c.660G>C (MAPT))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.44060605G>C
DNA change (hg38) g.45983239G>C
Published as MAPT(NM_001123066.3):c.435G>C (p.L145=)
ISCN -
DB-ID MAPT_000145
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) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2026-02-13 08:33:17 +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.-16041G>C r.(?) p.(=)
MAPT NM_001377265.1 -?/. - c.660G>C r.(?) p.(Leu220=)
MAPT NM_016835.4 -?/. - c.435G>C r.(?) p.(Leu145=)


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