Variant #0000291481 (NC_000017.10:g.44101601G>A, NM_001377265.1:c.*64G>A (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.44101601G>A
DNA change (hg38) g.46024235G>A
Published as MAPT(NM_005910.5):c.*64G>A
ISCN -
DB-ID MAPT_000110
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.*24569G>A r.(=) p.(=)
MAPT NM_001377265.1 ?/. - c.*64G>A r.(?) p.(=)
MAPT NM_016835.4 ?/. - c.*64G>A r.(=) p.(=)


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