Variant #0000658161 (NC_000017.10:g.44061060C>T, NM_001123066.3:c.890C>T (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.44061060C>T
DNA change (hg38) g.45983694C>T
Published as MAPT(NM_001123066.3):c.890C>T (p.A297V)
ISCN -
DB-ID MAPT_000138
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) 5.0E-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 2020-03-23 16:13:27 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
STH NM_001007532.2 -?/. - c.-15586C>T r.(?) p.(=)
MAPT NM_001123066.3 -?/. - c.890C>T r.(?) p.(Ala297Val)
MAPT NM_016835.4 -?/. - c.890C>T r.(?) p.(Ala297Val)


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