Variant #0000562013 (NC_000017.10:g.44051788C>G, NM_001123066.3:c.258C>G (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.44051788C>G
DNA change (hg38) g.45974422C>G
Published as MAPT(NM_001123066.3):c.258C>G (p.G86=), MAPT(NM_005910.6):c.258C>G (p.G86=)
ISCN -
DB-ID MAPT_000089 See all 2 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) 6.0E-5 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +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.-24858C>G r.(?) p.(=)
MAPT NM_001123066.3 -?/. - c.258C>G r.(?) p.(Gly86=)
MAPT NM_016835.4 -?/. - c.258C>G r.(?) p.(Gly86=)


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