Variant #0000286119 (NC_000017.10:g.44071294T>C, NM_001123066.3:c.1512T>C (MAPT))

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.44071294T>C
DNA change (hg38) g.45993928T>C
Published as MAPT(NM_001123066.3):c.1512T>C (p.T504=), MAPT(NM_001123066.4):c.1512T>C (p.T504=)
ISCN -
DB-ID MAPT_000026 See all 4 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) 0.1443 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
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.-5352T>C r.(?) p.(=)
MAPT NM_001123066.3 -/. - c.1512T>C r.(?) p.(Thr504=)
MAPT NM_016835.4 -/. - c.1507+2342T>C r.(=) p.(=)


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