Variant #0000251494 (NC_000011.9:g.6637499A>T, NC_000011.9(NM_000391.3):c.1075+47T>A (TPP1))

Chromosome 11
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.6637499A>T
DNA change (hg38) g.6616268A>T
Published as TPP1(NM_000391.4):c.1075+47T>A
ISCN -
DB-ID TPP1_000129
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) 3.0E-5 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 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TPP1 NM_000391.3 -/. - c.1075+47T>A r.(=) p.(=)
TAF10 NM_006284.3 -/. - c.-4079T>A r.(?) p.(=)


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