Variant #0000314807 (NC_000011.9:g.6636668C>T, NC_000011.9(NM_000391.3):c.1266+5G>A (TPP1))

Chromosome 11
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.6636668C>T
DNA change (hg38) g.6615437C>T
Published as TPP1(NM_000391.3):c.1266+5G>A (p.?), TPP1(NM_000391.4):c.1266+5G>A
ISCN -
DB-ID TPP1_000005 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) 0.00474 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 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TPP1 NM_000391.3 -?/. - c.1266+5G>A r.spl? p.?
ILK NM_004517.2 -?/. - c.*4826C>T r.(=) p.(=)
TAF10 NM_006284.3 -?/. - c.-3248G>A r.(?) p.(=)


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