Variant #0000255637 (NC_000011.9:g.6636430A>C, NM_000391.3:c.1397T>G (TPP1))

Chromosome 11
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.6636430A>C
DNA change (hg38) g.6615199A>C
Published as TPP1(NM_000391.3):c.1397T>G (p.V466G), TPP1(NM_000391.4):c.1397T>G (p.V466G)
ISCN -
DB-ID TPP1_000113 See all 13 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 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 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.1397T>G r.(?) p.(Val466Gly)
ILK NM_004517.2 +/. - c.*4588A>C r.(=) p.(=)
TAF10 NM_006284.3 +/. - c.-3010T>G r.(?) p.(=)


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