Variant #0000723613 (NC_000011.9:g.6638382C>T, NM_000391.3:c.511G>A (TPP1))

Chromosome 11
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.6638382C>T
DNA change (hg38) -
Published as TPP1(NM_000391.3):c.511G>A (p.G171R)
ISCN -
DB-ID DCHS1_000273
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TPP1 NM_000391.3 ?/. - c.511G>A r.(?) p.(Gly171Arg)
DCHS1 NM_003737.2 ?/. - c.*4628G>A r.(=) p.(=)
TAF10 NM_006284.3 ?/. - c.-4962G>A r.(?) p.(=)


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