Variant #0000723612 (NC_000011.9:g.6637606G>A, NM_000391.3:c.1015C>T (TPP1))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.6637606G>A
DNA change (hg38) -
Published as TPP1(NM_000391.3):c.1015C>T (p.R339W)
ISCN -
DB-ID TPP1_000047 See all 7 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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TPP1 NM_000391.3 +?/. - c.1015C>T r.(?) p.(Arg339Trp)
DCHS1 NM_003737.2 +?/. - c.*5404C>T r.(=) p.(=)
TAF10 NM_006284.3 +?/. - c.-4186C>T r.(?) p.(=)


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