Variant #0001037025 (NC_000008.10:g.63978501_63978502insAA, NM_000370.3:c.513_514insTT (TTPA))

Chromosome 8
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.63978501_63978502insAA
DNA change (hg38) -
Published as TTPA(NM_000370.3):c.513_514insTT (p.(Thr172LeufsTer5))
ISCN -
DB-ID TTPA_000012 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) 0.00015 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TTPA NM_000370.3 +/. - c.513_514insTT r.(?) p.(Thr172LeufsTer5)


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