Variant #0000570758 (NC_000021.8:g.45528884C>T, NM_003274.4:c.*5472C>T (TRAPPC10))

Chromosome 21
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.45528884C>T
DNA change (hg38) g.44109003C>T
Published as PWP2(NM_005049.3):c.38C>T (p.T13M)
ISCN -
DB-ID PWP2_000001
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRAPPC10 NM_003274.4 ?/. - c.*5472C>T r.(=) p.(=)
PWP2 NM_005049.2 ?/. - c.38C>T r.(?) p.(Thr13Met)


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