Variant #0000309450 (NC_000004.11:g.184585165G>C, NM_021942.5:c.145G>C (TRAPPC11))

Chromosome 4
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.184585165G>C
DNA change (hg38) g.183664012G>C
Published as TRAPPC11(NM_021942.5):c.145G>C (p.(Val49Leu)), TRAPPC11(NM_021942.6):c.145G>C (p.V49L)
ISCN -
DB-ID TRAPPC11_000010 See all 2 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) 0.01418 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRAPPC11 NM_021942.5 -?/. - c.145G>C r.(?) p.(Val49Leu)
RWDD4 NM_152682.2 -?/. - c.-5060C>G r.(?) p.(=)


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