Variant #0000994227 (NC_000004.11:g.184614210C>G, NM_021942.5:c.2147C>G (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.184614210C>G
DNA change (hg38) -
Published as TRAPPC11(NM_021942.5):c.2147C>G (p.A716G, p.(Ala716Gly)), TRAPPC11(NM_021942.6):c.2147C>G (p.A716G)
ISCN -
DB-ID TRAPPC11_000048 See all 3 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) 0.00059 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2024-08-28 13:16:32 +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     
TRAPPC11 NM_021942.5 -?/. - c.2147C>G r.(?) p.(Ala716Gly)


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