Variant #0000567683 (NC_000019.9:g.45681351C>T, NM_212550.3:c.-748C>T (BLOC1S3))

Chromosome 19
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.45681351C>T
DNA change (hg38) g.45178093C>T
Published as TRAPPC6A(NM_024108.2):c.126G>A (p.(Lys42Lys))
ISCN -
DB-ID BLOC1S3_000006
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRAPPC6A NM_024108.2 ?/. - c.126G>A r.(?) p.(Lys42=)
BLOC1S3 NM_212550.3 ?/. - c.-748C>T r.(?) p.(=)


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