Variant #0000567686 (NC_000019.9:g.45683032G>T, NM_212550.3:c.478G>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.45683032G>T
DNA change (hg38) g.45179774G>T
Published as BLOC1S3(NM_212550.4):c.478G>T (p.V160L), BLOC1S3(NM_212550.5):c.478G>T (p.V160L)
ISCN -
DB-ID BLOC1S3_000008 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) 0.00166 View details
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 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     
TRAPPC6A NM_024108.2 ?/. - c.-1556C>A r.(?) p.(=)
BLOC1S3 NM_212550.3 ?/. - c.478G>T r.(?) p.(Val160Leu)


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