Variant #0000314407 (NC_000006.11:g.13316856G>A, NM_030948.2:c.*29546G>A (PHACTR1))

Chromosome 6
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.13316856G>A
DNA change (hg38) g.13316624G>A
Published as TBC1D7(NM_016495.6):c.466C>T (p.R156*)
ISCN -
DB-ID TBC1D7_000005
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) 1.0E-5 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TBC1D7 NM_016495.4 +/. - c.466C>T r.(?) p.(Arg156Ter)
PHACTR1 NM_030948.2 +/. - c.*29546G>A r.(=) p.(=)


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