Variant #0000677623 (NC_000006.11:g.13306723del, NM_030948.2:c.*19413del (PHACTR1))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.13306723del
DNA change (hg38) -
Published as TBC1D7(NM_016495.5):c.703delC (p.L235*)
ISCN -
DB-ID PHACTR1_000011 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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2021-02-08 18:36:18 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TBC1D7 NM_016495.4 +?/. - c.703del r.(?) p.(Leu235Ter)
PHACTR1 NM_030948.2 +?/. - c.*19413del r.(?) p.(=)


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