Variant #0001052262 (NC_000006.11:g.13283682_13283684dup, NM_030948.2:c.1538_1540dup (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.13283682_13283684dup
DNA change (hg38) -
Published as PHACTR1(NM_030948.6):c.1538_1540dup (p.(Leu513dup))
ISCN -
DB-ID TBC1D7_000022
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TBC1D7 NM_016495.4 +?/. - c.*21650_*21652dup r.(=) p.(=)
PHACTR1 NM_030948.2 +?/. - c.1538_1540dup r.(?) p.(Leu513dup)


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