Variant #0000316267 (NC_000006.11:g.13321202C>T, NM_030948.2:c.*33892C>T (PHACTR1))

Chromosome 6
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.13321202C>T
DNA change (hg38) g.13320970C>T
Published as TBC1D7(NM_001318806.1):c.238G>A (p.V80I), TBC1D7(NM_016495.4):c.319G>A (p.(Val107Ile))
ISCN -
DB-ID TBC1D7_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) 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 2018-01-15 20:58:59 +01:00 (CET)
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     
TBC1D7 NM_016495.4 ?/. - c.319G>A r.(?) p.(Val107Ile)
PHACTR1 NM_030948.2 ?/. - c.*33892C>T r.(=) p.(=)


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