Variant #0000655483 (NC_000006.11:g.13316909G>T, NM_030948.2:c.*29599G>T (PHACTR1))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.13316909G>T
DNA change (hg38) g.13316677G>T
Published as TBC1D7(NM_001143964.2):c.413C>A (p.(Ala138Asp))
ISCN -
DB-ID PHACTR1_000010
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) 0.00265 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2020-03-23 16:13:27 +01:00 (CET)
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.413C>A r.(?) p.(Ala138Asp)
PHACTR1 NM_030948.2 -?/. - c.*29599G>T r.(=) p.(=)


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