Variant #0000249080 (NC_000006.11:g.13288648A>G, NM_030948.2:c.*1338A>G (PHACTR1))

Chromosome 6
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.13288648A>G
DNA change (hg38) g.13288416A>G
Published as TBC1D7-LOC100130357(NM_001318809.2):c.*39+16646T>C
ISCN -
DB-ID PHACTR1_000002
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) 0.85246 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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.*16685T>C r.(=) p.(=)
PHACTR1 NM_030948.2 -/. - c.*1338A>G r.(=) p.(=)


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