Variant #0000802317 (NC_000006.11:g.13316902G>A, NM_030948.2:c.*29592G>A (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.13316902G>A
DNA change (hg38) -
Published as TBC1D7(NM_016495.5):c.420C>T (p.A140=)
ISCN -
DB-ID TBC1D7_000016
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 2021-09-17 14:40:49 +02:00 (CEST)
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.420C>T r.(?) p.(Ala140=)
PHACTR1 NM_030948.2 -?/. - c.*29592G>A r.(=) p.(=)


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