Variant #0000330816 (NC_000006.11:g.13325357C>G, NM_030948.2:c.*38047C>G (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.13325357C>G
DNA change (hg38) g.13325125C>G
Published as TBC1D7(NM_001143964.2):c.162G>C (p.(Met54Ile))
ISCN -
DB-ID TBC1D7_000011
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 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 2018-01-15 20:58:59 +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.162G>C r.(?) p.(Met54Ile)
PHACTR1 NM_030948.2 ?/. - c.*38047C>G r.(=) p.(=)


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