Variant #0000887481 (NC_000006.11:g.82461760_82461789dup, NM_017633.2:c.102_131dup (FAM46A))

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.82461760_82461789dup
DNA change (hg38) -
Published as FAM46A(NM_017633.2):c.87_116dupCGGCGACTTCGGCGGCGGCGACTTCGGCGG (p.(Gly39_Gly40insGlyAspPheGlyGlyGlyAspPheGlyGly)), TENT5A(NM_017633.3):c.72_101dupCG...
ISCN -
DB-ID FAM46A_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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FAM46A NM_017633.2 -/. - c.102_131dup r.(?) p.(Asp36_Gly45dup)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.