Variant #0000721124 (NC_000006.11:g.82461775_82461789dup, NM_017633.2:c.117_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.82461775_82461789dup
DNA change (hg38) -
Published as TENT5A(NM_017633.2):c.117_131dupCGGCGACTTCGGCGG (p.D41_G45dup), TENT5A(NM_017633.3):c.117_131dupCGGCGACTTCGGCGG (p.D41_G45dup)
ISCN -
DB-ID FAM46A_000010 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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FAM46A NM_017633.2 -/. - c.117_131dup r.(?) p.(Asp41_Gly45dup)


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