Variant #0000964927 (NC_000008.10:g.145699895C>T, NM_032902.5:c.-22683C>T (PPP1R16A))

Chromosome 8
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.145699895C>T
DNA change (hg38) -
Published as FOXH1(NM_003923.3):c.824G>A (p.G275E)
ISCN -
DB-ID FOXH1_000021 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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FOXH1 NM_003923.2 ?/. - c.824G>A r.(?) p.(Gly275Glu)
PPP1R16A NM_032902.5 ?/. - c.-22683C>T r.(?) p.(=)
KIFC2 NM_145754.2 ?/. - c.*1062C>T r.(=) p.(=)


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