Variant #0001025493 (NC_000008.10:g.145700385C>T, NM_032902.5:c.-22193C>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.145700385C>T
DNA change (hg38) -
Published as FOXH1(NM_003923.3):c.334G>A (p.V112M)
ISCN -
DB-ID FOXH1_000032
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) 8.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2025-02-07 18:57:27 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FOXH1 NM_003923.2 ?/. - c.334G>A r.(?) p.(Val112Met)
PPP1R16A NM_032902.5 ?/. - c.-22193C>T r.(?) p.(=)
KIFC2 NM_145754.2 ?/. - c.*1552C>T r.(=) p.(=)


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