Variant #0000287855 (NC_000008.10:g.145700267C>T, NM_032902.5:c.-22311C>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.145700267C>T
DNA change (hg38) g.144474884C>T
Published as FOXH1(NM_003923.2):c.452G>A (p.G151D)
ISCN -
DB-ID FOXH1_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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2019-12-04 15:24:38 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FOXH1 NM_003923.2 ?/. - c.452G>A r.(?) p.(Gly151Asp)
PPP1R16A NM_032902.5 ?/. - c.-22311C>T r.(?) p.(=)
KIFC2 NM_145754.2 ?/. - c.*1434C>T r.(=) p.(=)


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