Variant #0000287852 (NC_000008.10:g.145699601T>C, NM_032902.5:c.-22977T>C (PPP1R16A))

Chromosome 8
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.145699601T>C
DNA change (hg38) g.144474218T>C
Published as FOXH1(NM_003923.2):c.*20A>G
ISCN -
DB-ID FOXH1_000001
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) 0.96554 View details
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 2020-03-23 16:13:27 +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.*20A>G r.(=) p.(=)
PPP1R16A NM_032902.5 -/. - c.-22977T>C r.(?) p.(=)
KIFC2 NM_145754.2 -/. - c.*768T>C r.(=) p.(=)


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