Variant #0000534243 (NC_000008.10:g.145694209C>T, NM_003923.2:c.*5412G>A (FOXH1))

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.145694209C>T
DNA change (hg38) g.144468826C>T
Published as KIFC2(NM_145754.3):c.1105C>T (p.R369W)
ISCN -
DB-ID CYHR1_000003
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) 9.0E-5 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 2019-07-18 18:22:55 +02:00 (CEST)
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.*5412G>A r.(=) p.(=)
CYHR1 NM_138496.1 ?/. - c.-3925G>A r.(?) p.(=)
KIFC2 NM_145754.2 ?/. - c.1105C>T r.(?) p.(Arg369Trp)


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