Variant #0000864878 (NC_000016.9:g.67203121_67203125del, NC_000016.9(NM_001374675.1):c.1255-61_1255-57del (HSF4))

Chromosome 16
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.67203121_67203125del
DNA change (hg38) -
Published as -
ISCN -
DB-ID FBXL8_000017
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KIAA0895L NM_001040715.1 ?/. - c.*7590_*7594del r.(=) p.(=)
HSF4 NM_001374675.1 ?/. - c.1255-61_1255-57del r.(=) p.(=)
FBXL8 NM_018378.2 ?/. - c.*5398_*5402del r.(=) p.(=)


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