Variant #0000330095 (NC_000004.11:g.126237751G>C, NM_024582.4:c.185G>C (FAT4))

Chromosome 4
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.126237751G>C
DNA change (hg38) g.125316596G>C
Published as FAT4(NM_001291303.3):c.185G>C (p.G62A), FAT4(NM_024582.4):c.185G>C (p.(Gly62Ala)), FAT4(NM_024582.5):c.185G>C (p.G62A)
ISCN -
DB-ID FAT4_000007 See all 3 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) 0.00106 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-11-27 17:27:23 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FAT4 NM_024582.4 ?/. - c.185G>C r.(?) p.(Gly62Ala)


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