Variant #0001072327 (NC_000004.11:g.187557185T>C, NM_005245.3:c.4177A>G (FAT1))

Chromosome 4
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.187557185T>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID FAT1_000160
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs753226094
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00023 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-04-10 14:40:01 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FAT1 NM_005245.3 -?/. - c.4177A>G r.(?) p.(Ile1393Val)


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