Variant #0000522298 (NC_000004.11:g.187542899G>A, NM_005245.3:c.4841C>T (FAT1))

Chromosome 4
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.187542899G>A
DNA change (hg38) g.186621745G>A
Published as FAT1(NM_005245.3):c.4841C>T (p.P1614L, p.(Pro1614Leu)), FAT1(NM_005245.4):c.4841C>T (p.P1614L)
ISCN -
DB-ID FAT1_000023 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) 0.00332 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FAT1 NM_005245.3 -/. - c.4841C>T r.(?) p.(Pro1614Leu)


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