Variant #0000250611 (NC_000006.11:g.110064928A>T, NM_014845.5:c.1090A>T (FIG4))

Chromosome 6
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.110064928A>T
DNA change (hg38) g.109743725A>T
Published as FIG4(NM_014845.5):c.1090A>T (p.M364L), FIG4(NM_014845.6):c.1090A>T (p.M364L)
ISCN -
DB-ID FIG4_000062 See all 4 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) 0.07893 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FIG4 NM_014845.5 -/. - c.1090A>T r.(?) p.(Met364Leu)


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