Variant #0000283214 (NC_000006.11:g.110012665C>T, NM_014845.5:c.27C>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.110012665C>T
DNA change (hg38) g.109691462C>T
Published as FIG4(NM_014845.5):c.27C>T (p.I9=), FIG4(NM_014845.6):c.27C>T (p.I9=)
ISCN -
DB-ID FIG4_000033 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) 0.00479 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
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     
AKD1 NM_001145128.2 -/. - c.-327G>A r.(?) p.(=)
FIG4 NM_014845.5 -/. - c.27C>T r.(?) p.(Ile9=)


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