Variant #0000975212 (NC_000002.11:g.27716888G>T, NM_015662.1:c.-4368C>A (IFT172))

Chromosome 2
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.27716888G>T
DNA change (hg38) -
Published as FNDC4(NM_022823.3):c.363C>A (p.(Ile121=))
ISCN -
DB-ID FNDC4_000003
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) 0.00316 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 2024-04-19 20:20:39 +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     
GCKR NM_001486.3 -?/. - c.-2884G>T r.(?) p.(=)
IFT172 NM_015662.1 -?/. - c.-4368C>A r.(?) p.(=)
FNDC4 NM_022823.2 -?/. - c.363C>A r.(?) p.(=)


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