Variant #0000557024 (NC_000016.9:g.1841532C>T, IGFALS(NM_004970.2):c.887G>A)

Chromosome 16
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.1841532C>T
DNA change (hg38) g.1791531C>T
Published as IGFALS(NM_004970.2):c.887G>A (p.(Arg296Gln))
ISCN -
DB-ID NUBP2_000005
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) 3.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IGFALS NM_004970.2 ?/. - c.887G>A r.(?) p.(Arg296Gln)
NUBP2 NM_012225.2 ?/. - c.*2817C>T r.(=) p.(=)