Variant #0000680436 (NC_000016.9:g.1840983C>T, IGFALS(NM_004970.2):c.1436G>A)

Chromosome 16
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.1840983C>T
DNA change (hg38) -
Published as IGFALS(NM_001146006.1):c.1550G>A (p.(Gly517Asp))
ISCN -
DB-ID NUBP2_000012
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) 0.00141 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.1436G>A r.(?) p.(Gly479Asp)
NUBP2 NM_012225.2 -?/. - c.*2268C>T r.(=) p.(=)