Variant #0000691961 (NC_000016.9:g.1841424C>G, IGFALS(NM_004970.2):c.995G>C)

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.1841424C>G
DNA change (hg38) -
Published as IGFALS(NM_001146006.1):c.1109G>C (p.(Arg370Pro))
ISCN -
DB-ID NUBP2_000013
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) 1.0E-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
Date created 2020-09-15 15:50:26 +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     
IGFALS NM_004970.2 ?/. - c.995G>C r.(?) p.(Arg332Pro)
NUBP2 NM_012225.2 ?/. - c.*2709C>G r.(=) p.(=)