Variant #0000557026 (NC_000016.9:g.1841559G>A, IGFALS(NM_004970.2):c.860C>T)

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.1841559G>A
DNA change (hg38) g.1791558G>A
Published as IGFALS(NM_001146006.1):c.974C>T (p.(Pro325Leu)), IGFALS(NM_004970.2):c.860C>T (p.P287L)
ISCN -
DB-ID IGFALS_000033 See all 2 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) 0.00349 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2019-12-04 15:24:38 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IGFALS NM_004970.2 -?/. - c.860C>T r.(?) p.(Pro287Leu)
NUBP2 NM_012225.2 -?/. - c.*2844G>A r.(=) p.(=)