Variant #0000557025 (NC_000016.9:g.1841533G>A, NM_004970.2:c.886C>T (IGFALS))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.1841533G>A
DNA change (hg38) g.1791532G>A
Published as IGFALS(NM_001146006.1):c.1000C>T (p.(Arg334Trp))
ISCN -
DB-ID NUBP2_000006
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) 2.0E-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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-11-01 13:01:21 +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.886C>T r.(?) p.(Arg296Trp)
NUBP2 NM_012225.2 +?/. - c.*2818G>A r.(=) p.(=)


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