Variant #0000615815 (NC_000016.9:g.1840801A>G, NM_004970.2:c.1618T>C (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.1840801A>G
DNA change (hg38) g.1790800A>G
Published as IGFALS(NM_001146006.1):c.1732T>C (p.(Cys578Arg))
ISCN -
DB-ID IGFALS_000005 See all 4 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) 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +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.1618T>C r.(?) p.(Cys540Arg)
NUBP2 NM_012225.2 +?/. - c.*2086A>G r.(=) p.(=)


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