Variant #0000619005 (NC_000023.10:g.130417174C>T, NM_001170961.1:c.732G>A (IGSF1))

Chromosome X
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.130417174C>T
DNA change (hg38) g.131283200C>T
Published as IGSF1(NM_001170961.1):c.732G>A (p.L244=), IGSF1(NM_001170961.2):c.732G>A (p.L244=)
ISCN -
DB-ID IGSF1_000007 See all 3 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) 0.00584 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IGSF1 NM_001170961.1 -/. - c.732G>A r.(?) p.(Leu244=)


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