Variant #0000573546 (NC_000023.10:g.130416480A>C, NM_001170961.1:c.1184T>G (IGSF1))

Chromosome X
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.130416480A>C
DNA change (hg38) g.131282506A>C
Published as IGSF1(NM_001170961.1):c.1184T>G (p.(Leu395Arg)), IGSF1(NM_001170961.2):c.1184T>G (p.L395R)
ISCN -
DB-ID IGSF1_000001 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) 0.00916 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 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.1184T>G r.(?) p.(Leu395Arg)


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