Variant #0001006428 (NC_000023.10:g.130412003_130412029del, NM_001170961.1:c.2138_2164del (IGSF1))

Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.130412003_130412029del
DNA change (hg38) -
Published as IGSF1(NM_001170961.1):c.2138_2164delCAGGCATGGGGTTTGCTCTGTATAAGG (p.(Ala713_Lys721del)), IGSF1(NM_001170961.1):c.2138_2164delCAGGCATGGGGTTTGCTCTGTAT...
ISCN -
DB-ID IGSF1_000010 See all 7 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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IGSF1 NM_001170961.1 +/. - c.2138_2164del r.(?) p.(Ala713_Lys721del)


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