Variant #0000984453 (NC_000023.10:g.130413265A>G, NM_001170961.1:c.1697T>C (IGSF1))

Chromosome X
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.130413265A>G
DNA change (hg38) -
Published as IGSF1(NM_001170961.1):c.1697T>C (p.V566A), IGSF1(NM_001555.5):c.1697T>C (p.(Val566Ala))
ISCN -
DB-ID IGSF1_000079 See all 2 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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IGSF1 NM_001170961.1 ?/. - c.1697T>C r.(?) p.(Val566Ala)


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