Variant #0000335532 (NC_000023.10:g.130419111G>C, NC_000023.10(NM_001170961.1):c.667+42C>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.130419111G>C
DNA change (hg38) g.131285137G>C
Published as IGSF1(NM_001170963.1):c.709C>G (p.(Pro237Ala)), IGSF1(NM_205833.3):c.709C>G (p.P237A), IGSF1(NM_205833.4):c.709C>G (p.P237A)
ISCN -
DB-ID IGSF1_000067 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) 0.0006 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IGSF1 NM_001170961.1 -?/. - c.667+42C>G r.(=) p.(=)


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