Variant #0000285336 (NC_000023.10:g.53349744C>G, IQSEC2(NM_001111125.1):c.578G>C)

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.53349744C>G
DNA change (hg38) g.53320546C>G
Published as IQSEC2(NM_001111125.2):c.578G>C (p.G193A, p.(Gly193Ala)), IQSEC2(NM_001111125.3):c.578G>C (p.G193A)
ISCN -
DB-ID IQSEC2_000049 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) 0.00036 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
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     
IQSEC2 NM_001111125.1 -?/. - c.578G>C r.(?) p.(Gly193Ala)