Variant #0000810068 (NC_000023.10:g.153060138_153060146dup, NM_004135.3:c.-364_-356dup (IDH3G))

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.153060138_153060146dup
DNA change (hg38) -
Published as SSR4(NM_001204527.1):c.20_28dupAGGCGATGG (p.E7_M9dup)
ISCN -
DB-ID SSR4_000024
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IDH3G NM_004135.3 ?/. - c.-364_-356dup r.(?) p.(=)
SSR4 NM_006280.2 ?/. - c.-5_4dup r.(?) p.(Ala2Aspfs*40)


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