Variant #0000574377 (NC_000023.10:g.153063536_153063545del, NM_004135.3:c.-3759_-3750del (IDH3G))

Chromosome X
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.153063536_153063545del
DNA change (hg38) g.153798081_153798090del
Published as SSR4(NM_001204526.1):c.390_399del (p.(Asn132ThrfsTer36))
ISCN -
DB-ID SSR4_000019
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-21 13:38:42 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IDH3G NM_004135.3 +?/. - c.-3759_-3750del r.(?) p.(=)
SSR4 NM_006280.2 +?/. - c.362_371del r.(?) p.(Asn121ThrfsTer36)
PDZD4 NM_032512.2 +?/. - c.*5268_*5277del r.(=) p.(=)


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