Variant #0000563939 (NC_000018.9:g.11881059_11881060del, GNAL(NM_001142339.2):c.1071_1072del)

Chromosome 18
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.11881059_11881060del
DNA change (hg38) g.11881060_11881061del
Published as GNAL(NM_182978.4):c.1302_1303delGA (p.N435Hfs*21)
ISCN -
DB-ID GNAL_000022
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) Variant not found in online data sets
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GNAL NM_001142339.2 +?/. - c.1071_1072del r.(?) p.(Asn358HisfsTer21)
CHMP1B NM_020412.4 +?/. - c.*28949_*28950del r.(=) p.(=)
MPPE1 NM_023075.5 +?/. - c.*3387_*3388del r.(=) p.(=)