Variant #0001003924 (NC_000018.9:g.11872396C>T, NM_001142339.2:c.930C>T (GNAL))

Chromosome 18
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.11872396C>T
DNA change (hg38) -
Published as GNAL(NM_182978.3):c.1161C>T (p.(Asp387Asp))
ISCN -
DB-ID GNAL_000036
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) 9.0E-5 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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GNAL NM_001142339.2 ?/. - c.930C>T r.(?) p.(=)
CHMP1B NM_020412.4 ?/. - c.*20286C>T r.(=) p.(=)
MPPE1 NM_023075.5 ?/. - c.*12048G>A r.(=) p.(=)


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