Variant #0001055755 (NC_000016.9:g.90089130A>G, NM_001481.2:c.1A>G (GAS8))

Chromosome 16
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.90089130A>G
DNA change (hg38) -
Published as GAS8(NM_001481.3):c.1A>G (p.(Met1?))
ISCN -
DB-ID C16orf3_000021
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 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C16orf3 NM_001214.3 ?/. - c.*6267T>C r.(=) p.(=)
GAS8 NM_001481.2 ?/. - c.1A>G r.(?) p.?
DBNDD1 NM_024043.2 ?/. - c.-12675T>C r.(?) p.(=)


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