Variant #0000288217 (NC_000016.9:g.90095646C>G, NC_000016.9(NM_001481.2):c.90+1516C>G (GAS8))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.90095646C>G
DNA change (hg38) g.90029238C>G
Published as GAS8-AS1(NR_122031.1):n.664G>C
ISCN -
DB-ID C16orf3_000001
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-10 18:04:47 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C16orf3 NM_001214.3 -?/. - c.105G>C r.(?) p.(Ala35=)
GAS8 NM_001481.2 -?/. - c.90+1516C>G r.(=) p.(=)


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