Variant #0000560044 (NC_000016.9:g.90103716G>A, NM_001481.2:c.833G>A (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.90103716G>A
DNA change (hg38) g.90037308G>A
Published as GAS8(NM_001481.2):c.833G>A (p.(Arg278His))
ISCN -
DB-ID C16orf3_000005
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) 0.00769 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C16orf3 NM_001214.3 -?/. - c.-7966C>T r.(?) p.(=)
GAS8 NM_001481.2 -?/. - c.833G>A r.(?) p.(Arg278His)


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