Variant #0000323949 (NC_000015.9:g.28947208C>G, NM_001282468.1:c.1791G>C (GOLGA8M))

Chromosome 15
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.28947208C>G
DNA change (hg38) g.28702062C>G
Published as GOLGA8M(XM_003118930.4):c.1752G>C (p.(Lys584Asn))
ISCN -
DB-ID GOLGA8M_000002
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) 0.00211 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 2018-01-15 20:58:59 +01:00 (CET)
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     
GOLGA8M NM_001282468.1 -?/. - c.1791G>C r.(?) p.(Lys597Asn)


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