{{Rsnum
|rsid=1040835
|Gene=GOLGA5
|Chromosome=14
|position=92810309
|Orientation=plus
|ReferenceAllele=T
|MissenseAllele=C
|GMAF=0.1832
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=GOLGA5
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 12.3 | 43.1 | 44.6
| HCB | 6.7 | 28.9 | 64.4
| JPT | 2.3 | 45.5 | 52.3
| YRI | 0.0 | 3.2 | 96.8
| ASW | 0.0 | 0.0 | 0.0
| CHB | 6.7 | 28.9 | 64.4
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{Venter SNP
|rsid=1040835
|allele=C
|frequency=0.667
|uid=1103649130466
|type=homozygous_SNP
|hugo=GOLGA5
|ensembl gene=ENSG00000066455
|ensembl transcript=ENST00000163416
|sift=TOLERATED
|disease=A chromosomal aberration involving GOLGA5 is a cause of thyroid papillary carcinomas (PACT) (MIM:188550). Translocation t(10;14)(q11;q32) with RET. The translocation generates the RET/GOLGA5 (PTC5) oncogene which was found in 2 cases of PACT in children exposed to radioactive fallout after Chernobyl.
}}

{{GET Evidence
|gene=GOLGA5
|aa_change=Phe350Leu
|aa_change_short=F350L
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1040835
|overall_frequency_n=8603
|overall_frequency_d=10758
|overall_frequency=0.799684
|n_genomes=47
|n_genomes_annotated=0
|n_haplomes=81
|n_articles=0
|n_articles_annotated=0
|nblosum100=0
|autoscore=0
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}