{{Rsnum
|rsid=103612
|Gene=NUP214
|Chromosome=9
|position=131144705
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=T
|GMAF=0.3343
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=NUP214
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 10.6 | 50.4 | 38.9
| HCB | 13.9 | 42.3 | 43.8
| JPT | 15.9 | 50.4 | 33.6
| YRI | 8.2 | 50.3 | 41.5
| ASW | 8.8 | 59.6 | 31.6
| CHB | 13.9 | 42.3 | 43.8
| CHD | 12.8 | 45.9 | 41.3
| GIH | 24.8 | 49.5 | 25.7
| LWK | 16.4 | 50.0 | 33.6
| MEX | 8.6 | 36.2 | 55.2
| MKK | 5.1 | 42.9 | 51.9
| TSI | 5.9 | 47.5 | 46.5
| HapMapRevision=28
}}

{{Venter SNP
|rsid=103612
|allele=T
|frequency=0.683
|uid=1103652194601
|type=homozygous_SNP
|hugo=NUP214
|ensembl gene=ENSG00000126883
|ensembl transcript=ENST00000372284
|sift=TOLERATED
|disease=A chromosomal aberration involving NUP214 is found in some cases of acute undifferentiated leukemia (AUL). Translocation t(6;9)(q21;q34.1) with SET.
}}

{{GET Evidence
|gene=NUP214
|aa_change=Pro574Ser
|aa_change_short=P574S
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs103612
|overall_frequency_n=7236
|overall_frequency_d=10758
|overall_frequency=0.672616
|n_genomes=46
|n_genomes_annotated=0
|n_haplomes=67
|n_articles=0
|n_articles_annotated=0
|nblosum100=3
|autoscore=0
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}