Version: 8.0.0
Date: Tue Jan 28 2025
7 results
Allele/Variant Genes: POLDIP2 (Hsa)

(GRCh38)17:28352988G>C

(Homo sapiens)
Allele/Variant
Source: rs34126265
Genes: POLDIP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)17:28352988G>C

(GRCh38)17:28357342G>A

(Homo sapiens)
Allele/Variant
Source: rs11555978
Genes: POLDIP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)17:28357342G>A

(GRCh38)17:28357347G>A

(Homo sapiens)
Allele/Variant
Source: rs201357006
Genes: POLDIP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)17:28357347G>A

(GRCh38)17:28357368T>G

(Homo sapiens)
Allele/Variant
Source: rs17856014
Genes: POLDIP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)17:28357368T>G

(GRCh38)17:28348239C>T

(Homo sapiens)
Allele/Variant
Source: rs2073868
Genes: POLDIP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:28348239C>T

(GRCh38)17:28349133C>T

(Homo sapiens)
Allele/Variant
Source: rs34881086
Genes: POLDIP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)17:28349133C>T

(GRCh38)17:28349157T>C

(Homo sapiens)
Allele/Variant
Source: rs34108350
Genes: POLDIP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)17:28349157T>C