Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: GSPT2 (Hsa)
(GRCh38)X:51744647G>A
(Homo sapiens)Allele/Variant
Source: rs1057519440
Genes: GSPT2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)X:51744647G>A
(GRCh38)X:51745367G>A
(Homo sapiens)Allele/Variant
Source: rs782096390
Genes: GSPT2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)X:51745367G>A
(GRCh38)X:51743814T>C
(Homo sapiens)Allele/Variant
Source: rs1033702848
Genes: GSPT2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)X:51743814T>C
(GRCh38)X:51743916G>T
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.51743916G>T
Genes: GSPT2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)X:51743916G>T
(GRCh38)X:51745147C>T
(Homo sapiens)Allele/Variant
Source: rs781793704
Genes: GSPT2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:51745147C>T
(GRCh38)X:51744293A>G
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.51744293A>G
Genes: GSPT2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)X:51744293A>G
(GRCh38)X:51744784C>T
(Homo sapiens)Allele/Variant
Source: rs797044501
Genes: GSPT2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:51744784C>T
(GRCh38)X:51743694C>T
(Homo sapiens)Allele/Variant
Source: rs147103223
Genes: GSPT2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)X:51743694C>T
(GRCh38)X:51744836T>G
(Homo sapiens)Allele/Variant
Source: rs782790209
Genes: GSPT2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)X:51744836T>G
(GRCh38)X:51744014A>G
(Homo sapiens)Allele/Variant
Source: rs782797091
Genes: GSPT2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)X:51744014A>G
(GRCh38)X:51744714A>T
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.51744714A>T
Genes: GSPT2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)X:51744714A>T
(GRCh38)X:51744104G>A
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.51744104G>A
Genes: GSPT2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)X:51744104G>A
(GRCh38)X:51743672G>A
(Homo sapiens)Allele/Variant
Source: rs199733827
Genes: GSPT2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)X:51743672G>A
(GRCh38)X:51744049G>A
(Homo sapiens)Allele/Variant
Source: rs58066621
Genes: GSPT2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:51744049G>A
(GRCh38)X:51745085C>T
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.51745085C>T
Genes: GSPT2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)X:51745085C>T
(GRCh38)X:51743886G>A
(Homo sapiens)Allele/Variant
Source: rs782600305
Genes: GSPT2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)X:51743886G>A
(GRCh38)X:51743896T>G
(Homo sapiens)Allele/Variant
Source: rs782692534
Genes: GSPT2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)X:51743896T>G
(GRCh38)X:51745186C>T
(Homo sapiens)Allele/Variant
Source: rs782194813
Genes: GSPT2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:51745186C>T