Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: OGT (Hsa)
(GRCh38)X:71563492C>G
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.71563492C>G
Genes: OGT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:71563492C>G
(GRCh38)X:71557585G>A
(Homo sapiens)Allele/Variant
Source: rs34739713
Genes: OGT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:71557585G>A
(GRCh38)X:71563199G>A
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.71563199G>A
Genes: OGT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:71563199G>A
(GRCh38)X:71537962C>T
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.71537962C>T
Genes: OGT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:71537962C>T
(GRCh38)X:71557640G>A
(Homo sapiens)Allele/Variant
Source: rs1556069426
Genes: OGT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:71557640G>A
(GRCh38)X:71557066A>C
(Homo sapiens)Allele/Variant
Source: rs34350994
Genes: OGT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:71557066A>C
(GRCh38)X:71561897T>G
(Homo sapiens)Allele/Variant
Source: rs2147688604
Genes: OGT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:71561897T>G
(GRCh38)X:71557606A>G
(Homo sapiens)Allele/Variant
Source: rs143784248
Genes: OGT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:71557606A>G
(GRCh38)X:71561912A>G
(Homo sapiens)Allele/Variant
Source: rs374294708
Genes: OGT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:71561912A>G
(GRCh38)X:71563516A>G
(Homo sapiens)Allele/Variant
Source: rs191361286
Genes: OGT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:71563516A>G
(GRCh38)X:71547971G>A
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.71547971G>A
Genes: OGT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:71547971G>A
(GRCh38)X:71555223G>T
(Homo sapiens)Allele/Variant
Source: rs1131692155
Genes: OGT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:71555223G>T
(GRCh38)X:71533302G>A
(Homo sapiens)Allele/Variant
Source: rs2147664566
Genes: OGT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, start_lost
Diseases: Not Available
Variant Name: (GRCh38)X:71533302G>A
(GRCh38)X:71536191T>C
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.71536191T>C
Genes: OGT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:71536191T>C
(GRCh38)X:71537959C>T
(Homo sapiens)Allele/Variant
Source: rs1317050680
Genes: OGT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:71537959C>T
(GRCh38)X:71533327G>A
(Homo sapiens)Allele/Variant
Source: rs2147664606
Genes: OGT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:71533327G>A
(GRCh38)X:71536350G>T
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.71536350G>T
Genes: OGT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:71536350G>T
(GRCh38)X:71567606G>A
(Homo sapiens)Allele/Variant
Source: rs773673612
Genes: OGT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:71567606G>A
(GRCh38)X:71568005C>T
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.71568005C>T
Genes: OGT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:71568005C>T
(GRCh38)X:71559373C>T
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.71559373C>T
Genes: OGT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:71559373C>T
(GRCh38)X:71563001T>C
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.71563001T>C
Genes: OGT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:71563001T>C
(GRCh38)X:71567519A>G
(Homo sapiens)Allele/Variant
Source: rs1393034082
Genes: OGT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:71567519A>G
(GRCh38)X:71567603A>G
(Homo sapiens)Allele/Variant
Source: rs899091443
Genes: OGT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:71567603A>G
(GRCh38)X:71557080A>G
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.71557080A>G
Genes: OGT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:71557080A>G
(GRCh38)X:71559267A>G
(Homo sapiens)Allele/Variant
Source: rs2040366519
Genes: OGT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:71559267A>G
(GRCh38)X:71554548T>C
(Homo sapiens)Allele/Variant
Source: rs745898524
Genes: OGT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:71554548T>C
(GRCh38)X:71556045A>G
(Homo sapiens)Allele/Variant
Source: rs1602147880
Genes: OGT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:71556045A>G
(GRCh38)X:71557524G>A
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.71557524G>A
Genes: OGT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:71557524G>A
(GRCh38)X:71557231C>G
(Homo sapiens)Allele/Variant
Source: rs763636681
Genes: OGT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:71557231C>G
(GRCh38)X:71559327C>T
(Homo sapiens)Allele/Variant
Source: rs776506519
Genes: OGT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:71559327C>T
(GRCh38)X:71555296A>G
(Homo sapiens)Allele/Variant
Source: rs777634651
Genes: OGT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:71555296A>G
(GRCh38)X:71556755C>T
(Homo sapiens)Allele/Variant
Source: rs755051797
Genes: OGT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:71556755C>T
(GRCh38)X:71557039T>C
(Homo sapiens)Allele/Variant
Source: rs780141528
Genes: OGT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:71557039T>C
(GRCh38)X:71537851G>A
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.71537851G>A
Genes: OGT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:71537851G>A
(GRCh38)X:71544626A>C
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.71544626A>C
Genes: OGT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:71544626A>C
(GRCh38)X:71562982A>G
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.71562982A>G
Genes: OGT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:71562982A>G
(GRCh38)X:71564705T>G
(Homo sapiens)Allele/Variant
Source: rs2147691095
Genes: OGT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:71564705T>G
(GRCh38)X:71538037G>A
(Homo sapiens)Allele/Variant
Source: rs948915983
Genes: OGT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:71538037G>A
(GRCh38)X:71538068A>G
(Homo sapiens)Allele/Variant
Source: rs149977750
Genes: OGT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:71538068A>G
(GRCh38)X:71555236G>A
(Homo sapiens)Allele/Variant
Source: rs797044898
Genes: OGT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:71555236G>A
(GRCh38)X:71573628A>T
(Homo sapiens)Allele/Variant
Source: rs2040472529
Genes: OGT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:71573628A>T
(GRCh38)X:71559249A>G
(Homo sapiens)Allele/Variant
Source: rs778311896
Genes: OGT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:71559249A>G
(GRCh38)X:71556108G>A
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.71556108G>A
Genes: OGT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:71556108G>A
(GRCh38)X:71555984G>A
(Homo sapiens)Allele/Variant
Source: rs1602147851
Genes: OGT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:71555984G>A
(GRCh38)X:71533318A>C
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.71533318A>C
Genes: OGT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:71533318A>C
(GRCh38)X:71536280T>G
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.71536280T>G
Genes: OGT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:71536280T>G
(GRCh38)X:71537917G>A
(Homo sapiens)Allele/Variant
Source: rs1556046834
Genes: OGT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:71537917G>A
(GRCh38)X:71556003C>T
(Homo sapiens)Allele/Variant
Source: rs1222893946
Genes: OGT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:71556003C>T
(GRCh38)X:71557599G>A
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.71557599G>A
Genes: OGT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:71557599G>A
(GRCh38)X:71557637A>G
(Homo sapiens)Allele/Variant
Source: rs2147684242
Genes: OGT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:71557637A>G