Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: DDX3X (Hsa)
(GRCh38)X:41347406C>A
(Homo sapiens)Allele/Variant
Source: rs2063941047
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41347406C>A
(GRCh38)X:41347415G>A
(Homo sapiens)Allele/Variant
Source: rs1200557241
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41347415G>A
(GRCh38)X:41347652G>A
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.41347652G>A
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41347652G>A
(GRCh38)X:41346607C>G
(Homo sapiens)Allele/Variant
Source: rs1555954284
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41346607C>G
(GRCh38)X:41346608G>A
(Homo sapiens)Allele/Variant
Source: rs2147359333
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41346608G>A
(GRCh38)X:41346379C>G
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.41346379C>G
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, stop_gained, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41346379C>G
(GRCh38)X:41333711G>C
(Homo sapiens)Allele/Variant
Source: rs186005081
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41333711G>C
(GRCh38)X:41347349C>T
(Homo sapiens)Allele/Variant
Source: rs886041705
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, stop_gained, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41347349C>T
(GRCh38)X:41347426C>T
(Homo sapiens)Allele/Variant
Source: rs779341057
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41347426C>T
(GRCh38)X:41346842T>C
(Homo sapiens)Allele/Variant
Source: rs1454645098
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41346842T>C
(GRCh38)X:41334255G>A
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.41334255G>A
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, start_lost, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41334255G>A
(GRCh38)X:41341494T>C
(Homo sapiens)Allele/Variant
Source: rs2147348601
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41341494T>C
(GRCh38)X:41341556G>A
(Homo sapiens)Allele/Variant
Source: rs1569236301
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41341556G>A
(GRCh38)X:41341688T>G
(Homo sapiens)Allele/Variant
Source: rs146299715
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41341688T>G
(GRCh38)X:41344278G>A
(Homo sapiens)Allele/Variant
Source: rs875989802
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41344278G>A
(GRCh38)X:41345536C>T
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.41345536C>T
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41345536C>T
(GRCh38)X:41345558T>C
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.41345558T>C
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41345558T>C
(GRCh38)X:41346589C>T
(Homo sapiens)Allele/Variant
Source: rs1064795323
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41346589C>T
(GRCh38)X:41346428T>G
(Homo sapiens)Allele/Variant
Source: rs112884433
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41346428T>G
(GRCh38)X:41346953G>A
(Homo sapiens)Allele/Variant
Source: rs1555954388
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, stop_gained, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41346953G>A
(GRCh38)X:41339203T>C
(Homo sapiens)Allele/Variant
Source: rs2275943
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41339203T>C
(GRCh38)X:41342653A>G
(Homo sapiens)Allele/Variant
Source: rs1064794404
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41342653A>G
(GRCh38)X:41341465T>C
(Homo sapiens)Allele/Variant
Source: rs769031608
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41341465T>C
(GRCh38)X:41341566A>C
(Homo sapiens)Allele/Variant
Source: rs143627607
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41341566A>C
(GRCh38)X:41342492C>T
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.41342492C>T
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41342492C>T
(GRCh38)X:41343268G>A
(Homo sapiens)Allele/Variant
Source: rs755750366
Genes: DDX3X (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:41343268G>A
(GRCh38)X:41343278C>T
(Homo sapiens)Allele/Variant
Source: rs1358728169
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41343278C>T
(GRCh38)X:41344393T>A
(Homo sapiens)Allele/Variant
Source: rs2063893678
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41344393T>A
(GRCh38)X:41344551C>T
(Homo sapiens)Allele/Variant
Source: rs776834725
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41344551C>T
(GRCh38)X:41345091T>A
(Homo sapiens)Allele/Variant
Source: rs146259535
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41345091T>A
(GRCh38)X:41337391A>G
(Homo sapiens)Allele/Variant
Source: rs770884779
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41337391A>G
(GRCh38)X:41337431T>C
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.41337431T>C
Genes: DDX3X (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:41337431T>C
(GRCh38)X:41342638G>A
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.41342638G>A
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41342638G>A
(GRCh38)X:41345174T>C
(Homo sapiens)Allele/Variant
Source: rs755959550
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41345174T>C
(GRCh38)X:41345177C>T
(Homo sapiens)Allele/Variant
Source: rs1288221968
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41345177C>T
(GRCh38)X:41343802G>A
(Homo sapiens)Allele/Variant
Source: rs752738546
Genes: DDX3X (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:41343802G>A
(GRCh38)X:41344138A>C
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.41344138A>C
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41344138A>C
(GRCh38)X:41343828T>A
(Homo sapiens)Allele/Variant
Source: rs1277122647
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41343828T>A
(GRCh38)X:41344243C>G
(Homo sapiens)Allele/Variant
Source: rs1555953482
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41344243C>G
(GRCh38)X:41345537T>C
(Homo sapiens)Allele/Variant
Source: rs2063911698
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, stop_lost
Diseases: Not Available
Variant Name: (GRCh38)X:41345537T>C
(GRCh38)X:41346525C>G
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.41346525C>G
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41346525C>G
(GRCh38)X:41341526A>G
(Homo sapiens)Allele/Variant
Source: rs2063850443
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41341526A>G
(GRCh38)X:41341577C>G
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.41341577C>G
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41341577C>G
(GRCh38)X:41341595G>A
(Homo sapiens)Allele/Variant
Source: rs763397133
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41341595G>A
(GRCh38)X:41345206G>A
(Homo sapiens)Allele/Variant
Source: rs1057518707
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41345206G>A
(GRCh38)X:41345186G>C
(Homo sapiens)Allele/Variant
Source: rs2063907779
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41345186G>C
(GRCh38)X:41345266C>T
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.41345266C>T
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41345266C>T
(GRCh38)X:41334255G>C
(Homo sapiens)Allele/Variant
Source: rs1555950665
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, start_lost, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41334255G>C
(GRCh38)X:41342656A>T
(Homo sapiens)Allele/Variant
Source: rs2147350644
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41342656A>T
(GRCh38)X:41342841G>A
(Homo sapiens)Allele/Variant
Source: rs1555953039
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41342841G>A