Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: DDX3X (Hsa) Molecular Consequence: non coding transcript variant
(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: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>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
(GRCh38)X:41341173C>T
(Homo sapiens)Allele/Variant
Source: rs149501085
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:41341173C>T
(GRCh38)X:41343199A>G
(Homo sapiens)Allele/Variant
Source: rs762956543
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:41343199A>G
(GRCh38)X:41344400G>A
(Homo sapiens)Allele/Variant
Source: rs2147354193
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41344400G>A
(GRCh38)X:41343801C>T
(Homo sapiens)Allele/Variant
Source: rs1569238002
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:41343801C>T
(GRCh38)X:41334279G>A
(Homo sapiens)Allele/Variant
Source: rs761774074
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:41334279G>A
(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: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: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: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:41337461C>T
(Homo sapiens)Allele/Variant
Source: rs1326601263
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:41337461C>T
(GRCh38)X:41343786T>C
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.41343786T>C
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:41343786T>C
(GRCh38)X:41344237A>G
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.41344237A>G
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_acceptor_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41344237A>G
(GRCh38)X:41346224G>A
(Homo sapiens)Allele/Variant
Source: rs768513094
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:41346224G>A
(GRCh38)X:41337467T>C
(Homo sapiens)Allele/Variant
Source: rs2063787817
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41337467T>C
(GRCh38)X:41339051C>G
(Homo sapiens)Allele/Variant
Source: rs1064793858
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41339051C>G
(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: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: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: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:41343755C>T
(Homo sapiens)Allele/Variant
Source: rs796052223
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:41343755C>T
(GRCh38)X:41343771C>T
(Homo sapiens)Allele/Variant
Source: rs774264628
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:41343771C>T
(GRCh38)X:41345561A>G
(Homo sapiens)Allele/Variant
Source: rs1177433387
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41345561A>G
(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: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:41345400T>C
(Homo sapiens)Allele/Variant
Source: rs756329794
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:41345400T>C
(GRCh38)X:41346227A>G
(Homo sapiens)Allele/Variant
Source: rs1602135698
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, splice_acceptor_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41346227A>G
(GRCh38)X:41346497T>C
(Homo sapiens)Allele/Variant
Source: rs762048074
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:41346497T>C
(GRCh38)X:41337389C>T
(Homo sapiens)Allele/Variant
Source: rs762809683
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41337389C>T
(GRCh38)X:41337420G>T
(Homo sapiens)Allele/Variant
Source: rs1569233520
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41337420G>T
(GRCh38)X:41339054C>A
(Homo sapiens)Allele/Variant
Source: rs1341824034
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41339054C>A
(GRCh38)X:41342667G>A
(Homo sapiens)Allele/Variant
Source: rs2063867246
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:41342667G>A
(GRCh38)X:41341617G>C
(Homo sapiens)Allele/Variant
Source: rs1555952710
Genes: DDX3X (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
Diseases: Not Available
Variant Name: (GRCh38)X:41341617G>C
(GRCh38)X:41341625T>A
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.41341625T>A
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:41341625T>A
(GRCh38)X:41343257T>G
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.41343257T>G
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:41343257T>G
(GRCh38)X:41344403T>G
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.41344403T>G
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:41344403T>G
(GRCh38)X:41343726T>C
(Homo sapiens)Allele/Variant
Source: rs1463374308
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:41343726T>C
(GRCh38)X:41344234T>G
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.41344234T>G
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:41344234T>G