Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: DHX34 (Hsa)
(GRCh38)19:47353040C>G
(Homo sapiens)Allele/Variant
Source: NC_000019.10:g.47353040C>G
Genes: DHX34 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:47353040C>G
(GRCh38)19:47353136C>T
(Homo sapiens)Allele/Variant
Source: rs748157892
Genes: DHX34 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:47353136C>T
(GRCh38)19:47376521G>A
(Homo sapiens)Allele/Variant
Source: rs200310017
Genes: DHX34 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:47376521G>A
(GRCh38)19:47382097G>C
(Homo sapiens)Allele/Variant
Source: NC_000019.10:g.47382097G>C
Genes: DHX34 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:47382097G>C
(GRCh38)19:47353668G>A
(Homo sapiens)Allele/Variant
Source: rs745607167
Genes: DHX34 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:47353668G>A
(GRCh38)19:47353723G>T
(Homo sapiens)Allele/Variant
Source: rs199814292
Genes: DHX34 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:47353723G>T
(GRCh38)19:47355091T>C
(Homo sapiens)Allele/Variant
Source: NC_000019.10:g.47355091T>C
Genes: DHX34 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:47355091T>C
(GRCh38)19:47376558G>A
(Homo sapiens)Allele/Variant
Source: rs1970169010
Genes: DHX34 (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)19:47376558G>A
(GRCh38)19:47379829T>G
(Homo sapiens)Allele/Variant
Source: rs28522883
Genes: DHX34 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)19:47379829T>G
(GRCh38)19:47379962C>T
(Homo sapiens)Allele/Variant
Source: NC_000019.10:g.47379962C>T
Genes: DHX34 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:47379962C>T
(GRCh38)19:47375508G>A
(Homo sapiens)Allele/Variant
Source: rs748080729
Genes: DHX34 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:47375508G>A
(GRCh38)19:47375553C>T
(Homo sapiens)Allele/Variant
Source: rs764820314
Genes: DHX34 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:47375553C>T
(GRCh38)19:47382083G>A
(Homo sapiens)Allele/Variant
Source: rs199562453
Genes: DHX34 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)19:47382083G>A
(GRCh38)19:47367018C>T
(Homo sapiens)Allele/Variant
Source: NC_000019.10:g.47367018C>T
Genes: DHX34 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:47367018C>T
(GRCh38)19:47372846G>A
(Homo sapiens)Allele/Variant
Source: rs548006217
Genes: DHX34 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:47372846G>A
(GRCh38)19:47353431G>A
(Homo sapiens)Allele/Variant
Source: rs775183244
Genes: DHX34 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:47353431G>A
(GRCh38)19:47375467A>G
(Homo sapiens)Allele/Variant
Source: rs760979886
Genes: DHX34 (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)19:47375467A>G
(GRCh38)19:47375493G>A
(Homo sapiens)Allele/Variant
Source: rs371979299
Genes: DHX34 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:47375493G>A
(GRCh38)19:47375585C>T
(Homo sapiens)Allele/Variant
Source: rs79484248
Genes: DHX34 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)19:47375585C>T
(GRCh38)19:47353436G>T
(Homo sapiens)Allele/Variant
Source: rs1969352540
Genes: DHX34 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:47353436G>T
(GRCh38)19:47362702T>C
(Homo sapiens)Allele/Variant
Source: rs2547389
Genes: DHX34 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:47362702T>C
(GRCh38)19:47358058C>T
(Homo sapiens)Allele/Variant
Source: rs141497944
Genes: DHX34 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:47358058C>T
(GRCh38)19:47358094G>A
(Homo sapiens)Allele/Variant
Source: rs146802153
Genes: DHX34 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:47358094G>A
(GRCh38)19:47353538C>T
(Homo sapiens)Allele/Variant
Source: rs113879151
Genes: DHX34 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:47353538C>T
(GRCh38)19:47355129C>T
(Homo sapiens)Allele/Variant
Source: rs371092274
Genes: DHX34 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:47355129C>T
(GRCh38)19:47375483C>T
(Homo sapiens)Allele/Variant
Source: rs112720936
Genes: DHX34 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)19:47375483C>T
(GRCh38)19:47375620G>A
(Homo sapiens)Allele/Variant
Source: rs7251713
Genes: DHX34 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:47375620G>A
(GRCh38)19:47379825C>A
(Homo sapiens)Allele/Variant
Source: rs139543869
Genes: DHX34 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:47379825C>A
(GRCh38)19:47362640C>T
(Homo sapiens)Allele/Variant
Source: rs149264949
Genes: DHX34 (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)19:47362640C>T
(GRCh38)19:47380834C>T
(Homo sapiens)Allele/Variant
Source: rs145868005
Genes: DHX34 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:47380834C>T
(GRCh38)19:47381974C>T
(Homo sapiens)Allele/Variant
Source: rs374537824
Genes: DHX34 (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)19:47381974C>T
(GRCh38)19:47381977T>C
(Homo sapiens)Allele/Variant
Source: rs113840347
Genes: DHX34 (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)19:47381977T>C
(GRCh38)19:47375481C>T
(Homo sapiens)Allele/Variant
Source: rs764616742
Genes: DHX34 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:47375481C>T
(GRCh38)19:47375598G>A
(Homo sapiens)Allele/Variant
Source: rs1970118036
Genes: DHX34 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:47375598G>A
(GRCh38)19:47382015A>G
(Homo sapiens)Allele/Variant
Source: rs770270856
Genes: DHX34 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:47382015A>G
(GRCh38)19:47367030C>G
(Homo sapiens)Allele/Variant
Source: NC_000019.10:g.47367030C>G
Genes: DHX34 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:47367030C>G
(GRCh38)19:47372763T>C
(Homo sapiens)Allele/Variant
Source: rs755019006
Genes: DHX34 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:47372763T>C
(GRCh38)19:47353145T>G
(Homo sapiens)Allele/Variant
Source: rs746020227
Genes: DHX34 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:47353145T>G
(GRCh38)19:47355237C>T
(Homo sapiens)Allele/Variant
Source: rs61757592
Genes: DHX34 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:47355237C>T
(GRCh38)19:47358023G>A
(Homo sapiens)Allele/Variant
Source: NC_000019.10:g.47358023G>A
Genes: DHX34 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:47358023G>A
(GRCh38)19:47360017A>G
(Homo sapiens)Allele/Variant
Source: rs549149043
Genes: DHX34 (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)19:47360017A>G
(GRCh38)19:47362620C>T
(Homo sapiens)Allele/Variant
Source: rs374782101
Genes: DHX34 (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)19:47362620C>T
(GRCh38)19:47367056G>A
(Homo sapiens)Allele/Variant
Source: rs1403342992
Genes: DHX34 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:47367056G>A
(GRCh38)19:47372751C>T
(Homo sapiens)Allele/Variant
Source: rs761628939
Genes: DHX34 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:47372751C>T
(GRCh38)19:47373612G>A
(Homo sapiens)Allele/Variant
Source: rs769923444
Genes: DHX34 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:47373612G>A
(GRCh38)19:47373644C>T
(Homo sapiens)Allele/Variant
Source: rs150311568
Genes: DHX34 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:47373644C>T
(GRCh38)19:47355232C>G
(Homo sapiens)Allele/Variant
Source: rs34802163
Genes: DHX34 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:47355232C>G
(GRCh38)19:47355260C>T
(Homo sapiens)Allele/Variant
Source: rs774630959
Genes: DHX34 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)19:47355260C>T
(GRCh38)19:47358112C>G
(Homo sapiens)Allele/Variant
Source: rs751138024
Genes: DHX34 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:47358112C>G
(GRCh38)19:47375688A>G
(Homo sapiens)Allele/Variant
Source: rs749826686
Genes: DHX34 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:47375688A>G