Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: RARB (Hsa)
(GRCh38)3:25461323C>T
(Homo sapiens)Allele/Variant
Source: rs138872395
Genes: RARB (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)3:25461323C>T
(GRCh38)3:25596489T>C
(Homo sapiens)Allele/Variant
Source: NC_000003.12:g.25596489T>C
Genes: RARB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)3:25596489T>C
(GRCh38)3:24725121C>A
(Homo sapiens)Allele/Variant
Source: rs207463060
Genes: RARB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:24725121C>A
(GRCh38)3:25430783G>A
(Homo sapiens)Allele/Variant
Source: rs1381205738
Genes: RARB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:25430783G>A
(GRCh38)3:25501080G>A
(Homo sapiens)Allele/Variant
Source: rs2116703
Genes: RARB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:25501080G>A
(GRCh38)3:25580610C>T
(Homo sapiens)Allele/Variant
Source: NC_000003.12:g.25580610C>T
Genes: RARB (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)3:25580610C>T
(GRCh38)3:25593677C>A
(Homo sapiens)Allele/Variant
Source: rs1436425031
Genes: RARB (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)3:25593677C>A
(GRCh38)3:25501230C>T
(Homo sapiens)Allele/Variant
Source: rs397518481
Genes: RARB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:25501230C>T
(GRCh38)3:25596479C>T
(Homo sapiens)Allele/Variant
Source: rs1575553547
Genes: RARB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)3:25596479C>T
(GRCh38)3:25461192G>A
(Homo sapiens)Allele/Variant
Source: NC_000003.12:g.25461192G>A
Genes: RARB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, splice_acceptor_variant
Diseases: Not Available
Variant Name: (GRCh38)3:25461192G>A
(GRCh38)3:25596420G>A
(Homo sapiens)Allele/Variant
Source: rs1701834292
Genes: RARB (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)3:25596420G>A
(GRCh38)3:25593557G>T
(Homo sapiens)Allele/Variant
Source: rs1701697256
Genes: RARB (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)3:25593557G>T
(GRCh38)3:25501284C>T
(Homo sapiens)Allele/Variant
Source: rs1553624279
Genes: RARB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:25501284C>T
(GRCh38)3:25580678G>T
(Homo sapiens)Allele/Variant
Source: rs773216330
Genes: RARB (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)3:25580678G>T
(GRCh38)3:25580704C>T
(Homo sapiens)Allele/Variant
Source: rs115482149
Genes: RARB (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)3:25580704C>T
(GRCh38)3:25461178C>A
(Homo sapiens)Allele/Variant
Source: rs374770716
Genes: RARB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:25461178C>A
(GRCh38)3:25580677C>T
(Homo sapiens)Allele/Variant
Source: rs139584096
Genes: RARB (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)3:25580677C>T
(GRCh38)3:25593561G>T
(Homo sapiens)Allele/Variant
Source: NC_000003.12:g.25593561G>T
Genes: RARB (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)3:25593561G>T
(GRCh38)3:25596498C>A
(Homo sapiens)Allele/Variant
Source: rs1701838268
Genes: RARB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)3:25596498C>A
(GRCh38)3:25264468G>T
(Homo sapiens)Allele/Variant
Source: rs146746728
Genes: RARB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:25264468G>T
(GRCh38)3:25593588A>T
(Homo sapiens)Allele/Variant
Source: rs1553637470
Genes: RARB (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)3:25593588A>T
(GRCh38)3:25501285G>A
(Homo sapiens)Allele/Variant
Source: rs1387195672
Genes: RARB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:25501285G>A
(GRCh38)3:25580574T>C
(Homo sapiens)Allele/Variant
Source: rs869025222
Genes: RARB (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)3:25580574T>C
(GRCh38)3:25594422A>C
(Homo sapiens)Allele/Variant
Source: rs57466864
Genes: RARB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:25594422A>C
(GRCh38)3:25461184C>G
(Homo sapiens)Allele/Variant
Source: rs78470280
Genes: RARB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:25461184C>G
(GRCh38)3:25590187A>G
(Homo sapiens)Allele/Variant
Source: rs207463062
Genes: RARB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:25590187A>G
(GRCh38)3:25501097A>G
(Homo sapiens)Allele/Variant
Source: rs7623934
Genes: RARB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:25501097A>G
(GRCh38)3:25580619G>T
(Homo sapiens)Allele/Variant
Source: NC_000003.12:g.25580619G>T
Genes: RARB (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)3:25580619G>T
(GRCh38)3:25596585G>C
(Homo sapiens)Allele/Variant
Source: rs368432868
Genes: RARB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)3:25596585G>C
(GRCh38)3:25593495C>T
(Homo sapiens)Allele/Variant
Source: rs780963962
Genes: RARB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:25593495C>T
(GRCh38)3:25593560G>A
(Homo sapiens)Allele/Variant
Source: rs1553637463
Genes: RARB (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)3:25593560G>A
(GRCh38)3:25593563C>G
(Homo sapiens)Allele/Variant
Source: rs1559483735
Genes: RARB (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)3:25593563C>G
(GRCh38)3:25569854A>G
(Homo sapiens)Allele/Variant
Source: rs1044203022
Genes: RARB (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)3:25569854A>G
(GRCh38)3:25593552T>C
(Homo sapiens)Allele/Variant
Source: rs1701697098
Genes: RARB (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)3:25593552T>C
(GRCh38)3:25593570T>C
(Homo sapiens)Allele/Variant
Source: rs2125325427
Genes: RARB (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)3:25593570T>C
(GRCh38)3:25593676C>A
(Homo sapiens)Allele/Variant
Source: rs775637491
Genes: RARB (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)3:25593676C>A
(GRCh38)3:25596419G>C
(Homo sapiens)Allele/Variant
Source: NC_000003.12:g.25596419G>C
Genes: RARB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, splice_acceptor_variant
Diseases: Not Available
Variant Name: (GRCh38)3:25596419G>C
(GRCh38)3:25461005C>T
(Homo sapiens)Allele/Variant
Source: rs74820342
Genes: RARB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:25461005C>T
(GRCh38)3:25461378T>G
(Homo sapiens)Allele/Variant
Source: rs2067964
Genes: RARB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:25461378T>G
(GRCh38)3:25461186A>G
(Homo sapiens)Allele/Variant
Source: rs182336010
Genes: RARB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:25461186A>G
(GRCh38)3:25461266G>C
(Homo sapiens)Allele/Variant
Source: rs138754945
Genes: RARB (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)3:25461266G>C
(GRCh38)3:25596450A>G
(Homo sapiens)Allele/Variant
Source: rs2125330280
Genes: RARB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)3:25596450A>G
(GRCh38)3:25596462C>G
(Homo sapiens)Allele/Variant
Source: rs1701836507
Genes: RARB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)3:25596462C>G
(GRCh38)3:25596480A>C
(Homo sapiens)Allele/Variant
Source: rs1559485305
Genes: RARB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)3:25596480A>C
(GRCh38)3:25596620A>G
(Homo sapiens)Allele/Variant
Source: rs150640333
Genes: RARB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)3:25596620A>G
(GRCh38)3:25594570T>C
(Homo sapiens)Allele/Variant
Source: rs1351277479
Genes: RARB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:25594570T>C
(GRCh38)3:25593596G>A
(Homo sapiens)Allele/Variant
Source: NC_000003.12:g.25593596G>A
Genes: RARB (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)3:25593596G>A
(GRCh38)3:25594587A>G
(Homo sapiens)Allele/Variant
Source: rs757567712
Genes: RARB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:25594587A>G
(GRCh38)3:25596449G>T
(Homo sapiens)Allele/Variant
Source: rs1575553528
Genes: RARB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)3:25596449G>T
(GRCh38)3:24914817T>C
(Homo sapiens)Allele/Variant
Source: rs207463061
Genes: RARB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:24914817T>C