Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: TYR (Hsa) Molecular Consequence: missense variant
(GRCh38)11:89227830T>C
(Homo sapiens)Allele/Variant
Source: rs771720319
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89227830T>C
(GRCh38)11:89178211T>C
(Homo sapiens)Allele/Variant
Source: rs1464099781
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89178211T>C
(GRCh38)11:89178226C>T
(Homo sapiens)Allele/Variant
Source: rs2135242041
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89178226C>T
(GRCh38)11:89178559T>C
(Homo sapiens)Allele/Variant
Source: NC_000011.10:g.89178559T>C
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89178559T>C
(GRCh38)11:89178560G>T
(Homo sapiens)Allele/Variant
Source: rs778881311
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89178560G>T
(GRCh38)11:89227918C>T
(Homo sapiens)Allele/Variant
Source: rs61754390
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: (GRCh38)11:89227918C>T
(GRCh38)11:89178238C>T
(Homo sapiens)Allele/Variant
Source: rs1943251591
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89178238C>T
(GRCh38)11:89284926C>T
(Homo sapiens)Allele/Variant
Source: rs749924379
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89284926C>T
(GRCh38)11:89284863C>G
(Homo sapiens)Allele/Variant
Source: rs1590902378
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89284863C>G
(GRCh38)11:89284863C>T
(Homo sapiens)Allele/Variant
Source: rs1590902378
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89284863C>T
(GRCh38)11:89284958A>G
(Homo sapiens)Allele/Variant
Source: rs61754398
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89284958A>G
(GRCh38)11:89227953C>T
(Homo sapiens)Allele/Variant
Source: rs13312743
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89227953C>T
(GRCh38)11:89295596G>A
(Homo sapiens)Allele/Variant
Source: rs532489606
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89295596G>A
(GRCh38)11:89177980G>A
(Homo sapiens)Allele/Variant
Source: rs1325874647
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89177980G>A
(GRCh38)11:89178712A>T
(Homo sapiens)Allele/Variant
Source: rs200936835
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89178712A>T
(GRCh38)11:89178763C>T
(Homo sapiens)Allele/Variant
Source: rs1398673169
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89178763C>T
(GRCh38)11:89178780A>G
(Homo sapiens)Allele/Variant
Source: rs371040611
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89178780A>G
(GRCh38)11:89178783C>T
(Homo sapiens)Allele/Variant
Source: rs1943263803
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89178783C>T
(GRCh38)11:89178789A>G
(Homo sapiens)Allele/Variant
Source: rs1943263875
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89178789A>G
(GRCh38)11:89191214C>T
(Homo sapiens)Allele/Variant
Source: rs62645904
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89191214C>T
(GRCh38)11:89178631A>G
(Homo sapiens)Allele/Variant
Source: rs746685788
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89178631A>G
(GRCh38)11:89178736C>T
(Homo sapiens)Allele/Variant
Source: rs751135308
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89178736C>T
(GRCh38)11:89191204T>C
(Homo sapiens)Allele/Variant
Source: rs1241007197
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89191204T>C
(GRCh38)11:89191210T>C
(Homo sapiens)Allele/Variant
Source: NC_000011.10:g.89191210T>C
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89191210T>C
(GRCh38)11:89191285T>C
(Homo sapiens)Allele/Variant
Source: NC_000011.10:g.89191285T>C
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89191285T>C
(GRCh38)11:89178337C>A
(Homo sapiens)Allele/Variant
Source: rs56414416
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89178337C>A
(GRCh38)11:89178337C>G
(Homo sapiens)Allele/Variant
Source: rs56414416
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89178337C>G
(GRCh38)11:89178409C>T
(Homo sapiens)Allele/Variant
Source: rs61753257
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89178409C>T
(GRCh38)11:89177974C>T
(Homo sapiens)Allele/Variant
Source: rs1943245244
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89177974C>T
(GRCh38)11:89178785A>G
(Homo sapiens)Allele/Variant
Source: NC_000011.10:g.89178785A>G
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89178785A>G
(GRCh38)11:89177962G>T
(Homo sapiens)Allele/Variant
Source: NC_000011.10:g.89177962G>T
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89177962G>T
(GRCh38)11:89178599T>C
(Homo sapiens)Allele/Variant
Source: rs61754363
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89178599T>C
(GRCh38)11:89178614G>T
(Homo sapiens)Allele/Variant
Source: rs758115945
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89178614G>T
(GRCh38)11:89178637T>C
(Homo sapiens)Allele/Variant
Source: NC_000011.10:g.89178637T>C
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89178637T>C
(GRCh38)11:89178640A>G
(Homo sapiens)Allele/Variant
Source: rs1943260698
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89178640A>G
(GRCh38)11:89178658T>C
(Homo sapiens)Allele/Variant
Source: rs138817690
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89178658T>C
(GRCh38)11:89178658T>G
(Homo sapiens)Allele/Variant
Source: rs138817690
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89178658T>G
(GRCh38)11:89178660G>A
(Homo sapiens)Allele/Variant
Source: rs61754367
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89178660G>A
(GRCh38)11:89178751A>G
(Homo sapiens)Allele/Variant
Source: rs1360472075
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89178751A>G
(GRCh38)11:89178787A>C
(Homo sapiens)Allele/Variant
Source: rs1943263851
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89178787A>C
(GRCh38)11:89284955G>A
(Homo sapiens)Allele/Variant
Source: rs369610829
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, splice_donor_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89284955G>A
(GRCh38)11:89178091T>C
(Homo sapiens)Allele/Variant
Source: NC_000011.10:g.89178091T>C
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89178091T>C
(GRCh38)11:89178133G>A
(Homo sapiens)Allele/Variant
Source: rs746279486
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89178133G>A
(GRCh38)11:89191430C>A
(Homo sapiens)Allele/Variant
Source: NC_000011.10:g.89191430C>A
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89191430C>A
(GRCh38)11:89178325C>T
(Homo sapiens)Allele/Variant
Source: rs935942144
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89178325C>T
(GRCh38)11:89178388C>T
(Homo sapiens)Allele/Variant
Source: NC_000011.10:g.89178388C>T
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89178388C>T
(GRCh38)11:89284759C>T
(Homo sapiens)Allele/Variant
Source: NC_000011.10:g.89284759C>T
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89284759C>T
(GRCh38)11:89284959A>G
(Homo sapiens)Allele/Variant
Source: rs61754397
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89284959A>G
(GRCh38)11:89284833T>C
(Homo sapiens)Allele/Variant
Source: NC_000011.10:g.89284833T>C
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89284833T>C
(GRCh38)11:89284848T>C
(Homo sapiens)Allele/Variant
Source: rs375283211
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89284848T>C