Version: 8.0.0
Date: Tue Jan 28 2025
566 results
Allele/Variant Genes: TYR (Hsa)

(GRCh38)11:89227825T>C

(Homo sapiens)
Allele/Variant
Source: rs2135281765
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89227825T>C

(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)11:89178183G>A

(Homo sapiens)
Allele/Variant
Source: rs61753185
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89178183G>A

(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)11:89178495A>T

(Homo sapiens)
Allele/Variant
Source: NC_000011.10:g.89178495A>T
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89178495A>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)11:89178573T>G

(Homo sapiens)
Allele/Variant
Source: NC_000011.10:g.89178573T>G
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89178573T>G

(GRCh38)11:89191379G>T

(Homo sapiens)
Allele/Variant
Source: rs896650424
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89191379G>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)11:89177964C>T

(Homo sapiens)
Allele/Variant
Source: rs1254138989
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89177964C>T

(GRCh38)11:89177979T>C

(Homo sapiens)
Allele/Variant
Source: rs1238837002
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89177979T>C

(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)11:89178609A>C

(Homo sapiens)
Allele/Variant
Source: rs2135242551
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89178609A>C

(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)11:89178719C>T

(Homo sapiens)
Allele/Variant
Source: rs61754370
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89178719C>T

(GRCh38)11:89178720A>G

(Homo sapiens)
Allele/Variant
Source: rs1289102976
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89178720A>G

(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)11:89178689A>T

(Homo sapiens)
Allele/Variant
Source: rs2135242705
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89178689A>T

(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)11:89191215G>T

(Homo sapiens)
Allele/Variant
Source: NC_000011.10:g.89191215G>T
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89191215G>T

(GRCh38)11:89191278G>A

(Homo sapiens)
Allele/Variant
Source: rs61754375
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89191278G>A

(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)11:89191297C>A

(Homo sapiens)
Allele/Variant
Source: rs142170797
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89191297C>A

(GRCh38)11:89178483T>A

(Homo sapiens)
Allele/Variant
Source: rs571810545
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89178483T>A

(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)11:89178602C>T

(Homo sapiens)
Allele/Variant
Source: rs63159160
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89178602C>T

(GRCh38)11:89178608G>A

(Homo sapiens)
Allele/Variant
Source: rs747995722
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89178608G>A

(GRCh38)11:89178612A>G

(Homo sapiens)
Allele/Variant
Source: rs2135242554
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89178612A>G

(GRCh38)11:89178614G>A

(Homo sapiens)
Allele/Variant
Source: rs758115945
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89178614G>A

(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)11:89178657A>G

(Homo sapiens)
Allele/Variant
Source: NC_000011.10:g.89178657A>G
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89178657A>G

(GRCh38)11:89191409A>G

(Homo sapiens)
Allele/Variant
Source: rs1172024364
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89191409A>G

(GRCh38)11:89227907T>C

(Homo sapiens)
Allele/Variant
Source: rs769024531
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89227907T>C

(GRCh38)11:89227915G>T

(Homo sapiens)
Allele/Variant
Source: rs1394026490
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89227915G>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)11:89227924T>C

(Homo sapiens)
Allele/Variant
Source: rs61754391
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89227924T>C

(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)11:89178242G>A

(Homo sapiens)
Allele/Variant
Source: rs61753252
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89178242G>A

(GRCh38)11:89178386A>G

(Homo sapiens)
Allele/Variant
Source: rs758570611
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89178386A>G

(GRCh38)11:89178054A>C

(Homo sapiens)
Allele/Variant
Source: rs1555083355
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89178054A>C

(GRCh38)11:89284907T>C

(Homo sapiens)
Allele/Variant
Source: rs762831445
Genes: TYR (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)11:89284907T>C