Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: SNCA (Hsa) Molecular Consequence: non coding transcript exon variant
(GRCh38)4:89822309T>C
(Homo sapiens)Allele/Variant
Source: rs568436589
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89822309T>C
(GRCh38)4:89835563C>T
(Homo sapiens)Allele/Variant
Source: rs768334864
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89835563C>T
(GRCh38)4:89822301C>A
(Homo sapiens)Allele/Variant
Source: rs386352363
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89822301C>A
(GRCh38)4:89835569T>C
(Homo sapiens)Allele/Variant
Source: rs766497794
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89835569T>C
(GRCh38)4:89835624A>G
(Homo sapiens)Allele/Variant
Source: rs1739238968
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89835624A>G
(GRCh38)4:89835562C>G
(Homo sapiens)Allele/Variant
Source: rs1342686707
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89835562C>G
(GRCh38)4:89835566T>C
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.89835566T>C
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89835566T>C
(GRCh38)4:89729225G>A
(Homo sapiens)Allele/Variant
Source: rs1024288001
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89729225G>A
(GRCh38)4:89822265T>C
(Homo sapiens)Allele/Variant
Source: rs548523899
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89822265T>C
(GRCh38)4:89822349C>T
(Homo sapiens)Allele/Variant
Source: rs752981956
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89822349C>T
(GRCh38)4:89729202G>T
(Homo sapiens)Allele/Variant
Source: rs750899874
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89729202G>T
(GRCh38)4:89729209A>G
(Homo sapiens)Allele/Variant
Source: rs367556974
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89729209A>G
(GRCh38)4:89828150C>A
(Homo sapiens)Allele/Variant
Source: rs148108612
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89828150C>A
(GRCh38)4:89828170C>T
(Homo sapiens)Allele/Variant
Source: rs104893875
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89828170C>T
(GRCh38)4:89835637C>A
(Homo sapiens)Allele/Variant
Source: rs1219278381
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89835637C>A
(GRCh38)4:89835659T>C
(Homo sapiens)Allele/Variant
Source: rs370989462
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89835659T>C
(GRCh38)4:89822254A>G
(Homo sapiens)Allele/Variant
Source: rs138969470
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89822254A>G
(GRCh38)4:89835568T>C
(Homo sapiens)Allele/Variant
Source: rs1330229174
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89835568T>C
(GRCh38)4:89835597T>C
(Homo sapiens)Allele/Variant
Source: rs1739236610
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89835597T>C
(GRCh38)4:89724951G>A
(Homo sapiens)Allele/Variant
Source: rs17016072
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89724951G>A
(GRCh38)4:89822305C>G
(Homo sapiens)Allele/Variant
Source: rs2110460484
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89822305C>G
(GRCh38)4:89726660C>G
(Homo sapiens)Allele/Variant
Source: rs2110065132
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89726660C>G
(GRCh38)4:89822378C>G
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.89822378C>G
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89822378C>G
(GRCh38)4:89729214C>A
(Homo sapiens)Allele/Variant
Source: rs1358566725
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89729214C>A
(GRCh38)4:89822303C>T
(Homo sapiens)Allele/Variant
Source: rs1737224483
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89822303C>T
(GRCh38)4:89729242T>G
(Homo sapiens)Allele/Variant
Source: rs770804878
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89729242T>G
(GRCh38)4:89726643G>A
(Homo sapiens)Allele/Variant
Source: rs76642636
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89726643G>A
(GRCh38)4:89822336C>T
(Homo sapiens)Allele/Variant
Source: rs144758871
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89822336C>T
(GRCh38)4:89828149C>T
(Homo sapiens)Allele/Variant
Source: rs104893877
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89828149C>T
(GRCh38)4:89828159C>T
(Homo sapiens)Allele/Variant
Source: rs141859659
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89828159C>T
(GRCh38)4:89822327T>A
(Homo sapiens)Allele/Variant
Source: rs149401968
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89822327T>A
(GRCh38)4:89835560A>G
(Homo sapiens)Allele/Variant
Source: rs1407062582
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89835560A>G
(GRCh38)4:89729203C>T
(Homo sapiens)Allele/Variant
Source: rs191055637
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89729203C>T
(GRCh38)4:89822306C>T
(Homo sapiens)Allele/Variant
Source: rs775179895
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89822306C>T
(GRCh38)4:89726650T>C
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.89726650T>C
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89726650T>C
(GRCh38)4:89828156A>C
(Homo sapiens)Allele/Variant
Source: rs201106962
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89828156A>C
(GRCh38)4:89835621A>G
(Homo sapiens)Allele/Variant
Source: rs1289802008
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89835621A>G
(GRCh38)4:89828154C>T
(Homo sapiens)Allele/Variant
Source: rs431905511
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89828154C>T
(GRCh38)4:89835579G>C
(Homo sapiens)Allele/Variant
Source: rs2110525413
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89835579G>C
(GRCh38)4:89729235G>T
(Homo sapiens)Allele/Variant
Source: rs145138372
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89729235G>T
(GRCh38)4:89835562C>T
(Homo sapiens)Allele/Variant
Source: rs1342686707
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89835562C>T
(GRCh38)4:89822365C>G
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.89822365C>G
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89822365C>G
(GRCh38)4:89822369C>T
(Homo sapiens)Allele/Variant
Source: rs1737231816
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89822369C>T
(GRCh38)4:89725998A>C
(Homo sapiens)Allele/Variant
Source: rs886059725
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89725998A>C
(GRCh38)4:89835580C>G
(Homo sapiens)Allele/Variant
Source: rs104893878
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89835580C>G
(GRCh38)4:89729217C>T
(Homo sapiens)Allele/Variant
Source: rs200056149
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89729217C>T
(GRCh38)4:89822335C>T
(Homo sapiens)Allele/Variant
Source: rs774113587
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89822335C>T
(GRCh38)4:89724591A>G
(Homo sapiens)Allele/Variant
Source: rs553070344
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89724591A>G
(GRCh38)4:89724926C>T
(Homo sapiens)Allele/Variant
Source: rs886059714
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89724926C>T
(GRCh38)4:89725110A>G
(Homo sapiens)Allele/Variant
Source: rs1724761878
Genes: SNCA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:89725110A>G