Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: SOD2 (Hsa)
(GRCh38)6:159682529C>A
(Homo sapiens)Allele/Variant
Source: rs1780005831
Genes: SOD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)6:159682529C>A
(GRCh38)6:159748228G>C
(Homo sapiens)Allele/Variant
Source: rs755677301
Genes: SOD2 (Hsa), WTAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:159748228G>C
(GRCh38)6:159685006T>A
(Homo sapiens)Allele/Variant
Source: rs530833676
Genes: SOD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:159685006T>A
(GRCh38)6:159692705T>G
(Homo sapiens)Allele/Variant
Source: NC_000006.12:g.159692705T>G
Genes: SOD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)6:159692705T>G
(GRCh38)6:159682620C>A
(Homo sapiens)Allele/Variant
Source: rs1469862592
Genes: SOD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)6:159682620C>A
(GRCh38)6:159755270C>T
(Homo sapiens)Allele/Variant
Source: rs747375621
Genes: SOD2 (Hsa), WTAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:159755270C>T
(GRCh38)6:159688239T>A
(Homo sapiens)Allele/Variant
Source: NC_000006.12:g.159688239T>A
Genes: SOD2 (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)6:159688239T>A
(GRCh38)6:159682506G>A
(Homo sapiens)Allele/Variant
Source: rs1188104649
Genes: SOD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)6:159682506G>A
(GRCh38)6:159692840A>G
(Homo sapiens)Allele/Variant
Source: rs4880
Genes: SOD2 (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)6:159692840A>G
(GRCh38)6:159684953C>A
(Homo sapiens)Allele/Variant
Source: rs376398472
Genes: SOD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:159684953C>A
(GRCh38)6:159684910C>T
(Homo sapiens)Allele/Variant
Source: rs372335332
Genes: SOD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:159684910C>T
(GRCh38)6:159684978C>G
(Homo sapiens)Allele/Variant
Source: rs372173830
Genes: SOD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:159684978C>G
(GRCh38)6:159692774A>T
(Homo sapiens)Allele/Variant
Source: rs375884951
Genes: SOD2 (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)6:159692774A>T
(GRCh38)6:159748286A>T
(Homo sapiens)Allele/Variant
Source: NC_000006.12:g.159748286A>T
Genes: SOD2 (Hsa), WTAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:159748286A>T
(GRCh38)6:159685010G>A
(Homo sapiens)Allele/Variant
Source: rs143582231
Genes: SOD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:159685010G>A
(GRCh38)6:159692756G>C
(Homo sapiens)Allele/Variant
Source: rs763954620
Genes: SOD2 (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)6:159692756G>C
(GRCh38)6:159682531C>T
(Homo sapiens)Allele/Variant
Source: rs1395235141
Genes: SOD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)6:159682531C>T
(GRCh38)6:159685012T>A
(Homo sapiens)Allele/Variant
Source: rs756111347
Genes: SOD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:159685012T>A
(GRCh38)6:159755213G>A
(Homo sapiens)Allele/Variant
Source: rs1395757040
Genes: SOD2 (Hsa), WTAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:159755213G>A
(GRCh38)6:159682612C>T
(Homo sapiens)Allele/Variant
Source: rs564741623
Genes: SOD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)6:159682612C>T
(GRCh38)6:159684965C>A
(Homo sapiens)Allele/Variant
Source: NC_000006.12:g.159684965C>A
Genes: SOD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:159684965C>A
(GRCh38)6:159682583A>G
(Homo sapiens)Allele/Variant
Source: rs557996027
Genes: SOD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)6:159682583A>G
(GRCh38)6:159692671C>T
(Homo sapiens)Allele/Variant
Source: rs200264201
Genes: SOD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)6:159692671C>T
(GRCh38)6:159755210G>A
(Homo sapiens)Allele/Variant
Source: NC_000006.12:g.159755210G>A
Genes: SOD2 (Hsa), WTAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:159755210G>A
(GRCh38)6:159685031C>G
(Homo sapiens)Allele/Variant
Source: rs1047426562
Genes: SOD2 (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)6:159685031C>G
(GRCh38)6:159755211A>G
(Homo sapiens)Allele/Variant
Source: NC_000006.12:g.159755211A>G
Genes: SOD2 (Hsa), WTAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:159755211A>G
(GRCh38)6:159755280C>T
(Homo sapiens)Allele/Variant
Source: rs762690654
Genes: SOD2 (Hsa), WTAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:159755280C>T