Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: SOD1 (Hsa)
(GRCh38)21:31663814T>C
(Homo sapiens)Allele/Variant
Source: rs2049569572
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31663814T>C
(GRCh38)21:31663833T>A
(Homo sapiens)Allele/Variant
Source: rs1555836520
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31663833T>A
(GRCh38)21:31663839A>G
(Homo sapiens)Allele/Variant
Source: rs1568809149
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31663839A>G
(GRCh38)21:31663841G>A
(Homo sapiens)Allele/Variant
Source: rs121912433
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31663841G>A
(GRCh38)21:31667378A>G
(Homo sapiens)Allele/Variant
Source: rs746682134
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31667378A>G
(GRCh38)21:31666552A>C
(Homo sapiens)Allele/Variant
Source: rs2234694
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31666552A>C
(GRCh38)21:31667273G>C
(Homo sapiens)Allele/Variant
Source: rs1315541036
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31667273G>C
(GRCh38)21:31667280G>A
(Homo sapiens)Allele/Variant
Source: rs1568810641
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31667280G>A
(GRCh38)21:31668525A>G
(Homo sapiens)Allele/Variant
Source: rs1568811445
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31668525A>G
(GRCh38)21:31659788T>A
(Homo sapiens)Allele/Variant
Source: rs1312702973
Genes: SOD1-DT (Hsa), SOD1 (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)21:31659788T>A
(GRCh38)21:31666458G>A
(Homo sapiens)Allele/Variant
Source: rs1413388444
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31666458G>A
(GRCh38)21:31666524A>C
(Homo sapiens)Allele/Variant
Source: rs374610141
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31666524A>C
(GRCh38)21:31667373G>C
(Homo sapiens)Allele/Variant
Source: rs1235629842
Genes: SOD1 (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)21:31667373G>C
(GRCh38)21:31668490A>C
(Homo sapiens)Allele/Variant
Source: rs1164911383
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31668490A>C
(GRCh38)21:31668548G>C
(Homo sapiens)Allele/Variant
Source: rs1482760341
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31668548G>C
(GRCh38)21:31659683G>A
(Homo sapiens)Allele/Variant
Source: rs139202139
Genes: SOD1-DT (Hsa), SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31659683G>A
(GRCh38)21:31666495C>T
(Homo sapiens)Allele/Variant
Source: rs368042695
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31666495C>T
(GRCh38)21:31667844C>A
(Homo sapiens)Allele/Variant
Source: rs17881732
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31667844C>A
(GRCh38)21:31668487A>T
(Homo sapiens)Allele/Variant
Source: rs1568811366
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31668487A>T
(GRCh38)21:31668489G>C
(Homo sapiens)Allele/Variant
Source: rs1568811372
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31668489G>C
(GRCh38)21:31666493C>T
(Homo sapiens)Allele/Variant
Source: rs2049594311
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31666493C>T
(GRCh38)21:31667305C>T
(Homo sapiens)Allele/Variant
Source: rs1568810690
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31667305C>T
(GRCh38)21:31668514A>G
(Homo sapiens)Allele/Variant
Source: NC_000021.9:g.31668514A>G
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31668514A>G
(GRCh38)21:31668556G>A
(Homo sapiens)Allele/Variant
Source: rs1555836950
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31668556G>A
(GRCh38)21:31668058C>T
(Homo sapiens)Allele/Variant
Source: rs4817420
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31668058C>T
(GRCh38)21:31666429T>C
(Homo sapiens)Allele/Variant
Source: rs17885833
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31666429T>C
(GRCh38)21:31666472T>C
(Homo sapiens)Allele/Variant
Source: rs1030039318
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31666472T>C
(GRCh38)21:31666509A>T
(Homo sapiens)Allele/Variant
Source: rs1568810316
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31666509A>T
(GRCh38)21:31666535C>G
(Homo sapiens)Allele/Variant
Source: rs2123434677
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31666535C>G
(GRCh38)21:31667242G>A
(Homo sapiens)Allele/Variant
Source: rs779802862
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31667242G>A
(GRCh38)21:31659854A>G
(Homo sapiens)Allele/Variant
Source: rs754347852
Genes: SOD1-DT (Hsa), SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31659854A>G
(GRCh38)21:31663813G>A
(Homo sapiens)Allele/Variant
Source: rs769715106
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31663813G>A
(GRCh38)21:31663857A>G
(Homo sapiens)Allele/Variant
Source: rs121912443
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31663857A>G
(GRCh38)21:31666508G>T
(Homo sapiens)Allele/Variant
Source: rs1601157750
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31666508G>T
(GRCh38)21:31666533A>T
(Homo sapiens)Allele/Variant
Source: rs766574368
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31666533A>T
(GRCh38)21:31668172A>G
(Homo sapiens)Allele/Variant
Source: rs2049614155
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31668172A>G
(GRCh38)21:31668487A>C
(Homo sapiens)Allele/Variant
Source: rs1568811366
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31668487A>C
(GRCh38)21:31659679C>G
(Homo sapiens)Allele/Variant
Source: rs568985632
Genes: SOD1-DT (Hsa), SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31659679C>G
(GRCh38)21:31659714T>A
(Homo sapiens)Allele/Variant
Source: rs535066119
Genes: SOD1-DT (Hsa), SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31659714T>A
(GRCh38)21:31659722T>A
(Homo sapiens)Allele/Variant
Source: rs142752986
Genes: SOD1-DT (Hsa), SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31659722T>A
(GRCh38)21:31659789G>T
(Homo sapiens)Allele/Variant
Source: rs121912448
Genes: SOD1-DT (Hsa), SOD1 (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)21:31659789G>T
(GRCh38)21:31659783C>T
(Homo sapiens)Allele/Variant
Source: rs121912442
Genes: SOD1-DT (Hsa), SOD1 (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)21:31659783C>T
(GRCh38)21:31659974C>T
(Homo sapiens)Allele/Variant
Source: rs17881180
Genes: SOD1-DT (Hsa), SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31659974C>T
(GRCh38)21:31667691T>G
(Homo sapiens)Allele/Variant
Source: rs17883234
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31667691T>G
(GRCh38)21:31668475A>T
(Homo sapiens)Allele/Variant
Source: rs1410925719
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31668475A>T
(GRCh38)21:31668570G>A
(Homo sapiens)Allele/Variant
Source: rs747094021
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31668570G>A
(GRCh38)21:31668552T>C
(Homo sapiens)Allele/Variant
Source: rs1568811515
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31668552T>C
(GRCh38)21:31659779A>G
(Homo sapiens)Allele/Variant
Source: rs1568807297
Genes: SOD1-DT (Hsa), SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31659779A>G
(GRCh38)21:31668341G>C
(Homo sapiens)Allele/Variant
Source: rs117304270
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31668341G>C
(GRCh38)21:31668563T>C
(Homo sapiens)Allele/Variant
Source: NC_000021.9:g.31668563T>C
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31668563T>C