Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: SOD1 (Hsa) Molecular Consequence: synonymous variant
(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
(GRCh38)21:31663792A>G
(Homo sapiens)Allele/Variant
Source: rs2049569274
Genes: SOD1 (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)21:31663792A>G
(GRCh38)21:31667330G>A
(Homo sapiens)Allele/Variant
Source: rs2049603364
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31667330G>A
(GRCh38)21:31667336A>T
(Homo sapiens)Allele/Variant
Source: rs763963373
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31667336A>T
(GRCh38)21:31667306C>T
(Homo sapiens)Allele/Variant
Source: rs557930089
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31667306C>T
(GRCh38)21:31668557T>C
(Homo sapiens)Allele/Variant
Source: rs372540831
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31668557T>C
(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)21:31663804A>G
(Homo sapiens)Allele/Variant
Source: rs145198224
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31663804A>G
(GRCh38)21:31659823C>A
(Homo sapiens)Allele/Variant
Source: rs1447729350
Genes: SOD1-DT (Hsa), SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31659823C>A
(GRCh38)21:31663867G>A
(Homo sapiens)Allele/Variant
Source: rs201045805
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31663867G>A
(GRCh38)21:31668500A>G
(Homo sapiens)Allele/Variant
Source: NC_000021.9:g.31668500A>G
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31668500A>G
(GRCh38)21:31666459T>C
(Homo sapiens)Allele/Variant
Source: rs373888553
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31666459T>C
(GRCh38)21:31666474T>C
(Homo sapiens)Allele/Variant
Source: rs147620646
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31666474T>C
(GRCh38)21:31659829T>C
(Homo sapiens)Allele/Variant
Source: rs1601153464
Genes: SOD1-DT (Hsa), SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31659829T>C
(GRCh38)21:31663876T>C
(Homo sapiens)Allele/Variant
Source: rs1276917683
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31663876T>C
(GRCh38)21:31668521A>G
(Homo sapiens)Allele/Variant
Source: NC_000021.9:g.31668521A>G
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31668521A>G
(GRCh38)21:31667369A>C
(Homo sapiens)Allele/Variant
Source: rs757951479
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31667369A>C
(GRCh38)21:31667315T>C
(Homo sapiens)Allele/Variant
Source: rs1432013430
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31667315T>C
(GRCh38)21:31659784C>T
(Homo sapiens)Allele/Variant
Source: rs199766524
Genes: SOD1-DT (Hsa), SOD1 (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)21:31659784C>T
(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)21:31663882A>G
(Homo sapiens)Allele/Variant
Source: NC_000021.9:g.31663882A>G
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31663882A>G
(GRCh38)21:31667271T>C
(Homo sapiens)Allele/Variant
Source: rs121912452
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31667271T>C
(GRCh38)21:31668527A>G
(Homo sapiens)Allele/Variant
Source: rs752378382
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31668527A>G
(GRCh38)21:31668536T>A
(Homo sapiens)Allele/Variant
Source: rs143100660
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31668536T>A
(GRCh38)21:31668533C>T
(Homo sapiens)Allele/Variant
Source: rs1804449
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31668533C>T
(GRCh38)21:31667339C>T
(Homo sapiens)Allele/Variant
Source: rs377269573
Genes: SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31667339C>T
(GRCh38)21:31659796G>A
(Homo sapiens)Allele/Variant
Source: rs772764888
Genes: SOD1-DT (Hsa), SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31659796G>A
(GRCh38)21:31659808C>T
(Homo sapiens)Allele/Variant
Source: rs377178013
Genes: SOD1-DT (Hsa), SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31659808C>T
(GRCh38)21:31659835G>A
(Homo sapiens)Allele/Variant
Source: rs756458346
Genes: SOD1-DT (Hsa), SOD1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)21:31659835G>A