Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: WARS2 (Hsa) Molecular Consequence: synonymous variant
(GRCh38)1:119076551C>G
(Homo sapiens)Allele/Variant
Source: rs139975529
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119076551C>G
(GRCh38)1:119033196C>T
(Homo sapiens)Allele/Variant
Source: rs768587458
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119033196C>T
(GRCh38)1:119042326G>A
(Homo sapiens)Allele/Variant
Source: rs33960696
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119042326G>A
(GRCh38)1:119140561A>T
(Homo sapiens)Allele/Variant
Source: rs749282492
Genes: WARS2 (Hsa), WARS2-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119140561A>T
(GRCh38)1:119076587T>C
(Homo sapiens)Allele/Variant
Source: rs780986003
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119076587T>C
(GRCh38)1:119076503T>C
(Homo sapiens)Allele/Variant
Source: rs1224122076
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119076503T>C
(GRCh38)1:119034108G>A
(Homo sapiens)Allele/Variant
Source: rs932112855
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119034108G>A
(GRCh38)1:119045639A>G
(Homo sapiens)Allele/Variant
Source: rs184828552
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119045639A>G
(GRCh38)1:119042278G>A
(Homo sapiens)Allele/Variant
Source: NC_000001.11:g.119042278G>A
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119042278G>A
(GRCh38)1:119033310C>T
(Homo sapiens)Allele/Variant
Source: rs77497675
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119033310C>T
(GRCh38)1:119033109C>T
(Homo sapiens)Allele/Variant
Source: rs946355135
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119033109C>T
(GRCh38)1:119076542G>A
(Homo sapiens)Allele/Variant
Source: rs1163806887
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119076542G>A
(GRCh38)1:119042296T>C
(Homo sapiens)Allele/Variant
Source: rs149281638
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119042296T>C
(GRCh38)1:119033112G>A
(Homo sapiens)Allele/Variant
Source: rs1165413282
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119033112G>A
(GRCh38)1:119033136G>C
(Homo sapiens)Allele/Variant
Source: NC_000001.11:g.119033136G>C
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119033136G>C
(GRCh38)1:119033163C>G
(Homo sapiens)Allele/Variant
Source: rs1003432838
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119033163C>G
(GRCh38)1:119042310G>A
(Homo sapiens)Allele/Variant
Source: rs762541487
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119042310G>A
(GRCh38)1:119076401A>G
(Homo sapiens)Allele/Variant
Source: NC_000001.11:g.119076401A>G
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119076401A>G
(GRCh38)1:119076524G>A
(Homo sapiens)Allele/Variant
Source: NC_000001.11:g.119076524G>A
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119076524G>A
(GRCh38)1:119045612T>C
(Homo sapiens)Allele/Variant
Source: rs777267723
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119045612T>C
(GRCh38)1:119033064C>T
(Homo sapiens)Allele/Variant
Source: rs139467678
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119033064C>T
(GRCh38)1:119140594C>T
(Homo sapiens)Allele/Variant
Source: rs141898658
Genes: WARS2 (Hsa), WARS2-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119140594C>T
(GRCh38)1:119045645T>C
(Homo sapiens)Allele/Variant
Source: rs778680858
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119045645T>C
(GRCh38)1:119076377T>C
(Homo sapiens)Allele/Variant
Source: rs745462502
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119076377T>C
(GRCh38)1:119076380C>T
(Homo sapiens)Allele/Variant
Source: rs758130195
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119076380C>T
(GRCh38)1:119045648T>C
(Homo sapiens)Allele/Variant
Source: rs745550081
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119045648T>C
(GRCh38)1:119033145C>G
(Homo sapiens)Allele/Variant
Source: rs772131113
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119033145C>G
(GRCh38)1:119076557G>A
(Homo sapiens)Allele/Variant
Source: rs2101319588
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119076557G>A
(GRCh38)1:119140618C>A
(Homo sapiens)Allele/Variant
Source: rs587745035
Genes: WARS2 (Hsa), WARS2-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119140618C>A
(GRCh38)1:119140636C>T
(Homo sapiens)Allele/Variant
Source: rs1656904108
Genes: WARS2 (Hsa), WARS2-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119140636C>T
(GRCh38)1:119033031A>T
(Homo sapiens)Allele/Variant
Source: NC_000001.11:g.119033031A>T
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119033031A>T
(GRCh38)1:119033142C>G
(Homo sapiens)Allele/Variant
Source: rs202238245
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119033142C>G
(GRCh38)1:119034204G>A
(Homo sapiens)Allele/Variant
Source: rs199831668
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119034204G>A
(GRCh38)1:119076581G>A
(Homo sapiens)Allele/Variant
Source: rs371681806
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119076581G>A