Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: WARS2 (Hsa)
(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)1:119076555T>C
(Homo sapiens)Allele/Variant
Source: rs1296437426
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119076555T>C
(GRCh38)1:119032981C>G
(Homo sapiens)Allele/Variant
Source: rs1370759242
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119032981C>G
(GRCh38)1:119032984A>G
(Homo sapiens)Allele/Variant
Source: rs1448970558
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119032984A>G
(GRCh38)1:119033006G>A
(Homo sapiens)Allele/Variant
Source: NC_000001.11:g.119033006G>A
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119033006G>A
(GRCh38)1:119033038C>T
(Homo sapiens)Allele/Variant
Source: rs376728283
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119033038C>T
(GRCh38)1:119076381G>A
(Homo sapiens)Allele/Variant
Source: rs753188889
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119076381G>A
(GRCh38)1:119076493C>G
(Homo sapiens)Allele/Variant
Source: NC_000001.11:g.119076493C>G
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119076493C>G
(GRCh38)1:119033197G>A
(Homo sapiens)Allele/Variant
Source: rs368914534
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119033197G>A
(GRCh38)1:119033203T>C
(Homo sapiens)Allele/Variant
Source: rs139194636
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119033203T>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)1:119032915A>G
(Homo sapiens)Allele/Variant
Source: rs17023101
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119032915A>G
(GRCh38)1:119033056T>A
(Homo sapiens)Allele/Variant
Source: rs145867327
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119033056T>A
(GRCh38)1:119033110G>A
(Homo sapiens)Allele/Variant
Source: rs140469836
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119033110G>A
(GRCh38)1:119033112G>T
(Homo sapiens)Allele/Variant
Source: NC_000001.11:g.119033112G>T
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119033112G>T
(GRCh38)1:119033314A>G
(Homo sapiens)Allele/Variant
Source: rs2101095108
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119033314A>G
(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)1:119034107C>A
(Homo sapiens)Allele/Variant
Source: rs137890886
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119034107C>A
(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)1:119076549C>T
(Homo sapiens)Allele/Variant
Source: rs1571323203
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119076549C>T
(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)1:119032964C>A
(Homo sapiens)Allele/Variant
Source: rs1647552297
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119032964C>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)1:119076433G>A
(Homo sapiens)Allele/Variant
Source: rs374597293
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119076433G>A
(GRCh38)1:119076445G>A
(Homo sapiens)Allele/Variant
Source: rs776400244
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119076445G>A
(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)1:119033282C>T
(Homo sapiens)Allele/Variant
Source: rs1300524106
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119033282C>T
(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)1:119045653G>T
(Homo sapiens)Allele/Variant
Source: rs1648735933
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119045653G>T
(GRCh38)1:119033150C>T
(Homo sapiens)Allele/Variant
Source: NC_000001.11:g.119033150C>T
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119033150C>T
(GRCh38)1:119033153C>T
(Homo sapiens)Allele/Variant
Source: rs952768523
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119033153C>T
(GRCh38)1:119033095G>A
(Homo sapiens)Allele/Variant
Source: rs370628159
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119033095G>A
(GRCh38)1:119033120G>A
(Homo sapiens)Allele/Variant
Source: rs201132666
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119033120G>A
(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)1:119076467G>C
(Homo sapiens)Allele/Variant
Source: rs766501807
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119076467G>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)1:119140598A>G
(Homo sapiens)Allele/Variant
Source: rs1204105967
Genes: WARS2 (Hsa), WARS2-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119140598A>G
(GRCh38)1:119140599T>A
(Homo sapiens)Allele/Variant
Source: NC_000001.11:g.119140599T>A
Genes: WARS2 (Hsa), WARS2-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119140599T>A
(GRCh38)1:119033243A>G
(Homo sapiens)Allele/Variant
Source: NC_000001.11:g.119033243A>G
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119033243A>G
(GRCh38)1:119033290A>T
(Homo sapiens)Allele/Variant
Source: NC_000001.11:g.119033290A>T
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119033290A>T
(GRCh38)1:119033329T>C
(Homo sapiens)Allele/Variant
Source: rs1647601318
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119033329T>C
(GRCh38)1:119034281G>A
(Homo sapiens)Allele/Variant
Source: rs17023108
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119034281G>A
(GRCh38)1:119076332C>T
(Homo sapiens)Allele/Variant
Source: rs1651726480
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119076332C>T
(GRCh38)1:119032978G>A
(Homo sapiens)Allele/Variant
Source: rs1647554050
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119032978G>A
(GRCh38)1:119032979A>T
(Homo sapiens)Allele/Variant
Source: rs1332510652
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119032979A>T
(GRCh38)1:119076499C>G
(Homo sapiens)Allele/Variant
Source: rs149515458
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119076499C>G
(GRCh38)1:119076484T>C
(Homo sapiens)Allele/Variant
Source: rs1376745156
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119076484T>C
(GRCh38)1:119076505C>A
(Homo sapiens)Allele/Variant
Source: rs2101319201
Genes: WARS2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:119076505C>A