Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Molecular Consequence: missense variant
(GRCh38)5:140115050C>T
(Homo sapiens)Allele/Variant
Source: NC_000005.10:g.140115050C>T
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140115050C>T
(GRCh38)5:140114915G>C
(Homo sapiens)Allele/Variant
Source: rs1554129118
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114915G>C
(GRCh38)5:140114753C>T
(Homo sapiens)Allele/Variant
Source: rs1064795165
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114753C>T
(GRCh38)5:140114819A>T
(Homo sapiens)Allele/Variant
Source: rs1763052435
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114819A>T
(GRCh38)5:140114765T>A
(Homo sapiens)Allele/Variant
Source: rs1763051158
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114765T>A
(GRCh38)5:140114786T>C
(Homo sapiens)Allele/Variant
Source: rs1561793336
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114786T>C
(GRCh38)5:140114797A>T
(Homo sapiens)Allele/Variant
Source: rs786204834
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114797A>T
(GRCh38)5:140114776C>T
(Homo sapiens)Allele/Variant
Source: rs1763051347
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114776C>T
(GRCh38)5:140114944A>G
(Homo sapiens)Allele/Variant
Source: NC_000005.10:g.140114944A>G
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114944A>G
(GRCh38)5:140115053C>T
(Homo sapiens)Allele/Variant
Source: NC_000005.10:g.140115053C>T
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140115053C>T
(GRCh38)5:140115101C>T
(Homo sapiens)Allele/Variant
Source: rs1554129135
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140115101C>T
(GRCh38)5:140115132A>C
(Homo sapiens)Allele/Variant
Source: NC_000005.10:g.140115132A>C
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140115132A>C
(GRCh38)5:140115100G>A
(Homo sapiens)Allele/Variant
Source: rs751843411
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140115100G>A
(GRCh38)5:140115104C>T
(Homo sapiens)Allele/Variant
Source: rs780035820
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140115104C>T
(GRCh38)5:140114839G>A
(Homo sapiens)Allele/Variant
Source: NC_000005.10:g.140114839G>A
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114839G>A
(GRCh38)5:140114795T>C
(Homo sapiens)Allele/Variant
Source: rs1581036537
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114795T>C
(GRCh38)5:140115106G>C
(Homo sapiens)Allele/Variant
Source: rs1273916819
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140115106G>C
(GRCh38)5:140114744T>C
(Homo sapiens)Allele/Variant
Source: rs793888527
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114744T>C
(GRCh38)5:140114746G>C
(Homo sapiens)Allele/Variant
Source: rs1581036496
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114746G>C
(GRCh38)5:140114873T>C
(Homo sapiens)Allele/Variant
Source: rs1554129113
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114873T>C
(GRCh38)5:140114938T>G
(Homo sapiens)Allele/Variant
Source: NC_000005.10:g.140114938T>G
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114938T>G
(GRCh38)5:140115030G>C
(Homo sapiens)Allele/Variant
Source: rs181348692
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140115030G>C
(GRCh38)5:140114789C>T
(Homo sapiens)Allele/Variant
Source: rs2126749271
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114789C>T
(GRCh38)5:140114853G>C
(Homo sapiens)Allele/Variant
Source: rs1187486679
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114853G>C
(GRCh38)5:140114864A>G
(Homo sapiens)Allele/Variant
Source: rs1554129110
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114864A>G
(GRCh38)5:140114891C>T
(Homo sapiens)Allele/Variant
Source: rs886039899
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114891C>T
(GRCh38)5:140114777G>C
(Homo sapiens)Allele/Variant
Source: rs587783001
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114777G>C
(GRCh38)5:140114728A>G
(Homo sapiens)Allele/Variant
Source: rs1386400193
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114728A>G
(GRCh38)5:140114950A>G
(Homo sapiens)Allele/Variant
Source: rs770307150
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114950A>G
(GRCh38)5:140114832G>T
(Homo sapiens)Allele/Variant
Source: NC_000005.10:g.140114832G>T
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114832G>T
(GRCh38)5:140114855C>T
(Homo sapiens)Allele/Variant
Source: rs1763053031
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114855C>T
(GRCh38)5:140114873T>G
(Homo sapiens)Allele/Variant
Source: rs1554129113
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114873T>G
(GRCh38)5:140114974G>A
(Homo sapiens)Allele/Variant
Source: NC_000005.10:g.140114974G>A
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114974G>A
(GRCh38)5:140115028G>C
(Homo sapiens)Allele/Variant
Source: rs750482815
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140115028G>C
(GRCh38)5:140115032A>C
(Homo sapiens)Allele/Variant
Source: NC_000005.10:g.140115032A>C
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140115032A>C
(GRCh38)5:140115056G>C
(Homo sapiens)Allele/Variant
Source: NC_000005.10:g.140115056G>C
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140115056G>C
(GRCh38)5:140115103G>A
(Homo sapiens)Allele/Variant
Source: rs1286829864
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140115103G>A
(GRCh38)5:140115122A>C
(Homo sapiens)Allele/Variant
Source: rs1763059029
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140115122A>C
(GRCh38)5:140114815G>C
(Homo sapiens)Allele/Variant
Source: rs1561793355
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114815G>C
(GRCh38)5:140114960C>T
(Homo sapiens)Allele/Variant
Source: rs1064795567
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114960C>T
(GRCh38)5:140115131A>T
(Homo sapiens)Allele/Variant
Source: rs1581036746
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140115131A>T
(GRCh38)5:140115136G>C
(Homo sapiens)Allele/Variant
Source: rs1763059359
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140115136G>C
(GRCh38)5:140114885T>G
(Homo sapiens)Allele/Variant
Source: rs1057524051
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114885T>G
(GRCh38)5:140114806T>G
(Homo sapiens)Allele/Variant
Source: NC_000005.10:g.140114806T>G
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114806T>G
(GRCh38)5:140114807A>T
(Homo sapiens)Allele/Variant
Source: rs1763052181
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114807A>T
(GRCh38)5:140114960C>G
(Homo sapiens)Allele/Variant
Source: rs1064795567
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114960C>G
(GRCh38)5:140114608C>G
(Homo sapiens)Allele/Variant
Source: rs1554129084
Genes: MALINC1 (Hsa), PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114608C>G
(GRCh38)5:140114617G>A
(Homo sapiens)Allele/Variant
Source: rs1763047012
Genes: MALINC1 (Hsa), PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114617G>A
(GRCh38)5:140114639G>C
(Homo sapiens)Allele/Variant
Source: rs886039610
Genes: MALINC1 (Hsa), PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114639G>C
(R6)3L:7603070G>A
(Drosophila melanogaster)Allele/Variant
Source: NT_037436.4:g.7603070G>A
Genes: Pura (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)3L:7603070G>A