Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: PURA (Hsa)
(GRCh38)5:140114676C>G
(Homo sapiens)Allele/Variant
Source: rs1455936459
Genes: MALINC1 (Hsa), PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114676C>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)5:140114835G>T
(Homo sapiens)Allele/Variant
Source: rs1040360891
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114835G>T
(GRCh38)5:140114847C>T
(Homo sapiens)Allele/Variant
Source: NC_000005.10:g.140114847C>T
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114847C>T
(GRCh38)5:140114907G>C
(Homo sapiens)Allele/Variant
Source: rs1581036621
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114907G>C
(GRCh38)5:140114697G>A
(Homo sapiens)Allele/Variant
Source: rs1480387613
Genes: MALINC1 (Hsa), PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114697G>A
(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
(GRCh38)5:140114766C>G
(Homo sapiens)Allele/Variant
Source: rs1581036515
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114766C>G
(GRCh38)5:140114778T>C
(Homo sapiens)Allele/Variant
Source: rs762183564
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114778T>C
(GRCh38)5:140114658C>G
(Homo sapiens)Allele/Variant
Source: rs1453429129
Genes: MALINC1 (Hsa), PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114658C>G
(GRCh38)5:140114674G>A
(Homo sapiens)Allele/Variant
Source: rs1561793272
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)5:140114674G>A
(GRCh38)5:140114687G>A
(Homo sapiens)Allele/Variant
Source: NC_000005.10:g.140114687G>A
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)5:140114687G>A
(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)5:140114604G>A
(Homo sapiens)Allele/Variant
Source: rs1160252551
Genes: MALINC1 (Hsa), PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114604G>A
(GRCh38)5:140114642A>G
(Homo sapiens)Allele/Variant
Source: NC_000005.10:g.140114642A>G
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)5:140114642A>G
(GRCh38)5:140114874C>T
(Homo sapiens)Allele/Variant
Source: rs750557574
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114874C>T
(GRCh38)5:140114661G>A
(Homo sapiens)Allele/Variant
Source: rs759194196
Genes: MALINC1 (Hsa), PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114661G>A
(GRCh38)5:140114684T>C
(Homo sapiens)Allele/Variant
Source: rs1581036449
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)5:140114684T>C
(GRCh38)5:140114575C>G
(Homo sapiens)Allele/Variant
Source: rs746218892
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)5:140114575C>G
(GRCh38)5:140114653G>T
(Homo sapiens)Allele/Variant
Source: rs797044866
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)5:140114653G>T
(GRCh38)5:140114656C>G
(Homo sapiens)Allele/Variant
Source: rs1763048369
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)5:140114656C>G
(GRCh38)5:140114676C>T
(Homo sapiens)Allele/Variant
Source: rs1455936459
Genes: MALINC1 (Hsa), PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114676C>T
(GRCh38)5:140114677C>A
(Homo sapiens)Allele/Variant
Source: rs1554129096
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)5:140114677C>A
(GRCh38)5:140114602C>A
(Homo sapiens)Allele/Variant
Source: rs1413692088
Genes: MALINC1 (Hsa), PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114602C>A
(GRCh38)5:140114907G>A
(Homo sapiens)Allele/Variant
Source: rs1581036621
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114907G>A
(GRCh38)5:140114636A>T
(Homo sapiens)Allele/Variant
Source: rs2126749099
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)5:140114636A>T
(GRCh38)5:140114977A>T
(Homo sapiens)Allele/Variant
Source: rs1554129129
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: (GRCh38)5:140114977A>T
(GRCh38)5:140114983G>T
(Homo sapiens)Allele/Variant
Source: rs2126749415
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: (GRCh38)5:140114983G>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)5:140114405T>C
(Homo sapiens)Allele/Variant
Source: rs1554129049
Genes: MALINC1 (Hsa), PURA (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)5:140114405T>C
(GRCh38)5:140114422G>A
(Homo sapiens)Allele/Variant
Source: rs1581036224
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)5:140114422G>A
(GRCh38)5:140114487C>T
(Homo sapiens)Allele/Variant
Source: rs762714935
Genes: MALINC1 (Hsa), PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114487C>T
(GRCh38)5:140114520C>G
(Homo sapiens)Allele/Variant
Source: rs1581036318
Genes: MALINC1 (Hsa), PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114520C>G
(GRCh38)5:140114224C>A
(Homo sapiens)Allele/Variant
Source: rs923665124
Genes: MALINC1 (Hsa), PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114224C>A
(GRCh38)5:140114260G>C
(Homo sapiens)Allele/Variant
Source: rs1470806491
Genes: MALINC1 (Hsa), PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, coding_sequence_variant, non_coding_transcript_variant, incomplete_terminal_codon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114260G>C
(GRCh38)5:140114391C>T
(Homo sapiens)Allele/Variant
Source: rs373688524
Genes: MALINC1 (Hsa), PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114391C>T
(GRCh38)5:140114291G>C
(Homo sapiens)Allele/Variant
Source: rs1430796646
Genes: MALINC1 (Hsa), PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114291G>C
(GRCh38)5:140114292C>G
(Homo sapiens)Allele/Variant
Source: NC_000005.10:g.140114292C>G
Genes: MALINC1 (Hsa), PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114292C>G
(GRCh38)5:140114320G>A
(Homo sapiens)Allele/Variant
Source: rs1763039495
Genes: MALINC1 (Hsa), PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114320G>A
(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)5:140114272G>A
(Homo sapiens)Allele/Variant
Source: NC_000005.10:g.140114272G>A
Genes: MALINC1 (Hsa), PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114272G>A
(GRCh38)5:140114371A>T
(Homo sapiens)Allele/Variant
Source: NC_000005.10:g.140114371A>T
Genes: MALINC1 (Hsa), PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114371A>T
(GRCh38)5:140114446G>A
(Homo sapiens)Allele/Variant
Source: rs587782999
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)5:140114446G>A
(GRCh38)5:140114659A>G
(Homo sapiens)Allele/Variant
Source: rs2126749118
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)5:140114659A>G
(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)5:140114985A>G
(Homo sapiens)Allele/Variant
Source: rs1581036671
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114985A>G
(GRCh38)5:140114405T>G
(Homo sapiens)Allele/Variant
Source: rs1554129049
Genes: MALINC1 (Hsa), PURA (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)5:140114405T>G
(GRCh38)5:140114408A>T
(Homo sapiens)Allele/Variant
Source: NC_000005.10:g.140114408A>T
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)5:140114408A>T
(GRCh38)5:140114412G>T
(Homo sapiens)Allele/Variant
Source: rs2126748841
Genes: MALINC1 (Hsa), PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114412G>T