Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: PURA (Hsa) Molecular Consequence: non coding transcript variant
(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)5:140114220G>A
(Homo sapiens)Allele/Variant
Source: NC_000005.10:g.140114220G>A
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)5:140114220G>A
(GRCh38)5:140114236G>A
(Homo sapiens)Allele/Variant
Source: rs2126748559
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)5:140114236G>A
(GRCh38)5:140114253C>T
(Homo sapiens)Allele/Variant
Source: rs1763036127
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)5:140114253C>T
(GRCh38)5:140114280C>T
(Homo sapiens)Allele/Variant
Source: rs2126748624
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)5:140114280C>T
(GRCh38)5:140114224C>G
(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>G
(GRCh38)5:140114286T>G
(Homo sapiens)Allele/Variant
Source: rs1282359377
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)5:140114286T>G
(GRCh38)5:140114336G>A
(Homo sapiens)Allele/Variant
Source: rs763614822
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)5:140114336G>A
(GRCh38)5:140114210A>T
(Homo sapiens)Allele/Variant
Source: NC_000005.10:g.140114210A>T
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)5:140114210A>T
(GRCh38)5:140114182A>G
(Homo sapiens)Allele/Variant
Source: rs793888530
Genes: MALINC1 (Hsa), PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, start_lost, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114182A>G
(GRCh38)5:140114222C>T
(Homo sapiens)Allele/Variant
Source: rs1282141695
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)5:140114222C>T
(GRCh38)5:140114388G>A
(Homo sapiens)Allele/Variant
Source: rs758197840
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)5:140114388G>A
(GRCh38)5:140114402A>G
(Homo sapiens)Allele/Variant
Source: rs2126748837
Genes: MALINC1 (Hsa), PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, splice_donor_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114402A>G
(GRCh38)5:140114336G>T
(Homo sapiens)Allele/Variant
Source: rs763614822
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)5:140114336G>T
(GRCh38)5:140114344C>T
(Homo sapiens)Allele/Variant
Source: rs1085307472
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)5:140114344C>T
(GRCh38)5:140114223G>A
(Homo sapiens)Allele/Variant
Source: rs1350220385
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)5:140114223G>A
(GRCh38)5:140114231C>A
(Homo sapiens)Allele/Variant
Source: rs1346561117
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)5:140114231C>A
(GRCh38)5:140114244G>T
(Homo sapiens)Allele/Variant
Source: rs935069923
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)5:140114244G>T
(GRCh38)5:140114259G>A
(Homo sapiens)Allele/Variant
Source: rs1156498095
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)5:140114259G>A
(GRCh38)5:140114208G>A
(Homo sapiens)Allele/Variant
Source: rs1481319515
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)5:140114208G>A
(GRCh38)5:140114263T>C
(Homo sapiens)Allele/Variant
Source: rs1554129019
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)5:140114263T>C
(GRCh38)5:140114327G>T
(Homo sapiens)Allele/Variant
Source: rs773489265
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)5:140114327G>T
(GRCh38)5:140114225T>C
(Homo sapiens)Allele/Variant
Source: rs2126748545
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)5:140114225T>C
(GRCh38)5:140114235C>T
(Homo sapiens)Allele/Variant
Source: NC_000005.10:g.140114235C>T
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)5:140114235C>T
(GRCh38)5:140114382C>T
(Homo sapiens)Allele/Variant
Source: NC_000005.10:g.140114382C>T
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)5:140114382C>T
(GRCh38)5:140114386C>T
(Homo sapiens)Allele/Variant
Source: rs1554129045
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)5:140114386C>T
(GRCh38)5:140114392A>C
(Homo sapiens)Allele/Variant
Source: NC_000005.10:g.140114392A>C
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)5:140114392A>C
(GRCh38)5:140114349C>T
(Homo sapiens)Allele/Variant
Source: rs750111075
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)5:140114349C>T
(GRCh38)5:140114239T>C
(Homo sapiens)Allele/Variant
Source: rs1763035593
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)5:140114239T>C
(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)5:140114322C>T
(Homo sapiens)Allele/Variant
Source: rs769972776
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)5:140114322C>T
(GRCh38)5:140114219C>T
(Homo sapiens)Allele/Variant
Source: rs533257824
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)5:140114219C>T
(GRCh38)5:140114242C>T
(Homo sapiens)Allele/Variant
Source: rs1437420883
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)5:140114242C>T
(GRCh38)5:140114251C>G
(Homo sapiens)Allele/Variant
Source: rs1064795164
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)5:140114251C>G
(GRCh38)5:140114359G>T
(Homo sapiens)Allele/Variant
Source: rs1763041722
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)5:140114359G>T
(GRCh38)5:140114375G>T
(Homo sapiens)Allele/Variant
Source: NC_000005.10:g.140114375G>T
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)5:140114375G>T
(GRCh38)5:140114367C>T
(Homo sapiens)Allele/Variant
Source: rs963675770
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)5:140114367C>T
(GRCh38)5:140114283T>C
(Homo sapiens)Allele/Variant
Source: rs1446546980
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)5:140114283T>C
(GRCh38)5:140114283T>G
(Homo sapiens)Allele/Variant
Source: rs1446546980
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)5:140114283T>G
(GRCh38)5:140114286T>C
(Homo sapiens)Allele/Variant
Source: rs1282359377
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)5:140114286T>C
(GRCh38)5:140114298C>T
(Homo sapiens)Allele/Variant
Source: rs1025358715
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)5:140114298C>T
(GRCh38)5:140114249A>G
(Homo sapiens)Allele/Variant
Source: rs1319701255
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)5:140114249A>G
(GRCh38)5:140114328G>C
(Homo sapiens)Allele/Variant
Source: rs1388309889
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)5:140114328G>C
(GRCh38)5:140114346G>A
(Homo sapiens)Allele/Variant
Source: rs764979877
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)5:140114346G>A