Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: IL10 (Hsa)
(GRCh38)1:206773062T>G
(Homo sapiens)Allele/Variant
Source: rs1800872
Genes: IL10 (Hsa), IL19 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:206773062T>G
(GRCh38)1:206771516A>C
(Homo sapiens)Allele/Variant
Source: rs1518110
Genes: IL10 (Hsa), IL19 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:206771516A>C
(GRCh38)1:206769887A>T
(Homo sapiens)Allele/Variant
Source: rs1319282028
Genes: IL10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:206769887A>T
(GRCh38)1:206770942T>A
(Homo sapiens)Allele/Variant
Source: rs150423829
Genes: IL10 (Hsa), IL19 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:206770942T>A
(GRCh38)1:206768639G>C
(Homo sapiens)Allele/Variant
Source: rs771277922
Genes: IL10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:206768639G>C
(GRCh38)1:206768643C>T
(Homo sapiens)Allele/Variant
Source: rs376415487
Genes: IL10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:206768643C>T
(GRCh38)1:206770958C>T
(Homo sapiens)Allele/Variant
Source: rs750441744
Genes: IL10 (Hsa), IL19 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:206770958C>T
(GRCh38)1:206772406C>G
(Homo sapiens)Allele/Variant
Source: rs762421652
Genes: IL10 (Hsa), IL19 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:206772406C>G
(GRCh38)1:206771366T>C
(Homo sapiens)Allele/Variant
Source: rs545228684
Genes: IL10 (Hsa), IL19 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:206771366T>C
(GRCh38)1:206771380C>T
(Homo sapiens)Allele/Variant
Source: rs2102439750
Genes: IL10 (Hsa), IL19 (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)1:206771380C>T
(GRCh38)1:206769809C>T
(Homo sapiens)Allele/Variant
Source: NC_000001.11:g.206769809C>T
Genes: IL10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:206769809C>T
(GRCh38)1:206769880G>A
(Homo sapiens)Allele/Variant
Source: rs1229974502
Genes: IL10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:206769880G>A
(GRCh38)1:206768519A>G
(Homo sapiens)Allele/Variant
Source: rs3024496
Genes: IL10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)1:206768519A>G
(GRCh38)1:206770915G>A
(Homo sapiens)Allele/Variant
Source: rs746523858
Genes: IL10 (Hsa), IL19 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:206770915G>A
(GRCh38)1:206770949C>G
(Homo sapiens)Allele/Variant
Source: rs767727378
Genes: IL10 (Hsa), IL19 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:206770949C>G
(GRCh38)1:206768663G>A
(Homo sapiens)Allele/Variant
Source: rs142093260
Genes: IL10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:206768663G>A
(GRCh38)1:206768702G>A
(Homo sapiens)Allele/Variant
Source: rs1674735790
Genes: IL10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:206768702G>A
(GRCh38)1:206768702G>T
(Homo sapiens)Allele/Variant
Source: rs1674735790
Genes: IL10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:206768702G>T
(GRCh38)1:206771336C>T
(Homo sapiens)Allele/Variant
Source: rs1372528108
Genes: IL10 (Hsa), IL19 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:206771336C>T
(GRCh38)1:206771338C>T
(Homo sapiens)Allele/Variant
Source: rs376490444
Genes: IL10 (Hsa), IL19 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:206771338C>T
(GRCh38)1:206768736G>A
(Homo sapiens)Allele/Variant
Source: NC_000001.11:g.206768736G>A
Genes: IL10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:206768736G>A
(GRCh38)1:206768670A>T
(Homo sapiens)Allele/Variant
Source: NC_000001.11:g.206768670A>T
Genes: IL10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:206768670A>T
(GRCh38)1:206769890C>A
(Homo sapiens)Allele/Variant
Source: rs760677075
Genes: IL10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:206769890C>A
(GRCh38)1:206771044G>T
(Homo sapiens)Allele/Variant
Source: rs2102439318
Genes: IL10 (Hsa), IL19 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:206771044G>T
(GRCh38)1:206772256A>G
(Homo sapiens)Allele/Variant
Source: rs373813224
Genes: IL10 (Hsa), IL19 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:206772256A>G
(GRCh38)1:206771341C>T
(Homo sapiens)Allele/Variant
Source: rs1342823726
Genes: IL10 (Hsa), IL19 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:206771341C>T
(GRCh38)1:206772393C>T
(Homo sapiens)Allele/Variant
Source: rs145922845
Genes: IL10 (Hsa), IL19 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:206772393C>T
(GRCh38)1:206772430G>A
(Homo sapiens)Allele/Variant
Source: rs140486772
Genes: IL10 (Hsa), IL19 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:206772430G>A
(GRCh38)1:206773289A>G
(Homo sapiens)Allele/Variant
Source: rs1800871
Genes: IL10 (Hsa), IL19 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:206773289A>G
(GRCh38)1:206769849C>G
(Homo sapiens)Allele/Variant
Source: rs1674768626
Genes: IL10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:206769849C>G
(GRCh38)1:206772380C>T
(Homo sapiens)Allele/Variant
Source: rs139073251
Genes: IL10 (Hsa), IL19 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:206772380C>T
(GRCh38)1:206772418C>T
(Homo sapiens)Allele/Variant
Source: rs760242157
Genes: IL10 (Hsa), IL19 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:206772418C>T
(GRCh38)1:206769839G>A
(Homo sapiens)Allele/Variant
Source: rs774072665
Genes: IL10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:206769839G>A
(GRCh38)1:206770940G>A
(Homo sapiens)Allele/Variant
Source: rs5743626
Genes: IL10 (Hsa), IL19 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:206770940G>A
(GRCh38)1:206768666T>G
(Homo sapiens)Allele/Variant
Source: rs568879359
Genes: IL10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:206768666T>G
(GRCh38)1:206770888A>G
(Homo sapiens)Allele/Variant
Source: rs1554286
Genes: IL10 (Hsa), IL19 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:206770888A>G
(GRCh38)1:206771028A>T
(Homo sapiens)Allele/Variant
Source: NC_000001.11:g.206771028A>T
Genes: IL10 (Hsa), IL19 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, start_lost, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:206771028A>T
(GRCh38)1:206770006T>C
(Homo sapiens)Allele/Variant
Source: rs3024494
Genes: IL10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:206770006T>C
(GRCh38)1:206770623C>A
(Homo sapiens)Allele/Variant
Source: rs3024493
Genes: IL10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:206770623C>A
(GRCh38)1:206772251C>T
(Homo sapiens)Allele/Variant
Source: rs749899175
Genes: IL10 (Hsa), IL19 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:206772251C>T
(GRCh38)1:206772315G>A
(Homo sapiens)Allele/Variant
Source: rs750010814
Genes: IL10 (Hsa), IL19 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:206772315G>A
(GRCh38)1:206770965G>A
(Homo sapiens)Allele/Variant
Source: rs755490123
Genes: IL10 (Hsa), IL19 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:206770965G>A
(GRCh38)1:206771024G>A
(Homo sapiens)Allele/Variant
Source: NC_000001.11:g.206771024G>A
Genes: IL10 (Hsa), IL19 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:206771024G>A
(GRCh38)1:206771339C>T
(Homo sapiens)Allele/Variant
Source: rs1674832645
Genes: IL10 (Hsa), IL19 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:206771339C>T
(GRCh38)1:206772378G>A
(Homo sapiens)Allele/Variant
Source: rs141219090
Genes: IL10 (Hsa), IL19 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:206772378G>A
(GRCh38)1:206771430A>G
(Homo sapiens)Allele/Variant
Source: rs191140520
Genes: IL10 (Hsa), IL19 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:206771430A>G
(GRCh38)1:206772299T>C
(Homo sapiens)Allele/Variant
Source: rs769965755
Genes: IL10 (Hsa), IL19 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:206772299T>C
(GRCh38)1:206772318T>C
(Homo sapiens)Allele/Variant
Source: rs755837237
Genes: IL10 (Hsa), IL19 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, start_lost, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:206772318T>C
(GRCh38)1:206770971A>C
(Homo sapiens)Allele/Variant
Source: rs372883095
Genes: IL10 (Hsa), IL19 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:206770971A>C
(GRCh38)1:206770910G>T
(Homo sapiens)Allele/Variant
Source: rs755403362
Genes: IL10 (Hsa), IL19 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:206770910G>T