Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: CD96 (Hsa)
(GRCh38)3:111652186C>A
(Homo sapiens)Allele/Variant
Source: rs80033730
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111652186C>A
(GRCh38)3:111649767C>T
(Homo sapiens)Allele/Variant
Source: rs148525569
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111649767C>T
(GRCh38)3:111649966C>T
(Homo sapiens)Allele/Variant
Source: rs3733176
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111649966C>T
(GRCh38)3:111649978G>T
(Homo sapiens)Allele/Variant
Source: rs886057770
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111649978G>T
(GRCh38)3:111649997G>A
(Homo sapiens)Allele/Variant
Source: rs886057771
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111649997G>A
(GRCh38)3:111623820A>T
(Homo sapiens)Allele/Variant
Source: rs148659928
Genes: CD96 (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)3:111623820A>T
(GRCh38)3:111637211C>T
(Homo sapiens)Allele/Variant
Source: rs886057767
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111637211C>T
(GRCh38)3:111567528G>C
(Homo sapiens)Allele/Variant
Source: rs2276872
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111567528G>C
(GRCh38)3:111577516G>A
(Homo sapiens)Allele/Variant
Source: rs142203509
Genes: CD96 (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)3:111577516G>A
(GRCh38)3:111542198A>G
(Homo sapiens)Allele/Variant
Source: rs370450188
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111542198A>G
(GRCh38)3:111585337C>T
(Homo sapiens)Allele/Variant
Source: rs1462219495
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111585337C>T
(GRCh38)3:111593595G>A
(Homo sapiens)Allele/Variant
Source: rs200140607
Genes: CD96 (Hsa), ZBED2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111593595G>A
(GRCh38)3:111545313G>A
(Homo sapiens)Allele/Variant
Source: rs372870533
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111545313G>A
(GRCh38)3:111567556T>C
(Homo sapiens)Allele/Variant
Source: rs147832650
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111567556T>C
(GRCh38)3:111579058C>T
(Homo sapiens)Allele/Variant
Source: rs267599539
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111579058C>T
(GRCh38)3:111606750C>T
(Homo sapiens)Allele/Variant
Source: rs201962401
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111606750C>T
(GRCh38)3:111651621G>A
(Homo sapiens)Allele/Variant
Source: rs146712540
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111651621G>A
(GRCh38)3:111623809C>T
(Homo sapiens)Allele/Variant
Source: rs1162310451
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111623809C>T
(GRCh38)3:111638128T>C
(Homo sapiens)Allele/Variant
Source: rs766329053
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111638128T>C
(GRCh38)3:111637236G>C
(Homo sapiens)Allele/Variant
Source: rs1533270
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111637236G>C
(GRCh38)3:111651609G>A
(Homo sapiens)Allele/Variant
Source: rs184317872
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111651609G>A
(GRCh38)3:111579058C>G
(Homo sapiens)Allele/Variant
Source: NC_000003.12:g.111579058C>G
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111579058C>G
(GRCh38)3:111598166T>C
(Homo sapiens)Allele/Variant
Source: rs781311611
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111598166T>C
(GRCh38)3:111650486C>G
(Homo sapiens)Allele/Variant
Source: rs886057772
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111650486C>G
(GRCh38)3:111649714C>T
(Homo sapiens)Allele/Variant
Source: rs1939992902
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111649714C>T
(GRCh38)3:111623812C>G
(Homo sapiens)Allele/Variant
Source: rs1002521009
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111623812C>G
(GRCh38)3:111623823G>A
(Homo sapiens)Allele/Variant
Source: rs1021804713
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, splice_donor_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111623823G>A
(GRCh38)3:111652186C>T
(Homo sapiens)Allele/Variant
Source: rs80033730
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111652186C>T
(GRCh38)3:111579224C>T
(Homo sapiens)Allele/Variant
Source: rs879595027
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111579224C>T
(GRCh38)3:111579062A>T
(Homo sapiens)Allele/Variant
Source: NC_000003.12:g.111579062A>T
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, stop_gained, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111579062A>T
(GRCh38)3:111545165G>A
(Homo sapiens)Allele/Variant
Source: rs150450686
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111545165G>A
(GRCh38)3:111567638A>G
(Homo sapiens)Allele/Variant
Source: rs759813586
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111567638A>G
(GRCh38)3:111606700G>T
(Homo sapiens)Allele/Variant
Source: rs1283203445
Genes: CD96 (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)3:111606700G>T
(GRCh38)3:111579061A>C
(Homo sapiens)Allele/Variant
Source: rs61733706
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111579061A>C
(GRCh38)3:111579189G>A
(Homo sapiens)Allele/Variant
Source: rs751482008
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111579189G>A
(GRCh38)3:111594078T>A
(Homo sapiens)Allele/Variant
Source: NC_000003.12:g.111594078T>A
Genes: CD96 (Hsa), ZBED2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111594078T>A
(GRCh38)3:111650647G>C
(Homo sapiens)Allele/Variant
Source: rs886057775
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111650647G>C
(GRCh38)3:111651605G>A
(Homo sapiens)Allele/Variant
Source: rs535247425
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111651605G>A
(GRCh38)3:111647649T>C
(Homo sapiens)Allele/Variant
Source: rs111262991
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111647649T>C
(GRCh38)3:111650202C>T
(Homo sapiens)Allele/Variant
Source: rs543716163
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111650202C>T
(GRCh38)3:111600920T>C
(Homo sapiens)Allele/Variant
Source: rs776048679
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111600920T>C
(GRCh38)3:111593841G>C
(Homo sapiens)Allele/Variant
Source: rs139937578
Genes: CD96 (Hsa), ZBED2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111593841G>C
(GRCh38)3:111594078T>C
(Homo sapiens)Allele/Variant
Source: rs370951160
Genes: CD96 (Hsa), ZBED2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111594078T>C
(GRCh38)3:111650675G>C
(Homo sapiens)Allele/Variant
Source: rs566078679
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111650675G>C
(GRCh38)3:111651243A>G
(Homo sapiens)Allele/Variant
Source: rs886057780
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111651243A>G
(GRCh38)3:111651359C>T
(Homo sapiens)Allele/Variant
Source: rs6763154
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111651359C>T
(GRCh38)3:111651896A>G
(Homo sapiens)Allele/Variant
Source: rs868287764
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111651896A>G
(GRCh38)3:111651170G>A
(Homo sapiens)Allele/Variant
Source: rs368097665
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111651170G>A
(GRCh38)3:111501532C>G
(Homo sapiens)Allele/Variant
Source: rs207463536
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111501532C>G
(GRCh38)3:111649718T>G
(Homo sapiens)Allele/Variant
Source: rs760873204
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111649718T>G