Version: 8.0.0
Date: Tue Jan 28 2025
96 results
Allele/Variant Genes: CD96 (Hsa) Molecular Consequence: non coding transcript variant

(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)3:111623820A>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)3:111542198A>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)3:111501532C>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

(GRCh38)3:111542132G>A

(Homo sapiens)
Allele/Variant
Source: rs886057762
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111542132G>A

(GRCh38)3:111579097A>G

(Homo sapiens)
Allele/Variant
Source: rs200541974
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)3:111579097A>G

(GRCh38)3:111585365A>G

(Homo sapiens)
Allele/Variant
Source: rs1936662124
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111585365A>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)3:111545313G>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)3:111623809C>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)3:111638080C>T

(Homo sapiens)
Allele/Variant
Source: rs374379667
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111638080C>T

(GRCh38)3:111649741A>G

(Homo sapiens)
Allele/Variant
Source: rs765701422
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111649741A>G

(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)3:111649714C>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)3:111579224C>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)3:111545144G>A

(Homo sapiens)
Allele/Variant
Source: rs149258762
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111545144G>A

(GRCh38)3:111567604G>C

(Homo sapiens)
Allele/Variant
Source: rs532537422
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, stop_lost
Diseases: Not Available
Variant Name: (GRCh38)3:111567604G>C

(GRCh38)3:111606778G>A

(Homo sapiens)
Allele/Variant
Source: rs138396447
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111606778G>A

(GRCh38)3:111624334C>A

(Homo sapiens)
Allele/Variant
Source: rs76343124
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111624334C>A

(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)3:111647649T>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)3:111624356C>T

(Homo sapiens)
Allele/Variant
Source: rs201691670
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111624356C>T

(GRCh38)3:111638081A>G

(Homo sapiens)
Allele/Variant
Source: rs1939421281
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)3:111638081A>G

(GRCh38)3:111649795G>C

(Homo sapiens)
Allele/Variant
Source: rs979289215
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111649795G>C

(GRCh38)3:111623789G>T

(Homo sapiens)
Allele/Variant
Source: rs200767318
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111623789G>T

(GRCh38)3:111567526C>A

(Homo sapiens)
Allele/Variant
Source: rs1410223124
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111567526C>A

(GRCh38)3:111606738A>G

(Homo sapiens)
Allele/Variant
Source: rs147445900
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111606738A>G

(GRCh38)3:111567553C>T

(Homo sapiens)
Allele/Variant
Source: rs149798144
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111567553C>T

(GRCh38)3:111600863C>T

(Homo sapiens)
Allele/Variant
Source: rs200729689
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111600863C>T

(GRCh38)3:111545070C>G

(Homo sapiens)
Allele/Variant
Source: rs1004724022
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111545070C>G

(GRCh38)3:111598160C>G

(Homo sapiens)
Allele/Variant
Source: NC_000003.12:g.111598160C>G
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111598160C>G

(GRCh38)3:111600762A>G

(Homo sapiens)
Allele/Variant
Source: rs886057765
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111600762A>G

(GRCh38)3:111600797G>A

(Homo sapiens)
Allele/Variant
Source: rs149013704
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111600797G>A

(GRCh38)3:111606763C>T

(Homo sapiens)
Allele/Variant
Source: rs980174274
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111606763C>T

(GRCh38)3:111545161C>A

(Homo sapiens)
Allele/Variant
Source: rs145133367
Genes: CD96 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)3:111545161C>A