Version: 8.0.0
Date: Tue Jan 28 2025
5 results
Allele/Variant Genes: THAP12 (Hsa)

(GRCh38)11:76351044C>T

(Homo sapiens)
Allele/Variant
Source: rs752359040
Genes: THAP12 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)11:76351044C>T

(GRCh38)11:76352213T>C

(Homo sapiens)
Allele/Variant
Source: rs148924079
Genes: THAP12 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)11:76352213T>C

(GRCh38)11:76351421T>C

(Homo sapiens)
Allele/Variant
Source: rs754184061
Genes: THAP12 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)11:76351421T>C

(GRCh38)11:76350960T>G

(Homo sapiens)
Allele/Variant
Source: NC_000011.10:g.76350960T>G
Genes: THAP12 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)11:76350960T>G

(GRCh38)11:76352354C>T

(Homo sapiens)
Allele/Variant
Source: rs1169353709
Genes: THAP12 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)11:76352354C>T