Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: BCL2 (Hsa) Molecular Consequence: missense variant
(GRCh38)18:63318208G>A
(Homo sapiens)Allele/Variant
Source: rs137945099
Genes: BCL2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)18:63318208G>A
(GRCh38)18:63318367G>A
(Homo sapiens)Allele/Variant
Source: rs61733416
Genes: BCL2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)18:63318367G>A
(GRCh38)18:63318646T>C
(Homo sapiens)Allele/Variant
Source: rs1801018
Genes: BCL2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)18:63318646T>C