Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: CFAP57 (Hsa) Molecular Consequence: synonymous variant
(GRCh38)1:43215266C>T
(Homo sapiens)Allele/Variant
Source: rs541310801
Genes: EBNA1BP2 (Hsa), CFAP57 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:43215266C>T
(GRCh38)1:43234551G>A
(Homo sapiens)Allele/Variant
Source: rs544184490
Genes: EBNA1BP2 (Hsa), CFAP57 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:43234551G>A
(GRCh38)1:43181742A>G
(Homo sapiens)Allele/Variant
Source: rs376782182
Genes: EBNA1BP2 (Hsa), CFAP57 (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)1:43181742A>G
(GRCh38)1:43197606C>T
(Homo sapiens)Allele/Variant
Source: rs117105091
Genes: EBNA1BP2 (Hsa), CFAP57 (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)1:43197606C>T
(GRCh38)1:43199500G>A
(Homo sapiens)Allele/Variant
Source: rs151207529
Genes: EBNA1BP2 (Hsa), CFAP57 (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)1:43199500G>A
(GRCh38)1:43206869C>T
(Homo sapiens)Allele/Variant
Source: rs143175489
Genes: EBNA1BP2 (Hsa), CFAP57 (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)1:43206869C>T
(GRCh38)1:43185326G>A
(Homo sapiens)Allele/Variant
Source: rs267598609
Genes: EBNA1BP2 (Hsa), CFAP57 (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)1:43185326G>A
(GRCh38)1:43209829G>A
(Homo sapiens)Allele/Variant
Source: rs143009991
Genes: EBNA1BP2 (Hsa), CFAP57 (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)1:43209829G>A
(GRCh38)1:43222925T>C
(Homo sapiens)Allele/Variant
Source: rs184439522
Genes: EBNA1BP2 (Hsa), CFAP57 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:43222925T>C
(GRCh38)1:43185164A>G
(Homo sapiens)Allele/Variant
Source: rs140557499
Genes: EBNA1BP2 (Hsa), CFAP57 (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)1:43185164A>G
(GRCh38)1:43227015T>C
(Homo sapiens)Allele/Variant
Source: rs540417591
Genes: EBNA1BP2 (Hsa), CFAP57 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:43227015T>C
(GRCh38)1:43227018A>G
(Homo sapiens)Allele/Variant
Source: rs995524509
Genes: EBNA1BP2 (Hsa), CFAP57 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:43227018A>G
(GRCh38)1:43254161C>T
(Homo sapiens)Allele/Variant
Source: rs752372030
Genes: EBNA1BP2 (Hsa), CFAP57 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:43254161C>T