Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: CLEC3B (Hsa)
(GRCh38)3:45007541G>C
(Homo sapiens)Allele/Variant
Source: rs35502907
Genes: CLEC3B (Hsa), EXOSC7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:45007541G>C
(GRCh38)3:45035772G>T
(Homo sapiens)Allele/Variant
Source: rs754348525
Genes: CLEC3B (Hsa), EXOSC7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:45035772G>T
(GRCh38)3:45007433A>G
(Homo sapiens)Allele/Variant
Source: rs141843360
Genes: CLEC3B (Hsa), EXOSC7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:45007433A>G
(GRCh38)3:45011299G>A
(Homo sapiens)Allele/Variant
Source: rs757197931
Genes: CLEC3B (Hsa), EXOSC7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:45011299G>A
(GRCh38)3:45035688G>T
(Homo sapiens)Allele/Variant
Source: NC_000003.12:g.45035688G>T
Genes: CLEC3B (Hsa), EXOSC7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:45035688G>T
(GRCh38)3:45035800C>T
(Homo sapiens)Allele/Variant
Source: NC_000003.12:g.45035800C>T
Genes: CLEC3B (Hsa), EXOSC7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:45035800C>T
(GRCh38)3:45026394G>A
(Homo sapiens)Allele/Variant
Source: rs777844887
Genes: CLEC3B (Hsa), EXOSC7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:45026394G>A
(GRCh38)3:45007567A>T
(Homo sapiens)Allele/Variant
Source: rs561294281
Genes: CLEC3B (Hsa), EXOSC7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:45007567A>T
(GRCh38)3:45035703G>A
(Homo sapiens)Allele/Variant
Source: rs979391813
Genes: CLEC3B (Hsa), EXOSC7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:45035703G>A
(GRCh38)3:45035854C>A
(Homo sapiens)Allele/Variant
Source: NC_000003.12:g.45035854C>A
Genes: CLEC3B (Hsa), EXOSC7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:45035854C>A
(GRCh38)3:45005354C>G
(Homo sapiens)Allele/Variant
Source: rs1707004830
Genes: CLEC3B (Hsa), EXOSC7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:45005354C>G
(GRCh38)3:45005319G>A
(Homo sapiens)Allele/Variant
Source: rs138979902
Genes: CLEC3B (Hsa), EXOSC7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:45005319G>A
(GRCh38)3:45035684G>C
(Homo sapiens)Allele/Variant
Source: NC_000003.12:g.45035684G>C
Genes: CLEC3B (Hsa), EXOSC7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:45035684G>C
(GRCh38)3:45035536G>A
(Homo sapiens)Allele/Variant
Source: rs758667999
Genes: CLEC3B (Hsa), EXOSC7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:45035536G>A
(GRCh38)3:45035736G>A
(Homo sapiens)Allele/Variant
Source: NC_000003.12:g.45035736G>A
Genes: CLEC3B (Hsa), EXOSC7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:45035736G>A
(GRCh38)3:45007567A>G
(Homo sapiens)Allele/Variant
Source: rs561294281
Genes: CLEC3B (Hsa), EXOSC7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:45007567A>G
(GRCh38)3:45035919G>A
(Homo sapiens)Allele/Variant
Source: rs770774345
Genes: CLEC3B (Hsa), EXOSC7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:45035919G>A
(GRCh38)3:45005371G>A
(Homo sapiens)Allele/Variant
Source: rs557489049
Genes: CLEC3B (Hsa), EXOSC7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:45005371G>A
(GRCh38)3:45026426G>A
(Homo sapiens)Allele/Variant
Source: rs1455334649
Genes: CLEC3B (Hsa), EXOSC7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:45026426G>A