Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: WDR54 (Hsa)
(GRCh38)2:74424974G>C
(Homo sapiens)Allele/Variant
Source: rs1381474654
Genes: WDR54 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:74424974G>C
(GRCh38)2:74423869C>T
(Homo sapiens)Allele/Variant
Source: rs767574359
Genes: WDR54 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:74423869C>T
(GRCh38)2:74424930G>A
(Homo sapiens)Allele/Variant
Source: rs144082439
Genes: WDR54 (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)2:74424930G>A
(GRCh38)2:74424960G>A
(Homo sapiens)Allele/Variant
Source: rs771889482
Genes: WDR54 (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)2:74424960G>A
(GRCh38)2:74422163T>C
(Homo sapiens)Allele/Variant
Source: rs370158222
Genes: WDR54 (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)2:74422163T>C
(GRCh38)2:74423940G>T
(Homo sapiens)Allele/Variant
Source: NC_000002.12:g.74423940G>T
Genes: WDR54 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:74423940G>T
(GRCh38)2:74424879G>T
(Homo sapiens)Allele/Variant
Source: rs754346230
Genes: WDR54 (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)2:74424879G>T
(GRCh38)2:74425486A>G
(Homo sapiens)Allele/Variant
Source: NC_000002.12:g.74425486A>G
Genes: WDR54 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:74425486A>G
(GRCh38)2:74422276C>A
(Homo sapiens)Allele/Variant
Source: rs138373911
Genes: WDR54 (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)2:74422276C>A
(GRCh38)2:74423332A>G
(Homo sapiens)Allele/Variant
Source: rs755226668
Genes: WDR54 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:74423332A>G
(GRCh38)2:74423971G>A
(Homo sapiens)Allele/Variant
Source: rs376456333
Genes: WDR54 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:74423971G>A
(GRCh38)2:74422185G>C
(Homo sapiens)Allele/Variant
Source: rs763968610
Genes: WDR54 (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)2:74422185G>C
(GRCh38)2:74423938C>G
(Homo sapiens)Allele/Variant
Source: NC_000002.12:g.74423938C>G
Genes: WDR54 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:74423938C>G
(GRCh38)2:74425197G>A
(Homo sapiens)Allele/Variant
Source: rs779965597
Genes: WDR54 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)2:74425197G>A
(GRCh38)2:74422344G>T
(Homo sapiens)Allele/Variant
Source: rs746088546
Genes: WDR54 (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)2:74422344G>T
(GRCh38)2:74423881T>C
(Homo sapiens)Allele/Variant
Source: NC_000002.12:g.74423881T>C
Genes: WDR54 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:74423881T>C
(GRCh38)2:74423967G>A
(Homo sapiens)Allele/Variant
Source: rs1180683986
Genes: WDR54 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)2:74423967G>A
(GRCh38)2:74425202A>G
(Homo sapiens)Allele/Variant
Source: rs750716117
Genes: WDR54 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)2:74425202A>G
(GRCh38)2:74422238C>T
(Homo sapiens)Allele/Variant
Source: rs145359287
Genes: WDR54 (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)2:74422238C>T
(GRCh38)2:74422191C>T
(Homo sapiens)Allele/Variant
Source: rs1023176123
Genes: WDR54 (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)2:74422191C>T
(GRCh38)2:74425157A>G
(Homo sapiens)Allele/Variant
Source: rs929596868
Genes: WDR54 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)2:74425157A>G
(GRCh38)2:74422916C>T
(Homo sapiens)Allele/Variant
Source: rs1441509953
Genes: WDR54 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:74422916C>T
(GRCh38)2:74423870G>A
(Homo sapiens)Allele/Variant
Source: rs753843700
Genes: WDR54 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:74423870G>A
(GRCh38)2:74423924A>G
(Homo sapiens)Allele/Variant
Source: NC_000002.12:g.74423924A>G
Genes: WDR54 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:74423924A>G
(GRCh38)2:74423963C>T
(Homo sapiens)Allele/Variant
Source: rs370273315
Genes: WDR54 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:74423963C>T
(GRCh38)2:74425681C>T
(Homo sapiens)Allele/Variant
Source: rs766235102
Genes: WDR54 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)2:74425681C>T
(GRCh38)2:74422355A>C
(Homo sapiens)Allele/Variant
Source: rs775681644
Genes: WDR54 (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)2:74422355A>C
(GRCh38)2:74422175A>T
(Homo sapiens)Allele/Variant
Source: NC_000002.12:g.74422175A>T
Genes: WDR54 (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)2:74422175A>T
(GRCh38)2:74424948C>T
(Homo sapiens)Allele/Variant
Source: rs774364950
Genes: WDR54 (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)2:74424948C>T
(GRCh38)2:74425600G>A
(Homo sapiens)Allele/Variant
Source: rs200440850
Genes: WDR54 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:74425600G>A
(GRCh38)2:74425478G>C
(Homo sapiens)Allele/Variant
Source: rs1573228715
Genes: WDR54 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:74425478G>C