Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: PRPF3 (Hsa)
(GRCh38)1:150325557C>T
(Homo sapiens)Allele/Variant
Source: rs34964511
Genes: PRPF3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:150325557C>T
(GRCh38)1:150325871G>A
(Homo sapiens)Allele/Variant
Source: rs782194993
Genes: PRPF3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:150325871G>A
(GRCh38)1:150325872A>G
(Homo sapiens)Allele/Variant
Source: rs782538822
Genes: PRPF3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:150325872A>G
(GRCh38)1:150334986G>C
(Homo sapiens)Allele/Variant
Source: rs80201355
Genes: PRPF3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:150334986G>C
(GRCh38)1:150335091A>G
(Homo sapiens)Allele/Variant
Source: rs138240814
Genes: PRPF3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:150335091A>G
(GRCh38)1:150338275T>C
(Homo sapiens)Allele/Variant
Source: rs1657267180
Genes: PRPF3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:150338275T>C
(GRCh38)1:150328378G>A
(Homo sapiens)Allele/Variant
Source: NC_000001.11:g.150328378G>A
Genes: PRPF3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:150328378G>A
(GRCh38)1:150328421C>T
(Homo sapiens)Allele/Variant
Source: rs59082627
Genes: PRPF3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:150328421C>T
(GRCh38)1:150332991T>C
(Homo sapiens)Allele/Variant
Source: rs1656586815
Genes: PRPF3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:150332991T>C
(GRCh38)1:150344160A>C
(Homo sapiens)Allele/Variant
Source: rs1658057278
Genes: PRPF3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, splice_acceptor_variant
Diseases: Not Available
Variant Name: (GRCh38)1:150344160A>C
(GRCh38)1:150346087A>G
(Homo sapiens)Allele/Variant
Source: rs782130614
Genes: PRPF3 (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)1:150346087A>G
(GRCh38)1:150343313C>G
(Homo sapiens)Allele/Variant
Source: rs782511773
Genes: PRPF3 (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)1:150343313C>G
(GRCh38)1:150343372G>A
(Homo sapiens)Allele/Variant
Source: rs1053201955
Genes: PRPF3 (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)1:150343372G>A
(GRCh38)1:150344446G>A
(Homo sapiens)Allele/Variant
Source: rs782715866
Genes: PRPF3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:150344446G>A
(GRCh38)1:150344542A>G
(Homo sapiens)Allele/Variant
Source: rs782490570
Genes: PRPF3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:150344542A>G
(GRCh38)1:150352849G>A
(Homo sapiens)Allele/Variant
Source: rs201590000
Genes: PRPF3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:150352849G>A
(GRCh38)1:150352957C>T
(Homo sapiens)Allele/Variant
Source: NC_000001.11:g.150352957C>T
Genes: PRPF3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:150352957C>T
(GRCh38)1:150325050C>T
(Homo sapiens)Allele/Variant
Source: rs1553863345
Genes: PRPF3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:150325050C>T
(GRCh38)1:150349160A>T
(Homo sapiens)Allele/Variant
Source: rs587704985
Genes: PRPF3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:150349160A>T
(GRCh38)1:150349204G>A
(Homo sapiens)Allele/Variant
Source: rs782042725
Genes: PRPF3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:150349204G>A
(GRCh38)1:150335165C>T
(Homo sapiens)Allele/Variant
Source: rs1553866975
Genes: PRPF3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:150335165C>T
(GRCh38)1:150335182A>G
(Homo sapiens)Allele/Variant
Source: rs782792715
Genes: PRPF3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:150335182A>G
(GRCh38)1:150335007A>G
(Homo sapiens)Allele/Variant
Source: rs958240141
Genes: PRPF3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:150335007A>G
(GRCh38)1:150340399A>G
(Homo sapiens)Allele/Variant
Source: rs142080861
Genes: PRPF3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:150340399A>G
(GRCh38)1:150332747A>G
(Homo sapiens)Allele/Variant
Source: rs1282813411
Genes: PRPF3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:150332747A>G
(GRCh38)1:150343416G>A
(Homo sapiens)Allele/Variant
Source: rs1657984645
Genes: PRPF3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:150343416G>A
(GRCh38)1:150343425G>T
(Homo sapiens)Allele/Variant
Source: NC_000001.11:g.150343425G>T
Genes: PRPF3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:150343425G>T
(GRCh38)1:150343430G>T
(Homo sapiens)Allele/Variant
Source: NC_000001.11:g.150343430G>T
Genes: PRPF3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:150343430G>T
(GRCh38)1:150343455G>T
(Homo sapiens)Allele/Variant
Source: rs2102010164
Genes: PRPF3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:150343455G>T
(GRCh38)1:150344212C>G
(Homo sapiens)Allele/Variant
Source: NC_000001.11:g.150344212C>G
Genes: PRPF3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:150344212C>G
(GRCh38)1:150325069G>A
(Homo sapiens)Allele/Variant
Source: rs781967322
Genes: PRPF3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:150325069G>A
(GRCh38)1:150325070A>G
(Homo sapiens)Allele/Variant
Source: rs375882146
Genes: PRPF3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:150325070A>G
(GRCh38)1:150325093T>C
(Homo sapiens)Allele/Variant
Source: rs1363821930
Genes: PRPF3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:150325093T>C
(GRCh38)1:150325809G>C
(Homo sapiens)Allele/Variant
Source: NC_000001.11:g.150325809G>C
Genes: PRPF3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:150325809G>C
(GRCh38)1:150328335G>A
(Homo sapiens)Allele/Variant
Source: NC_000001.11:g.150328335G>A
Genes: PRPF3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:150328335G>A
(GRCh38)1:150335067T>C
(Homo sapiens)Allele/Variant
Source: rs782226725
Genes: PRPF3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:150335067T>C
(GRCh38)1:150335132C>A
(Homo sapiens)Allele/Variant
Source: rs782644120
Genes: PRPF3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:150335132C>A
(GRCh38)1:150338256G>A
(Homo sapiens)Allele/Variant
Source: rs1043744478
Genes: PRPF3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:150338256G>A
(GRCh38)1:150338324T>C
(Homo sapiens)Allele/Variant
Source: NC_000001.11:g.150338324T>C
Genes: PRPF3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:150338324T>C
(GRCh38)1:150332761A>G
(Homo sapiens)Allele/Variant
Source: rs146995242
Genes: PRPF3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:150332761A>G
(GRCh38)1:150344212C>T
(Homo sapiens)Allele/Variant
Source: rs121434242
Genes: PRPF3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:150344212C>T
(GRCh38)1:150344275G>T
(Homo sapiens)Allele/Variant
Source: rs376006808
Genes: PRPF3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:150344275G>T
(GRCh38)1:150325086C>T
(Homo sapiens)Allele/Variant
Source: rs370220628
Genes: PRPF3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:150325086C>T
(GRCh38)1:150325787G>A
(Homo sapiens)Allele/Variant
Source: rs782061609
Genes: PRPF3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:150325787G>A
(GRCh38)1:150335172C>T
(Homo sapiens)Allele/Variant
Source: rs781991178
Genes: PRPF3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:150335172C>T
(GRCh38)1:150335238A>G
(Homo sapiens)Allele/Variant
Source: rs143350315
Genes: PRPF3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:150335238A>G
(GRCh38)1:150338154T>C
(Homo sapiens)Allele/Variant
Source: rs1553868765
Genes: PRPF3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:150338154T>C
(GRCh38)1:150335097A>G
(Homo sapiens)Allele/Variant
Source: rs146124055
Genes: PRPF3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:150335097A>G
(GRCh38)1:150335143C>T
(Homo sapiens)Allele/Variant
Source: rs1489549828
Genes: PRPF3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:150335143C>T
(GRCh38)1:150338304A>C
(Homo sapiens)Allele/Variant
Source: rs2101990462
Genes: PRPF3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:150338304A>C