Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: PRMT9 (Hsa)
(GRCh38)4:147654033T>A
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.147654033T>A
Genes: PRMT9 (Hsa), TMEM184C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:147654033T>A
(GRCh38)4:147654057G>C
(Homo sapiens)Allele/Variant
Source: rs141544929
Genes: PRMT9 (Hsa), TMEM184C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:147654057G>C
(GRCh38)4:147657804G>A
(Homo sapiens)Allele/Variant
Source: rs142189908
Genes: PRMT9 (Hsa), TMEM184C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:147657804G>A
(GRCh38)4:147657869T>C
(Homo sapiens)Allele/Variant
Source: rs145625390
Genes: PRMT9 (Hsa), TMEM184C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:147657869T>C
(GRCh38)4:147660967G>A
(Homo sapiens)Allele/Variant
Source: rs1734908853
Genes: PRMT9 (Hsa), TMEM184C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:147660967G>A
(GRCh38)4:147654125A>G
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.147654125A>G
Genes: PRMT9 (Hsa), TMEM184C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:147654125A>G
(GRCh38)4:147654303G>C
(Homo sapiens)Allele/Variant
Source: rs759003872
Genes: PRMT9 (Hsa), TMEM184C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:147654303G>C
(GRCh38)4:147654395C>T
(Homo sapiens)Allele/Variant
Source: rs1176271058
Genes: PRMT9 (Hsa), TMEM184C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:147654395C>T
(GRCh38)4:147683936C>T
(Homo sapiens)Allele/Variant
Source: rs139397245
Genes: PRMT9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:147683936C>T
(GRCh38)4:147683942C>G
(Homo sapiens)Allele/Variant
Source: rs201765298
Genes: PRMT9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:147683942C>G
(GRCh38)4:147654111C>G
(Homo sapiens)Allele/Variant
Source: rs751553388
Genes: PRMT9 (Hsa), TMEM184C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:147654111C>G
(GRCh38)4:147673648C>T
(Homo sapiens)Allele/Variant
Source: rs769164317
Genes: PRMT9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:147673648C>T
(GRCh38)4:147680442C>T
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.147680442C>T
Genes: PRMT9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:147680442C>T
(GRCh38)4:147683898C>G
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.147683898C>G
Genes: PRMT9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:147683898C>G
(GRCh38)4:147654422G>A
(Homo sapiens)Allele/Variant
Source: rs944272685
Genes: PRMT9 (Hsa), TMEM184C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:147654422G>A
(GRCh38)4:147668542T>C
(Homo sapiens)Allele/Variant
Source: rs761553983
Genes: PRMT9 (Hsa), TMEM184C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:147668542T>C
(GRCh38)4:147672990C>G
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.147672990C>G
Genes: PRMT9 (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)4:147672990C>G
(GRCh38)4:147642831G>A
(Homo sapiens)Allele/Variant
Source: rs138286974
Genes: PRMT9 (Hsa), TMEM184C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:147642831G>A
(GRCh38)4:147654011G>A
(Homo sapiens)Allele/Variant
Source: rs780664768
Genes: PRMT9 (Hsa), TMEM184C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:147654011G>A
(GRCh38)4:147638651A>T
(Homo sapiens)Allele/Variant
Source: rs142086610
Genes: PRMT9 (Hsa), TMEM184C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:147638651A>T
(GRCh38)4:147660848G>T
(Homo sapiens)Allele/Variant
Source: rs543162347
Genes: PRMT9 (Hsa), TMEM184C (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)4:147660848G>T
(GRCh38)4:147660947T>G
(Homo sapiens)Allele/Variant
Source: rs753882873
Genes: PRMT9 (Hsa), TMEM184C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:147660947T>G
(GRCh38)4:147673000C>T
(Homo sapiens)Allele/Variant
Source: rs145578256
Genes: PRMT9 (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)4:147673000C>T
(GRCh38)4:147673128T>C
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.147673128T>C
Genes: PRMT9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, splice_acceptor_variant
Diseases: Not Available
Variant Name: (GRCh38)4:147673128T>C
(GRCh38)4:147657960C>T
(Homo sapiens)Allele/Variant
Source: rs145050413
Genes: PRMT9 (Hsa), TMEM184C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:147657960C>T
(GRCh38)4:147654050C>T
(Homo sapiens)Allele/Variant
Source: rs1426399494
Genes: PRMT9 (Hsa), TMEM184C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:147654050C>T
(GRCh38)4:147654266A>G
(Homo sapiens)Allele/Variant
Source: rs199827425
Genes: PRMT9 (Hsa), TMEM184C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:147654266A>G
(GRCh38)4:147638546T>C
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.147638546T>C
Genes: PRMT9 (Hsa), TMEM184C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:147638546T>C
(GRCh38)4:147657959G>C
(Homo sapiens)Allele/Variant
Source: rs78250904
Genes: PRMT9 (Hsa), TMEM184C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:147657959G>C
(GRCh38)4:147654194C>T
(Homo sapiens)Allele/Variant
Source: rs368438347
Genes: PRMT9 (Hsa), TMEM184C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:147654194C>T
(GRCh38)4:147680404A>T
(Homo sapiens)Allele/Variant
Source: rs1392285676
Genes: PRMT9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:147680404A>T
(GRCh38)4:147657807C>T
(Homo sapiens)Allele/Variant
Source: rs564517370
Genes: PRMT9 (Hsa), TMEM184C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:147657807C>T
(GRCh38)4:147654117G>C
(Homo sapiens)Allele/Variant
Source: rs139425779
Genes: PRMT9 (Hsa), TMEM184C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:147654117G>C
(GRCh38)4:147654111C>T
(Homo sapiens)Allele/Variant
Source: rs751553388
Genes: PRMT9 (Hsa), TMEM184C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:147654111C>T
(GRCh38)4:147660979G>A
(Homo sapiens)Allele/Variant
Source: rs143783342
Genes: PRMT9 (Hsa), TMEM184C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:147660979G>A
(GRCh38)4:147670646G>A
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.147670646G>A
Genes: PRMT9 (Hsa), TMEM184C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:147670646G>A
(GRCh38)4:147680450A>G
(Homo sapiens)Allele/Variant
Source: rs201893952
Genes: PRMT9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:147680450A>G
(GRCh38)4:147654056T>C
(Homo sapiens)Allele/Variant
Source: rs760098991
Genes: PRMT9 (Hsa), TMEM184C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:147654056T>C
(GRCh38)4:147660917G>A
(Homo sapiens)Allele/Variant
Source: rs552399598
Genes: PRMT9 (Hsa), TMEM184C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:147660917G>A
(GRCh38)4:147673007A>G
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.147673007A>G
Genes: PRMT9 (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)4:147673007A>G
(GRCh38)4:147638605A>G
(Homo sapiens)Allele/Variant
Source: rs748662468
Genes: PRMT9 (Hsa), TMEM184C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:147638605A>G
(GRCh38)4:147642866G>A
(Homo sapiens)Allele/Variant
Source: rs778872333
Genes: PRMT9 (Hsa), TMEM184C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:147642866G>A
(GRCh38)4:147673798C>A
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.147673798C>A
Genes: PRMT9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:147673798C>A
(GRCh38)4:147683927G>A
(Homo sapiens)Allele/Variant
Source: rs754402059
Genes: PRMT9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:147683927G>A
(GRCh38)4:147673659C>T
(Homo sapiens)Allele/Variant
Source: rs141216537
Genes: PRMT9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:147673659C>T
(GRCh38)4:147673677T>C
(Homo sapiens)Allele/Variant
Source: rs760056625
Genes: PRMT9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:147673677T>C
(GRCh38)4:147642879C>G
(Homo sapiens)Allele/Variant
Source: rs200715429
Genes: PRMT9 (Hsa), TMEM184C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:147642879C>G
(GRCh38)4:147673798C>T
(Homo sapiens)Allele/Variant
Source: rs747281440
Genes: PRMT9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:147673798C>T
(GRCh38)4:147680391A>C
(Homo sapiens)Allele/Variant
Source: rs756105948
Genes: PRMT9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:147680391A>C
(GRCh38)4:147639076T>G
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.147639076T>G
Genes: PRMT9 (Hsa), TMEM184C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:147639076T>G