Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: PRMT9 (Hsa) Molecular Consequence: non coding transcript variant
(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)4:147680442C>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)4:147673128T>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)4:147680404A>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)4:147680450A>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)4:147673127C>T
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.147673127C>T
Genes: PRMT9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, splice_acceptor_variant
Diseases: Not Available
Variant Name: (GRCh38)4:147673127C>T