Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: SRSF3 (Hsa)
(GRCh38)6:36596796G>C
(Homo sapiens)Allele/Variant
Source: NC_000006.12:g.36596796G>C
Genes: SRSF3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)6:36596796G>C
(GRCh38)6:36598910C>T
(Homo sapiens)Allele/Variant
Source: rs142398173
Genes: SRSF3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)6:36598910C>T
(GRCh38)6:36601740C>T
(Homo sapiens)Allele/Variant
Source: NC_000006.12:g.36601740C>T
Genes: SRSF3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)6:36601740C>T