In Depth Mutation Analysis: C.316G>C (p.Gly106Arg) - Factor IX ...

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In Depth Mutation Analysis: c.316G>C (p.Gly106Arg) c.316G>C p.Gly106Arg (60) Mutation Type: Point Mutation Effect: Missense Domain: EGF1 Location: Exon 4 No. of bases: 1 CpG: Y Comments: - No. of patients reported: 4

Patient Information : Show

Patient	FIX:C(%)	FIX:Ag(%)	Inheritance	Severity	Type	Inhibitors	Country	Comments	Reference
1	Từ khóa » F9 C.316g A NM_000133.3(F9):c.316G>A (p.Gly106Ser) AND Multiple Conditions NM_000133.3(F9):c.316G>A (p.Gly106Ser) AND Hereditary Factor ... List Of Variants In Gene F9 Studied For Hemophilia B - ClinVar Miner [XLS] CHBMP US Database - CDC Mutation Analysis Of A Cohort Of US Patients With ... - CDC Stacks Mutation Analysis Of A Cohort Of US Patients ... - Wiley Online Library Mutation Analysis Of A Cohort Of US Patients With Hemophilia B - Li Noninvasive Detection Of F8 Int22h-related Inversions And Sequence ... Genotype-Phenotype Heterogeneity In Haemophilia - IntechOpen Low Frequency Of Treatable Pediatric Disease Alleles In GnomAD Splicing Dysregulation Contributes To The Pathogenicity Of Several F9 ... [PDF] Splicing Dysregulation Contributes To The Pathogenicity Of Several ... Factor IX Gene (F9) Variant Database Liên Hệ TRUYỀN HÌNH CÁP SÔNG THU ĐÀ NẴNG Địa Chỉ: 58 Hàm Nghi - Đà Nẵng Phone: 0905 989 xxx Web: truyenhinhcapsongthu.net Facebook: https://fb.com/truyenhinhcapsongthu/ Twitter: @ Capsongthu Copyright © 2022 \| Thiết Kế Truyền Hình Cáp Sông Thu

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