Feb 20, 2024 · NM_000546.6(TP53):c.673-1G>T. Gene: TP53:tumor protein p53 [Gene - OMIM - HGNC]; Variant type: single nucleotide variant ...

The mutation database ClinVar contains entries for this variant (Variation ID:379336). ... Comment: The c.673-1G>A intronic pathogenic mutation results from a G ...

The c.673-1G>A intronic pathogenic mutation results from a G to A substitution one nucleotide upstream from coding exon 6 of the TP53 gene. ... J Med Genet. 2001 ...

Jun 9, 2023 · 993 + 1G > A were the youngest variants shared in an individual in Turkey dated 450 years BP (Table 1). High sharing rate. Eleven (24.4%) shared ...

COSM43751; Gene name: TP53; AA mutation: p.? (Unknown); CDS mutation: c.673-1G>A (Substitution); Nucleotides inserted: n/a; Genomic coordinates: GRCh38, ...

673-1G>T/C/A), are capable of reprogramming cells inducing the acquisition of pro-metastatic features [60,61]. A recent study evaluated the amount of TP53 ...

673-1G>A, rs878854073. NM_000546.6(TP53):c.673-1G>C, rs878854073. NM_000546.6(TP53):c.673-1G>T, rs878854073. NM_000546.6(TP53):c.673-2A>G, rs1555525585.

Nov 16, 2018 · ... 673-1G>A and Arg249Lys) identified in both cases, BALCL3 and BALCL6 respectively. The TP53 c.673-1G>A mutation affects the canonical splice ...

673-1G= ENST00000652225.2:c.673-1G= (ERCC5) MANE Select, ENSP00000498881.2:n.673-1G= ENST00000652613.1:c.169-1G= (ERCC5), ENSP00000498357.1:n.169-1G ...

673-1G>A and c.733G>A, respectively; supplemental Table 2), and again, both of them displayed a loss of the wild-type allele in leukemic specimens. Personal ...