Webatm q13315 d831g cancer y1124f y2437h atr q13535 r2074i q1226h brca1 p38398 g1048v brca2 p51587 f590c p3280h s384f g1771d chek2 o96017 t138i fanca o15360 a416d l1143v fancc q00597 v60i fancg o15287 ... g2891d m1628v i2888t e461d y2334d g529v g2695c v1581l n1314d i1014s d1560y l1307f s191l n484k s2313c w2094l d558y t2461i r1762m … Webp.G2891D (Substitution - Missense, position 2891 ... {ATM_ENST00000452508}, 169409213{C11orf65} Tissue distribution. This section displays the distribution of mutated samples and tissue types (top 5). You can see more information on our help pages. Samples. This section displays a table of mutated samples, with tissue, histology and …
ATM G2891D - My Cancer Genome
WebNov 5, 2024 · 82 ATM p.G2891D 12% 13% Kinase domain. 81 ATM c.2921 + 1G>A 78% 65% Not germline based on tumor testing. 87 ATM p.L2492R 7% 9% CHIP hotspot. 76 BRCA2 p.T3310Nfs*17 3% 3% Reported by outside lab, WebAug 28, 2014 · Rearrangements between the TCL1A/B locus on chromosome 14 4,5 or its homolog MTCP1 on chromosome X and the T-cell receptor locus on chromosome 14 3,6,7 are characteristic of T-PLL. Additionally, the ATM gene located at chromosome 11q23 is frequently deleted or mutated, 8-10 and trisomies of the long arm of chromosome 8 are … the only thing new in the world
Identification of Clonal Hematopoiesis Mutations in Solid Tumor ...
WebJul 1, 2000 · Thirteen aberrations of ATM transcripts were identified in 12 patients. Case TP15, without detectable LOH using polymorphic markers, was found homozygote for an A7499G mutation (single-letter amino acid code), which was absent in germline DNA. This was interpreted as a small-sized allelic deletion of the ATM gene. WebIt describes the source of the mutation i.e gene name/sample name/tissue name with unique ID, and also shows the mutation syntax at the amino acid and nucleotide sequence level. You can see more information on our help pages . Genomic Mutation ID COSV99215400 Legacy Identifier COSM7869597 Gene name BMPR1B_ENST00000264568 AA mutation WebThe p.G2891D variant (also known as c.8672G>A), located in coding exon 59 of the ATM gene, results from a G to A substitution at nucleotide position 8672. This variant impacts … microaggression handout