SSBP2 c.203T>G ;(p.F68C)

Variant ID: 5-80911371-A-C

NM_001256732.1(SSBP2):c.203T>G;(p.F68C)

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Endometrioid endometrial cancer "recurring" as high-grade serous adenocarcinoma in the inguinal lymph nodes in a patient with germline MLH1 mutated Lynch syndrome: consequence or coincidence?

Hereditary Cancer In Clinical Practice
Jiang, Wei W; Gao, Tong T; Tao, Xiang X; Zhu, Menghan M; Yao, Liangqing L; Feng, Weiwei W
Publication Date: 2019

Variant appearance in text: SSBP2: F68C
PubMed Link: 31139268
Variant Present in the following documents:
  • 13053_2019_112_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page