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. 2019 Jul 5;9:574. doi: 10.3389/fonc.2019.00574

Table 4.

The variants with lower Prm found in COSMIC.

Gene Chr: GRCh38 Pos rsid COSMIC ids Tissue*
DLGAP4-AS1 20:36525992 rs971669684 COSM5601362, COSM5601361 Skin
RBM12 20:35652667 rs747020729 COSM5039294 Liver
DLGAP4-AS1 20:36548162 rs7273824 COSM3693464 Large intestine, prostate
RFX3 9:3247951 rs2229356 COSM3763880 Large intestine
DLGAP4-AS1 20:36526879 rs114982034 COSM4098029, COSM4098028 Stomach
ATP6V1A 3:113795187 rs771311957 COSM4583806, COSM1036559 Bone, endometrium
ATP8A1 4:42485617 rs370223580 COSM1184146, COSM1184145 Large intestine
RECK 9:36083487 rs754745207 COSM1177811 Endometrium
SLC35E1 19:16553901 rs773244448 COSM1391284, COSM1391283 Large intestine
ATP8A1 4:42586383 COSM3603994, COSM3603993 Skin
RECK 9:36110029 rs772507584 COSM1462342 Large intestine
ATP8A1 4:42443590 rs140420171 COSM1184148, COSM1184147 Large intestine, skin

Somatic mutation in variant rs771311957 in ATP6V1A and variant rs754745207 in RECK were discovered in Endometrium.

*

Primary tissue where the somatic mutations were found as cataloged by COSMIC database.

The tissue source where the somatic mutations were found in endometrium in COSMIC database are marked in bold.