Colon Cancer: Gene >> GRIP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000619221
Start	14511261:14511261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143935537
CDS Mutation	c.2128C>T
AA Mutation	p.Arg710Cys(p.R710C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000619221
Start	14517853:14517853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs532400436
CDS Mutation	c.1366G>A
AA Mutation	p.Val456Met(p.V456M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000619221
Start	14509880:14509880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774195468
CDS Mutation	c.2309C>T
AA Mutation	p.Thr770Met(p.T770M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000619221
Start	14506875:14506875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369531639
CDS Mutation	c.2615C>T
AA Mutation	p.Pro872Leu(p.P872L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000619221
Start	14493721:14493721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781001244
CDS Mutation	c.3367G>A
AA Mutation	p.Ala1123Thr(p.A1123T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000619221
Start	14493808:14493808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765627113
CDS Mutation	c.3280C>T
AA Mutation	p.Arg1094Trp(p.R1094W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000619221
Start	14509941:14509941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746354259
CDS Mutation	c.2248G>A
AA Mutation	p.Val750Ile(p.V750I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000619221
Start	14520489:14520489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763795271
CDS Mutation	c.1052C>T
AA Mutation	p.Thr351Met(p.T351M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000619221
Start	14517874:14517874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1345C>A
AA Mutation	p.Leu449Met(p.L449M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000619221
Start	14517076:14517076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1585C>T
AA Mutation	p.His529Tyr(p.H529Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000619221
Start	14507607:14507607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2463G>T
AA Mutation	p.Gln821His(p.Q821H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000619221
Start	14541987:14541987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.95C>A
AA Mutation	p.Ser32Tyr(p.S32Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000619221
Start	14506975:14506975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2515C>A
AA Mutation	p.Leu839Ile(p.L839I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000619221
Start	14521696:14521696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755847798
CDS Mutation	c.949C>T
AA Mutation	p.Arg317Trp(p.R317W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000619221
Start	14509831:14509831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2358C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000619221
Start	14513693:14513693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761172020
CDS Mutation	c.1902C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000619221
Start	14521766:14521766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.879C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000619221
Start	14493764:14493764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371141235
CDS Mutation	c.3324G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000619221
Start	14507649:14507649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2421C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000619221
Start	14521709:14521709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.936C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000619221
Start	14514395:14514395(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1681delC
AA Mutation	p.Leu561SerfsTer95(p.L561Sfs*95)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> GRIP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000619221
Start	14493730:14493730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3358C>T
AA Mutation	p.Pro1120Ser(p.P1120S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000619221
Start	14523041:14523041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368903779
CDS Mutation	c.816G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000619221
Start	14514327:14514327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762030891
CDS Mutation	c.1749C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000619221
Start	14520464:14520464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766736884
CDS Mutation	c.1077G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000619221
Start	14506898:14506898(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2592C>T
Mutation Classification	Silent
Feature Type	Transcript