Colon Cancer: Gene >> GRM2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000395052
Start	51712813:51712813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.791G>A
AA Mutation	p.Arg264His(p.R264H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000395052
Start	51715740:51715740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767625940
CDS Mutation	c.1967G>A
AA Mutation	p.Arg656His(p.R656H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000395052
Start	51709186:51709186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.203C>T
AA Mutation	p.Ala68Val(p.A68V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000395052
Start	51717773:51717773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764654881
CDS Mutation	c.2501G>A
AA Mutation	p.Arg834His(p.R834H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000395052
Start	51715385:51715385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201981098
CDS Mutation	c.1612G>A
AA Mutation	p.Ala538Thr(p.A538T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000395052
Start	51717658:51717658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200496822
CDS Mutation	c.2386G>A
AA Mutation	p.Val796Met(p.V796M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000395052
Start	51712548:51712548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.526T>C
AA Mutation	p.Ser176Pro(p.S176P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000395052
Start	51713059:51713059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200432452
CDS Mutation	c.1037G>A
AA Mutation	p.Arg346His(p.R346H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000395052
Start	51715425:51715425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1652C>T
AA Mutation	p.Thr551Ile(p.T551I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000395052
Start	51716033:51716033(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2260G>A
AA Mutation	p.Glu754Lys(p.E754K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000395052
Start	51709374:51709374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.391G>A
AA Mutation	p.Asp131Asn(p.D131N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000395052
Start	51709288:51709288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.305C>T
AA Mutation	p.Ala102Val(p.A102V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000395052
Start	51709192:51709192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.209A>G
AA Mutation	p.Asp70Gly(p.D70G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000395052
Start	51715775:51715775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2002G>A
AA Mutation	p.Ala668Thr(p.A668T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395052
Start	51709424:51709424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.441C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395052
Start	51715261:51715261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777119324
CDS Mutation	c.1488C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395052
Start	51709115:51709115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.132C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395052
Start	51715906:51715906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201665578
CDS Mutation	c.2133C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395052
Start	51712976:51712976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.954G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> GRM2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000395052
Start	51712714:51712714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147501226
CDS Mutation	c.692G>A
AA Mutation	p.Arg231His(p.R231H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000395052
Start	51709363:51709363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764682062
CDS Mutation	c.380C>T
AA Mutation	p.Ala127Val(p.A127V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395052
Start	51715528:51715528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1755G>A
Mutation Classification	Silent
Feature Type	Transcript