Colon Cancer: Gene >> GRM4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000538487
Start	34133366:34133366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143062959
CDS Mutation	c.131G>A
AA Mutation	p.Arg44His(p.R44H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000538487
Start	34056639:34056639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1073G>A
AA Mutation	p.Arg358His(p.R358H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000538487
Start	34133454:34133454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.43C>T
AA Mutation	p.Pro15Ser(p.P15S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000538487
Start	34133115:34133115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773888824
CDS Mutation	c.382G>A
AA Mutation	p.Glu128Lys(p.E128K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000538487
Start	34133148:34133148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757871136
CDS Mutation	c.349G>A
AA Mutation	p.Glu117Lys(p.E117K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000538487
Start	34028210:34028210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2599G>A
AA Mutation	p.Ala867Thr(p.A867T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000538487
Start	34036345:34036345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377004554
CDS Mutation	c.1765G>A
AA Mutation	p.Val589Met(p.V589M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000538487
Start	34036447:34036447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1663T>C
AA Mutation	p.Tyr555His(p.Y555H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000538487
Start	34133186:34133186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.311G>A
AA Mutation	p.Arg104His(p.R104H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000538487
Start	34040263:34040263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs528782611
CDS Mutation	c.1421G>A
AA Mutation	p.Arg474His(p.R474H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000538487
Start	34035706:34035706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2404A>C
AA Mutation	p.Ile802Leu(p.I802L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000538487
Start	34133198:34133198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.299C>T
AA Mutation	p.Thr100Met(p.T100M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000538487
Start	34035913:34035913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774098056
CDS Mutation	c.2197C>T
AA Mutation	p.Arg733Trp(p.R733W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000538487
Start	34092029:34092029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.590G>A
AA Mutation	p.Arg197His(p.R197H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000538487
Start	34133094:34133094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368604495
CDS Mutation	c.403C>T
AA Mutation	p.Arg135Cys(p.R135C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000538487
Start	34028138:34028138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2671G>A
AA Mutation	p.Glu891Lys(p.E891K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000538487
Start	34133223:34133223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs536244500
CDS Mutation	c.274G>A
AA Mutation	p.Asp92Asn(p.D92N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000538487
Start	34035677:34035677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2433G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000538487
Start	34091920:34091920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147871838
CDS Mutation	c.699C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000538487
Start	34035935:34035935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2175G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000538487
Start	34035812:34035812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2298G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000538487
Start	34036022:34036022(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2088delC
AA Mutation	p.Ala697ProfsTer126(p.A697Pfs*126)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> GRM4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000538487
Start	34061938:34061938(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200915496
CDS Mutation	c.827C>T
AA Mutation	p.Ser276Leu(p.S276L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000538487
Start	34040272:34040272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1412C>T
AA Mutation	p.Ala471Val(p.A471V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000538487
Start	34061956:34061956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148055958
CDS Mutation	c.809G>A
AA Mutation	p.Arg270His(p.R270H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000538487
Start	34036259:34036259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781063155
CDS Mutation	c.1851C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000538487
Start	34040223:34040223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760818778
CDS Mutation	c.1461C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000538487
Start	34040660:34040660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151094606
CDS Mutation	c.1257G>A
Mutation Classification	Silent
Feature Type	Transcript