Colon Cancer: Gene >> MRVI1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000423302
Start	10593590:10593590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2077C>T
AA Mutation	p.Arg693Cys(p.R693C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000423302
Start	10603217:10603217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199928205
CDS Mutation	c.1778G>A
AA Mutation	p.Arg593Gln(p.R593Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000423302
Start	10652095:10652095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.155C>T
AA Mutation	p.Ala52Val(p.A52V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000423302
Start	10626201:10626201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1133C>G
AA Mutation	p.Ala378Gly(p.A378G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000423302
Start	10628007:10628007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.671G>A
AA Mutation	p.Gly224Asp(p.G224D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000423302
Start	10604464:10604464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767130215
CDS Mutation	c.1684C>T
AA Mutation	p.Arg562Cys(p.R562C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000423302
Start	10626120:10626120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374041885
CDS Mutation	c.1214G>A
AA Mutation	p.Arg405Gln(p.R405Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000423302
Start	10626393:10626393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.941G>T
AA Mutation	p.Gly314Val(p.G314V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000423302
Start	10626073:10626073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755206470
CDS Mutation	c.1261C>T
AA Mutation	p.Arg421Cys(p.R421C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000423302
Start	10604463:10604463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368966460
CDS Mutation	c.1685G>A
AA Mutation	p.Arg562His(p.R562H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000423302
Start	10594183:10594183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2030C>A
AA Mutation	p.Pro677His(p.P677H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000423302
Start	10629627:10629627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375197703
CDS Mutation	c.485C>T
AA Mutation	p.Ala162Val(p.A162V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000423302
Start	10626022:10626022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1312G>T
AA Mutation	p.Asp438Tyr(p.D438Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000423302
Start	10600989:10600989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1946A>G
AA Mutation	p.Lys649Arg(p.K649R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000423302
Start	10626359:10626359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.975C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000423302
Start	10652124:10652124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.126C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000423302
Start	10594158:10594158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2055C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000423302
Start	10629629:10629629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.483G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000423302
Start	10576389:10576389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2682C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000423302
Start	10600979:10600979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs540632213
CDS Mutation	c.1956G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000423302
Start	10603149:10603149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1846C>T
AA Mutation	p.Arg616Ter(p.R616*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000423302
Start	10626133:10626133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1201G>T
AA Mutation	p.Glu401Ter(p.E401*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	protein_altering_variant
Transcription ID	ENST00000423302
Start	10626561:10626562(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.772_773insCTGTTTGTA
AA Mutation	p.Asp258delinsAlaValCysAsn(p.D258delinsAVCN)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MRVI1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000423302
Start	10601046:10601046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369932235
CDS Mutation	c.1889C>T
AA Mutation	p.Ser630Leu(p.S630L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000423302
Start	10601052:10601052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs558392649
CDS Mutation	c.1883G>A
AA Mutation	p.Arg628His(p.R628H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000423302
Start	10626432:10626432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.902C>T
AA Mutation	p.Thr301Ile(p.T301I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript