Colon Cancer: Gene >> TYR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263321
Start	89295218:89295218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1442C>T
AA Mutation	p.Ala481Val(p.A481V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263321
Start	89178317:89178317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.364A>C
AA Mutation	p.Asn122His(p.N122H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263321
Start	89191278:89191278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61754375
CDS Mutation	c.896G>A
AA Mutation	p.Arg299His(p.R299H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000263321
Start	89178521:89178521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.568G>T
AA Mutation	p.Gly190Trp(p.G190W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000263321
Start	89178183:89178183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61753185
CDS Mutation	c.230G>A
AA Mutation	p.Arg77Gln(p.R77Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000263321
Start	89178736:89178736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.783C>G
AA Mutation	p.Asn261Lys(p.N261K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000263321
Start	89227889:89227889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1103T>A
AA Mutation	p.Ile368Asn(p.I368N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000263321
Start	89178352:89178352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.399A>T
AA Mutation	p.Lys133Asn(p.K133N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000263321
Start	89191344:89191344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.962G>A
AA Mutation	p.Cys321Tyr(p.C321Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000263321
Start	89227928:89227928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1142C>T
AA Mutation	p.Ala381Val(p.A381V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000263321
Start	89284907:89284907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1319T>G
AA Mutation	p.Ile440Ser(p.I440S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263321
Start	89178190:89178190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376813190
CDS Mutation	c.237G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263321
Start	89227893:89227893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1107T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263321
Start	89178043:89178043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.90G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263321
Start	89178199:89178199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139926589
CDS Mutation	c.246C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263321
Start	89178353:89178353(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.405delT
AA Mutation	p.Phe135LeufsTer6(p.F135Lfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TYR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263321
Start	89227850:89227850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151206295
CDS Mutation	c.1064C>T
AA Mutation	p.Ala355Val(p.A355V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263321
Start	89178098:89178098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.145C>T
AA Mutation	p.Leu49Phe(p.L49F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263321
Start	89295235:89295235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1459G>T
AA Mutation	p.Val487Phe(p.V487F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript