Colon Cancer: Gene >> VCAM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000294728
Start	100731476:100731476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757451312
CDS Mutation	c.1483G>A
AA Mutation	p.Glu495Lys(p.E495K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000294728
Start	100738270:100738270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2207A>C
AA Mutation	p.Lys736Thr(p.K736T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000294728
Start	100723145:100723145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.466G>T
AA Mutation	p.Asp156Tyr(p.D156Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000294728
Start	100734663:100734663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200910233
CDS Mutation	c.1954G>A
AA Mutation	p.Ala652Thr(p.A652T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000294728
Start	100734546:100734546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1837G>T
AA Mutation	p.Val613Phe(p.V613F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000294728
Start	100723193:100723193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.514T>C
AA Mutation	p.Ser172Pro(p.S172P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000294728
Start	100723166:100723166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779073619
CDS Mutation	c.487G>A
AA Mutation	p.Glu163Lys(p.E163K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000294728
Start	100731297:100731297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769528923
CDS Mutation	c.1304G>A
AA Mutation	p.Arg435Gln(p.R435Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000294728
Start	100720626:100720626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754424141
CDS Mutation	c.215C>T
AA Mutation	p.Thr72Met(p.T72M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000294728
Start	100734617:100734617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1908G>T
AA Mutation	p.Lys636Asn(p.K636N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000294728
Start	100724727:100724727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.765G>T
AA Mutation	p.Glu255Asp(p.E255D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000294728
Start	100738263:100738263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2200G>A
AA Mutation	p.Ala734Thr(p.A734T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000294728
Start	100724888:100724888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759683632
CDS Mutation	c.926A>G
AA Mutation	p.Gln309Arg(p.Q309R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000294728
Start	100723220:100723220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.541A>G
AA Mutation	p.Thr181Ala(p.T181A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294728
Start	100723177:100723177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.498G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294728
Start	100720627:100720627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.216G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294728
Start	100724835:100724835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.873T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294728
Start	100734644:100734644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758175606
CDS Mutation	c.1935A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294728
Start	100731451:100731451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1458G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000294728
Start	100731346:100731347(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1358dupT
AA Mutation	p.Leu453PhefsTer23(p.L453Ffs*23)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000294728
Start	100729370:100729371(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1192_1193insAGAAAGA
AA Mutation	p.Val398GlufsTer10(p.V398Efs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> VCAM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000294728
Start	100731281:100731281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781641145
CDS Mutation	c.1288G>A
AA Mutation	p.Val430Met(p.V430M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000294728
Start	100729319:100729319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1141T>C
AA Mutation	p.Tyr381His(p.Y381H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000294728
Start	100732517:100732517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745882659
CDS Mutation	c.1625C>T
AA Mutation	p.Pro542Leu(p.P542L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000294728
Start	100724634:100724634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.672G>T
AA Mutation	p.Lys224Asn(p.K224N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000294728
Start	100738145:100738145(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2086delT
AA Mutation	p.Ser696LeufsTer13(p.S696Lfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript