Colon Cancer: Gene >> COL4A6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372216
Start	108175739:108175739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2748T>G
AA Mutation	p.Ile916Met(p.I916M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372216
Start	108159664:108159664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763836649
CDS Mutation	c.4613G>A
AA Mutation	p.Arg1538His(p.R1538H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000372216
Start	108187970:108187970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1648C>A
AA Mutation	p.Leu550Ile(p.L550I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000372216
Start	108170827:108170827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3371G>T
AA Mutation	p.Gly1124Val(p.G1124V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000372216
Start	108191440:108191440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1277C>T
AA Mutation	p.Pro426Leu(p.P426L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000372216
Start	108187108:108187108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745484454
CDS Mutation	c.1942C>A
AA Mutation	p.Pro648Thr(p.P648T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000372216
Start	108221293:108221293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.229G>A
AA Mutation	p.Gly77Arg(p.G77R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000372216
Start	108164894:108164894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3956G>C
AA Mutation	p.Gly1319Ala(p.G1319A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000372216
Start	108175201:108175201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2848C>T
AA Mutation	p.Pro950Ser(p.P950S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000372216
Start	108188545:108188545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1562G>A
AA Mutation	p.Gly521Glu(p.G521E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000372216
Start	108188612:108188612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1495C>T
AA Mutation	p.Pro499Ser(p.P499S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000372216
Start	108169596:108169596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3593G>T
AA Mutation	p.Gly1198Val(p.G1198V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000372216
Start	108179247:108179247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2326C>A
AA Mutation	p.Leu776Ile(p.L776I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000372216
Start	108188642:108188642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1465C>T
AA Mutation	p.Pro489Ser(p.P489S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000372216
Start	108214152:108214152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.404T>G
AA Mutation	p.Phe135Cys(p.F135C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000372216
Start	108188015:108188015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1603C>T
AA Mutation	p.Pro535Ser(p.P535S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000372216
Start	108174502:108174502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3079G>T
AA Mutation	p.Gly1027Cys(p.G1027C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000372216
Start	108159701:108159701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4576T>C
AA Mutation	p.Tyr1526His(p.Y1526H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000372216
Start	108161649:108161649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4306C>T
AA Mutation	p.Pro1436Ser(p.P1436S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000372216
Start	108162910:108162910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4201G>A
AA Mutation	p.Gly1401Ser(p.G1401S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372216
Start	108160635:108160635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4356C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372216
Start	108175775:108175775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs187774618
CDS Mutation	c.2712C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372216
Start	108209987:108209987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.531T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372216
Start	108171427:108171427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3240C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372216
Start	108175169:108175169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770801415
CDS Mutation	c.2880T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372216
Start	108157177:108157177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4899C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372216
Start	108160629:108160629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139555294
CDS Mutation	c.4362C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372216
Start	108176929:108176929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2601C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372216
Start	108175211:108175211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762315690
CDS Mutation	c.2838C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000372216
Start	108187220:108187220(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs771066852
CDS Mutation	c.1830delA
AA Mutation	p.Gly611AlafsTer127(p.G611Afs*127)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	stop_gained
Transcription ID	ENST00000372216
Start	108221371:108221371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.151C>T
AA Mutation	p.Arg51Ter(p.R51*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	stop_gained
Transcription ID	ENST00000372216
Start	108195087:108195087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.946C>T
AA Mutation	p.Gln316Ter(p.Q316*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	stop_gained
Transcription ID	ENST00000372216
Start	108169498:108169498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3691C>T
AA Mutation	p.Arg1231Ter(p.R1231*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000372216
Start	108176931:108176932(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2598dupA
AA Mutation	p.Gly867ArgfsTer77(p.G867Rfs*77)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> COL4A6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372216
Start	108159623:108159623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4654C>A
AA Mutation	p.Pro1552Thr(p.P1552T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372216
Start	108164884:108164884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3966A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372216
Start	108202943:108202943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.822C>T
Mutation Classification	Silent
Feature Type	Transcript