Colon Cancer: Gene >> ITGA7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000555728
Start	55697011:55697011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs17854598
CDS Mutation	c.1757G>A
AA Mutation	p.Arg586His(p.R586H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000555728
Start	55703158:55703158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.227A>T
AA Mutation	p.Gln76Leu(p.Q76L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000555728
Start	55701141:55701141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs537937026
CDS Mutation	c.428G>A
AA Mutation	p.Arg143Gln(p.R143Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000555728
Start	55696299:55696299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2003G>T
AA Mutation	p.Ser668Ile(p.S668I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000555728
Start	55695597:55695597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748345970
CDS Mutation	c.2060G>A
AA Mutation	p.Cys687Tyr(p.C687Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000555728
Start	55697008:55697008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1760T>C
AA Mutation	p.Val587Ala(p.V587A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000555728
Start	55698461:55698461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752464052
CDS Mutation	c.1246C>T
AA Mutation	p.Arg416Trp(p.R416W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000555728
Start	55698846:55698846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771929107
CDS Mutation	c.994G>A
AA Mutation	p.Ala332Thr(p.A332T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000555728
Start	55694622:55694622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2402G>A
AA Mutation	p.Gly801Asp(p.G801D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000555728
Start	55697530:55697530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1558C>A
AA Mutation	p.His520Asn(p.H520N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000555728
Start	55694079:55694079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2609G>A
AA Mutation	p.Gly870Asp(p.G870D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000555728
Start	55685185:55685185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200485048
CDS Mutation	c.3419C>T
AA Mutation	p.Thr1140Met(p.T1140M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000555728
Start	55694839:55694839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771597583
CDS Mutation	c.2267A>T
AA Mutation	p.Gln756Leu(p.Q756L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000555728
Start	55703071:55703071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.314G>A
AA Mutation	p.Arg105Lys(p.R105K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000555728
Start	55698786:55698786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746101495
CDS Mutation	c.1054G>A
AA Mutation	p.Glu352Lys(p.E352K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000555728
Start	55702926:55702926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.360G>T
AA Mutation	p.Glu120Asp(p.E120D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000555728
Start	55707586:55707586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.97G>A
AA Mutation	p.Ala33Thr(p.A33T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000555728
Start	55697491:55697491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1597G>T
AA Mutation	p.Asp533Tyr(p.D533Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000555728
Start	55703131:55703131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150476577
CDS Mutation	c.254C>T
AA Mutation	p.Ala85Val(p.A85V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000555728
Start	55698901:55698901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199699185
CDS Mutation	c.939G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000555728
Start	55696926:55696926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1842C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000555728
Start	55707626:55707626(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.57delT
AA Mutation	p.Phe19LeufsTer20(p.F19Lfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000555728
Start	55698517:55698517(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1190delG
AA Mutation	p.Gly397ValfsTer7(p.G397Vfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000555728
Start	55707618:55707619(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.64dupC
AA Mutation	p.Leu22ProfsTer81(p.L22Pfs*81)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000555728
Start	55698516:55698517(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1190dupG
AA Mutation	p.Ala398CysfsTer25(p.A398Cfs*25)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000555728
Start	55698848:55698849(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.991dupC
AA Mutation	p.Arg331ProfsTer42(p.R331Pfs*42)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000555728
Start	55697026:55697027(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1741_1742insAA
AA Mutation	p.Arg581GlnfsTer8(p.R581Qfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ITGA7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000555728
Start	55700321:55700321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776189266
CDS Mutation	c.743C>T
AA Mutation	p.Ala248Val(p.A248V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000555728
Start	55694457:55694457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2475G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000555728
Start	55693297:55693297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138301131
CDS Mutation	c.2688G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000555728
Start	55688943:55688943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2991C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000555728
Start	55698530:55698530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1177G>T
AA Mutation	p.Glu393Ter(p.E393*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript