Colon Cancer: Gene >> ITGB7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000267082
Start	53200352:53200352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.92C>A
AA Mutation	p.Ala31Asp(p.A31D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000267082
Start	53195378:53195378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1157A>G
AA Mutation	p.Tyr386Cys(p.Y386C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000267082
Start	53197568:53197568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.499G>A
AA Mutation	p.Asp167Asn(p.D167N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000267082
Start	53191911:53191911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755135151
CDS Mutation	c.2264G>A
AA Mutation	p.Arg755His(p.R755H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000267082
Start	53196739:53196739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748193418
CDS Mutation	c.656G>A
AA Mutation	p.Arg219Gln(p.R219Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000267082
Start	53193792:53193792(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1418T>G
AA Mutation	p.Leu473Arg(p.L473R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000267082
Start	53191989:53191989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2186T>C
AA Mutation	p.Leu729Pro(p.L729P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267082
Start	53196125:53196125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372436147
CDS Mutation	c.891C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267082
Start	53196624:53196624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370057719
CDS Mutation	c.771G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267082
Start	53191928:53191928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771753910
CDS Mutation	c.2247G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267082
Start	53194330:53194330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773859000
CDS Mutation	c.1176C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267082
Start	53196681:53196681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.714C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267082
Start	53192501:53192501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1984C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267082
Start	53191982:53191982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370893853
CDS Mutation	c.2193C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000267082
Start	53192333:53192333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2152G>T
AA Mutation	p.Glu718Ter(p.E718*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ITGB7

Mutation ID	1
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000267082
Start	53193207:53193245(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1621_1659delGGTCACTGTCAATGTGGACGCTGCAGCTGCAGTGGACAG
AA Mutation	p.Gly541_Gln553del(p.G541_Q553del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript