Colon Cancer: Gene >> RASAL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000462775
Start	178445644:178445644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1165T>A
AA Mutation	p.Tyr389Asn(p.Y389N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367649
Start	178094682:178094682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750926173
CDS Mutation	c.190G>A
AA Mutation	p.Val64Ile(p.V64I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367649
Start	178283638:178283638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.277A>C
AA Mutation	p.Lys93Gln(p.K93Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000462775
Start	178452627:178452627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1540A>C
AA Mutation	p.Ile514Leu(p.I514L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000462775
Start	178458465:178458465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs552212761
CDS Mutation	c.2750G>A
AA Mutation	p.Arg917Gln(p.R917Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000462775
Start	178457907:178457907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2192T>A
AA Mutation	p.Ile731Lys(p.I731K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000462775
Start	178442907:178442907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.716A>G
AA Mutation	p.Lys239Arg(p.K239R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000462775
Start	178452522:178452522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1435C>A
AA Mutation	p.Leu479Ile(p.L479I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000462775
Start	178458408:178458408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2693G>T
AA Mutation	p.Gly898Val(p.G898V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000462775
Start	178443044:178443044(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.853C>T
AA Mutation	p.Arg285Trp(p.R285W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000462775
Start	178458054:178458054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750183203
CDS Mutation	c.2339C>T
AA Mutation	p.Ser780Leu(p.S780L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000462775
Start	178458497:178458497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2782A>G
AA Mutation	p.Ser928Gly(p.S928G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000462775
Start	178445519:178445519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1040A>G
AA Mutation	p.Asp347Gly(p.D347G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000462775
Start	178443171:178443171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.980A>G
AA Mutation	p.Asn327Ser(p.N327S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000462775
Start	178473116:178473116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3297G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000462775
Start	178442906:178442906(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs775329137
CDS Mutation	c.722delA
AA Mutation	p.Lys241ArgfsTer7(p.K241Rfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000462775
Start	178442759:178442760(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.568_569insGTCTTGCTGGTTGTACGAGCAAAGAGGGTATCATC
AA Mutation	p.Glu190GlyfsTer70(p.E190Gfs*70)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000462775
Start	178442758:178442759(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.567_568insTTT
AA Mutation	p.Cys189_Glu190insPhe(p.C189_E190insF)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> RASAL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367649
Start	178283645:178283645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.284G>A
AA Mutation	p.Cys95Tyr(p.C95Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000462775
Start	178439507:178439507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.316G>C
AA Mutation	p.Gly106Arg(p.G106R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000462775
Start	178445554:178445554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772116589
CDS Mutation	c.1075C>T
AA Mutation	p.Arg359Cys(p.R359C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000462775
Start	178454519:178454519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1638C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000462775
Start	178458304:178458304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2589T>C
Mutation Classification	Silent
Feature Type	Transcript