Colon Cancer: Gene >> GPSM2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264126
Start	108914344:108914344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754166364
CDS Mutation	c.1199G>A
AA Mutation	p.Arg400His(p.R400H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264126
Start	108901836:108901836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753366137
CDS Mutation	c.844G>A
AA Mutation	p.Ala282Thr(p.A282T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264126
Start	108897026:108897026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.219C>G
AA Mutation	p.Phe73Leu(p.F73L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264126
Start	108922518:108922518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1542G>T
AA Mutation	p.Lys514Asn(p.K514N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264126
Start	108896931:108896931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780911321
CDS Mutation	c.124G>A
AA Mutation	p.Ala42Thr(p.A42T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000264126
Start	108924030:108924030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs191870755
CDS Mutation	c.1631C>T
AA Mutation	p.Thr544Met(p.T544M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000264126
Start	108918614:108918614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs571651862
CDS Mutation	c.1265T>C
AA Mutation	p.Val422Ala(p.V422A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000264126
Start	108929794:108929794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs189033496
CDS Mutation	c.1909C>T
AA Mutation	p.Arg637Trp(p.R637W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000264126
Start	108897986:108897986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.442C>A
AA Mutation	p.Leu148Ile(p.L148I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000264126
Start	108929830:108929830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1945C>A
AA Mutation	p.Leu649Ile(p.L649I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000264126
Start	108901810:108901810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs77121685
CDS Mutation	c.818G>A
AA Mutation	p.Arg273Gln(p.R273Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000264126
Start	108897998:108897998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.454T>C
AA Mutation	p.Tyr152His(p.Y152H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264126
Start	108922524:108922524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1548C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264126
Start	108918681:108918681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1332A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264126
Start	108918651:108918651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1302A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264126
Start	108929776:108929776(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1895delT
AA Mutation	p.Phe632SerfsTer31(p.F632Sfs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264126
Start	108901888:108901888(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.899delA
AA Mutation	p.Lys300ArgfsTer7(p.K300Rfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000264126
Start	108918769:108918769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776770855
CDS Mutation	c.1420C>T
AA Mutation	p.Arg474Ter(p.R474*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000264126
Start	108898897:108898897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.700G>T
AA Mutation	p.Glu234Ter(p.E234*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264126
Start	108918705:108918706(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1362dupA
AA Mutation	p.Tyr455IlefsTer8(p.Y455Ifs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000264126
Start	108903125:108903125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.954-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> GPSM2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264126
Start	108898960:108898960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.763C>A
AA Mutation	p.Leu255Ile(p.L255I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264126
Start	108922469:108922469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762107426
CDS Mutation	c.1493G>A
AA Mutation	p.Arg498Gln(p.R498Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript