Colon Cancer: Gene >> RASGRF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265080
Start	81068064:81068064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.428T>C
AA Mutation	p.Leu143Ser(p.L143S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265080
Start	81180228:81180228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2740G>T
AA Mutation	p.Ala914Ser(p.A914S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265080
Start	81112707:81112707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1936C>T
AA Mutation	p.Arg646Cys(p.R646C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265080
Start	81180261:81180261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2773T>C
AA Mutation	p.Trp925Arg(p.W925R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265080
Start	81113776:81113776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2326T>G
AA Mutation	p.Ser776Ala(p.S776A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265080
Start	81217399:81217399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3478G>T
AA Mutation	p.Asp1160Tyr(p.D1160Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000265080
Start	81112813:81112813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2042A>C
AA Mutation	p.Lys681Thr(p.K681T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000265080
Start	81080596:81080596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.968C>A
AA Mutation	p.Ala323Asp(p.A323D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000265080
Start	81070555:81070555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.607G>T
AA Mutation	p.Asp203Tyr(p.D203Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000265080
Start	81112635:81112635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1864G>A
AA Mutation	p.Asp622Asn(p.D622N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000265080
Start	81208398:81208398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3116G>A
AA Mutation	p.Arg1039Lys(p.R1039K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000265080
Start	81092851:81092851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749203214
CDS Mutation	c.1441C>T
AA Mutation	p.Arg481Cys(p.R481C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000265080
Start	81113704:81113704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2254A>G
AA Mutation	p.Asn752Asp(p.N752D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000265080
Start	81208394:81208394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs556120453
CDS Mutation	c.3112G>A
AA Mutation	p.Glu1038Lys(p.E1038K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000265080
Start	81207348:81207348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs545786297
CDS Mutation	c.3070G>A
AA Mutation	p.Glu1024Lys(p.E1024K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265080
Start	81225725:81225725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3669G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265080
Start	81217416:81217416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3495A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265080
Start	81201431:81201431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2895G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000265080
Start	81201390:81201390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2854C>T
AA Mutation	p.Arg952Ter(p.R952*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000265080
Start	81086848:81086848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1285G>T
AA Mutation	p.Glu429Ter(p.E429*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265080
Start	81092871:81092872(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1466dupA
AA Mutation	p.Glu490GlyfsTer42(p.E490Gfs*42)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> RASGRF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265080
Start	81112797:81112797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376549001
CDS Mutation	c.2026G>T
AA Mutation	p.Ala676Ser(p.A676S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265080
Start	81123690:81123690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2519C>T
AA Mutation	p.Pro840Leu(p.P840L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265080
Start	81094889:81094889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1652A>T
AA Mutation	p.Asp551Val(p.D551V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265080
Start	81201336:81201336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747659788
CDS Mutation	c.2800G>A
AA Mutation	p.Glu934Lys(p.E934K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265080
Start	81070565:81070565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.617T>C
AA Mutation	p.Ile206Thr(p.I206T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265080
Start	81085900:81085900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1260G>T
AA Mutation	p.Glu420Asp(p.E420D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265080
Start	81180227:81180227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2739G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265080
Start	81201428:81201428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751578295
CDS Mutation	c.2892C>T
Mutation Classification	Silent
Feature Type	Transcript