Colon Cancer: Gene >> SRRT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000611405
Start	100887345:100887345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2001G>T
AA Mutation	p.Glu667Asp(p.E667D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000611405
Start	100885278:100885278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1225G>A
AA Mutation	p.Gly409Arg(p.G409R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000611405
Start	100881288:100881288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.126G>C
AA Mutation	p.Glu42Asp(p.E42D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000611405
Start	100888104:100888104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2389C>T
AA Mutation	p.Pro797Ser(p.P797S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000611405
Start	100882151:100882151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.497C>T
AA Mutation	p.Thr166Met(p.T166M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000611405
Start	100886858:100886858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760285736
CDS Mutation	c.1711G>A
AA Mutation	p.Ala571Thr(p.A571T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000611405
Start	100887767:100887767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2234A>G
AA Mutation	p.Lys745Arg(p.K745R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000611405
Start	100884479:100884479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.869G>A
AA Mutation	p.Arg290Gln(p.R290Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000611405
Start	100882099:100882099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.445A>G
AA Mutation	p.Met149Val(p.M149V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000611405
Start	100888274:100888274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775643465
CDS Mutation	c.2446G>A
AA Mutation	p.Ala816Thr(p.A816T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000611405
Start	100885873:100885873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1390C>T
AA Mutation	p.Arg464Cys(p.R464C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000611405
Start	100887114:100887114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1889A>G
AA Mutation	p.Tyr630Cys(p.Y630C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000611405
Start	100885219:100885219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs113298167
CDS Mutation	c.1166C>T
AA Mutation	p.Ala389Val(p.A389V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000611405
Start	100888052:100888052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2337A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000611405
Start	100886339:100886339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1551G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000611405
Start	100885358:100885358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1305C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000611405
Start	100884123:100884123(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.646delG
AA Mutation	p.Ala216ProfsTer6(p.A216Pfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000611405
Start	100887778:100887778(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2250delT
AA Mutation	p.Phe750LeufsTer32(p.F750Lfs*32)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SRRT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000611405
Start	100887481:100887481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2137T>G
AA Mutation	p.Trp713Gly(p.W713G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript