Colon Cancer: Gene >> MEIS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000272369
Start	66440565:66440565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.385C>T
AA Mutation	p.Arg129Cys(p.R129C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000272369
Start	66437911:66437911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.187A>G
AA Mutation	p.Met63Val(p.M63V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000272369
Start	66464188:66464188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758233459
CDS Mutation	c.710C>T
AA Mutation	p.Thr237Met(p.T237M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000272369
Start	66512210:66512210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.804G>T
AA Mutation	p.Lys268Asn(p.K268N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000272369
Start	66512236:66512236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.830G>A
AA Mutation	p.Gly277Asp(p.G277D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000272369
Start	66437789:66437789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.65C>T
AA Mutation	p.Thr22Met(p.T22M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000272369
Start	66443026:66443026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.608G>T
AA Mutation	p.Arg203Ile(p.R203I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000272369
Start	66512199:66512199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.793G>T
AA Mutation	p.Asp265Tyr(p.D265Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000272369
Start	66568718:66568718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1076T>C
AA Mutation	p.Val359Ala(p.V359A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000272369
Start	66464195:66464195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.717C>G
AA Mutation	p.His239Gln(p.H239Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000272369
Start	66464190:66464190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.712T>C
AA Mutation	p.Ser238Pro(p.S238P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000272369
Start	66437749:66437749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.25C>T
AA Mutation	p.Pro9Ser(p.P9S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000272369
Start	66439909:66439909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.306C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000272369
Start	66437742:66437742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.18C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000272369
Start	66439902:66439902(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.304delC
AA Mutation	p.Arg102AlafsTer20(p.R102Afs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000272369
Start	66512176:66512176(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.774delC
AA Mutation	p.Ser259AlafsTer24(p.S259Afs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000272369
Start	66439901:66439902(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.304dupC
AA Mutation	p.Arg102ProfsTer18(p.R102Pfs*18)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MEIS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000272369
Start	66437743:66437743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.19G>A
AA Mutation	p.Asp7Asn(p.D7N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000272369
Start	66440568:66440568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.388G>A
AA Mutation	p.Ala130Thr(p.A130T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000272369
Start	66567473:66567473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.986G>T
AA Mutation	p.Arg329Ile(p.R329I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript