Colon Cancer: Gene >> MAPK8IP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000241014
Start	45903044:45903044(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1277C>T
AA Mutation	p.Ala426Val(p.A426V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000241014
Start	45904125:45904125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1630G>A
AA Mutation	p.Ala544Thr(p.A544T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000241014
Start	45905033:45905033(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1956G>T
AA Mutation	p.Lys652Asn(p.K652N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000241014
Start	45902957:45902957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1190G>A
AA Mutation	p.Arg397Gln(p.R397Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000241014
Start	45902480:45902480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746604189
CDS Mutation	c.713G>A
AA Mutation	p.Arg238His(p.R238H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000241014
Start	45902741:45902741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774929831
CDS Mutation	c.974C>T
AA Mutation	p.Pro325Leu(p.P325L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000241014
Start	45902737:45902737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749687015
CDS Mutation	c.970C>T
AA Mutation	p.Arg324Trp(p.R324W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000241014
Start	45905159:45905159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1973G>A
AA Mutation	p.Gly658Glu(p.G658E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000241014
Start	45903073:45903073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375735836
CDS Mutation	c.1306C>T
AA Mutation	p.Arg436Trp(p.R436W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000241014
Start	45902642:45902642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.875C>T
AA Mutation	p.Ala292Val(p.A292V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000241014
Start	45904722:45904722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1781C>T
AA Mutation	p.Ala594Val(p.A594V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000241014
Start	45904130:45904130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1635C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000241014
Start	45905178:45905178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs544815653
CDS Mutation	c.1992C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000241014
Start	45902914:45902914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1147C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000241014
Start	45902640:45902640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138625751
CDS Mutation	c.873C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000241014
Start	45905000:45905000(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1928delA
AA Mutation	p.Asn643ThrfsTer91(p.N643Tfs*91)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000241014
Start	45902518:45902518(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.755delC
AA Mutation	p.Pro252LeufsTer24(p.P252Lfs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MAPK8IP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000241014
Start	45904011:45904011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1516G>A
AA Mutation	p.Glu506Lys(p.E506K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000241014
Start	45902684:45902684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771448062
CDS Mutation	c.917G>A
AA Mutation	p.Arg306Gln(p.R306Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript