Colon Cancer: Gene >> MYCN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000281043
Start	15945772:15945772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1070G>A
AA Mutation	p.Arg357His(p.R357H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000281043
Start	15945685:15945685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.983A>G
AA Mutation	p.Gln328Arg(p.Q328R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000281043
Start	15942191:15942191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.127A>G
AA Mutation	p.Thr43Ala(p.T43A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000281043
Start	15945741:15945741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1039C>A
AA Mutation	p.Gln347Lys(p.Q347K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000281043
Start	15945606:15945606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144939456
CDS Mutation	c.904C>T
AA Mutation	p.Arg302Cys(p.R302C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000281043
Start	15945771:15945771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1069C>T
AA Mutation	p.Arg357Cys(p.R357C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000281043
Start	15945558:15945558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776847158
CDS Mutation	c.856C>T
AA Mutation	p.Arg286Cys(p.R286C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000281043
Start	15945548:15945548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.846G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000281043
Start	15942340:15942340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.276C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000281043
Start	15942673:15942673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.609G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000281043
Start	15945923:15945923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs190053841
CDS Mutation	c.1221C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000281043
Start	15942192:15942192(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.134delC
AA Mutation	p.Pro45ArgfsTer86(p.P45Rfs*86)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MYCN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000281043
Start	15945606:15945606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144939456
CDS Mutation	c.904C>T
AA Mutation	p.Arg302Cys(p.R302C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000281043
Start	15945601:15945601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.899C>T
AA Mutation	p.Thr300Ile(p.T300I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000281043
Start	15942164:15942164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.100G>T
AA Mutation	p.Asp34Tyr(p.D34Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000281043
Start	15945820:15945820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1118G>A
AA Mutation	p.Arg373Gln(p.R373Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000281043
Start	15945542:15945542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.840C>G
Mutation Classification	Silent
Feature Type	Transcript