Colon Cancer: Gene >> MYBPH

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000255416
Start	203168921:203168921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201112460
CDS Mutation	c.1402C>T
AA Mutation	p.Arg468Trp(p.R468W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000255416
Start	203170368:203170368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769884152
CDS Mutation	c.1016G>A
AA Mutation	p.Arg339Gln(p.R339Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000255416
Start	203174471:203174471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770005031
CDS Mutation	c.467C>T
AA Mutation	p.Pro156Leu(p.P156L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000255416
Start	203174507:203174507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146696842
CDS Mutation	c.431G>A
AA Mutation	p.Arg144His(p.R144H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000255416
Start	203169037:203169037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750570762
CDS Mutation	c.1286G>A
AA Mutation	p.Arg429His(p.R429H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000255416
Start	203169276:203169276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1207T>C
AA Mutation	p.Cys403Arg(p.C403R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000255416
Start	203171511:203171511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.665T>G
AA Mutation	p.Met222Arg(p.M222R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255416
Start	203174548:203174548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.390G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000255416
Start	203175742:203175742(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs752878638
CDS Mutation	c.14delA
AA Mutation	p.Asn5ThrfsTer73(p.N5Tfs*73)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000255416
Start	203168939:203168939(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1384delG
AA Mutation	p.Glu462ArgfsTer114(p.E462Rfs*114)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000255416
Start	203175679:203175680(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.76dupA
AA Mutation	p.Thr26AsnfsTer37(p.T26Nfs*37)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MYBPH

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255416
Start	203175343:203175343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.324G>A
Mutation Classification	Silent
Feature Type	Transcript