Colon Cancer: Gene >> MYNN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000349841
Start	169779013:169779013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764466451
CDS Mutation	c.512C>T
AA Mutation	p.Ala171Val(p.A171V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000349841
Start	169784642:169784642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374143807
CDS Mutation	c.1504G>A
AA Mutation	p.Glu502Lys(p.E502K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000349841
Start	169784685:169784685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1547A>C
AA Mutation	p.Lys516Thr(p.K516T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000349841
Start	169778850:169778850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.349G>T
AA Mutation	p.Asp117Tyr(p.D117Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000349841
Start	169779293:169779293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.792G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000349841
Start	169779068:169779068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760353149
CDS Mutation	c.567G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000349841
Start	169782525:169782525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1281C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000349841
Start	169774478:169774478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.183C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000349841
Start	169786656:169786656(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1817delT
AA Mutation	p.Leu606TyrfsTer19(p.L606Yfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MYNN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000349841
Start	169774306:169774306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763197153
CDS Mutation	c.11C>T
AA Mutation	p.Ser4Leu(p.S4L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000349841
Start	169783520:169783520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1443T>G
AA Mutation	p.Ile481Met(p.I481M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000349841
Start	169778905:169778905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.404A>C
AA Mutation	p.Asn135Thr(p.N135T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000349841
Start	169778982:169778982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.481G>T
AA Mutation	p.Asp161Tyr(p.D161Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000349841
Start	169779478:169779478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.977G>A
AA Mutation	p.Gly326Glu(p.G326E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000349841
Start	169778958:169778958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.457C>T
AA Mutation	p.Arg153Ter(p.R153*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000349841
Start	169778781:169778781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.280G>T
AA Mutation	p.Glu94Ter(p.E94*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript