Colon Cancer: Gene >> MSX1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000382723
Start	4863040:4863040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.809C>T
AA Mutation	p.Ser270Leu(p.S270L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000382723
Start	4860335:4860335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.436A>G
AA Mutation	p.Met146Val(p.M146V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000382723
Start	4862953:4862953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.722C>A
AA Mutation	p.Ala241Asp(p.A241D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000382723
Start	4862805:4862805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.574C>T
AA Mutation	p.Arg192Cys(p.R192C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000382723
Start	4860152:4860152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.253G>A
AA Mutation	p.Gly85Ser(p.G85S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382723
Start	4862762:4862762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144660633
CDS Mutation	c.531G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000382723
Start	4860042:4860043(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.148dupG
AA Mutation	p.Ala50GlyfsTer125(p.A50Gfs*125)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MSX1

No Mutation Annotation!