Colon Cancer: Gene >> ASMT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000381229
Start	1642833:1642833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.857T>C
AA Mutation	p.Leu286Pro(p.L286P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000381229
Start	1629897:1629897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs189062200
CDS Mutation	c.520G>A
AA Mutation	p.Ala174Thr(p.A174T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000381229
Start	1623166:1623166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149222772
CDS Mutation	c.97G>A
AA Mutation	p.Val33Met(p.V33M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000381229
Start	1642937:1642937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.961C>A
AA Mutation	p.Leu321Ile(p.L321I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000381229
Start	1636494:1636494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.760C>A
AA Mutation	p.Leu254Ile(p.L254I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381229
Start	1636463:1636463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756221219
CDS Mutation	c.729G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381229
Start	1627706:1627706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.378A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381229
Start	1623252:1623252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.183G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381229
Start	1627745:1627745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.417T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000381229
Start	1636473:1636473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.739C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000381229
Start	1623188:1623188(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.122delC
AA Mutation	p.Pro41GlnfsTer13(p.P41Qfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000381229
Start	1642907:1642907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.931G>T
AA Mutation	p.Glu311Ter(p.E311*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ASMT

No Mutation Annotation!