Colon Cancer: Gene >> DCTN2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000548249
Start	57535827:57535827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.124A>C
AA Mutation	p.Ser42Arg(p.S42R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000548249
Start	57534364:57534364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.452C>T
AA Mutation	p.Ala151Val(p.A151V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000548249
Start	57533988:57533988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374804015
CDS Mutation	c.634C>T
AA Mutation	p.Arg212Trp(p.R212W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000548249
Start	57534371:57534371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.445C>A
AA Mutation	p.Leu149Met(p.L149M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000548249
Start	57533957:57533957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.665C>T
AA Mutation	p.Ala222Val(p.A222V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000548249
Start	57534022:57534023(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs774424233
CDS Mutation	c.599dupC
AA Mutation	p.Asp201ArgfsTer2(p.D201Rfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> DCTN2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000548249
Start	57533993:57533993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.629A>G
AA Mutation	p.His210Arg(p.H210R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript