Colon Cancer: Gene >> FBLIM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375766
Start	15784552:15784552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1013G>A
AA Mutation	p.Cys338Tyr(p.C338Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375766
Start	15777178:15777178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757119431
CDS Mutation	c.899C>T
AA Mutation	p.Ala300Val(p.A300V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000375766
Start	15765015:15765015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145692215
CDS Mutation	c.32C>T
AA Mutation	p.Ser11Leu(p.S11L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000375766
Start	15774726:15774726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767546555
CDS Mutation	c.820C>T
AA Mutation	p.Arg274Trp(p.R274W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375766
Start	15767452:15767452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138682032
CDS Mutation	c.327G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375766
Start	15774785:15774785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150817626
CDS Mutation	c.879C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375766
Start	15784619:15784619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1080C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000375766
Start	15767546:15767546(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.425delC
AA Mutation	p.Pro142ArgfsTer59(p.P142Rfs*59)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000375766
Start	15777267:15777268(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.992dupA
AA Mutation	p.Asn331LysfsTer6(p.N331Kfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> FBLIM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375766
Start	15765220:15765220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.237G>C
AA Mutation	p.Gln79His(p.Q79H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375766
Start	15777242:15777242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.963C>T
Mutation Classification	Silent
Feature Type	Transcript