Colon Cancer: Gene >> SFTPB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000393822
Start	85665694:85665694(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370750455
CDS Mutation	c.494G>A
AA Mutation	p.Arg165Gln(p.R165Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000393822
Start	85663669:85663669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.851G>T
AA Mutation	p.Gly284Val(p.G284V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000393822
Start	85665326:85665326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.635G>T
AA Mutation	p.Arg212Met(p.R212M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000393822
Start	85665695:85665695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370715446
CDS Mutation	c.493C>T
AA Mutation	p.Arg165Trp(p.R165W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000393822
Start	85663464:85663464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780787602
CDS Mutation	c.884G>A
AA Mutation	p.Arg295Gln(p.R295Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000393822
Start	85665769:85665769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.419T>G
AA Mutation	p.Leu140Arg(p.L140R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393822
Start	85663674:85663674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.846C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393822
Start	85668165:85668165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.19C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393822
Start	85666707:85666707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772677222
CDS Mutation	c.303C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393822
Start	85665671:85665671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.517C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393822
Start	85662053:85662053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1059C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393822
Start	85666668:85666668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.342A>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SFTPB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000393822
Start	85663420:85663420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201986026
CDS Mutation	c.928G>A
AA Mutation	p.Gly310Arg(p.G310R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000393822
Start	85668177:85668177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7G>A
AA Mutation	p.Glu3Lys(p.E3K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000393822
Start	85665644:85665644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138274558
CDS Mutation	c.544C>T
AA Mutation	p.Pro182Ser(p.P182S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript