Colon Cancer: Gene >> PITPNC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000581322
Start	67578235:67578235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.344A>G
AA Mutation	p.Asp115Gly(p.D115G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000581322
Start	67692593:67692593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751106529
CDS Mutation	c.704G>A
AA Mutation	p.Arg235Gln(p.R235Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000581322
Start	67632219:67632219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.443G>A
AA Mutation	p.Arg148His(p.R148H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000581322
Start	67692632:67692632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.743A>G
AA Mutation	p.Lys248Arg(p.K248R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000581322
Start	67692694:67692694(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752172631
CDS Mutation	c.805C>T
AA Mutation	p.Arg269Cys(p.R269C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000581322
Start	67532927:67532927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs529862745
CDS Mutation	c.174C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000581322
Start	67692641:67692641(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.755delT
AA Mutation	p.Phe252SerfsTer64(p.F252Sfs*64)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PITPNC1

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000581322
Start	67532844:67532844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.91G>T
AA Mutation	p.Glu31Ter(p.E31*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript