Colon Cancer: Gene >> PODN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000312553
Start	53080842:53080842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs534137326
CDS Mutation	c.1771G>A
AA Mutation	p.Asp591Asn(p.D591N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000312553
Start	53069820:53069820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778944420
CDS Mutation	c.109C>A
AA Mutation	p.Pro37Thr(p.P37T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000312553
Start	53070151:53070151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.440A>C
AA Mutation	p.Asn147Thr(p.N147T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000312553
Start	53080794:53080794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1723C>A
AA Mutation	p.Leu575Met(p.L575M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000312553
Start	53078546:53078546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781706326
CDS Mutation	c.1180C>T
AA Mutation	p.Arg394Trp(p.R394W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000312553
Start	53069934:53069934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.223G>A
AA Mutation	p.Ala75Thr(p.A75T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000312553
Start	53078919:53078919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763567428
CDS Mutation	c.1553C>T
AA Mutation	p.Ala518Val(p.A518V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312553
Start	53078629:53078629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373979403
CDS Mutation	c.1263C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312553
Start	53080841:53080841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1770C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312553
Start	53080850:53080850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs547822345
CDS Mutation	c.1779G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312553
Start	53078620:53078620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370467120
CDS Mutation	c.1254G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312553
Start	53077732:53077732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.930C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312553
Start	53080823:53080823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773271095
CDS Mutation	c.1752G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000312553
Start	53077705:53077705(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.908delC
AA Mutation	p.Pro303ArgfsTer7(p.P303Rfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000312553
Start	53078989:53078989(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1627delC
AA Mutation	p.Arg543ValfsTer77(p.R543Vfs*77)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000312553
Start	53078499:53078499(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1137delC
AA Mutation	p.Ile380SerfsTer55(p.I380Sfs*55)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PODN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000312553
Start	53069932:53069932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.221G>C
AA Mutation	p.Arg74Thr(p.R74T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000312553
Start	53078753:53078753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780959803
CDS Mutation	c.1387C>T
AA Mutation	p.Arg463Cys(p.R463C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000312553
Start	53071591:53071591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.513G>T
AA Mutation	p.Glu171Asp(p.E171D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript