Colon Cancer: Gene >> PCDHB16

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000609684
Start	141184693:141184693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2134C>T
AA Mutation	p.Arg712Trp(p.R712W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000609684
Start	141184504:141184504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1945G>A
AA Mutation	p.Glu649Lys(p.E649K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000609684
Start	141184655:141184655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2096C>T
AA Mutation	p.Ser699Leu(p.S699L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000609684
Start	141182987:141182987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.428C>T
AA Mutation	p.Pro143Leu(p.P143L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000609684
Start	141183076:141183076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.517A>G
AA Mutation	p.Ser173Gly(p.S173G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000609684
Start	141184730:141184730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2171G>A
AA Mutation	p.Arg724His(p.R724H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000609684
Start	141183633:141183633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1074G>T
AA Mutation	p.Glu358Asp(p.E358D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000609684
Start	141184178:141184178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1619C>T
AA Mutation	p.Ala540Val(p.A540V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000609684
Start	141184511:141184511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1952C>T
AA Mutation	p.Pro651Leu(p.P651L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000609684
Start	141184292:141184292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781886261
CDS Mutation	c.1733G>A
AA Mutation	p.Arg578Gln(p.R578Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000609684
Start	141183486:141183486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.927C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000609684
Start	141184716:141184716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781822956
CDS Mutation	c.2157G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000609684
Start	141184653:141184653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2094G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000609684
Start	141184035:141184035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1476G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000609684
Start	141184458:141184458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1899C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000609684
Start	141182871:141182871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.312A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000609684
Start	141184597:141184597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2038C>T
AA Mutation	p.Gln680Ter(p.Q680*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000609684
Start	141183463:141183463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.904C>T
AA Mutation	p.Arg302Ter(p.R302*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000609684
Start	141183223:141183223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.664C>T
AA Mutation	p.Arg222Ter(p.R222*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PCDHB16

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000609684
Start	141182977:141182977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.418C>A
AA Mutation	p.Leu140Ile(p.L140I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000609684
Start	141184586:141184586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2027C>T
AA Mutation	p.Ala676Val(p.A676V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000609684
Start	141184525:141184525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1966G>A
AA Mutation	p.Ala656Thr(p.A656T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000609684
Start	141184331:141184331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1772C>T
AA Mutation	p.Ala591Val(p.A591V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000609684
Start	141184526:141184526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1967C>T
AA Mutation	p.Ala656Val(p.A656V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript