Colon Cancer: Gene >> PRKCD

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000330452
Start	53183186:53183186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.637G>A
AA Mutation	p.Ala213Thr(p.A213T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000330452
Start	53179631:53179631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.170C>T
AA Mutation	p.Ser57Leu(p.S57L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000330452
Start	53188836:53188836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1532C>A
AA Mutation	p.Thr511Asn(p.T511N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000330452
Start	53179683:53179683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.222G>A
AA Mutation	p.Met74Ile(p.M74I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000330452
Start	53178526:53178526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782070830
CDS Mutation	c.104C>T
AA Mutation	p.Ala35Val(p.A35V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000330452
Start	53186276:53186276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781872957
CDS Mutation	c.1196G>A
AA Mutation	p.Arg399Gln(p.R399Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000330452
Start	53183483:53183483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.689C>T
AA Mutation	p.Pro230Leu(p.P230L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000330452
Start	53189092:53189092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1589A>G
AA Mutation	p.Asp530Gly(p.D530G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000330452
Start	53179660:53179660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.199C>T
AA Mutation	p.Arg67Cys(p.R67C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000330452
Start	53183148:53183148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.599G>A
AA Mutation	p.Cys200Tyr(p.C200Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330452
Start	53179593:53179593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.132G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330452
Start	53192245:53192245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781808423
CDS Mutation	c.2010C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330452
Start	53189195:53189195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs564128768
CDS Mutation	c.1692G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000330452
Start	53186637:53186637(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1300delG
AA Mutation	p.Asp434ThrfsTer2(p.D434Tfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000330452
Start	53181452:53181452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.385C>T
AA Mutation	p.Gln129Ter(p.Q129*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000330452
Start	53186636:53186637(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1300dupG
AA Mutation	p.Asp434GlyfsTer13(p.D434Gfs*13)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> PRKCD

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000330452
Start	53181501:53181501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.434G>A
AA Mutation	p.Arg145His(p.R145H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330452
Start	53188795:53188795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1491G>A
Mutation Classification	Silent
Feature Type	Transcript