Colon Cancer: Gene >> PANK2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000316562
Start	3889350:3889350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.250C>G
AA Mutation	p.Arg84Gly(p.R84G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000316562
Start	3912472:3912472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1250C>T
AA Mutation	p.Thr417Ile(p.T417I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000316562
Start	3889149:3889149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.49C>A
AA Mutation	p.Pro17Thr(p.P17T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000316562
Start	3912556:3912556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1334A>G
AA Mutation	p.Lys445Arg(p.K445R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316562
Start	3917017:3917017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1503T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316562
Start	3912611:3912611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1389G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316562
Start	3923291:3923291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762044608
CDS Mutation	c.1710G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316562
Start	3908266:3908266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.969G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PANK2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000316562
Start	3908048:3908048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.751T>G
AA Mutation	p.Tyr251Asp(p.Y251D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000316562
Start	3908202:3908202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.905A>C
AA Mutation	p.Lys302Thr(p.K302T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316562
Start	3908212:3908212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751910368
CDS Mutation	c.915G>A
Mutation Classification	Silent
Feature Type	Transcript