Colon Cancer: Gene >> NPAS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000335681
Start	100964137:100964137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.678C>A
AA Mutation	p.Phe226Leu(p.F226L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000335681
Start	100964151:100964151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749630318
CDS Mutation	c.692G>A
AA Mutation	p.Arg231His(p.R231H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000335681
Start	100964130:100964130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.671T>G
AA Mutation	p.Val224Gly(p.V224G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000335681
Start	100988187:100988187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368846782
CDS Mutation	c.1738G>A
AA Mutation	p.Gly580Arg(p.G580R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000335681
Start	100977785:100977785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778685112
CDS Mutation	c.1468G>A
AA Mutation	p.Ala490Thr(p.A490T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000335681
Start	100993475:100993475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751284957
CDS Mutation	c.2240C>T
AA Mutation	p.Ser747Leu(p.S747L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000335681
Start	100932925:100932925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775528411
CDS Mutation	c.197C>T
AA Mutation	p.Thr66Met(p.T66M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000335681
Start	100937774:100937774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753351516
CDS Mutation	c.295G>A
AA Mutation	p.Ala99Thr(p.A99T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335681
Start	100993407:100993407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143542914
CDS Mutation	c.2172C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335681
Start	100990354:100990354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776277664
CDS Mutation	c.1926G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335681
Start	100990297:100990297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371612685
CDS Mutation	c.1869C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335681
Start	100975549:100975549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1374C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> NPAS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000335681
Start	100937774:100937774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753351516
CDS Mutation	c.295G>A
AA Mutation	p.Ala99Thr(p.A99T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000335681
Start	100982235:100982235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs530175072
CDS Mutation	c.1487C>T
AA Mutation	p.Ser496Leu(p.S496L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript