Colon Cancer: Gene >> SLC14A2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000255226
Start	45667038:45667038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1661G>T
AA Mutation	p.Ser554Ile(p.S554I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000255226
Start	45663790:45663790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs556141911
CDS Mutation	c.1357G>A
AA Mutation	p.Gly453Ser(p.G453S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000255226
Start	45625689:45625689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200534486
CDS Mutation	c.157C>T
AA Mutation	p.Arg53Trp(p.R53W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000255226
Start	45667841:45667841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1726C>T
AA Mutation	p.Pro576Ser(p.P576S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000255226
Start	45639809:45639809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767386635
CDS Mutation	c.907G>A
AA Mutation	p.Gly303Ser(p.G303S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000255226
Start	45639803:45639803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.901A>G
AA Mutation	p.Thr301Ala(p.T301A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000255226
Start	45673695:45673695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776377373
CDS Mutation	c.2390C>T
AA Mutation	p.Ala797Val(p.A797V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000255226
Start	45667959:45667959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779206322
CDS Mutation	c.1844C>T
AA Mutation	p.Ala615Val(p.A615V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000255226
Start	45637141:45637141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.802T>G
AA Mutation	p.Ser268Ala(p.S268A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255226
Start	45667912:45667912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369173950
CDS Mutation	c.1797C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255226
Start	45639772:45639772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777983375
CDS Mutation	c.870C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255226
Start	45639817:45639817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753723423
CDS Mutation	c.915C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255226
Start	45627115:45627115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367796494
CDS Mutation	c.489G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255226
Start	45632422:45632422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143328575
CDS Mutation	c.594G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SLC14A2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000255226
Start	45639840:45639840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758464911
CDS Mutation	c.938C>T
AA Mutation	p.Ser313Leu(p.S313L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000255226
Start	45625825:45625825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.293T>C
AA Mutation	p.Leu98Pro(p.L98P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000255226
Start	45666139:45666139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1477T>A
AA Mutation	p.Phe493Ile(p.F493I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000255226
Start	45667959:45667959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779206322
CDS Mutation	c.1844C>T
AA Mutation	p.Ala615Val(p.A615V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255226
Start	45673810:45673810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139049054
CDS Mutation	c.2505C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000255226
Start	45625724:45625724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767916603
CDS Mutation	c.192C>T
Mutation Classification	Silent
Feature Type	Transcript