Colon Cancer: Gene >> SLC22A16

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368919
Start	110442495:110442495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs557250493
CDS Mutation	c.932T>C
AA Mutation	p.Met311Thr(p.M311T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368919
Start	110442268:110442268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1159G>A
AA Mutation	p.Glu387Lys(p.E387K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368919
Start	110456789:110456789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.282G>T
AA Mutation	p.Glu94Asp(p.E94D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000368919
Start	110446957:110446957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.567C>A
AA Mutation	p.Ser189Arg(p.S189R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000368919
Start	110438809:110438809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144862556
CDS Mutation	c.1222G>A
AA Mutation	p.Ala408Thr(p.A408T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000368919
Start	110424913:110424913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757260946
CDS Mutation	c.1694C>T
AA Mutation	p.Thr565Met(p.T565M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000368919
Start	110442603:110442603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.824C>A
AA Mutation	p.Ser275Tyr(p.S275Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000368919
Start	110424964:110424964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1643G>T
AA Mutation	p.Ser548Ile(p.S548I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368919
Start	110425049:110425049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1558T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368919
Start	110424906:110424906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748989233
CDS Mutation	c.1701G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368919
Start	110442359:110442359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201904861
CDS Mutation	c.1068G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368919
Start	110424914:110424914(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1693delA
AA Mutation	p.Thr565ArgfsTer21(p.T565Rfs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SLC22A16

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368919
Start	110442715:110442715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.712T>A
AA Mutation	p.Ser238Thr(p.S238T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368919
Start	110442343:110442343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149834139
CDS Mutation	c.1084G>A
AA Mutation	p.Val362Ile(p.V362I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368919
Start	110425081:110425081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1526T>G
AA Mutation	p.Phe509Cys(p.F509C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript