Colon Cancer: Gene >> SLC16A7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261187
Start	59774887:59774887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759736305
CDS Mutation	c.592C>A
AA Mutation	p.Leu198Ile(p.L198I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261187
Start	59775230:59775230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752116486
CDS Mutation	c.935G>A
AA Mutation	p.Arg312Gln(p.R312Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261187
Start	59779434:59779434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1192G>A
AA Mutation	p.Asp398Asn(p.D398N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261187
Start	59774779:59774779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.484G>A
AA Mutation	p.Ala162Thr(p.A162T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261187
Start	59779544:59779544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1302G>T
AA Mutation	p.Lys434Asn(p.K434N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261187
Start	59775096:59775096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.801C>A
AA Mutation	p.Phe267Leu(p.F267L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000261187
Start	59779476:59779476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1234G>A
AA Mutation	p.Ala412Thr(p.A412T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000261187
Start	59704985:59704985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.184T>C
AA Mutation	p.Ser62Pro(p.S62P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000261187
Start	59775410:59775410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1115C>T
AA Mutation	p.Ser372Phe(p.S372F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261187
Start	59774685:59774685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201840996
CDS Mutation	c.390C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261187
Start	59775339:59775339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1044C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261187
Start	59774849:59774849(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.557delT
AA Mutation	p.Leu186Ter(p.L186*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261187
Start	59775075:59775075(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.786delT
AA Mutation	p.Phe262LeufsTer39(p.F262Lfs*39)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261187
Start	59774937:59774938(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.643_644delGA
AA Mutation	p.Glu215ArgfsTer2(p.E215Rfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000261187
Start	59779446:59779446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1204G>T
AA Mutation	p.Glu402Ter(p.E402*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000261187
Start	59779581:59779581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1339G>T
AA Mutation	p.Glu447Ter(p.E447*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000261187
Start	59774722:59774722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755179284
CDS Mutation	c.427C>T
AA Mutation	p.Arg143Ter(p.R143*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261187
Start	59775074:59775075(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.786dupT
AA Mutation	p.Ala263CysfsTer11(p.A263Cfs*11)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261187
Start	59775247:59775248(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.952_953insATTCCTTG
AA Mutation	p.Ser318AsnfsTer85(p.S318Nfs*85)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261187
Start	59775249:59775250(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.954_955insC
AA Mutation	p.Phe319LeufsTer37(p.F319Lfs*37)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SLC16A7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261187
Start	59775091:59775091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.796A>T
AA Mutation	p.Ile266Leu(p.I266L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261187
Start	59704884:59704884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.83T>G
AA Mutation	p.Ile28Ser(p.I28S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261187
Start	59775137:59775137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766674596
CDS Mutation	c.842C>T
AA Mutation	p.Ser281Leu(p.S281L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261187
Start	59774686:59774686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs543596862
CDS Mutation	c.391G>A
AA Mutation	p.Ala131Thr(p.A131T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261187
Start	59775404:59775404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1109G>T
AA Mutation	p.Arg370Ile(p.R370I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261187
Start	59775006:59775006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.711A>C
AA Mutation	p.Leu237Phe(p.L237F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261187
Start	59775075:59775075(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.786delT
AA Mutation	p.Phe262LeufsTer39(p.F262Lfs*39)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript