Colon Cancer: Gene >> TRPV6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359396
Start	142885480:142885480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.37C>A
AA Mutation	p.Leu13Ile(p.L13I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359396
Start	142875617:142875617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.973G>A
AA Mutation	p.Gly325Arg(p.G325R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359396
Start	142876790:142876790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.535G>A
AA Mutation	p.Val179Met(p.V179M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000359396
Start	142872450:142872450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751323691
CDS Mutation	c.1817G>A
AA Mutation	p.Arg606Gln(p.R606Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000359396
Start	142877717:142877717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs111318322
CDS Mutation	c.283G>A
AA Mutation	p.Ala95Thr(p.A95T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000359396
Start	142875581:142875581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1009C>A
AA Mutation	p.Leu337Met(p.L337M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000359396
Start	142877755:142877755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375523215
CDS Mutation	c.245C>T
AA Mutation	p.Ala82Val(p.A82V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000359396
Start	142872418:142872418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs576385529
CDS Mutation	c.1849G>A
AA Mutation	p.Gly617Arg(p.G617R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000359396
Start	142871733:142871733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757082631
CDS Mutation	c.2152G>A
AA Mutation	p.Gly718Arg(p.G718R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000359396
Start	142875133:142875133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1154G>A
AA Mutation	p.Arg385Gln(p.R385Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000359396
Start	142875866:142875866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.801G>T
AA Mutation	p.Gln267His(p.Q267H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000359396
Start	142875676:142875676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745408146
CDS Mutation	c.914G>A
AA Mutation	p.Arg305His(p.R305H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000359396
Start	142876551:142876551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.619C>G
AA Mutation	p.Pro207Ala(p.P207A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000359396
Start	142871828:142871828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2057G>A
AA Mutation	p.Arg686Gln(p.R686Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000359396
Start	142875161:142875161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1126G>A
AA Mutation	p.Ala376Thr(p.A376T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000359396
Start	142876427:142876427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.743G>A
AA Mutation	p.Gly248Glu(p.G248E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000359396
Start	142877259:142877259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769078836
CDS Mutation	c.370G>A
AA Mutation	p.Ala124Thr(p.A124T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000359396
Start	142877771:142877771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.229G>A
AA Mutation	p.Ala77Thr(p.A77T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000359396
Start	142875894:142875894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.773A>G
AA Mutation	p.His258Arg(p.H258R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359396
Start	142877170:142877170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.459C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359396
Start	142875657:142875657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369054271
CDS Mutation	c.933G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359396
Start	142876791:142876791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138110961
CDS Mutation	c.534C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359396
Start	142874569:142874569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1374C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TRPV6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359396
Start	142877162:142877162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.467C>A
AA Mutation	p.Pro156His(p.P156H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359396
Start	142871949:142871949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763838443
CDS Mutation	c.1936C>T
AA Mutation	p.Arg646Cys(p.R646C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359396
Start	142871763:142871763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762397125
CDS Mutation	c.2122C>T
AA Mutation	p.Arg708Cys(p.R708C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000359396
Start	142874139:142874139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1456A>G
AA Mutation	p.Ile486Val(p.I486V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000359396
Start	142877265:142877265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.364C>G
AA Mutation	p.His122Asp(p.H122D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000359396
Start	142885483:142885483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.34A>G
AA Mutation	p.Ile12Val(p.I12V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript