Colon Cancer: Gene >> JRK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000612905
Start	142665263:142665263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.796A>T
AA Mutation	p.Ile266Phe(p.I266F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000612905
Start	142664614:142664614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1445G>A
AA Mutation	p.Gly482Asp(p.G482D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000612905
Start	142666015:142666015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.44G>A
AA Mutation	p.Arg15Gln(p.R15Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000612905
Start	142664930:142664930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375018716
CDS Mutation	c.1129G>A
AA Mutation	p.Val377Ile(p.V377I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000612905
Start	142665145:142665145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.914C>T
AA Mutation	p.Pro305Leu(p.P305L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000612905
Start	142665564:142665564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.495C>G
AA Mutation	p.Phe165Leu(p.F165L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000612905
Start	142665574:142665574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781950867
CDS Mutation	c.485C>T
AA Mutation	p.Ala162Val(p.A162V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000612905
Start	142665746:142665746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782306597
CDS Mutation	c.313G>A
AA Mutation	p.Val105Ile(p.V105I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000612905
Start	142664504:142664504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs2978972
CDS Mutation	c.1555C>T
AA Mutation	p.Arg519Cys(p.R519C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000612905
Start	142664945:142664945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782289704
CDS Mutation	c.1114G>A
AA Mutation	p.Ala372Thr(p.A372T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000612905
Start	142665341:142665341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782134634
CDS Mutation	c.718G>A
AA Mutation	p.Gly240Ser(p.G240S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000612905
Start	142665628:142665628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.431G>A
AA Mutation	p.Gly144Asp(p.G144D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000612905
Start	142664890:142664890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782654867
CDS Mutation	c.1169C>T
AA Mutation	p.Ala390Val(p.A390V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000612905
Start	142664370:142664370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1689C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000612905
Start	142665837:142665837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781865813
CDS Mutation	c.222G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000612905
Start	142665256:142665257(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.802dupT
AA Mutation	p.Ser268PhefsTer47(p.S268Ffs*47)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> JRK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000612905
Start	142664920:142664920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782712137
CDS Mutation	c.1139G>A
AA Mutation	p.Arg380Gln(p.R380Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000612905
Start	142664978:142664978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199539351
CDS Mutation	c.1081G>A
AA Mutation	p.Asp361Asn(p.D361N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000612905
Start	142664772:142664772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1287G>A
Mutation Classification	Silent
Feature Type	Transcript