Colon Cancer: Gene >> RAG1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000299440
Start	36576081:36576081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2777A>C
AA Mutation	p.Lys926Thr(p.K926T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000299440
Start	36573404:36573404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778391388
CDS Mutation	c.100C>T
AA Mutation	p.Arg34Trp(p.R34W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000299440
Start	36575399:36575399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199474676
CDS Mutation	c.2095C>T
AA Mutation	p.Arg699Trp(p.R699W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000299440
Start	36575030:36575030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1726G>T
AA Mutation	p.Asp576Tyr(p.D576Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000299440
Start	36575513:36575513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760816389
CDS Mutation	c.2209C>T
AA Mutation	p.Arg737Cys(p.R737C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000299440
Start	36574103:36574103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148393376
CDS Mutation	c.799G>A
AA Mutation	p.Ala267Thr(p.A267T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000299440
Start	36573429:36573429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.125C>A
AA Mutation	p.Pro42His(p.P42H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000299440
Start	36575480:36575480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2176T>C
AA Mutation	p.Ser726Pro(p.S726P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000299440
Start	36575287:36575287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1983G>A
AA Mutation	p.Met661Ile(p.M661I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000299440
Start	36575313:36575313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139863630
CDS Mutation	c.2009C>T
AA Mutation	p.Thr670Met(p.T670M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000299440
Start	36574509:36574509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1205T>C
AA Mutation	p.Leu402Pro(p.L402P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000299440
Start	36574211:36574211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.907C>A
AA Mutation	p.Pro303Thr(p.P303T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000299440
Start	36575652:36575652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2348C>T
AA Mutation	p.Ser783Leu(p.S783L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000299440
Start	36573867:36573867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.563G>A
AA Mutation	p.Ser188Asn(p.S188N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000299440
Start	36574794:36574794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1490G>A
AA Mutation	p.Arg497Lys(p.R497K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000299440
Start	36576343:36576343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3039A>C
AA Mutation	p.Lys1013Asn(p.K1013N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000299440
Start	36575994:36575994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2690G>A
AA Mutation	p.Arg897Gln(p.R897Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299440
Start	36574834:36574834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1530G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299440
Start	36573586:36573586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148700564
CDS Mutation	c.282C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299440
Start	36573982:36573982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.678T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299440
Start	36576094:36576094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2790G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299440
Start	36574873:36574873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1569G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299440
Start	36573901:36573901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148288583
CDS Mutation	c.597C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299440
Start	36573857:36573857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.553A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000299440
Start	36575240:36575240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1936G>T
AA Mutation	p.Glu646Ter(p.E646*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RAG1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000299440
Start	36573627:36573627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748211230
CDS Mutation	c.323G>A
AA Mutation	p.Arg108Gln(p.R108Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000299440
Start	36573451:36573451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.147G>T
AA Mutation	p.Lys49Asn(p.K49N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000299440
Start	36574964:36574964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1660G>A
AA Mutation	p.Asp554Asn(p.D554N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299440
Start	36576211:36576211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2907A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299440
Start	36573790:36573790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753042511
CDS Mutation	c.486T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299440
Start	36573811:36573811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.507G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000299440
Start	36576197:36576197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2893G>T
AA Mutation	p.Glu965Ter(p.E965*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript