Colon Cancer: Gene >> IL7R

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000303115
Start	35873510:35873510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.568C>T
AA Mutation	p.Leu190Phe(p.L190F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000303115
Start	35867354:35867354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.270G>T
AA Mutation	p.Glu90Asp(p.E90D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000303115
Start	35871157:35871157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.481A>C
AA Mutation	p.Lys161Gln(p.K161Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000303115
Start	35856990:35856990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.13G>T
AA Mutation	p.Gly5Cys(p.G5C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000303115
Start	35876371:35876371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1265A>T
AA Mutation	p.Gln422Leu(p.Q422L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000303115
Start	35867347:35867347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.263T>C
AA Mutation	p.Leu88Pro(p.L88P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000303115
Start	35873632:35873632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.690G>T
AA Mutation	p.Glu230Asp(p.E230D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000303115
Start	35867421:35867421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.337G>A
AA Mutation	p.Glu113Lys(p.E113K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000303115
Start	35867321:35867321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs552630274
CDS Mutation	c.237G>T
AA Mutation	p.Glu79Asp(p.E79D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000303115
Start	35873620:35873620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.678C>A
AA Mutation	p.Phe226Leu(p.F226L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303115
Start	35876382:35876382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1276C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303115
Start	35867381:35867381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.297C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303115
Start	35873533:35873533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201431556
CDS Mutation	c.591G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303115
Start	35874501:35874501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201268331
CDS Mutation	c.759C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000303115
Start	35867439:35867439(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.361delA
AA Mutation	p.Ile121Ter(p.I121*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> IL7R

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000303115
Start	35871121:35871121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.445A>G
AA Mutation	p.Thr149Ala(p.T149A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000303115
Start	35873609:35873609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.667A>C
AA Mutation	p.Ser223Arg(p.S223R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000303115
Start	35860854:35860854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.85G>T
AA Mutation	p.Asp29Tyr(p.D29Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript