Colon Cancer: Gene >> IL17RD

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296318
Start	57098414:57098414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1289T>C
AA Mutation	p.Val430Ala(p.V430A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000296318
Start	57097725:57097725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756741660
CDS Mutation	c.1978C>T
AA Mutation	p.Arg660Trp(p.R660W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000296318
Start	57098295:57098295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1408G>A
AA Mutation	p.Ala470Thr(p.A470T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000296318
Start	57098073:57098073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1630G>A
AA Mutation	p.Val544Ile(p.V544I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000296318
Start	57098130:57098130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1573A>G
AA Mutation	p.Thr525Ala(p.T525A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000296318
Start	57098453:57098453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1250T>C
AA Mutation	p.Phe417Ser(p.F417S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000296318
Start	57097667:57097667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2036T>C
AA Mutation	p.Met679Thr(p.M679T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000296318
Start	57098421:57098421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750856460
CDS Mutation	c.1282T>C
AA Mutation	p.Tyr428His(p.Y428H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000296318
Start	57097988:57097988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1715T>C
AA Mutation	p.Leu572Pro(p.L572P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296318
Start	57097726:57097726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1977G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296318
Start	57098215:57098215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1488C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296318
Start	57098128:57098128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1575G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296318
Start	57097651:57097651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2052G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296318
Start	57098296:57098296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746897778
CDS Mutation	c.1407C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000296318
Start	57096419:57096419(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2194delG
AA Mutation	p.Glu732AsnfsTer40(p.E732Nfs*40)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> IL17RD

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296318
Start	57097952:57097952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1751C>T
AA Mutation	p.Ser584Leu(p.S584L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000296318
Start	57110288:57110288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.334C>T
AA Mutation	p.Arg112Trp(p.R112W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000296318
Start	57098090:57098090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1613C>T
AA Mutation	p.Ser538Leu(p.S538L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000296318
Start	57102518:57102518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.940G>A
AA Mutation	p.Ala314Thr(p.A314T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000296318
Start	57103120:57103120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.839G>T
AA Mutation	p.Arg280Ile(p.R280I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000296318
Start	57104389:57104389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.766A>G
AA Mutation	p.Thr256Ala(p.T256A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296318
Start	57098011:57098011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200249733
CDS Mutation	c.1692C>T
Mutation Classification	Silent
Feature Type	Transcript