Colon Cancer: Gene >> CHRNA4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370263
Start	63349711:63349711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs76895198
CDS Mutation	c.1700C>T
AA Mutation	p.Ala567Val(p.A567V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370263
Start	63350885:63350885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.526A>G
AA Mutation	p.Thr176Ala(p.T176A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370263
Start	63350224:63350224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1187G>T
AA Mutation	p.Ser396Ile(p.S396I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000370263
Start	63359613:63359613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.163G>A
AA Mutation	p.Val55Met(p.V55M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000370263
Start	63349979:63349979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1432G>A
AA Mutation	p.Val478Met(p.V478M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000370263
Start	63349777:63349777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121912282
CDS Mutation	c.1634C>T
AA Mutation	p.Thr545Met(p.T545M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000370263
Start	63350227:63350227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121912269
CDS Mutation	c.1184C>T
AA Mutation	p.Thr395Met(p.T395M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000370263
Start	63350599:63350599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.812G>A
AA Mutation	p.Cys271Tyr(p.C271Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000370263
Start	63350654:63350654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.757C>A
AA Mutation	p.Pro253Thr(p.P253T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000370263
Start	63350921:63350921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.490G>A
AA Mutation	p.Asp164Asn(p.D164N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000370263
Start	63359678:63359678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201575409
CDS Mutation	c.98G>A
AA Mutation	p.Arg33Gln(p.R33Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000370263
Start	63350194:63350194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777222517
CDS Mutation	c.1217C>T
AA Mutation	p.Pro406Leu(p.P406L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000370263
Start	63350918:63350918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762764855
CDS Mutation	c.493G>A
AA Mutation	p.Val165Ile(p.V165I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370263
Start	63350682:63350682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121912253
CDS Mutation	c.729G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370263
Start	63350517:63350517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.894C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370263
Start	63350679:63350679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752054605
CDS Mutation	c.732C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370263
Start	63350193:63350193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200528988
CDS Mutation	c.1218G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370263
Start	63350730:63350730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs45588436
CDS Mutation	c.681C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370263
Start	63356386:63356386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140239470
CDS Mutation	c.258C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370263
Start	63349683:63349683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1728C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CHRNA4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370263
Start	63350822:63350822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144716263
CDS Mutation	c.589C>T
AA Mutation	p.Arg197Cys(p.R197C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370263
Start	63350527:63350527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.884T>G
AA Mutation	p.Ile295Ser(p.I295S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370263
Start	63349886:63349886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142137599
CDS Mutation	c.1525G>A
AA Mutation	p.Ala509Thr(p.A509T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370263
Start	63350124:63350124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1287C>A
Mutation Classification	Silent
Feature Type	Transcript