Colon Cancer: Gene >> ARMCX1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372829
Start	101553345:101553345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.415G>A
AA Mutation	p.Ala139Thr(p.A139T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372829
Start	101554045:101554045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1115A>C
AA Mutation	p.Glu372Ala(p.E372A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000372829
Start	101553229:101553229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.299G>A
AA Mutation	p.Ser100Asn(p.S100N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000372829
Start	101553580:101553580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.650C>T
AA Mutation	p.Thr217Ile(p.T217I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000372829
Start	101554002:101554002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1072C>T
AA Mutation	p.Pro358Ser(p.P358S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000372829
Start	101552943:101552943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.13C>T
AA Mutation	p.Arg5Trp(p.R5W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000372829
Start	101553910:101553910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.980A>G
AA Mutation	p.Tyr327Cys(p.Y327C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000372829
Start	101553390:101553390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.460C>T
AA Mutation	p.Pro154Ser(p.P154S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000372829
Start	101553364:101553364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.434C>A
AA Mutation	p.Pro145Gln(p.P145Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000372829
Start	101553424:101553424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.494C>T
AA Mutation	p.Ala165Val(p.A165V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000372829
Start	101553192:101553192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.262C>T
AA Mutation	p.Pro88Ser(p.P88S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372829
Start	101552957:101552957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.27C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372829
Start	101553908:101553908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.978C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372829
Start	101553878:101553878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.948T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372829
Start	101553113:101553113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.183C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000372829
Start	101553482:101553483(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.555_559dupGCCTG
AA Mutation	p.Val187GlyfsTer18(p.V187Gfs*18)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ARMCX1

No Mutation Annotation!