Colon Cancer: Gene >> ARHGEF28

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000426542
Start	73858204:73858204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2032T>C
AA Mutation	p.Ser678Pro(p.S678P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000426542
Start	73885900:73885900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750588590
CDS Mutation	c.3106G>T
AA Mutation	p.Asp1036Tyr(p.D1036Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000426542
Start	73892104:73892104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3440C>T
AA Mutation	p.Ala1147Val(p.A1147V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000426542
Start	73904237:73904237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4090T>G
AA Mutation	p.Phe1364Val(p.F1364V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000426542
Start	73909539:73909539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4289C>T
AA Mutation	p.Ala1430Val(p.A1430V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000426542
Start	73858139:73858139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777295435
CDS Mutation	c.1967C>T
AA Mutation	p.Ala656Val(p.A656V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000426542
Start	73909616:73909616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4366C>T
AA Mutation	p.Arg1456Cys(p.R1456C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000426542
Start	73840552:73840552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767417665
CDS Mutation	c.1219T>C
AA Mutation	p.Cys407Arg(p.C407R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000426542
Start	73883794:73883794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747665438
CDS Mutation	c.2965C>T
AA Mutation	p.Arg989Cys(p.R989C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000426542
Start	73867999:73867999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2276T>C
AA Mutation	p.Val759Ala(p.V759A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000426542
Start	73901214:73901214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4004G>A
AA Mutation	p.Gly1335Asp(p.G1335D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000426542
Start	73776655:73776655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.799C>G
AA Mutation	p.Leu267Val(p.L267V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000426542
Start	73868016:73868016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2293G>A
AA Mutation	p.Glu765Lys(p.E765K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000426542
Start	73909608:73909608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139349480
CDS Mutation	c.4358G>A
AA Mutation	p.Arg1453His(p.R1453H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000426542
Start	73898006:73898006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368673332
CDS Mutation	c.3886G>A
AA Mutation	p.Val1296Met(p.V1296M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000426542
Start	73867931:73867931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2208C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000426542
Start	73852672:73852672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs535155177
CDS Mutation	c.1770G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000426542
Start	73753120:73753120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.393C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000426542
Start	73883797:73883797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771514690
CDS Mutation	c.2968C>T
AA Mutation	p.Arg990Ter(p.R990*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ARHGEF28

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000426542
Start	73901210:73901210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762965898
CDS Mutation	c.4000A>G
AA Mutation	p.Arg1334Gly(p.R1334G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000426542
Start	73873119:73873119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2687G>T
AA Mutation	p.Cys896Phe(p.C896F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000426542
Start	73885854:73885854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3060A>C
AA Mutation	p.Arg1020Ser(p.R1020S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000426542
Start	73753010:73753010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.283A>T
AA Mutation	p.Met95Leu(p.M95L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000426542
Start	73840698:73840698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759407440
CDS Mutation	c.1365C>G
AA Mutation	p.Asn455Lys(p.N455K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000426542
Start	73840664:73840664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1331C>G
AA Mutation	p.Ser444Cys(p.S444C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000426542
Start	73893245:73893245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3615G>T
AA Mutation	p.Lys1205Asn(p.K1205N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000426542
Start	73780741:73780741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.906A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000426542
Start	73752961:73752961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.234T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000426542
Start	73832444:73832444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1131T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000426542
Start	73870184:73870184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2541C>T
Mutation Classification	Silent
Feature Type	Transcript