Colon Cancer: Gene >> ROBO3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000397801
Start	124865642:124865642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.65A>T
AA Mutation	p.Asp22Val(p.D22V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000397801
Start	124875974:124875974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2442G>T
AA Mutation	p.Glu814Asp(p.E814D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000397801
Start	124875238:124875238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2201T>A
AA Mutation	p.Leu734His(p.L734H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000397801
Start	124870168:124870168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750349831
CDS Mutation	c.770G>A
AA Mutation	p.Arg257His(p.R257H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000397801
Start	124868897:124868897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.256C>T
AA Mutation	p.Arg86Cys(p.R86C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000397801
Start	124877527:124877527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2855T>C
AA Mutation	p.Met952Thr(p.M952T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000397801
Start	124876437:124876437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2756G>A
AA Mutation	p.Arg919His(p.R919H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000397801
Start	124868825:124868825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.184G>A
AA Mutation	p.Ala62Thr(p.A62T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000397801
Start	124873754:124873754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1676C>A
AA Mutation	p.Pro559His(p.P559H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000397801
Start	124875211:124875211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2174G>A
AA Mutation	p.Ser725Asn(p.S725N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000397801
Start	124872462:124872462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1240G>A
AA Mutation	p.Val414Met(p.V414M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000397801
Start	124877179:124877179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201504479
CDS Mutation	c.2798C>T
AA Mutation	p.Pro933Leu(p.P933L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000397801
Start	124870045:124870045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.743C>T
AA Mutation	p.Ala248Val(p.A248V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000397801
Start	124868994:124868994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.353T>C
AA Mutation	p.Leu118Pro(p.L118P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397801
Start	124875248:124875248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2211G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397801
Start	124872455:124872455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1233C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397801
Start	124874861:124874861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2025G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397801
Start	124872937:124872937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1384C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397801
Start	124874229:124874229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1944T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397801
Start	124880530:124880530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4071C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397801
Start	124874903:124874903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2067C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397801
Start	124865661:124865661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.84G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397801
Start	124868947:124868947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.306G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397801
Start	124877277:124877277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2814G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397801
Start	124873372:124873372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752023556
CDS Mutation	c.1599C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000397801
Start	124869527:124869527(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.571delC
AA Mutation	p.Arg191AlafsTer31(p.R191Afs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000397801
Start	124878121:124878121(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3175delG
AA Mutation	p.Asp1059ThrfsTer9(p.D1059Tfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	stop_gained
Transcription ID	ENST00000397801
Start	124869596:124869596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.634G>T
AA Mutation	p.Gly212Ter(p.G212*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000397801
Start	124871098:124871099(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1124dupC
AA Mutation	p.Pro376ThrfsTer35(p.P376Tfs*35)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000397801
Start	124869526:124869527(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs756837590
CDS Mutation	c.571dupC
AA Mutation	p.Arg191ProfsTer61(p.R191Pfs*61)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ROBO3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000397801
Start	124880459:124880459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374478103
CDS Mutation	c.4000C>T
AA Mutation	p.Arg1334Trp(p.R1334W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000397801
Start	124879300:124879300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3644T>G
AA Mutation	p.Leu1215Arg(p.L1215R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000397801
Start	124872381:124872381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1159G>A
AA Mutation	p.Val387Ile(p.V387I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000397801
Start	124875304:124875304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2267G>A
AA Mutation	p.Ser756Asn(p.S756N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000397801
Start	124870696:124870696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373820994
CDS Mutation	c.1001G>A
AA Mutation	p.Arg334His(p.R334H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397801
Start	124877277:124877277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2814G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397801
Start	124871057:124871057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1077T>A
Mutation Classification	Silent
Feature Type	Transcript