Colon Cancer: Gene >> ADGRB2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373658
Start	31728201:31728201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749337394
CDS Mutation	c.4496G>A
AA Mutation	p.Arg1499His(p.R1499H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373658
Start	31756188:31756188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747551189
CDS Mutation	c.649G>A
AA Mutation	p.Gly217Ser(p.G217S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373658
Start	31730906:31730906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4274C>T
AA Mutation	p.Pro1425Leu(p.P1425L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000373658
Start	31730882:31730882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368168880
CDS Mutation	c.4298G>A
AA Mutation	p.Arg1433His(p.R1433H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000373658
Start	31731011:31731011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4169C>T
AA Mutation	p.Ala1390Val(p.A1390V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000373658
Start	31735214:31735214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3421C>A
AA Mutation	p.Leu1141Met(p.L1141M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000373658
Start	31727598:31727598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4580C>T
AA Mutation	p.Pro1527Leu(p.P1527L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000373658
Start	31756743:31756743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754770509
CDS Mutation	c.94G>A
AA Mutation	p.Ala32Thr(p.A32T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000373658
Start	31744731:31744731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.839G>T
AA Mutation	p.Gly280Val(p.G280V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000373658
Start	31756229:31756229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774342144
CDS Mutation	c.608G>A
AA Mutation	p.Arg203His(p.R203H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000373658
Start	31730900:31730900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146789434
CDS Mutation	c.4280C>T
AA Mutation	p.Pro1427Leu(p.P1427L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000373658
Start	31730852:31730852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761734906
CDS Mutation	c.4328G>A
AA Mutation	p.Arg1443Gln(p.R1443Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000373658
Start	31756592:31756592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.245G>A
AA Mutation	p.Arg82His(p.R82H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000373658
Start	31742994:31742994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1096G>A
AA Mutation	p.Val366Met(p.V366M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000373658
Start	31738894:31738894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2539C>T
AA Mutation	p.Arg847Cys(p.R847C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000373658
Start	31756217:31756217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199605095
CDS Mutation	c.620A>G
AA Mutation	p.Glu207Gly(p.E207G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000373658
Start	31739431:31739431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774818699
CDS Mutation	c.2372C>T
AA Mutation	p.Thr791Met(p.T791M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000373658
Start	31741865:31741865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774040499
CDS Mutation	c.1520C>T
AA Mutation	p.Thr507Met(p.T507M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000373658
Start	31730883:31730883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776687412
CDS Mutation	c.4297C>T
AA Mutation	p.Arg1433Cys(p.R1433C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000373658
Start	31739615:31739615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2188C>T
AA Mutation	p.Pro730Ser(p.P730S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000373658
Start	31732980:31732980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151028224
CDS Mutation	c.3616C>T
AA Mutation	p.Arg1206Cys(p.R1206C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000373658
Start	31756335:31756335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773280182
CDS Mutation	c.502G>A
AA Mutation	p.Glu168Lys(p.E168K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000373658
Start	31741937:31741937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1448C>T
AA Mutation	p.Ala483Val(p.A483V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373658
Start	31742914:31742914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1176G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373658
Start	31736335:31736335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766161972
CDS Mutation	c.3186C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373658
Start	31756327:31756327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745764525
CDS Mutation	c.510G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373658
Start	31739996:31739996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781573880
CDS Mutation	c.2097G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373658
Start	31728239:31728239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143976016
CDS Mutation	c.4458C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373658
Start	31730923:31730923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs577696912
CDS Mutation	c.4257T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373658
Start	31732544:31732544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201162344
CDS Mutation	c.3693G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373658
Start	31740518:31740518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1818G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373658
Start	31735214:31735214(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3421delC
AA Mutation	p.Leu1141CysfsTer35(p.L1141Cfs*35)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	stop_gained
Transcription ID	ENST00000373658
Start	31731030:31731030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4150C>T
AA Mutation	p.Arg1384Ter(p.R1384*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000373658
Start	31738631:31738631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2602-1G>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ADGRB2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373658
Start	31736334:31736334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3187G>A
AA Mutation	p.Gly1063Ser(p.G1063S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373658
Start	31728072:31728072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749363644
CDS Mutation	c.4525C>T
AA Mutation	p.Arg1509Trp(p.R1509W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373658
Start	31756366:31756366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751925666
CDS Mutation	c.471C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373658
Start	31742129:31742129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs530331422
CDS Mutation	c.1341C>T
Mutation Classification	Silent
Feature Type	Transcript