Colon Cancer: Gene >> RAPGEF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372189
Start	131584376:131584376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2791G>T
AA Mutation	p.Ala931Ser(p.A931S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372189
Start	131621898:131621898(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1752G>T
AA Mutation	p.Lys584Asn(p.K584N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000372189
Start	131643258:131643258(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760601332
CDS Mutation	c.424G>A
AA Mutation	p.Asp142Asn(p.D142N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000372189
Start	131638706:131638706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.529G>A
AA Mutation	p.Val177Met(p.V177M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000372189
Start	131584521:131584521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2751G>A
AA Mutation	p.Met917Ile(p.M917I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000372189
Start	131579513:131579513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs34330901
CDS Mutation	c.3218G>A
AA Mutation	p.Arg1073Gln(p.R1073Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000372189
Start	131592178:131592178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2137G>A
AA Mutation	p.Val713Met(p.V713M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000372189
Start	131626230:131626230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1343A>C
AA Mutation	p.Gln448Pro(p.Q448P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000372189
Start	131643312:131643312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.370C>T
AA Mutation	p.Leu124Phe(p.L124F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000372189
Start	131579501:131579501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3230C>G
AA Mutation	p.Thr1077Ser(p.T1077S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000372189
Start	131630312:131630312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.613C>T
AA Mutation	p.Leu205Phe(p.L205F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000372189
Start	131579514:131579514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747478083
CDS Mutation	c.3217C>T
AA Mutation	p.Arg1073Trp(p.R1073W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000372189
Start	131582693:131582693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2866G>A
AA Mutation	p.Glu956Lys(p.E956K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000372189
Start	131584591:131584591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779896256
CDS Mutation	c.2681G>A
AA Mutation	p.Arg894Gln(p.R894Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000372189
Start	131625957:131625957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1616A>C
AA Mutation	p.Lys539Thr(p.K539T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000372189
Start	131602128:131602128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762417571
CDS Mutation	c.1876G>A
AA Mutation	p.Gly626Arg(p.G626R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372189
Start	131626217:131626217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370830882
CDS Mutation	c.1356G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372189
Start	131596365:131596365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200827749
CDS Mutation	c.2064C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372189
Start	131584566:131584566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2706G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372189
Start	131626334:131626334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201940435
CDS Mutation	c.1239G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372189
Start	131589936:131589936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2259C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372189
Start	131592167:131592167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759382126
CDS Mutation	c.2148C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372189
Start	131602105:131602105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs549201601
CDS Mutation	c.1899G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372189
Start	131596356:131596356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372772375
CDS Mutation	c.2073C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RAPGEF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372189
Start	131589908:131589908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2287G>A
AA Mutation	p.Val763Ile(p.V763I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372189
Start	131625984:131625984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763837636
CDS Mutation	c.1589C>T
AA Mutation	p.Ala530Val(p.A530V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000372189
Start	131650864:131650864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374143304
CDS Mutation	c.96G>T
AA Mutation	p.Lys32Asn(p.K32N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000372189
Start	131650154:131650154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.239T>G
AA Mutation	p.Val80Gly(p.V80G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372189
Start	131589909:131589909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2286G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372189
Start	131589915:131589915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2280C>T
Mutation Classification	Silent
Feature Type	Transcript