Colon Cancer: Gene >> RANGAP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356244
Start	41268131:41268131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.266C>T
AA Mutation	p.Thr89Met(p.T89M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000356244
Start	41256022:41256022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1072A>T
AA Mutation	p.Ser358Cys(p.S358C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356244
Start	41268120:41268120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776060557
CDS Mutation	c.277C>T
AA Mutation	p.Arg93Trp(p.R93W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356244
Start	41256042:41256042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1052C>T
AA Mutation	p.Ala351Val(p.A351V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000356244
Start	41268104:41268104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.293C>A
AA Mutation	p.Pro98Gln(p.P98Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000356244
Start	41249342:41249342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748108526
CDS Mutation	c.1682C>T
AA Mutation	p.Ala561Val(p.A561V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000356244
Start	41268098:41268098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.299T>C
AA Mutation	p.Leu100Pro(p.L100P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000356244
Start	41258077:41258077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.645G>A
AA Mutation	p.Met215Ile(p.M215I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000356244
Start	41256728:41256728(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143560227
CDS Mutation	c.871G>A
AA Mutation	p.Gly291Ser(p.G291S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356244
Start	41254431:41254431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1137G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356244
Start	41249786:41249786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376593623
CDS Mutation	c.1515G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356244
Start	41256732:41256732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs531001209
CDS Mutation	c.867C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356244
Start	41246642:41246642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs555171214
CDS Mutation	c.1725C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356244
Start	41254383:41254383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771108482
CDS Mutation	c.1185A>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RANGAP1

No Mutation Annotation!