Colon Cancer: Gene >> ELMO3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000393997
Start	67200264:67200264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.475C>T
AA Mutation	p.Arg159Cys(p.R159C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000393997
Start	67203806:67203806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750093350
CDS Mutation	c.2251C>T
AA Mutation	p.Arg751Trp(p.R751W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000393997
Start	67203354:67203354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1967T>C
AA Mutation	p.Leu656Pro(p.L656P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000393997
Start	67202016:67202016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1249G>A
AA Mutation	p.Gly417Ser(p.G417S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000393997
Start	67202005:67202005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765459031
CDS Mutation	c.1238G>A
AA Mutation	p.Arg413His(p.R413H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000393997
Start	67200515:67200515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.637T>C
AA Mutation	p.Ser213Pro(p.S213P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000393997
Start	67203771:67203771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200461796
CDS Mutation	c.2216G>A
AA Mutation	p.Arg739His(p.R739H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000393997
Start	67199709:67199709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.304T>C
AA Mutation	p.Tyr102His(p.Y102H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393997
Start	67203790:67203790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763019732
CDS Mutation	c.2235C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393997
Start	67199230:67199230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.63A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000393997
Start	67203827:67203827(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2277delC
AA Mutation	p.Thr760ProfsTer31(p.T760Pfs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ELMO3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000393997
Start	67202233:67202233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1369A>C
AA Mutation	p.Ser457Arg(p.S457R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript