Colon Cancer: Gene >> IGFALS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000215539
Start	1791748:1791748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.670G>A
AA Mutation	p.Asp224Asn(p.D224N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000215539
Start	1791495:1791495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201622145
CDS Mutation	c.923G>A
AA Mutation	p.Arg308His(p.R308H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000215539
Start	1790641:1790641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1777G>A
AA Mutation	p.Asp593Asn(p.D593N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000215539
Start	1792195:1792195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779943562
CDS Mutation	c.223G>A
AA Mutation	p.Gly75Ser(p.G75S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000215539
Start	1790778:1790778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1640T>C
AA Mutation	p.Leu547Pro(p.L547P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000215539
Start	1791564:1791564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.854C>T
AA Mutation	p.Thr285Met(p.T285M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000215539
Start	1791454:1791454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.964G>T
AA Mutation	p.Gly322Cys(p.G322C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000215539
Start	1791151:1791151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200564045
CDS Mutation	c.1267G>A
AA Mutation	p.Val423Met(p.V423M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000215539
Start	1791873:1791873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.545T>C
AA Mutation	p.Leu182Pro(p.L182P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000215539
Start	1791774:1791774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.644G>A
AA Mutation	p.Ser215Asn(p.S215N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000215539
Start	1791501:1791501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201176815
CDS Mutation	c.917G>A
AA Mutation	p.Arg306Gln(p.R306Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000215539
Start	1790699:1790699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1719G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000215539
Start	1791617:1791617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs35632685
CDS Mutation	c.801G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> IGFALS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000215539
Start	1791727:1791727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.691C>T
AA Mutation	p.Arg231Trp(p.R231W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000215539
Start	1791429:1791429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.989C>G
AA Mutation	p.Ala330Gly(p.A330G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript