Colon Cancer: Gene >> FEM1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306917
Start	68289986:68289986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138980106
CDS Mutation	c.628C>T
AA Mutation	p.Arg210Cys(p.R210C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000306917
Start	68290343:68290343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.985C>A
AA Mutation	p.Leu329Ile(p.L329I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000306917
Start	68290020:68290020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.662C>T
AA Mutation	p.Thr221Met(p.T221M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000306917
Start	68290037:68290037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.679G>A
AA Mutation	p.Ala227Thr(p.A227T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000306917
Start	68290797:68290797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1439G>A
AA Mutation	p.Arg480Lys(p.R480K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000306917
Start	68290940:68290940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757432489
CDS Mutation	c.1582G>A
AA Mutation	p.Val528Met(p.V528M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306917
Start	68290651:68290651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1293T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306917
Start	68291221:68291221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1863A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306917
Start	68289733:68289733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.375G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> FEM1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306917
Start	68290739:68290739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775266107
CDS Mutation	c.1381G>A
AA Mutation	p.Glu461Lys(p.E461K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000306917
Start	68290725:68290725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1367A>C
AA Mutation	p.Lys456Thr(p.K456T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000306917
Start	68290272:68290272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.914G>T
AA Mutation	p.Arg305Ile(p.R305I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript