Colon Cancer: Gene >> MPHOSPH8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361479
Start	19659054:19659054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1636G>A
AA Mutation	p.Glu546Lys(p.E546K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361479
Start	19666505:19666505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2100G>T
AA Mutation	p.Gln700His(p.Q700H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361479
Start	19647227:19647227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1154C>T
AA Mutation	p.Thr385Met(p.T385M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361479
Start	19668456:19668456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145688067
CDS Mutation	c.2254G>A
AA Mutation	p.Ala752Thr(p.A752T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000361479
Start	19646743:19646743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.670A>G
AA Mutation	p.Thr224Ala(p.T224A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000361479
Start	19646684:19646684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.611C>A
AA Mutation	p.Ser204Tyr(p.S204Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000361479
Start	19650136:19650136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1452G>T
AA Mutation	p.Lys484Asn(p.K484N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000361479
Start	19647053:19647053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.980G>C
AA Mutation	p.Arg327Thr(p.R327T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361479
Start	19650151:19650151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751322867
CDS Mutation	c.1467A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361479
Start	19646667:19646667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.594G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361479
Start	19642183:19642183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.282T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361479
Start	19650054:19650054(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1376delA
AA Mutation	p.Asn459MetfsTer20(p.N459Mfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361479
Start	19647154:19647154(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1085delA
AA Mutation	p.Lys362SerfsTer14(p.K362Sfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361479
Start	19646577:19646578(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.504_505insC
AA Mutation	p.Lys169GlnfsTer28(p.K169Qfs*28)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361479
Start	19633957:19633958(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.213+1dupG
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MPHOSPH8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361479
Start	19642262:19642262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.361G>T
AA Mutation	p.Asp121Tyr(p.D121Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript