Colon Cancer: Gene >> MARK4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262891
Start	45287522:45287522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1352G>A
AA Mutation	p.Arg451Gln(p.R451Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262891
Start	45251596:45251596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8C>T
AA Mutation	p.Ser3Leu(p.S3L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262891
Start	45271626:45271626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.704C>T
AA Mutation	p.Pro235Leu(p.P235L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262891
Start	45297773:45297773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1696C>T
AA Mutation	p.Arg566Cys(p.R566C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262891
Start	45297774:45297774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1697G>A
AA Mutation	p.Arg566His(p.R566H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262891
Start	45297908:45297908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1831C>A
AA Mutation	p.Pro611Thr(p.P611T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262891
Start	45280711:45280711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755396651
CDS Mutation	c.1253G>A
AA Mutation	p.Arg418His(p.R418H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000262891
Start	45302451:45302451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745321890
CDS Mutation	c.2000C>T
AA Mutation	p.Ser667Leu(p.S667L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000262891
Start	45266232:45266232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs534682723
CDS Mutation	c.500C>T
AA Mutation	p.Ser167Leu(p.S167L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000262891
Start	45287495:45287495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778118260
CDS Mutation	c.1325C>T
AA Mutation	p.Thr442Met(p.T442M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000262891
Start	45294417:45294417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1563G>T
AA Mutation	p.Glu521Asp(p.E521D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262891
Start	45271693:45271693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756565152
CDS Mutation	c.771C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262891
Start	45278027:45278027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.891A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262891
Start	45302406:45302406(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1960delC
AA Mutation	p.Arg654GlyfsTer9(p.R654Gfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262891
Start	45271576:45271576(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.659delC
AA Mutation	p.Pro220HisfsTer74(p.P220Hfs*74)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MARK4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262891
Start	45287527:45287527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1357C>T
AA Mutation	p.Pro453Ser(p.P453S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262891
Start	45264877:45264877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.459G>T
AA Mutation	p.Met153Ile(p.M153I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262891
Start	45266232:45266232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs534682723
CDS Mutation	c.500C>T
AA Mutation	p.Ser167Leu(p.S167L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262891
Start	45280687:45280687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756740251
CDS Mutation	c.1229G>A
AA Mutation	p.Arg410Gln(p.R410Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262891
Start	45280462:45280462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1095C>A
Mutation Classification	Silent
Feature Type	Transcript