Colon Cancer: Gene >> MAP7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000354570
Start	136362609:136362609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1367C>T
AA Mutation	p.Ala456Val(p.A456V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000354570
Start	136389481:136389481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150235721
CDS Mutation	c.281G>A
AA Mutation	p.Arg94Gln(p.R94Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000354570
Start	136346020:136346020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2075T>G
AA Mutation	p.Phe692Cys(p.F692C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000354570
Start	136421754:136421754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.113G>A
AA Mutation	p.Arg38His(p.R38H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000354570
Start	136388446:136388446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.473A>G
AA Mutation	p.Asn158Ser(p.N158S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000354570
Start	136362628:136362628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1348A>G
AA Mutation	p.Thr450Ala(p.T450A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000354570
Start	136389380:136389380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755861106
CDS Mutation	c.382C>T
AA Mutation	p.Arg128Trp(p.R128W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000354570
Start	136389504:136389504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770208353
CDS Mutation	c.258A>G
AA Mutation	p.Ile86Met(p.I86M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000354570
Start	136365899:136365899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764720646
CDS Mutation	c.1109G>A
AA Mutation	p.Arg370His(p.R370H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000354570
Start	136383745:136383745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371940141
CDS Mutation	c.563C>T
AA Mutation	p.Ser188Leu(p.S188L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000354570
Start	136360746:136360746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372519059
CDS Mutation	c.1754G>A
AA Mutation	p.Arg585Gln(p.R585Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000354570
Start	136365764:136365764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148466707
CDS Mutation	c.1244G>A
AA Mutation	p.Arg415Gln(p.R415Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000354570
Start	136356762:136356762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1945C>T
AA Mutation	p.Pro649Ser(p.P649S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000354570
Start	136366428:136366428(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.888delA
AA Mutation	p.Glu297LysfsTer102(p.E297Kfs*102)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000354570
Start	136362460:136362460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1516G>T
AA Mutation	p.Glu506Ter(p.E506*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000354570
Start	136360031:136360031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1804C>T
AA Mutation	p.Arg602Ter(p.R602*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> MAP7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000354570
Start	136372574:136372574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.803C>T
AA Mutation	p.Ser268Leu(p.S268L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000354570
Start	136365836:136365836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1172A>C
AA Mutation	p.Lys391Thr(p.K391T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000354570
Start	136383682:136383682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.626C>A
AA Mutation	p.Ser209Tyr(p.S209Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354570
Start	136361113:136361113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1593G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354570
Start	136389417:136389417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.345G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000354570
Start	136421772:136421773(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.93_94dupTA
AA Mutation	p.Lys32IlefsTer51(p.K32Ifs*51)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000354570
Start	136366326:136366326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.989+1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript