Colon Cancer: Gene >> KIF27

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000297814
Start	83891493:83891493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1611A>C
AA Mutation	p.Lys537Asn(p.K537N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000297814
Start	83870592:83870592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777539862
CDS Mutation	c.2684C>T
AA Mutation	p.Pro895Leu(p.P895L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000297814
Start	83842333:83842333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3625G>T
AA Mutation	p.Asp1209Tyr(p.D1209Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000297814
Start	83883864:83883864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2394A>C
AA Mutation	p.Lys798Asn(p.K798N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000297814
Start	83908639:83908639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.312G>T
AA Mutation	p.Glu104Asp(p.E104D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000297814
Start	83889201:83889201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375590529
CDS Mutation	c.1862G>A
AA Mutation	p.Arg621Gln(p.R621Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000297814
Start	83891338:83891338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1766T>C
AA Mutation	p.Leu589Ser(p.L589S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297814
Start	83887114:83887114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2166T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297814
Start	83903513:83903513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1005C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000297814
Start	83842289:83842290(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3668_3669delAA
AA Mutation	p.Lys1223ThrfsTer2(p.K1223Tfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000297814
Start	83850249:83850249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3406G>T
AA Mutation	p.Glu1136Ter(p.E1136*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000297814
Start	83903869:83903869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.649C>T
AA Mutation	p.Gln217Ter(p.Q217*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000297814
Start	83887103:83887104(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2176dupA
AA Mutation	p.Met726AsnfsTer7(p.M726Nfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> KIF27

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000297814
Start	83891444:83891444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1660A>C
AA Mutation	p.Lys554Gln(p.K554Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000297814
Start	83837284:83837284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3923C>A
AA Mutation	p.Ser1308Tyr(p.S1308Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000297814
Start	83842261:83842261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3697C>T
AA Mutation	p.Arg1233Trp(p.R1233W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000297814
Start	83899783:83899783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1480G>T
AA Mutation	p.Val494Leu(p.V494L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000297814
Start	83903221:83903221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs77150451
CDS Mutation	c.1297G>A
AA Mutation	p.Glu433Lys(p.E433K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000297814
Start	83837123:83837123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4084G>T
AA Mutation	p.Glu1362Ter(p.E1362*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript