Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> FSTL5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306100
Start	161385827:161385827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2464G>C
AA Mutation	p.Asp822His(p.D822H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000306100
Start	161386166:161386166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2125A>C
AA Mutation	p.Ile709Leu(p.I709L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000306100
Start	161481097:161481097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1531G>T
AA Mutation	p.Asp511Tyr(p.D511Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000306100
Start	161538268:161538268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs186644009
CDS Mutation	c.1210C>T
AA Mutation	p.Arg404Cys(p.R404C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000306100
Start	161542690:161542690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1019C>A
AA Mutation	p.Pro340His(p.P340H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000306100
Start	161920502:161920502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.311A>G
AA Mutation	p.Asp104Gly(p.D104G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000306100
Start	161656378:161656378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.844T>A
AA Mutation	p.Trp282Arg(p.W282R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000306100
Start	161920460:161920460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.353C>A
AA Mutation	p.Ala118Asp(p.A118D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000306100
Start	162111352:162111352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.45T>G
AA Mutation	p.Phe15Leu(p.F15L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000306100
Start	161656396:161656396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.826C>A
AA Mutation	p.Leu276Met(p.L276M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000306100
Start	162033640:162033640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.145A>T
AA Mutation	p.Ser49Cys(p.S49C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000306100
Start	161386074:161386074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2217A>G
AA Mutation	p.Ile739Met(p.I739M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000306100
Start	162111309:162111309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.88C>T
AA Mutation	p.Leu30Phe(p.L30F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000306100
Start	161775970:161775970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199735797
CDS Mutation	c.514G>A
AA Mutation	p.Asp172Asn(p.D172N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000306100
Start	161587482:161587482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.988T>C
AA Mutation	p.Tyr330His(p.Y330H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000306100
Start	161386316:161386316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1975G>A
AA Mutation	p.Gly659Ser(p.G659S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000306100
Start	161759513:161759513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.625C>T
AA Mutation	p.Leu209Phe(p.L209F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000306100
Start	161759449:161759449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.689A>T
AA Mutation	p.Asp230Val(p.D230V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306100
Start	161385795:161385795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2496C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306100
Start	161386167:161386167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2124C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306100
Start	161386278:161386278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201123322
CDS Mutation	c.2013A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306100
Start	161920582:161920582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.231T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306100
Start	161386251:161386251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368625257
CDS Mutation	c.2040C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306100
Start	161386020:161386020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755415491
CDS Mutation	c.2271C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000306100
Start	161538191:161538191(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1287delT
AA Mutation	p.Phe429LeufsTer10(p.F429Lfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000306100
Start	161500102:161500102(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1372delT
AA Mutation	p.Tyr458MetfsTer7(p.Y458Mfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000306100
Start	161481029:161481029(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs779560788
CDS Mutation	c.1599delA
AA Mutation	p.Val534LeufsTer5(p.V534Lfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000306100
Start	161500043:161500043(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1431delG
AA Mutation	p.Lys477AsnfsTer62(p.K477Nfs*62)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	stop_gained
Transcription ID	ENST00000306100
Start	161510404:161510404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1333G>T
AA Mutation	p.Glu445Ter(p.E445*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	stop_gained
Transcription ID	ENST00000306100
Start	162111279:162111279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141917472
CDS Mutation	c.118C>T
AA Mutation	p.Arg40Ter(p.R40*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	stop_gained
Transcription ID	ENST00000306100
Start	161775994:161775994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.490G>T
AA Mutation	p.Glu164Ter(p.E164*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000306100
Start	161920446:161920447(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.366dupA
AA Mutation	p.Gln123ThrfsTer9(p.Q123Tfs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000306100
Start	161920580:161920581(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.232dupA
AA Mutation	p.Thr78AsnfsTer27(p.T78Nfs*27)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000306100
Start	161538276:161538277(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1201_1202insAATCTATTTGTTATAAT
AA Mutation	p.Ser401LysfsTer44(p.S401Kfs*44)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> FSTL5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306100
Start	161386349:161386349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150697984
CDS Mutation	c.1942G>A
AA Mutation	p.Val648Ile(p.V648I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000306100
Start	161455050:161455050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745600368
CDS Mutation	c.1795G>A
AA Mutation	p.Asp599Asn(p.D599N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000306100
Start	161759512:161759512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.626T>G
AA Mutation	p.Leu209Arg(p.L209R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000306100
Start	161386436:161386436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1855C>A
AA Mutation	p.Leu619Ile(p.L619I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000306100
Start	161500038:161500038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1436G>T
AA Mutation	p.Ser479Ile(p.S479I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000306100
Start	161920578:161920578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.235A>C
AA Mutation	p.Ser79Arg(p.S79R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306100
Start	161656477:161656477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.745C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000306100
Start	161656376:161656376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.846G>A
AA Mutation	p.Trp282Ter(p.W282*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000306100
Start	161385821:161385821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776031059
CDS Mutation	c.2470C>T
AA Mutation	p.Arg824Ter(p.R824*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000306100
Start	162111351:162111352(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.45dupT
AA Mutation	p.Leu16SerfsTer16(p.L16Sfs*16)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript