Colon Cancer: Gene >> SH3BP4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000344528
Start	235042319:235042319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1550C>T
AA Mutation	p.Ala517Val(p.A517V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000344528
Start	235042117:235042117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1348T>C
AA Mutation	p.Tyr450His(p.Y450H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000344528
Start	235042073:235042073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1304G>T
AA Mutation	p.Gly435Val(p.G435V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000344528
Start	235043247:235043247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2478G>A
AA Mutation	p.Met826Ile(p.M826I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000344528
Start	235043183:235043183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2414T>A
AA Mutation	p.Leu805Gln(p.L805Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000344528
Start	235052656:235052656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754479794
CDS Mutation	c.2573G>A
AA Mutation	p.Arg858Gln(p.R858Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000344528
Start	235042120:235042120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780291299
CDS Mutation	c.1351G>A
AA Mutation	p.Val451Met(p.V451M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000344528
Start	235042825:235042825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2056C>T
AA Mutation	p.Leu686Phe(p.L686F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000344528
Start	235041311:235041311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.542T>C
AA Mutation	p.Leu181Pro(p.L181P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000344528
Start	235042258:235042258(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1489C>T
AA Mutation	p.His497Tyr(p.H497Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000344528
Start	235042903:235042903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2134G>A
AA Mutation	p.Gly712Ser(p.G712S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000344528
Start	235052647:235052647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2564A>C
AA Mutation	p.Gln855Pro(p.Q855P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000344528
Start	235042039:235042039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1270C>T
AA Mutation	p.Pro424Ser(p.P424S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000344528
Start	235043084:235043084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2315T>C
AA Mutation	p.Phe772Ser(p.F772S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000344528
Start	235041892:235041892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1123A>C
AA Mutation	p.Ser375Arg(p.S375R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344528
Start	235035101:235035101(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138260268
CDS Mutation	c.99G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344528
Start	235041399:235041399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376738527
CDS Mutation	c.630G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344528
Start	235042488:235042488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1719C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344528
Start	235041441:235041441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.672C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344528
Start	235041901:235041901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1132C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344528
Start	235042356:235042356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765228030
CDS Mutation	c.1587C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000344528
Start	235042628:235042628(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1860delC
AA Mutation	p.Gln622LysfsTer114(p.Q622Kfs*114)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	stop_gained
Transcription ID	ENST00000344528
Start	235042447:235042447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1678C>T
AA Mutation	p.Arg560Ter(p.R560*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000344528
Start	235041971:235041972(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs766163019
CDS Mutation	c.1208dupA
AA Mutation	p.Asn403LysfsTer2(p.N403Kfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SH3BP4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000344528
Start	235035060:235035060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756321673
CDS Mutation	c.58G>A
AA Mutation	p.Glu20Lys(p.E20K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000344528
Start	235041421:235041421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.652G>T
AA Mutation	p.Asp218Tyr(p.D218Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344528
Start	235042203:235042203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1434C>G
Mutation Classification	Silent
Feature Type	Transcript