Colon Cancer: Gene >> STAT5B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000293328
Start	42207722:42207722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1913G>T
AA Mutation	p.Arg638Ile(p.R638I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000293328
Start	42218300:42218300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1020G>T
AA Mutation	p.Gln340His(p.Q340H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000293328
Start	42207660:42207660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1975C>T
AA Mutation	p.Arg659Cys(p.R659C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000293328
Start	42223492:42223492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.440C>T
AA Mutation	p.Thr147Met(p.T147M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000293328
Start	42217239:42217239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1301C>T
AA Mutation	p.Ser434Leu(p.S434L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000293328
Start	42212113:42212113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373036522
CDS Mutation	c.1551C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000293328
Start	42219829:42219829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747457595
CDS Mutation	c.564G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000293328
Start	42217392:42217392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1242C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000293328
Start	42217431:42217431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200710135
CDS Mutation	c.1203C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000293328
Start	42210429:42210429(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1749delA
AA Mutation	p.Lys583AsnfsTer16(p.K583Nfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000293328
Start	42223441:42223441(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.491delA
AA Mutation	p.Lys164SerfsTer17(p.K164Sfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000293328
Start	42210428:42210429(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1749dupA
AA Mutation	p.His584ThrfsTer8(p.H584Tfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000293328
Start	42210303:42210303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1776-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> STAT5B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000293328
Start	42217224:42217224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1316A>C
AA Mutation	p.Lys439Thr(p.K439T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000293328
Start	42202342:42202342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2235G>T
AA Mutation	p.Gln745His(p.Q745H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000293328
Start	42212173:42212173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1491C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000293328
Start	42210244:42210244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1833A>G
Mutation Classification	Silent
Feature Type	Transcript