Colon Cancer: Gene >> STAT5A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000345506
Start	42308319:42308319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2048A>C
AA Mutation	p.Tyr683Ser(p.Y683S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000345506
Start	42307705:42307705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1888G>A
AA Mutation	p.Ala630Thr(p.A630T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000345506
Start	42310617:42310617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762056710
CDS Mutation	c.2333G>A
AA Mutation	p.Arg778His(p.R778H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000345506
Start	42289529:42289529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.118A>T
AA Mutation	p.Ser40Cys(p.S40C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000345506
Start	42292006:42292006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs575765283
CDS Mutation	c.320G>A
AA Mutation	p.Arg107His(p.R107H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000345506
Start	42301339:42301339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777748961
CDS Mutation	c.1054G>A
AA Mutation	p.Val352Ile(p.V352I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000345506
Start	42299759:42299759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.559G>T
AA Mutation	p.Ala187Ser(p.A187S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345506
Start	42300267:42300267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.819C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345506
Start	42304574:42304574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150767426
CDS Mutation	c.1302C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345506
Start	42306418:42306418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1651C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345506
Start	42304375:42304375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375505587
CDS Mutation	c.1203C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000345506
Start	42301381:42301381(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs759027671
CDS Mutation	c.1102delC
AA Mutation	p.Gln368ArgfsTer2(p.Q368Rfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000345506
Start	42307400:42307400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1681-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000345506
Start	42301274:42301274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.990-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> STAT5A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000345506
Start	42308289:42308289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2018G>A
AA Mutation	p.Arg673His(p.R673H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000345506
Start	42301343:42301343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372745237
CDS Mutation	c.1058G>A
AA Mutation	p.Arg353His(p.R353H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript