Colon Cancer: Gene >> SP4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000222584
Start	21430673:21430673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1508G>C
AA Mutation	p.Gly503Ala(p.G503A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000222584
Start	21511223:21511223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748277058
CDS Mutation	c.2309C>T
AA Mutation	p.Ser770Leu(p.S770L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000222584
Start	21511082:21511082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2168C>T
AA Mutation	p.Ser723Phe(p.S723F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222584
Start	21481957:21481957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1941T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222584
Start	21511224:21511224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200932303
CDS Mutation	c.2310G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000222584
Start	21481942:21481942(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1931delA
AA Mutation	p.Lys644ArgfsTer195(p.K644Rfs*195)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000222584
Start	21429579:21429579(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.418delA
AA Mutation	p.Thr140LeufsTer28(p.T140Lfs*28)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000222584
Start	21482009:21482009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1993C>T
AA Mutation	p.Arg665Ter(p.R665*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SP4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000222584
Start	21428706:21428706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.37G>A
AA Mutation	p.Ala13Thr(p.A13T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222584
Start	21477167:21477167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774052513
CDS Mutation	c.1767G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222584
Start	21430311:21430311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1146A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000222584
Start	21429663:21429664(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.498_499insTTTT
AA Mutation	p.Val167PhefsTer20(p.V167Ffs*20)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript