Colon Cancer: Gene >> ITIH4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000266041
Start	52824471:52824471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.971C>A
AA Mutation	p.Pro324Gln(p.P324Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000266041
Start	52814347:52814347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2488G>A
AA Mutation	p.Asp830Asn(p.D830N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000266041
Start	52823665:52823665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1430T>C
AA Mutation	p.Val477Ala(p.V477A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000266041
Start	52825911:52825911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768593175
CDS Mutation	c.734G>A
AA Mutation	p.Arg245Gln(p.R245Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000266041
Start	52829145:52829145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.225G>T
AA Mutation	p.Lys75Asn(p.K75N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000266041
Start	52819404:52819404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143285865
CDS Mutation	c.2066G>A
AA Mutation	p.Arg689His(p.R689H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000266041
Start	52819407:52819407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769039012
CDS Mutation	c.2063G>A
AA Mutation	p.Arg688His(p.R688H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000266041
Start	52819408:52819408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2062C>A
AA Mutation	p.Arg688Ser(p.R688S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266041
Start	52826875:52826875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.435C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266041
Start	52816904:52816904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755043796
CDS Mutation	c.2451G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266041
Start	52813481:52813481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2733G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266041
Start	52818146:52818146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2202C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266041
Start	52827101:52827101(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.348C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ITIH4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000266041
Start	52825912:52825912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs550860646
CDS Mutation	c.733C>T
AA Mutation	p.Arg245Trp(p.R245W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript