Colon Cancer: Gene >> SOCS5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306503
Start	46758993:46758993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.463C>T
AA Mutation	p.Arg155Cys(p.R155C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000306503
Start	46759002:46759002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373780921
CDS Mutation	c.472G>A
AA Mutation	p.Val158Ile(p.V158I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000306503
Start	46758661:46758661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.131A>G
AA Mutation	p.Asn44Ser(p.N44S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000306503
Start	46758596:46758596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.66G>T
AA Mutation	p.Glu22Asp(p.E22D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000306503
Start	46759589:46759589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1059A>T
AA Mutation	p.Arg353Ser(p.R353S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000306503
Start	46758938:46758938(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.408G>T
AA Mutation	p.Leu136Phe(p.L136F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000306503
Start	46759491:46759491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.961A>G
AA Mutation	p.Asn321Asp(p.N321D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000306503
Start	46759493:46759493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370456653
CDS Mutation	c.963T>G
AA Mutation	p.Asn321Lys(p.N321K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000306503
Start	46760106:46760106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1576C>T
AA Mutation	p.Arg526Cys(p.R526C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000306503
Start	46758783:46758783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.253G>A
AA Mutation	p.Glu85Lys(p.E85K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000306503
Start	46758829:46758829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.299C>A
AA Mutation	p.Ser100Tyr(p.S100Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306503
Start	46759361:46759361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.831T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306503
Start	46759979:46759979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1449C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306503
Start	46759637:46759637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1107C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000306503
Start	46758876:46758876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.346C>T
AA Mutation	p.Arg116Ter(p.R116*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000306503
Start	46758600:46758600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.70G>T
AA Mutation	p.Gly24Ter(p.G24*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SOCS5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306503
Start	46759921:46759921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149307689
CDS Mutation	c.1391C>T
AA Mutation	p.Ser464Leu(p.S464L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000306503
Start	46760101:46760101(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1571G>C
AA Mutation	p.Arg524Thr(p.R524T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306503
Start	46758875:46758875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.345T>C
Mutation Classification	Silent
Feature Type	Transcript