Mutation

Primary Site >> Stomach Cancer

Gene >> MSH6

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000234420
Start	47783363:47783363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.130C>A
AA Mutation	p.Pro44Thr(p.P44T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000234420
Start	47798999:47798999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1016C>A
AA Mutation	p.Ala339Asp(p.A339D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000234420
Start	47798839:47798839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.856G>A
AA Mutation	p.Glu286Lys(p.E286K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000234420
Start	47799172:47799172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs587779913
CDS Mutation	c.1189T>C
AA Mutation	p.Tyr397His(p.Y397H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000234420
Start	47791049:47791049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.383G>A
AA Mutation	p.Arg128His(p.R128H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000234420
Start	47801011:47801011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3028A>G
AA Mutation	p.Thr1010Ala(p.T1010A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000234420
Start	47804974:47804974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3503C>T
AA Mutation	p.Thr1168Ile(p.T1168I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000234420
Start	47798789:47798789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs587779322
CDS Mutation	c.806C>G
AA Mutation	p.Thr269Ser(p.T269S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000234420
Start	47800910:47800910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs63751113
CDS Mutation	c.2927G>A
AA Mutation	p.Arg976His(p.R976H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000234420
Start	47800729:47800729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2746T>C
AA Mutation	p.Phe916Leu(p.F916L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000234420
Start	47799983:47799983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2000A>T
AA Mutation	p.Asp667Val(p.D667V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000234420
Start	47800586:47800586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780280765
CDS Mutation	c.2603T>C
AA Mutation	p.Met868Thr(p.M868T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000234420
Start	47798940:47798940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375210430
CDS Mutation	c.957G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000234420
Start	47798865:47798865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.882C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000234420
Start	47800668:47800668(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2690delA
AA Mutation	p.Asn897IlefsTer9(p.N897Ifs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000234420
Start	47803553:47803553(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3312delT
AA Mutation	p.Phe1104LeufsTer11(p.F1104Lfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript