Product Details

SNP ID

rs140351413

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.15:58880046 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCCTTAAATGGCTTAAATCCGGAGC[C/T]ACTTCCTCTTGGCATGGAATTGCCA

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SLTM PubMed Links

Gene Details

Gene

SLTM

Gene Name

SAFB like transcription modulator

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001013843.2	2965	Missense Mutation	AGC,GGC	S1002G	NP_001013865.1
NM_024755.3	2965	Missense Mutation	AGC,GGC	S1020G	NP_079031.2
XM_006720686.3	2965	Missense Mutation	AGC,GGC	S1073G	XP_006720749.3
XM_006720690.1	2965	Missense Mutation	AGC,GGC	S589G	XP_006720753.1
XM_011522022.1	2965	Missense Mutation	AGC,GGC	S1162G	XP_011520324.1
XM_011522023.1	2965	Missense Mutation	AGC,GGC	S1144G	XP_011520325.1
XM_011522024.1	2965	Missense Mutation	AGC,GGC	S1112G	XP_011520326.1
XM_011522025.1	2965	Missense Mutation	AGC,GGC	S1096G	XP_011520327.1
XM_011522026.2	2965	Missense Mutation	AGC,GGC	S1089G	XP_011520328.2
XM_011522027.1	2965	Missense Mutation	AGC,GGC	S1080G	XP_011520329.1
XM_011522028.1	2965	Missense Mutation	AGC,GGC	S1062G	XP_011520330.1
XM_011522029.2	2965	Missense Mutation	AGC,GGC	S974G	XP_011520331.1
XM_011522030.2	2965	Intron			XP_011520332.1
XM_011522031.2	2965	Missense Mutation	AGC,GGC	S792G	XP_011520333.1
XM_017022576.1	2965	Missense Mutation	AGC,GGC	S952G	XP_016878065.1
XM_017022577.1	2965	Missense Mutation	AGC,GGC	S1071G	XP_016878066.1
XM_017022578.1	2965	Missense Mutation	AGC,GGC	S1055G	XP_016878067.1
XM_017022579.1	2965	Missense Mutation	AGC,GGC	S967G	XP_016878068.1
XM_017022580.1	2965	Missense Mutation	AGC,GGC	S589G	XP_016878069.1

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