Product Details

SNP ID

rs150851735

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.15:56921042 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATTTTGCAGATGTTTTCCCCACCTG[C/T]TAATAGTGGGAAAACTAGACCAACT

Phenotype

MIM: 600480

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

LOC145783 PubMed Links

Gene Details

Gene

LOC145783

Gene Name

uncharacterized LOC145783

There are no transcripts associated with this gene.

Gene

TCF12

Gene Name

transcription factor 12

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001306219.2	233	Intron			NP_001293148.1
NM_001306220.2	233	Intron			NP_001293149.1
NM_001322151.1	233	Missense Mutation	GCT,GTT	A31V	NP_001309080.1
NM_001322152.1	233	Missense Mutation	GCT,GTT	A31V	NP_001309081.1
NM_001322154.1	233	UTR 5			NP_001309083.1
NM_001322156.1	233	UTR 5			NP_001309085.1
NM_001322157.1	233	Missense Mutation	GCT,GTT	A31V	NP_001309086.1
NM_001322158.1	233	UTR 5			NP_001309087.1
NM_001322159.1	233	Missense Mutation	GCT,GTT	A31V	NP_001309088.1
NM_001322161.1	233	Missense Mutation	GCT,GTT	A31V	NP_001309090.1
NM_001322162.1	233	Missense Mutation	GCT,GTT	A31V	NP_001309091.1
NM_001322164.1	233	Missense Mutation	GCT,GTT	A31V	NP_001309093.1
NM_001322165.1	233	Missense Mutation	GCT,GTT	A31V	NP_001309094.1
NM_003205.3	233	Missense Mutation	GCT,GTT	A31V	NP_003196.1
NM_207036.1	233	Missense Mutation	GCT,GTT	A31V	NP_996919.1
NM_207037.1	233	Missense Mutation	GCT,GTT	A31V	NP_996920.1
NM_207038.1	233	Missense Mutation	GCT,GTT	A31V	NP_996921.1
NM_207040.1	233	Intron			NP_996923.1
XM_011521959.2	233	Missense Mutation	GCT,GTT	A31V	XP_011520261.1
XM_011521960.2	233	Missense Mutation	GCT,GTT	A31V	XP_011520262.1
XM_011521961.2	233	Missense Mutation	GCT,GTT	A31V	XP_011520263.1
XM_011521962.2	233	Missense Mutation	GCT,GTT	A31V	XP_011520264.1
XM_011521963.2	233	Missense Mutation	GCT,GTT	A31V	XP_011520265.1
XM_011521965.1	233	UTR 5			XP_011520267.1
XM_011521966.2	233	Intron			XP_011520268.1
XM_011521967.1	233	UTR 5			XP_011520269.1
XM_011521969.1	233	Intron			XP_011520271.1
XM_017022520.1	233	Missense Mutation	GCT,GTT	A31V	XP_016878009.1

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