Product Details

SNP ID

rs145697435

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.16:89883413 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACGGGGAGAGGTCTGGCTGTGCGCT[C/G]ACAGACGCTGTGGCACCAGGGAACA

Phenotype

MIM: 612326

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

TCF25 PubMed Links

Gene Details

Gene

TCF25

Gene Name

transcription factor 25

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_014972.2	938	Silent Mutation	CTC,CTG	L85L	NP_055787.1
XM_005256297.2	938	Silent Mutation	CTC,CTG	L85L	XP_005256354.1
XM_005256298.2	938	Silent Mutation	CTC,CTG	L85L	XP_005256355.1
XM_005256299.2	938	Silent Mutation	CTC,CTG	L85L	XP_005256356.1
XM_011522956.2	938	Silent Mutation	CTC,CTG	L85L	XP_011521258.1
XM_011522957.2	938	Silent Mutation	CTC,CTG	L85L	XP_011521259.1
XM_011522958.2	938	Silent Mutation	CTC,CTG	L85L	XP_011521260.1
XM_011522959.2	938	Silent Mutation	CTC,CTG	L85L	XP_011521261.1
XM_011522960.2	938	Silent Mutation	CTC,CTG	L85L	XP_011521262.1
XM_011522961.2	938	UTR 5			XP_011521263.1
XM_017023047.1	938	Silent Mutation	CTC,CTG	L85L	XP_016878536.1
XM_017023048.1	938	Silent Mutation	CTC,CTG	L85L	XP_016878537.1
XM_017023049.1	938	Silent Mutation	CTC,CTG	L85L	XP_016878538.1
XM_017023050.1	938	Silent Mutation	CTC,CTG	L85L	XP_016878539.1
XM_017023051.1	938	Silent Mutation	CTC,CTG	L85L	XP_016878540.1
XM_017023052.1	938	Silent Mutation	CTC,CTG	L85L	XP_016878541.1
XM_017023053.1	938	UTR 5			XP_016878542.1
XM_017023054.1	938	UTR 5			XP_016878543.1
XM_017023055.1	938	UTR 5			XP_016878544.1
XM_017023056.1	938	UTR 5			XP_016878545.1
XM_017023057.1	938	UTR 5			XP_016878546.1
XM_017023058.1	938	UTR 5			XP_016878547.1

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