Product Details

SNP ID

rs138286826

Assay Type

Functionally tested

NCBI dbSNP Submissions

18

Location

Chr.1:117060509 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGCGATGGCCCGAATAAAGGAAAGA[A/G]CTTCTACGTGTGCCGGGCAGACACG

Phenotype

MIM: 604718

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

LOC101929099 PubMed Links

Gene Details

Gene

LOC101929099

Gene Name

uncharacterized LOC101929099

There are no transcripts associated with this gene.

Gene

TTF2

Gene Name

transcription termination factor 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_003594.3	142	Missense Mutation	AAC,AGC	N28S	NP_003585.3
XM_005271277.3	142	Missense Mutation	AAC,AGC	N28S	XP_005271334.1
XM_011542303.2	142	Missense Mutation	AAC,AGC	N28S	XP_011540605.1
XM_017002549.1	142	Missense Mutation	AAC,AGC	N28S	XP_016858038.1
XM_017002550.1	142	Missense Mutation	AAC,AGC	N28S	XP_016858039.1
XM_017002551.1	142	Missense Mutation	AAC,AGC	N28S	XP_016858040.1
XM_017002552.1	142	Missense Mutation	AAC,AGC	N28S	XP_016858041.1
XM_017002553.1	142	Missense Mutation	AAC,AGC	N28S	XP_016858042.1
XM_017002554.1	142	Missense Mutation	AAC,AGC	N28S	XP_016858043.1
XM_017002555.1	142	Missense Mutation	AAC,AGC	N28S	XP_016858044.1

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