Product Details

SNP ID

rs202052204

Assay Type

Functionally tested

NCBI dbSNP Submissions

6

Location

Chr.1:117060353 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACTTGGGGGACCCAGCGAAATGGAA[C/G]AAGTTAGGTGTCCAGAGCACGGTAA

Phenotype

MIM: 604718

Polymorphism

C/G, Transversion 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	66	Missense Mutation	CAA,GAA	Q3E	NP_003585.3
XM_005271277.3	66	Missense Mutation	CAA,GAA	Q3E	XP_005271334.1
XM_011542303.2	66	Missense Mutation	CAA,GAA	Q3E	XP_011540605.1
XM_017002549.1	66	Missense Mutation	CAA,GAA	Q3E	XP_016858038.1
XM_017002550.1	66	Missense Mutation	CAA,GAA	Q3E	XP_016858039.1
XM_017002551.1	66	Missense Mutation	CAA,GAA	Q3E	XP_016858040.1
XM_017002552.1	66	Missense Mutation	CAA,GAA	Q3E	XP_016858041.1
XM_017002553.1	66	Missense Mutation	CAA,GAA	Q3E	XP_016858042.1
XM_017002554.1	66	Missense Mutation	CAA,GAA	Q3E	XP_016858043.1
XM_017002555.1	66	Nonsense Mutation	CAA,GAA	Q3E	XP_016858044.1

View Full Product Details