Product Details

SNP ID

rs201783756

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:103331548 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCTGCTTCAGTCTCTCGAAGAATTT[A/G]AAGAGGACATAGACTATAGGCATTT

Phenotype

MIM: 300771

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

TCEAL7 PubMed Links

Gene Details

Gene

TCEAL7

Gene Name

transcription elongation factor A like 7

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_152278.3	350	Missense Mutation	AAA,GAA	K49E	NP_689491.1
XM_017029655.1	350	Missense Mutation	AAA,GAA	K49E	XP_016885144.1

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