Product Details

SNP ID

rs200374529

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:103630031 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AAAGCAGTCCCCCGAGGAGCAGTCT[C/T]CGGAGGAGCAGTCCTCGGAGGAGGA

Phenotype

MIM: 300237

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

TCEAL1 PubMed Links

Gene Details

Gene

TCEAL1

Gene Name

transcription elongation factor A like 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001006639.1	277	Missense Mutation	CCG,TCG	P39S	NP_001006640.1
NM_001006640.1	277	Missense Mutation	CCG,TCG	P39S	NP_001006641.1
NM_004780.2	277	Missense Mutation	CCG,TCG	P39S	NP_004771.2

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