Product Details

SNP ID
rs202054247
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:103587300 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGGCTGCAGGGCCCCACGAAGGGAC[A/G]TTGAAGACATTCCTTATGTGTAGTG
Phenotype
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
TCEAL4 PubMed Links

Gene Details

Gene
TCEAL4
Gene Name
transcription elongation factor A like 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001006935.2 919 Missense Mutation ATT,GTT I209V NP_001006936.1
NM_001006937.2 919 Missense Mutation ATT,GTT I209V NP_001006938.1
NM_001300901.1 919 Missense Mutation ATT,GTT I352V NP_001287830.1
NM_001305840.1 919 Missense Mutation ATT,GTT I209V NP_001292769.1
NM_001305841.1 919 Missense Mutation ATT,GTT I209V NP_001292770.1
NM_001305842.1 919 Missense Mutation ATT,GTT I209V NP_001292771.1
NM_024863.5 919 Missense Mutation ATT,GTT I209V NP_079139.4
XM_017029856.1 919 Missense Mutation ATT,GTT I271V XP_016885345.1
XM_017029857.1 919 Missense Mutation ATT,GTT I209V XP_016885346.1

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