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SNP ID: rs151214675
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.20:63661882 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CACGGACATCCCAAAGATTATTTAC[A/G]CCTCCAGGACCCACTCGCAACTCAC
Phenotype: MIM: 608833 MIM: 608362
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: RTEL1 PubMed Links

Gene Details

Gene: RTEL1
Gene Name: regulator of telomere elongation helicase 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001283009.1	1161	Missense Mutation	ACC,GCC	T112A	NP_001269938.1
NM_001283010.1	1161	UTR 5			NP_001269939.1
NM_016434.3	1161	Missense Mutation	ACC,GCC	T112A	NP_057518.1
NM_032957.4	1161	Missense Mutation	ACC,GCC	T112A	NP_116575.3

Gene: RTEL1-TNFRSF6B
Gene Name: RTEL1-TNFRSF6B readthrough (NMD candidate)

There are no transcripts associated with this gene.

Gene: STMN3
Gene Name: stathmin 3

There are no transcripts associated with this gene.

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