Product Details

SNP ID

rs34353835

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.15:73985325 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTCCCCAGGGCTCCTCACCTGGCCC[C/T]GGGGACGGGGCACCTCCTGCCATTG

Phenotype

MIM: 102578 MIM: 608326

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

PML PubMed Links

Gene Details

Gene

PML

Gene Name

promyelocytic leukemia

There are no transcripts associated with this gene.

Gene

STOML1

Gene Name

stomatin like 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001256672.1	1813	Silent Mutation	CCA,CCG	P261P	NP_001243601.1
NM_001256673.1	1813	Silent Mutation	CCA,CCG	P211P	NP_001243602.1
NM_001256674.1	1813	Silent Mutation	CCA,CCG	P211P	NP_001243603.1
NM_001256675.1	1813	Silent Mutation	CCA,CCG	P261P	NP_001243604.1
NM_001256676.1	1813	Silent Mutation	CCA,CCG	P174P	NP_001243605.1
NM_001256677.1	1813	Silent Mutation	CCA,CCG	P219P	NP_001243606.1
NM_001324226.1	1813	Silent Mutation	CCA,CCG	P105P	NP_001311155.1
NM_001324227.1	1813	Silent Mutation	CCA,CCG	P174P	NP_001311156.1
NM_001324228.1	1813	Silent Mutation	CCA,CCG	P174P	NP_001311157.1
NM_001324229.1	1813	Silent Mutation	CCA,CCG	P105P	NP_001311158.1
NM_001324230.1	1813	Silent Mutation	CCA,CCG	P219P	NP_001311159.1
NM_004809.4	1813	Silent Mutation	CCA,CCG	P261P	NP_004800.2
XM_005254792.4	1813	Silent Mutation	CCA,CCG	P219P	XP_005254849.1
XM_006720773.3	1813	Silent Mutation	CCA,CCG	P219P	XP_006720836.1

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