Product Details

SNP ID

rs188195414

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.22:41714045 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGCAGCTGAAGCTGGAGCAGACTAT[C/T]CGTTGCCTGCTGGATGAGTGCCACA

Phenotype

MIM: 608797

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

MEI1 PubMed Links

Gene Details

Gene

MEI1

Gene Name

meiotic double-stranded break formation protein 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_152513.3	427	Silent Mutation	ATC,ATT	I131I	NP_689726.3
XM_011529935.1	427	Silent Mutation	ATC,ATT	I131I	XP_011528237.1
XM_011529936.1	427	Silent Mutation	ATC,ATT	I131I	XP_011528238.1
XM_011529937.1	427	Silent Mutation	ATC,ATT	I131I	XP_011528239.1
XM_011529938.1	427	Silent Mutation	ATC,ATT	I131I	XP_011528240.1
XM_011529939.1	427	Silent Mutation	ATC,ATT	I131I	XP_011528241.1
XM_011529940.1	427	Silent Mutation	ATC,ATT	I131I	XP_011528242.1
XM_011529941.1	427	Silent Mutation	ATC,ATT	I131I	XP_011528243.1
XM_011529942.2	427	Silent Mutation	ATC,ATT	I67I	XP_011528244.1
XM_011529943.1	427	Silent Mutation	ATC,ATT	I131I	XP_011528245.1
XM_011529944.1	427	Silent Mutation	ATC,ATT	I131I	XP_011528246.1
XM_011529945.2	427	Silent Mutation	ATC,ATT	I131I	XP_011528247.1
XM_011529946.1	427	Silent Mutation	ATC,ATT	I131I	XP_011528248.1
XM_011529947.1	427	Silent Mutation	ATC,ATT	I131I	XP_011528249.1
XM_011529948.2	427	Intron			XP_011528250.1
XM_011529949.1	427	UTR 5			XP_011528251.1
XM_011529950.1	427	Silent Mutation	ATC,ATT	I131I	XP_011528252.1
XM_011529952.1	427	Intron			XP_011528254.1
XM_011529954.1	427	Intron			XP_011528256.1
XM_011529955.1	427	Silent Mutation	ATC,ATT	I131I	XP_011528257.1
XM_011529956.2	427	Silent Mutation	ATC,ATT	I131I	XP_011528258.1
XM_017028633.1	427	Silent Mutation	ATC,ATT	I131I	XP_016884122.1
XM_017028635.1	427	Intron			XP_016884124.1

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