Product Details

SNP ID

rs147772907

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:127869521 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGACACCTTTTTCATTAATGAATTC[A/G]ATTCGAATCCCATGGACCCCTACCT

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

AMMECR1L PubMed Links

Gene Details

Gene

AMMECR1L

Gene Name

AMMECR1 like

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001199140.1	1289	Silent Mutation	ATC,ATT	I219I	NP_001186069.1
NM_031445.2	1289	Intron			NP_113633.2
XM_005263804.4	1289	Silent Mutation	ATC,ATT	I219I	XP_005263861.1
XM_005263806.4	1289	Silent Mutation	ATC,ATT	I182I	XP_005263863.1
XM_005263807.4	1289	Silent Mutation	ATC,ATT	I182I	XP_005263864.1
XM_011511952.2	1289	Silent Mutation	ATC,ATT	I219I	XP_011510254.1
XM_011511954.2	1289	Silent Mutation	ATC,ATT	I91I	XP_011510256.1
XM_011511955.2	1289	Intron			XP_011510257.1
XM_011511956.2	1289	Intron			XP_011510258.1
XM_017005063.1	1289	UTR 3			XP_016860552.1

Gene

LOC107985803

Gene Name

uncharacterized LOC107985803

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
XM_017005446.1	1289	Intron			XP_016860935.1

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