Product Details

SNP ID

rs191680400

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:11277251 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCCTCACTGCTGTGGATTGCCTTTA[C/T]TAAAATAGAGATCTATGCAGAAATA

Phenotype

MIM: 608760

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

ATG7 PubMed Links

Gene Details

Gene

ATG7

Gene Name

autophagy related 7

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001136031.2		Intron			NP_001129503.2
NM_001144912.1		Intron			NP_001138384.1
NM_006395.2		Intron			NP_006386.1
XM_006712931.3		Intron			XP_006712994.1
XM_006712932.3		Intron			XP_006712995.1
XM_006712933.3		Intron			XP_006712996.1
XM_011533277.2		Intron			XP_011531579.1
XM_011533278.2		Intron			XP_011531580.1
XM_011533279.2		Intron			XP_011531581.1
XM_011533280.2		Intron			XP_011531582.1
XM_011533281.2		Intron			XP_011531583.1
XM_011533282.2		Intron			XP_011531584.1
XM_011533283.2		Intron			XP_011531585.1
XM_011533284.2		Intron			XP_011531586.1
XM_011533285.2		Intron			XP_011531587.1
XM_011533286.2		Intron			XP_011531588.1
XM_017005542.1		Intron			XP_016861031.1
XM_017005543.1		Intron			XP_016861032.1
XM_017005544.1		Intron			XP_016861033.1
XM_017005545.1		Intron			XP_016861034.1
XM_017005546.1		Intron			XP_016861035.1
XM_017005547.1		Intron			XP_016861036.1
XM_017005548.1		Intron			XP_016861037.1
XM_017005549.1		Intron			XP_016861038.1
XM_017005550.1		Intron			XP_016861039.1
XM_017005551.1		Intron			XP_016861040.1
XM_017005552.1		Intron			XP_016861041.1
XM_017005553.1		Intron			XP_016861042.1
XM_017005554.1		Intron			XP_016861043.1

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