Product Details

SNP ID

rs7725623

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.5:102758794 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ACATTGCCAGTATACAGCTATTGCT[C/T]TATGACTCAAGTAGTTATTTTAGTT

Phenotype

MIM: 170270

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

PAM PubMed Links

Gene Details

Gene

PAM

Gene Name

peptidylglycine alpha-amidating monooxygenase

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000919.3		Intron			NP_000910.2
NM_001177306.1		Intron			NP_001170777.1
NM_001319943.1		Intron			NP_001306872.1
NM_138766.2		Intron			NP_620121.1
NM_138821.2		Intron			NP_620176.1
NM_138822.2		Intron			NP_620177.1
XM_011543419.2		Intron			XP_011541721.1
XM_017009495.1		Intron			XP_016864984.1
XM_017009496.1		Intron			XP_016864985.1
XM_017009497.1		Intron			XP_016864986.1
XM_017009498.1		Intron			XP_016864987.1
XM_017009499.1		Intron			XP_016864988.1
XM_017009500.1		Intron			XP_016864989.1
XM_017009501.1		Intron			XP_016864990.1
XM_017009502.1		Intron			XP_016864991.1
XM_017009503.1		Intron			XP_016864992.1
XM_017009504.1		Intron			XP_016864993.1
XM_017009505.1		Intron			XP_016864994.1
XM_017009506.1		Intron			XP_016864995.1
XM_017009507.1		Intron			XP_016864996.1
XM_017009508.1		Intron			XP_016864997.1
XM_017009509.1		Intron			XP_016864998.1
XM_017009510.1		Intron			XP_016864999.1
XM_017009511.1		Intron			XP_016865000.1
XM_017009512.1		Intron			XP_016865001.1
XM_017009513.1		Intron			XP_016865002.1
XM_017009514.1		Intron			XP_016865003.1
XM_017009515.1		Intron			XP_016865004.1
XM_017009516.1		Intron			XP_016865005.1

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