NT5C1B

5'-nucleotidase, cytosolic IB

Summary

Cytosolic 5-prime nucleotidases, such as NT5C1B, catalyze production of adenosine, which regulates diverse physiologic processes (Sala-Newby and Newby, 2001 [PubMed 11690631]).[supplied by OMIM, Mar 2008]

Known Variants56 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs1036003032	2:18,745,072	A/G	—	uncertain significance
rs760038236	2:18,745,084	A/G	—	uncertain significance
rs79501117	2:18,745,087	C/A	—	uncertain significance
rs1271872801	2:18,745,097	C/T	—	likely benign
rs147939092	2:18,745,126	A/G	—	uncertain significance
rs1300002168	2:18,745,241	G/A	—	uncertain significance
rs772555868	2:18,745,304	T/C	—	uncertain significance
rs201315955	2:18,745,319	G/A	—	uncertain significance
rs533460102	2:18,745,370	A/G	—	uncertain significance
rs774249364	2:18,757,507	A/T	—	uncertain significance
rs1273130658	2:18,757,508	T/C	—	uncertain significance
rs117487981	2:18,757,575	G/A	—	uncertain significance
rs140510680	2:18,758,085	C/G	—	uncertain significance
rs922468689	2:18,758,901	G/A	—	—
rs113497432	2:18,764,236	G/A	—	uncertain significance
rs773168634	2:18,765,364	C/G	—	uncertain significance
rs140827083	2:18,765,398	C/T	—	uncertain significance
rs749149800	2:18,765,431	G/T	—	uncertain significance
rs1666451877	2:18,765,463	A/C	—	uncertain significance
rs766665062	2:18,765,465	C/G	—	uncertain significance
rs1004574912	2:18,765,484	G/A	—	uncertain significance
rs2528272233	2:18,765,485	A/T	—	uncertain significance
rs763669295	2:18,765,800	T/C	—	uncertain significance
rs200906490	2:18,765,866	C/G	—	uncertain significance
rs781054410	2:18,765,887	C/G	—	uncertain significance
rs752681908	2:18,765,893	G/C	—	uncertain significance
rs201047201	2:18,765,970	G/A	—	uncertain significance
rs373347393	2:18,766,001	G/A	—	uncertain significance
rs764194785	2:18,766,070	G/A	—	uncertain significance
rs528905701	2:18,766,085	C/T	—	uncertain significance
rs775147320	2:18,766,141	G/C	—	uncertain significance
rs760451943	2:18,766,142	C/G	—	uncertain significance
rs200689028	2:18,766,173	C/T	—	benign
rs117298882	2:18,766,191	A/G	—	benign
rs779702855	2:18,766,220	G/A	—	uncertain significance
rs751170359	2:18,767,526	A/C	—	uncertain significance
rs928525179	2:18,767,539	C/T	—	uncertain significance
rs368550960	2:18,767,561	G/A	—	uncertain significance
rs202225134	2:18,767,581	C/T	—	uncertain significance
rs747025354	2:18,767,582	G/A	—	uncertain significance
rs367871143	2:18,767,605	C/A	—	uncertain significance
rs114622083	2:18,767,621	G/A	—	benign
rs147855918	2:18,767,638	A/G	—	likely benign
rs765397825	2:18,768,302	C/A	—	uncertain significance
rs113913452	2:18,768,319	G/A	—	uncertain significance
rs761277392	2:18,768,321	A/G	—	uncertain significance
rs367989070	2:18,768,348	C/G	—	uncertain significance
rs199544140	2:18,768,370	G/A	—	uncertain significance
rs1447978953	2:18,768,391	G/C	—	uncertain significance
rs76041976	2:18,768,410	C/T	—	benign
rs373286312	2:18,768,411	G/A	—	uncertain significance
rs140803100	2:18,768,421	G/C	—	likely benign
rs368786487	2:18,768,782	C/T	—	uncertain significance
rs750593394	2:18,768,783	G/A	—	uncertain significance
rs1010471319	2:18,768,829	C/G	—	likely benign
rs139661780	2:18,768,853	C/G	—	uncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.