CD79A

CD79a molecule

Summary

The B lymphocyte antigen receptor is a multimeric complex that includes the antigen-specific component, surface immunoglobulin (Ig). Surface Ig non-covalently associates with two other proteins, Ig-alpha and Ig-beta, which are necessary for expression and function of the B-cell antigen receptor. This gene encodes the Ig-alpha protein of the B-cell antigen component. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]

Known Variants145 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs1428922	19:42,379,780	G/A	regulatory region variant	—
rs530102496	19:42,380,226	C/T	—	—
rs782206373	19:42,381,382	G/C	—	uncertain significance
rs782195967	19:42,381,386	T/G	—	likely benign
rs146480366	19:42,381,387	C/T	—	uncertain significance
rs782746615	19:42,381,395	C/T	—	likely benign
rs2123301467	19:42,381,398	C/T	—	likely benign
rs371184689	19:42,381,402	G/A	—	conflicting classifications of pathogenicity
rs782716159	19:42,381,404	T/C	—	likely benign
rs2513695999	19:42,381,425	C/A	—	likely benign
rs141033669	19:42,381,428	C/A	—	likely benign
rs1044944143	19:42,381,435	C/T	—	likely benign
rs1600629998	19:42,381,438	T/A	—	uncertain significance
rs377608483	19:42,381,459	T/C	—	uncertain significance
rs782176112	19:42,381,461	G/A	—	likely benign
rs782665303	19:42,381,467	G/A	—	likely benign
rs76983681	19:42,382,757	G/A	—	benign
rs1555843439	19:42,383,048	G/A	—	likely benign
rs781874528	19:42,383,057	C/T	—	uncertain significance
rs2074204427	19:42,383,060	G/T	—	uncertain significance
rs2513698671	19:42,383,061	C/G	—	likely benign
rs2123303737	19:42,383,067	G/C	—	likely benign
rs2513698746	19:42,383,088	C/T	—	likely benign
rs2513698783	19:42,383,100	A/C	—	likely benign
rs782421590	19:42,383,108	T/A	—	uncertain significance
rs199603062	19:42,383,114	G/C	—	uncertain significance
rs2074204859	19:42,383,117	T/C	—	uncertain significance
rs782302503	19:42,383,127	C/T	—	likely benign
rs1600631081	19:42,383,130	C/T	—	likely benign
rs764758292	19:42,383,144	C/T	—	conflicting classifications of pathogenicity
rs144847382	19:42,383,145	G/A	—	likely benign
rs370313642	19:42,383,159	A/G	—	uncertain significance
rs2074205317	19:42,383,162	A/T	—	uncertain significance
rs781792305	19:42,383,163	C/T	—	likely benign
rs782467376	19:42,383,164	G/A	—	uncertain significance
rs151224661	19:42,383,168	A/G	—	uncertain significance
rs140047688	19:42,383,169	C/T	—	likely benign
rs374041941	19:42,383,170	G/A	—	uncertain significance
rs1568801716	19:42,383,178	G/A	—	pathogenic
rs782657641	19:42,383,182	C/T	—	uncertain significance
rs782507150	19:42,383,183	G/A	—	conflicting classifications of pathogenicity
rs150297110	19:42,383,184	C/T	—	likely benign
rs2074205615	19:42,383,190	C/A	—	likely benign
rs199967393	19:42,383,204	C/A	—	uncertain significance
rs1487166711	19:42,383,205	G/A	—	likely benign
rs2074205887	19:42,383,222	T/C	—	uncertain significance
rs781949432	19:42,383,233	G/A	—	uncertain significance
rs587778166	19:42,383,238	C/A	—	uncertain significance
rs1383830014	19:42,383,239	C/T	—	uncertain significance
rs570673845	19:42,383,243	A/G	—	uncertain significance
rs137953079	19:42,383,249	C/T	—	uncertain significance
rs781875393	19:42,383,250	G/A	—	likely benign
rs117078414	19:42,383,281	G/A	—	likely benign
rs113019286	19:42,383,289	A/G	—	conflicting classifications of pathogenicity
rs2123304241	19:42,383,290	T/C	—	uncertain significance
rs200667174	19:42,383,292	C/T	—	likely benign
rs782661874	19:42,383,293	G/A	—	uncertain significance
rs143511203	19:42,383,300	G/A	—	uncertain significance
rs1600631294	19:42,383,303	T/G	—	pathogenic
rs782492918	19:42,383,307	G/A	—	likely benign
rs782207639	19:42,383,315	A/G	—	uncertain significance
rs1600631316	19:42,383,316	C/T	—	likely benign
rs2513699406	19:42,383,318	A/G	—	uncertain significance
rs145895409	19:42,383,321	C/T	—	uncertain significance
rs138454344	19:42,383,337	C/T	—	likely benign
rs782282654	19:42,383,338	G/A	—	uncertain significance
rs144006380	19:42,383,350	C/T	—	uncertain significance
rs144367487	19:42,383,351	G/A	—	uncertain significance
rs377615732	19:42,383,352	C/T	—	likely benign
rs548487112	19:42,383,353	G/A	—	uncertain significance
rs2123304410	19:42,383,354	T/G	—	uncertain significance
rs1600631350	19:42,383,355	G/A	—	likely benign
rs782709381	19:42,383,357	G/A	—	uncertain significance
rs1555843601	19:42,383,360	G/A	—	likely pathogenic
rs2513699525	19:42,383,362	G/A	—	uncertain significance
rs563307867	19:42,383,378	G/T	—	likely benign
rs1334158948	19:42,383,591	C/A	—	likely benign
rs1555843684	19:42,383,597	C/T	—	likely benign
rs1600631593	19:42,383,603	A/G	—	pathogenic
rs782014534	19:42,383,609	G/A	—	likely benign
rs1174888211	19:42,383,612	C/T	—	likely benign
rs782751776	19:42,383,619	C/A	—	uncertain significance
rs201206281	19:42,383,620	C/T	—	uncertain significance
rs2123304949	19:42,383,625	C/T	—	likely benign
rs1462257912	19:42,383,641	G/A	—	uncertain significance
rs148797987	19:42,383,644	C/A	—	conflicting classifications of pathogenicity
rs2513700301	19:42,383,652	C/A	—	likely benign
rs1555843732	19:42,383,653	G/A	—	uncertain significance
rs2074209426	19:42,383,667	G/A	—	uncertain significance
rs1221821073	19:42,383,677	T/C	—	uncertain significance
rs1349692713	19:42,383,678	C/T	—	likely benign
rs1555843760	19:42,383,684	G/A	—	likely benign
rs537675914	19:42,383,690	C/T	—	likely benign
rs782150073	19:42,383,691	G/A	—	uncertain significance
rs202097187	19:42,383,692	C/T	—	uncertain significance
rs1320852597	19:42,383,694	G/A	—	uncertain significance
rs781984117	19:42,383,708	G/A	—	likely benign
rs782244248	19:42,383,718	T/C	—	uncertain significance
rs2123305225	19:42,383,723	G/C	—	uncertain significance
rs1487832415	19:42,383,729	C/A	—	uncertain significance

Showing 100 of 145 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.