CLIP1

CAP-Gly domain containing linker protein 1

Summary

The protein encoded by this gene links endocytic vesicles to microtubules. This gene is highly expressed in Reed-Sternberg cells of Hodgkin disease. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]

Known Variants118 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs10270	12:122,756,342	G/A	downstream gene variant	—
rs756787282	12:122,757,476	G/C	—	uncertain significance
rs780582171	12:122,757,480	T/A	—	uncertain significance
rs765475076	12:122,757,513	T/C	—	uncertain significance
rs2547195726	12:122,757,558	G/C	—	uncertain significance
rs374978178	12:122,757,621	T/C	—	uncertain significance
rs201297279	12:122,758,610	C/T	—	uncertain significance
rs2547205225	12:122,758,669	T/C	—	uncertain significance
rs2547205348	12:122,758,678	A/G	—	uncertain significance
rs7968420	12:122,760,191	G/A	—	—
rs1592957865	12:122,762,725	C/G	—	uncertain significance
rs78676307	12:122,762,743	T/C	—	benign
rs370225545	12:122,763,330	G/A	—	likely benign
rs766333607	12:122,763,347	C/G	—	uncertain significance
rs142499667	12:122,763,406	G/C	—	likely benign
rs771499354	12:122,763,427	T/C	—	likely benign
rs372003670	12:122,763,455	T/C	—	uncertain significance
rs148653401	12:122,763,466	G/A	—	likely benign
rs1566069686	12:122,763,631	T/A	—	uncertain significance
rs17881033	12:122,763,670	C/A	—	likely benign
rs375267504	12:122,794,336	G/A	—	likely benign
rs200110148	12:122,794,381	C/T	—	likely benign
rs1242730063	12:122,801,328	C/A	—	uncertain significance
rs748125127	12:122,801,333	C/T	—	uncertain significance
rs532538060	12:122,801,355	G/C	—	uncertain significance
rs1481199665	12:122,803,785	C/A	—	likely benign
rs201714257	12:122,803,809	G/A	—	likely benign
rs757261205	12:122,803,881	C/T	—	likely benign
rs781272448	12:122,803,882	G/A	—	uncertain significance
rs201275758	12:122,803,890	A/G	—	likely benign
rs368149044	12:122,812,484	C/T	—	uncertain significance
rs755593779	12:122,812,558	C/T	—	likely benign
rs570410484	12:122,812,563	G/A	—	benign
rs773140799	12:122,812,594	G/A	—	likely benign
rs145767151	12:122,812,630	G/C	—	uncertain significance
rs1555264879	12:122,812,646	T/A	—	uncertain significance
rs875989820	12:122,812,682	G/A	—	uncertain significance
rs924615128	12:122,812,684	T/C	—	uncertain significance
rs574120310	12:122,812,687	T/C	—	uncertain significance
rs766914209	12:122,812,867	C/G	—	uncertain significance
rs199619793	12:122,812,919	A/T	—	uncertain significance
rs377320132	12:122,817,556	C/T	—	uncertain significance
rs143777418	12:122,817,561	A/C	—	uncertain significance
rs1283328324	12:122,819,210	G/C	—	uncertain significance
rs34177347	12:122,819,250	T/C	—	conflicting classifications of pathogenicity
rs137857498	12:122,821,194	T/C	—	likely benign
rs375698666	12:122,821,200	C/T	—	likely benign
rs748959643	12:122,821,262	C/G	—	uncertain significance
rs144240398	12:122,825,299	C/A	—	uncertain significance
rs776825338	12:122,825,310	T/C	—	uncertain significance
rs76532232	12:122,825,315	A/G	—	likely benign
rs3741447	12:122,825,413	G/A	—	conflicting classifications of pathogenicity
rs757189888	12:122,825,522	C/T	—	uncertain significance
rs774622840	12:122,825,559	G/C	—	uncertain significance
rs373375564	12:122,825,575	C/T	—	uncertain significance
rs545710606	12:122,825,597	G/T	—	uncertain significance
rs201352592	12:122,825,734	C/T	—	uncertain significance
rs140672946	12:122,825,793	G/A	—	uncertain significance
rs1302205735	12:122,825,796	T/C	—	uncertain significance
rs139321433	12:122,825,858	G/T	—	likely benign
rs1952485958	12:122,825,860	T/C	—	uncertain significance
rs2547556680	12:122,825,893	T/C	—	uncertain significance
rs371231033	12:122,825,967	G/A	—	uncertain significance
rs771496362	12:122,825,974	T/C	—	likely benign
rs751767143	12:122,825,995	T/C	—	uncertain significance
rs780646864	12:122,826,024	T/C	—	uncertain significance
rs549426099	12:122,826,137	A/G	—	likely benign
rs2136344211	12:122,826,143	A/T	—	uncertain significance
rs201330075	12:122,826,144	T/C	—	uncertain significance
rs1158251525	12:122,826,151	C/T	—	uncertain significance
rs1324172594	12:122,826,162	C/T	—	uncertain significance
rs1012699618	12:122,826,167	C/T	—	likely benign
rs10773088	12:122,828,069	A/G	—	—
rs899229922	12:122,831,970	A/C	—	uncertain significance
rs149025674	12:122,832,002	G/A	—	uncertain significance
rs746134099	12:122,835,678	T/C	—	uncertain significance
rs117592229	12:122,835,688	T/C	—	benign
rs1406976858	12:122,839,025	G/C	—	uncertain significance
rs1430348466	12:122,839,106	G/A	—	uncertain significance
rs1320593798	12:122,839,673	C/T	—	uncertain significance
rs758749763	12:122,839,676	C/T	—	uncertain significance
rs1593144293	12:122,839,704	C/T	—	likely benign
rs138064731	12:122,839,710	C/A	—	likely benign
rs759562298	12:122,839,712	C/T	—	uncertain significance
rs764436620	12:122,839,717	C/T	—	uncertain significance
rs751868310	12:122,839,719	C/T	—	uncertain significance
rs149345437	12:122,839,841	G/A	—	uncertain significance
rs547632811	12:122,839,848	G/A	—	likely benign
rs757843503	12:122,845,602	C/T	—	likely benign
rs115643125	12:122,845,608	C/T	—	benign
rs775992825	12:122,845,615	A/G	—	uncertain significance
rs930512802	12:122,845,657	G/A	—	uncertain significance
rs372196407	12:122,848,536	C/G	—	uncertain significance
rs754102187	12:122,848,597	C/T	—	uncertain significance
rs146627539	12:122,848,601	G/A	—	benign
rs758764782	12:122,848,612	T/A	—	uncertain significance
rs958782845	12:122,848,627	G/A	—	uncertain significance
rs769477406	12:122,848,628	G/T	—	uncertain significance
rs779820660	12:122,848,636	C/A	—	uncertain significance
rs140634925	12:122,861,989	C/G	—	likely benign

Showing 100 of 118 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.