AKNAD1

AKNA domain containing 1

Summary

This gene encodes a protein which contains a domain found in an AT-hook-containing transcription factor. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2012]

Known Variants59 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs145949871	1:109,358,799	T/G	—	uncertain significance
rs756248528	1:109,358,806	C/T	—	likely benign
rs966666421	1:109,358,848	G/A	—	likely benign
rs753254641	1:109,359,679	T/C	—	uncertain significance
rs1663635922	1:109,359,699	A/C	—	uncertain significance
rs142355297	1:109,359,765	C/T	—	uncertain significance
rs377132841	1:109,363,180	G/A	—	uncertain significance
rs779539017	1:109,363,213	C/T	—	uncertain significance
rs541057411	1:109,366,003	T/C	—	uncertain significance
rs1023388636	1:109,366,055	G/A	—	uncertain significance
rs866205366	1:109,366,208	C/A	—	uncertain significance
rs775377275	1:109,369,851	C/T	—	uncertain significance
rs762177802	1:109,369,859	T/C	—	uncertain significance
rs779270486	1:109,369,914	C/A	—	uncertain significance
rs143433407	1:109,373,196	C/A	—	uncertain significance
rs140157073	1:109,373,208	C/T	—	uncertain significance
rs199923486	1:109,373,226	G/A	—	uncertain significance
rs544090925	1:109,373,253	G/A	—	uncertain significance
rs972630568	1:109,377,118	G/A	—	likely benign
rs201355205	1:109,377,148	T/C	—	uncertain significance
rs771542694	1:109,377,606	G/T	—	uncertain significance
rs1346565298	1:109,377,653	G/A	—	uncertain significance
rs2524646250	1:109,377,677	A/G	—	uncertain significance
rs370267672	1:109,380,191	A/C	—	uncertain significance
rs143468067	1:109,385,778	C/T	—	uncertain significance
rs754345409	1:109,385,784	T/C	—	uncertain significance
rs146735362	1:109,385,810	T/G	—	uncertain significance
rs745826129	1:109,385,844	A/G	—	uncertain significance
rs576852391	1:109,391,402	G/A	—	uncertain significance
rs754895224	1:109,391,436	C/A	—	uncertain significance
rs1375389362	1:109,391,558	T/G	—	uncertain significance
rs138642492	1:109,391,658	G/A	—	likely benign
rs370187001	1:109,392,186	C/T	—	uncertain significance
rs1277203	1:109,392,837	C/T	intron variant	—
rs372577805	1:109,394,376	T/C	—	uncertain significance
rs768759491	1:109,394,383	T/C	—	uncertain significance
rs879429112	1:109,394,428	T/C	—	uncertain significance
rs777288194	1:109,394,465	C/G	—	likely benign
rs772310438	1:109,394,583	T/A	—	uncertain significance
rs553089987	1:109,394,721	G/A	—	likely benign
rs2524695914	1:109,394,755	C/T	—	uncertain significance
rs1212674940	1:109,394,759	C/G	—	uncertain significance
rs140527469	1:109,394,793	G/A	—	uncertain significance
rs774838943	1:109,394,850	G/A	—	uncertain significance
rs1273548236	1:109,394,889	A/G	—	uncertain significance
rs147800238	1:109,394,923	A/G	—	uncertain significance
rs748027442	1:109,394,938	G/T	—	uncertain significance
rs1664892986	1:109,394,952	A/T	—	uncertain significance
rs367694753	1:109,394,980	C/A	—	uncertain significance
rs1193296540	1:109,394,984	T/G	—	uncertain significance
rs2524696932	1:109,395,015	C/T	—	uncertain significance
rs375477243	1:109,395,025	C/G	—	uncertain significance
rs142028863	1:109,395,031	C/T	—	uncertain significance
rs2524697027	1:109,395,041	G/C	—	uncertain significance
rs769224939	1:109,395,049	C/A	—	uncertain significance
rs933712579	1:109,395,062	T/G	—	uncertain significance
rs774264243	1:109,395,163	C/T	—	uncertain significance
rs41279674	1:109,395,258	G/A	—	uncertain significance
rs138948369	1:109,395,280	C/T	—	uncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.