SEC31B
SEC31 homolog B, COPII component
Summary
This gene encodes a protein of unknown function. The protein has moderate similarity to rat VAP1 protein which is an endosomal membrane-associated protein, containing a putative Ca2+/calmodulin-dependent kinase II phosphorylation site. [provided by RefSeq, Jul 2008]
Known Variants85 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs542973878 | 10:102,247,392 | G/A | — | uncertain significance |
| rs561655156 | 10:102,247,393 | C/T | — | uncertain significance |
| rs2492833947 | 10:102,247,396 | T/C | — | uncertain significance |
| rs1162224522 | 10:102,247,423 | T/G | — | uncertain significance |
| rs150586701 | 10:102,247,438 | C/T | — | uncertain significance |
| rs532079426 | 10:102,247,448 | G/C | — | uncertain significance |
| rs767865962 | 10:102,247,502 | A/C | — | uncertain significance |
| rs140998456 | 10:102,247,548 | G/A | — | uncertain significance |
| rs140504657 | 10:102,247,813 | A/G | — | likely benign |
| rs527366544 | 10:102,248,625 | G/A | — | uncertain significance |
| rs367572736 | 10:102,248,689 | G/A | — | uncertain significance |
| rs201352890 | 10:102,249,037 | G/A | — | uncertain significance |
| rs531498743 | 10:102,249,041 | G/T | — | uncertain significance |
| rs148697151 | 10:102,249,083 | T/A | — | uncertain significance |
| rs750563008 | 10:102,249,088 | T/C | — | likely benign |
| rs1424628398 | 10:102,249,136 | G/A | — | uncertain significance |
| rs139252999 | 10:102,249,137 | G/A | — | uncertain significance |
| rs764443825 | 10:102,249,475 | G/T | — | uncertain significance |
| rs2492841488 | 10:102,249,831 | G/A | — | uncertain significance |
| rs774756323 | 10:102,249,852 | T/C | — | uncertain significance |
| rs146812157 | 10:102,249,885 | G/A | — | uncertain significance |
| rs1312379711 | 10:102,249,896 | A/G | — | likely benign |
| rs149977742 | 10:102,249,920 | A/G | — | uncertain significance |
| rs780079597 | 10:102,249,923 | A/G | — | uncertain significance |
| rs748408887 | 10:102,249,948 | T/C | — | likely benign |
| rs761231588 | 10:102,249,959 | C/T | — | likely benign |
| rs767261666 | 10:102,249,975 | A/G | — | uncertain significance |
| rs373986067 | 10:102,249,980 | A/G | — | uncertain significance |
| rs368613786 | 10:102,249,984 | G/A | — | uncertain significance |
| rs773946652 | 10:102,250,028 | G/A | — | uncertain significance |
| rs2492842091 | 10:102,250,030 | G/C | — | uncertain significance |
| rs778009464 | 10:102,250,469 | T/C | — | uncertain significance |
| rs201605633 | 10:102,250,472 | C/T | — | uncertain significance |
| rs138360654 | 10:102,250,606 | G/T | — | uncertain significance |
| rs1167850594 | 10:102,255,206 | A/T | — | uncertain significance |
| rs201699532 | 10:102,255,210 | C/A | — | uncertain significance |
| rs1404768411 | 10:102,255,213 | T/C | — | likely benign |
| rs145944362 | 10:102,255,251 | A/G | — | uncertain significance |
| rs368290309 | 10:102,255,255 | C/T | — | uncertain significance |
| rs747944272 | 10:102,255,275 | A/C | — | uncertain significance |
| rs1355822073 | 10:102,255,303 | G/A | — | uncertain significance |
| rs758067644 | 10:102,256,047 | C/T | — | uncertain significance |
| rs777642860 | 10:102,256,049 | G/A | — | uncertain significance |
| rs746877100 | 10:102,256,053 | C/T | — | uncertain significance |
| rs9420790 | 10:102,256,197 | G/T | — | — |
| rs149062257 | 10:102,257,022 | C/A | — | uncertain significance |
| rs2492860838 | 10:102,257,472 | C/A | — | uncertain significance |
| rs765372360 | 10:102,257,498 | C/A | — | uncertain significance |
| rs191855412 | 10:102,257,821 | G/A | — | likely benign |
| rs138105588 | 10:102,257,827 | G/C | — | uncertain significance |
| rs1589733872 | 10:102,257,853 | C/T | — | uncertain significance |
| rs2492865270 | 10:102,258,984 | A/G | — | uncertain significance |
| rs185616140 | 10:102,259,004 | C/A | — | uncertain significance |
| rs571312370 | 10:102,259,009 | T/C | — | uncertain significance |
| rs1315313164 | 10:102,262,172 | G/A | — | uncertain significance |
| rs2492872814 | 10:102,262,210 | G/C | — | uncertain significance |
| rs372919677 | 10:102,265,153 | T/C | — | uncertain significance |
| rs778023087 | 10:102,265,186 | C/T | — | uncertain significance |
| rs2492878739 | 10:102,265,191 | G/A | — | uncertain significance |
| rs770270783 | 10:102,265,224 | G/A | — | uncertain significance |
| rs1331719030 | 10:102,265,816 | T/C | — | uncertain significance |
| rs1487776272 | 10:102,265,843 | A/G | — | uncertain significance |
| rs2295774 | 10:102,265,847 | A/T | missense variant | — |
| rs375086611 | 10:102,265,865 | C/T | — | uncertain significance |
| rs1427297728 | 10:102,265,954 | A/G | — | uncertain significance |
| rs1452175193 | 10:102,266,113 | T/C | — | uncertain significance |
| rs11190587 | 10:102,266,638 | C/G | — | — |
| rs775770577 | 10:102,267,224 | C/T | — | uncertain significance |
| rs753277513 | 10:102,267,246 | C/T | — | uncertain significance |
| rs2492884086 | 10:102,267,269 | C/T | — | uncertain significance |
| rs751891158 | 10:102,267,691 | T/C | — | uncertain significance |
| rs764671612 | 10:102,267,754 | G/C | — | uncertain significance |
| rs375862494 | 10:102,267,772 | G/A | — | uncertain significance |
| rs112097675 | 10:102,267,805 | G/C | — | uncertain significance |
| rs773941606 | 10:102,268,771 | T/A | — | uncertain significance |
| rs1851689316 | 10:102,268,859 | C/T | — | uncertain significance |
| rs761948301 | 10:102,269,138 | G/A | — | uncertain significance |
| rs148779271 | 10:102,269,149 | G/A | — | uncertain significance |
| rs142391082 | 10:102,269,168 | C/G | — | uncertain significance |
| rs745484505 | 10:102,269,174 | A/T | — | uncertain significance |
| rs146423915 | 10:102,269,183 | G/A | — | uncertain significance |
| rs1269493982 | 10:102,269,248 | C/G | — | uncertain significance |
| rs4917902 | 10:102,274,998 | G/A | — | — |
| rs747139486 | 10:102,275,926 | C/T | — | uncertain significance |
| rs201874203 | 10:102,276,687 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.