DSCAML1
DS cell adhesion molecule like 1
Summary
The protein encoded by this gene is a member of the Ig superfamily of cell adhesion molecules and is involved in neuronal differentiation. The encoded membrane-bound protein localizes to the cell surface, where it forms aggregates that repel neuronal processes of the same cell type. [provided by RefSeq, Sep 2016]
Known Variants1,108 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs3741283 | 11:117,299,039 | G/C | — | benign |
| rs752650717 | 11:117,299,053 | G/C | — | likely benign |
| rs2542948544 | 11:117,299,061 | A/G | — | uncertain significance |
| rs2047703935 | 11:117,299,066 | G/C | — | uncertain significance |
| rs764358636 | 11:117,299,067 | A/G | — | uncertain significance |
| rs754158750 | 11:117,299,068 | G/A | — | likely benign |
| rs146675916 | 11:117,299,072 | G/A | — | uncertain significance |
| rs199968404 | 11:117,299,073 | C/T | — | uncertain significance |
| rs140170178 | 11:117,299,077 | G/A | — | likely benign |
| rs2047704439 | 11:117,299,078 | G/A | — | uncertain significance |
| rs143875346 | 11:117,299,079 | C/T | — | likely benign |
| rs1484500272 | 11:117,299,080 | C/T | — | likely benign |
| rs371134042 | 11:117,299,103 | C/A | — | uncertain significance |
| rs202136721 | 11:117,299,106 | C/T | — | uncertain significance |
| rs764313532 | 11:117,299,107 | C/T | — | likely benign |
| rs762186342 | 11:117,299,121 | C/T | — | uncertain significance |
| rs142254786 | 11:117,299,122 | G/A | — | benign |
| rs536857940 | 11:117,299,128 | C/T | — | likely benign |
| rs151330891 | 11:117,299,143 | C/T | — | likely benign |
| rs1327920172 | 11:117,299,144 | C/T | — | uncertain significance |
| rs2047706822 | 11:117,299,146 | C/T | — | uncertain significance |
| rs1288543114 | 11:117,299,156 | T/C | — | uncertain significance |
| rs916593525 | 11:117,299,162 | C/T | — | uncertain significance |
| rs746166512 | 11:117,299,166 | C/T | — | uncertain significance |
| rs201303561 | 11:117,299,167 | G/A | — | likely benign |
| rs1201470618 | 11:117,299,169 | C/T | — | uncertain significance |
| rs1272931015 | 11:117,299,170 | T/C | — | likely benign |
| rs1024856803 | 11:117,299,171 | C/T | — | uncertain significance |
| rs370252456 | 11:117,299,175 | G/A | — | uncertain significance |
| rs2542950190 | 11:117,299,177 | G/T | — | uncertain significance |
| rs747590806 | 11:117,299,181 | C/T | — | uncertain significance |
| rs576671392 | 11:117,299,182 | G/A | — | likely benign |
| rs776798501 | 11:117,299,188 | G/A | — | likely benign |
| rs773507353 | 11:117,299,192 | G/A | — | uncertain significance |
| rs752617299 | 11:117,299,194 | C/T | — | likely benign |
| rs755988012 | 11:117,299,195 | G/A | — | uncertain significance |
| rs764021953 | 11:117,299,200 | G/A | — | likely benign |
| rs753302101 | 11:117,299,201 | G/T | — | uncertain significance |
| rs778403842 | 11:117,299,205 | C/T | — | uncertain significance |
| rs750127893 | 11:117,299,206 | G/A | — | likely benign |
| rs1038729722 | 11:117,299,209 | G/A | — | likely benign |
| rs769222169 | 11:117,299,214 | C/T | — | uncertain significance |
| rs1452210417 | 11:117,299,218 | G/A | — | likely benign |
| rs2047709644 | 11:117,299,219 | G/A | — | uncertain significance |
| rs1476374021 | 11:117,299,233 | G/T | — | likely benign |
| rs2542950835 | 11:117,299,234 | G/C | — | uncertain significance |
| rs1284730958 | 11:117,299,236 | G/A | — | likely benign |
| rs748130077 | 11:117,299,237 | G/A | — | uncertain significance |
| rs1384317034 | 11:117,299,241 | C/G | — | uncertain significance |
| rs769966155 | 11:117,299,242 | G/A | — | likely benign |
| rs2047710804 | 11:117,299,243 | G/A | — | uncertain significance |
| rs1021902671 | 11:117,299,246 | G/A | — | uncertain significance |
| rs1381143446 | 11:117,299,250 | G/A | — | uncertain significance |
| rs763293056 | 11:117,299,251 | G/A | — | likely benign |
| rs967064423 | 11:117,299,253 | G/A | — | uncertain significance |
| rs373112304 | 11:117,299,254 | G/A | — | likely benign |
| rs760492346 | 11:117,299,255 | G/T | — | uncertain significance |
| rs2137050100 | 11:117,299,256 | C/T | — | uncertain significance |
| rs960537269 | 11:117,299,262 | C/T | — | uncertain significance |
| rs558725278 | 11:117,299,263 | G/A | — | likely benign |
| rs1165612080 | 11:117,299,265 | C/T | — | uncertain significance |
| rs572391937 | 11:117,299,266 | T/C | — | likely benign |
| rs549967851 | 11:117,299,267 | G/T | — | uncertain significance |
| rs750034909 | 11:117,299,268 | G/C | — | uncertain significance |
| rs779859656 | 11:117,299,270 | G/A | — | uncertain significance |
| rs751935158 | 11:117,299,271 | G/A | — | uncertain significance |
| rs561070197 | 11:117,299,272 | G/T | — | likely benign |
| rs200329592 | 11:117,299,273 | G/T | — | uncertain significance |
| rs769760089 | 11:117,299,276 | G/A | — | uncertain significance |
| rs112326789 | 11:117,299,278 | C/T | — | uncertain significance |
| rs777851211 | 11:117,299,282 | G/A | — | uncertain significance |
| rs930221363 | 11:117,299,283 | C/T | — | uncertain significance |
| rs749332074 | 11:117,299,290 | C/A | — | uncertain significance |
| rs774575847 | 11:117,299,303 | G/A | — | uncertain significance |
| rs760438880 | 11:117,299,304 | T/C | — | uncertain significance |
| rs954870089 | 11:117,299,306 | G/T | — | uncertain significance |
| rs2542952013 | 11:117,299,314 | G/A | — | likely benign |
| rs1259189993 | 11:117,299,315 | G/C | — | uncertain significance |
| rs761872269 | 11:117,299,316 | C/T | — | uncertain significance |
| rs563097187 | 11:117,299,317 | G/A | — | likely benign |
| rs532349976 | 11:117,299,322 | C/T | — | uncertain significance |
| rs140530446 | 11:117,299,323 | G/A | — | likely benign |
| rs2047715190 | 11:117,299,325 | G/A | — | uncertain significance |
| rs546069251 | 11:117,299,327 | G/A | — | uncertain significance |
| rs768061825 | 11:117,299,328 | C/A | — | uncertain significance |
| rs559119644 | 11:117,299,329 | C/G | — | benign |
| rs778172814 | 11:117,299,330 | C/T | — | uncertain significance |
| rs2542952247 | 11:117,299,334 | G/T | — | uncertain significance |
| rs779073642 | 11:117,299,338 | G/A | — | likely benign |
| rs2047716054 | 11:117,299,343 | G/A | — | uncertain significance |
| rs1256518161 | 11:117,299,361 | C/T | — | uncertain significance |
| rs766028547 | 11:117,299,362 | A/T | — | likely benign |
| rs759321410 | 11:117,299,366 | T/C | — | uncertain significance |
| rs1198060014 | 11:117,299,377 | G/T | — | uncertain significance |
| rs1426667540 | 11:117,299,379 | G/A | — | uncertain significance |
| rs767282357 | 11:117,299,381 | C/T | — | uncertain significance |
| rs753066184 | 11:117,299,382 | G/A | — | uncertain significance |
| rs1461779264 | 11:117,299,385 | C/T | — | uncertain significance |
| rs2047717734 | 11:117,299,390 | G/A | — | uncertain significance |
| rs2542952798 | 11:117,299,395 | G/A | — | likely benign |
Showing 100 of 1,108 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.