RIN3
Ras and Rab interactor 3
Summary
Summary: This protein encoded by this gene is a member of the RIN family of Ras interaction-interference proteins, which are binding partners to the RAB5 small GTPases. The protein functions as a guanine nucleotide exchange for RAB5B and RAB31. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]
Known Variants84 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1896362245 | 14:92,980,270 | C/A | — | uncertain significance |
| rs61409971 | 14:93,012,625 | G/A | intron variant | — |
| rs10131197 | 14:93,015,394 | A/G | intron variant | — |
| rs10131290 | 14:93,015,479 | A/G | — | — |
| rs190161374 | 14:93,016,350 | G/A | regulatory region variant | — |
| rs7157029 | 14:93,017,566 | G/A | regulatory region variant | — |
| rs1184429170 | 14:93,022,173 | A/G | — | uncertain significance |
| rs2503649321 | 14:93,022,205 | A/G | — | likely benign |
| rs201845332 | 14:93,022,287 | G/A | — | likely benign |
| rs56098450 | 14:93,027,166 | C/A | regulatory region variant | — |
| rs200444790 | 14:93,043,781 | C/T | — | uncertain significance |
| rs2503424569 | 14:93,043,873 | A/T | — | uncertain significance |
| rs72697295 | 14:93,069,980 | G/A | — | — |
| rs72697297 | 14:93,069,989 | T/C | regulatory region variant | — |
| rs78440108 | 14:93,070,286 | C/T | regulatory region variant | — |
| rs72697299 | 14:93,070,367 | C/T | regulatory region variant | — |
| rs35629566 | 14:93,072,317 | C/A | — | — |
| rs72699818 | 14:93,077,611 | T/C | regulatory region variant | — |
| rs1232646323 | 14:93,081,803 | T/C | — | uncertain significance |
| rs149187226 | 14:93,088,100 | G/A | intron variant | — |
| rs7141996 | 14:93,094,298 | G/A | intron variant | — |
| rs11623779 | 14:93,096,391 | T/C | intron variant | — |
| rs11621587 | 14:93,098,339 | G/C | intron variant | — |
| rs17184313 | 14:93,102,251 | C/G | — | — |
| rs10498635 | 14:93,103,309 | C/T | intron variant | — |
| rs11627032 | 14:93,104,072 | T/A | — | — |
| rs146503912 | 14:93,107,620 | A/C | — | uncertain significance |
| rs1342060411 | 14:93,107,642 | C/T | — | uncertain significance |
| rs2503538727 | 14:93,107,697 | G/T | — | uncertain significance |
| rs2503539266 | 14:93,107,906 | A/C | — | uncertain significance |
| rs1075472 | 14:93,108,131 | A/G | intron variant | — |
| rs734206 | 14:93,108,464 | T/A | — | — |
| rs578113254 | 14:93,112,311 | G/A | — | — |
| rs112560164 | 14:93,112,924 | G/A | intron variant | — |
| rs754388 | 14:93,115,410 | G/A | — | — |
| rs967095052 | 14:93,117,950 | C/A | — | uncertain significance |
| rs141011280 | 14:93,117,953 | C/T | — | uncertain significance |
| rs762604956 | 14:93,117,957 | A/C | — | uncertain significance |
| rs779236886 | 14:93,118,001 | G/A | — | uncertain significance |
| rs368941632 | 14:93,118,004 | T/C | — | uncertain significance |
| rs763772852 | 14:93,118,037 | C/T | — | uncertain significance |
| rs28663978 | 14:93,118,043 | G/A | — | uncertain significance |
| rs761172106 | 14:93,118,190 | T/A | — | uncertain significance |
| rs2503559655 | 14:93,118,274 | C/G | — | uncertain significance |
| rs776128263 | 14:93,118,371 | C/T | — | uncertain significance |
| rs764937631 | 14:93,118,398 | A/G | — | uncertain significance |
| rs1407735267 | 14:93,118,430 | T/C | — | likely benign |
| rs139992127 | 14:93,118,562 | C/T | — | uncertain significance |
| rs145578489 | 14:93,118,565 | G/A | — | likely benign |
| rs765997699 | 14:93,118,571 | G/A | — | uncertain significance |
| rs201333399 | 14:93,118,617 | G/A | — | uncertain significance |
| rs141595077 | 14:93,118,673 | C/T | — | likely benign |
| rs751810271 | 14:93,118,743 | C/T | — | uncertain significance |
| rs757802317 | 14:93,118,747 | G/C | — | uncertain significance |
| rs1887489440 | 14:93,118,761 | C/T | — | uncertain significance |
| rs750573436 | 14:93,118,770 | C/T | — | uncertain significance |
| rs143884398 | 14:93,118,797 | G/C | — | uncertain significance |
| rs149919482 | 14:93,119,093 | G/C | — | uncertain significance |
| rs147614557 | 14:93,119,123 | A/G | — | uncertain significance |
| rs374091561 | 14:93,119,189 | C/T | — | uncertain significance |
| rs1225046492 | 14:93,119,198 | T/C | — | uncertain significance |
| rs746203523 | 14:93,119,214 | A/G | — | uncertain significance |
| rs770243392 | 14:93,119,220 | C/T | — | uncertain significance |
| rs2503564668 | 14:93,119,319 | A/C | — | uncertain significance |
| rs764082541 | 14:93,119,333 | A/G | — | uncertain significance |
| rs751154201 | 14:93,119,335 | G/A | — | uncertain significance |
| rs199975411 | 14:93,119,372 | G/A | — | uncertain significance |
| rs768762308 | 14:93,119,417 | C/T | — | uncertain significance |
| rs747857960 | 14:93,125,619 | G/A | — | uncertain significance |
| rs779497612 | 14:93,125,685 | G/A | — | uncertain significance |
| rs1046031104 | 14:93,125,809 | A/G | — | uncertain significance |
| rs147042536 | 14:93,142,861 | T/C | — | likely benign |
| rs754628613 | 14:93,142,874 | G/A | — | uncertain significance |
| rs56208303 | 14:93,142,887 | G/A | — | benign |
| rs752209042 | 14:93,151,346 | A/T | — | uncertain significance |
| rs2503640375 | 14:93,151,452 | G/A | — | uncertain significance |
| rs773247649 | 14:93,153,866 | C/A | — | — |
| rs2503648544 | 14:93,154,302 | A/G | — | uncertain significance |
| rs368234737 | 14:93,154,388 | C/T | — | uncertain significance |
| rs368824511 | 14:93,154,424 | G/C | — | uncertain significance |
| rs748050403 | 14:93,154,431 | G/A | — | uncertain significance |
| rs759158028 | 14:93,154,458 | C/T | — | uncertain significance |
| rs202018881 | 14:93,154,487 | A/C | — | uncertain significance |
| rs766595882 | 14:93,154,577 | C/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.