SUGP2
SURP and G-patch domain containing 2
Summary
This gene encodes a member of the arginine/serine-rich family of splicing factors. The encoded protein functions in mRNA processing. Alternatively spliced transcript variants have been described. [provided by RefSeq, Feb 2009]
Known Variants62 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs183027848 | 19:19,105,258 | C/T | — | uncertain significance |
| rs201431527 | 19:19,106,050 | C/T | — | uncertain significance |
| rs1003803618 | 19:19,106,068 | C/T | — | uncertain significance |
| rs539312588 | 19:19,109,536 | G/C | — | — |
| rs73006914 | 19:19,110,422 | C/A | — | — |
| rs752897249 | 19:19,112,441 | C/T | — | uncertain significance |
| rs371121890 | 19:19,112,442 | G/A | — | uncertain significance |
| rs751621128 | 19:19,112,468 | C/T | — | uncertain significance |
| rs140411225 | 19:19,113,360 | T/C | intron variant | — |
| rs145157655 | 19:19,115,072 | C/A | — | uncertain significance |
| rs368160175 | 19:19,115,130 | C/T | — | likely benign |
| rs763972693 | 19:19,115,142 | C/T | — | uncertain significance |
| rs760714207 | 19:19,115,171 | G/A | — | uncertain significance |
| rs141675288 | 19:19,115,202 | C/T | — | uncertain significance |
| rs932735663 | 19:19,115,220 | C/T | — | uncertain significance |
| rs2513410892 | 19:19,115,231 | G/A | — | uncertain significance |
| rs1296684554 | 19:19,115,277 | C/T | — | uncertain significance |
| rs550419254 | 19:19,115,333 | G/A | — | uncertain significance |
| rs139157473 | 19:19,115,337 | T/C | — | uncertain significance |
| rs999611321 | 19:19,119,193 | C/T | — | uncertain significance |
| rs549354023 | 19:19,119,222 | A/G | — | uncertain significance |
| rs144992117 | 19:19,119,232 | T/C | — | uncertain significance |
| rs772860547 | 19:19,120,741 | G/A | — | uncertain significance |
| rs2513505767 | 19:19,120,822 | A/G | — | uncertain significance |
| rs759499277 | 19:19,120,858 | C/T | — | uncertain significance |
| rs376121808 | 19:19,120,952 | G/A | — | uncertain significance |
| rs755641426 | 19:19,120,964 | G/A | — | uncertain significance |
| rs369530300 | 19:19,121,008 | C/T | — | uncertain significance |
| rs774333053 | 19:19,121,087 | G/A | — | uncertain significance |
| rs764665379 | 19:19,129,927 | G/C | — | uncertain significance |
| rs764498444 | 19:19,130,032 | G/A | — | uncertain significance |
| rs12981035 | 19:19,130,871 | T/A | intron variant | — |
| rs189998358 | 19:19,131,834 | G/A | intron variant | — |
| rs773499718 | 19:19,135,443 | T/C | — | uncertain significance |
| rs766777240 | 19:19,135,515 | C/T | — | uncertain significance |
| rs759764812 | 19:19,135,520 | T/C | — | uncertain significance |
| rs771639087 | 19:19,135,603 | T/A | — | uncertain significance |
| rs759346528 | 19:19,135,767 | C/G | — | uncertain significance |
| rs908952965 | 19:19,135,781 | A/T | — | uncertain significance |
| rs184057440 | 19:19,136,139 | T/C | — | uncertain significance |
| rs2513775794 | 19:19,136,199 | C/T | — | uncertain significance |
| rs753112571 | 19:19,136,202 | T/C | — | likely benign |
| rs2513776001 | 19:19,136,206 | G/C | — | uncertain significance |
| rs747055033 | 19:19,136,213 | C/T | — | uncertain significance |
| rs2513776468 | 19:19,136,226 | T/C | — | uncertain significance |
| rs576858379 | 19:19,136,234 | C/T | — | uncertain significance |
| rs1377246854 | 19:19,136,330 | G/A | — | uncertain significance |
| rs1568455897 | 19:19,136,393 | A/T | — | uncertain significance |
| rs148151679 | 19:19,136,516 | C/T | — | uncertain significance |
| rs953329830 | 19:19,136,591 | C/T | — | uncertain significance |
| rs2058902262 | 19:19,136,602 | C/A | — | uncertain significance |
| rs537778892 | 19:19,136,636 | C/T | — | uncertain significance |
| rs777073523 | 19:19,136,763 | G/A | — | uncertain significance |
| rs2513794417 | 19:19,136,838 | A/G | — | uncertain significance |
| rs373340429 | 19:19,136,913 | T/G | — | uncertain significance |
| rs2058923057 | 19:19,136,971 | T/G | — | uncertain significance |
| rs375114418 | 19:19,137,001 | C/G | — | likely benign |
| rs2513799403 | 19:19,137,014 | C/A | — | uncertain significance |
| rs750988612 | 19:19,137,033 | G/T | — | uncertain significance |
| rs531945811 | 19:19,139,644 | A/G | — | — |
| rs541734593 | 19:19,141,774 | T/A | — | uncertain significance |
| rs768546522 | 19:19,141,853 | T/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.