HAUS6
HAUS augmin like complex subunit 6
Summary
The protein encoded by this gene is a subunit of the augmin complex. The augmin complex plays a role in microtubule attachment to the kinetochore and central spindle formation. This protein may have a role in efficient chromosome congression and segregation by promoting microtubule-dependent microtubule amplification. Pseudogenes of this gene are located on chromosomes 7 and 20. Alternative splicing results in multiple transcript variants that encode different protein isoforms. [provided by RefSeq, Aug 2012]
Known Variants75 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs201056474 | 9:19,056,398 | T/G | — | uncertain significance |
| rs2489222277 | 9:19,057,991 | G/A | — | uncertain significance |
| rs373281093 | 9:19,058,049 | A/G | — | uncertain significance |
| rs148788726 | 9:19,058,072 | G/A | — | likely benign |
| rs763959516 | 9:19,058,075 | C/T | — | uncertain significance |
| rs1386036468 | 9:19,058,076 | G/A | — | uncertain significance |
| rs537866681 | 9:19,058,154 | G/C | — | uncertain significance |
| rs149710112 | 9:19,058,204 | G/A | — | uncertain significance |
| rs754485651 | 9:19,058,250 | C/A | — | uncertain significance |
| rs376889777 | 9:19,058,264 | C/T | — | uncertain significance |
| rs762141378 | 9:19,058,295 | G/C | — | uncertain significance |
| rs1208138874 | 9:19,058,297 | G/A | — | uncertain significance |
| rs370946839 | 9:19,058,327 | A/G | — | likely benign |
| rs1398613680 | 9:19,058,346 | T/G | — | uncertain significance |
| rs776427843 | 9:19,058,420 | T/C | — | uncertain significance |
| rs1476458428 | 9:19,058,423 | G/A | — | uncertain significance |
| rs527919595 | 9:19,058,471 | G/C | — | uncertain significance |
| rs199727248 | 9:19,058,474 | C/T | — | uncertain significance |
| rs1379905446 | 9:19,058,601 | T/C | — | uncertain significance |
| rs554017283 | 9:19,058,699 | T/G | — | uncertain significance |
| rs750669925 | 9:19,058,708 | A/G | — | uncertain significance |
| rs554778233 | 9:19,058,723 | T/C | — | uncertain significance |
| rs2489224449 | 9:19,058,739 | C/G | — | uncertain significance |
| rs750439820 | 9:19,058,766 | G/C | — | uncertain significance |
| rs769268526 | 9:19,058,931 | G/C | — | uncertain significance |
| rs60269255 | 9:19,059,865 | G/A | — | — |
| rs2171955 | 9:19,061,658 | T/C | downstream gene variant | — |
| rs2171954 | 9:19,061,659 | C/T | — | — |
| rs199958062 | 9:19,063,081 | A/T | — | uncertain significance |
| rs146554163 | 9:19,063,088 | G/C | — | uncertain significance |
| rs199865674 | 9:19,063,098 | C/T | — | uncertain significance |
| rs1836666798 | 9:19,063,101 | C/T | — | likely benign |
| rs2489233694 | 9:19,063,568 | A/G | — | uncertain significance |
| rs13287117 | 9:19,064,068 | C/G | — | — |
| rs13287517 | 9:19,064,129 | G/C | upstream gene variant | — |
| rs558093369 | 9:19,070,238 | G/A | — | uncertain significance |
| rs1360725788 | 9:19,070,268 | C/G | — | uncertain significance |
| rs148336635 | 9:19,070,278 | G/C | — | uncertain significance |
| rs12380322 | 9:19,074,538 | A/G | downstream gene variant | — |
| rs1168535736 | 9:19,076,674 | G/A | — | uncertain significance |
| rs562719033 | 9:19,076,687 | G/A | — | uncertain significance |
| rs748828305 | 9:19,078,175 | G/A | — | uncertain significance |
| rs149255370 | 9:19,078,233 | T/C | — | uncertain significance |
| rs544499565 | 9:19,078,274 | G/C | — | uncertain significance |
| rs768251644 | 9:19,078,284 | C/T | — | uncertain significance |
| rs146004976 | 9:19,080,482 | A/C | — | uncertain significance |
| rs143462027 | 9:19,080,490 | G/T | — | uncertain significance |
| rs778993432 | 9:19,080,523 | C/G | — | uncertain significance |
| rs1454273813 | 9:19,080,559 | C/T | — | uncertain significance |
| rs974130115 | 9:19,080,663 | A/G | — | uncertain significance |
| rs371706932 | 9:19,082,884 | T/G | — | uncertain significance |
| rs138226659 | 9:19,082,890 | A/G | — | uncertain significance |
| rs199750812 | 9:19,082,912 | G/A | — | uncertain significance |
| rs142571406 | 9:19,082,930 | T/G | — | uncertain significance |
| rs780117142 | 9:19,082,945 | C/A | — | uncertain significance |
| rs146901356 | 9:19,082,988 | C/A | — | uncertain significance |
| rs148389196 | 9:19,083,005 | T/C | — | uncertain significance |
| rs570643336 | 9:19,086,743 | T/G | — | uncertain significance |
| rs7037714 | 9:19,088,820 | G/A | upstream gene variant | — |
| rs139911174 | 9:19,089,430 | T/G | — | uncertain significance |
| rs775413265 | 9:19,089,454 | C/A | — | uncertain significance |
| rs755574064 | 9:19,089,545 | T/A | — | uncertain significance |
| rs899296946 | 9:19,089,551 | G/A | — | uncertain significance |
| rs148483833 | 9:19,093,191 | T/G | — | uncertain significance |
| rs2489277364 | 9:19,093,216 | T/C | — | uncertain significance |
| rs765450053 | 9:19,093,219 | T/C | — | uncertain significance |
| rs151253216 | 9:19,093,229 | G/A | — | uncertain significance |
| rs370117102 | 9:19,093,291 | C/T | — | uncertain significance |
| rs772854146 | 9:19,093,295 | A/T | — | uncertain significance |
| rs1044441591 | 9:19,094,334 | T/C | — | uncertain significance |
| rs147703808 | 9:19,094,344 | G/A | — | uncertain significance |
| rs1817816687 | 9:19,094,359 | T/A | — | uncertain significance |
| rs189824591 | 9:19,096,666 | C/G | — | likely benign |
| rs146772121 | 9:19,096,698 | G/C | — | uncertain significance |
| rs112107457 | 9:19,103,774 | C/G | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.