| 405285247 | CV3202617 | single nucleotide variant | NM_018137.3(PRMT6):c.-8C>T | PRMT6-related disorder [RCV003909872] | likely benign | 1 | 107056708 | 107056708 | Human | | name , trait , alternate_id |
| 405260402 | CV3209141 | single nucleotide variant | NM_018137.3(PRMT6):c.36G>C (p.Gly12=) | PRMT6-related disorder [RCV003943846] | likely benign | 1 | 107056751 | 107056751 | Human | | name , trait , alternate_id |
| 156043334 | CV2387968 | single nucleotide variant | NM_018137.3(PRMT6):c.14A>G (p.Lys5Arg) | not specified [RCV004236506] | uncertain significance | 1 | 107056729 | 107056729 | Human | | name |
| 405255679 | CV3210768 | single nucleotide variant | NM_018137.3(PRMT6):c.25C>G (p.Leu9Val) | PRMT6-related disorder [RCV003939284] | likely benign | 1 | 107056740 | 107056740 | Human | | name , trait , alternate_id |
| 155987421 | CV2275590 | single nucleotide variant | NM_018137.3(PRMT6):c.34G>C (p.Gly12Arg) | not specified [RCV004137225] | uncertain significance | 1 | 107056749 | 107056749 | Human | | name |
| 405292782 | CV3192591 | single nucleotide variant | NM_018137.3(PRMT6):c.942G>A (p.Pro314=) | PRMT6-related disorder [RCV003929840] | benign | 1 | 107057657 | 107057657 | Human | | name , trait , alternate_id |
| 405671786 | CV3377279 | single nucleotide variant | NM_018137.3(PRMT6):c.34G>T (p.Gly12Trp) | not specified [RCV004515312] | uncertain significance | 1 | 107056749 | 107056749 | Human | | name |
| 598203009 | CV3904600 | single nucleotide variant | NM_018137.3(PRMT6):c.67G>C (p.Glu23Gln) | not specified [RCV005269307] | uncertain significance | 1 | 107056782 | 107056782 | Human | | name |
| 405671776 | CV3377277 | single nucleotide variant | NM_018137.3(PRMT6):c.109C>G (p.Arg37Gly) | not specified [RCV004515310] | uncertain significance | 1 | 107056824 | 107056824 | Human | | name |
| 405671779 | CV3377278 | single nucleotide variant | NM_018137.3(PRMT6):c.160G>T (p.Val54Phe) | not specified [RCV004515311] | uncertain significance | 1 | 107056875 | 107056875 | Human | | name |
| 597780829 | CV3588031 | single nucleotide variant | NM_018137.3(PRMT6):c.236C>T (p.Ala79Val) | not specified [RCV004853587] | uncertain significance | 1 | 107056951 | 107056951 | Human | | name |
| 597780847 | CV3588035 | single nucleotide variant | NM_018137.3(PRMT6):c.127C>T (p.Arg43Trp) | not specified [RCV004853591] | uncertain significance | 1 | 107056842 | 107056842 | Human | | name |
| 598247329 | CV3904601 | single nucleotide variant | NM_018137.3(PRMT6):c.247G>A (p.Gly83Ser) | not specified [RCV005258623] | uncertain significance | 1 | 107056962 | 107056962 | Human | | name |
| 156401286 | CV2210817 | single nucleotide variant | NM_018137.3(PRMT6):c.892G>C (p.Gly298Arg) | not specified [RCV004085908] | uncertain significance | 1 | 107057607 | 107057607 | Human | | name |
| 156138378 | CV2211896 | single nucleotide variant | NM_018137.3(PRMT6):c.688C>T (p.Leu230Phe) | not specified [RCV004087029] | uncertain significance | 1 | 107057403 | 107057403 | Human | | name |
| 156119399 | CV2275808 | single nucleotide variant | NM_018137.3(PRMT6):c.349T>A (p.Trp117Arg) | not specified [RCV004139477] | uncertain significance | 1 | 107057064 | 107057064 | Human | | name |
| 155996556 | CV2288524 | single nucleotide variant | NM_018137.3(PRMT6):c.450T>A (p.Asp150Glu) | not specified [RCV004152056] | uncertain significance | 1 | 107057165 | 107057165 | Human | | name |
| 156098424 | CV2294549 | single nucleotide variant | NM_018137.3(PRMT6):c.818G>T (p.Gly273Val) | not specified [RCV004161821] | uncertain significance | 1 | 107057533 | 107057533 | Human | | name |
| 156266147 | CV2312304 | single nucleotide variant | NM_018137.3(PRMT6):c.597G>C (p.Gln199His) | not specified [RCV004167011] | uncertain significance | 1 | 107057312 | 107057312 | Human | | name |
| 155978510 | CV2321515 | single nucleotide variant | NM_018137.3(PRMT6):c.503G>A (p.Ser168Asn) | not specified [RCV004177483] | uncertain significance | 1 | 107057218 | 107057218 | Human | | name |
| 155918296 | CV2332975 | single nucleotide variant | NM_018137.3(PRMT6):c.316C>T (p.Arg106Trp) | not specified [RCV004194276] | uncertain significance | 1 | 107057031 | 107057031 | Human | | name |
| 155923750 | CV2351848 | single nucleotide variant | NM_018137.3(PRMT6):c.574T>C (p.Phe192Leu) | not specified [RCV004197992] | uncertain significance | 1 | 107057289 | 107057289 | Human | | name |
| 156387654 | CV2372814 | single nucleotide variant | NM_018137.3(PRMT6):c.730G>A (p.Glu244Lys) | not specified [RCV004221997] | uncertain significance | 1 | 107057445 | 107057445 | Human | | name |
| 329375855 | CV2431645 | single nucleotide variant | NM_018137.3(PRMT6):c.788T>C (p.Leu263Ser) | not specified [RCV004254790] | uncertain significance | 1 | 107057503 | 107057503 | Human | | name |
| 401744181 | CV2688112 | single nucleotide variant | NM_018137.3(PRMT6):c.853A>G (p.Met285Val) | not specified [RCV004305167] | uncertain significance | 1 | 107057568 | 107057568 | Human | | name |
| 401773958 | CV2727686 | single nucleotide variant | NM_018137.3(PRMT6):c.892G>A (p.Gly298Arg) | not specified [RCV004329858] | uncertain significance | 1 | 107057607 | 107057607 | Human | | name |
| 401863418 | CV2765781 | single nucleotide variant | NM_018137.3(PRMT6):c.979G>A (p.Glu327Lys) | not specified [RCV004335781] | uncertain significance | 1 | 107057694 | 107057694 | Human | | name |
| 405287842 | CV3217989 | single nucleotide variant | NM_018137.3(PRMT6):c.581C>T (p.Ala194Val) | PRMT6-related disorder [RCV003982113] | benign | 1 | 107057296 | 107057296 | Human | 13 | name , trait , alternate_id |
| 405671792 | CV3377280 | single nucleotide variant | NM_018137.3(PRMT6):c.395G>A (p.Arg132Gln) | not specified [RCV004515313] | uncertain significance | 1 | 107057110 | 107057110 | Human | | name |
| 405672512 | CV3377281 | single nucleotide variant | NM_018137.3(PRMT6):c.410C>T (p.Pro137Leu) | not specified [RCV004515314] | uncertain significance | 1 | 107057125 | 107057125 | Human | | name |
| 405672507 | CV3377282 | single nucleotide variant | NM_018137.3(PRMT6):c.631G>C (p.Val211Leu) | not specified [RCV004515315] | uncertain significance | 1 | 107057346 | 107057346 | Human | | name |
| 405672504 | CV3377283 | single nucleotide variant | NM_018137.3(PRMT6):c.761C>G (p.Ala254Gly) | not specified [RCV004515316] | uncertain significance | 1 | 107057476 | 107057476 | Human | | name |
| 405672500 | CV3377284 | single nucleotide variant | NM_018137.3(PRMT6):c.781G>C (p.Ala261Pro) | not specified [RCV004515317] | uncertain significance | 1 | 107057496 | 107057496 | Human | | name |
| 405672496 | CV3377285 | single nucleotide variant | NM_018137.3(PRMT6):c.853A>C (p.Met285Leu) | not specified [RCV004515318] | likely benign | 1 | 107057568 | 107057568 | Human | | name |
| 405672492 | CV3377286 | single nucleotide variant | NM_018137.3(PRMT6):c.858T>G (p.His286Gln) | not specified [RCV004515319] | uncertain significance | 1 | 107057573 | 107057573 | Human | | name |
| 405672488 | CV3377287 | single nucleotide variant | NM_018137.3(PRMT6):c.893G>A (p.Gly298Glu) | not specified [RCV004515320] | uncertain significance | 1 | 107057608 | 107057608 | Human | | name |
| 405672485 | CV3377288 | single nucleotide variant | NM_018137.3(PRMT6):c.943G>T (p.Ala315Ser) | not specified [RCV004515321] | uncertain significance | 1 | 107057658 | 107057658 | Human | | name |
| 407465786 | CV3464610 | single nucleotide variant | NM_018137.3(PRMT6):c.536A>G (p.Lys179Arg) | not specified [RCV004660319] | uncertain significance | 1 | 107057251 | 107057251 | Human | | name |
| 597780825 | CV3588030 | single nucleotide variant | NM_018137.3(PRMT6):c.964C>T (p.Leu322Phe) | not specified [RCV004853586] | uncertain significance | 1 | 107057679 | 107057679 | Human | | name |
| 597780833 | CV3588032 | single nucleotide variant | NM_018137.3(PRMT6):c.322G>A (p.Val108Met) | not specified [RCV004853588] | uncertain significance | 1 | 107057037 | 107057037 | Human | | name |
| 597780837 | CV3588033 | single nucleotide variant | NM_018137.3(PRMT6):c.659G>A (p.Ser220Asn) | not specified [RCV004853589] | uncertain significance | 1 | 107057374 | 107057374 | Human | | name |
| 597780856 | CV3588037 | single nucleotide variant | NM_018137.3(PRMT6):c.624G>C (p.Trp208Cys) | not specified [RCV004853593] | uncertain significance | 1 | 107057339 | 107057339 | Human | | name |
| 597780860 | CV3588038 | single nucleotide variant | NM_018137.3(PRMT6):c.962C>G (p.Ala321Gly) | not specified [RCV004853594] | uncertain significance | 1 | 107057677 | 107057677 | Human | | name |
| 598247321 | CV3904599 | single nucleotide variant | NM_018137.3(PRMT6):c.870C>G (p.Ile290Met) | not specified [RCV005258622] | uncertain significance | 1 | 107057585 | 107057585 | Human | | name |
| 598203016 | CV3904604 | single nucleotide variant | NM_018137.3(PRMT6):c.794A>T (p.Gln265Leu) | not specified [RCV005269308] | uncertain significance | 1 | 107057509 | 107057509 | Human | | name |
| 405671765 | CV3377275 | single nucleotide variant | NM_018137.3(PRMT6):c.1039C>G (p.Arg347Gly) | not specified [RCV004515308] | uncertain significance | 1 | 107057754 | 107057754 | Human | | name |
| 405671770 | CV3377276 | single nucleotide variant | NM_018137.3(PRMT6):c.1039C>T (p.Arg347Trp) | not specified [RCV004515309] | uncertain significance | 1 | 107057754 | 107057754 | Human | | name |
| 597780851 | CV3588036 | single nucleotide variant | NM_018137.3(PRMT6):c.1047C>G (p.Asn349Lys) | not specified [RCV004853592] | uncertain significance | 1 | 107057762 | 107057762 | Human | | name |
| 598247338 | CV3904602 | single nucleotide variant | NM_018137.3(PRMT6):c.1052G>A (p.Arg351His) | not specified [RCV005258624] | uncertain significance | 1 | 107057767 | 107057767 | Human | | name |
| 598247346 | CV3904603 | single nucleotide variant | NM_018137.3(PRMT6):c.1099A>C (p.Lys367Gln) | not specified [RCV005258625] | uncertain significance | 1 | 107057814 | 107057814 | Human | | name |
