| 329359038 | CV2450810 | single nucleotide variant | NM_014573.3(TMEM97):c.147G>C (p.Trp49Cys) | not specified [RCV004267727] | uncertain significance | 17 | 28325523 | 28325523 | Human | | name |
| 401783036 | CV2716098 | single nucleotide variant | NM_014573.3(TMEM97):c.179A>G (p.Gln60Arg) | not specified [RCV004323342] | uncertain significance | 17 | 28325555 | 28325555 | Human | | name |
| 405772879 | CV3343370 | single nucleotide variant | NM_014573.3(TMEM97):c.107G>T (p.Arg36Leu) | not specified [RCV004470597] | uncertain significance | 17 | 28319346 | 28319346 | Human | | name |
| 597800824 | CV3610782 | single nucleotide variant | NM_014573.3(TMEM97):c.187C>T (p.Pro63Ser) | not specified [RCV004880410] | uncertain significance | 17 | 28325563 | 28325563 | Human | | name |
| 401736652 | CV2688845 | single nucleotide variant | NM_014573.3(TMEM97):c.364G>A (p.Asp122Asn) | not specified [RCV004303861] | uncertain significance | 17 | 28326626 | 28326626 | Human | | name |
| 405772885 | CV3343371 | single nucleotide variant | NM_014573.3(TMEM97):c.411G>C (p.Leu137Phe) | not specified [RCV004470598] | likely benign | 17 | 28326673 | 28326673 | Human | | name |
| 405772890 | CV3343372 | single nucleotide variant | NM_014573.3(TMEM97):c.419G>A (p.Arg140Gln) | not specified [RCV004470599] | uncertain significance | 17 | 28326681 | 28326681 | Human | | name |
| 597800820 | CV3610780 | single nucleotide variant | NM_014573.3(TMEM97):c.337C>T (p.Pro113Ser) | not specified [RCV004880408] | uncertain significance | 17 | 28326599 | 28326599 | Human | | name |
| 597800822 | CV3610781 | single nucleotide variant | NM_014573.3(TMEM97):c.482T>A (p.Met161Lys) | not specified [RCV004880409] | uncertain significance | 17 | 28326744 | 28326744 | Human | | name |