| 15107073 | CV748278 | single nucleotide variant | NM_001135179.2(ZDHHC3):c.306+504G>A | not provided [RCV000915880] | likely benign | 3 | 44958627 | 44958627 | Human | | name |
| 8644853 | CV104260 | single nucleotide variant | NM_001135179.2(ZDHHC3):c.147C>T (p.Ile49=) | not provided [RCV000084658] | not provided | 3 | 44959290 | 44959290 | Human | | name |
| 8644854 | CV104261 | single nucleotide variant | NM_001135179.2(ZDHHC3):c.86A>G (p.Tyr29Cys) | not provided [RCV000084659]|not specified [RCV004019584] | uncertain significance|not provided | 3 | 44959351 | 44959351 | Human | | name |
| 401741832 | CV2676536 | single nucleotide variant | NM_001135179.2(ZDHHC3):c.83C>G (p.Pro28Arg) | not specified [RCV004288727] | uncertain significance | 3 | 44959354 | 44959354 | Human | | name |
| 597724832 | CV3631083 | single nucleotide variant | NM_001135179.2(ZDHHC3):c.83C>A (p.Pro28His) | not specified [RCV004888204] | uncertain significance | 3 | 44959354 | 44959354 | Human | | name |
| 155924833 | CV2211660 | single nucleotide variant | NM_001135179.2(ZDHHC3):c.136G>A (p.Ala46Thr) | not specified [RCV004084552] | uncertain significance | 3 | 44959301 | 44959301 | Human | | name |
| 155933698 | CV2228975 | single nucleotide variant | NM_001135179.2(ZDHHC3):c.241A>G (p.Ile81Val) | not specified [RCV004098764] | uncertain significance | 3 | 44959196 | 44959196 | Human | | name |
| 155921016 | CV2340379 | single nucleotide variant | NM_001135179.2(ZDHHC3):c.212G>A (p.Arg71Gln) | not specified [RCV004197110] | uncertain significance | 3 | 44959225 | 44959225 | Human | | name |
| 329365456 | CV2444890 | single nucleotide variant | NM_001135179.2(ZDHHC3):c.287G>A (p.Arg96Gln) | not specified [RCV004259126] | uncertain significance | 3 | 44959150 | 44959150 | Human | | name |
| 405813036 | CV3349794 | single nucleotide variant | NM_001135179.2(ZDHHC3):c.220G>A (p.Val74Met) | not specified [RCV004483647] | uncertain significance | 3 | 44959217 | 44959217 | Human | | name |
| 8644852 | CV104259 | single nucleotide variant | NM_001135179.2(ZDHHC3):c.617G>C (p.Ser206Thr) | not provided [RCV000084657] | not provided | 3 | 44929430 | 44929430 | Human | | name |
| 155967689 | CV2265797 | single nucleotide variant | NM_001135179.2(ZDHHC3):c.346G>A (p.Glu116Lys) | not specified [RCV004126413] | uncertain significance | 3 | 44945253 | 44945253 | Human | | name |
| 405813038 | CV3349795 | single nucleotide variant | NM_001135179.2(ZDHHC3):c.398G>A (p.Cys133Tyr) | not specified [RCV004483648] | uncertain significance | 3 | 44945201 | 44945201 | Human | | name |
| 405813040 | CV3349796 | single nucleotide variant | NM_001135179.2(ZDHHC3):c.682C>T (p.Leu228Phe) | not specified [RCV004483649] | uncertain significance | 3 | 44929365 | 44929365 | Human | | name |
| 597793407 | CV3631082 | single nucleotide variant | NM_001135179.2(ZDHHC3):c.343A>G (p.Ile115Val) | not specified [RCV004877307] | uncertain significance | 3 | 44945256 | 44945256 | Human | | name |
| 598198259 | CV3927013 | single nucleotide variant | NM_001135179.2(ZDHHC3):c.386G>A (p.Cys129Tyr) | not specified [RCV005313762] | uncertain significance | 3 | 44945213 | 44945213 | Human | | name |
| 598198267 | CV3927014 | single nucleotide variant | NM_001135179.2(ZDHHC3):c.670G>A (p.Gly224Ser) | not specified [RCV005313763] | uncertain significance | 3 | 44929377 | 44929377 | Human | | name |