Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 129642 |
| ensemblid | ENSG00000143797.12 |
| hgncid | 25193 |
| symbol | MBOAT2 |
| name | membrane bound O-acyltransferase domain containing 2 |
| refseq_nuc | NM_138799.4 |
| refseq_prot | NP_620154.2 |
| ensembl_nuc | ENST00000305997.8 |
| ensembl_prot | ENSP00000302177.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 8852690 |
| end | 9003684 |
| strand | - |
| ver | v1.2 |
| region | chr2:8852690-9003684 |
| region5000 | chr2:8847690-9008684 |
| regionname0 | MBOAT2_chr2_8852690_9003684 |
| regionname5000 | MBOAT2_chr2_8847690_9008684 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 520 | 151 | 73 | 25 | 27 | 4 | 20 | 14 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | MATTS others(515): Show |
chr2 | 8847690 | 9008684 |
| a0002 | 0/0 | 520 | 7 | 4 | 2 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | MATTS others(515): Show |
chr2 | 8847690 | 9008684 |
| a0003 | 0/0 | 520 | 3 | 0 | 1 | 0 | 0 | 2 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | MATTS others(515): Show |
chr2 | 8847690 | 9008684 |
| a0004 | 0/0 | 520 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | MATTS others(515): Show |
chr2 | 8847690 | 9008684 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1560 | 150 | 72 | 25 | 27 | 4 | 20 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | ATGGC others(1555): Show |
chr2 | 8847690 | 9008684 | ||
| a0001c0004 | 0/0 | 1560 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | ATGGC others(1555): Show |
chr2 | 8847690 | 9008684 | ||
| a0002c0002 | 0/0 | 1560 | 7 | 4 | 2 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | ATGGC others(1555): Show |
chr2 | 8847690 | 9008684 | ||
| a0003c0003 | 0/0 | 1560 | 3 | 0 | 1 | 0 | 0 | 2 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | ATGGC others(1555): Show |
chr2 | 8847690 | 9008684 | ||
| a0004c0005 | 0/0 | 1560 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | ATGGC others(1555): Show |
chr2 | 8847690 | 9008684 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 7622 | 33 | 21 | 5 | 5 | 0 | 2 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | ATCCT others(7617): Show |
chr2 | 8847690 | 9008684 |
| a0001c0001t0002 | 0/1 | 7622 | 27 | 0 | 9 | 13 | 0 | 4 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | ATCCT others(7617): Show |
chr2 | 8847690 | 9008684 |
| a0001c0001t0003 | 0/0 | 7622 | 12 | 3 | 3 | 0 | 0 | 6 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | ATCCT others(7617): Show |
chr2 | 8847690 | 9008684 |
| a0001c0001t0004 | 0/0 | 7622 | 11 | 6 | 2 | 1 | 1 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | ATCCT others(7617): Show |
chr2 | 8847690 | 9008684 |
| a0001c0001t0005 | 0/0 | 7622 | 8 | 6 | 2 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | ATCCT others(7617): Show |
chr2 | 8847690 | 9008684 |
| a0001c0001t0006 | 0/0 | 7622 | 6 | 0 | 0 | 2 | 0 | 4 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | ATCCT others(7617): Show |
chr2 | 8847690 | 9008684 |
| a0001c0001t0007 | 1/0 | 7622 | 6 | 5 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | ATCCT others(7617): Show |
chr2 | 8847690 | 9008684 |
| a0001c0001t0008 | 0/0 | 7622 | 5 | 4 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | ATCCT others(7617): Show |
chr2 | 8847690 | 9008684 |
| a0001c0001t0009 | 0/0 | 7621 | 3 | 2 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | ATCCT others(7616): Show |
chr2 | 8847690 | 9008684 |
| a0001c0001t0011 | 0/0 | 7619 | 3 | 3 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | ATCCT others(7614): Show |
chr2 | 8847690 | 9008684 |
| a0001c0001t0012 | 0/0 | 7621 | 3 | 2 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | ATCCT others(7616): Show |
chr2 | 8847690 | 9008684 |
| a0001c0001t0013 | 0/0 | 7622 | 3 | 0 | 0 | 3 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | ATCCT others(7617): Show |
chr2 | 8847690 | 9008684 |
| a0001c0001t0014 | 0/0 | 7622 | 3 | 3 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | ATCCT others(7617): Show |
chr2 | 8847690 | 9008684 |
| a0001c0001t0016 | 0/0 | 7621 | 2 | 2 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | ATCCT others(7616): Show |
chr2 | 8847690 | 9008684 |
| a0001c0001t0018 | 0/0 | 7622 | 2 | 2 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | ATCCT others(7617): Show |
chr2 | 8847690 | 9008684 |
| a0001c0001t0019 | 0/0 | 7625 | 2 | 2 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | ATCCT others(7620): Show |
chr2 | 8847690 | 9008684 |
| a0001c0001t0020 | 0/0 | 7621 | 2 | 2 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | ATCCT others(7616): Show |
chr2 | 8847690 | 9008684 |
| a0001c0001t0021 | 0/0 | 7622 | 2 | 0 | 0 | 0 | 1 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | ATCCT others(7617): Show |
chr2 | 8847690 | 9008684 |
| a0001c0001t0022 | 0/0 | 7619 | 2 | 2 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | ATCCT others(7614): Show |
chr2 | 8847690 | 9008684 |
| a0001c0001t0023 | 0/0 | 7622 | 2 | 0 | 1 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | ATCCT others(7617): Show |
chr2 | 8847690 | 9008684 |
| a0001c0001t0025 | 0/0 | 7621 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | ATCCT others(7616): Show |
chr2 | 8847690 | 9008684 |
| a0001c0001t0026 | 0/0 | 7621 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | ATCCT others(7616): Show |
chr2 | 8847690 | 9008684 |
| a0001c0001t0029 | 0/0 | 7622 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | ATCCT others(7617): Show |
chr2 | 8847690 | 9008684 |
| a0001c0001t0030 | 0/0 | 7622 | 1 | 0 | 0 | 0 | 1 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | ATCCT others(7617): Show |
chr2 | 8847690 | 9008684 |
| a0001c0001t0031 | 0/0 | 7622 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | ATCCT others(7617): Show |
chr2 | 8847690 | 9008684 |
| a0001c0001t0032 | 0/0 | 7622 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | ATCCT others(7617): Show |
chr2 | 8847690 | 9008684 |
| a0001c0001t0033 | 0/0 | 7622 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | ATCCT others(7617): Show |
chr2 | 8847690 | 9008684 |
| a0001c0001t0034 | 0/0 | 7622 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | ATCCT others(7617): Show |
chr2 | 8847690 | 9008684 |
| a0001c0001t0035 | 0/0 | 7622 | 1 | 0 | 0 | 0 | 1 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | ATCCT others(7617): Show |
chr2 | 8847690 | 9008684 |
| a0001c0001t0036 | 0/0 | 7622 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | ATCCT others(7617): Show |
chr2 | 8847690 | 9008684 |
| a0001c0001t0037 | 0/0 | 7622 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | ATCCT others(7617): Show |
chr2 | 8847690 | 9008684 |
| a0001c0001t0038 | 0/0 | 7622 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | ATCCT others(7617): Show |
chr2 | 8847690 | 9008684 |
| a0001c0001t0039 | 0/0 | 7633 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | ATCCT others(7628): Show |
chr2 | 8847690 | 9008684 |
| a0001c0004t0015 | 0/0 | 7619 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | ATCCT others(7614): Show |
chr2 | 8847690 | 9008684 |
| a0002c0002t0015 | 0/0 | 7619 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | ATCCT others(7614): Show |
chr2 | 8847690 | 9008684 |
| a0002c0002t0017 | 0/0 | 7619 | 2 | 2 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | ATCCT others(7614): Show |
chr2 | 8847690 | 9008684 |
| a0002c0002t0024 | 0/0 | 7619 | 2 | 0 | 2 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | ATCCT others(7614): Show |
chr2 | 8847690 | 9008684 |
| a0002c0002t0027 | 0/0 | 7619 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | ATCCT others(7614): Show |
chr2 | 8847690 | 9008684 |
| a0002c0002t0040 | 0/0 | 7619 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | ATCCT others(7614): Show |
chr2 | 8847690 | 9008684 |
| a0003c0003t0010 | 0/0 | 7622 | 3 | 0 | 1 | 0 | 0 | 2 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | ATCCT others(7617): Show |
chr2 | 8847690 | 9008684 |
| a0004c0005t0028 | 0/0 | 7622 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | ATCCT others(7617): Show |
chr2 | 8847690 | 9008684 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0002g0105 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0003g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0004g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0004g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0005g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0005g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0005g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0005g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0005g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0005g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0005g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0006g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0006g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0006g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0006g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0006g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0006g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0007g0002 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0007g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0007g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0007g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0007g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0008g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0008g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0008g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0008g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0008g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0009g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0009g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0009g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0011g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0011g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0011g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0012g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0012g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0012g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0013g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0013g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0013g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0014g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0014g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0014g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0016g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0016g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0018g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0018g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0019g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0019g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0020g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0020g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0021g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0021g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0022g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0022g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0023g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0023g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0025g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0026g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0029g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0030g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0031g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0032g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0033g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0034g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0035g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0036g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0037g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0038g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0001t0039g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0001c0004t0015g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0002c0002t0015g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0002c0002t0017g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0002c0002t0017g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0002c0002t0024g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0002c0002t0024g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0002c0002t0027g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0002c0002t0040g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0003c0003t0010g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0003c0003t0010g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0003c0003t0010g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| a0004c0005t0028g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0035 | g0103 | EUR | GBR | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG00140 | hp2 | a0001 | c0001 | t0030 | g0095 | EUR | GBR | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG00558 | hp1 | a0001 | c0001 | t0013 | g0135 | EAS | CHS | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | CHS | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG00609 | hp2 | a0001 | c0001 | t0013 | g0003 | EAS | CHS | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | CHS | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | CHS | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG00639 | hp2 | a0001 | c0001 | t0009 | g0007 | AMR | PUR | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG00642 | hp1 | a0003 | c0003 | t0010 | g0155 | AMR | PUR | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0102 | AMR | PUR | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0065 | AMR | PUR | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG00738 | hp2 | a0001 | c0001 | t0012 | g0052 | AMR | PUR | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0066 | AMR | PUR | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG01070 | hp2 | a0001 | c0001 | t0008 | g0150 | AMR | PUR | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG01071 | hp1 | a0001 | c0001 | t0004 | g0067 | AMR | PUR | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG01071 | hp2 | a0001 | c0001 | t0023 | g0156 | AMR | PUR | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0118 | AMR | PUR | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG01167 | hp2 | a0002 | c0002 | t0024 | g0159 | AMR | PUR | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG01169 | hp1 | a0002 | c0002 | t0024 | g0160 | AMR | PUR | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0079 | AMR | PUR | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | PUR | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG01175 | hp2 | a0001 | c0001 | t0005 | g0042 | AMR | PUR | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0106 | AMR | CLM | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0131 | AMR | CLM | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG01884 | hp1 | a0001 | c0001 | t0025 | g0008 | AFR | ACB | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG01884 | hp2 | a0001 | c0001 | t0007 | g0086 | AFR | ACB | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0059 | AFR | ACB | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG01934 | hp1 | a0001 | c0001 | t0005 | g0037 | AMR | PEL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0107 | AMR | PEL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0114 | AMR | PEL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0030 | AMR | PEL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG02027 | hp1 | a0002 | c0002 | t0040 | g0158 | EAS | KHV | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG02055 | hp1 | a0001 | c0001 | t0007 | g0002 | AFR | ACB | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0056 | AFR | ACB | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | KHV | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG02080 | hp2 | a0001 | c0001 | t0038 | g0129 | EAS | KHV | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | KHV | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | KHV | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | KHV | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG02145 | hp1 | a0001 | c0001 | t0008 | g0151 | AFR | ACB | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG02145 | hp2 | a0001 | c0001 | t0011 | g0061 | AFR | ACB | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG02257 | hp1 | a0001 | c0001 | t0022 | g0083 | AFR | ACB | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG02257 | hp2 | a0002 | c0002 | t0015 | g0064 | AFR | ACB | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | ACB | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG02451 | hp1 | a0001 | c0001 | t0014 | g0014 | AFR | ACB | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG02572 | hp1 | a0002 | c0002 | t0017 | g0012 | AFR | GWD | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0040 | AFR | GWD | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG02622 | hp1 | a0001 | c0001 | t0007 | g0076 | AFR | GWD | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG02630 | hp2 | a0001 | c0001 | t0022 | g0084 | AFR | GWD | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG02647 | hp2 | a0002 | c0002 | t0017 | g0011 | AFR | GWD | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG02698 | hp2 | a0001 | c0001 | t0006 | g0122 | SAS | PJL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG02717 | hp2 | a0001 | c0001 | t0018 | g0025 | AFR | GWD | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG02735 | hp1 | a0001 | c0001 | t0006 | g0090 | SAS | PJL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0028 | SAS | PJL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0104 | SAS | PJL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0027 | SAS | PJL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG02809 | hp2 | a0001 | c0004 | t0015 | g0006 | AFR | GWD | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG02818 | hp1 | a0001 | c0001 | t0005 | g0044 | AFR | GWD | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG02886 | hp2 | a0001 | c0001 | t0012 | g0054 | AFR | GWD | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0045 | AFR | GWD | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG02895 | hp2 | a0001 | c0001 | t0016 | g0009 | AFR | GWD | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG02896 | hp1 | a0001 | c0001 | t0016 | g0010 | AFR | GWD | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG02896 | hp2 | a0001 | c0001 | t0014 | g0032 | AFR | GWD | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG02922 | hp2 | a0001 | c0001 | t0026 | g0005 | AFR | ESN | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG02976 | hp1 | a0001 | c0001 | t0019 | g0033 | AFR | ESN | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG02976 | hp2 | a0001 | c0001 | t0031 | g0038 | AFR | ESN | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG03017 | hp1 | a0001 | c0001 | t0034 | g0127 | SAS | PJL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0026 | SAS | PJL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0055 | AFR | GWD | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG03098 | hp1 | a0001 | c0001 | t0037 | g0111 | AFR | MSL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG03098 | hp2 | a0001 | c0001 | t0009 | g0034 | AFR | MSL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ESN | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG03130 | hp2 | a0001 | c0001 | t0007 | g0088 | AFR | ESN | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG03139 | hp1 | a0001 | c0001 | t0008 | g0152 | AFR | ESN | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG03195 | hp1 | a0001 | c0001 | t0020 | g0049 | AFR | ESN | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG03195 | hp2 | a0001 | c0001 | t0011 | g0062 | AFR | ESN | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | MSL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG03209 | hp2 | a0001 | c0001 | t0011 | g0063 | AFR | MSL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG03225 | hp1 | a0001 | c0001 | t0008 | g0108 | AFR | MSL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0022 | AFR | MSL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | MSL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG03453 | hp2 | a0001 | c0001 | t0039 | g0004 | AFR | MSL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | MSL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG03486 | hp2 | a0001 | c0001 | t0036 | g0112 | AFR | MSL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG03490 | hp1 | a0001 | c0001 | t0021 | g0078 | SAS | PJL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0080 | SAS | PJL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG03516 | hp1 | a0001 | c0001 | t0020 | g0048 | AFR | ESN | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0058 | AFR | ESN | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0057 | AFR | GWD | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0109 | SAS | PJL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG03654 | hp2 | a0003 | c0003 | t0010 | g0153 | SAS | PJL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0029 | SAS | PJL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG03710 | hp1 | a0001 | c0001 | t0023 | g0157 | SAS | PJL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG03710 | hp2 | a0003 | c0003 | t0010 | g0154 | SAS | PJL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0023 | SAS | STU | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG04115 | hp2 | a0001 | c0001 | t0006 | g0092 | SAS | STU | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0101 | SAS | BEB | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0050 | SAS | BEB | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| NA18522 | hp1 | a0001 | c0001 | t0019 | g0133 | AFR | YRI | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| NA18522 | hp2 | a0001 | c0001 | t0012 | g0053 | AFR | YRI | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | YRI | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0060 | AFR | YRI | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| NA18953 | hp2 | a0001 | c0001 | t0004 | g0051 | EAS | JPT | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| NA18956 | hp2 | a0001 | c0001 | t0006 | g0016 | EAS | JPT | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| NA18957 | hp1 | a0001 | c0001 | t0013 | g0134 | EAS | JPT | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| NA18982 | hp2 | a0001 | c0001 | t0006 | g0136 | EAS | JPT | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| NA19010 | hp1 | a0001 | c0001 | t0032 | g0094 | EAS | JPT | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| NA19030 | hp1 | a0001 | c0001 | t0029 | g0113 | AFR | LWK | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| NA19030 | hp2 | a0004 | c0005 | t0028 | g0013 | AFR | LWK | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| NA19043 | hp1 | a0001 | c0001 | t0018 | g0024 | AFR | LWK | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| NA19043 | hp2 | a0002 | c0002 | t0027 | g0036 | AFR | LWK | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| NA19063 | hp2 | a0001 | c0001 | t0033 | g0123 | EAS | JPT | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0046 | AFR | YRI | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| NA19240 | hp2 | a0001 | c0001 | t0009 | g0035 | AFR | YRI | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| NA20752 | hp1 | a0001 | c0001 | t0004 | g0047 | EUR | TSI | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| NA20752 | hp2 | a0001 | c0001 | t0021 | g0125 | EUR | TSI | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0019 | SAS | GIH | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| NA20905 | hp2 | a0001 | c0001 | t0006 | g0091 | SAS | GIH | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG02486 | hp1 | a0001 | c0001 | t0014 | g0031 | AFR | ACB | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG02486 | hp2 | a0001 | c0001 | t0007 | g0085 | AFR | ACB | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0041 | AFR | ACB | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG02559 | hp2 | a0001 | c0001 | t0008 | g0149 | AFR | ACB | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | MSL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | MSL | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | USA | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0039 | AFR | USA | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0105 | REF | REF | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0007 | g0002 | REF | REF | MBOAT2_chr2_8847690_9008684 | MBOAT2 | chr2 | 8847690 | 9008684 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:8858741 | T | C | 1 | a0003 | 3 | HG00642.hp1 HG03654.hp2 HG03710.hp2 |
missense_variant | MODERATE | c.1501A>G | p.Thr501Ala | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 1571/7622 | 1501/1563 | 501/520 | chr2 | 8858741 | |||
| chr2:8860626 | G | A | 1 | a0004 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.1324C>T | p.Leu442Phe | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 12/13 | 1394/7622 | 1324/1563 | 442/520 | chr2 | 8860626 | |||
| chr2:8873294 | C | T | 1 | a0002 | 7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
missense_variant | MODERATE | c.697G>A | p.Val233Ile | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 8/13 | 767/7622 | 697/1563 | 233/520 | chr2 | 8873294 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:8858841 | T | C | 2 | a0001c0004 a0002c0002 |
8 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(5): Show |
synonymous_variant | LOW | c.1401A>G | p.Lys467Lys | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 1471/7622 | 1401/1563 | 467/520 | chr2 | 8858841 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:8852770 | A | G | 1 | a0004c0005t0028 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5909T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 5909 | chr2 | 8852770 | ||||||
| chr2:8853102 | CA | C | 1 | a0001c0001t0020 | 2 | HG03195.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5576delT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 5576 | chr2 | 8853102 | ||||||
| chr2:8853209 | G | A | 1 | a0001c0001t0026 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5470C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 5470 | chr2 | 8853209 | ||||||
| chr2:8853212 | C | T | 5 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0020 others(2): Show |
22 | HG00642.hp1 HG01070.hp1 HG01070.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*5467G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 5467 | chr2 | 8853212 | ||||||
| chr2:8853375 | A | C | 9 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0008 others(6): Show |
31 | HG00140.hp1 HG00642.hp1 HG01070.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*5304T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 5304 | chr2 | 8853375 | ||||||
| chr2:8853646 | G | A | 1 | a0001c0001t0014 | 3 | HG02451.hp1 HG02486.hp1 HG02896.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5033C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 5033 | chr2 | 8853646 | ||||||
| chr2:8853664 | G | T | 5 | a0001c0001t0011 a0001c0004t0015 a0002c0002t0015 others(2): Show |
8 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5015C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 5015 | chr2 | 8853664 | ||||||
| chr2:8853879 | T | C | 1 | a0001c0001t0034 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4800A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 4800 | chr2 | 8853879 | ||||||
| chr2:8854078 | G | A | 3 | a0001c0004t0015 a0002c0002t0015 a0002c0002t0024 |
4 | HG01167.hp2 HG01169.hp1 HG02257.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4601C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 4601 | chr2 | 8854078 | ||||||
| chr2:8854080 | T | C | 1 | a0001c0001t0035 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4599A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 4599 | chr2 | 8854080 | ||||||
| chr2:8854172 | C | G | 1 | a0001c0001t0012 | 3 | HG00738.hp2 HG02886.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4507G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 4507 | chr2 | 8854172 | ||||||
| chr2:8854172 | CCT | C | 7 | a0001c0001t0011 a0001c0004t0015 a0002c0002t0015 others(4): Show |
11 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4505_*4506delAG | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 4505 | chr2 | 8854172 | ||||||
| chr2:8854470 | G | A | 1 | a0001c0001t0012 | 3 | HG00738.hp2 HG02886.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4209C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 4209 | chr2 | 8854470 | ||||||
| chr2:8855131 | A | C | 1 | a0001c0001t0008 | 5 | HG01070.hp2 HG02145.hp1 HG02559.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3548T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 3548 | chr2 | 8855131 | ||||||
| chr2:8855194 | G | A | 1 | a0001c0001t0031 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3485C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 3485 | chr2 | 8855194 | ||||||
| chr2:8855228 | G | C | 1 | a0001c0001t0029 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3451C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 3451 | chr2 | 8855228 | ||||||
| chr2:8855246 | G | A | 1 | a0001c0001t0030 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3433C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 3433 | chr2 | 8855246 | ||||||
| chr2:8855582 | G | A | 3 | a0001c0001t0006 a0001c0001t0032 a0001c0001t0035 |
8 | HG00140.hp1 HG02698.hp2 HG02735.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3097C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 3097 | chr2 | 8855582 | ||||||
| chr2:8855589 | A | T | 1 | a0001c0001t0032 | 1 | NA19010.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3090T>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 3090 | chr2 | 8855589 | ||||||
| chr2:8855855 | T | C | 1 | a0001c0001t0036 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2824A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 2824 | chr2 | 8855855 | ||||||
| chr2:8855961 | CAGG | C | 1 | a0001c0001t0022 | 2 | HG02257.hp1 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2715_*2717delCCT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 2715 | chr2 | 8855961 | ||||||
| chr2:8856033 | T | A | 2 | a0001c0001t0008 a0003c0003t0010 |
8 | HG00642.hp1 HG01070.hp2 HG02145.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2646A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 2646 | chr2 | 8856033 | ||||||
| chr2:8856110 | C | CA | 2 | a0001c0001t0008 a0003c0003t0010 |
8 | HG00642.hp1 HG01070.hp2 HG02145.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2568dupT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 2568 | chr2 | 8856110 | ||||||
| chr2:8856193 | G | A | 14 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0009 others(11): Show |
38 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2486C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 2486 | chr2 | 8856193 | ||||||
| chr2:8856196 | C | T | 27 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(24): Show |
75 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*2483G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 2483 | chr2 | 8856196 | ||||||
| chr2:8856247 | G | T | 6 | a0001c0004t0015 a0002c0002t0015 a0002c0002t0017 others(3): Show |
8 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2432C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 2432 | chr2 | 8856247 | ||||||
| chr2:8856308 | A | ACAC | 1 | a0001c0001t0019 | 2 | HG02976.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2370_*2371insGTG | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 2370 | chr2 | 8856308 | ||||||
| chr2:8856308 | A | ACACACAC others(4): Show |
1 | a0001c0001t0039 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2370_*2371insGTGT others(7): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 2370 | chr2 | 8856308 | ||||||
| chr2:8856310 | A | AC | 1 | a0001c0001t0016 | 2 | HG02895.hp2 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2368_*2369insG | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 2368 | chr2 | 8856310 | ||||||
| chr2:8856310 | A | ACAC | 5 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0014 others(2): Show |
10 | HG01070.hp1 HG01071.hp1 HG02055.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2368_*2369insGTG | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 2368 | chr2 | 8856310 | ||||||
| chr2:8856310 | A | ACACAC | 3 | a0001c0001t0003 a0001c0001t0030 a0004c0005t0028 |
12 | HG00140.hp2 HG01175.hp1 HG01256.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2368_*2369insGTGT others(1): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 2368 | chr2 | 8856310 | ||||||
| chr2:8856310 | A | C | 2 | a0001c0001t0019 a0001c0001t0039 |
3 | HG02976.hp1 HG03453.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2369T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 2369 | chr2 | 8856310 | ||||||
| chr2:8856312 | A | AAC | 5 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0007 others(2): Show |
11 | HG00609.hp2 HG00735.hp1 HG00735.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2365_*2366dupGT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 2366 | chr2 | 8856312 | ||||||
| chr2:8856312 | A | AC | 3 | a0001c0001t0009 a0001c0001t0026 a0001c0001t0033 |
5 | HG00639.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2366_*2367insG | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 2366 | chr2 | 8856312 | ||||||
| chr2:8856312 | A | ACAC | 4 | a0001c0001t0004 a0001c0001t0020 a0001c0001t0025 others(1): Show |
12 | HG01884.hp1 HG01891.hp1 HG03041.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2366_*2367insGTG | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 2366 | chr2 | 8856312 | ||||||
| chr2:8856312 | A | C | 14 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(11): Show |
33 | HG00140.hp2 HG01070.hp1 HG01071.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*2367T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 2367 | chr2 | 8856312 | ||||||
| chr2:8856312 | AAC | A | 4 | a0001c0001t0005 a0001c0001t0011 a0001c0001t0012 others(1): Show |
14 | HG00738.hp2 HG01934.hp1 HG02145.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2365_*2366delGT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 2365 | chr2 | 8856312 | ||||||
| chr2:8856314 | C | A | 2 | a0001c0001t0008 a0003c0003t0010 |
8 | HG00642.hp1 HG01070.hp2 HG02145.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2365G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 2365 | chr2 | 8856314 | ||||||
| chr2:8856316 | C | A | 4 | a0001c0001t0005 a0001c0001t0011 a0001c0001t0012 others(1): Show |
14 | HG00738.hp2 HG01934.hp1 HG02145.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2363G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 2363 | chr2 | 8856316 | ||||||
| chr2:8856598 | A | G | 3 | a0001c0001t0002 a0001c0001t0013 a0001c0001t0023 |
31 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*2081T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 2081 | chr2 | 8856598 | ||||||
| chr2:8856616 | A | G | 23 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0008 others(20): Show |
60 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*2063T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 2063 | chr2 | 8856616 | ||||||
| chr2:8856744 | G | A | 6 | a0001c0004t0015 a0002c0002t0015 a0002c0002t0017 others(3): Show |
8 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1935C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 1935 | chr2 | 8856744 | ||||||
| chr2:8856748 | A | T | 25 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0008 others(22): Show |
66 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*1931T>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 1931 | chr2 | 8856748 | ||||||
| chr2:8857175 | A | G | 2 | a0001c0001t0014 a0001c0001t0018 |
5 | HG02451.hp1 HG02486.hp1 HG02717.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1504T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 1504 | chr2 | 8857175 | ||||||
| chr2:8857824 | G | A | 1 | a0001c0001t0021 | 2 | HG03490.hp1 NA20752.hp2 |
3_prime_UTR_variant | MODIFIER | c.*855C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 855 | chr2 | 8857824 | ||||||
| chr2:8857900 | C | A | 1 | a0001c0001t0016 | 2 | HG02895.hp2 HG02896.hp1 |
3_prime_UTR_variant | MODIFIER | c.*779G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 779 | chr2 | 8857900 | ||||||
| chr2:8858024 | A | T | 1 | a0001c0001t0013 | 3 | HG00558.hp1 HG00609.hp2 NA18957.hp1 |
3_prime_UTR_variant | MODIFIER | c.*655T>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 655 | chr2 | 8858024 | ||||||
| chr2:8858030 | C | A | 2 | a0001c0001t0011 a0001c0001t0012 |
6 | HG00738.hp2 HG02145.hp2 HG02886.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*649G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 649 | chr2 | 8858030 | ||||||
| chr2:8858287 | G | C | 1 | a0001c0001t0037 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*392C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 392 | chr2 | 8858287 | ||||||
| chr2:8858480 | G | A | 1 | a0001c0001t0038 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*199C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 199 | chr2 | 8858480 | ||||||
| chr2:8858494 | A | G | 39 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(36): Show |
153 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(150): Show |
3_prime_UTR_variant | MODIFIER | c.*185T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 185 | chr2 | 8858494 | ||||||
| chr2:8858540 | T | A | 1 | a0002c0002t0017 | 2 | HG02572.hp1 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*139A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 139 | chr2 | 8858540 | ||||||
| chr2:8858556 | T | C | 1 | a0001c0001t0039 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*123A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 123 | chr2 | 8858556 | ||||||
| chr2:8858645 | CA | C | 14 | a0001c0001t0008 a0001c0001t0009 a0001c0001t0011 others(11): Show |
29 | HG00639.hp2 HG00642.hp1 HG00738.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*33delT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 13/13 | 33 | chr2 | 8858645 | ||||||
| chr2:9003634 | G | C | 1 | a0001c0001t0023 | 2 | HG01071.hp2 HG03710.hp1 |
5_prime_UTR_variant | MODIFIER | c.-20C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/13 | 20 | chr2 | 9003634 | ||||||
| chr2:9003671 | G | C | 2 | a0002c0002t0024 a0002c0002t0040 |
3 | HG01167.hp2 HG01169.hp1 HG02027.hp1 |
5_prime_UTR_variant | MODIFIER | c.-57C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/13 | 57 | chr2 | 9003671 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:8858923 | A | T | 2 | a0002c0002t0017g0011 a0002c0002t0017g0012 |
2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1338-19T>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 12/12 | chr2 | 8858923 | |||||||
| chr2:8859912 | T | C | 1 | a0001c0001t0001g0070 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1337+701A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 12/12 | chr2 | 8859912 | |||||||
| chr2:8860089 | G | T | 1 | a0001c0001t0002g0079 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1337+524C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 12/12 | chr2 | 8860089 | |||||||
| chr2:8860147 | C | T | 1 | a0001c0001t0039g0004 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1337+466G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 12/12 | chr2 | 8860147 | |||||||
| chr2:8860185 | C | T | 1 | a0001c0001t0029g0113 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1337+428G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 12/12 | chr2 | 8860185 | |||||||
| chr2:8860224 | ATAGCTGG others(64): Show |
A | 1 | a0001c0001t0001g0121 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1337+318_1337+388d others(73): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 12/12 | chr2 | 8860224 | |||||||
| chr2:8860243 | A | C | 1 | a0001c0001t0029g0113 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1337+370T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 12/12 | chr2 | 8860243 | |||||||
| chr2:8860318 | A | C | 1 | a0001c0001t0004g0047 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1337+295T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 12/12 | chr2 | 8860318 | |||||||
| chr2:8860407 | T | C | 1 | a0001c0001t0001g0082 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1337+206A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 12/12 | chr2 | 8860407 | |||||||
| chr2:8861137 | T | C | 7 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(4): Show |
7 | HG01070.hp1 HG01071.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.1186-373A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 11/12 | chr2 | 8861137 | |||||||
| chr2:8861362 | G | T | 42 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(39): Show |
42 | HG00639.hp2 HG00642.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.1186-598C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 11/12 | chr2 | 8861362 | |||||||
| chr2:8861659 | T | G | 1 | a0001c0001t0001g0120 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1186-895A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 11/12 | chr2 | 8861659 | |||||||
| chr2:8861662 | A | C | 7 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(4): Show |
7 | HG01070.hp1 HG01071.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.1186-898T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 11/12 | chr2 | 8861662 | |||||||
| chr2:8861749 | C | T | 2 | a0001c0001t0019g0033 a0001c0001t0019g0133 |
2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1185+841G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 11/12 | chr2 | 8861749 | |||||||
| chr2:8861779 | A | G | 31 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(28): Show |
31 | HG00642.hp1 HG00738.hp2 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.1185+811T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 11/12 | chr2 | 8861779 | |||||||
| chr2:8862015 | C | T | 7 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(4): Show |
7 | HG01070.hp1 HG01071.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185+575G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 11/12 | chr2 | 8862015 | |||||||
| chr2:8862016 | G | A | 1 | a0001c0001t0002g0144 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1185+574C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 11/12 | chr2 | 8862016 | |||||||
| chr2:8862379 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1185+211G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 11/12 | chr2 | 8862379 | |||||||
| chr2:8862390 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1185+200G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 11/12 | chr2 | 8862390 | |||||||
| chr2:8862474 | G | A | 10 | a0001c0001t0009g0007 a0001c0001t0009g0034 a0001c0001t0009g0035 others(7): Show |
10 | HG00639.hp2 HG01884.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1185+116C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 11/12 | chr2 | 8862474 | |||||||
| chr2:8862933 | TTATTGGT others(14): Show |
T | 3 | a0001c0001t0006g0090 a0001c0001t0006g0091 a0001c0001t0006g0092 |
3 | HG02735.hp1 HG04115.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1053-232_1053-212d others(23): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 10/12 | chr2 | 8862933 | |||||||
| chr2:8863084 | T | A | 3 | a0003c0003t0010g0153 a0003c0003t0010g0154 a0003c0003t0010g0155 |
3 | HG00642.hp1 HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1053-362A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 10/12 | chr2 | 8863084 | |||||||
| chr2:8863140 | A | T | 1 | a0001c0001t0033g0123 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1053-418T>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 10/12 | chr2 | 8863140 | |||||||
| chr2:8863184 | T | C | 1 | a0001c0001t0002g0131 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1053-462A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 10/12 | chr2 | 8863184 | |||||||
| chr2:8863186 | A | C | 1 | a0002c0002t0015g0064 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1053-464T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 10/12 | chr2 | 8863186 | |||||||
| chr2:8863250 | T | C | 1 | a0001c0001t0006g0122 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1053-528A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 10/12 | chr2 | 8863250 | |||||||
| chr2:8863331 | A | T | 1 | a0001c0001t0018g0025 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1053-609T>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 10/12 | chr2 | 8863331 | |||||||
| chr2:8863366 | C | T | 12 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(9): Show |
12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.1053-644G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 10/12 | chr2 | 8863366 | |||||||
| chr2:8863451 | G | A | 158 | a0001c0001t0001g0043 a0001c0001t0001g0070 a0001c0001t0001g0074 others(155): Show |
159 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(156): Show |
intron_variant | MODIFIER | c.1052+719C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 10/12 | chr2 | 8863451 | |||||||
| chr2:8863510 | T | C | 9 | a0001c0001t0001g0043 a0001c0001t0001g0082 a0001c0001t0001g0097 others(6): Show |
9 | HG00639.hp1 HG02451.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1052+660A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 10/12 | chr2 | 8863510 | |||||||
| chr2:8863653 | T | C | 33 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(30): Show |
33 | HG00642.hp1 HG00738.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.1052+517A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 10/12 | chr2 | 8863653 | |||||||
| chr2:8863913 | G | T | 2 | a0001c0001t0008g0149 a0001c0001t0008g0150 |
2 | HG01070.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.1052+257C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 10/12 | chr2 | 8863913 | |||||||
| chr2:8864063 | A | G | 3 | a0001c0001t0012g0052 a0001c0001t0012g0053 a0001c0001t0012g0054 |
3 | HG00738.hp2 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1052+107T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 10/12 | chr2 | 8864063 | |||||||
| chr2:8864140 | C | T | 1 | a0001c0001t0004g0058 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1052+30G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 10/12 | chr2 | 8864140 | |||||||
| chr2:8864252 | T | C | 3 | a0001c0001t0005g0044 a0001c0001t0005g0045 a0001c0001t0005g0046 |
3 | HG02818.hp1 HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.988-18A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8864252 | |||||||
| chr2:8864281 | C | T | 2 | a0001c0001t0002g0106 a0001c0001t0002g0114 |
2 | HG01256.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.988-47G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8864281 | |||||||
| chr2:8864422 | T | C | 1 | a0001c0001t0002g0104 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.988-188A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8864422 | |||||||
| chr2:8864536 | C | T | 22 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0002g0030 others(19): Show |
23 | HG00621.hp2 HG01175.hp1 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.988-302G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8864536 | |||||||
| chr2:8864801 | T | G | 2 | a0001c0001t0003g0021 a0001c0001t0003g0022 |
2 | HG03225.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.988-567A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8864801 | |||||||
| chr2:8864818 | C | T | 2 | a0001c0001t0023g0156 a0001c0001t0023g0157 |
2 | HG01071.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.988-584G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8864818 | |||||||
| chr2:8864902 | G | T | 1 | a0001c0001t0003g0021 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.988-668C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8864902 | |||||||
| chr2:8865246 | G | A | 2 | a0001c0001t0039g0004 a0004c0005t0028g0013 |
2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.988-1012C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8865246 | |||||||
| chr2:8865607 | A | G | 4 | a0002c0002t0015g0064 a0002c0002t0024g0159 a0002c0002t0024g0160 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.988-1373T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8865607 | |||||||
| chr2:8865701 | T | G | 1 | a0001c0001t0002g0071 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.988-1467A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8865701 | |||||||
| chr2:8865764 | C | T | 1 | a0002c0002t0027g0036 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.988-1530G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8865764 | |||||||
| chr2:8865894 | G | A | 19 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(16): Show |
19 | HG00738.hp2 HG01167.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.988-1660C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8865894 | |||||||
| chr2:8866000 | G | A | 2 | a0001c0001t0008g0151 a0001c0001t0008g0152 |
2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.988-1766C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8866000 | |||||||
| chr2:8866034 | C | T | 3 | a0003c0003t0010g0153 a0003c0003t0010g0154 a0003c0003t0010g0155 |
3 | HG00642.hp1 HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.988-1800G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8866034 | |||||||
| chr2:8866036 | C | A | 1 | a0001c0001t0036g0112 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.988-1802G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8866036 | |||||||
| chr2:8866036 | C | CAAAT | 5 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(2): Show |
5 | HG01891.hp2 HG02622.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.988-1806_988-1803d others(6): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8866036 | |||||||
| chr2:8866036 | C | CAAATAAA others(1): Show |
2 | a0001c0001t0001g0077 a0001c0001t0001g0137 |
2 | HG01109.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.988-1810_988-1803d others(10): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8866036 | |||||||
| chr2:8866036 | CAAAT | C | 3 | a0001c0001t0003g0027 a0001c0001t0003g0028 a0001c0001t0003g0029 |
3 | HG02735.hp2 HG02738.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.988-1806_988-1803d others(6): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8866036 | |||||||
| chr2:8866351 | T | C | 7 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(4): Show |
7 | HG01070.hp1 HG01071.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.987+2095A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8866351 | |||||||
| chr2:8866728 | T | C | 1 | a0001c0001t0009g0007 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.987+1718A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8866728 | |||||||
| chr2:8866759 | C | T | 1 | a0001c0001t0002g0131 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.987+1687G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8866759 | |||||||
| chr2:8866761 | T | C | 3 | a0002c0002t0017g0011 a0002c0002t0017g0012 a0002c0002t0027g0036 |
3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.987+1685A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8866761 | |||||||
| chr2:8866842 | GA | G | 7 | a0002c0002t0015g0064 a0002c0002t0017g0011 a0002c0002t0017g0012 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.987+1603delT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8866842 | |||||||
| chr2:8866875 | C | G | 7 | a0002c0002t0015g0064 a0002c0002t0017g0011 a0002c0002t0017g0012 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.987+1571G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8866875 | |||||||
| chr2:8866908 | C | T | 2 | a0001c0001t0004g0066 a0001c0001t0004g0067 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.987+1538G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8866908 | |||||||
| chr2:8866957 | T | C | 2 | a0002c0002t0017g0011 a0002c0002t0017g0012 |
2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.987+1489A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8866957 | |||||||
| chr2:8867047 | A | C | 2 | a0001c0001t0019g0033 a0001c0001t0019g0133 |
2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.987+1399T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8867047 | |||||||
| chr2:8867268 | T | C | 42 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(39): Show |
42 | HG00639.hp2 HG00642.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.987+1178A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8867268 | |||||||
| chr2:8867274 | A | C | 7 | a0002c0002t0015g0064 a0002c0002t0017g0011 a0002c0002t0017g0012 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.987+1172T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8867274 | |||||||
| chr2:8867444 | T | G | 2 | a0001c0001t0008g0151 a0001c0001t0008g0152 |
2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.987+1002A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8867444 | |||||||
| chr2:8867539 | A | G | 4 | a0002c0002t0015g0064 a0002c0002t0024g0159 a0002c0002t0024g0160 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.987+907T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8867539 | |||||||
| chr2:8867588 | G | A | 3 | a0003c0003t0010g0153 a0003c0003t0010g0154 a0003c0003t0010g0155 |
3 | HG00642.hp1 HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.987+858C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8867588 | |||||||
| chr2:8867807 | T | C | 2 | a0001c0001t0009g0034 a0001c0001t0009g0035 |
2 | HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.987+639A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8867807 | |||||||
| chr2:8868081 | T | G | 7 | a0002c0002t0015g0064 a0002c0002t0017g0011 a0002c0002t0017g0012 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.987+365A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8868081 | |||||||
| chr2:8868278 | G | C | 2 | a0001c0001t0003g0020 a0001c0001t0037g0111 |
2 | HG02280.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.987+168C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8868278 | |||||||
| chr2:8868372 | T | C | 2 | a0001c0001t0023g0156 a0001c0001t0023g0157 |
2 | HG01071.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.987+74A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 9/12 | chr2 | 8868372 | |||||||
| chr2:8868743 | A | G | 19 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(16): Show |
19 | HG00738.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.884-194T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 8/12 | chr2 | 8868743 | |||||||
| chr2:8868774 | A | G | 77 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0002g0030 others(74): Show |
78 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.884-225T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 8/12 | chr2 | 8868774 | |||||||
| chr2:8869208 | A | AT | 12 | a0001c0001t0002g0068 a0001c0001t0002g0081 a0001c0001t0004g0047 others(9): Show |
12 | HG00621.hp1 HG01070.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.884-660dupA | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 8/12 | chr2 | 8869208 | |||||||
| chr2:8869208 | AT | A | 20 | a0001c0001t0001g0096 a0001c0001t0001g0120 a0001c0001t0001g0126 others(17): Show |
20 | HG00735.hp2 HG01934.hp1 HG02027.hp2 others(17): Show |
intron_variant | MODIFIER | c.884-660delA | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 8/12 | chr2 | 8869208 | |||||||
| chr2:8869210 | T | A | 7 | a0002c0002t0015g0064 a0002c0002t0017g0011 a0002c0002t0017g0012 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.884-661A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 8/12 | chr2 | 8869210 | |||||||
| chr2:8869212 | T | A | 5 | a0002c0002t0015g0064 a0002c0002t0024g0159 a0002c0002t0024g0160 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.884-663A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 8/12 | chr2 | 8869212 | |||||||
| chr2:8869304 | C | G | 9 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(6): Show |
9 | HG01891.hp1 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.884-755G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 8/12 | chr2 | 8869304 | |||||||
| chr2:8869366 | C | A | 3 | a0002c0002t0017g0011 a0002c0002t0017g0012 a0002c0002t0027g0036 |
3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.884-817G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 8/12 | chr2 | 8869366 | |||||||
| chr2:8870429 | T | C | 3 | a0001c0001t0012g0052 a0001c0001t0012g0053 a0001c0001t0012g0054 |
3 | HG00738.hp2 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.884-1880A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 8/12 | chr2 | 8870429 | |||||||
| chr2:8870607 | C | T | 1 | a0001c0001t0003g0020 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.884-2058G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 8/12 | chr2 | 8870607 | |||||||
| chr2:8871002 | A | AT | 6 | a0001c0001t0002g0015 a0001c0001t0002g0093 a0001c0001t0005g0037 others(3): Show |
6 | HG01934.hp1 HG02135.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.883+2105dupA | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 8/12 | chr2 | 8871002 | |||||||
| chr2:8871756 | A | C | 1 | a0001c0001t0025g0008 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.883+1352T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 8/12 | chr2 | 8871756 | |||||||
| chr2:8872187 | C | T | 8 | a0001c0001t0009g0007 a0001c0001t0009g0034 a0001c0001t0009g0035 others(5): Show |
8 | HG00639.hp2 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.883+921G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 8/12 | chr2 | 8872187 | |||||||
| chr2:8872601 | G | A | 12 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(9): Show |
12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.883+507C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 8/12 | chr2 | 8872601 | |||||||
| chr2:8872824 | G | A | 9 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(6): Show |
9 | HG01891.hp1 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.883+284C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 8/12 | chr2 | 8872824 | |||||||
| chr2:8872885 | C | G | 2 | a0001c0001t0003g0018 a0001c0001t0003g0023 |
2 | HG01175.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.883+223G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 8/12 | chr2 | 8872885 | |||||||
| chr2:8873005 | T | G | 14 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(11): Show |
14 | HG00642.hp1 HG01070.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.883+103A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 8/12 | chr2 | 8873005 | |||||||
| chr2:8873475 | T | G | 2 | a0001c0001t0009g0007 a0001c0004t0015g0006 |
2 | HG00639.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.691-175A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 7/12 | chr2 | 8873475 | |||||||
| chr2:8873505 | A | G | 3 | a0002c0002t0024g0159 a0002c0002t0024g0160 a0002c0002t0040g0158 |
3 | HG01167.hp2 HG01169.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.691-205T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 7/12 | chr2 | 8873505 | |||||||
| chr2:8873620 | T | TA | 42 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(39): Show |
42 | HG00639.hp2 HG00642.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.691-321dupT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 7/12 | chr2 | 8873620 | |||||||
| chr2:8873761 | A | G | 2 | a0001c0001t0009g0034 a0001c0001t0009g0035 |
2 | HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.691-461T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 7/12 | chr2 | 8873761 | |||||||
| chr2:8874056 | A | T | 1 | a0004c0005t0028g0013 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.691-756T>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 7/12 | chr2 | 8874056 | |||||||
| chr2:8874206 | G | A | 4 | a0002c0002t0015g0064 a0002c0002t0024g0159 a0002c0002t0024g0160 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.691-906C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 7/12 | chr2 | 8874206 | |||||||
| chr2:8874774 | C | T | 1 | a0001c0001t0004g0051 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.691-1474G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 7/12 | chr2 | 8874774 | |||||||
| chr2:8874817 | T | C | 1 | a0001c0001t0005g0042 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.691-1517A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 7/12 | chr2 | 8874817 | |||||||
| chr2:8875054 | T | C | 10 | a0001c0001t0009g0007 a0001c0001t0026g0005 a0001c0004t0015g0006 others(7): Show |
10 | HG00639.hp2 HG01167.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.691-1754A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 7/12 | chr2 | 8875054 | |||||||
| chr2:8875122 | C | A | 1 | a0001c0001t0004g0057 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.691-1822G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 7/12 | chr2 | 8875122 | |||||||
| chr2:8875142 | G | A | 24 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0002g0030 others(21): Show |
25 | HG00621.hp2 HG01175.hp1 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.691-1842C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 7/12 | chr2 | 8875142 | |||||||
| chr2:8875386 | T | G | 42 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(39): Show |
42 | HG00639.hp2 HG00642.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.690+1644A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 7/12 | chr2 | 8875386 | |||||||
| chr2:8875510 | T | C | 1 | a0004c0005t0028g0013 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.690+1520A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 7/12 | chr2 | 8875510 | |||||||
| chr2:8875555 | T | G | 1 | a0001c0001t0002g0080 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.690+1475A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 7/12 | chr2 | 8875555 | |||||||
| chr2:8875774 | A | C | 8 | a0001c0001t0009g0007 a0001c0001t0009g0034 a0001c0001t0009g0035 others(5): Show |
8 | HG00639.hp2 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.690+1256T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 7/12 | chr2 | 8875774 | |||||||
| chr2:8875903 | T | C | 1 | a0002c0002t0027g0036 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.690+1127A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 7/12 | chr2 | 8875903 | |||||||
| chr2:8875952 | A | G | 1 | a0001c0001t0002g0065 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.690+1078T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 7/12 | chr2 | 8875952 | |||||||
| chr2:8876063 | A | C | 1 | a0001c0001t0003g0001 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.690+967T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 7/12 | chr2 | 8876063 | |||||||
| chr2:8876226 | C | A | 68 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0002g0030 others(65): Show |
69 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.690+804G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 7/12 | chr2 | 8876226 | |||||||
| chr2:8876904 | T | C | 98 | a0001c0001t0001g0070 a0001c0001t0001g0074 a0001c0001t0001g0075 others(95): Show |
99 | HG00609.hp1 HG00621.hp2 HG00639.hp2 others(96): Show |
intron_variant | MODIFIER | c.690+126A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 7/12 | chr2 | 8876904 | |||||||
| chr2:8876965 | T | C | 4 | a0001c0001t0008g0149 a0001c0001t0008g0150 a0001c0001t0008g0151 others(1): Show |
4 | HG01070.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.690+65A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 7/12 | chr2 | 8876965 | |||||||
| chr2:8877293 | C | T | 2 | a0002c0002t0017g0011 a0002c0002t0017g0012 |
2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.507-80G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8877293 | |||||||
| chr2:8877368 | T | C | 3 | a0001c0001t0012g0052 a0001c0001t0012g0053 a0001c0001t0012g0054 |
3 | HG00738.hp2 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.507-155A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8877368 | |||||||
| chr2:8877477 | G | A | 1 | a0002c0002t0027g0036 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.507-264C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8877477 | |||||||
| chr2:8877577 | C | T | 1 | a0001c0001t0002g0104 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.507-364G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8877577 | |||||||
| chr2:8877696 | G | A | 4 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(1): Show |
4 | HG03041.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.507-483C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8877696 | |||||||
| chr2:8877876 | T | C | 14 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(11): Show |
14 | HG00642.hp1 HG01070.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.507-663A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8877876 | |||||||
| chr2:8878125 | C | A | 7 | a0002c0002t0015g0064 a0002c0002t0017g0011 a0002c0002t0017g0012 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.507-912G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8878125 | |||||||
| chr2:8878281 | T | G | 1 | a0001c0001t0002g0119 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.507-1068A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8878281 | |||||||
| chr2:8878350 | C | T | 1 | a0002c0002t0027g0036 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.507-1137G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8878350 | |||||||
| chr2:8878434 | G | A | 2 | a0001c0001t0018g0024 a0001c0001t0018g0025 |
2 | HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.507-1221C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8878434 | |||||||
| chr2:8878712 | C | G | 2 | a0001c0001t0023g0156 a0001c0001t0023g0157 |
2 | HG01071.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.507-1499G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8878712 | |||||||
| chr2:8879075 | C | CA | 6 | a0001c0001t0002g0072 a0001c0001t0009g0034 a0001c0001t0009g0035 others(3): Show |
6 | HG03098.hp1 HG03098.hp2 NA18953.hp1 others(3): Show |
intron_variant | MODIFIER | c.507-1863dupT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8879075 | |||||||
| chr2:8879075 | CA | C | 11 | a0001c0001t0001g0070 a0001c0001t0001g0145 a0001c0001t0001g0146 others(8): Show |
11 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.507-1863delT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8879075 | |||||||
| chr2:8879382 | A | C | 1 | a0001c0001t0003g0023 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.507-2169T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8879382 | |||||||
| chr2:8879475 | C | T | 4 | a0001c0001t0008g0149 a0001c0001t0008g0150 a0001c0001t0008g0151 others(1): Show |
4 | HG01070.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.507-2262G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8879475 | |||||||
| chr2:8879741 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.507-2528G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8879741 | |||||||
| chr2:8880071 | T | C | 14 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(11): Show |
14 | HG00642.hp1 HG01070.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.506+2440A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8880071 | |||||||
| chr2:8880488 | T | C | 4 | a0001c0001t0008g0149 a0001c0001t0008g0150 a0001c0001t0008g0151 others(1): Show |
4 | HG01070.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.506+2023A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8880488 | |||||||
| chr2:8880535 | C | T | 3 | a0003c0003t0010g0153 a0003c0003t0010g0154 a0003c0003t0010g0155 |
3 | HG00642.hp1 HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.506+1976G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8880535 | |||||||
| chr2:8880536 | G | A | 1 | a0001c0001t0029g0113 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.506+1975C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8880536 | |||||||
| chr2:8880553 | C | T | 6 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0066 others(3): Show |
6 | HG01070.hp1 HG01071.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.506+1958G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8880553 | |||||||
| chr2:8880584 | G | A | 1 | a0001c0001t0029g0113 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.506+1927C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8880584 | |||||||
| chr2:8880680 | G | A | 6 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(3): Show |
6 | HG01109.hp1 HG01891.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.506+1831C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8880680 | |||||||
| chr2:8880696 | CAG | C | 1 | a0001c0001t0003g0001 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.506+1813_506+1814d others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8880696 | |||||||
| chr2:8880727 | A | G | 14 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(11): Show |
14 | HG00642.hp1 HG01070.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.506+1784T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8880727 | |||||||
| chr2:8880831 | G | A | 42 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(39): Show |
42 | HG00639.hp2 HG00642.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.506+1680C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8880831 | |||||||
| chr2:8880952 | C | T | 21 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(18): Show |
21 | HG00642.hp1 HG01070.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.506+1559G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8880952 | |||||||
| chr2:8881012 | G | A | 5 | a0002c0002t0015g0064 a0002c0002t0024g0159 a0002c0002t0024g0160 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.506+1499C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8881012 | |||||||
| chr2:8881024 | G | A | 3 | a0003c0003t0010g0153 a0003c0003t0010g0154 a0003c0003t0010g0155 |
3 | HG00642.hp1 HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.506+1487C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8881024 | |||||||
| chr2:8881108 | T | C | 2 | a0001c0001t0023g0156 a0001c0001t0023g0157 |
2 | HG01071.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.506+1403A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8881108 | |||||||
| chr2:8881159 | C | T | 1 | a0001c0001t0002g0109 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.506+1352G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8881159 | |||||||
| chr2:8881376 | G | A | 14 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(11): Show |
14 | HG00642.hp1 HG01070.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.506+1135C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8881376 | |||||||
| chr2:8881616 | G | C | 14 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(11): Show |
14 | HG00642.hp1 HG01070.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.506+895C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8881616 | |||||||
| chr2:8881971 | T | G | 1 | a0001c0001t0002g0109 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.506+540A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 6/12 | chr2 | 8881971 | |||||||
| chr2:8882764 | G | A | 1 | a0001c0001t0002g0015 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.452-199C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8882764 | |||||||
| chr2:8883194 | C | T | 33 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(30): Show |
33 | HG00642.hp1 HG00738.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.452-629G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8883194 | |||||||
| chr2:8883608 | T | A | 7 | a0002c0002t0015g0064 a0002c0002t0017g0011 a0002c0002t0017g0012 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.452-1043A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8883608 | |||||||
| chr2:8883660 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.452-1095G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8883660 | |||||||
| chr2:8883681 | C | G | 14 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(11): Show |
14 | HG00642.hp1 HG01070.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.452-1116G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8883681 | |||||||
| chr2:8883761 | T | G | 2 | a0001c0001t0018g0024 a0001c0001t0018g0025 |
2 | HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.452-1196A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8883761 | |||||||
| chr2:8883880 | A | G | 2 | a0001c0001t0003g0018 a0001c0001t0003g0023 |
2 | HG01175.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.452-1315T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8883880 | |||||||
| chr2:8883993 | C | T | 14 | a0001c0001t0008g0149 a0001c0001t0008g0150 a0001c0001t0008g0151 others(11): Show |
14 | HG00642.hp1 HG01070.hp2 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.452-1428G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8883993 | |||||||
| chr2:8884014 | G | C | 5 | a0001c0001t0005g0037 a0001c0001t0005g0039 a0001c0001t0005g0040 others(2): Show |
5 | HG01934.hp1 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.452-1449C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8884014 | |||||||
| chr2:8884195 | C | CA | 33 | a0001c0001t0001g0075 a0001c0001t0001g0128 a0001c0001t0001g0139 others(30): Show |
33 | HG01070.hp2 HG01884.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.452-1631dupT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8884195 | |||||||
| chr2:8884195 | C | CAA | 14 | a0001c0001t0004g0047 a0001c0001t0004g0051 a0001c0001t0004g0066 others(11): Show |
14 | HG00738.hp2 HG01070.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.452-1632_452-1631d others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8884195 | |||||||
| chr2:8884367 | C | G | 5 | a0001c0001t0005g0037 a0001c0001t0005g0039 a0001c0001t0005g0040 others(2): Show |
5 | HG01934.hp1 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.452-1802G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8884367 | |||||||
| chr2:8884381 | C | T | 4 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(1): Show |
4 | HG03041.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.452-1816G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8884381 | |||||||
| chr2:8884390 | A | G | 7 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(4): Show |
7 | HG01070.hp1 HG01071.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.452-1825T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8884390 | |||||||
| chr2:8884485 | T | TA | 117 | a0001c0001t0001g0043 a0001c0001t0001g0070 a0001c0001t0001g0074 others(114): Show |
118 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.452-1921dupT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8884485 | |||||||
| chr2:8884485 | T | TAA | 7 | a0002c0002t0015g0064 a0002c0002t0017g0011 a0002c0002t0017g0012 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.452-1922_452-1921d others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8884485 | |||||||
| chr2:8884721 | C | T | 1 | a0001c0001t0013g0134 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.452-2156G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8884721 | |||||||
| chr2:8885176 | T | C | 12 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(9): Show |
12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.452-2611A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8885176 | |||||||
| chr2:8885219 | G | C | 4 | a0001c0001t0008g0149 a0001c0001t0008g0150 a0001c0001t0008g0151 others(1): Show |
4 | HG01070.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.452-2654C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8885219 | |||||||
| chr2:8885258 | G | T | 1 | a0001c0001t0029g0113 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.452-2693C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8885258 | |||||||
| chr2:8885730 | T | C | 1 | a0001c0001t0004g0058 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.451+2288A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8885730 | |||||||
| chr2:8885855 | T | C | 12 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(9): Show |
12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.451+2163A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8885855 | |||||||
| chr2:8886019 | C | A | 1 | a0002c0002t0015g0064 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.451+1999G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8886019 | |||||||
| chr2:8886639 | T | A | 1 | a0001c0001t0012g0053 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.451+1379A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8886639 | |||||||
| chr2:8886794 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.451+1224T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8886794 | |||||||
| chr2:8886933 | C | T | 2 | a0001c0001t0001g0074 a0001c0001t0001g0075 |
2 | HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.451+1085G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8886933 | |||||||
| chr2:8887119 | C | A | 2 | a0001c0001t0008g0149 a0001c0001t0008g0150 |
2 | HG01070.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.451+899G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8887119 | |||||||
| chr2:8887303 | T | C | 7 | a0001c0001t0008g0149 a0001c0001t0008g0150 a0001c0001t0008g0151 others(4): Show |
7 | HG00642.hp1 HG01070.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.451+715A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8887303 | |||||||
| chr2:8887336 | CCT | C | 26 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(23): Show |
26 | HG00642.hp1 HG00738.hp2 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.451+680_451+681del others(2): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8887336 | |||||||
| chr2:8887355 | T | A | 26 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(23): Show |
26 | HG00642.hp1 HG00738.hp2 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.451+663A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8887355 | |||||||
| chr2:8887613 | A | G | 4 | a0001c0001t0008g0149 a0001c0001t0008g0150 a0001c0001t0008g0151 others(1): Show |
4 | HG01070.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.451+405T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8887613 | |||||||
| chr2:8887622 | G | T | 26 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(23): Show |
26 | HG00642.hp1 HG00738.hp2 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.451+396C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8887622 | |||||||
| chr2:8887782 | T | C | 1 | a0002c0002t0040g0158 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.451+236A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 5/12 | chr2 | 8887782 | |||||||
| chr2:8888100 | T | C | 4 | a0002c0002t0015g0064 a0002c0002t0024g0159 a0002c0002t0024g0160 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.396-27A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8888100 | |||||||
| chr2:8888228 | A | G | 14 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(11): Show |
14 | HG00642.hp1 HG01070.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.396-155T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8888228 | |||||||
| chr2:8888353 | C | A | 2 | a0001c0001t0008g0151 a0001c0001t0008g0152 |
2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.396-280G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8888353 | |||||||
| chr2:8888454 | C | A | 2 | a0002c0002t0017g0011 a0002c0002t0017g0012 |
2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.396-381G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8888454 | |||||||
| chr2:8888455 | T | A | 2 | a0002c0002t0017g0011 a0002c0002t0017g0012 |
2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.396-382A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8888455 | |||||||
| chr2:8888479 | C | A | 7 | a0002c0002t0015g0064 a0002c0002t0017g0011 a0002c0002t0017g0012 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.396-406G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8888479 | |||||||
| chr2:8888568 | G | C | 1 | a0002c0002t0027g0036 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.396-495C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8888568 | |||||||
| chr2:8888655 | G | GA | 7 | a0002c0002t0015g0064 a0002c0002t0017g0011 a0002c0002t0017g0012 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.396-583dupT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8888655 | |||||||
| chr2:8888807 | C | T | 1 | a0001c0001t0004g0055 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.396-734G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8888807 | |||||||
| chr2:8888992 | T | C | 1 | a0001c0001t0003g0020 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.396-919A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8888992 | |||||||
| chr2:8889092 | G | A | 2 | a0002c0002t0017g0011 a0002c0002t0017g0012 |
2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.396-1019C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8889092 | |||||||
| chr2:8889215 | G | A | 1 | a0001c0001t0002g0132 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.396-1142C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8889215 | |||||||
| chr2:8889300 | T | A | 1 | a0002c0002t0027g0036 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.396-1227A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8889300 | |||||||
| chr2:8889307 | T | C | 3 | a0001c0001t0005g0044 a0001c0001t0005g0045 a0001c0001t0005g0046 |
3 | HG02818.hp1 HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.396-1234A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8889307 | |||||||
| chr2:8889472 | T | A | 38 | a0001c0001t0001g0043 a0001c0001t0001g0077 a0001c0001t0001g0082 others(35): Show |
38 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.396-1399A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8889472 | |||||||
| chr2:8889582 | G | A | 1 | a0002c0002t0027g0036 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.396-1509C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8889582 | |||||||
| chr2:8889692 | T | C | 14 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(11): Show |
14 | HG00642.hp1 HG01070.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.396-1619A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8889692 | |||||||
| chr2:8889718 | C | T | 1 | a0001c0001t0005g0037 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.396-1645G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8889718 | |||||||
| chr2:8890304 | A | G | 19 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(16): Show |
19 | HG00738.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.396-2231T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8890304 | |||||||
| chr2:8890306 | G | A | 7 | a0002c0002t0015g0064 a0002c0002t0017g0011 a0002c0002t0017g0012 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.396-2233C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8890306 | |||||||
| chr2:8890458 | G | A | 2 | a0001c0001t0009g0034 a0001c0001t0009g0035 |
2 | HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.396-2385C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8890458 | |||||||
| chr2:8890466 | C | T | 1 | a0001c0001t0032g0094 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.396-2393G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8890466 | |||||||
| chr2:8890530 | T | A | 6 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(3): Show |
6 | HG01109.hp1 HG01891.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.396-2457A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8890530 | |||||||
| chr2:8890810 | C | T | 1 | a0001c0001t0012g0054 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.396-2737G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8890810 | |||||||
| chr2:8890891 | G | C | 7 | a0002c0002t0015g0064 a0002c0002t0017g0011 a0002c0002t0017g0012 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.396-2818C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8890891 | |||||||
| chr2:8891124 | T | A | 2 | a0001c0001t0009g0034 a0001c0001t0009g0035 |
2 | HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.396-3051A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8891124 | |||||||
| chr2:8891554 | C | G | 1 | a0002c0002t0027g0036 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.396-3481G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8891554 | |||||||
| chr2:8891555 | A | G | 7 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(4): Show |
7 | HG01070.hp1 HG01071.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.396-3482T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8891555 | |||||||
| chr2:8891691 | C | T | 1 | a0003c0003t0010g0155 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.396-3618G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8891691 | |||||||
| chr2:8891816 | G | A | 1 | a0001c0001t0004g0060 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.396-3743C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8891816 | |||||||
| chr2:8891853 | G | C | 1 | a0001c0001t0029g0113 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.396-3780C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8891853 | |||||||
| chr2:8891977 | A | G | 7 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(4): Show |
7 | HG01070.hp1 HG01071.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.396-3904T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8891977 | |||||||
| chr2:8892450 | T | G | 7 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(4): Show |
7 | HG01070.hp1 HG01071.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.396-4377A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8892450 | |||||||
| chr2:8892619 | A | G | 7 | a0001c0001t0008g0149 a0001c0001t0008g0150 a0001c0001t0008g0151 others(4): Show |
7 | HG00642.hp1 HG01070.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.396-4546T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8892619 | |||||||
| chr2:8892854 | A | G | 12 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(9): Show |
12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.396-4781T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8892854 | |||||||
| chr2:8892924 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.396-4851C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8892924 | |||||||
| chr2:8893411 | G | T | 2 | a0001c0001t0008g0149 a0001c0001t0008g0150 |
2 | HG01070.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.396-5338C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8893411 | |||||||
| chr2:8893466 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.396-5393T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8893466 | |||||||
| chr2:8893588 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.396-5515A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8893588 | |||||||
| chr2:8893621 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.396-5548A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8893621 | |||||||
| chr2:8893996 | G | T | 2 | a0001c0001t0005g0040 a0001c0001t0031g0038 |
2 | HG02572.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.396-5923C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8893996 | |||||||
| chr2:8894016 | T | C | 1 | a0001c0001t0006g0136 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.396-5943A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8894016 | |||||||
| chr2:8894143 | C | T | 1 | a0004c0005t0028g0013 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.396-6070G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8894143 | |||||||
| chr2:8894390 | A | G | 1 | a0002c0002t0027g0036 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.396-6317T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8894390 | |||||||
| chr2:8894419 | C | T | 2 | a0001c0001t0003g0021 a0001c0001t0003g0022 |
2 | HG03225.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.396-6346G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8894419 | |||||||
| chr2:8894447 | A | G | 1 | a0002c0002t0015g0064 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.396-6374T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8894447 | |||||||
| chr2:8894710 | G | A | 7 | a0002c0002t0015g0064 a0002c0002t0017g0011 a0002c0002t0017g0012 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.396-6637C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8894710 | |||||||
| chr2:8894878 | T | C | 12 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(9): Show |
12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.396-6805A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8894878 | |||||||
| chr2:8894899 | G | A | 2 | a0001c0001t0001g0089 a0001c0001t0001g0143 |
2 | HG00735.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.396-6826C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8894899 | |||||||
| chr2:8894991 | T | C | 25 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0002g0030 others(22): Show |
26 | HG00621.hp2 HG01175.hp1 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.396-6918A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8894991 | |||||||
| chr2:8895071 | G | A | 4 | a0001c0001t0002g0071 a0001c0001t0002g0072 a0001c0001t0002g0073 others(1): Show |
4 | HG02083.hp1 NA18953.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.396-6998C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8895071 | |||||||
| chr2:8895164 | T | G | 4 | a0001c0001t0008g0149 a0001c0001t0008g0150 a0001c0001t0008g0151 others(1): Show |
4 | HG01070.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.396-7091A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8895164 | |||||||
| chr2:8895321 | C | T | 1 | a0002c0002t0027g0036 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.396-7248G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8895321 | |||||||
| chr2:8895429 | T | C | 1 | a0001c0001t0030g0095 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.396-7356A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8895429 | |||||||
| chr2:8895460 | A | G | 2 | a0002c0002t0017g0011 a0002c0002t0017g0012 |
2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.396-7387T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8895460 | |||||||
| chr2:8895684 | C | T | 1 | a0001c0001t0001g0130 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.396-7611G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8895684 | |||||||
| chr2:8895713 | C | T | 9 | a0001c0001t0005g0037 a0001c0001t0005g0039 a0001c0001t0005g0040 others(6): Show |
9 | HG01175.hp2 HG01934.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.396-7640G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8895713 | |||||||
| chr2:8895780 | G | A | 1 | a0001c0001t0002g0101 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.396-7707C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8895780 | |||||||
| chr2:8895959 | C | T | 4 | a0001c0001t0008g0149 a0001c0001t0008g0150 a0001c0001t0008g0151 others(1): Show |
4 | HG01070.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.396-7886G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8895959 | |||||||
| chr2:8896003 | C | T | 3 | a0001c0001t0001g0070 a0001c0001t0001g0124 a0001c0001t0001g0130 |
3 | HG00609.hp1 NA18957.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.396-7930G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8896003 | |||||||
| chr2:8896099 | C | T | 3 | a0001c0001t0002g0093 a0001c0001t0006g0016 a0001c0001t0032g0094 |
3 | NA18956.hp1 NA18956.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.396-8026G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8896099 | |||||||
| chr2:8896234 | G | A | 2 | a0001c0001t0009g0034 a0001c0001t0009g0035 |
2 | HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.396-8161C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8896234 | |||||||
| chr2:8896238 | C | CA | 28 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0002g0030 others(25): Show |
29 | HG00621.hp2 HG01175.hp1 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.396-8166dupT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8896238 | |||||||
| chr2:8896357 | T | G | 3 | a0001c0001t0012g0052 a0001c0001t0012g0053 a0001c0001t0012g0054 |
3 | HG00738.hp2 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.396-8284A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8896357 | |||||||
| chr2:8896440 | C | CAA | 138 | a0001c0001t0001g0043 a0001c0001t0001g0070 a0001c0001t0001g0074 others(135): Show |
139 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(136): Show |
intron_variant | MODIFIER | c.396-8368_396-8367i others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8896440 | |||||||
| chr2:8896547 | G | C | 12 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(9): Show |
12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.396-8474C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8896547 | |||||||
| chr2:8896908 | C | CCT | 33 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(30): Show |
33 | HG00642.hp1 HG00738.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.396-8836_396-8835i others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8896908 | |||||||
| chr2:8896952 | C | T | 3 | a0001c0001t0002g0072 a0001c0001t0002g0073 a0001c0001t0002g0119 |
3 | HG02083.hp1 NA18953.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.396-8879G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8896952 | |||||||
| chr2:8896953 | G | A | 2 | a0001c0001t0014g0014 a0001c0001t0014g0032 |
2 | HG02451.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.396-8880C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8896953 | |||||||
| chr2:8897227 | T | TTC | 63 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0002g0030 others(60): Show |
64 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.396-9156_396-9155d others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8897227 | |||||||
| chr2:8897227 | T | TTCTCTTT others(58): Show |
4 | a0001c0001t0008g0149 a0001c0001t0008g0150 a0001c0001t0008g0151 others(1): Show |
4 | HG01070.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.396-9155_396-9154i others(67): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8897227 | |||||||
| chr2:8897260 | T | C | 3 | a0003c0003t0010g0153 a0003c0003t0010g0154 a0003c0003t0010g0155 |
3 | HG00642.hp1 HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.396-9187A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8897260 | |||||||
| chr2:8897437 | C | T | 1 | a0001c0001t0002g0073 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.396-9364G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8897437 | |||||||
| chr2:8897589 | G | A | 1 | a0002c0002t0015g0064 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.396-9516C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8897589 | |||||||
| chr2:8897638 | ACTAACTA others(4): Show |
A | 12 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(9): Show |
12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.396-9576_396-9566d others(13): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8897638 | |||||||
| chr2:8897658 | C | T | 12 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(9): Show |
12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.396-9585G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8897658 | |||||||
| chr2:8897676 | C | G | 2 | a0001c0001t0039g0004 a0004c0005t0028g0013 |
2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.396-9603G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8897676 | |||||||
| chr2:8898110 | C | A | 1 | a0001c0001t0001g0087 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.396-10037G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8898110 | |||||||
| chr2:8898847 | G | A | 3 | a0001c0001t0005g0044 a0001c0001t0005g0045 a0001c0001t0005g0046 |
3 | HG02818.hp1 HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.395+9774C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8898847 | |||||||
| chr2:8898990 | T | C | 1 | a0001c0001t0037g0111 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.395+9631A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8898990 | |||||||
| chr2:8899018 | G | A | 9 | a0001c0001t0002g0079 a0001c0001t0009g0007 a0001c0001t0009g0034 others(6): Show |
9 | HG00639.hp2 HG01169.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.395+9603C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8899018 | |||||||
| chr2:8899264 | C | T | 1 | a0001c0001t0038g0129 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.395+9357G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8899264 | |||||||
| chr2:8899308 | G | A | 3 | a0001c0001t0006g0090 a0001c0001t0006g0091 a0001c0001t0006g0092 |
3 | HG02735.hp1 HG04115.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.395+9313C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8899308 | |||||||
| chr2:8899332 | C | T | 14 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(11): Show |
14 | HG00642.hp1 HG01070.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.395+9289G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8899332 | |||||||
| chr2:8899341 | A | T | 1 | a0001c0001t0003g0001 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.395+9280T>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8899341 | |||||||
| chr2:8899414 | CA | C | 12 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(9): Show |
12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.395+9206delT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8899414 | |||||||
| chr2:8899714 | T | C | 2 | a0001c0001t0008g0149 a0001c0001t0008g0150 |
2 | HG01070.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.395+8907A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8899714 | |||||||
| chr2:8899813 | T | C | 3 | a0002c0002t0017g0011 a0002c0002t0017g0012 a0002c0002t0027g0036 |
3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.395+8808A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8899813 | |||||||
| chr2:8899859 | T | C | 2 | a0001c0001t0009g0034 a0001c0001t0009g0035 |
2 | HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.395+8762A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8899859 | |||||||
| chr2:8899961 | G | A | 1 | a0001c0001t0005g0042 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.395+8660C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8899961 | |||||||
| chr2:8900035 | G | GC | 12 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(9): Show |
12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.395+8585dupG | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8900035 | |||||||
| chr2:8900054 | G | T | 1 | a0001c0001t0005g0041 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.395+8567C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8900054 | |||||||
| chr2:8900171 | G | A | 1 | a0001c0001t0002g0073 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.395+8450C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8900171 | |||||||
| chr2:8900199 | G | T | 1 | a0001c0001t0001g0070 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.395+8422C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8900199 | |||||||
| chr2:8900243 | G | A | 5 | a0001c0001t0005g0037 a0001c0001t0005g0039 a0001c0001t0005g0040 others(2): Show |
5 | HG01934.hp1 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.395+8378C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8900243 | |||||||
| chr2:8900459 | C | T | 7 | a0001c0001t0008g0149 a0001c0001t0008g0150 a0001c0001t0008g0151 others(4): Show |
7 | HG00642.hp1 HG01070.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.395+8162G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8900459 | |||||||
| chr2:8901154 | T | C | 33 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(30): Show |
33 | HG00642.hp1 HG00738.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.395+7467A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8901154 | |||||||
| chr2:8901508 | AAAG | A | 3 | a0002c0002t0024g0159 a0002c0002t0024g0160 a0002c0002t0040g0158 |
3 | HG01167.hp2 HG01169.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.395+7110_395+7112d others(5): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8901508 | |||||||
| chr2:8901821 | G | T | 2 | a0001c0001t0002g0106 a0001c0001t0002g0114 |
2 | HG01256.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.395+6800C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8901821 | |||||||
| chr2:8901930 | G | A | 3 | a0003c0003t0010g0153 a0003c0003t0010g0154 a0003c0003t0010g0155 |
3 | HG00642.hp1 HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.395+6691C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8901930 | |||||||
| chr2:8901996 | G | A | 7 | a0001c0001t0008g0149 a0001c0001t0008g0150 a0001c0001t0008g0151 others(4): Show |
7 | HG00642.hp1 HG01070.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.395+6625C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8901996 | |||||||
| chr2:8902037 | G | A | 1 | a0001c0001t0002g0017 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.395+6584C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8902037 | |||||||
| chr2:8902332 | C | T | 1 | a0001c0001t0029g0113 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.395+6289G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8902332 | |||||||
| chr2:8902469 | G | A | 1 | a0001c0001t0005g0042 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.395+6152C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8902469 | |||||||
| chr2:8902570 | G | A | 1 | a0001c0001t0006g0136 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.395+6051C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8902570 | |||||||
| chr2:8902581 | A | G | 1 | a0002c0002t0015g0064 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.395+6040T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8902581 | |||||||
| chr2:8902780 | G | A | 1 | a0001c0001t0026g0005 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.395+5841C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8902780 | |||||||
| chr2:8902873 | T | C | 33 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(30): Show |
33 | HG00642.hp1 HG00738.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.395+5748A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8902873 | |||||||
| chr2:8903214 | C | T | 1 | a0002c0002t0040g0158 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.395+5407G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8903214 | |||||||
| chr2:8903476 | A | AT | 7 | a0002c0002t0015g0064 a0002c0002t0017g0011 a0002c0002t0017g0012 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.395+5144dupA | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8903476 | |||||||
| chr2:8903476 | AT | A | 23 | a0001c0001t0001g0120 a0001c0001t0002g0017 a0001c0001t0002g0030 others(20): Show |
24 | HG01175.hp1 HG01256.hp1 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.395+5144delA | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8903476 | |||||||
| chr2:8904018 | C | A | 2 | a0001c0001t0005g0037 a0001c0001t0005g0039 |
2 | HG01934.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.395+4603G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8904018 | |||||||
| chr2:8904071 | G | C | 1 | a0001c0001t0001g0087 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.395+4550C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8904071 | |||||||
| chr2:8904313 | T | A | 11 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(8): Show |
11 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.395+4308A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8904313 | |||||||
| chr2:8904316 | A | T | 16 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(13): Show |
16 | HG00738.hp2 HG01109.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.395+4305T>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8904316 | |||||||
| chr2:8904316 | AT | A | 66 | a0001c0001t0001g0098 a0001c0001t0002g0017 a0001c0001t0002g0030 others(63): Show |
67 | HG00609.hp2 HG00621.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.395+4304delA | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8904316 | |||||||
| chr2:8904317 | T | A | 7 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(4): Show |
7 | HG01891.hp1 HG02055.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.395+4304A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8904317 | |||||||
| chr2:8904415 | G | A | 2 | a0001c0001t0001g0074 a0001c0001t0001g0075 |
2 | HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.395+4206C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8904415 | |||||||
| chr2:8904997 | T | TAC | 2 | a0001c0001t0004g0051 a0001c0001t0035g0103 |
2 | HG00140.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.395+3622_395+3623d others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8904997 | |||||||
| chr2:8905010 | A | G | 8 | a0001c0001t0023g0157 a0002c0002t0015g0064 a0002c0002t0017g0011 others(5): Show |
8 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.395+3611T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8905010 | |||||||
| chr2:8905012 | G | A | 2 | a0001c0001t0016g0009 a0001c0001t0016g0010 |
2 | HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.395+3609C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8905012 | |||||||
| chr2:8905014 | G | A | 2 | a0001c0001t0004g0066 a0001c0001t0004g0067 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.395+3607C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8905014 | |||||||
| chr2:8905222 | G | A | 9 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(6): Show |
9 | HG01891.hp1 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.395+3399C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8905222 | |||||||
| chr2:8905750 | C | T | 14 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(11): Show |
14 | HG00642.hp1 HG01070.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.395+2871G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8905750 | |||||||
| chr2:8905776 | CACATGTA others(7): Show |
C | 7 | a0002c0002t0015g0064 a0002c0002t0017g0011 a0002c0002t0017g0012 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.395+2831_395+2844d others(16): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8905776 | |||||||
| chr2:8906033 | C | G | 1 | a0001c0001t0004g0059 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.395+2588G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8906033 | |||||||
| chr2:8906039 | C | T | 1 | a0001c0001t0002g0072 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.395+2582G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8906039 | |||||||
| chr2:8906100 | AGG | A | 26 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0002g0030 others(23): Show |
27 | HG00621.hp2 HG01175.hp1 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.395+2519_395+2520d others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8906100 | |||||||
| chr2:8906108 | G | A | 2 | a0001c0001t0008g0149 a0001c0001t0008g0150 |
2 | HG01070.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.395+2513C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8906108 | |||||||
| chr2:8906229 | A | G | 1 | a0001c0001t0002g0104 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.395+2392T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8906229 | |||||||
| chr2:8906279 | C | A | 1 | a0001c0001t0002g0080 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.395+2342G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8906279 | |||||||
| chr2:8907056 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.395+1565A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8907056 | |||||||
| chr2:8907194 | C | T | 1 | a0001c0001t0011g0063 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.395+1427G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8907194 | |||||||
| chr2:8907308 | C | T | 1 | a0003c0003t0010g0153 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.395+1313G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8907308 | |||||||
| chr2:8907907 | A | G | 2 | a0001c0001t0008g0149 a0001c0001t0008g0150 |
2 | HG01070.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.395+714T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8907907 | |||||||
| chr2:8908375 | C | G | 1 | a0004c0005t0028g0013 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.395+246G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8908375 | |||||||
| chr2:8908434 | T | G | 3 | a0001c0001t0012g0052 a0001c0001t0012g0053 a0001c0001t0012g0054 |
3 | HG00738.hp2 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.395+187A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 4/12 | chr2 | 8908434 | |||||||
| chr2:8909232 | C | T | 2 | a0001c0001t0018g0024 a0001c0001t0018g0025 |
2 | HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.300-516G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8909232 | |||||||
| chr2:8909266 | A | G | 6 | a0001c0001t0009g0007 a0001c0001t0016g0009 a0001c0001t0016g0010 others(3): Show |
6 | HG00639.hp2 HG01884.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.300-550T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8909266 | |||||||
| chr2:8909485 | T | G | 33 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(30): Show |
33 | HG00642.hp1 HG00738.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.300-769A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8909485 | |||||||
| chr2:8909597 | C | A | 1 | a0001c0001t0003g0001 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.300-881G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8909597 | |||||||
| chr2:8910170 | CAGAG | C | 12 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(9): Show |
12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.300-1458_300-1455d others(6): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8910170 | |||||||
| chr2:8910314 | A | G | 34 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(31): Show |
34 | HG00642.hp1 HG00738.hp2 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.300-1598T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8910314 | |||||||
| chr2:8910667 | T | A | 1 | a0001c0001t0029g0113 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.300-1951A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8910667 | |||||||
| chr2:8911082 | C | T | 1 | a0002c0002t0027g0036 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.300-2366G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8911082 | |||||||
| chr2:8911218 | T | C | 12 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(9): Show |
12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.300-2502A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8911218 | |||||||
| chr2:8911274 | T | C | 3 | a0003c0003t0010g0153 a0003c0003t0010g0154 a0003c0003t0010g0155 |
3 | HG00642.hp1 HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.300-2558A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8911274 | |||||||
| chr2:8911658 | T | G | 1 | a0001c0001t0012g0054 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.300-2942A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8911658 | |||||||
| chr2:8911659 | G | T | 1 | a0001c0001t0012g0054 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.300-2943C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8911659 | |||||||
| chr2:8911831 | C | A | 7 | a0001c0001t0008g0149 a0001c0001t0008g0150 a0001c0001t0008g0151 others(4): Show |
7 | HG00642.hp1 HG01070.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.300-3115G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8911831 | |||||||
| chr2:8911975 | A | G | 2 | a0001c0001t0001g0077 a0001c0001t0036g0112 |
2 | HG01109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.300-3259T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8911975 | |||||||
| chr2:8912298 | GA | G | 14 | a0001c0001t0002g0015 a0001c0001t0004g0047 a0001c0001t0004g0050 others(11): Show |
14 | HG00738.hp2 HG01167.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.300-3583delT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912298 | |||||||
| chr2:8912299 | A | AAAAG | 13 | a0001c0001t0001g0116 a0001c0001t0002g0030 a0001c0001t0002g0071 others(10): Show |
13 | HG01167.hp1 HG01256.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.300-3587_300-3584d others(6): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912299 | |||||||
| chr2:8912299 | A | AAAAGAAA others(1): Show |
11 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0124 others(8): Show |
11 | HG00609.hp1 HG02135.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.300-3591_300-3584d others(10): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912299 | |||||||
| chr2:8912299 | A | AAAAGAAA others(5): Show |
2 | a0001c0001t0002g0101 a0001c0001t0034g0127 |
2 | HG03017.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.300-3595_300-3584d others(14): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912299 | |||||||
| chr2:8912299 | A | AAAAGAAA others(13): Show |
2 | a0001c0001t0001g0070 a0001c0001t0001g0099 |
2 | HG03209.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.300-3603_300-3584d others(22): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912299 | |||||||
| chr2:8912299 | A | AAAAGAAA others(8): Show |
1 | a0001c0001t0001g0142 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.300-3584_300-3583i others(17): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912299 | |||||||
| chr2:8912299 | A | AAAG | 19 | a0001c0001t0001g0137 a0001c0001t0004g0055 a0001c0001t0004g0056 others(16): Show |
19 | HG00642.hp1 HG01070.hp1 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.300-3584_300-3583i others(5): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912299 | |||||||
| chr2:8912299 | AAAAG | A | 3 | a0001c0001t0001g0100 a0001c0001t0001g0115 a0001c0001t0003g0028 |
3 | HG02717.hp1 HG02735.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.300-3587_300-3584d others(6): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912299 | |||||||
| chr2:8912299 | AAAAGAAA others(5): Show |
A | 1 | a0001c0001t0002g0017 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.300-3595_300-3584d others(14): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912299 | |||||||
| chr2:8912301 | A | AGAAAGAA others(38): Show |
1 | a0001c0001t0011g0061 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.300-3586_300-3585i others(47): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912301 | |||||||
| chr2:8912303 | G | A | 1 | a0001c0001t0011g0061 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.300-3587C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912303 | |||||||
| chr2:8912328 | A | G | 1 | a0001c0001t0013g0134 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.300-3612T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912328 | |||||||
| chr2:8912329 | A | AAGAAAGA others(3): Show |
1 | a0001c0001t0005g0042 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.300-3623_300-3614d others(12): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912329 | |||||||
| chr2:8912333 | A | AAGAAAGA others(29): Show |
1 | a0001c0001t0005g0040 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.300-3618_300-3617i others(38): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912333 | |||||||
| chr2:8912337 | AAGAAAGA others(7): Show |
A | 1 | a0001c0001t0003g0023 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.300-3635_300-3622d others(16): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912337 | |||||||
| chr2:8912343 | GAA | G | 2 | a0001c0001t0001g0120 a0001c0001t0006g0016 |
2 | HG03704.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.300-3629_300-3628d others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912343 | |||||||
| chr2:8912345 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.300-3629T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912345 | |||||||
| chr2:8912345 | AAGAAAGA others(21): Show |
A | 1 | a0001c0001t0003g0018 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.300-3657_300-3630d others(30): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912345 | |||||||
| chr2:8912347 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.300-3631C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912347 | |||||||
| chr2:8912348 | A | AAAGAAAG others(3): Show |
1 | a0001c0001t0003g0027 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.300-3633_300-3632i others(12): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912348 | |||||||
| chr2:8912349 | A | G | 10 | a0001c0001t0001g0043 a0001c0001t0001g0087 a0001c0001t0001g0128 others(7): Show |
10 | HG00639.hp1 HG00738.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.300-3633T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912349 | |||||||
| chr2:8912349 | AAG | A | 13 | a0001c0001t0001g0120 a0001c0001t0001g0145 a0001c0001t0001g0146 others(10): Show |
13 | HG00609.hp2 HG01167.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.300-3635_300-3634d others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912349 | |||||||
| chr2:8912351 | G | A | 13 | a0001c0001t0001g0043 a0001c0001t0001g0087 a0001c0001t0001g0128 others(10): Show |
13 | HG00639.hp1 HG00738.hp2 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.300-3635C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912351 | |||||||
| chr2:8912351 | G | GAA | 17 | a0001c0001t0001g0110 a0001c0001t0002g0081 a0001c0001t0002g0104 others(14): Show |
17 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(14): Show |
intron_variant | MODIFIER | c.300-3636_300-3635i others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912351 | |||||||
| chr2:8912351 | G | GAAAGAA | 7 | a0001c0001t0001g0075 a0001c0001t0002g0102 a0001c0001t0002g0114 others(4): Show |
7 | HG00140.hp1 HG00642.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.300-3636_300-3635i others(8): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912351 | |||||||
| chr2:8912351 | G | GAAAGAAA others(3): Show |
3 | a0001c0001t0002g0065 a0001c0001t0002g0109 a0001c0001t0003g0021 |
3 | HG00738.hp1 HG03471.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.300-3636_300-3635i others(12): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912351 | |||||||
| chr2:8912351 | G | GAAAGAAA others(77): Show |
1 | a0001c0001t0011g0062 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.300-3636_300-3635i others(86): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912351 | |||||||
| chr2:8912351 | G | GAAAGAAA others(7): Show |
2 | a0001c0001t0002g0144 a0001c0001t0023g0156 |
2 | HG01071.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.300-3636_300-3635i others(16): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912351 | |||||||
| chr2:8912351 | G | GAAAGAAA others(12): Show |
1 | a0001c0001t0001g0121 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.300-3636_300-3635i others(21): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912351 | |||||||
| chr2:8912351 | G | GAAAGAAA others(13): Show |
1 | a0001c0001t0021g0125 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.300-3636_300-3635i others(22): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912351 | |||||||
| chr2:8912351 | G | GAAAGAAA others(31): Show |
1 | a0001c0001t0001g0130 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.300-3636_300-3635i others(40): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912351 | |||||||
| chr2:8912351 | G | GAAAGAGA others(5): Show |
1 | a0001c0001t0001g0096 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.300-3636_300-3635i others(14): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912351 | |||||||
| chr2:8912353 | G | A | 24 | a0001c0001t0001g0074 a0001c0001t0001g0077 a0001c0001t0001g0141 others(21): Show |
25 | HG00621.hp2 HG01109.hp2 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.300-3637C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912353 | |||||||
| chr2:8912355 | A | AAG | 18 | a0001c0001t0001g0075 a0001c0001t0001g0110 a0001c0001t0002g0081 others(15): Show |
18 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(15): Show |
intron_variant | MODIFIER | c.300-3641_300-3640d others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912355 | |||||||
| chr2:8912355 | A | G | 23 | a0001c0001t0001g0074 a0001c0001t0001g0077 a0001c0001t0001g0140 others(20): Show |
24 | HG00621.hp2 HG01109.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.300-3639T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912355 | |||||||
| chr2:8912357 | G | A | 2 | a0001c0001t0036g0112 a0003c0003t0010g0153 |
2 | HG03486.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.300-3641C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912357 | |||||||
| chr2:8912359 | A | AAG | 6 | a0001c0001t0002g0065 a0001c0001t0004g0047 a0001c0001t0030g0095 others(3): Show |
6 | HG00140.hp2 HG00738.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.300-3645_300-3644d others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912359 | |||||||
| chr2:8912359 | A | AAGAAAGA others(3): Show |
1 | a0001c0001t0001g0128 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.300-3653_300-3644d others(12): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912359 | |||||||
| chr2:8912359 | A | G | 2 | a0001c0001t0036g0112 a0003c0003t0010g0153 |
2 | HG03486.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.300-3643T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912359 | |||||||
| chr2:8912361 | GAA | G | 3 | a0001c0001t0018g0025 a0001c0001t0025g0008 a0001c0004t0015g0006 |
3 | HG01884.hp1 HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.300-3647_300-3646d others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912361 | |||||||
| chr2:8912363 | A | AAG | 3 | a0001c0001t0004g0050 a0001c0001t0008g0150 a0001c0001t0009g0007 |
3 | HG00639.hp2 HG01070.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.300-3649_300-3648d others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912363 | |||||||
| chr2:8912367 | A | AAG | 3 | a0001c0001t0001g0087 a0001c0001t0003g0029 a0001c0001t0014g0031 |
3 | HG02486.hp1 HG03453.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.300-3653_300-3652d others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912367 | |||||||
| chr2:8912367 | A | G | 4 | a0001c0001t0001g0146 a0001c0001t0001g0148 a0001c0001t0016g0009 others(1): Show |
4 | HG02895.hp2 HG02896.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.300-3651T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912367 | |||||||
| chr2:8912369 | G | A | 4 | a0001c0001t0001g0146 a0001c0001t0001g0148 a0001c0001t0016g0009 others(1): Show |
4 | HG02895.hp2 HG02896.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.300-3653C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912369 | |||||||
| chr2:8912369 | GAAAGAGA others(9): Show |
G | 1 | a0001c0001t0009g0034 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.300-3669_300-3654d others(18): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912369 | |||||||
| chr2:8912371 | A | G | 13 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0145 others(10): Show |
13 | HG00609.hp2 HG02080.hp2 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.300-3655T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912371 | |||||||
| chr2:8912371 | AAG | A | 6 | a0001c0001t0002g0072 a0001c0001t0008g0149 a0001c0001t0008g0152 others(3): Show |
6 | HG01884.hp1 HG02559.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.300-3657_300-3656d others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912371 | |||||||
| chr2:8912373 | G | A | 13 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0145 others(10): Show |
13 | HG00609.hp2 HG02080.hp2 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.300-3657C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912373 | |||||||
| chr2:8912373 | G | GAA | 12 | a0001c0001t0001g0043 a0001c0001t0001g0087 a0001c0001t0001g0096 others(9): Show |
12 | HG00140.hp2 HG00639.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.300-3658_300-3657i others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912373 | |||||||
| chr2:8912373 | G | GAAAGAAA others(7): Show |
1 | a0001c0001t0006g0122 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.300-3658_300-3657i others(16): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912373 | |||||||
| chr2:8912373 | G | GAAAGAAA others(63): Show |
1 | a0001c0001t0004g0058 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.300-3658_300-3657i others(72): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912373 | |||||||
| chr2:8912373 | G | GAAAGAAA others(59): Show |
1 | a0001c0001t0004g0060 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.300-3658_300-3657i others(68): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912373 | |||||||
| chr2:8912373 | G | GAAAGAAA others(71): Show |
1 | a0001c0001t0004g0059 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.300-3658_300-3657i others(80): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912373 | |||||||
| chr2:8912373 | G | GAAAGAAA others(39): Show |
1 | a0001c0001t0011g0063 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.300-3658_300-3657i others(48): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912373 | |||||||
| chr2:8912373 | G | GAAAGAAA others(51): Show |
2 | a0001c0001t0004g0056 a0001c0001t0004g0057 |
2 | HG02055.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.300-3658_300-3657i others(60): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912373 | |||||||
| chr2:8912373 | G | GAAAGAAA others(43): Show |
1 | a0001c0001t0012g0053 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.300-3658_300-3657i others(52): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912373 | |||||||
| chr2:8912373 | G | GAAAGAAA others(39): Show |
1 | a0001c0001t0012g0052 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.300-3658_300-3657i others(48): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912373 | |||||||
| chr2:8912373 | G | GAAAGAAA others(39): Show |
1 | a0001c0001t0004g0055 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.300-3658_300-3657i others(48): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912373 | |||||||
| chr2:8912373 | G | GAAAGAAG others(38): Show |
1 | a0001c0001t0012g0054 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.300-3658_300-3657i others(47): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912373 | |||||||
| chr2:8912373 | G | GAGAA | 14 | a0001c0001t0001g0082 a0001c0001t0001g0097 a0001c0001t0001g0116 others(11): Show |
14 | HG01884.hp2 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.300-3661_300-3658d others(6): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912373 | |||||||
| chr2:8912373 | G | GAGAAAGA others(1): Show |
9 | a0001c0001t0001g0070 a0001c0001t0001g0098 a0001c0001t0001g0143 others(6): Show |
9 | HG00735.hp1 HG02451.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.300-3665_300-3658d others(10): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912373 | |||||||
| chr2:8912373 | G | GAGAAAGA others(5): Show |
1 | a0001c0001t0001g0126 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.300-3669_300-3658d others(14): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912373 | |||||||
| chr2:8912373 | GAGAA | G | 5 | a0001c0001t0002g0017 a0001c0001t0003g0020 a0001c0001t0003g0022 others(2): Show |
5 | HG02280.hp2 HG02735.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.300-3661_300-3658d others(6): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912373 | |||||||
| chr2:8912373 | GAGAAAGA others(1): Show |
G | 11 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(8): Show |
11 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.300-3665_300-3658d others(10): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912373 | |||||||
| chr2:8912373 | GAGAAAGA others(5): Show |
G | 1 | a0001c0001t0009g0035 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.300-3669_300-3658d others(14): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912373 | |||||||
| chr2:8912373 | GAGAAAGA others(9): Show |
G | 1 | a0001c0001t0013g0134 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.300-3673_300-3658d others(18): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912373 | |||||||
| chr2:8912375 | G | A | 43 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0077 others(40): Show |
44 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.300-3659C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912375 | |||||||
| chr2:8912376 | A | AG | 2 | a0001c0001t0002g0073 a0001c0001t0035g0103 |
2 | HG00140.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.300-3661_300-3660i others(3): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912376 | |||||||
| chr2:8912377 | A | AAGAAAGA others(33): Show |
7 | a0001c0001t0005g0037 a0001c0001t0005g0039 a0001c0001t0005g0041 others(4): Show |
7 | HG01934.hp1 HG02559.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.300-3662_300-3661i others(42): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912377 | |||||||
| chr2:8912377 | A | G | 41 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0077 others(38): Show |
42 | HG00558.hp1 HG00558.hp2 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.300-3661T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912377 | |||||||
| chr2:8912379 | G | A | 6 | a0001c0001t0004g0047 a0001c0001t0009g0007 a0001c0001t0036g0112 others(3): Show |
6 | HG00639.hp2 HG02257.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.300-3663C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912379 | |||||||
| chr2:8912379 | GAA | G | 3 | a0001c0001t0002g0072 a0001c0001t0008g0149 a0001c0001t0008g0152 |
3 | HG02559.hp2 HG03139.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.300-3665_300-3664d others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912379 | |||||||
| chr2:8912380 | A | AAAGAAAG others(6): Show |
1 | a0001c0001t0038g0129 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.300-3665_300-3664i others(15): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912380 | |||||||
| chr2:8912381 | A | AAG | 2 | a0001c0001t0004g0050 a0001c0001t0008g0150 |
2 | HG01070.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.300-3667_300-3666d others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912381 | |||||||
| chr2:8912381 | A | AAGAAAGA others(7): Show |
1 | a0001c0001t0005g0042 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.300-3679_300-3666d others(16): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912381 | |||||||
| chr2:8912381 | A | G | 6 | a0001c0001t0004g0047 a0001c0001t0009g0007 a0001c0001t0036g0112 others(3): Show |
6 | HG00639.hp2 HG02257.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.300-3665T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912381 | |||||||
| chr2:8912383 | GAA | G | 5 | a0001c0001t0003g0018 a0001c0001t0016g0009 a0001c0001t0016g0010 others(2): Show |
5 | HG01175.hp1 HG01884.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.300-3669_300-3668d others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912383 | |||||||
| chr2:8912413 | A | C | 2 | a0001c0001t0039g0004 a0004c0005t0028g0013 |
2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.300-3697T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912413 | |||||||
| chr2:8912416 | A | G | 21 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(18): Show |
21 | HG00642.hp1 HG01070.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.300-3700T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912416 | |||||||
| chr2:8912417 | C | A | 12 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(9): Show |
12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.300-3701G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912417 | |||||||
| chr2:8912420 | G | A | 9 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(6): Show |
9 | HG01891.hp1 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.300-3704C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912420 | |||||||
| chr2:8912421 | C | A | 9 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(6): Show |
9 | HG01891.hp1 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.300-3705G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912421 | |||||||
| chr2:8912422 | C | A | 12 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(9): Show |
12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.300-3706G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912422 | |||||||
| chr2:8912559 | C | T | 1 | a0002c0002t0040g0158 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.300-3843G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912559 | |||||||
| chr2:8912650 | C | T | 1 | a0001c0001t0023g0157 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.300-3934G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912650 | |||||||
| chr2:8912651 | G | A | 8 | a0001c0001t0009g0007 a0001c0001t0009g0034 a0001c0001t0009g0035 others(5): Show |
8 | HG00639.hp2 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.300-3935C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912651 | |||||||
| chr2:8912672 | C | T | 8 | a0001c0001t0005g0037 a0001c0001t0005g0039 a0001c0001t0005g0040 others(5): Show |
8 | HG01934.hp1 HG02559.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.300-3956G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912672 | |||||||
| chr2:8912676 | G | A | 12 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(9): Show |
12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.300-3960C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912676 | |||||||
| chr2:8912874 | C | T | 12 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(9): Show |
12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.300-4158G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912874 | |||||||
| chr2:8912975 | G | A | 2 | a0002c0002t0017g0011 a0002c0002t0017g0012 |
2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.300-4259C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8912975 | |||||||
| chr2:8913101 | C | T | 1 | a0001c0001t0003g0020 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.300-4385G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8913101 | |||||||
| chr2:8913169 | T | G | 3 | a0001c0001t0012g0052 a0001c0001t0012g0053 a0001c0001t0012g0054 |
3 | HG00738.hp2 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.300-4453A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8913169 | |||||||
| chr2:8913403 | A | G | 7 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(4): Show |
7 | HG01070.hp1 HG01071.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.300-4687T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8913403 | |||||||
| chr2:8913475 | A | C | 2 | a0001c0001t0001g0089 a0001c0001t0001g0143 |
2 | HG00735.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.300-4759T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8913475 | |||||||
| chr2:8913526 | T | C | 3 | a0002c0002t0017g0011 a0002c0002t0017g0012 a0002c0002t0027g0036 |
3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.300-4810A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8913526 | |||||||
| chr2:8913585 | C | A | 7 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(4): Show |
7 | HG01070.hp1 HG01071.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.300-4869G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8913585 | |||||||
| chr2:8913675 | A | C | 14 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(11): Show |
14 | HG00642.hp1 HG01070.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.300-4959T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8913675 | |||||||
| chr2:8913835 | G | GA | 20 | a0001c0001t0001g0043 a0001c0001t0001g0082 a0001c0001t0001g0097 others(17): Show |
20 | HG00639.hp1 HG00642.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.300-5120dupT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8913835 | |||||||
| chr2:8914096 | C | T | 2 | a0001c0001t0001g0089 a0001c0001t0001g0143 |
2 | HG00735.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.300-5380G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8914096 | |||||||
| chr2:8914169 | G | C | 24 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0002g0030 others(21): Show |
25 | HG00621.hp2 HG01175.hp1 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.300-5453C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8914169 | |||||||
| chr2:8914415 | C | T | 1 | a0001c0001t0034g0127 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.300-5699G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8914415 | |||||||
| chr2:8914489 | GA | G | 21 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(18): Show |
21 | HG00642.hp1 HG00738.hp2 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.300-5774delT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8914489 | |||||||
| chr2:8914934 | C | CT | 43 | a0001c0001t0001g0070 a0001c0001t0001g0087 a0001c0001t0001g0096 others(40): Show |
43 | HG00140.hp1 HG00140.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.300-6219dupA | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8914934 | |||||||
| chr2:8914934 | C | CTT | 10 | a0001c0001t0001g0126 a0001c0001t0004g0056 a0001c0001t0004g0057 others(7): Show |
10 | HG00735.hp2 HG01884.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.300-6220_300-6219d others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8914934 | |||||||
| chr2:8914934 | CT | C | 32 | a0001c0001t0002g0017 a0001c0001t0002g0030 a0001c0001t0002g0093 others(29): Show |
33 | HG00621.hp2 HG00642.hp1 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.300-6219delA | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8914934 | |||||||
| chr2:8914939 | T | C | 2 | a0001c0001t0008g0149 a0001c0001t0008g0150 |
2 | HG01070.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.300-6223A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8914939 | |||||||
| chr2:8914999 | C | T | 44 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0002g0030 others(41): Show |
45 | HG00621.hp2 HG00639.hp2 HG01175.hp1 others(42): Show |
intron_variant | MODIFIER | c.300-6283G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8914999 | |||||||
| chr2:8915007 | C | T | 1 | a0002c0002t0040g0158 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.300-6291G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8915007 | |||||||
| chr2:8915228 | C | T | 1 | a0001c0001t0004g0060 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.300-6512G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8915228 | |||||||
| chr2:8915289 | T | C | 14 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(11): Show |
14 | HG00642.hp1 HG01070.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.300-6573A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8915289 | |||||||
| chr2:8915370 | A | T | 1 | a0001c0001t0002g0015 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.300-6654T>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8915370 | |||||||
| chr2:8915622 | G | A | 1 | a0001c0001t0002g0131 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.300-6906C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8915622 | |||||||
| chr2:8916025 | T | C | 1 | a0001c0001t0008g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.300-7309A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8916025 | |||||||
| chr2:8916112 | T | C | 3 | a0001c0001t0016g0009 a0001c0001t0016g0010 a0001c0001t0025g0008 |
3 | HG01884.hp1 HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.300-7396A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8916112 | |||||||
| chr2:8916117 | T | G | 2 | a0001c0001t0008g0151 a0001c0001t0008g0152 |
2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.300-7401A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8916117 | |||||||
| chr2:8916401 | T | C | 2 | a0001c0001t0001g0070 a0001c0001t0001g0124 |
2 | HG00609.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.300-7685A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8916401 | |||||||
| chr2:8916639 | G | C | 2 | a0002c0002t0024g0159 a0002c0002t0024g0160 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.300-7923C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8916639 | |||||||
| chr2:8916664 | T | C | 14 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(11): Show |
14 | HG00642.hp1 HG01070.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.300-7948A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8916664 | |||||||
| chr2:8916679 | T | C | 14 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(11): Show |
14 | HG00642.hp1 HG01070.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.300-7963A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8916679 | |||||||
| chr2:8916944 | G | C | 1 | a0001c0001t0002g0119 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.300-8228C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8916944 | |||||||
| chr2:8917999 | A | G | 3 | a0001c0001t0012g0052 a0001c0001t0012g0053 a0001c0001t0012g0054 |
3 | HG00738.hp2 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.300-9283T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8917999 | |||||||
| chr2:8918169 | A | C | 9 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(6): Show |
9 | HG01891.hp1 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.300-9453T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8918169 | |||||||
| chr2:8918400 | T | C | 1 | a0001c0001t0003g0019 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.300-9684A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8918400 | |||||||
| chr2:8918570 | G | A | 2 | a0001c0001t0004g0066 a0001c0001t0004g0067 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.300-9854C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8918570 | |||||||
| chr2:8918585 | C | A | 1 | a0001c0001t0001g0089 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.300-9869G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8918585 | |||||||
| chr2:8918741 | C | T | 12 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(9): Show |
12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.300-10025G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8918741 | |||||||
| chr2:8919002 | A | G | 1 | a0001c0001t0008g0108 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.300-10286T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8919002 | |||||||
| chr2:8919103 | C | T | 12 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(9): Show |
12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.300-10387G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8919103 | |||||||
| chr2:8919643 | C | A | 1 | a0001c0001t0002g0080 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.300-10927G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8919643 | |||||||
| chr2:8919756 | C | T | 33 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(30): Show |
33 | HG00642.hp1 HG00738.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.300-11040G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8919756 | |||||||
| chr2:8920035 | G | A | 9 | a0001c0001t0005g0037 a0001c0001t0005g0039 a0001c0001t0005g0040 others(6): Show |
9 | HG01175.hp2 HG01934.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.300-11319C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8920035 | |||||||
| chr2:8920060 | T | C | 33 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(30): Show |
33 | HG00642.hp1 HG00738.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.300-11344A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8920060 | |||||||
| chr2:8920089 | A | C | 33 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(30): Show |
33 | HG00642.hp1 HG00738.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.300-11373T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8920089 | |||||||
| chr2:8920186 | T | C | 1 | a0001c0001t0038g0129 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.300-11470A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8920186 | |||||||
| chr2:8920481 | A | T | 33 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(30): Show |
33 | HG00642.hp1 HG00738.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.300-11765T>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8920481 | |||||||
| chr2:8920560 | C | CA | 41 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(38): Show |
41 | HG00639.hp2 HG00642.hp1 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.300-11845dupT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8920560 | |||||||
| chr2:8920686 | ATCT | A | 9 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(6): Show |
9 | HG01891.hp1 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.300-11973_300-1197 others(7): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8920686 | |||||||
| chr2:8921179 | T | TA | 3 | a0002c0002t0017g0011 a0002c0002t0017g0012 a0002c0002t0027g0036 |
3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.300-12464dupT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8921179 | |||||||
| chr2:8921196 | G | C | 3 | a0003c0003t0010g0153 a0003c0003t0010g0154 a0003c0003t0010g0155 |
3 | HG00642.hp1 HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.300-12480C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8921196 | |||||||
| chr2:8921489 | A | G | 1 | a0001c0001t0029g0113 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.300-12773T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8921489 | |||||||
| chr2:8921888 | T | C | 7 | a0002c0002t0015g0064 a0002c0002t0017g0011 a0002c0002t0017g0012 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.300-13172A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8921888 | |||||||
| chr2:8922257 | T | C | 12 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(9): Show |
12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.300-13541A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8922257 | |||||||
| chr2:8922330 | T | C | 1 | a0001c0001t0029g0113 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.300-13614A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8922330 | |||||||
| chr2:8922497 | T | G | 1 | a0001c0001t0002g0101 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.300-13781A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8922497 | |||||||
| chr2:8922505 | T | C | 12 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(9): Show |
12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.300-13789A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8922505 | |||||||
| chr2:8922548 | T | A | 1 | a0001c0001t0002g0030 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.300-13832A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8922548 | |||||||
| chr2:8922549 | C | T | 1 | a0001c0001t0021g0125 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.300-13833G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8922549 | |||||||
| chr2:8922668 | G | C | 8 | a0001c0001t0009g0007 a0001c0001t0009g0034 a0001c0001t0009g0035 others(5): Show |
8 | HG00639.hp2 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.300-13952C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8922668 | |||||||
| chr2:8922785 | T | A | 2 | a0001c0001t0008g0151 a0001c0001t0008g0152 |
2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.300-14069A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8922785 | |||||||
| chr2:8922812 | C | T | 1 | a0001c0001t0029g0113 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.300-14096G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8922812 | |||||||
| chr2:8923001 | G | A | 1 | a0002c0002t0015g0064 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.300-14285C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8923001 | |||||||
| chr2:8923046 | G | T | 1 | a0001c0001t0002g0119 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.300-14330C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8923046 | |||||||
| chr2:8923105 | A | C | 7 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(4): Show |
7 | HG01070.hp1 HG01071.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.300-14389T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8923105 | |||||||
| chr2:8923194 | C | A | 1 | a0001c0001t0032g0094 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.300-14478G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8923194 | |||||||
| chr2:8923367 | T | C | 12 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(9): Show |
12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.300-14651A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8923367 | |||||||
| chr2:8923391 | G | A | 1 | a0001c0001t0002g0030 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.300-14675C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8923391 | |||||||
| chr2:8923499 | G | T | 1 | a0001c0001t0001g0096 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.300-14783C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8923499 | |||||||
| chr2:8923590 | C | G | 1 | a0001c0001t0001g0096 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.300-14874G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8923590 | |||||||
| chr2:8923634 | G | A | 2 | a0001c0001t0001g0097 a0001c0001t0001g0116 |
2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.300-14918C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8923634 | |||||||
| chr2:8923798 | T | C | 9 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(6): Show |
9 | HG01891.hp1 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.300-15082A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8923798 | |||||||
| chr2:8923981 | T | C | 1 | a0001c0001t0002g0069 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.300-15265A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8923981 | |||||||
| chr2:8924030 | G | A | 3 | a0002c0002t0017g0011 a0002c0002t0017g0012 a0002c0002t0027g0036 |
3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.300-15314C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8924030 | |||||||
| chr2:8924061 | A | G | 34 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(31): Show |
34 | HG00642.hp1 HG00738.hp2 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.300-15345T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8924061 | |||||||
| chr2:8924109 | CT | C | 7 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(4): Show |
7 | HG01070.hp1 HG01071.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.300-15394delA | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8924109 | |||||||
| chr2:8924159 | C | A | 1 | a0001c0001t0001g0128 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.300-15443G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8924159 | |||||||
| chr2:8924514 | T | A | 1 | a0001c0001t0001g0124 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.300-15798A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8924514 | |||||||
| chr2:8924515 | C | T | 7 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(4): Show |
7 | HG01070.hp1 HG01071.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.300-15799G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8924515 | |||||||
| chr2:8924591 | T | C | 7 | a0002c0002t0015g0064 a0002c0002t0017g0011 a0002c0002t0017g0012 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.300-15875A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8924591 | |||||||
| chr2:8924706 | CT | C | 42 | a0001c0001t0001g0075 a0001c0001t0004g0047 a0001c0001t0004g0050 others(39): Show |
42 | HG00639.hp2 HG00642.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.300-15991delA | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8924706 | |||||||
| chr2:8924748 | A | C | 34 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(31): Show |
34 | HG00642.hp1 HG00738.hp2 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.300-16032T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8924748 | |||||||
| chr2:8924753 | C | T | 2 | a0001c0001t0023g0156 a0001c0001t0023g0157 |
2 | HG01071.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.300-16037G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8924753 | |||||||
| chr2:8924922 | C | G | 1 | a0001c0001t0002g0101 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.300-16206G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8924922 | |||||||
| chr2:8925509 | G | C | 2 | a0001c0001t0001g0126 a0001c0001t0001g0128 |
2 | HG00735.hp2 HG02027.hp2 |
intron_variant | MODIFIER | c.300-16793C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8925509 | |||||||
| chr2:8925726 | T | C | 8 | a0001c0001t0009g0007 a0001c0001t0009g0034 a0001c0001t0009g0035 others(5): Show |
8 | HG00639.hp2 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.300-17010A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8925726 | |||||||
| chr2:8925765 | C | T | 1 | a0001c0001t0035g0103 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.300-17049G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8925765 | |||||||
| chr2:8926107 | CTTTG | C | 2 | a0001c0001t0019g0033 a0002c0002t0027g0036 |
2 | HG02976.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.299+17076_299+1707 others(8): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8926107 | |||||||
| chr2:8926227 | C | G | 7 | a0002c0002t0015g0064 a0002c0002t0017g0011 a0002c0002t0017g0012 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.299+16960G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8926227 | |||||||
| chr2:8926229 | A | G | 2 | a0001c0001t0009g0007 a0001c0004t0015g0006 |
2 | HG00639.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.299+16958T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8926229 | |||||||
| chr2:8926922 | C | T | 8 | a0001c0001t0009g0007 a0001c0001t0009g0034 a0001c0001t0009g0035 others(5): Show |
8 | HG00639.hp2 HG01884.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.299+16265G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8926922 | |||||||
| chr2:8926971 | T | C | 21 | a0001c0001t0001g0070 a0001c0001t0001g0074 a0001c0001t0001g0075 others(18): Show |
21 | HG00609.hp1 HG00735.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.299+16216A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8926971 | |||||||
| chr2:8927034 | G | A | 1 | a0001c0001t0004g0056 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.299+16153C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8927034 | |||||||
| chr2:8927161 | G | A | 1 | a0001c0001t0005g0042 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.299+16026C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8927161 | |||||||
| chr2:8927307 | G | A | 3 | a0001c0001t0012g0052 a0001c0001t0012g0053 a0001c0001t0012g0054 |
3 | HG00738.hp2 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.299+15880C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8927307 | |||||||
| chr2:8927524 | T | C | 1 | a0002c0002t0015g0064 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.299+15663A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8927524 | |||||||
| chr2:8927579 | C | T | 1 | a0001c0001t0005g0042 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.299+15608G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8927579 | |||||||
| chr2:8927637 | G | A | 6 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(3): Show |
6 | HG01109.hp1 HG01891.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.299+15550C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8927637 | |||||||
| chr2:8927904 | T | C | 1 | a0001c0001t0006g0016 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.299+15283A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8927904 | |||||||
| chr2:8928462 | A | G | 1 | a0001c0001t0004g0047 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.299+14725T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8928462 | |||||||
| chr2:8928564 | A | G | 3 | a0003c0003t0010g0153 a0003c0003t0010g0154 a0003c0003t0010g0155 |
3 | HG00642.hp1 HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.299+14623T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8928564 | |||||||
| chr2:8928587 | C | T | 2 | a0001c0001t0020g0048 a0001c0001t0020g0049 |
2 | HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.299+14600G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8928587 | |||||||
| chr2:8929131 | C | A | 14 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(11): Show |
14 | HG00642.hp1 HG01070.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.299+14056G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8929131 | |||||||
| chr2:8929245 | T | C | 1 | a0004c0005t0028g0013 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.299+13942A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8929245 | |||||||
| chr2:8929279 | G | A | 1 | a0001c0001t0039g0004 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.299+13908C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8929279 | |||||||
| chr2:8929281 | G | T | 14 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(11): Show |
14 | HG00642.hp1 HG01070.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.299+13906C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8929281 | |||||||
| chr2:8929330 | G | GTTCA | 6 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0002g0079 others(3): Show |
6 | HG00642.hp2 HG01169.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.299+13853_299+1385 others(8): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8929330 | |||||||
| chr2:8929330 | GTTCA | G | 29 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0096 others(26): Show |
29 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.299+13853_299+1385 others(8): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8929330 | |||||||
| chr2:8929330 | GTTCATTC others(1): Show |
G | 8 | a0001c0001t0026g0005 a0002c0002t0015g0064 a0002c0002t0017g0011 others(5): Show |
8 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.299+13849_299+1385 others(12): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8929330 | |||||||
| chr2:8929358 | A | ATTCG | 3 | a0001c0001t0012g0052 a0001c0001t0012g0053 a0001c0001t0012g0054 |
3 | HG00738.hp2 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.299+13828_299+1382 others(8): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8929358 | |||||||
| chr2:8929358 | A | G | 9 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(6): Show |
9 | HG01891.hp1 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.299+13829T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8929358 | |||||||
| chr2:8929436 | C | T | 1 | a0001c0001t0003g0028 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.299+13751G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8929436 | |||||||
| chr2:8929478 | A | G | 1 | a0001c0001t0002g0107 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.299+13709T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8929478 | |||||||
| chr2:8929502 | C | T | 1 | a0003c0003t0010g0153 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.299+13685G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8929502 | |||||||
| chr2:8929580 | T | C | 1 | a0001c0001t0002g0114 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.299+13607A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8929580 | |||||||
| chr2:8929581 | G | C | 9 | a0001c0001t0005g0037 a0001c0001t0005g0039 a0001c0001t0005g0040 others(6): Show |
9 | HG01175.hp2 HG01934.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.299+13606C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8929581 | |||||||
| chr2:8929739 | T | C | 42 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(39): Show |
42 | HG00639.hp2 HG00642.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.299+13448A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8929739 | |||||||
| chr2:8929942 | A | G | 1 | a0001c0001t0004g0051 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.299+13245T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8929942 | |||||||
| chr2:8930414 | C | CT | 33 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(30): Show |
33 | HG00642.hp1 HG00738.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.299+12772dupA | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8930414 | |||||||
| chr2:8930853 | T | C | 7 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(4): Show |
7 | HG01070.hp1 HG01071.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.299+12334A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8930853 | |||||||
| chr2:8930859 | T | C | 3 | a0003c0003t0010g0153 a0003c0003t0010g0154 a0003c0003t0010g0155 |
3 | HG00642.hp1 HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.299+12328A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8930859 | |||||||
| chr2:8930970 | G | A | 1 | a0001c0001t0002g0107 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.299+12217C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8930970 | |||||||
| chr2:8931085 | C | A | 1 | a0001c0001t0001g0120 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.299+12102G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8931085 | |||||||
| chr2:8931102 | C | T | 9 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(6): Show |
9 | HG01891.hp1 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.299+12085G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8931102 | |||||||
| chr2:8931113 | C | G | 1 | a0001c0001t0002g0102 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.299+12074G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8931113 | |||||||
| chr2:8931132 | A | G | 1 | a0001c0001t0021g0078 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.299+12055T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8931132 | |||||||
| chr2:8931298 | A | C | 78 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0002g0030 others(75): Show |
79 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.299+11889T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8931298 | |||||||
| chr2:8932128 | T | TA | 9 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(6): Show |
9 | HG01109.hp1 HG01934.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.299+11058dupT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8932128 | |||||||
| chr2:8932551 | C | A | 3 | a0002c0002t0024g0159 a0002c0002t0024g0160 a0002c0002t0040g0158 |
3 | HG01167.hp2 HG01169.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.299+10636G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8932551 | |||||||
| chr2:8932666 | G | T | 4 | a0001c0001t0008g0149 a0001c0001t0008g0150 a0001c0001t0008g0151 others(1): Show |
4 | HG01070.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.299+10521C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8932666 | |||||||
| chr2:8932885 | A | G | 2 | a0001c0001t0003g0021 a0001c0001t0003g0022 |
2 | HG03225.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.299+10302T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8932885 | |||||||
| chr2:8933089 | AT | A | 19 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(16): Show |
19 | HG00738.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.299+10097delA | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8933089 | |||||||
| chr2:8933116 | T | C | 5 | a0001c0001t0005g0037 a0001c0001t0005g0039 a0001c0001t0005g0040 others(2): Show |
5 | HG01934.hp1 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.299+10071A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8933116 | |||||||
| chr2:8933373 | G | C | 2 | a0001c0001t0011g0061 a0001c0001t0011g0063 |
2 | HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.299+9814C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8933373 | |||||||
| chr2:8933609 | T | G | 1 | a0002c0002t0015g0064 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.299+9578A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8933609 | |||||||
| chr2:8933645 | T | C | 2 | a0001c0001t0001g0082 a0001c0001t0001g0099 |
2 | HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.299+9542A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8933645 | |||||||
| chr2:8933866 | C | T | 1 | a0001c0001t0011g0062 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.299+9321G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8933866 | |||||||
| chr2:8933950 | A | C | 2 | a0001c0001t0001g0141 a0001c0001t0001g0142 |
2 | HG01891.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.299+9237T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8933950 | |||||||
| chr2:8934095 | C | T | 1 | a0002c0002t0015g0064 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.299+9092G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8934095 | |||||||
| chr2:8934218 | A | G | 4 | a0002c0002t0015g0064 a0002c0002t0024g0159 a0002c0002t0024g0160 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.299+8969T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8934218 | |||||||
| chr2:8934464 | A | G | 3 | a0002c0002t0017g0011 a0002c0002t0017g0012 a0002c0002t0027g0036 |
3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.299+8723T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8934464 | |||||||
| chr2:8934975 | T | A | 4 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(1): Show |
4 | HG03041.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.299+8212A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8934975 | |||||||
| chr2:8934989 | G | A | 1 | a0001c0001t0023g0157 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.299+8198C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8934989 | |||||||
| chr2:8935183 | G | A | 2 | a0001c0001t0001g0089 a0001c0001t0001g0143 |
2 | HG00735.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.299+8004C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8935183 | |||||||
| chr2:8935297 | TAA | T | 7 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(4): Show |
7 | HG01070.hp1 HG01071.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.299+7888_299+7889d others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8935297 | |||||||
| chr2:8935906 | TATC | T | 2 | a0001c0001t0004g0066 a0001c0001t0004g0067 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.299+7278_299+7280d others(5): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8935906 | |||||||
| chr2:8936289 | C | A | 1 | a0001c0001t0001g0087 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.299+6898G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8936289 | |||||||
| chr2:8936471 | C | T | 19 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(16): Show |
19 | HG00738.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.299+6716G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8936471 | |||||||
| chr2:8936602 | T | C | 4 | a0002c0002t0015g0064 a0002c0002t0024g0159 a0002c0002t0024g0160 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.299+6585A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8936602 | |||||||
| chr2:8936664 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.299+6523G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8936664 | |||||||
| chr2:8936711 | C | T | 2 | a0001c0001t0016g0009 a0001c0001t0016g0010 |
2 | HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.299+6476G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8936711 | |||||||
| chr2:8936735 | C | G | 1 | a0001c0001t0029g0113 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.299+6452G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8936735 | |||||||
| chr2:8936786 | C | CA | 11 | a0001c0001t0001g0096 a0001c0001t0002g0069 a0001c0001t0014g0014 others(8): Show |
11 | HG02027.hp1 HG02135.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.299+6400dupT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8936786 | |||||||
| chr2:8936801 | A | AG | 12 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(9): Show |
12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.299+6385_299+6386i others(3): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8936801 | |||||||
| chr2:8936822 | GAAAA | G | 7 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(4): Show |
7 | HG01070.hp1 HG01071.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.299+6361_299+6364d others(6): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8936822 | |||||||
| chr2:8936828 | A | AAAAG | 4 | a0002c0002t0015g0064 a0002c0002t0024g0159 a0002c0002t0024g0160 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.299+6355_299+6358d others(6): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8936828 | |||||||
| chr2:8936828 | AAAAG | A | 12 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(9): Show |
12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.299+6355_299+6358d others(6): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8936828 | |||||||
| chr2:8937104 | G | A | 7 | a0001c0001t0008g0149 a0001c0001t0008g0150 a0001c0001t0008g0151 others(4): Show |
7 | HG00642.hp1 HG01070.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.299+6083C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8937104 | |||||||
| chr2:8937815 | C | T | 12 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(9): Show |
12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.299+5372G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8937815 | |||||||
| chr2:8937922 | G | A | 1 | a0002c0002t0027g0036 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.299+5265C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8937922 | |||||||
| chr2:8937934 | G | A | 1 | a0003c0003t0010g0154 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.299+5253C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8937934 | |||||||
| chr2:8938015 | T | C | 7 | a0001c0001t0009g0007 a0001c0001t0016g0009 a0001c0001t0016g0010 others(4): Show |
7 | HG00639.hp2 HG01884.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.299+5172A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8938015 | |||||||
| chr2:8938080 | G | A | 3 | a0002c0002t0017g0011 a0002c0002t0017g0012 a0002c0002t0027g0036 |
3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.299+5107C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8938080 | |||||||
| chr2:8938548 | G | A | 7 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(4): Show |
7 | HG01070.hp1 HG01071.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.299+4639C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8938548 | |||||||
| chr2:8938673 | G | A | 2 | a0002c0002t0017g0011 a0002c0002t0017g0012 |
2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.299+4514C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8938673 | |||||||
| chr2:8938927 | C | T | 3 | a0002c0002t0017g0011 a0002c0002t0017g0012 a0002c0002t0027g0036 |
3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.299+4260G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8938927 | |||||||
| chr2:8939174 | T | A | 7 | a0001c0001t0008g0149 a0001c0001t0008g0150 a0001c0001t0008g0151 others(4): Show |
7 | HG00642.hp1 HG01070.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.299+4013A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8939174 | |||||||
| chr2:8939194 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.299+3993A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8939194 | |||||||
| chr2:8939396 | T | C | 7 | a0002c0002t0015g0064 a0002c0002t0017g0011 a0002c0002t0017g0012 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.299+3791A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8939396 | |||||||
| chr2:8939447 | G | C | 2 | a0001c0001t0009g0034 a0001c0001t0009g0035 |
2 | HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.299+3740C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8939447 | |||||||
| chr2:8939548 | G | A | 65 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0002g0030 others(62): Show |
66 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.299+3639C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8939548 | |||||||
| chr2:8939682 | G | A | 1 | a0001c0001t0002g0132 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.299+3505C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8939682 | |||||||
| chr2:8939773 | C | T | 2 | a0001c0001t0001g0097 a0001c0001t0001g0116 |
2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.299+3414G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8939773 | |||||||
| chr2:8939781 | A | G | 3 | a0002c0002t0017g0011 a0002c0002t0017g0012 a0002c0002t0027g0036 |
3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.299+3406T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8939781 | |||||||
| chr2:8940078 | G | A | 1 | a0001c0001t0002g0144 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.299+3109C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8940078 | |||||||
| chr2:8940078 | G | GCTTA | 19 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(16): Show |
19 | HG00738.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.299+3105_299+3108d others(6): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8940078 | |||||||
| chr2:8940138 | C | T | 1 | a0001c0001t0030g0095 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.299+3049G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8940138 | |||||||
| chr2:8940229 | T | C | 1 | a0004c0005t0028g0013 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.299+2958A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8940229 | |||||||
| chr2:8940683 | CAT | C | 25 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0002g0030 others(22): Show |
26 | HG00621.hp2 HG00639.hp2 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.299+2502_299+2503d others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8940683 | |||||||
| chr2:8940761 | C | T | 8 | a0001c0001t0001g0146 a0002c0002t0015g0064 a0002c0002t0017g0011 others(5): Show |
8 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.299+2426G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8940761 | |||||||
| chr2:8940898 | CGT | C | 2 | a0001c0001t0005g0040 a0001c0001t0031g0038 |
2 | HG02572.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.299+2287_299+2288d others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8940898 | |||||||
| chr2:8940899 | G | A | 4 | a0002c0002t0015g0064 a0002c0002t0024g0159 a0002c0002t0024g0160 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.299+2288C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8940899 | |||||||
| chr2:8941119 | T | C | 2 | a0001c0001t0003g0027 a0001c0001t0003g0029 |
2 | HG02738.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.299+2068A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8941119 | |||||||
| chr2:8941242 | C | T | 1 | a0001c0001t0031g0038 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.299+1945G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8941242 | |||||||
| chr2:8941416 | T | C | 1 | a0001c0001t0014g0031 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.299+1771A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8941416 | |||||||
| chr2:8941493 | G | C | 3 | a0002c0002t0017g0011 a0002c0002t0017g0012 a0002c0002t0027g0036 |
3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.299+1694C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8941493 | |||||||
| chr2:8941638 | A | G | 4 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0002g0132 others(1): Show |
4 | HG00621.hp2 HG02135.hp1 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.299+1549T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8941638 | |||||||
| chr2:8941654 | GA | G | 6 | a0001c0001t0001g0043 a0001c0001t0005g0042 a0002c0002t0015g0064 others(3): Show |
6 | HG00639.hp1 HG01167.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.299+1532delT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8941654 | |||||||
| chr2:8942005 | A | G | 2 | a0001c0001t0001g0043 a0001c0001t0005g0042 |
2 | HG00639.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.299+1182T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8942005 | |||||||
| chr2:8942009 | G | A | 3 | a0002c0002t0017g0011 a0002c0002t0017g0012 a0002c0002t0027g0036 |
3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.299+1178C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8942009 | |||||||
| chr2:8942038 | T | C | 3 | a0002c0002t0017g0011 a0002c0002t0017g0012 a0002c0002t0027g0036 |
3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.299+1149A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8942038 | |||||||
| chr2:8942201 | C | T | 1 | a0002c0002t0027g0036 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.299+986G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8942201 | |||||||
| chr2:8942202 | G | A | 2 | a0001c0001t0008g0151 a0001c0001t0008g0152 |
2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.299+985C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8942202 | |||||||
| chr2:8942285 | T | C | 2 | a0001c0001t0002g0131 a0001c0001t0021g0078 |
2 | HG01258.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.299+902A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8942285 | |||||||
| chr2:8942532 | T | C | 3 | a0001c0001t0012g0052 a0001c0001t0012g0053 a0001c0001t0012g0054 |
3 | HG00738.hp2 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.299+655A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8942532 | |||||||
| chr2:8942544 | A | C | 3 | a0003c0003t0010g0153 a0003c0003t0010g0154 a0003c0003t0010g0155 |
3 | HG00642.hp1 HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.299+643T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8942544 | |||||||
| chr2:8942563 | T | G | 3 | a0003c0003t0010g0153 a0003c0003t0010g0154 a0003c0003t0010g0155 |
3 | HG00642.hp1 HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.299+624A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8942563 | |||||||
| chr2:8942636 | G | C | 3 | a0002c0002t0017g0011 a0002c0002t0017g0012 a0002c0002t0027g0036 |
3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.299+551C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8942636 | |||||||
| chr2:8942693 | C | T | 140 | a0001c0001t0001g0043 a0001c0001t0001g0070 a0001c0001t0001g0074 others(137): Show |
141 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.299+494G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8942693 | |||||||
| chr2:8942987 | C | CA | 4 | a0002c0002t0015g0064 a0002c0002t0024g0159 a0002c0002t0024g0160 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.299+199dupT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8942987 | |||||||
| chr2:8943121 | T | C | 7 | a0001c0001t0008g0149 a0001c0001t0008g0150 a0001c0001t0008g0151 others(4): Show |
7 | HG00642.hp1 HG01070.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.299+66A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 3/12 | chr2 | 8943121 | |||||||
| chr2:8943294 | G | A | 3 | a0003c0003t0010g0153 a0003c0003t0010g0154 a0003c0003t0010g0155 |
3 | HG00642.hp1 HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.222-30C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8943294 | |||||||
| chr2:8943329 | T | G | 1 | a0001c0001t0005g0045 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.222-65A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8943329 | |||||||
| chr2:8943417 | C | A | 3 | a0001c0001t0005g0044 a0001c0001t0005g0045 a0001c0001t0005g0046 |
3 | HG02818.hp1 HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.222-153G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8943417 | |||||||
| chr2:8943933 | A | G | 33 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(30): Show |
33 | HG00642.hp1 HG00738.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.222-669T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8943933 | |||||||
| chr2:8943971 | C | T | 4 | a0002c0002t0015g0064 a0002c0002t0024g0159 a0002c0002t0024g0160 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.222-707G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8943971 | |||||||
| chr2:8944101 | G | C | 7 | a0001c0001t0008g0149 a0001c0001t0008g0150 a0001c0001t0008g0151 others(4): Show |
7 | HG00642.hp1 HG01070.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.222-837C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8944101 | |||||||
| chr2:8944320 | A | T | 4 | a0002c0002t0015g0064 a0002c0002t0024g0159 a0002c0002t0024g0160 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.222-1056T>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8944320 | |||||||
| chr2:8944353 | G | A | 1 | a0001c0004t0015g0006 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.222-1089C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8944353 | |||||||
| chr2:8944480 | T | G | 1 | a0001c0001t0037g0111 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.222-1216A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8944480 | |||||||
| chr2:8944580 | C | T | 7 | a0001c0001t0008g0149 a0001c0001t0008g0150 a0001c0001t0008g0151 others(4): Show |
7 | HG00642.hp1 HG01070.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.222-1316G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8944580 | |||||||
| chr2:8944605 | A | C | 1 | a0001c0001t0036g0112 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.222-1341T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8944605 | |||||||
| chr2:8944648 | G | GAC | 12 | a0001c0001t0001g0043 a0001c0001t0001g0141 a0001c0001t0001g0142 others(9): Show |
12 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.222-1386_222-1385d others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8944648 | |||||||
| chr2:8944648 | G | GACAC | 32 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0002g0132 others(29): Show |
33 | HG00621.hp2 HG01070.hp2 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.222-1388_222-1385d others(6): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8944648 | |||||||
| chr2:8944648 | G | GACACACA others(1): Show |
2 | a0002c0002t0017g0011 a0002c0002t0017g0012 |
2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.222-1392_222-1385d others(10): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8944648 | |||||||
| chr2:8944648 | G | GACACACA others(11): Show |
1 | a0002c0002t0027g0036 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.222-1402_222-1385d others(20): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8944648 | |||||||
| chr2:8944648 | GAC | G | 7 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(4): Show |
7 | HG01070.hp1 HG01071.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.222-1386_222-1385d others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8944648 | |||||||
| chr2:8944648 | GACACACA others(3): Show |
G | 13 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(10): Show |
13 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.222-1394_222-1385d others(12): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8944648 | |||||||
| chr2:8944726 | G | A | 2 | a0001c0001t0001g0074 a0001c0001t0001g0075 |
2 | HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.222-1462C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8944726 | |||||||
| chr2:8944878 | G | A | 1 | a0001c0001t0002g0132 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.222-1614C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8944878 | |||||||
| chr2:8944957 | G | A | 6 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(3): Show |
6 | HG01109.hp1 HG01891.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.222-1693C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8944957 | |||||||
| chr2:8945009 | T | C | 1 | a0003c0003t0010g0155 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.222-1745A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8945009 | |||||||
| chr2:8945266 | C | T | 2 | a0001c0001t0001g0043 a0001c0001t0005g0042 |
2 | HG00639.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.222-2002G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8945266 | |||||||
| chr2:8945497 | T | A | 3 | a0001c0001t0002g0118 a0001c0001t0013g0003 a0001c0001t0013g0135 |
3 | HG00558.hp1 HG00609.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.222-2233A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8945497 | |||||||
| chr2:8945612 | G | A | 1 | a0001c0001t0037g0111 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.222-2348C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8945612 | |||||||
| chr2:8945726 | T | G | 7 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(4): Show |
7 | HG01070.hp1 HG01071.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.222-2462A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8945726 | |||||||
| chr2:8946024 | C | T | 3 | a0002c0002t0017g0011 a0002c0002t0017g0012 a0002c0002t0027g0036 |
3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.222-2760G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8946024 | |||||||
| chr2:8946112 | G | A | 3 | a0001c0001t0012g0052 a0001c0001t0012g0053 a0001c0001t0012g0054 |
3 | HG00738.hp2 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.222-2848C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8946112 | |||||||
| chr2:8946800 | G | A | 12 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(9): Show |
12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.222-3536C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8946800 | |||||||
| chr2:8947015 | T | C | 1 | a0001c0001t0002g0107 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.222-3751A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8947015 | |||||||
| chr2:8947137 | C | T | 7 | a0002c0002t0015g0064 a0002c0002t0017g0011 a0002c0002t0017g0012 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.222-3873G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8947137 | |||||||
| chr2:8947221 | C | T | 4 | a0001c0001t0008g0149 a0001c0001t0008g0150 a0001c0001t0008g0151 others(1): Show |
4 | HG01070.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.222-3957G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8947221 | |||||||
| chr2:8947252 | T | C | 2 | a0001c0001t0009g0034 a0001c0001t0009g0035 |
2 | HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.222-3988A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8947252 | |||||||
| chr2:8947308 | A | G | 3 | a0002c0002t0017g0011 a0002c0002t0017g0012 a0002c0002t0027g0036 |
3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.222-4044T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8947308 | |||||||
| chr2:8947315 | T | C | 141 | a0001c0001t0001g0043 a0001c0001t0001g0070 a0001c0001t0001g0074 others(138): Show |
142 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(139): Show |
intron_variant | MODIFIER | c.222-4051A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8947315 | |||||||
| chr2:8947454 | A | T | 1 | a0001c0001t0001g0115 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.222-4190T>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8947454 | |||||||
| chr2:8947735 | GA | G | 7 | a0002c0002t0015g0064 a0002c0002t0017g0011 a0002c0002t0017g0012 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.222-4472delT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8947735 | |||||||
| chr2:8948324 | TAAC | T | 2 | a0002c0002t0024g0159 a0002c0002t0024g0160 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.222-5063_222-5061d others(5): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8948324 | |||||||
| chr2:8948482 | G | A | 3 | a0002c0002t0017g0011 a0002c0002t0017g0012 a0002c0002t0027g0036 |
3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.222-5218C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8948482 | |||||||
| chr2:8948531 | C | T | 4 | a0002c0002t0015g0064 a0002c0002t0024g0159 a0002c0002t0024g0160 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.222-5267G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8948531 | |||||||
| chr2:8948670 | A | C | 1 | a0001c0001t0002g0118 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.222-5406T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8948670 | |||||||
| chr2:8948725 | C | A | 1 | a0001c0001t0002g0079 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.222-5461G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8948725 | |||||||
| chr2:8948875 | G | A | 1 | a0001c0001t0014g0031 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.222-5611C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8948875 | |||||||
| chr2:8948935 | G | A | 3 | a0002c0002t0017g0011 a0002c0002t0017g0012 a0002c0002t0027g0036 |
3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.222-5671C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8948935 | |||||||
| chr2:8949144 | T | A | 1 | a0001c0001t0005g0041 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.222-5880A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8949144 | |||||||
| chr2:8949942 | C | T | 2 | a0001c0001t0002g0015 a0001c0001t0006g0016 |
2 | HG02135.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.222-6678G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8949942 | |||||||
| chr2:8950055 | T | C | 1 | a0001c0001t0004g0051 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.222-6791A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8950055 | |||||||
| chr2:8950084 | C | T | 33 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(30): Show |
33 | HG00642.hp1 HG00738.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.222-6820G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8950084 | |||||||
| chr2:8950369 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.222-7105C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8950369 | |||||||
| chr2:8950488 | C | T | 3 | a0001c0001t0005g0044 a0001c0001t0005g0045 a0001c0001t0005g0046 |
3 | HG02818.hp1 HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.222-7224G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8950488 | |||||||
| chr2:8950520 | C | T | 5 | a0001c0001t0001g0120 a0001c0001t0002g0131 a0001c0001t0008g0149 others(2): Show |
5 | HG01070.hp2 HG01258.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.222-7256G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8950520 | |||||||
| chr2:8950618 | G | A | 2 | a0001c0001t0034g0127 a0002c0002t0040g0158 |
2 | HG02027.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.222-7354C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8950618 | |||||||
| chr2:8951046 | T | C | 4 | a0001c0001t0008g0149 a0001c0001t0008g0150 a0001c0001t0008g0151 others(1): Show |
4 | HG01070.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.221+7451A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8951046 | |||||||
| chr2:8951085 | C | T | 2 | a0001c0001t0008g0151 a0001c0001t0008g0152 |
2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.221+7412G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8951085 | |||||||
| chr2:8951095 | T | C | 1 | a0001c0001t0019g0033 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.221+7402A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8951095 | |||||||
| chr2:8951161 | TCTC | T | 3 | a0002c0002t0024g0159 a0002c0002t0024g0160 a0002c0002t0040g0158 |
3 | HG01167.hp2 HG01169.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.221+7333_221+7335d others(5): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8951161 | |||||||
| chr2:8951207 | CT | C | 64 | a0001c0001t0001g0043 a0001c0001t0002g0015 a0001c0001t0002g0017 others(61): Show |
65 | HG00621.hp2 HG00639.hp1 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.221+7289delA | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8951207 | |||||||
| chr2:8951355 | T | C | 1 | a0001c0001t0019g0033 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.221+7142A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8951355 | |||||||
| chr2:8951358 | C | T | 1 | a0001c0001t0038g0129 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.221+7139G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8951358 | |||||||
| chr2:8951399 | C | T | 7 | a0002c0002t0015g0064 a0002c0002t0017g0011 a0002c0002t0017g0012 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.221+7098G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8951399 | |||||||
| chr2:8951989 | T | C | 1 | a0001c0001t0012g0054 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.221+6508A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8951989 | |||||||
| chr2:8952056 | T | G | 1 | a0001c0001t0002g0072 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.221+6441A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8952056 | |||||||
| chr2:8952384 | T | G | 4 | a0002c0002t0015g0064 a0002c0002t0024g0159 a0002c0002t0024g0160 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.221+6113A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8952384 | |||||||
| chr2:8952649 | T | C | 12 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(9): Show |
12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.221+5848A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8952649 | |||||||
| chr2:8952734 | C | T | 1 | a0001c0001t0003g0020 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.221+5763G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8952734 | |||||||
| chr2:8952764 | G | A | 1 | a0002c0002t0027g0036 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.221+5733C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8952764 | |||||||
| chr2:8952837 | A | G | 3 | a0003c0003t0010g0153 a0003c0003t0010g0154 a0003c0003t0010g0155 |
3 | HG00642.hp1 HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.221+5660T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8952837 | |||||||
| chr2:8952894 | C | T | 1 | a0002c0002t0027g0036 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.221+5603G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8952894 | |||||||
| chr2:8952905 | G | A | 7 | a0002c0002t0015g0064 a0002c0002t0017g0011 a0002c0002t0017g0012 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.221+5592C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8952905 | |||||||
| chr2:8953173 | T | C | 1 | a0001c0001t0033g0123 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.221+5324A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8953173 | |||||||
| chr2:8953591 | T | C | 1 | a0001c0001t0021g0125 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.221+4906A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8953591 | |||||||
| chr2:8953623 | T | C | 1 | a0001c0001t0002g0117 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.221+4874A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8953623 | |||||||
| chr2:8954193 | T | G | 1 | a0002c0002t0027g0036 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.221+4304A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8954193 | |||||||
| chr2:8954293 | C | T | 1 | a0001c0001t0003g0026 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.221+4204G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8954293 | |||||||
| chr2:8954505 | G | A | 5 | a0001c0001t0002g0109 a0002c0002t0015g0064 a0002c0002t0024g0159 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.221+3992C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8954505 | |||||||
| chr2:8954749 | T | C | 2 | a0001c0001t0002g0068 a0001c0001t0002g0081 |
2 | HG00621.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.221+3748A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8954749 | |||||||
| chr2:8954776 | T | G | 46 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(43): Show |
46 | HG00639.hp2 HG00642.hp1 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.221+3721A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8954776 | |||||||
| chr2:8954866 | A | G | 33 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(30): Show |
33 | HG00642.hp1 HG00738.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.221+3631T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8954866 | |||||||
| chr2:8954907 | A | G | 21 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0002g0030 others(18): Show |
22 | HG00621.hp2 HG01175.hp1 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.221+3590T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8954907 | |||||||
| chr2:8954938 | T | G | 21 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0002g0030 others(18): Show |
22 | HG00621.hp2 HG01175.hp1 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.221+3559A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8954938 | |||||||
| chr2:8954985 | G | A | 1 | a0001c0001t0002g0073 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.221+3512C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8954985 | |||||||
| chr2:8954997 | G | A | 1 | a0004c0005t0028g0013 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.221+3500C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8954997 | |||||||
| chr2:8955117 | C | G | 9 | a0001c0001t0009g0007 a0001c0001t0009g0034 a0001c0001t0009g0035 others(6): Show |
9 | HG00639.hp2 HG01884.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.221+3380G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8955117 | |||||||
| chr2:8955365 | C | A | 6 | a0001c0001t0009g0007 a0001c0001t0016g0009 a0001c0001t0016g0010 others(3): Show |
6 | HG00639.hp2 HG01884.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.221+3132G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8955365 | |||||||
| chr2:8955736 | C | G | 1 | a0003c0003t0010g0155 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.221+2761G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8955736 | |||||||
| chr2:8955997 | A | T | 9 | a0001c0001t0009g0007 a0001c0001t0009g0034 a0001c0001t0009g0035 others(6): Show |
9 | HG00639.hp2 HG01884.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.221+2500T>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8955997 | |||||||
| chr2:8956131 | T | C | 33 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(30): Show |
33 | HG00642.hp1 HG00738.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.221+2366A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8956131 | |||||||
| chr2:8956205 | T | C | 4 | a0001c0001t0001g0100 a0001c0001t0001g0110 a0001c0001t0001g0115 others(1): Show |
4 | HG02717.hp1 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.221+2292A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8956205 | |||||||
| chr2:8956416 | C | A | 1 | a0001c0001t0002g0069 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.221+2081G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8956416 | |||||||
| chr2:8956456 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.221+2041A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8956456 | |||||||
| chr2:8956658 | C | G | 1 | a0002c0002t0015g0064 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.221+1839G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8956658 | |||||||
| chr2:8956775 | G | A | 2 | a0001c0001t0001g0043 a0001c0001t0005g0042 |
2 | HG00639.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.221+1722C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8956775 | |||||||
| chr2:8956820 | C | T | 1 | a0001c0001t0003g0001 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.221+1677G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8956820 | |||||||
| chr2:8956915 | T | C | 140 | a0001c0001t0001g0043 a0001c0001t0001g0070 a0001c0001t0001g0074 others(137): Show |
141 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.221+1582A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8956915 | |||||||
| chr2:8957141 | G | A | 2 | a0001c0001t0001g0043 a0001c0001t0005g0042 |
2 | HG00639.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.221+1356C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8957141 | |||||||
| chr2:8957274 | A | G | 7 | a0001c0001t0008g0149 a0001c0001t0008g0150 a0001c0001t0008g0151 others(4): Show |
7 | HG00642.hp1 HG01070.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.221+1223T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8957274 | |||||||
| chr2:8957475 | T | C | 3 | a0002c0002t0017g0011 a0002c0002t0017g0012 a0002c0002t0027g0036 |
3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.221+1022A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8957475 | |||||||
| chr2:8957716 | G | A | 3 | a0002c0002t0017g0011 a0002c0002t0017g0012 a0002c0002t0027g0036 |
3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.221+781C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8957716 | |||||||
| chr2:8957752 | C | T | 4 | a0001c0001t0008g0149 a0001c0001t0008g0150 a0001c0001t0008g0151 others(1): Show |
4 | HG01070.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.221+745G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8957752 | |||||||
| chr2:8957754 | C | G | 2 | a0001c0001t0003g0021 a0001c0001t0003g0022 |
2 | HG03225.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.221+743G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8957754 | |||||||
| chr2:8957755 | G | C | 2 | a0001c0001t0003g0021 a0001c0001t0003g0022 |
2 | HG03225.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.221+742C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8957755 | |||||||
| chr2:8957778 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.221+719C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8957778 | |||||||
| chr2:8957844 | T | C | 1 | a0004c0005t0028g0013 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.221+653A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8957844 | |||||||
| chr2:8957922 | C | T | 1 | a0003c0003t0010g0155 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.221+575G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8957922 | |||||||
| chr2:8957923 | G | A | 2 | a0001c0001t0001g0126 a0001c0001t0001g0128 |
2 | HG00735.hp2 HG02027.hp2 |
intron_variant | MODIFIER | c.221+574C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8957923 | |||||||
| chr2:8958288 | A | C | 2 | a0001c0001t0001g0077 a0001c0001t0036g0112 |
2 | HG01109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.221+209T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 2/12 | chr2 | 8958288 | |||||||
| chr2:8958862 | G | A | 7 | a0001c0001t0008g0149 a0001c0001t0008g0150 a0001c0001t0008g0151 others(4): Show |
7 | HG00642.hp1 HG01070.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.76-220C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8958862 | |||||||
| chr2:8958903 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.76-261G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8958903 | |||||||
| chr2:8958917 | A | G | 7 | a0002c0002t0015g0064 a0002c0002t0017g0011 a0002c0002t0017g0012 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.76-275T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8958917 | |||||||
| chr2:8958985 | G | T | 33 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(30): Show |
33 | HG00642.hp1 HG00738.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.76-343C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8958985 | |||||||
| chr2:8959185 | T | C | 3 | a0002c0002t0017g0011 a0002c0002t0017g0012 a0002c0002t0027g0036 |
3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.76-543A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8959185 | |||||||
| chr2:8959376 | C | G | 13 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0002g0030 others(10): Show |
14 | HG00621.hp2 HG01175.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.76-734G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8959376 | |||||||
| chr2:8959464 | C | CT | 15 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0002g0030 others(12): Show |
16 | HG00621.hp2 HG00738.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.76-823dupA | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8959464 | |||||||
| chr2:8959713 | T | C | 3 | a0002c0002t0017g0011 a0002c0002t0017g0012 a0002c0002t0027g0036 |
3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.76-1071A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8959713 | |||||||
| chr2:8959727 | T | C | 1 | a0001c0001t0036g0112 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.76-1085A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8959727 | |||||||
| chr2:8959837 | A | G | 3 | a0001c0001t0002g0093 a0001c0001t0032g0094 a0001c0001t0033g0123 |
3 | NA18956.hp1 NA19010.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.76-1195T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8959837 | |||||||
| chr2:8960007 | C | T | 7 | a0002c0002t0015g0064 a0002c0002t0017g0011 a0002c0002t0017g0012 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.76-1365G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8960007 | |||||||
| chr2:8960008 | A | G | 76 | a0001c0001t0001g0043 a0001c0001t0002g0015 a0001c0001t0002g0017 others(73): Show |
77 | HG00621.hp2 HG00639.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.76-1366T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8960008 | |||||||
| chr2:8960565 | C | A | 18 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0055 others(15): Show |
18 | HG00738.hp2 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.76-1923G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8960565 | |||||||
| chr2:8960728 | C | T | 2 | a0001c0001t0001g0043 a0001c0001t0005g0042 |
2 | HG00639.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.76-2086G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8960728 | |||||||
| chr2:8961590 | GA | G | 7 | a0001c0001t0008g0149 a0001c0001t0008g0150 a0001c0001t0008g0151 others(4): Show |
7 | HG00642.hp1 HG01070.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.76-2949delT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8961590 | |||||||
| chr2:8961592 | A | C | 3 | a0003c0003t0010g0153 a0003c0003t0010g0154 a0003c0003t0010g0155 |
3 | HG00642.hp1 HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.76-2950T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8961592 | |||||||
| chr2:8961692 | G | A | 1 | a0001c0001t0011g0062 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.76-3050C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8961692 | |||||||
| chr2:8961802 | G | C | 65 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0002g0030 others(62): Show |
66 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.76-3160C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8961802 | |||||||
| chr2:8961829 | C | G | 1 | a0001c0001t0013g0003 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.76-3187G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8961829 | |||||||
| chr2:8961844 | T | G | 7 | a0001c0001t0008g0149 a0001c0001t0008g0150 a0001c0001t0008g0151 others(4): Show |
7 | HG00642.hp1 HG01070.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.76-3202A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8961844 | |||||||
| chr2:8962070 | C | A | 2 | a0002c0002t0017g0011 a0002c0002t0017g0012 |
2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.76-3428G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8962070 | |||||||
| chr2:8962566 | C | A | 19 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(16): Show |
19 | HG00738.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.76-3924G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8962566 | |||||||
| chr2:8962603 | C | T | 1 | a0002c0002t0015g0064 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.76-3961G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8962603 | |||||||
| chr2:8962724 | T | C | 1 | a0001c0001t0004g0059 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.76-4082A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8962724 | |||||||
| chr2:8962810 | C | A | 2 | a0001c0001t0009g0034 a0001c0001t0009g0035 |
2 | HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.76-4168G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8962810 | |||||||
| chr2:8962969 | G | A | 12 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(9): Show |
12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.76-4327C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8962969 | |||||||
| chr2:8963142 | G | A | 1 | a0001c0001t0021g0078 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.76-4500C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8963142 | |||||||
| chr2:8963194 | C | T | 1 | a0001c0001t0025g0008 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.76-4552G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8963194 | |||||||
| chr2:8963221 | G | A | 2 | a0002c0002t0017g0011 a0002c0002t0017g0012 |
2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.76-4579C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8963221 | |||||||
| chr2:8963287 | C | A | 3 | a0002c0002t0017g0011 a0002c0002t0017g0012 a0002c0002t0027g0036 |
3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.76-4645G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8963287 | |||||||
| chr2:8963288 | G | A | 2 | a0001c0001t0008g0151 a0001c0001t0008g0152 |
2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.76-4646C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8963288 | |||||||
| chr2:8963352 | A | G | 1 | a0003c0003t0010g0154 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.76-4710T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8963352 | |||||||
| chr2:8963353 | G | C | 3 | a0002c0002t0017g0011 a0002c0002t0017g0012 a0002c0002t0027g0036 |
3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.76-4711C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8963353 | |||||||
| chr2:8963365 | A | G | 1 | a0001c0001t0002g0131 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.76-4723T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8963365 | |||||||
| chr2:8963366 | C | T | 2 | a0002c0002t0024g0159 a0002c0002t0024g0160 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.76-4724G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8963366 | |||||||
| chr2:8963397 | G | A | 1 | a0001c0001t0004g0050 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.76-4755C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8963397 | |||||||
| chr2:8963554 | T | C | 32 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0002g0030 others(29): Show |
33 | HG00621.hp2 HG00639.hp2 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.76-4912A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8963554 | |||||||
| chr2:8963594 | C | T | 1 | a0001c0001t0038g0129 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.76-4952G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8963594 | |||||||
| chr2:8963898 | G | A | 19 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(16): Show |
19 | HG00738.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.76-5256C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8963898 | |||||||
| chr2:8964218 | G | A | 4 | a0002c0002t0015g0064 a0002c0002t0024g0159 a0002c0002t0024g0160 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.76-5576C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8964218 | |||||||
| chr2:8964306 | G | A | 1 | a0001c0001t0039g0004 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.76-5664C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8964306 | |||||||
| chr2:8964403 | T | C | 2 | a0001c0001t0008g0151 a0001c0001t0008g0152 |
2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.76-5761A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8964403 | |||||||
| chr2:8964411 | T | G | 2 | a0002c0002t0024g0159 a0002c0002t0024g0160 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.76-5769A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8964411 | |||||||
| chr2:8964840 | C | A | 3 | a0003c0003t0010g0153 a0003c0003t0010g0154 a0003c0003t0010g0155 |
3 | HG00642.hp1 HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.76-6198G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8964840 | |||||||
| chr2:8964902 | A | G | 2 | a0001c0001t0001g0043 a0001c0001t0005g0042 |
2 | HG00639.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.76-6260T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8964902 | |||||||
| chr2:8965001 | C | G | 3 | a0003c0003t0010g0153 a0003c0003t0010g0154 a0003c0003t0010g0155 |
3 | HG00642.hp1 HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.76-6359G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8965001 | |||||||
| chr2:8965113 | G | A | 1 | a0001c0001t0004g0050 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.76-6471C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8965113 | |||||||
| chr2:8965126 | C | T | 2 | a0001c0001t0039g0004 a0004c0005t0028g0013 |
2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.76-6484G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8965126 | |||||||
| chr2:8965264 | T | C | 9 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(6): Show |
9 | HG01891.hp1 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.76-6622A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8965264 | |||||||
| chr2:8965371 | G | A | 7 | a0001c0001t0008g0149 a0001c0001t0008g0150 a0001c0001t0008g0151 others(4): Show |
7 | HG00642.hp1 HG01070.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.76-6729C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8965371 | |||||||
| chr2:8965382 | T | C | 1 | a0002c0002t0015g0064 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.76-6740A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8965382 | |||||||
| chr2:8965803 | G | A | 7 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(4): Show |
7 | HG01070.hp1 HG01071.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.76-7161C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8965803 | |||||||
| chr2:8965879 | T | G | 3 | a0002c0002t0017g0011 a0002c0002t0017g0012 a0002c0002t0027g0036 |
3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.76-7237A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8965879 | |||||||
| chr2:8966130 | G | A | 3 | a0002c0002t0017g0011 a0002c0002t0017g0012 a0002c0002t0027g0036 |
3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.76-7488C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8966130 | |||||||
| chr2:8966165 | T | C | 7 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(4): Show |
7 | HG01070.hp1 HG01071.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.76-7523A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8966165 | |||||||
| chr2:8966199 | A | G | 1 | a0001c0001t0006g0091 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.76-7557T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8966199 | |||||||
| chr2:8966336 | G | T | 6 | a0001c0001t0009g0007 a0001c0001t0016g0009 a0001c0001t0016g0010 others(3): Show |
6 | HG00639.hp2 HG01884.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.76-7694C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8966336 | |||||||
| chr2:8966378 | C | T | 2 | a0001c0001t0009g0034 a0001c0001t0009g0035 |
2 | HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.76-7736G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8966378 | |||||||
| chr2:8966544 | G | A | 4 | a0002c0002t0015g0064 a0002c0002t0024g0159 a0002c0002t0024g0160 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.76-7902C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8966544 | |||||||
| chr2:8966722 | T | C | 1 | a0004c0005t0028g0013 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.76-8080A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8966722 | |||||||
| chr2:8966906 | G | C | 3 | a0002c0002t0017g0011 a0002c0002t0017g0012 a0002c0002t0027g0036 |
3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.76-8264C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8966906 | |||||||
| chr2:8967015 | T | C | 1 | a0001c0001t0004g0060 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.76-8373A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8967015 | |||||||
| chr2:8967041 | T | A | 65 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0002g0030 others(62): Show |
66 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.76-8399A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8967041 | |||||||
| chr2:8967426 | T | C | 3 | a0002c0002t0017g0011 a0002c0002t0017g0012 a0002c0002t0027g0036 |
3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.76-8784A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8967426 | |||||||
| chr2:8967585 | TA | T | 23 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0002g0030 others(20): Show |
24 | HG00621.hp2 HG01175.hp1 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.76-8944delT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8967585 | |||||||
| chr2:8967761 | T | C | 7 | a0001c0001t0008g0149 a0001c0001t0008g0150 a0001c0001t0008g0151 others(4): Show |
7 | HG00642.hp1 HG01070.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.76-9119A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8967761 | |||||||
| chr2:8968041 | G | C | 14 | a0001c0001t0008g0149 a0001c0001t0008g0150 a0001c0001t0008g0151 others(11): Show |
14 | HG00642.hp1 HG01070.hp2 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.76-9399C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8968041 | |||||||
| chr2:8968193 | C | A | 12 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(9): Show |
12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.76-9551G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8968193 | |||||||
| chr2:8968492 | G | A | 3 | a0002c0002t0017g0011 a0002c0002t0017g0012 a0002c0002t0027g0036 |
3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.76-9850C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8968492 | |||||||
| chr2:8968800 | G | T | 12 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(9): Show |
12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.76-10158C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8968800 | |||||||
| chr2:8968810 | G | A | 7 | a0002c0002t0015g0064 a0002c0002t0017g0011 a0002c0002t0017g0012 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.76-10168C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8968810 | |||||||
| chr2:8968847 | C | T | 1 | a0003c0003t0010g0154 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.76-10205G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8968847 | |||||||
| chr2:8968977 | T | G | 1 | a0001c0001t0001g0121 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.76-10335A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8968977 | |||||||
| chr2:8969135 | T | C | 65 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0002g0030 others(62): Show |
66 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.76-10493A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8969135 | |||||||
| chr2:8969197 | A | C | 3 | a0003c0003t0010g0153 a0003c0003t0010g0154 a0003c0003t0010g0155 |
3 | HG00642.hp1 HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.76-10555T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8969197 | |||||||
| chr2:8969401 | T | C | 141 | a0001c0001t0001g0043 a0001c0001t0001g0070 a0001c0001t0001g0074 others(138): Show |
142 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(139): Show |
intron_variant | MODIFIER | c.76-10759A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8969401 | |||||||
| chr2:8969557 | T | A | 72 | a0001c0001t0001g0043 a0001c0001t0002g0015 a0001c0001t0002g0017 others(69): Show |
73 | HG00621.hp2 HG00639.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.76-10915A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8969557 | |||||||
| chr2:8969580 | T | C | 1 | a0001c0001t0012g0054 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.76-10938A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8969580 | |||||||
| chr2:8969729 | G | A | 2 | a0001c0001t0008g0151 a0001c0001t0008g0152 |
2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.76-11087C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8969729 | |||||||
| chr2:8969796 | G | A | 3 | a0002c0002t0017g0011 a0002c0002t0017g0012 a0002c0002t0027g0036 |
3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.76-11154C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8969796 | |||||||
| chr2:8969814 | A | C | 3 | a0002c0002t0017g0011 a0002c0002t0017g0012 a0002c0002t0027g0036 |
3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.76-11172T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8969814 | |||||||
| chr2:8970180 | A | C | 3 | a0002c0002t0024g0159 a0002c0002t0024g0160 a0002c0002t0040g0158 |
3 | HG01167.hp2 HG01169.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.76-11538T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8970180 | |||||||
| chr2:8970236 | A | G | 4 | a0002c0002t0015g0064 a0002c0002t0024g0159 a0002c0002t0024g0160 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.76-11594T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8970236 | |||||||
| chr2:8970778 | T | C | 2 | a0001c0001t0008g0151 a0001c0001t0008g0152 |
2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.76-12136A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8970778 | |||||||
| chr2:8970791 | C | T | 2 | a0001c0001t0001g0043 a0001c0001t0005g0042 |
2 | HG00639.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.76-12149G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8970791 | |||||||
| chr2:8970910 | C | G | 7 | a0002c0002t0015g0064 a0002c0002t0017g0011 a0002c0002t0017g0012 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.76-12268G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8970910 | |||||||
| chr2:8970951 | G | C | 2 | a0002c0002t0017g0011 a0002c0002t0017g0012 |
2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.76-12309C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8970951 | |||||||
| chr2:8971100 | C | T | 2 | a0001c0001t0008g0151 a0001c0001t0008g0152 |
2 | HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.76-12458G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8971100 | |||||||
| chr2:8971135 | G | T | 1 | a0001c0001t0002g0119 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.76-12493C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8971135 | |||||||
| chr2:8971256 | C | T | 6 | a0001c0001t0001g0082 a0001c0001t0001g0097 a0001c0001t0001g0098 others(3): Show |
6 | HG02451.hp2 HG02717.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.76-12614G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8971256 | |||||||
| chr2:8971277 | C | T | 4 | a0002c0002t0015g0064 a0002c0002t0024g0159 a0002c0002t0024g0160 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.76-12635G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8971277 | |||||||
| chr2:8971375 | TAA | T | 3 | a0001c0001t0016g0009 a0001c0001t0016g0010 a0001c0001t0025g0008 |
3 | HG01884.hp1 HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.76-12735_76-12734d others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8971375 | |||||||
| chr2:8971473 | G | C | 7 | a0001c0001t0008g0149 a0001c0001t0008g0150 a0001c0001t0008g0151 others(4): Show |
7 | HG00642.hp1 HG01070.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.76-12831C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8971473 | |||||||
| chr2:8971477 | C | T | 1 | a0001c0001t0013g0134 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.76-12835G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8971477 | |||||||
| chr2:8971595 | C | T | 1 | a0001c0001t0002g0132 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.76-12953G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8971595 | |||||||
| chr2:8971600 | T | C | 1 | a0001c0001t0011g0062 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.76-12958A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8971600 | |||||||
| chr2:8971856 | C | T | 5 | a0001c0001t0005g0037 a0001c0001t0005g0039 a0001c0001t0005g0040 others(2): Show |
5 | HG01934.hp1 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.76-13214G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8971856 | |||||||
| chr2:8972004 | T | C | 2 | a0001c0001t0009g0034 a0001c0001t0009g0035 |
2 | HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.76-13362A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8972004 | |||||||
| chr2:8972902 | C | A | 19 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(16): Show |
19 | HG00738.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.76-14260G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8972902 | |||||||
| chr2:8972918 | A | G | 2 | a0001c0001t0022g0083 a0001c0001t0022g0084 |
2 | HG02257.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.76-14276T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8972918 | |||||||
| chr2:8972978 | C | A | 1 | a0001c0001t0001g0121 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.76-14336G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8972978 | |||||||
| chr2:8973079 | C | T | 141 | a0001c0001t0001g0043 a0001c0001t0001g0070 a0001c0001t0001g0074 others(138): Show |
142 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(139): Show |
intron_variant | MODIFIER | c.76-14437G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8973079 | |||||||
| chr2:8973289 | T | C | 9 | a0001c0001t0009g0007 a0001c0001t0009g0034 a0001c0001t0009g0035 others(6): Show |
9 | HG00639.hp2 HG01884.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.76-14647A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8973289 | |||||||
| chr2:8973375 | G | T | 4 | a0001c0001t0008g0149 a0001c0001t0008g0150 a0001c0001t0008g0151 others(1): Show |
4 | HG01070.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-14733C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8973375 | |||||||
| chr2:8973444 | A | G | 4 | a0002c0002t0015g0064 a0002c0002t0024g0159 a0002c0002t0024g0160 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.76-14802T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8973444 | |||||||
| chr2:8973552 | TA | T | 61 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0002g0030 others(58): Show |
62 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.76-14911delT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8973552 | |||||||
| chr2:8973562 | A | G | 3 | a0001c0001t0006g0090 a0001c0001t0006g0091 a0001c0001t0006g0092 |
3 | HG02735.hp1 HG04115.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.76-14920T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8973562 | |||||||
| chr2:8973614 | G | T | 141 | a0001c0001t0001g0043 a0001c0001t0001g0070 a0001c0001t0001g0074 others(138): Show |
142 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(139): Show |
intron_variant | MODIFIER | c.76-14972C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8973614 | |||||||
| chr2:8973750 | C | T | 2 | a0001c0001t0004g0066 a0001c0001t0004g0067 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.76-15108G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8973750 | |||||||
| chr2:8973894 | T | G | 14 | a0001c0001t0008g0149 a0001c0001t0008g0150 a0001c0001t0008g0151 others(11): Show |
14 | HG00642.hp1 HG01070.hp2 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.76-15252A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8973894 | |||||||
| chr2:8973909 | T | C | 23 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0002g0030 others(20): Show |
24 | HG00621.hp2 HG01175.hp1 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.76-15267A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8973909 | |||||||
| chr2:8974129 | A | G | 7 | a0002c0002t0015g0064 a0002c0002t0017g0011 a0002c0002t0017g0012 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.76-15487T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8974129 | |||||||
| chr2:8974378 | C | A | 1 | a0001c0001t0002g0118 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.76-15736G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8974378 | |||||||
| chr2:8974414 | C | T | 3 | a0003c0003t0010g0153 a0003c0003t0010g0154 a0003c0003t0010g0155 |
3 | HG00642.hp1 HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.76-15772G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8974414 | |||||||
| chr2:8974635 | T | G | 33 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(30): Show |
33 | HG00642.hp1 HG00738.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.76-15993A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8974635 | |||||||
| chr2:8974663 | A | T | 4 | a0001c0001t0008g0149 a0001c0001t0008g0150 a0001c0001t0008g0151 others(1): Show |
4 | HG01070.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-16021T>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8974663 | |||||||
| chr2:8974918 | G | A | 7 | a0002c0002t0015g0064 a0002c0002t0017g0011 a0002c0002t0017g0012 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.76-16276C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8974918 | |||||||
| chr2:8975303 | C | A | 5 | a0001c0001t0005g0037 a0001c0001t0005g0039 a0001c0001t0005g0040 others(2): Show |
5 | HG01934.hp1 HG02559.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.76-16661G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8975303 | |||||||
| chr2:8975462 | C | A | 2 | a0001c0001t0001g0074 a0001c0001t0001g0075 |
2 | HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.76-16820G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8975462 | |||||||
| chr2:8975788 | T | G | 1 | a0001c0001t0025g0008 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.76-17146A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8975788 | |||||||
| chr2:8975797 | C | CA | 61 | a0001c0001t0001g0089 a0001c0001t0001g0128 a0001c0001t0001g0145 others(58): Show |
62 | HG00621.hp1 HG00621.hp2 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.76-17156dupT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8975797 | |||||||
| chr2:8975797 | C | CAA | 6 | a0001c0001t0003g0023 a0001c0001t0004g0056 a0001c0001t0008g0151 others(3): Show |
6 | HG02055.hp2 HG02145.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.76-17157_76-17156d others(4): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8975797 | |||||||
| chr2:8975849 | T | C | 9 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(6): Show |
9 | HG01891.hp1 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.76-17207A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8975849 | |||||||
| chr2:8975909 | C | A | 1 | a0001c0001t0003g0026 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.76-17267G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8975909 | |||||||
| chr2:8976695 | G | A | 1 | a0001c0001t0019g0033 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.76-18053C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8976695 | |||||||
| chr2:8976789 | C | T | 3 | a0003c0003t0010g0153 a0003c0003t0010g0154 a0003c0003t0010g0155 |
3 | HG00642.hp1 HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.76-18147G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8976789 | |||||||
| chr2:8977010 | C | T | 9 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(6): Show |
9 | HG01891.hp1 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.76-18368G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8977010 | |||||||
| chr2:8977050 | A | T | 1 | a0001c0001t0004g0058 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.76-18408T>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8977050 | |||||||
| chr2:8977299 | T | C | 4 | a0002c0002t0015g0064 a0002c0002t0024g0159 a0002c0002t0024g0160 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.76-18657A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8977299 | |||||||
| chr2:8977461 | A | G | 1 | a0001c0001t0006g0122 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.76-18819T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8977461 | |||||||
| chr2:8977558 | T | C | 2 | a0001c0001t0001g0043 a0001c0001t0005g0042 |
2 | HG00639.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.76-18916A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8977558 | |||||||
| chr2:8977581 | C | T | 19 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(16): Show |
19 | HG00738.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.76-18939G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8977581 | |||||||
| chr2:8977829 | T | A | 1 | a0001c0001t0001g0115 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.76-19187A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8977829 | |||||||
| chr2:8977841 | C | T | 4 | a0002c0002t0015g0064 a0002c0002t0024g0159 a0002c0002t0024g0160 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.76-19199G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8977841 | |||||||
| chr2:8977945 | C | T | 3 | a0001c0001t0005g0044 a0001c0001t0005g0045 a0001c0001t0005g0046 |
3 | HG02818.hp1 HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.76-19303G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8977945 | |||||||
| chr2:8978086 | T | C | 33 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(30): Show |
33 | HG00642.hp1 HG00738.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.76-19444A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8978086 | |||||||
| chr2:8978308 | T | C | 33 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(30): Show |
33 | HG00642.hp1 HG00738.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.76-19666A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8978308 | |||||||
| chr2:8978610 | T | C | 32 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(29): Show |
32 | HG00642.hp1 HG00738.hp2 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.76-19968A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8978610 | |||||||
| chr2:8978686 | A | G | 2 | a0002c0002t0017g0011 a0002c0002t0017g0012 |
2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.76-20044T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8978686 | |||||||
| chr2:8978756 | C | G | 1 | a0001c0001t0019g0033 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.76-20114G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8978756 | |||||||
| chr2:8978853 | TA | T | 65 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0002g0030 others(62): Show |
66 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.76-20212delT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8978853 | |||||||
| chr2:8978854 | A | T | 1 | a0001c0001t0002g0080 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.76-20212T>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8978854 | |||||||
| chr2:8979251 | G | C | 1 | a0001c0001t0001g0116 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.76-20609C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8979251 | |||||||
| chr2:8979449 | C | T | 2 | a0001c0001t0009g0007 a0001c0004t0015g0006 |
2 | HG00639.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.76-20807G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8979449 | |||||||
| chr2:8979564 | T | G | 12 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(9): Show |
12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.76-20922A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8979564 | |||||||
| chr2:8979605 | G | A | 6 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(3): Show |
6 | HG01109.hp1 HG01891.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.76-20963C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8979605 | |||||||
| chr2:8979916 | G | A | 23 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0002g0030 others(20): Show |
24 | HG00621.hp2 HG01175.hp1 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.76-21274C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8979916 | |||||||
| chr2:8980069 | T | C | 1 | a0002c0002t0015g0064 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.76-21427A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8980069 | |||||||
| chr2:8980254 | A | AG | 3 | a0002c0002t0024g0159 a0002c0002t0024g0160 a0002c0002t0040g0158 |
3 | HG01167.hp2 HG01169.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.76-21613dupC | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8980254 | |||||||
| chr2:8980356 | CA | C | 2 | a0001c0001t0003g0027 a0001c0001t0003g0029 |
2 | HG02738.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.76-21715delT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8980356 | |||||||
| chr2:8980418 | T | C | 3 | a0001c0001t0003g0027 a0001c0001t0003g0028 a0001c0001t0003g0029 |
3 | HG02735.hp2 HG02738.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.76-21776A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8980418 | |||||||
| chr2:8980925 | A | T | 3 | a0002c0002t0017g0011 a0002c0002t0017g0012 a0002c0002t0027g0036 |
3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.76-22283T>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8980925 | |||||||
| chr2:8981007 | T | C | 7 | a0001c0001t0008g0149 a0001c0001t0008g0150 a0001c0001t0008g0151 others(4): Show |
7 | HG00642.hp1 HG01070.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.76-22365A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8981007 | |||||||
| chr2:8981041 | AAGAT | A | 9 | a0001c0001t0001g0043 a0001c0001t0005g0039 a0001c0001t0005g0040 others(6): Show |
9 | HG00639.hp1 HG01175.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-22403_76-22400d others(6): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8981041 | |||||||
| chr2:8981049 | T | C | 1 | a0001c0001t0002g0117 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.76-22407A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8981049 | |||||||
| chr2:8981207 | G | T | 1 | a0001c0001t0001g0121 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.75+22333C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8981207 | |||||||
| chr2:8981215 | C | T | 14 | a0001c0001t0008g0149 a0001c0001t0008g0150 a0001c0001t0008g0151 others(11): Show |
14 | HG00642.hp1 HG01070.hp2 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.75+22325G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8981215 | |||||||
| chr2:8981436 | T | TGTCGCCC others(34): Show |
1 | a0002c0002t0027g0036 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.75+22063_75+22103d others(43): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8981436 | |||||||
| chr2:8981682 | G | T | 2 | a0001c0001t0009g0007 a0001c0004t0015g0006 |
2 | HG00639.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.75+21858C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8981682 | |||||||
| chr2:8982030 | C | T | 4 | a0001c0001t0008g0149 a0001c0001t0008g0150 a0001c0001t0008g0151 others(1): Show |
4 | HG01070.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+21510G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8982030 | |||||||
| chr2:8982102 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.75+21438G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8982102 | |||||||
| chr2:8982164 | A | T | 2 | a0002c0002t0017g0011 a0002c0002t0017g0012 |
2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.75+21376T>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8982164 | |||||||
| chr2:8982289 | C | T | 7 | a0002c0002t0015g0064 a0002c0002t0017g0011 a0002c0002t0017g0012 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+21251G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8982289 | |||||||
| chr2:8982932 | C | A | 12 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(9): Show |
12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.75+20608G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8982932 | |||||||
| chr2:8982994 | A | G | 7 | a0002c0002t0015g0064 a0002c0002t0017g0011 a0002c0002t0017g0012 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+20546T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8982994 | |||||||
| chr2:8983031 | G | A | 1 | a0001c0001t0002g0080 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.75+20509C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8983031 | |||||||
| chr2:8983274 | T | A | 1 | a0001c0001t0019g0033 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.75+20266A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8983274 | |||||||
| chr2:8983363 | A | G | 4 | a0001c0001t0008g0149 a0001c0001t0008g0150 a0001c0001t0008g0151 others(1): Show |
4 | HG01070.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+20177T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8983363 | |||||||
| chr2:8983393 | A | C | 9 | a0001c0001t0009g0007 a0001c0001t0009g0034 a0001c0001t0009g0035 others(6): Show |
9 | HG00639.hp2 HG01884.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.75+20147T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8983393 | |||||||
| chr2:8983425 | C | T | 4 | a0002c0002t0015g0064 a0002c0002t0024g0159 a0002c0002t0024g0160 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+20115G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8983425 | |||||||
| chr2:8984043 | T | C | 7 | a0002c0002t0015g0064 a0002c0002t0017g0011 a0002c0002t0017g0012 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+19497A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8984043 | |||||||
| chr2:8984189 | G | A | 3 | a0002c0002t0024g0159 a0002c0002t0024g0160 a0002c0002t0040g0158 |
3 | HG01167.hp2 HG01169.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.75+19351C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8984189 | |||||||
| chr2:8984202 | C | G | 2 | a0002c0002t0017g0011 a0002c0002t0017g0012 |
2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.75+19338G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8984202 | |||||||
| chr2:8984349 | G | C | 1 | a0001c0001t0039g0004 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.75+19191C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8984349 | |||||||
| chr2:8984417 | G | C | 1 | a0001c0001t0019g0033 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.75+19123C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8984417 | |||||||
| chr2:8984469 | G | C | 2 | a0002c0002t0024g0159 a0002c0002t0024g0160 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.75+19071C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8984469 | |||||||
| chr2:8984539 | G | GTGAAAGC others(10): Show |
1 | a0001c0001t0038g0129 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.75+19000_75+19001i others(19): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8984539 | |||||||
| chr2:8984541 | G | C | 1 | a0001c0001t0038g0129 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.75+18999C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8984541 | |||||||
| chr2:8984602 | C | A | 6 | a0001c0001t0002g0118 a0001c0001t0013g0003 a0001c0001t0013g0134 others(3): Show |
6 | HG00558.hp1 HG00609.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+18938G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8984602 | |||||||
| chr2:8984663 | A | G | 2 | a0002c0002t0017g0011 a0002c0002t0017g0012 |
2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.75+18877T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8984663 | |||||||
| chr2:8984683 | G | GA | 3 | a0002c0002t0017g0011 a0002c0002t0017g0012 a0002c0002t0027g0036 |
3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.75+18856dupT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8984683 | |||||||
| chr2:8984779 | G | A | 1 | a0002c0002t0027g0036 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.75+18761C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8984779 | |||||||
| chr2:8985033 | C | T | 2 | a0001c0001t0002g0068 a0001c0001t0002g0081 |
2 | HG00621.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.75+18507G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8985033 | |||||||
| chr2:8985084 | GA | G | 8 | a0001c0001t0008g0149 a0001c0001t0008g0150 a0001c0001t0008g0151 others(5): Show |
8 | HG00642.hp1 HG01070.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.75+18455delT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8985084 | |||||||
| chr2:8985118 | C | T | 1 | a0001c0001t0002g0069 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.75+18422G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8985118 | |||||||
| chr2:8985246 | G | A | 1 | a0001c0001t0019g0133 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.75+18294C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8985246 | |||||||
| chr2:8985561 | A | G | 7 | a0001c0001t0008g0149 a0001c0001t0008g0150 a0001c0001t0008g0151 others(4): Show |
7 | HG00642.hp1 HG01070.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+17979T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8985561 | |||||||
| chr2:8985829 | T | C | 1 | a0001c0001t0003g0029 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.75+17711A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8985829 | |||||||
| chr2:8985895 | C | T | 23 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0002g0030 others(20): Show |
24 | HG00621.hp2 HG01175.hp1 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.75+17645G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8985895 | |||||||
| chr2:8985991 | A | G | 4 | a0002c0002t0015g0064 a0002c0002t0024g0159 a0002c0002t0024g0160 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+17549T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8985991 | |||||||
| chr2:8986114 | A | T | 15 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0124 others(12): Show |
15 | HG00609.hp1 HG00735.hp2 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.75+17426T>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8986114 | |||||||
| chr2:8986207 | CA | C | 5 | a0001c0001t0001g0120 a0001c0001t0002g0119 a0001c0001t0006g0090 others(2): Show |
5 | HG02735.hp1 HG02895.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.75+17332delT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8986207 | |||||||
| chr2:8986378 | A | C | 3 | a0002c0002t0017g0011 a0002c0002t0017g0012 a0002c0002t0027g0036 |
3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.75+17162T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8986378 | |||||||
| chr2:8986565 | T | TA | 8 | a0001c0001t0001g0096 a0001c0001t0002g0093 a0001c0001t0006g0090 others(5): Show |
8 | HG00140.hp2 HG02698.hp1 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.75+16974dupT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8986565 | |||||||
| chr2:8986811 | G | A | 11 | a0001c0001t0008g0149 a0001c0001t0008g0150 a0001c0001t0008g0151 others(8): Show |
11 | HG00642.hp1 HG01070.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.75+16729C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8986811 | |||||||
| chr2:8987016 | C | A | 12 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(9): Show |
12 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.75+16524G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8987016 | |||||||
| chr2:8987063 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.75+16477C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8987063 | |||||||
| chr2:8987079 | T | C | 15 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0124 others(12): Show |
15 | HG00609.hp1 HG00735.hp2 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.75+16461A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8987079 | |||||||
| chr2:8987095 | A | G | 1 | a0001c0001t0002g0030 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.75+16445T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8987095 | |||||||
| chr2:8987122 | T | A | 1 | a0001c0001t0002g0080 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.75+16418A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8987122 | |||||||
| chr2:8987213 | C | T | 19 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(16): Show |
19 | HG00738.hp2 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.75+16327G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8987213 | |||||||
| chr2:8987422 | T | A | 1 | a0001c0001t0001g0130 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.75+16118A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8987422 | |||||||
| chr2:8987591 | C | A | 3 | a0002c0002t0024g0159 a0002c0002t0024g0160 a0002c0002t0040g0158 |
3 | HG01167.hp2 HG01169.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.75+15949G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8987591 | |||||||
| chr2:8987591 | C | G | 2 | a0002c0002t0017g0011 a0002c0002t0017g0012 |
2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.75+15949G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8987591 | |||||||
| chr2:8987692 | C | T | 4 | a0001c0001t0008g0149 a0001c0001t0008g0150 a0001c0001t0008g0151 others(1): Show |
4 | HG01070.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+15848G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8987692 | |||||||
| chr2:8987766 | G | A | 1 | a0001c0001t0004g0051 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.75+15774C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8987766 | |||||||
| chr2:8988301 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.75+15239C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8988301 | |||||||
| chr2:8988563 | T | C | 2 | a0001c0001t0002g0131 a0001c0001t0021g0078 |
2 | HG01258.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.75+14977A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8988563 | |||||||
| chr2:8988905 | G | A | 65 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0002g0030 others(62): Show |
66 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.75+14635C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8988905 | |||||||
| chr2:8988995 | G | T | 4 | a0001c0001t0008g0149 a0001c0001t0008g0150 a0001c0001t0008g0151 others(1): Show |
4 | HG01070.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+14545C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8988995 | |||||||
| chr2:8989196 | T | C | 1 | a0001c0001t0019g0033 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.75+14344A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8989196 | |||||||
| chr2:8989523 | T | C | 3 | a0002c0002t0017g0011 a0002c0002t0017g0012 a0002c0002t0027g0036 |
3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.75+14017A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8989523 | |||||||
| chr2:8989953 | G | T | 1 | a0001c0001t0001g0070 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.75+13587C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8989953 | |||||||
| chr2:8989999 | A | G | 3 | a0002c0002t0017g0011 a0002c0002t0017g0012 a0002c0002t0027g0036 |
3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.75+13541T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8989999 | |||||||
| chr2:8990053 | G | A | 14 | a0001c0001t0008g0149 a0001c0001t0008g0150 a0001c0001t0008g0151 others(11): Show |
14 | HG00642.hp1 HG01070.hp2 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.75+13487C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8990053 | |||||||
| chr2:8990417 | T | C | 141 | a0001c0001t0001g0043 a0001c0001t0001g0070 a0001c0001t0001g0074 others(138): Show |
142 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(139): Show |
intron_variant | MODIFIER | c.75+13123A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8990417 | |||||||
| chr2:8990773 | T | C | 1 | a0001c0001t0002g0073 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.75+12767A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8990773 | |||||||
| chr2:8990902 | A | C | 14 | a0001c0001t0008g0149 a0001c0001t0008g0150 a0001c0001t0008g0151 others(11): Show |
14 | HG00642.hp1 HG01070.hp2 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.75+12638T>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8990902 | |||||||
| chr2:8991051 | A | T | 1 | a0001c0001t0005g0046 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.75+12489T>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8991051 | |||||||
| chr2:8991510 | G | A | 6 | a0001c0001t0009g0007 a0001c0001t0016g0009 a0001c0001t0016g0010 others(3): Show |
6 | HG00639.hp2 HG01884.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+12030C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8991510 | |||||||
| chr2:8992309 | G | A | 1 | a0001c0001t0019g0033 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.75+11231C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8992309 | |||||||
| chr2:8992705 | C | T | 1 | a0001c0001t0021g0078 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.75+10835G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8992705 | |||||||
| chr2:8992879 | C | T | 1 | a0001c0001t0004g0057 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.75+10661G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8992879 | |||||||
| chr2:8993440 | G | A | 3 | a0003c0003t0010g0153 a0003c0003t0010g0154 a0003c0003t0010g0155 |
3 | HG00642.hp1 HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.75+10100C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8993440 | |||||||
| chr2:8993595 | C | T | 7 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(4): Show |
7 | HG01070.hp1 HG01071.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+9945G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8993595 | |||||||
| chr2:8993680 | T | C | 3 | a0002c0002t0024g0159 a0002c0002t0024g0160 a0002c0002t0040g0158 |
3 | HG01167.hp2 HG01169.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.75+9860A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8993680 | |||||||
| chr2:8993839 | C | G | 3 | a0002c0002t0017g0011 a0002c0002t0017g0012 a0002c0002t0027g0036 |
3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.75+9701G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8993839 | |||||||
| chr2:8994151 | T | C | 3 | a0002c0002t0017g0011 a0002c0002t0017g0012 a0002c0002t0027g0036 |
3 | HG02572.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.75+9389A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8994151 | |||||||
| chr2:8994240 | CA | C | 7 | a0002c0002t0015g0064 a0002c0002t0017g0011 a0002c0002t0017g0012 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+9299delT | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8994240 | |||||||
| chr2:8994483 | T | C | 3 | a0001c0001t0005g0044 a0001c0001t0005g0045 a0001c0001t0005g0046 |
3 | HG02818.hp1 HG02895.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.75+9057A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8994483 | |||||||
| chr2:8994530 | C | T | 4 | a0002c0002t0015g0064 a0002c0002t0024g0159 a0002c0002t0024g0160 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+9010G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8994530 | |||||||
| chr2:8994795 | A | G | 3 | a0003c0003t0010g0153 a0003c0003t0010g0154 a0003c0003t0010g0155 |
3 | HG00642.hp1 HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.75+8745T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8994795 | |||||||
| chr2:8994803 | T | C | 1 | a0001c0001t0019g0133 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.75+8737A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8994803 | |||||||
| chr2:8994988 | T | A | 4 | a0002c0002t0015g0064 a0002c0002t0024g0159 a0002c0002t0024g0160 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+8552A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8994988 | |||||||
| chr2:8995011 | C | T | 1 | a0001c0001t0004g0056 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.75+8529G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8995011 | |||||||
| chr2:8995302 | T | C | 74 | a0001c0001t0001g0043 a0001c0001t0002g0015 a0001c0001t0002g0017 others(71): Show |
75 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.75+8238A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8995302 | |||||||
| chr2:8995589 | C | CT | 3 | a0001c0001t0009g0007 a0001c0001t0026g0005 a0001c0004t0015g0006 |
3 | HG00639.hp2 HG02809.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.75+7950_75+7951ins others(1): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8995589 | |||||||
| chr2:8995590 | A | AT | 58 | a0001c0001t0001g0043 a0001c0001t0001g0082 a0001c0001t0002g0015 others(55): Show |
59 | HG00621.hp1 HG00639.hp1 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.75+7949dupA | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8995590 | |||||||
| chr2:8995590 | A | T | 3 | a0001c0001t0009g0007 a0001c0001t0026g0005 a0001c0004t0015g0006 |
3 | HG00639.hp2 HG02809.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.75+7950T>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8995590 | |||||||
| chr2:8995645 | T | C | 1 | a0001c0001t0002g0080 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.75+7895A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8995645 | |||||||
| chr2:8995652 | A | G | 1 | a0001c0001t0002g0080 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.75+7888T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8995652 | |||||||
| chr2:8995653 | C | G | 1 | a0001c0001t0002g0080 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.75+7887G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8995653 | |||||||
| chr2:8995673 | C | T | 1 | a0001c0001t0002g0079 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.75+7867G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8995673 | |||||||
| chr2:8995689 | C | T | 1 | a0001c0001t0021g0078 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.75+7851G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8995689 | |||||||
| chr2:8995768 | G | T | 2 | a0001c0001t0013g0134 a0001c0001t0019g0033 |
2 | HG02976.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.75+7772C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8995768 | |||||||
| chr2:8995804 | A | G | 77 | a0001c0001t0001g0043 a0001c0001t0001g0074 a0001c0001t0001g0075 others(74): Show |
78 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.75+7736T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8995804 | |||||||
| chr2:8995879 | T | C | 157 | a0001c0001t0001g0043 a0001c0001t0001g0070 a0001c0001t0001g0074 others(154): Show |
158 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(155): Show |
intron_variant | MODIFIER | c.75+7661A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8995879 | |||||||
| chr2:8995886 | C | T | 2 | a0001c0001t0001g0074 a0001c0001t0001g0075 |
2 | HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.75+7654G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8995886 | |||||||
| chr2:8996348 | TGACAACA | T | 4 | a0001c0001t0001g0070 a0001c0001t0002g0071 a0001c0001t0002g0072 others(1): Show |
4 | HG02083.hp1 NA18953.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+7185_75+7191del others(7): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8996348 | |||||||
| chr2:8996361 | T | C | 4 | a0002c0002t0015g0064 a0002c0002t0024g0159 a0002c0002t0024g0160 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+7179A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8996361 | |||||||
| chr2:8996531 | G | A | 2 | a0001c0001t0016g0009 a0001c0001t0016g0010 |
2 | HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.75+7009C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8996531 | |||||||
| chr2:8996557 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.75+6983G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8996557 | |||||||
| chr2:8996666 | G | A | 1 | a0001c0001t0011g0062 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.75+6874C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8996666 | |||||||
| chr2:8996843 | T | C | 3 | a0001c0001t0013g0003 a0001c0001t0013g0134 a0001c0001t0013g0135 |
3 | HG00558.hp1 HG00609.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.75+6697A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8996843 | |||||||
| chr2:8996901 | C | T | 1 | a0001c0001t0002g0069 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.75+6639G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8996901 | |||||||
| chr2:8997017 | C | T | 2 | a0001c0001t0014g0014 a0001c0001t0014g0032 |
2 | HG02451.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.75+6523G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8997017 | |||||||
| chr2:8997512 | C | T | 1 | a0001c0001t0002g0068 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.75+6028G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8997512 | |||||||
| chr2:8997831 | T | A | 9 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(6): Show |
9 | HG01891.hp1 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.75+5709A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8997831 | |||||||
| chr2:8998015 | C | T | 2 | a0001c0001t0004g0066 a0001c0001t0004g0067 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.75+5525G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8998015 | |||||||
| chr2:8998093 | A | T | 3 | a0001c0001t0012g0052 a0001c0001t0012g0053 a0001c0001t0012g0054 |
3 | HG00738.hp2 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.75+5447T>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8998093 | |||||||
| chr2:8998131 | T | G | 29 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0002g0030 others(26): Show |
30 | HG00639.hp2 HG01175.hp1 HG01256.hp1 others(27): Show |
intron_variant | MODIFIER | c.75+5409A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8998131 | |||||||
| chr2:8998179 | C | T | 1 | a0001c0001t0002g0065 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.75+5361G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8998179 | |||||||
| chr2:8998277 | C | A | 1 | a0001c0001t0006g0136 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.75+5263G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8998277 | |||||||
| chr2:8998358 | T | C | 3 | a0001c0001t0012g0052 a0001c0001t0012g0053 a0001c0001t0012g0054 |
3 | HG00738.hp2 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.75+5182A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8998358 | |||||||
| chr2:8998609 | C | T | 22 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0002g0030 others(19): Show |
23 | HG01175.hp1 HG01256.hp1 HG01258.hp1 others(20): Show |
intron_variant | MODIFIER | c.75+4931G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8998609 | |||||||
| chr2:8998624 | G | C | 6 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(3): Show |
6 | HG01109.hp1 HG01891.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+4916C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8998624 | |||||||
| chr2:8998905 | G | C | 1 | a0002c0002t0015g0064 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.75+4635C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8998905 | |||||||
| chr2:8998921 | G | A | 1 | a0001c0001t0011g0063 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.75+4619C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8998921 | |||||||
| chr2:8999159 | A | G | 17 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(14): Show |
17 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.75+4381T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8999159 | |||||||
| chr2:8999188 | C | T | 1 | a0001c0001t0004g0055 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.75+4352G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8999188 | |||||||
| chr2:8999454 | G | A | 7 | a0001c0001t0008g0149 a0001c0001t0008g0150 a0001c0001t0008g0151 others(4): Show |
7 | HG00642.hp1 HG01070.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+4086C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8999454 | |||||||
| chr2:8999526 | T | C | 19 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(16): Show |
19 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.75+4014A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8999526 | |||||||
| chr2:8999731 | A | G | 1 | a0002c0002t0040g0158 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.75+3809T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8999731 | |||||||
| chr2:8999818 | G | C | 4 | a0001c0001t0008g0149 a0001c0001t0008g0150 a0001c0001t0008g0151 others(1): Show |
4 | HG01070.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+3722C>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8999818 | |||||||
| chr2:8999839 | T | C | 9 | a0001c0001t0004g0055 a0001c0001t0004g0056 a0001c0001t0004g0057 others(6): Show |
9 | HG01891.hp1 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.75+3701A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8999839 | |||||||
| chr2:8999867 | T | C | 1 | a0001c0001t0014g0032 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.75+3673A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 8999867 | |||||||
| chr2:9000041 | C | T | 1 | a0001c0001t0026g0005 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.75+3499G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 9000041 | |||||||
| chr2:9000156 | C | T | 4 | a0002c0002t0015g0064 a0002c0002t0024g0159 a0002c0002t0024g0160 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+3384G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 9000156 | |||||||
| chr2:9000192 | T | A | 1 | a0001c0001t0001g0143 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.75+3348A>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 9000192 | |||||||
| chr2:9000320 | T | G | 9 | a0001c0001t0009g0007 a0001c0001t0009g0034 a0001c0001t0009g0035 others(6): Show |
9 | HG00639.hp2 HG01884.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.75+3220A>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 9000320 | |||||||
| chr2:9000358 | C | T | 61 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0002g0030 others(58): Show |
62 | HG00639.hp2 HG00642.hp1 HG00738.hp2 others(59): Show |
intron_variant | MODIFIER | c.75+3182G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 9000358 | |||||||
| chr2:9000560 | G | A | 17 | a0001c0001t0004g0047 a0001c0001t0004g0050 a0001c0001t0004g0051 others(14): Show |
17 | HG00738.hp2 HG01891.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.75+2980C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 9000560 | |||||||
| chr2:9000785 | C | T | 2 | a0002c0002t0017g0011 a0002c0002t0017g0012 |
2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.75+2755G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 9000785 | |||||||
| chr2:9000889 | A | G | 6 | a0001c0001t0009g0007 a0001c0001t0016g0009 a0001c0001t0016g0010 others(3): Show |
6 | HG00639.hp2 HG01884.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+2651T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 9000889 | |||||||
| chr2:9000987 | A | G | 1 | a0001c0001t0039g0004 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.75+2553T>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 9000987 | |||||||
| chr2:9001054 | T | C | 4 | a0002c0002t0015g0064 a0002c0002t0024g0159 a0002c0002t0024g0160 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02027.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+2486A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 9001054 | |||||||
| chr2:9002045 | CAT | C | 4 | a0001c0001t0008g0149 a0001c0001t0008g0150 a0001c0001t0008g0151 others(1): Show |
4 | HG01070.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+1493_75+1494del others(2): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 9002045 | |||||||
| chr2:9002053 | G | T | 4 | a0001c0001t0008g0149 a0001c0001t0008g0150 a0001c0001t0008g0151 others(1): Show |
4 | HG01070.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+1487C>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 9002053 | |||||||
| chr2:9002054 | C | T | 4 | a0001c0001t0008g0149 a0001c0001t0008g0150 a0001c0001t0008g0151 others(1): Show |
4 | HG01070.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+1486G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 9002054 | |||||||
| chr2:9002055 | ACACCAGT others(31): Show |
A | 4 | a0001c0001t0008g0149 a0001c0001t0008g0150 a0001c0001t0008g0151 others(1): Show |
4 | HG01070.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+1447_75+1484del others(38): Show |
MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 9002055 | |||||||
| chr2:9002094 | C | G | 4 | a0001c0001t0008g0149 a0001c0001t0008g0150 a0001c0001t0008g0151 others(1): Show |
4 | HG01070.hp2 HG02145.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+1446G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 9002094 | |||||||
| chr2:9002419 | G | A | 1 | a0001c0001t0002g0144 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.75+1121C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 9002419 | |||||||
| chr2:9002430 | T | C | 3 | a0003c0003t0010g0153 a0003c0003t0010g0154 a0003c0003t0010g0155 |
3 | HG00642.hp1 HG03654.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.75+1110A>G | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 9002430 | |||||||
| chr2:9002883 | A | T | 72 | a0001c0001t0001g0043 a0001c0001t0002g0015 a0001c0001t0002g0017 others(69): Show |
73 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.75+657T>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 9002883 | |||||||
| chr2:9002928 | C | G | 2 | a0001c0001t0008g0149 a0001c0001t0008g0150 |
2 | HG01070.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.75+612G>C | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 9002928 | |||||||
| chr2:9002993 | C | T | 1 | a0001c0001t0013g0003 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.75+547G>A | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 9002993 | |||||||
| chr2:9003366 | G | A | 4 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(1): Show |
4 | HG03041.hp2 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.75+174C>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 9003366 | |||||||
| chr2:9003515 | C | A | 7 | a0001c0001t0008g0149 a0001c0001t0008g0150 a0001c0001t0008g0151 others(4): Show |
7 | HG00642.hp1 HG01070.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+25G>T | MBOAT2 | ENSG00000143797.12 | transcript | ENST00000305997.8 | protein_coding | 1/12 | chr2 | 9003515 |