Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 83752 |
| ensemblid | ENSG00000102910.14 |
| hgncid | 20598 |
| symbol | LONP2 |
| name | lon peptidase 2, peroxisomal |
| refseq_nuc | NM_031490.5 |
| refseq_prot | NP_113678.2 |
| ensembl_nuc | ENST00000285737.9 |
| ensembl_prot | ENSP00000285737.4 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 48244300 |
| end | 48357349 |
| strand | + |
| ver | v1.2 |
| region | chr16:48244300-48357349 |
| region5000 | chr16:48239300-48362349 |
| regionname0 | LONP2_chr16_48244300_48357349 |
| regionname5000 | LONP2_chr16_48239300_48362349 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 852 | 152 | 77 | 34 | 18 | 5 | 16 | 6 | LONP2_chr16_48239300_48362349 | LONP2 | MSSVS others(847): Show |
chr16 | 48239300 | 48362349 |
| a0002 | 0/0 | 852 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | MSSVS others(847): Show |
chr16 | 48239300 | 48362349 |
| a0003 | 0/0 | 852 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | MSSVS others(847): Show |
chr16 | 48239300 | 48362349 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2556 | 135 | 61 | 34 | 17 | 5 | 16 | LONP2_chr16_48239300_48362349 | LONP2 | ATGTC others(2551): Show |
chr16 | 48239300 | 48362349 | ||
| a0001c0002 | 0/0 | 2556 | 10 | 10 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | ATGTC others(2551): Show |
chr16 | 48239300 | 48362349 | ||
| a0001c0003 | 0/0 | 2556 | 4 | 4 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | ATGTC others(2551): Show |
chr16 | 48239300 | 48362349 | ||
| a0001c0004 | 0/0 | 2556 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | ATGTC others(2551): Show |
chr16 | 48239300 | 48362349 | ||
| a0001c0006 | 0/0 | 2556 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | ATGTC others(2551): Show |
chr16 | 48239300 | 48362349 | ||
| a0001c0008 | 0/0 | 2556 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | ATGTC others(2551): Show |
chr16 | 48239300 | 48362349 | ||
| a0002c0005 | 0/0 | 2556 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | ATGTC others(2551): Show |
chr16 | 48239300 | 48362349 | ||
| a0003c0007 | 0/0 | 2556 | 1 | 0 | 0 | 0 | 1 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | ATGTC others(2551): Show |
chr16 | 48239300 | 48362349 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 8194 | 17 | 5 | 8 | 4 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8189): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0002 | 0/0 | 8195 | 15 | 10 | 2 | 0 | 0 | 3 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8190): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0003 | 0/0 | 8194 | 7 | 0 | 2 | 1 | 2 | 2 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8189): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0004 | 0/0 | 8198 | 4 | 1 | 2 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8193): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0005 | 0/0 | 8200 | 4 | 1 | 2 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8195): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0006 | 0/0 | 8201 | 3 | 2 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8196): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0007 | 0/0 | 8200 | 2 | 0 | 1 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8195): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0008 | 0/0 | 8196 | 3 | 1 | 0 | 2 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8191): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0009 | 0/0 | 8194 | 3 | 3 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8189): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0010 | 0/0 | 8195 | 2 | 2 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8190): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0011 | 0/0 | 8196 | 3 | 0 | 0 | 2 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8191): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0012 | 0/0 | 8194 | 3 | 0 | 0 | 3 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8189): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0013 | 0/0 | 8199 | 2 | 2 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8194): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0014 | 0/0 | 8200 | 2 | 2 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8195): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0015 | 0/0 | 8199 | 2 | 0 | 2 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8194): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0016 | 0/0 | 8199 | 2 | 0 | 1 | 0 | 1 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8194): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0017 | 0/0 | 8195 | 2 | 0 | 1 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8190): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0018 | 0/0 | 8199 | 2 | 2 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8194): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0019 | 0/0 | 8194 | 2 | 2 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8189): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0020 | 0/0 | 8199 | 2 | 0 | 1 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8194): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0021 | 0/0 | 8196 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8191): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0022 | 0/0 | 8198 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8193): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0023 | 0/0 | 8197 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8192): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0024 | 0/0 | 8196 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8191): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0025 | 0/0 | 8195 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8190): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0026 | 0/0 | 8196 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8191): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0027 | 0/0 | 8199 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8194): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0028 | 0/0 | 8198 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8193): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0029 | 0/0 | 8195 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8190): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0030 | 0/0 | 8209 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8204): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0031 | 0/0 | 8201 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8196): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0032 | 0/0 | 8185 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8180): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0033 | 0/0 | 8189 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8184): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0034 | 0/0 | 8188 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8183): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0035 | 0/0 | 8187 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8182): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0036 | 0/0 | 8200 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8195): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0037 | 0/0 | 8187 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8182): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0039 | 0/0 | 8200 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8195): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0040 | 0/0 | 8197 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8192): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0051 | 0/0 | 8203 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8198): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0053 | 0/0 | 8203 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8198): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0054 | 0/0 | 8201 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8196): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0055 | 0/0 | 8202 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8197): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0056 | 0/0 | 8200 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8195): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0057 | 0/0 | 8200 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8195): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0062 | 0/0 | 8201 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8196): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0064 | 0/0 | 8200 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8195): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0065 | 0/0 | 8195 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8190): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0066 | 1/0 | 8195 | 1 | 0 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8190): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0067 | 0/0 | 8193 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8188): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0068 | 0/0 | 8195 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8190): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0069 | 0/0 | 8196 | 1 | 0 | 0 | 0 | 1 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8191): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0070 | 0/0 | 8198 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8193): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0071 | 0/0 | 8195 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8190): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0072 | 0/0 | 8194 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8189): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0073 | 0/0 | 8195 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8190): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0074 | 0/0 | 8196 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8191): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0075 | 0/0 | 8197 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8192): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0076 | 0/0 | 8197 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8192): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0077 | 0/0 | 8192 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8187): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0078 | 0/0 | 8193 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8188): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0079 | 0/1 | 8194 | 1 | 0 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8189): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0080 | 0/0 | 8194 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8189): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0081 | 0/0 | 8193 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8188): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0082 | 0/0 | 8193 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8188): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0083 | 0/0 | 8194 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8189): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0084 | 0/0 | 8195 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8190): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0085 | 0/0 | 8196 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8191): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0086 | 0/0 | 8196 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8191): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0087 | 0/0 | 8196 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8191): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0088 | 0/0 | 8194 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8189): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0089 | 0/0 | 8193 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8188): Show |
chr16 | 48239300 | 48362349 |
| a0001c0001t0090 | 0/0 | 8199 | 1 | 0 | 0 | 0 | 1 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8194): Show |
chr16 | 48239300 | 48362349 |
| a0001c0002t0041 | 0/0 | 8217 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8212): Show |
chr16 | 48239300 | 48362349 |
| a0001c0002t0042 | 0/0 | 8209 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8204): Show |
chr16 | 48239300 | 48362349 |
| a0001c0002t0043 | 0/0 | 8192 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8187): Show |
chr16 | 48239300 | 48362349 |
| a0001c0002t0044 | 0/0 | 8208 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8203): Show |
chr16 | 48239300 | 48362349 |
| a0001c0002t0045 | 0/0 | 8206 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8201): Show |
chr16 | 48239300 | 48362349 |
| a0001c0002t0046 | 0/0 | 8207 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8202): Show |
chr16 | 48239300 | 48362349 |
| a0001c0002t0047 | 0/0 | 8217 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8212): Show |
chr16 | 48239300 | 48362349 |
| a0001c0002t0048 | 0/0 | 8207 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8202): Show |
chr16 | 48239300 | 48362349 |
| a0001c0002t0049 | 0/0 | 8195 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8190): Show |
chr16 | 48239300 | 48362349 |
| a0001c0002t0050 | 0/0 | 8193 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8188): Show |
chr16 | 48239300 | 48362349 |
| a0001c0003t0058 | 0/0 | 8200 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8195): Show |
chr16 | 48239300 | 48362349 |
| a0001c0003t0059 | 0/0 | 8201 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8196): Show |
chr16 | 48239300 | 48362349 |
| a0001c0003t0060 | 0/0 | 8199 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8194): Show |
chr16 | 48239300 | 48362349 |
| a0001c0003t0061 | 0/0 | 8199 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8194): Show |
chr16 | 48239300 | 48362349 |
| a0001c0004t0063 | 0/0 | 8196 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8191): Show |
chr16 | 48239300 | 48362349 |
| a0001c0006t0038 | 0/0 | 8208 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8203): Show |
chr16 | 48239300 | 48362349 |
| a0001c0008t0010 | 0/0 | 8195 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8190): Show |
chr16 | 48239300 | 48362349 |
| a0002c0005t0052 | 0/0 | 8200 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8195): Show |
chr16 | 48239300 | 48362349 |
| a0003c0007t0007 | 0/0 | 8200 | 1 | 0 | 0 | 0 | 1 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | GGGTC others(8195): Show |
chr16 | 48239300 | 48362349 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0002g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0004g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0004g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0005g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0005g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0005g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0005g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0006g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0006g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0006g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0007g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0007g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0008g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0008g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0008g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0009g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0009g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0009g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0010g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0010g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0011g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0011g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0011g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0012g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0012g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0012g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0013g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0013g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0014g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0014g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0015g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0015g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0016g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0016g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0017g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0017g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0018g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0018g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0019g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0019g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0020g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0020g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0021g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0022g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0023g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0024g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0025g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0026g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0027g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0028g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0029g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0030g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0031g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0032g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0033g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0034g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0035g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0036g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0037g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0039g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0040g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0051g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0053g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0054g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0055g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0056g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0057g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0062g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0064g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0065g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0066g0049 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0067g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0068g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0069g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0070g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0071g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0072g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0073g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0074g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0075g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0076g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0077g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0078g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0079g0097 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0080g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0081g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0082g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0083g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0084g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0085g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0086g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0087g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0088g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0089g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0001t0090g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0002t0041g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0002t0042g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0002t0043g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0002t0044g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0002t0045g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0002t0046g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0002t0047g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0002t0048g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0002t0049g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0002t0050g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0003t0058g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0003t0059g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0003t0060g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0003t0061g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0004t0063g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0006t0038g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0001c0008t0010g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0002c0005t0052g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| a0003c0007t0007g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0024 | EUR | FIN | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG00323 | hp2 | a0001 | c0001 | t0016 | g0131 | EUR | FIN | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | CHS | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG00621 | hp1 | a0001 | c0001 | t0011 | g0051 | EAS | CHS | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG00621 | hp2 | a0001 | c0001 | t0011 | g0096 | EAS | CHS | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG00642 | hp1 | a0001 | c0001 | t0021 | g0039 | AMR | PUR | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG00642 | hp2 | a0001 | c0001 | t0084 | g0032 | AMR | PUR | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0028 | AMR | PUR | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG00733 | hp2 | a0001 | c0001 | t0056 | g0001 | AMR | PUR | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG00738 | hp1 | a0001 | c0001 | t0087 | g0027 | AMR | PUR | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG00738 | hp2 | a0001 | c0001 | t0015 | g0109 | AMR | PUR | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG00741 | hp1 | a0001 | c0001 | t0015 | g0108 | AMR | PUR | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG00741 | hp2 | a0001 | c0001 | t0020 | g0063 | AMR | PUR | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0065 | AMR | PUR | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01070 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | PUR | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01071 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | PUR | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01081 | hp2 | a0001 | c0001 | t0005 | g0132 | AMR | PUR | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0074 | AMR | PUR | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01099 | hp2 | a0001 | c0001 | t0007 | g0130 | AMR | PUR | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01106 | hp1 | a0001 | c0001 | t0073 | g0022 | AMR | PUR | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01106 | hp2 | a0001 | c0001 | t0016 | g0001 | AMR | PUR | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0111 | AMR | PUR | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01109 | hp2 | a0001 | c0001 | t0076 | g0064 | AMR | PUR | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01175 | hp1 | a0001 | c0001 | t0054 | g0139 | AMR | PUR | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0078 | AMR | PUR | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01243 | hp2 | a0001 | c0001 | t0006 | g0129 | AMR | PUR | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01515 | hp1 | a0001 | c0001 | t0069 | g0066 | EUR | IBS | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01515 | hp2 | a0001 | c0001 | t0090 | g0106 | EUR | IBS | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01884 | hp1 | a0001 | c0002 | t0043 | g0011 | AFR | ACB | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01884 | hp2 | a0001 | c0001 | t0024 | g0118 | AFR | ACB | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01891 | hp1 | a0001 | c0001 | t0034 | g0125 | AFR | ACB | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01891 | hp2 | a0001 | c0001 | t0014 | g0101 | AFR | ACB | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01975 | hp1 | a0001 | c0001 | t0017 | g0004 | AMR | PEL | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01975 | hp2 | a0001 | c0001 | t0077 | g0002 | AMR | PEL | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01993 | hp1 | a0001 | c0001 | t0088 | g0071 | AMR | PEL | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01993 | hp2 | a0001 | c0001 | t0072 | g0035 | AMR | PEL | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02055 | hp1 | a0001 | c0001 | t0006 | g0136 | AFR | ACB | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02055 | hp2 | a0001 | c0001 | t0010 | g0021 | AFR | ACB | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02074 | hp1 | a0001 | c0001 | t0055 | g0141 | EAS | KHV | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02074 | hp2 | a0001 | c0008 | t0010 | g0057 | EAS | KHV | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02083 | hp1 | a0001 | c0001 | t0008 | g0089 | EAS | KHV | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02083 | hp2 | a0001 | c0001 | t0057 | g0140 | EAS | KHV | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02129 | hp1 | a0001 | c0001 | t0012 | g0044 | EAS | KHV | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02129 | hp2 | a0001 | c0001 | t0012 | g0055 | EAS | KHV | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02145 | hp1 | a0001 | c0001 | t0006 | g0133 | AFR | ACB | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02145 | hp2 | a0001 | c0001 | t0023 | g0115 | AFR | ACB | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | CDX | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02155 | hp2 | a0001 | c0001 | t0082 | g0026 | EAS | CDX | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02258 | hp1 | a0001 | c0001 | t0027 | g0102 | AFR | ACB | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02258 | hp2 | a0001 | c0001 | t0068 | g0077 | AFR | ACB | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02280 | hp1 | a0001 | c0001 | t0029 | g0113 | AFR | ACB | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02280 | hp2 | a0001 | c0001 | t0065 | g0030 | AFR | ACB | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02572 | hp1 | a0001 | c0001 | t0013 | g0099 | AFR | GWD | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02615 | hp1 | a0001 | c0001 | t0018 | g0040 | AFR | GWD | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02615 | hp2 | a0002 | c0005 | t0052 | g0138 | AFR | GWD | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0085 | AFR | GWD | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02622 | hp2 | a0001 | c0002 | t0050 | g0007 | AFR | GWD | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02647 | hp1 | a0001 | c0001 | t0009 | g0076 | AFR | GWD | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02647 | hp2 | a0001 | c0002 | t0042 | g0009 | AFR | GWD | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02723 | hp1 | a0001 | c0002 | t0045 | g0012 | AFR | GWD | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02723 | hp2 | a0001 | c0002 | t0049 | g0017 | AFR | GWD | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02735 | hp1 | a0001 | c0001 | t0083 | g0112 | SAS | PJL | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02735 | hp2 | a0001 | c0001 | t0064 | g0088 | SAS | PJL | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02818 | hp2 | a0001 | c0002 | t0048 | g0008 | AFR | GWD | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02886 | hp1 | a0001 | c0001 | t0026 | g0114 | AFR | GWD | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02895 | hp1 | a0001 | c0003 | t0061 | g0120 | AFR | GWD | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | GWD | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02896 | hp1 | a0001 | c0001 | t0030 | g0143 | AFR | GWD | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0086 | AFR | GWD | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02897 | hp1 | a0001 | c0003 | t0060 | g0122 | AFR | GWD | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0087 | AFR | GWD | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02922 | hp1 | a0001 | c0001 | t0009 | g0019 | AFR | ESN | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | ESN | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02965 | hp1 | a0001 | c0001 | t0067 | g0068 | AFR | ESN | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02965 | hp2 | a0001 | c0001 | t0035 | g0127 | AFR | ESN | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02970 | hp1 | a0001 | c0001 | t0037 | g0126 | AFR | ESN | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02970 | hp2 | a0001 | c0004 | t0063 | g0094 | AFR | ESN | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02976 | hp1 | a0001 | c0001 | t0008 | g0093 | AFR | ESN | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02976 | hp2 | a0001 | c0002 | t0044 | g0014 | AFR | ESN | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03098 | hp1 | a0001 | c0001 | t0022 | g0117 | AFR | MSL | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03098 | hp2 | a0001 | c0001 | t0014 | g0005 | AFR | MSL | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03130 | hp1 | a0001 | c0001 | t0028 | g0005 | AFR | ESN | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0062 | AFR | ESN | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0083 | AFR | ESN | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03139 | hp2 | a0001 | c0002 | t0046 | g0013 | AFR | ESN | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03195 | hp1 | a0001 | c0001 | t0053 | g0134 | AFR | ESN | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03195 | hp2 | a0001 | c0001 | t0089 | g0067 | AFR | ESN | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03209 | hp1 | a0001 | c0001 | t0080 | g0025 | AFR | MSL | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03209 | hp2 | a0001 | c0003 | t0058 | g0123 | AFR | MSL | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0128 | AFR | MSL | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03225 | hp2 | a0001 | c0001 | t0009 | g0020 | AFR | MSL | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0029 | SAS | PJL | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03239 | hp2 | a0001 | c0001 | t0005 | g0001 | SAS | PJL | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03453 | hp1 | a0001 | c0001 | t0019 | g0018 | AFR | MSL | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03453 | hp2 | a0001 | c0006 | t0038 | g0144 | AFR | MSL | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03486 | hp1 | a0001 | c0001 | t0032 | g0124 | AFR | MSL | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03486 | hp2 | a0001 | c0001 | t0019 | g0069 | AFR | MSL | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0107 | SAS | PJL | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0016 | SAS | PJL | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03540 | hp1 | a0001 | c0001 | t0081 | g0070 | AFR | GWD | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03540 | hp2 | a0001 | c0001 | t0074 | g0081 | AFR | GWD | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03927 | hp1 | a0001 | c0001 | t0075 | g0082 | SAS | BEB | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03927 | hp2 | a0001 | c0001 | t0086 | g0080 | SAS | BEB | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03942 | hp1 | a0001 | c0001 | t0007 | g0137 | SAS | BEB | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0043 | SAS | BEB | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG04115 | hp1 | a0001 | c0001 | t0011 | g0056 | SAS | STU | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0023 | SAS | STU | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG04199 | hp1 | a0001 | c0001 | t0071 | g0098 | SAS | STU | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG04199 | hp2 | a0001 | c0001 | t0070 | g0061 | SAS | STU | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG04204 | hp1 | a0001 | c0001 | t0020 | g0036 | SAS | STU | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0075 | SAS | STU | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| NA18906 | hp1 | a0001 | c0001 | t0040 | g0119 | AFR | YRI | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| NA18906 | hp2 | a0001 | c0001 | t0051 | g0146 | AFR | YRI | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| NA18986 | hp1 | a0001 | c0001 | t0012 | g0092 | EAS | JPT | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| NA18986 | hp2 | a0001 | c0001 | t0008 | g0090 | EAS | JPT | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| NA19043 | hp1 | a0001 | c0001 | t0025 | g0116 | AFR | LWK | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| NA19043 | hp2 | a0001 | c0001 | t0018 | g0042 | AFR | LWK | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| NA19068 | hp1 | a0001 | c0001 | t0085 | g0045 | EAS | JPT | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| NA19068 | hp2 | a0001 | c0001 | t0017 | g0054 | EAS | JPT | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0095 | AFR | YRI | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| NA19240 | hp2 | a0001 | c0001 | t0033 | g0147 | AFR | YRI | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| NA20129 | hp1 | a0001 | c0001 | t0078 | g0048 | AFR | ASW | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| NA20129 | hp2 | a0001 | c0002 | t0047 | g0010 | AFR | ASW | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0053 | EUR | TSI | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| NA20752 | hp2 | a0003 | c0007 | t0007 | g0135 | EUR | TSI | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01123 | hp1 | a0001 | c0001 | t0039 | g0105 | AMR | CLM | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0060 | AFR | ACB | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02109 | hp2 | a0001 | c0001 | t0031 | g0103 | AFR | ACB | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02486 | hp1 | a0001 | c0001 | t0013 | g0100 | AFR | ACB | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02486 | hp2 | a0001 | c0003 | t0059 | g0121 | AFR | ACB | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02559 | hp1 | a0001 | c0001 | t0036 | g0104 | AFR | ACB | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03471 | hp1 | a0001 | c0001 | t0062 | g0142 | AFR | MSL | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | MSL | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0110 | AFR | USA | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| HG06807 | hp2 | a0001 | c0001 | t0010 | g0041 | AFR | USA | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | USA | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| NA20300 | hp2 | a0001 | c0002 | t0041 | g0015 | AFR | USA | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0079 | g0097 | REF | REF | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0066 | g0049 | REF | REF | LONP2_chr16_48239300_48362349 | LONP2 | chr16 | 48239300 | 48362349 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:48296051 | C | T | 1 | a0003 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.1420C>T | p.His474Tyr | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/15 | 1509/8195 | 1420/2559 | 474/852 | chr16 | 48296051 | |||
| chr16:48351717 | G | A | 1 | a0002 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.2474G>A | p.Ser825Asn | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2563/8195 | 2474/2559 | 825/852 | chr16 | 48351717 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:48244556 | C | T | 1 | a0001c0008 | 1 | HG02074.hp2 | synonymous_variant | LOW | c.168C>T | p.Ile56Ile | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/15 | 257/8195 | 168/2559 | 56/852 | chr16 | 48244556 | |||
| chr16:48244580 | T | C | 1 | a0001c0003 | 4 | HG02486.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
synonymous_variant | LOW | c.192T>C | p.Pro64Pro | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/15 | 281/8195 | 192/2559 | 64/852 | chr16 | 48244580 | |||
| chr16:48347536 | A | C | 1 | a0001c0006 | 1 | HG03453.hp2 | synonymous_variant | LOW | c.1968A>C | p.Val656Val | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 13/15 | 2057/8195 | 1968/2559 | 656/852 | chr16 | 48347536 | |||
| chr16:48351607 | G | C | 1 | a0001c0004 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.2364G>C | p.Leu788Leu | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2453/8195 | 2364/2559 | 788/852 | chr16 | 48351607 | |||
| chr16:48351622 | G | A | 1 | a0001c0002 | 10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
synonymous_variant | LOW | c.2379G>A | p.Ala793Ala | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2468/8195 | 2379/2559 | 793/852 | chr16 | 48351622 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:48244331 | C | A | 1 | a0001c0001t0021 | 1 | HG00642.hp1 | 5_prime_UTR_variant | MODIFIER | c.-58C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/15 | 58 | chr16 | 48244331 | ||||||
| chr16:48244380 | G | T | 1 | a0001c0001t0090 | 1 | HG01515.hp2 | 5_prime_UTR_variant | MODIFIER | c.-9G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/15 | 9 | chr16 | 48244380 | ||||||
| chr16:48352046 | T | C | 51 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(48): Show |
64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*244T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 244 | chr16 | 48352046 | ||||||
| chr16:48352115 | G | A | 5 | a0001c0001t0022 a0001c0001t0023 a0001c0001t0024 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 HG02886.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*313G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 313 | chr16 | 48352115 | ||||||
| chr16:48352225 | A | C | 1 | a0001c0001t0062 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*423A>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 423 | chr16 | 48352225 | ||||||
| chr16:48352234 | C | T | 4 | a0001c0003t0058 a0001c0003t0059 a0001c0003t0060 others(1): Show |
4 | HG02486.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*432C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 432 | chr16 | 48352234 | ||||||
| chr16:48352353 | A | G | 12 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0007 others(9): Show |
19 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*551A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 551 | chr16 | 48352353 | ||||||
| chr16:48352368 | G | A | 4 | a0001c0001t0013 a0001c0001t0014 a0001c0001t0027 others(1): Show |
6 | HG01891.hp2 HG02258.hp1 HG02486.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*566G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 566 | chr16 | 48352368 | ||||||
| chr16:48352372 | G | A | 5 | a0001c0001t0022 a0001c0001t0023 a0001c0001t0024 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 HG02886.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*570G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 570 | chr16 | 48352372 | ||||||
| chr16:48352464 | G | C | 5 | a0001c0001t0022 a0001c0001t0023 a0001c0001t0024 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 HG02886.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*662G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 662 | chr16 | 48352464 | ||||||
| chr16:48352720 | A | G | 10 | a0001c0002t0041 a0001c0002t0042 a0001c0002t0043 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*918A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 918 | chr16 | 48352720 | ||||||
| chr16:48352821 | A | G | 1 | a0001c0001t0089 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1019A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 1019 | chr16 | 48352821 | ||||||
| chr16:48353271 | C | T | 1 | a0001c0001t0040 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1469C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 1469 | chr16 | 48353271 | ||||||
| chr16:48353392 | C | A | 1 | a0001c0004t0063 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1590C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 1590 | chr16 | 48353392 | ||||||
| chr16:48353408 | TG | T | 8 | a0001c0002t0041 a0001c0002t0042 a0001c0002t0043 others(5): Show |
8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1609delG | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 1609 | INFO_REALIGN_3_PRIME | chr16 | 48353408 | |||||
| chr16:48353440 | G | A | 1 | a0001c0001t0029 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1638G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 1638 | chr16 | 48353440 | ||||||
| chr16:48353443 | A | C | 1 | a0001c0001t0088 | 1 | HG01993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1641A>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 1641 | chr16 | 48353443 | ||||||
| chr16:48353465 | G | A | 4 | a0001c0003t0058 a0001c0003t0059 a0001c0003t0060 others(1): Show |
4 | HG02486.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1663G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 1663 | chr16 | 48353465 | ||||||
| chr16:48353496 | C | CA | 12 | a0001c0001t0022 a0001c0001t0023 a0001c0002t0041 others(9): Show |
12 | HG01884.hp1 HG02145.hp2 HG02622.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1715dupA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 1716 | INFO_REALIGN_3_PRIME | chr16 | 48353496 | |||||
| chr16:48353496 | CA | C | 62 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(59): Show |
122 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*1715delA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 1715 | INFO_REALIGN_3_PRIME | chr16 | 48353496 | |||||
| chr16:48353571 | T | C | 1 | a0002c0005t0052 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1769T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 1769 | chr16 | 48353571 | ||||||
| chr16:48353769 | C | T | 4 | a0001c0001t0004 a0001c0001t0015 a0001c0001t0039 others(1): Show |
8 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1967C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 1967 | chr16 | 48353769 | ||||||
| chr16:48353998 | TG | T | 10 | a0001c0002t0041 a0001c0002t0042 a0001c0002t0043 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2197delG | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2197 | chr16 | 48353998 | ||||||
| chr16:48353999 | G | GT | 5 | a0001c0001t0013 a0001c0001t0014 a0001c0001t0027 others(2): Show |
7 | HG01891.hp2 HG02258.hp1 HG02486.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2207dupT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2208 | INFO_REALIGN_3_PRIME | chr16 | 48353999 | |||||
| chr16:48353999 | G | T | 1 | a0001c0001t0003 | 1 | NA18983.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2197G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2197 | chr16 | 48353999 | ||||||
| chr16:48354000 | T | A | 10 | a0001c0002t0041 a0001c0002t0042 a0001c0002t0043 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2198T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2198 | chr16 | 48354000 | ||||||
| chr16:48354078 | T | TG | 5 | a0001c0001t0013 a0001c0001t0068 a0001c0001t0090 others(2): Show |
6 | HG01515.hp2 HG02258.hp2 HG02486.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2276_*2277insG | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2277 | chr16 | 48354078 | ||||||
| chr16:48354078 | T | TGG | 3 | a0001c0002t0041 a0001c0003t0058 a0001c0003t0059 |
3 | HG02486.hp2 HG03209.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2276_*2277insGG | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2277 | chr16 | 48354078 | ||||||
| chr16:48354079 | T | G | 14 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0013 others(11): Show |
21 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2277T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2277 | chr16 | 48354079 | ||||||
| chr16:48354079 | T | TG | 25 | a0001c0001t0010 a0001c0001t0011 a0001c0001t0016 others(22): Show |
29 | HG00323.hp2 HG00621.hp1 HG00621.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*2285dupG | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2286 | INFO_REALIGN_3_PRIME | chr16 | 48354079 | |||||
| chr16:48354079 | T | TGG | 19 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0007 others(16): Show |
26 | HG01081.hp2 HG01099.hp2 HG01109.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*2284_*2285dupGG | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2286 | INFO_REALIGN_3_PRIME | chr16 | 48354079 | |||||
| chr16:48354184 | C | A | 4 | a0001c0001t0004 a0001c0001t0015 a0001c0001t0039 others(1): Show |
8 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2382C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2382 | chr16 | 48354184 | ||||||
| chr16:48354194 | C | T | 5 | a0001c0001t0007 a0001c0001t0054 a0001c0001t0055 others(2): Show |
6 | HG01099.hp2 HG01175.hp1 HG02074.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2392C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2392 | chr16 | 48354194 | ||||||
| chr16:48354196 | C | CT | 14 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0011 others(11): Show |
36 | HG00621.hp1 HG00621.hp2 HG00642.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*2423dupT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2424 | INFO_REALIGN_3_PRIME | chr16 | 48354196 | |||||
| chr16:48354196 | C | CTT | 7 | a0001c0001t0069 a0001c0001t0070 a0001c0001t0075 others(4): Show |
7 | HG00738.hp1 HG01109.hp2 HG01515.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2422_*2423dupTT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2424 | INFO_REALIGN_3_PRIME | chr16 | 48354196 | |||||
| chr16:48354196 | C | CTTTTT | 4 | a0001c0001t0020 a0001c0001t0030 a0001c0001t0064 others(1): Show |
5 | HG00741.hp2 HG02735.hp2 HG02896.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2419_*2423dupTTTT others(1): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2424 | INFO_REALIGN_3_PRIME | chr16 | 48354196 | |||||
| chr16:48354196 | C | CTTTTTTT others(6): Show |
1 | a0001c0002t0045 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2411_*2423dupTTTT others(9): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2424 | INFO_REALIGN_3_PRIME | chr16 | 48354196 | |||||
| chr16:48354196 | C | CTTTTTTT others(7): Show |
3 | a0001c0002t0042 a0001c0002t0044 a0001c0002t0046 |
3 | HG02647.hp2 HG02976.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2410_*2423dupTTTT others(10): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2424 | INFO_REALIGN_3_PRIME | chr16 | 48354196 | |||||
| chr16:48354196 | C | CTTTTTTT others(8): Show |
1 | a0001c0002t0048 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2409_*2423dupTTTT others(11): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2424 | INFO_REALIGN_3_PRIME | chr16 | 48354196 | |||||
| chr16:48354196 | C | CTTTTTTT others(16): Show |
1 | a0001c0002t0041 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2401_*2423dupTTTT others(19): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2424 | INFO_REALIGN_3_PRIME | chr16 | 48354196 | |||||
| chr16:48354196 | C | CTTTTTTT others(17): Show |
1 | a0001c0002t0047 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2400_*2423dupTTTT others(20): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2424 | INFO_REALIGN_3_PRIME | chr16 | 48354196 | |||||
| chr16:48354196 | CT | C | 7 | a0001c0001t0023 a0001c0001t0027 a0001c0001t0040 others(4): Show |
7 | HG02074.hp1 HG02145.hp2 HG02258.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2423delT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2423 | INFO_REALIGN_3_PRIME | chr16 | 48354196 | |||||
| chr16:48354196 | CTT | C | 10 | a0001c0001t0006 a0001c0001t0022 a0001c0001t0026 others(7): Show |
12 | HG00733.hp2 HG01175.hp1 HG01243.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2422_*2423delTT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2422 | INFO_REALIGN_3_PRIME | chr16 | 48354196 | |||||
| chr16:48354196 | CTTT | C | 9 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0016 others(6): Show |
14 | HG00323.hp2 HG01081.hp2 HG01099.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2421_*2423delTTT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2421 | INFO_REALIGN_3_PRIME | chr16 | 48354196 | |||||
| chr16:48354351 | G | T | 1 | a0001c0001t0027 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2549G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2549 | chr16 | 48354351 | ||||||
| chr16:48354424 | G | A | 5 | a0001c0001t0032 a0001c0001t0033 a0001c0001t0034 others(2): Show |
5 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2622G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2622 | chr16 | 48354424 | ||||||
| chr16:48354489 | G | A | 8 | a0001c0002t0041 a0001c0002t0042 a0001c0002t0043 others(5): Show |
8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2687G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2687 | chr16 | 48354489 | ||||||
| chr16:48354510 | A | G | 1 | a0001c0001t0074 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2708A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2708 | chr16 | 48354510 | ||||||
| chr16:48354606 | ACTTT | A | 5 | a0001c0001t0032 a0001c0001t0033 a0001c0001t0034 others(2): Show |
5 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2811_*2814delTTCT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2811 | INFO_REALIGN_3_PRIME | chr16 | 48354606 | |||||
| chr16:48354678 | C | T | 1 | a0001c0001t0040 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2876C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 2876 | chr16 | 48354678 | ||||||
| chr16:48354876 | A | AGT | 5 | a0001c0001t0022 a0001c0001t0023 a0001c0001t0024 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 HG02886.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3074_*3075insGT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 3075 | chr16 | 48354876 | ||||||
| chr16:48354877 | C | CAGTT | 28 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(25): Show |
41 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*3078_*3081dupTTAG | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 3082 | INFO_REALIGN_3_PRIME | chr16 | 48354877 | |||||
| chr16:48354877 | C | CAGTTAGT others(1): Show |
3 | a0001c0001t0030 a0001c0001t0062 a0001c0006t0038 |
3 | HG02896.hp1 HG03453.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3081_*3082insTTAG others(4): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 3082 | INFO_REALIGN_3_PRIME | chr16 | 48354877 | |||||
| chr16:48354877 | C | T | 5 | a0001c0001t0022 a0001c0001t0023 a0001c0001t0024 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 HG02886.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3075C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 3075 | chr16 | 48354877 | ||||||
| chr16:48355036 | G | A | 5 | a0001c0001t0032 a0001c0001t0033 a0001c0001t0034 others(2): Show |
5 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3234G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 3234 | chr16 | 48355036 | ||||||
| chr16:48355125 | G | GAAGT | 12 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0007 others(9): Show |
19 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*3324_*3327dupAAGT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 3328 | INFO_REALIGN_3_PRIME | chr16 | 48355125 | |||||
| chr16:48355691 | A | G | 4 | a0001c0001t0032 a0001c0001t0034 a0001c0001t0035 others(1): Show |
4 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3889A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 3889 | chr16 | 48355691 | ||||||
| chr16:48355927 | A | G | 12 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0007 others(9): Show |
19 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*4125A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 4125 | chr16 | 48355927 | ||||||
| chr16:48355954 | TTTGC | T | 5 | a0001c0001t0032 a0001c0001t0033 a0001c0001t0034 others(2): Show |
5 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4155_*4158delGCTT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 4155 | INFO_REALIGN_3_PRIME | chr16 | 48355954 | |||||
| chr16:48356006 | T | C | 2 | a0001c0001t0031 a0001c0001t0036 |
2 | HG02109.hp2 HG02559.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4204T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 4204 | chr16 | 48356006 | ||||||
| chr16:48356034 | G | A | 6 | a0001c0001t0013 a0001c0001t0014 a0001c0001t0027 others(3): Show |
8 | HG01891.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4232G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 4232 | chr16 | 48356034 | ||||||
| chr16:48356161 | G | A | 3 | a0001c0001t0012 a0001c0001t0075 a0001c0001t0085 |
5 | HG02129.hp1 HG02129.hp2 HG03927.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4359G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 4359 | chr16 | 48356161 | ||||||
| chr16:48356187 | C | A | 8 | a0001c0002t0041 a0001c0002t0042 a0001c0002t0043 others(5): Show |
8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*4385C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 4385 | chr16 | 48356187 | ||||||
| chr16:48356324 | C | T | 1 | a0001c0001t0083 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4522C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 4522 | chr16 | 48356324 | ||||||
| chr16:48356466 | T | G | 2 | a0001c0001t0065 a0001c0001t0080 |
2 | HG02280.hp2 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4664T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 4664 | chr16 | 48356466 | ||||||
| chr16:48356512 | T | TA | 8 | a0001c0001t0017 a0001c0001t0018 a0001c0001t0032 others(5): Show |
10 | HG01891.hp1 HG01975.hp1 HG02615.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4731dupA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 4732 | INFO_REALIGN_3_PRIME | chr16 | 48356512 | |||||
| chr16:48356512 | TA | T | 8 | a0001c0001t0012 a0001c0001t0019 a0001c0001t0030 others(5): Show |
11 | HG01106.hp1 HG01993.hp2 HG02129.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4731delA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 4731 | INFO_REALIGN_3_PRIME | chr16 | 48356512 | |||||
| chr16:48356512 | TAA | T | 11 | a0001c0001t0062 a0001c0001t0067 a0001c0002t0041 others(8): Show |
11 | HG01884.hp1 HG02622.hp2 HG02723.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4730_*4731delAA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 4730 | INFO_REALIGN_3_PRIME | chr16 | 48356512 | |||||
| chr16:48356601 | G | T | 12 | a0001c0001t0003 a0001c0001t0020 a0001c0001t0064 others(9): Show |
19 | HG00323.hp1 HG00642.hp2 HG00733.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*4799G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 4799 | chr16 | 48356601 | ||||||
| chr16:48356869 | TA | T | 11 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0007 others(8): Show |
18 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*5070delA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 5070 | INFO_REALIGN_3_PRIME | chr16 | 48356869 | |||||
| chr16:48356980 | C | T | 51 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(48): Show |
64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*5178C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 5178 | chr16 | 48356980 | ||||||
| chr16:48357046 | A | G | 5 | a0001c0001t0022 a0001c0001t0023 a0001c0001t0024 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 HG02886.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5244A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 5244 | chr16 | 48357046 | ||||||
| chr16:48357237 | C | T | 35 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(32): Show |
48 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*5435C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 5435 | chr16 | 48357237 | ||||||
| chr16:48357263 | C | CTGTT | 1 | a0001c0001t0018 | 2 | HG02615.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5464_*5467dupTTTG | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 15/15 | 5468 | INFO_REALIGN_3_PRIME | chr16 | 48357263 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:48244714 | A | G | 38 | a0001c0001t0001g0145 a0001c0001t0005g0001 a0001c0001t0005g0128 others(35): Show |
38 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.233+93A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48244714 | |||||||
| chr16:48244751 | T | C | 38 | a0001c0001t0001g0145 a0001c0001t0005g0001 a0001c0001t0005g0128 others(35): Show |
38 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.233+130T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48244751 | |||||||
| chr16:48244790 | C | T | 3 | a0001c0001t0001g0145 a0001c0001t0033g0147 a0001c0001t0051g0146 |
3 | HG02818.hp1 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.233+169C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48244790 | |||||||
| chr16:48244798 | C | G | 1 | a0001c0001t0083g0112 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.233+177C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48244798 | |||||||
| chr16:48244812 | G | T | 3 | a0001c0001t0030g0143 a0001c0001t0062g0142 a0001c0006t0038g0144 |
3 | HG02896.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.233+191G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48244812 | |||||||
| chr16:48244889 | T | C | 1 | a0001c0001t0029g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.233+268T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48244889 | |||||||
| chr16:48244897 | T | C | 1 | a0001c0002t0050g0007 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.233+276T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48244897 | |||||||
| chr16:48245107 | C | A | 8 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(5): Show |
8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.233+486C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48245107 | |||||||
| chr16:48245181 | C | G | 18 | a0001c0001t0005g0001 a0001c0001t0005g0111 a0001c0001t0005g0128 others(15): Show |
18 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.233+560C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48245181 | |||||||
| chr16:48245241 | C | T | 3 | a0001c0001t0030g0143 a0001c0001t0062g0142 a0001c0006t0038g0144 |
3 | HG02896.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.233+620C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48245241 | |||||||
| chr16:48245333 | G | C | 1 | a0001c0001t0003g0016 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.233+712G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48245333 | |||||||
| chr16:48245339 | T | C | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+718T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48245339 | |||||||
| chr16:48245422 | A | T | 52 | a0001c0001t0001g0145 a0001c0001t0004g0006 a0001c0001t0004g0107 others(49): Show |
53 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.233+801A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48245422 | |||||||
| chr16:48245512 | T | C | 1 | a0001c0001t0019g0018 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.233+891T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48245512 | |||||||
| chr16:48245600 | C | T | 4 | a0001c0001t0032g0124 a0001c0001t0034g0125 a0001c0001t0035g0127 others(1): Show |
4 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.233+979C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48245600 | |||||||
| chr16:48245604 | C | T | 8 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(5): Show |
8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.233+983C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48245604 | |||||||
| chr16:48245621 | GGA | G | 4 | a0001c0003t0058g0123 a0001c0003t0059g0121 a0001c0003t0060g0122 others(1): Show |
4 | HG02486.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.233+1002_233+1003d others(4): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 48245621 | ||||||
| chr16:48245635 | C | T | 1 | a0001c0002t0050g0007 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.233+1014C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48245635 | |||||||
| chr16:48245895 | C | T | 7 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(4): Show |
8 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.233+1274C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48245895 | |||||||
| chr16:48245926 | T | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+1305T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48245926 | |||||||
| chr16:48245944 | C | T | 8 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(5): Show |
8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.233+1323C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48245944 | |||||||
| chr16:48246004 | C | T | 1 | a0001c0001t0040g0119 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.233+1383C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48246004 | |||||||
| chr16:48246044 | G | C | 3 | a0001c0001t0030g0143 a0001c0001t0062g0142 a0001c0006t0038g0144 |
3 | HG02896.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.233+1423G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48246044 | |||||||
| chr16:48246211 | C | A | 7 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(4): Show |
8 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.233+1590C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48246211 | |||||||
| chr16:48246334 | C | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+1713C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48246334 | |||||||
| chr16:48246368 | A | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+1747A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48246368 | |||||||
| chr16:48246493 | A | C | 7 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(4): Show |
8 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.233+1872A>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48246493 | |||||||
| chr16:48246706 | C | T | 1 | a0001c0001t0071g0098 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.233+2085C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48246706 | |||||||
| chr16:48246715 | T | C | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+2094T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48246715 | |||||||
| chr16:48246799 | T | C | 6 | a0001c0001t0013g0099 a0001c0001t0013g0100 a0001c0001t0014g0005 others(3): Show |
6 | HG01891.hp2 HG02258.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.233+2178T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48246799 | |||||||
| chr16:48246883 | T | C | 6 | a0001c0001t0029g0113 a0001c0001t0040g0119 a0001c0003t0058g0123 others(3): Show |
6 | HG02280.hp1 HG02486.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.233+2262T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48246883 | |||||||
| chr16:48247053 | G | A | 1 | a0001c0001t0029g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.233+2432G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48247053 | |||||||
| chr16:48247155 | A | G | 1 | a0001c0001t0029g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.233+2534A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48247155 | |||||||
| chr16:48247217 | T | TAA | 6 | a0001c0001t0022g0117 a0001c0001t0023g0115 a0001c0001t0024g0118 others(3): Show |
6 | HG01884.hp2 HG02145.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.233+2614_233+2615d others(4): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 48247217 | ||||||
| chr16:48247217 | T | TAAAGA | 8 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(5): Show |
8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.233+2599_233+2600i others(7): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 48247217 | ||||||
| chr16:48247217 | TA | T | 13 | a0001c0001t0013g0099 a0001c0001t0013g0100 a0001c0001t0014g0005 others(10): Show |
13 | HG01891.hp2 HG02074.hp1 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.233+2615delA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 48247217 | ||||||
| chr16:48247238 | G | C | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+2617G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48247238 | |||||||
| chr16:48247283 | T | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+2662T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48247283 | |||||||
| chr16:48247353 | C | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+2732C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48247353 | |||||||
| chr16:48247412 | A | AGAGCAGC others(451): Show |
10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+2831_233+2832i others(460): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 48247412 | ||||||
| chr16:48247412 | A | AGAGCAGC others(450): Show |
3 | a0001c0001t0030g0143 a0001c0001t0062g0142 a0001c0006t0038g0144 |
3 | HG02896.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.233+2831_233+2832i others(459): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 48247412 | ||||||
| chr16:48247412 | A | AGAGCAGC others(451): Show |
1 | a0001c0001t0011g0096 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.233+2831_233+2832i others(460): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 48247412 | ||||||
| chr16:48247455 | G | C | 6 | a0001c0001t0013g0099 a0001c0001t0013g0100 a0001c0001t0014g0005 others(3): Show |
6 | HG01891.hp2 HG02258.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.233+2834G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48247455 | |||||||
| chr16:48247491 | T | C | 7 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(4): Show |
8 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.233+2870T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48247491 | |||||||
| chr16:48247527 | C | G | 1 | a0001c0001t0002g0095 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.233+2906C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48247527 | |||||||
| chr16:48247705 | G | T | 1 | a0001c0004t0063g0094 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.233+3084G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48247705 | |||||||
| chr16:48247803 | A | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+3182A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48247803 | |||||||
| chr16:48247818 | C | T | 1 | a0001c0001t0008g0093 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.233+3197C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48247818 | |||||||
| chr16:48247860 | A | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.233+3239A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48247860 | |||||||
| chr16:48247946 | T | C | 2 | a0001c0001t0009g0019 a0001c0001t0009g0020 |
2 | HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.233+3325T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48247946 | |||||||
| chr16:48248377 | C | T | 1 | a0001c0001t0012g0092 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.234-3754C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48248377 | |||||||
| chr16:48248610 | G | A | 1 | a0001c0001t0062g0142 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.234-3521G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48248610 | |||||||
| chr16:48248725 | T | G | 1 | a0001c0001t0029g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.234-3406T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48248725 | |||||||
| chr16:48248757 | C | G | 1 | a0001c0001t0001g0091 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.234-3374C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48248757 | |||||||
| chr16:48248885 | G | GA | 19 | a0001c0001t0002g0023 a0001c0001t0004g0006 a0001c0001t0004g0107 others(16): Show |
20 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.234-3227dupA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 48248885 | ||||||
| chr16:48248885 | GAAA | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-3229_234-3227d others(5): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 48248885 | ||||||
| chr16:48249123 | C | T | 2 | a0001c0001t0008g0089 a0001c0001t0008g0090 |
2 | HG02083.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.234-3008C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48249123 | |||||||
| chr16:48249159 | A | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-2972A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48249159 | |||||||
| chr16:48249182 | G | T | 1 | a0001c0001t0029g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.234-2949G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48249182 | |||||||
| chr16:48249532 | G | C | 15 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(12): Show |
16 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.234-2599G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48249532 | |||||||
| chr16:48249642 | A | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-2489A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48249642 | |||||||
| chr16:48249730 | A | T | 1 | a0001c0001t0064g0088 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.234-2401A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48249730 | |||||||
| chr16:48249731 | T | A | 1 | a0001c0001t0007g0130 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.234-2400T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48249731 | |||||||
| chr16:48249813 | T | C | 1 | a0001c0001t0003g0016 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.234-2318T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48249813 | |||||||
| chr16:48249915 | G | A | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-2216G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48249915 | |||||||
| chr16:48249934 | G | A | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-2197G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48249934 | |||||||
| chr16:48250050 | G | A | 1 | a0001c0001t0007g0130 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.234-2081G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48250050 | |||||||
| chr16:48250082 | G | C | 17 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(14): Show |
18 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.234-2049G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48250082 | |||||||
| chr16:48250095 | G | A | 6 | a0001c0001t0005g0001 a0001c0001t0005g0132 a0001c0001t0006g0129 others(3): Show |
6 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.234-2036G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48250095 | |||||||
| chr16:48250146 | C | T | 1 | a0001c0001t0071g0098 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.234-1985C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48250146 | |||||||
| chr16:48250162 | G | C | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-1969G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48250162 | |||||||
| chr16:48250279 | G | C | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-1852G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48250279 | |||||||
| chr16:48250434 | A | T | 18 | a0001c0001t0005g0001 a0001c0001t0005g0111 a0001c0001t0005g0128 others(15): Show |
18 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.234-1697A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48250434 | |||||||
| chr16:48250476 | G | A | 1 | a0001c0001t0011g0096 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.234-1655G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48250476 | |||||||
| chr16:48250480 | C | CAA | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-1640_234-1639d others(4): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 48250480 | ||||||
| chr16:48250510 | C | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-1621C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48250510 | |||||||
| chr16:48250538 | A | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-1593A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48250538 | |||||||
| chr16:48250632 | T | C | 5 | a0001c0001t0029g0113 a0001c0003t0058g0123 a0001c0003t0059g0121 others(2): Show |
5 | HG02280.hp1 HG02486.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.234-1499T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48250632 | |||||||
| chr16:48251033 | A | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-1098A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48251033 | |||||||
| chr16:48251160 | C | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-971C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48251160 | |||||||
| chr16:48251195 | GTTC | G | 4 | a0001c0003t0058g0123 a0001c0003t0059g0121 a0001c0003t0060g0122 others(1): Show |
4 | HG02486.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.234-931_234-929del others(3): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 48251195 | ||||||
| chr16:48251390 | A | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-741A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48251390 | |||||||
| chr16:48251628 | C | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-503C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48251628 | |||||||
| chr16:48251639 | G | A | 1 | a0001c0001t0003g0024 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.234-492G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48251639 | |||||||
| chr16:48251862 | C | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.234-269C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48251862 | |||||||
| chr16:48251891 | C | T | 1 | a0001c0001t0002g0023 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.234-240C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48251891 | |||||||
| chr16:48251949 | A | G | 1 | a0001c0004t0063g0094 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.234-182A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 1/14 | chr16 | 48251949 | |||||||
| chr16:48252546 | A | G | 6 | a0001c0001t0013g0099 a0001c0001t0013g0100 a0001c0001t0014g0005 others(3): Show |
6 | HG01891.hp2 HG02258.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+181A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48252546 | |||||||
| chr16:48252589 | C | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.468+224C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48252589 | |||||||
| chr16:48252998 | T | A | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.468+633T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48252998 | |||||||
| chr16:48253113 | T | C | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.468+748T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48253113 | |||||||
| chr16:48253142 | A | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.468+777A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48253142 | |||||||
| chr16:48253299 | G | A | 4 | a0001c0003t0058g0123 a0001c0003t0059g0121 a0001c0003t0060g0122 others(1): Show |
4 | HG02486.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.468+934G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48253299 | |||||||
| chr16:48253368 | G | A | 2 | a0001c0001t0013g0099 a0001c0001t0013g0100 |
2 | HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.468+1003G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48253368 | |||||||
| chr16:48253469 | C | CA | 6 | a0001c0001t0013g0099 a0001c0001t0013g0100 a0001c0001t0014g0005 others(3): Show |
6 | HG01891.hp2 HG02258.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+1117dupA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 48253469 | ||||||
| chr16:48253556 | T | C | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.468+1191T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48253556 | |||||||
| chr16:48253782 | A | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.468+1417A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48253782 | |||||||
| chr16:48253925 | A | G | 4 | a0001c0001t0001g0084 a0001c0001t0002g0085 a0001c0001t0002g0086 others(1): Show |
4 | HG02622.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.468+1560A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48253925 | |||||||
| chr16:48254073 | C | T | 1 | a0001c0001t0002g0083 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.468+1708C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48254073 | |||||||
| chr16:48254117 | C | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.468+1752C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48254117 | |||||||
| chr16:48254346 | A | G | 2 | a0001c0001t0074g0081 a0001c0001t0075g0082 |
2 | HG03540.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.468+1981A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48254346 | |||||||
| chr16:48254364 | AT | A | 11 | a0001c0001t0003g0024 a0001c0001t0003g0028 a0001c0001t0003g0029 others(8): Show |
11 | HG00323.hp1 HG00621.hp2 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.468+2016delT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 48254364 | ||||||
| chr16:48254457 | G | A | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.468+2092G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48254457 | |||||||
| chr16:48254513 | G | A | 1 | a0001c0001t0030g0143 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.469-2097G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48254513 | |||||||
| chr16:48254520 | C | T | 8 | a0001c0001t0013g0099 a0001c0001t0013g0100 a0001c0001t0014g0005 others(5): Show |
8 | HG01891.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.469-2090C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48254520 | |||||||
| chr16:48254539 | G | A | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-2071G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48254539 | |||||||
| chr16:48254565 | A | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-2045A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48254565 | |||||||
| chr16:48254610 | G | A | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-2000G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48254610 | |||||||
| chr16:48254811 | C | G | 1 | a0001c0006t0038g0144 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.469-1799C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48254811 | |||||||
| chr16:48254832 | T | A | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-1778T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48254832 | |||||||
| chr16:48254898 | C | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-1712C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48254898 | |||||||
| chr16:48255053 | T | C | 2 | a0001c0001t0023g0115 a0001c0001t0025g0116 |
2 | HG02145.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.469-1557T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48255053 | |||||||
| chr16:48255101 | C | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-1509C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48255101 | |||||||
| chr16:48255167 | T | C | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-1443T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48255167 | |||||||
| chr16:48255239 | G | A | 1 | a0001c0001t0006g0129 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.469-1371G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48255239 | |||||||
| chr16:48255289 | A | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-1321A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48255289 | |||||||
| chr16:48255389 | C | G | 8 | a0001c0001t0013g0099 a0001c0001t0013g0100 a0001c0001t0014g0005 others(5): Show |
8 | HG01891.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.469-1221C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48255389 | |||||||
| chr16:48255586 | T | A | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-1024T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48255586 | |||||||
| chr16:48255599 | G | A | 2 | a0001c0001t0031g0103 a0001c0001t0036g0104 |
2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.469-1011G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48255599 | |||||||
| chr16:48255667 | C | T | 1 | a0001c0001t0084g0032 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.469-943C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48255667 | |||||||
| chr16:48255777 | G | T | 1 | a0001c0001t0003g0031 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.469-833G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48255777 | |||||||
| chr16:48255789 | G | A | 1 | a0001c0001t0011g0096 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.469-821G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48255789 | |||||||
| chr16:48256155 | G | A | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-455G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48256155 | |||||||
| chr16:48256193 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.469-417G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48256193 | |||||||
| chr16:48256252 | C | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-358C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48256252 | |||||||
| chr16:48256259 | T | C | 4 | a0001c0001t0001g0084 a0001c0001t0002g0085 a0001c0001t0002g0086 others(1): Show |
4 | HG02622.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.469-351T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48256259 | |||||||
| chr16:48256435 | T | C | 1 | a0001c0001t0006g0133 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.469-175T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 2/14 | chr16 | 48256435 | |||||||
| chr16:48256895 | GTTTTATA others(27): Show |
G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.600+192_600+225del others(34): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 48256895 | ||||||
| chr16:48257182 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.600+441G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 3/14 | chr16 | 48257182 | |||||||
| chr16:48257311 | TAAATA | T | 8 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(5): Show |
8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.600+573_600+577del others(5): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 48257311 | ||||||
| chr16:48257367 | C | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.600+626C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 3/14 | chr16 | 48257367 | |||||||
| chr16:48257538 | A | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.600+797A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 3/14 | chr16 | 48257538 | |||||||
| chr16:48257582 | TTTAAG | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.600+844_600+848del others(5): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 48257582 | ||||||
| chr16:48257612 | A | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.600+871A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 3/14 | chr16 | 48257612 | |||||||
| chr16:48257625 | A | G | 1 | a0001c0001t0005g0132 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.600+884A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 3/14 | chr16 | 48257625 | |||||||
| chr16:48257718 | T | C | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.601-900T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 3/14 | chr16 | 48257718 | |||||||
| chr16:48257878 | G | A | 5 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0034 others(2): Show |
5 | HG01175.hp2 HG01496.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.601-740G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 3/14 | chr16 | 48257878 | |||||||
| chr16:48258036 | G | A | 3 | a0001c0001t0030g0143 a0001c0001t0062g0142 a0001c0006t0038g0144 |
3 | HG02896.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.601-582G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 3/14 | chr16 | 48258036 | |||||||
| chr16:48258118 | T | C | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.601-500T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 3/14 | chr16 | 48258118 | |||||||
| chr16:48258122 | A | C | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.601-496A>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 3/14 | chr16 | 48258122 | |||||||
| chr16:48258150 | A | G | 2 | a0001c0002t0049g0017 a0001c0002t0050g0007 |
2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.601-468A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 3/14 | chr16 | 48258150 | |||||||
| chr16:48258338 | T | G | 2 | a0001c0001t0013g0099 a0001c0001t0013g0100 |
2 | HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.601-280T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 3/14 | chr16 | 48258338 | |||||||
| chr16:48258345 | CA | C | 53 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(50): Show |
54 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.601-262delA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 48258345 | ||||||
| chr16:48258355 | A | AG | 2 | a0001c0002t0049g0017 a0001c0002t0050g0007 |
2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.601-263_601-262ins others(1): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 3/14 | chr16 | 48258355 | |||||||
| chr16:48258355 | AAG | A | 8 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(5): Show |
8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.601-261_601-260del others(2): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 48258355 | ||||||
| chr16:48258357 | G | A | 2 | a0001c0002t0049g0017 a0001c0002t0050g0007 |
2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.601-261G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 3/14 | chr16 | 48258357 | |||||||
| chr16:48258358 | A | G | 8 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(5): Show |
8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.601-260A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 3/14 | chr16 | 48258358 | |||||||
| chr16:48258364 | A | G | 1 | a0001c0001t0006g0133 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.601-254A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 3/14 | chr16 | 48258364 | |||||||
| chr16:48258519 | T | TG | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.601-99_601-98insG | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 3/14 | chr16 | 48258519 | |||||||
| chr16:48258594 | A | G | 1 | a0001c0001t0040g0119 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.601-24A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 3/14 | chr16 | 48258594 | |||||||
| chr16:48258602 | A | G | 47 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(44): Show |
48 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.601-16A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 3/14 | chr16 | 48258602 | |||||||
| chr16:48258839 | C | T | 3 | a0001c0001t0030g0143 a0001c0001t0062g0142 a0001c0006t0038g0144 |
3 | HG02896.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.723+99C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 4/14 | chr16 | 48258839 | |||||||
| chr16:48258877 | C | A | 1 | a0001c0001t0080g0025 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.723+137C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 4/14 | chr16 | 48258877 | |||||||
| chr16:48258973 | G | A | 1 | a0001c0001t0005g0132 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.723+233G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 4/14 | chr16 | 48258973 | |||||||
| chr16:48259206 | C | A | 1 | a0001c0001t0082g0026 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.723+466C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 4/14 | chr16 | 48259206 | |||||||
| chr16:48259353 | C | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.723+613C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 4/14 | chr16 | 48259353 | |||||||
| chr16:48259401 | T | C | 8 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(5): Show |
8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.723+661T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 4/14 | chr16 | 48259401 | |||||||
| chr16:48259553 | A | C | 1 | a0001c0001t0040g0119 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.723+813A>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 4/14 | chr16 | 48259553 | |||||||
| chr16:48259613 | A | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.723+873A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 4/14 | chr16 | 48259613 | |||||||
| chr16:48259736 | G | A | 1 | a0001c0002t0050g0007 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.723+996G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 4/14 | chr16 | 48259736 | |||||||
| chr16:48259799 | A | C | 1 | a0001c0001t0025g0116 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.723+1059A>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 4/14 | chr16 | 48259799 | |||||||
| chr16:48259837 | G | A | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.723+1097G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 4/14 | chr16 | 48259837 | |||||||
| chr16:48259871 | A | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.723+1131A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 4/14 | chr16 | 48259871 | |||||||
| chr16:48259890 | T | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.723+1150T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 4/14 | chr16 | 48259890 | |||||||
| chr16:48259999 | C | T | 1 | a0001c0001t0086g0080 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.723+1259C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 4/14 | chr16 | 48259999 | |||||||
| chr16:48260350 | A | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.724-1074A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 4/14 | chr16 | 48260350 | |||||||
| chr16:48260376 | T | C | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.724-1048T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 4/14 | chr16 | 48260376 | |||||||
| chr16:48260641 | A | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.724-783A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 4/14 | chr16 | 48260641 | |||||||
| chr16:48260660 | G | A | 64 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(61): Show |
65 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(62): Show |
intron_variant | MODIFIER | c.724-764G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 4/14 | chr16 | 48260660 | |||||||
| chr16:48260691 | T | C | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.724-733T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 4/14 | chr16 | 48260691 | |||||||
| chr16:48260712 | G | A | 1 | a0001c0001t0003g0024 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.724-712G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 4/14 | chr16 | 48260712 | |||||||
| chr16:48260746 | G | A | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.724-678G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 4/14 | chr16 | 48260746 | |||||||
| chr16:48261373 | G | A | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.724-51G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 4/14 | chr16 | 48261373 | |||||||
| chr16:48261693 | A | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.887+106A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 5/14 | chr16 | 48261693 | |||||||
| chr16:48262153 | A | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.887+566A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 5/14 | chr16 | 48262153 | |||||||
| chr16:48262170 | T | A | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.887+583T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 5/14 | chr16 | 48262170 | |||||||
| chr16:48262193 | T | C | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.888-585T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 5/14 | chr16 | 48262193 | |||||||
| chr16:48262244 | G | A | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.888-534G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 5/14 | chr16 | 48262244 | |||||||
| chr16:48262286 | A | G | 1 | a0001c0001t0029g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.888-492A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 5/14 | chr16 | 48262286 | |||||||
| chr16:48262303 | T | C | 3 | a0001c0001t0001g0038 a0001c0001t0001g0145 a0001c0001t0002g0037 |
3 | HG02572.hp2 HG02818.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.888-475T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 5/14 | chr16 | 48262303 | |||||||
| chr16:48262570 | T | A | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.888-208T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 5/14 | chr16 | 48262570 | |||||||
| chr16:48262589 | G | T | 1 | a0001c0001t0033g0147 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.888-189G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 5/14 | chr16 | 48262589 | |||||||
| chr16:48262628 | C | T | 2 | a0001c0002t0049g0017 a0001c0002t0050g0007 |
2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.888-150C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 5/14 | chr16 | 48262628 | |||||||
| chr16:48262748 | A | G | 1 | a0001c0001t0020g0036 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.888-30A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 5/14 | chr16 | 48262748 | |||||||
| chr16:48263043 | T | A | 15 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(12): Show |
16 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.982+171T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48263043 | |||||||
| chr16:48263045 | A | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.982+173A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48263045 | |||||||
| chr16:48263078 | A | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.982+206A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48263078 | |||||||
| chr16:48263277 | T | C | 2 | a0001c0002t0049g0017 a0001c0002t0050g0007 |
2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.982+405T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48263277 | |||||||
| chr16:48263339 | C | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.982+467C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48263339 | |||||||
| chr16:48263522 | C | T | 1 | a0001c0002t0041g0015 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.982+650C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48263522 | |||||||
| chr16:48263597 | C | T | 18 | a0001c0001t0005g0001 a0001c0001t0005g0111 a0001c0001t0005g0128 others(15): Show |
18 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.982+725C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48263597 | |||||||
| chr16:48263648 | T | C | 4 | a0001c0001t0005g0111 a0001c0001t0005g0128 a0001c0001t0006g0133 others(1): Show |
4 | HG01109.hp1 HG02145.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.982+776T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48263648 | |||||||
| chr16:48263876 | A | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.982+1004A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48263876 | |||||||
| chr16:48263932 | C | T | 8 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(5): Show |
8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.982+1060C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48263932 | |||||||
| chr16:48263944 | C | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.982+1072C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48263944 | |||||||
| chr16:48264001 | G | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.982+1129G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48264001 | |||||||
| chr16:48264011 | G | C | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.982+1139G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48264011 | |||||||
| chr16:48264075 | A | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.982+1203A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48264075 | |||||||
| chr16:48264155 | C | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.982+1283C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48264155 | |||||||
| chr16:48264178 | G | A | 63 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(60): Show |
64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.982+1306G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48264178 | |||||||
| chr16:48264193 | C | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.982+1321C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48264193 | |||||||
| chr16:48264249 | C | T | 6 | a0001c0001t0013g0099 a0001c0001t0013g0100 a0001c0001t0014g0005 others(3): Show |
6 | HG01891.hp2 HG02258.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.982+1377C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48264249 | |||||||
| chr16:48264312 | C | CG | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.982+1447dupG | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr16 | 48264312 | ||||||
| chr16:48264388 | A | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.982+1516A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48264388 | |||||||
| chr16:48264404 | T | C | 63 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(60): Show |
64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.982+1532T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48264404 | |||||||
| chr16:48264444 | G | A | 1 | a0001c0001t0021g0039 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.982+1572G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48264444 | |||||||
| chr16:48264604 | C | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.982+1732C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48264604 | |||||||
| chr16:48264607 | A | G | 2 | a0001c0001t0014g0101 a0001c0001t0027g0102 |
2 | HG01891.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.982+1735A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48264607 | |||||||
| chr16:48264674 | A | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.982+1802A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48264674 | |||||||
| chr16:48264682 | A | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.982+1810A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48264682 | |||||||
| chr16:48264786 | T | C | 1 | a0001c0001t0029g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.982+1914T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48264786 | |||||||
| chr16:48264902 | T | TTCGGTAC others(7): Show |
6 | a0001c0001t0032g0124 a0001c0001t0033g0147 a0001c0001t0034g0125 others(3): Show |
6 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.982+2030_982+2031i others(16): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48264902 | |||||||
| chr16:48264904 | C | A | 6 | a0001c0001t0032g0124 a0001c0001t0033g0147 a0001c0001t0034g0125 others(3): Show |
6 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.982+2032C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48264904 | |||||||
| chr16:48264982 | G | A | 8 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(5): Show |
8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.982+2110G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48264982 | |||||||
| chr16:48265012 | C | T | 1 | a0001c0001t0054g0139 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.982+2140C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48265012 | |||||||
| chr16:48265245 | C | T | 1 | a0001c0001t0002g0023 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.982+2373C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48265245 | |||||||
| chr16:48265335 | GT | G | 8 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(5): Show |
8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.982+2467delT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr16 | 48265335 | ||||||
| chr16:48265357 | AT | A | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.982+2488delT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr16 | 48265357 | ||||||
| chr16:48265533 | AACTTTAT others(2): Show |
A | 39 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(36): Show |
40 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.982+2662_982+2670d others(11): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48265533 | |||||||
| chr16:48265628 | C | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.982+2756C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48265628 | |||||||
| chr16:48265797 | A | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.982+2925A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48265797 | |||||||
| chr16:48265828 | A | G | 1 | a0001c0001t0040g0119 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.982+2956A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48265828 | |||||||
| chr16:48265952 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.982+3080A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48265952 | |||||||
| chr16:48266050 | C | G | 15 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(12): Show |
16 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.982+3178C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48266050 | |||||||
| chr16:48266063 | G | A | 3 | a0001c0001t0010g0041 a0001c0001t0018g0040 a0001c0001t0018g0042 |
3 | HG02615.hp1 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.982+3191G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48266063 | |||||||
| chr16:48266152 | T | C | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.982+3280T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48266152 | |||||||
| chr16:48266275 | G | A | 1 | a0001c0001t0023g0115 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.982+3403G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48266275 | |||||||
| chr16:48266297 | G | A | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.982+3425G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48266297 | |||||||
| chr16:48266327 | GTT | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.982+3468_982+3469d others(4): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr16 | 48266327 | ||||||
| chr16:48266467 | C | A | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.983-3549C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48266467 | |||||||
| chr16:48266562 | G | A | 6 | a0001c0001t0032g0124 a0001c0001t0033g0147 a0001c0001t0034g0125 others(3): Show |
6 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.983-3454G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48266562 | |||||||
| chr16:48266789 | T | C | 1 | a0001c0004t0063g0094 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.983-3227T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48266789 | |||||||
| chr16:48266828 | T | C | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.983-3188T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48266828 | |||||||
| chr16:48267027 | G | T | 16 | a0001c0001t0032g0124 a0001c0001t0033g0147 a0001c0001t0034g0125 others(13): Show |
16 | HG01884.hp1 HG01891.hp1 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.983-2989G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48267027 | |||||||
| chr16:48267322 | T | C | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.983-2694T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48267322 | |||||||
| chr16:48267626 | C | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.983-2390C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48267626 | |||||||
| chr16:48267655 | G | A | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.983-2361G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48267655 | |||||||
| chr16:48267656 | G | C | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.983-2360G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48267656 | |||||||
| chr16:48267664 | G | A | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.983-2352G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48267664 | |||||||
| chr16:48267665 | T | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.983-2351T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48267665 | |||||||
| chr16:48267699 | C | T | 63 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(60): Show |
64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.983-2317C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48267699 | |||||||
| chr16:48267721 | C | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.983-2295C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48267721 | |||||||
| chr16:48267730 | C | T | 1 | a0001c0001t0003g0078 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.983-2286C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48267730 | |||||||
| chr16:48267760 | C | T | 1 | a0001c0001t0035g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.983-2256C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48267760 | |||||||
| chr16:48267817 | T | C | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.983-2199T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48267817 | |||||||
| chr16:48267905 | C | T | 1 | a0001c0001t0029g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.983-2111C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48267905 | |||||||
| chr16:48268001 | G | C | 1 | a0001c0002t0048g0008 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.983-2015G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48268001 | |||||||
| chr16:48268372 | A | C | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.983-1644A>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48268372 | |||||||
| chr16:48268390 | A | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.983-1626A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48268390 | |||||||
| chr16:48268450 | A | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.983-1566A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48268450 | |||||||
| chr16:48268476 | C | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.983-1540C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48268476 | |||||||
| chr16:48268497 | A | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.983-1519A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48268497 | |||||||
| chr16:48268523 | T | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.983-1493T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48268523 | |||||||
| chr16:48268730 | T | C | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.983-1286T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48268730 | |||||||
| chr16:48268748 | A | G | 6 | a0001c0001t0002g0086 a0001c0001t0002g0087 a0001c0001t0009g0019 others(3): Show |
6 | HG02258.hp2 HG02647.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.983-1268A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48268748 | |||||||
| chr16:48268913 | G | GA | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.983-1102dupA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr16 | 48268913 | ||||||
| chr16:48269019 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.983-997C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48269019 | |||||||
| chr16:48269125 | G | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.983-891G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48269125 | |||||||
| chr16:48269182 | C | A | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.983-834C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48269182 | |||||||
| chr16:48269199 | TG | T | 8 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(5): Show |
8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.983-816delG | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48269199 | |||||||
| chr16:48269200 | G | T | 2 | a0001c0002t0049g0017 a0001c0002t0050g0007 |
2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.983-816G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48269200 | |||||||
| chr16:48269200 | GT | G | 8 | a0001c0001t0008g0090 a0001c0001t0012g0055 a0001c0001t0012g0092 others(5): Show |
8 | HG02129.hp2 HG02486.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.983-799delT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr16 | 48269200 | ||||||
| chr16:48269386 | T | A | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.983-630T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48269386 | |||||||
| chr16:48269434 | T | C | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.983-582T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48269434 | |||||||
| chr16:48269522 | A | G | 4 | a0001c0001t0032g0124 a0001c0001t0034g0125 a0001c0001t0035g0127 others(1): Show |
4 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.983-494A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48269522 | |||||||
| chr16:48269628 | G | A | 63 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(60): Show |
64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.983-388G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48269628 | |||||||
| chr16:48269638 | T | C | 1 | a0001c0001t0002g0043 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.983-378T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48269638 | |||||||
| chr16:48269700 | T | A | 6 | a0001c0001t0032g0124 a0001c0001t0033g0147 a0001c0001t0034g0125 others(3): Show |
6 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.983-316T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48269700 | |||||||
| chr16:48269701 | A | T | 18 | a0001c0001t0005g0001 a0001c0001t0005g0111 a0001c0001t0005g0128 others(15): Show |
18 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.983-315A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48269701 | |||||||
| chr16:48269748 | A | G | 4 | a0001c0003t0058g0123 a0001c0003t0059g0121 a0001c0003t0060g0122 others(1): Show |
4 | HG02486.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.983-268A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48269748 | |||||||
| chr16:48269765 | C | T | 4 | a0001c0001t0009g0019 a0001c0001t0009g0020 a0001c0001t0009g0076 others(1): Show |
4 | HG02258.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.983-251C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48269765 | |||||||
| chr16:48269799 | T | C | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.983-217T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48269799 | |||||||
| chr16:48269890 | A | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.983-126A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 6/14 | chr16 | 48269890 | |||||||
| chr16:48270320 | A | G | 1 | a0001c0001t0040g0119 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1241+46A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48270320 | |||||||
| chr16:48270377 | G | A | 1 | a0001c0001t0012g0044 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1241+103G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48270377 | |||||||
| chr16:48270477 | A | G | 1 | a0002c0005t0052g0138 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1241+203A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48270477 | |||||||
| chr16:48270594 | G | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1241+320G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48270594 | |||||||
| chr16:48270945 | T | C | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1241+671T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48270945 | |||||||
| chr16:48270959 | T | C | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1241+685T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48270959 | |||||||
| chr16:48270989 | T | A | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1241+715T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48270989 | |||||||
| chr16:48271034 | T | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1241+760T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48271034 | |||||||
| chr16:48271110 | G | C | 2 | a0001c0002t0049g0017 a0001c0002t0050g0007 |
2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1241+836G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48271110 | |||||||
| chr16:48271174 | TCAAA | T | 2 | a0001c0001t0007g0137 a0001c0006t0038g0144 |
2 | HG03453.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1241+920_1241+923d others(6): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 48271174 | ||||||
| chr16:48271174 | TCAAACAA others(1): Show |
T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1241+916_1241+923d others(10): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 48271174 | ||||||
| chr16:48271270 | G | A | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1241+996G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48271270 | |||||||
| chr16:48271294 | T | A | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1241+1020T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48271294 | |||||||
| chr16:48271341 | T | C | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1241+1067T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48271341 | |||||||
| chr16:48271364 | A | G | 7 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(4): Show |
8 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.1241+1090A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48271364 | |||||||
| chr16:48271390 | A | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1241+1116A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48271390 | |||||||
| chr16:48271461 | A | G | 2 | a0001c0001t0033g0147 a0001c0001t0051g0146 |
2 | NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1241+1187A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48271461 | |||||||
| chr16:48271463 | G | T | 143 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0033 others(140): Show |
145 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(142): Show |
intron_variant | MODIFIER | c.1241+1189G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48271463 | |||||||
| chr16:48271656 | G | A | 2 | a0001c0002t0049g0017 a0001c0002t0050g0007 |
2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1241+1382G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48271656 | |||||||
| chr16:48271721 | A | C | 2 | a0001c0002t0049g0017 a0001c0002t0050g0007 |
2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1241+1447A>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48271721 | |||||||
| chr16:48271784 | G | A | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1241+1510G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48271784 | |||||||
| chr16:48271819 | T | A | 1 | a0001c0001t0040g0119 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1241+1545T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48271819 | |||||||
| chr16:48272292 | A | G | 1 | a0001c0001t0062g0142 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1241+2018A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48272292 | |||||||
| chr16:48272319 | C | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1241+2045C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48272319 | |||||||
| chr16:48272330 | T | C | 1 | a0001c0001t0003g0053 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1241+2056T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48272330 | |||||||
| chr16:48272396 | C | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1241+2122C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48272396 | |||||||
| chr16:48272397 | A | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1241+2123A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48272397 | |||||||
| chr16:48272475 | ATGCTTT | A | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1241+2204_1241+220 others(10): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 48272475 | ||||||
| chr16:48272483 | G | T | 53 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(50): Show |
54 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.1241+2209G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48272483 | |||||||
| chr16:48272642 | A | G | 1 | a0001c0001t0029g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1241+2368A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48272642 | |||||||
| chr16:48272735 | C | T | 1 | a0001c0006t0038g0144 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1241+2461C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48272735 | |||||||
| chr16:48272754 | C | A | 8 | a0001c0001t0029g0113 a0001c0001t0030g0143 a0001c0001t0062g0142 others(5): Show |
8 | HG02280.hp1 HG02486.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1241+2480C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48272754 | |||||||
| chr16:48273064 | C | T | 1 | a0001c0001t0062g0142 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1241+2790C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48273064 | |||||||
| chr16:48273223 | C | T | 1 | a0002c0005t0052g0138 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1241+2949C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48273223 | |||||||
| chr16:48273268 | G | A | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1241+2994G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48273268 | |||||||
| chr16:48273650 | G | A | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1241+3376G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48273650 | |||||||
| chr16:48273728 | TAATGTTT others(1): Show |
T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1241+3455_1241+346 others(12): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48273728 | |||||||
| chr16:48273767 | AAAG | A | 3 | a0001c0001t0030g0143 a0001c0001t0062g0142 a0001c0006t0038g0144 |
3 | HG02896.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1241+3496_1241+349 others(7): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 48273767 | ||||||
| chr16:48273771 | A | T | 1 | a0001c0001t0029g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1241+3497A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48273771 | |||||||
| chr16:48273851 | A | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1242-3487A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48273851 | |||||||
| chr16:48273918 | G | A | 5 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0034 others(2): Show |
5 | HG01175.hp2 HG01496.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1242-3420G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48273918 | |||||||
| chr16:48274057 | G | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1242-3281G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48274057 | |||||||
| chr16:48274163 | G | A | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1242-3175G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48274163 | |||||||
| chr16:48274176 | A | G | 48 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(45): Show |
49 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.1242-3162A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48274176 | |||||||
| chr16:48274201 | C | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1242-3137C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48274201 | |||||||
| chr16:48274274 | T | G | 1 | a0001c0001t0040g0119 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1242-3064T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48274274 | |||||||
| chr16:48274451 | TA | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1242-2886delA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48274451 | |||||||
| chr16:48274494 | A | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1242-2844A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48274494 | |||||||
| chr16:48274608 | T | C | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1242-2730T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48274608 | |||||||
| chr16:48274609 | T | C | 3 | a0001c0001t0030g0143 a0001c0001t0062g0142 a0001c0006t0038g0144 |
3 | HG02896.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1242-2729T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48274609 | |||||||
| chr16:48274728 | A | G | 1 | a0001c0001t0002g0075 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1242-2610A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48274728 | |||||||
| chr16:48274747 | G | A | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1242-2591G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48274747 | |||||||
| chr16:48274923 | C | T | 1 | a0001c0001t0062g0142 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1242-2415C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48274923 | |||||||
| chr16:48274970 | A | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1242-2368A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48274970 | |||||||
| chr16:48275000 | C | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1242-2338C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48275000 | |||||||
| chr16:48275137 | C | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1242-2201C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48275137 | |||||||
| chr16:48275186 | TTC | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1242-2147_1242-214 others(6): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 48275186 | ||||||
| chr16:48275332 | G | A | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1242-2006G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48275332 | |||||||
| chr16:48275475 | A | G | 2 | a0001c0001t0014g0005 a0001c0001t0028g0005 |
2 | HG03098.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1242-1863A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48275475 | |||||||
| chr16:48275541 | A | G | 1 | a0001c0001t0009g0020 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1242-1797A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48275541 | |||||||
| chr16:48275698 | T | A | 64 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(61): Show |
65 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(62): Show |
intron_variant | MODIFIER | c.1242-1640T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48275698 | |||||||
| chr16:48275747 | G | C | 2 | a0001c0002t0049g0017 a0001c0002t0050g0007 |
2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1242-1591G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48275747 | |||||||
| chr16:48275829 | G | A | 1 | a0001c0001t0074g0081 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1242-1509G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48275829 | |||||||
| chr16:48276053 | T | C | 1 | a0001c0001t0062g0142 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1242-1285T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48276053 | |||||||
| chr16:48276107 | G | T | 1 | a0001c0001t0004g0006 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1242-1231G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48276107 | |||||||
| chr16:48276283 | T | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1242-1055T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48276283 | |||||||
| chr16:48276473 | G | A | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1242-865G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48276473 | |||||||
| chr16:48276508 | G | A | 1 | a0001c0001t0040g0119 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1242-830G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48276508 | |||||||
| chr16:48276513 | G | A | 3 | a0001c0001t0030g0143 a0001c0001t0062g0142 a0001c0006t0038g0144 |
3 | HG02896.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1242-825G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48276513 | |||||||
| chr16:48276775 | T | C | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1242-563T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48276775 | |||||||
| chr16:48276833 | TTTG | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1242-496_1242-494d others(5): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr16 | 48276833 | ||||||
| chr16:48276872 | G | T | 5 | a0001c0001t0022g0117 a0001c0001t0023g0115 a0001c0001t0024g0118 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1242-466G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48276872 | |||||||
| chr16:48276957 | G | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1242-381G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48276957 | |||||||
| chr16:48277190 | A | G | 1 | a0001c0001t0006g0136 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1242-148A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48277190 | |||||||
| chr16:48277246 | A | G | 1 | a0001c0001t0003g0024 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1242-92A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 7/14 | chr16 | 48277246 | |||||||
| chr16:48277670 | T | C | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+191T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48277670 | |||||||
| chr16:48277677 | T | A | 47 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(44): Show |
48 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.1383+198T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48277677 | |||||||
| chr16:48277781 | C | T | 3 | a0001c0001t0030g0143 a0001c0001t0062g0142 a0001c0006t0038g0144 |
3 | HG02896.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1383+302C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48277781 | |||||||
| chr16:48277807 | C | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+328C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48277807 | |||||||
| chr16:48277830 | C | T | 4 | a0001c0003t0058g0123 a0001c0003t0059g0121 a0001c0003t0060g0122 others(1): Show |
4 | HG02486.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1383+351C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48277830 | |||||||
| chr16:48277855 | C | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+376C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48277855 | |||||||
| chr16:48277892 | ATT | A | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+426_1383+427d others(4): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr16 | 48277892 | ||||||
| chr16:48278024 | CTTGTTTT others(4): Show |
C | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+556_1383+566d others(13): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr16 | 48278024 | ||||||
| chr16:48278038 | GT | G | 3 | a0001c0001t0012g0055 a0001c0001t0012g0092 a0001c0001t0017g0054 |
3 | HG02129.hp2 NA18986.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1383+566delT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr16 | 48278038 | ||||||
| chr16:48278121 | C | T | 8 | a0001c0001t0029g0113 a0001c0001t0030g0143 a0001c0001t0062g0142 others(5): Show |
8 | HG02280.hp1 HG02486.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1383+642C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48278121 | |||||||
| chr16:48278147 | G | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+668G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48278147 | |||||||
| chr16:48278253 | A | G | 1 | a0001c0001t0068g0077 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1383+774A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48278253 | |||||||
| chr16:48278291 | C | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+812C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48278291 | |||||||
| chr16:48278296 | G | A | 63 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(60): Show |
64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.1383+817G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48278296 | |||||||
| chr16:48278335 | T | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+856T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48278335 | |||||||
| chr16:48278496 | A | G | 2 | a0001c0001t0001g0073 a0001c0001t0002g0074 |
2 | HG01081.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.1383+1017A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48278496 | |||||||
| chr16:48278577 | T | C | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+1098T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48278577 | |||||||
| chr16:48278796 | G | A | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+1317G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48278796 | |||||||
| chr16:48278934 | C | T | 1 | a0001c0001t0013g0100 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1383+1455C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48278934 | |||||||
| chr16:48279084 | A | G | 1 | a0001c0001t0075g0082 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1383+1605A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48279084 | |||||||
| chr16:48279178 | A | T | 3 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0017g0004 |
3 | HG01496.hp2 HG01975.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.1383+1699A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48279178 | |||||||
| chr16:48279194 | C | CTCTG | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+1718_1383+171 others(8): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr16 | 48279194 | ||||||
| chr16:48279421 | A | ACT | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+1943_1383+194 others(6): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr16 | 48279421 | ||||||
| chr16:48279526 | G | A | 7 | a0001c0002t0042g0009 a0001c0002t0043g0011 a0001c0002t0044g0014 others(4): Show |
7 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1383+2047G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48279526 | |||||||
| chr16:48279528 | G | A | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+2049G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48279528 | |||||||
| chr16:48279576 | A | C | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+2097A>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48279576 | |||||||
| chr16:48279684 | G | A | 1 | a0001c0001t0029g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1383+2205G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48279684 | |||||||
| chr16:48279703 | G | A | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+2224G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48279703 | |||||||
| chr16:48279837 | C | T | 1 | a0001c0001t0001g0052 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1383+2358C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48279837 | |||||||
| chr16:48280099 | C | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+2620C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48280099 | |||||||
| chr16:48280700 | AAATGAAG others(4): Show |
A | 1 | a0001c0001t0088g0071 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1383+3223_1383+323 others(15): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr16 | 48280700 | ||||||
| chr16:48280744 | G | C | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+3265G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48280744 | |||||||
| chr16:48280753 | C | G | 6 | a0001c0001t0032g0124 a0001c0001t0033g0147 a0001c0001t0034g0125 others(3): Show |
6 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1383+3274C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48280753 | |||||||
| chr16:48280827 | G | A | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+3348G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48280827 | |||||||
| chr16:48280906 | C | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+3427C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48280906 | |||||||
| chr16:48280907 | A | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+3428A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48280907 | |||||||
| chr16:48280927 | C | T | 63 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(60): Show |
64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.1383+3448C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48280927 | |||||||
| chr16:48280957 | A | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+3478A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48280957 | |||||||
| chr16:48281042 | A | G | 4 | a0001c0001t0032g0124 a0001c0001t0034g0125 a0001c0001t0035g0127 others(1): Show |
4 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1383+3563A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48281042 | |||||||
| chr16:48281260 | A | T | 3 | a0001c0001t0012g0055 a0001c0001t0012g0092 a0001c0001t0017g0054 |
3 | HG02129.hp2 NA18986.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1383+3781A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48281260 | |||||||
| chr16:48281581 | C | A | 1 | a0001c0001t0064g0088 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1383+4102C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48281581 | |||||||
| chr16:48281703 | G | A | 11 | a0001c0001t0072g0035 a0001c0002t0041g0015 a0001c0002t0042g0009 others(8): Show |
11 | HG01884.hp1 HG01993.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.1383+4224G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48281703 | |||||||
| chr16:48281872 | T | C | 19 | a0001c0001t0005g0001 a0001c0001t0005g0111 a0001c0001t0005g0128 others(16): Show |
19 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.1383+4393T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48281872 | |||||||
| chr16:48282224 | C | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+4745C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48282224 | |||||||
| chr16:48282272 | A | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+4793A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48282272 | |||||||
| chr16:48282277 | C | G | 63 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(60): Show |
64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.1383+4798C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48282277 | |||||||
| chr16:48282410 | CA | C | 79 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0033 others(76): Show |
81 | HG00733.hp2 HG00738.hp2 HG00741.hp1 others(78): Show |
intron_variant | MODIFIER | c.1383+4950delA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr16 | 48282410 | ||||||
| chr16:48282429 | AG | A | 4 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(1): Show |
4 | HG01884.hp1 HG02647.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.1383+4951delG | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48282429 | |||||||
| chr16:48282430 | G | A | 2 | a0001c0002t0049g0017 a0001c0002t0050g0007 |
2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1383+4951G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48282430 | |||||||
| chr16:48282474 | A | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+4995A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48282474 | |||||||
| chr16:48282820 | A | ATC | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+5344_1383+534 others(6): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr16 | 48282820 | ||||||
| chr16:48283039 | C | G | 39 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(36): Show |
40 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.1383+5560C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48283039 | |||||||
| chr16:48283063 | G | A | 63 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(60): Show |
64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.1383+5584G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48283063 | |||||||
| chr16:48283081 | A | G | 5 | a0001c0001t0001g0073 a0001c0001t0001g0091 a0001c0001t0002g0065 others(2): Show |
5 | HG00558.hp2 HG01070.hp1 HG01081.hp1 others(2): Show |
intron_variant | MODIFIER | c.1383+5602A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48283081 | |||||||
| chr16:48283089 | A | G | 1 | a0001c0001t0062g0142 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1383+5610A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48283089 | |||||||
| chr16:48283313 | A | AT | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+5838dupT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr16 | 48283313 | ||||||
| chr16:48283436 | G | C | 1 | a0001c0001t0032g0124 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1383+5957G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48283436 | |||||||
| chr16:48284043 | T | A | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+6564T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48284043 | |||||||
| chr16:48284070 | A | T | 2 | a0001c0001t0055g0141 a0001c0001t0057g0140 |
2 | HG02074.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.1383+6591A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48284070 | |||||||
| chr16:48284273 | A | G | 1 | a0001c0001t0011g0051 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1383+6794A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48284273 | |||||||
| chr16:48284299 | A | C | 2 | a0001c0001t0031g0103 a0001c0001t0036g0104 |
2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1383+6820A>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48284299 | |||||||
| chr16:48284342 | A | T | 2 | a0001c0001t0055g0141 a0001c0001t0057g0140 |
2 | HG02074.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.1383+6863A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48284342 | |||||||
| chr16:48284482 | C | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+7003C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48284482 | |||||||
| chr16:48284506 | A | G | 4 | a0001c0003t0058g0123 a0001c0003t0059g0121 a0001c0003t0060g0122 others(1): Show |
4 | HG02486.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1383+7027A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48284506 | |||||||
| chr16:48284525 | C | T | 1 | a0001c0001t0029g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1383+7046C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48284525 | |||||||
| chr16:48284737 | C | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+7258C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48284737 | |||||||
| chr16:48284817 | C | A | 63 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(60): Show |
64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.1383+7338C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48284817 | |||||||
| chr16:48284865 | T | A | 8 | a0001c0001t0013g0099 a0001c0001t0013g0100 a0001c0001t0014g0005 others(5): Show |
8 | HG01891.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1383+7386T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48284865 | |||||||
| chr16:48284865 | T | G | 40 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(37): Show |
41 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.1383+7386T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48284865 | |||||||
| chr16:48285221 | G | A | 2 | a0001c0001t0013g0099 a0001c0001t0013g0100 |
2 | HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1383+7742G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48285221 | |||||||
| chr16:48285399 | G | A | 2 | a0001c0001t0002g0075 a0001c0001t0011g0056 |
2 | HG04115.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1383+7920G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48285399 | |||||||
| chr16:48285474 | G | A | 5 | a0001c0001t0029g0113 a0001c0003t0058g0123 a0001c0003t0059g0121 others(2): Show |
5 | HG02280.hp1 HG02486.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1383+7995G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48285474 | |||||||
| chr16:48285560 | A | T | 4 | a0001c0001t0032g0124 a0001c0001t0034g0125 a0001c0001t0035g0127 others(1): Show |
4 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1383+8081A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48285560 | |||||||
| chr16:48285658 | G | A | 3 | a0001c0001t0030g0143 a0001c0001t0062g0142 a0001c0006t0038g0144 |
3 | HG02896.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1383+8179G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48285658 | |||||||
| chr16:48285756 | C | G | 9 | a0001c0001t0003g0016 a0001c0001t0003g0053 a0001c0001t0003g0078 others(6): Show |
9 | HG00741.hp2 HG01109.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.1383+8277C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48285756 | |||||||
| chr16:48285894 | T | C | 1 | a0001c0001t0064g0088 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1383+8415T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48285894 | |||||||
| chr16:48285994 | C | T | 3 | a0001c0001t0030g0143 a0001c0001t0062g0142 a0001c0006t0038g0144 |
3 | HG02896.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1383+8515C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48285994 | |||||||
| chr16:48286142 | C | A | 1 | a0001c0001t0085g0045 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1383+8663C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48286142 | |||||||
| chr16:48286142 | C | CT | 54 | a0001c0001t0001g0091 a0001c0001t0004g0006 a0001c0001t0004g0107 others(51): Show |
55 | HG00323.hp2 HG00558.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.1383+8680dupT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr16 | 48286142 | ||||||
| chr16:48286164 | C | T | 1 | a0001c0001t0004g0006 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1383+8685C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48286164 | |||||||
| chr16:48286440 | C | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1383+8961C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48286440 | |||||||
| chr16:48286693 | C | T | 2 | a0001c0002t0049g0017 a0001c0002t0050g0007 |
2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1383+9214C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48286693 | |||||||
| chr16:48286804 | C | CTT | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1384-9200_1384-919 others(6): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr16 | 48286804 | ||||||
| chr16:48286898 | A | T | 1 | a0001c0001t0029g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1384-9117A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48286898 | |||||||
| chr16:48286941 | C | T | 1 | a0001c0001t0011g0056 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1384-9074C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48286941 | |||||||
| chr16:48287062 | T | C | 1 | a0001c0001t0051g0146 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1384-8953T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48287062 | |||||||
| chr16:48287094 | A | T | 2 | a0001c0002t0049g0017 a0001c0002t0050g0007 |
2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1384-8921A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48287094 | |||||||
| chr16:48287121 | C | T | 24 | a0001c0001t0005g0001 a0001c0001t0005g0111 a0001c0001t0005g0128 others(21): Show |
24 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.1384-8894C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48287121 | |||||||
| chr16:48287358 | C | T | 1 | a0003c0007t0007g0135 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1384-8657C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48287358 | |||||||
| chr16:48287437 | A | G | 1 | a0001c0001t0030g0143 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1384-8578A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48287437 | |||||||
| chr16:48287554 | C | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1384-8461C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48287554 | |||||||
| chr16:48287591 | T | G | 1 | a0001c0001t0007g0130 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1384-8424T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48287591 | |||||||
| chr16:48287621 | C | T | 4 | a0001c0003t0058g0123 a0001c0003t0059g0121 a0001c0003t0060g0122 others(1): Show |
4 | HG02486.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1384-8394C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48287621 | |||||||
| chr16:48287640 | A | G | 1 | a0001c0001t0015g0109 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1384-8375A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48287640 | |||||||
| chr16:48287673 | G | A | 1 | a0001c0001t0018g0040 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1384-8342G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48287673 | |||||||
| chr16:48287847 | A | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1384-8168A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48287847 | |||||||
| chr16:48288020 | C | T | 24 | a0001c0001t0005g0001 a0001c0001t0005g0111 a0001c0001t0005g0128 others(21): Show |
24 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.1384-7995C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48288020 | |||||||
| chr16:48288150 | C | CT | 6 | a0001c0001t0002g0085 a0001c0001t0002g0086 a0001c0001t0015g0108 others(3): Show |
6 | HG00741.hp1 HG02622.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1384-7844dupT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr16 | 48288150 | ||||||
| chr16:48288153 | T | C | 1 | a0001c0001t0040g0119 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1384-7862T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48288153 | |||||||
| chr16:48288224 | G | A | 8 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(5): Show |
8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1384-7791G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48288224 | |||||||
| chr16:48288481 | C | T | 1 | a0001c0001t0021g0039 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1384-7534C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48288481 | |||||||
| chr16:48288562 | T | G | 63 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(60): Show |
64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.1384-7453T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48288562 | |||||||
| chr16:48288629 | G | A | 19 | a0001c0001t0002g0037 a0001c0001t0005g0001 a0001c0001t0005g0111 others(16): Show |
19 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.1384-7386G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48288629 | |||||||
| chr16:48288778 | TAC | T | 3 | a0001c0001t0030g0143 a0001c0001t0062g0142 a0001c0006t0038g0144 |
3 | HG02896.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1384-7235_1384-723 others(6): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr16 | 48288778 | ||||||
| chr16:48289200 | A | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1384-6815A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48289200 | |||||||
| chr16:48289428 | T | C | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1384-6587T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48289428 | |||||||
| chr16:48289692 | A | G | 6 | a0001c0001t0013g0099 a0001c0001t0013g0100 a0001c0001t0014g0005 others(3): Show |
6 | HG01891.hp2 HG02258.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1384-6323A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48289692 | |||||||
| chr16:48289744 | TA | T | 2 | a0001c0001t0030g0143 a0001c0006t0038g0144 |
2 | HG02896.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1384-6270delA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48289744 | |||||||
| chr16:48289879 | C | A | 2 | a0001c0001t0001g0073 a0001c0001t0002g0074 |
2 | HG01081.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.1384-6136C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48289879 | |||||||
| chr16:48289904 | T | C | 1 | a0001c0001t0086g0080 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1384-6111T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48289904 | |||||||
| chr16:48289960 | A | G | 2 | a0001c0001t0065g0030 a0001c0001t0080g0025 |
2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1384-6055A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48289960 | |||||||
| chr16:48290163 | G | A | 7 | a0001c0002t0042g0009 a0001c0002t0043g0011 a0001c0002t0044g0014 others(4): Show |
7 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1384-5852G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48290163 | |||||||
| chr16:48290210 | G | T | 2 | a0001c0002t0043g0011 a0001c0002t0047g0010 |
2 | HG01884.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1384-5805G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48290210 | |||||||
| chr16:48290335 | G | A | 4 | a0001c0001t0032g0124 a0001c0001t0034g0125 a0001c0001t0035g0127 others(1): Show |
4 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1384-5680G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48290335 | |||||||
| chr16:48290555 | G | A | 4 | a0001c0001t0032g0124 a0001c0001t0034g0125 a0001c0001t0035g0127 others(1): Show |
4 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1384-5460G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48290555 | |||||||
| chr16:48290589 | GAA | G | 18 | a0001c0001t0005g0001 a0001c0001t0005g0111 a0001c0001t0005g0128 others(15): Show |
18 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.1384-5424_1384-542 others(6): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr16 | 48290589 | ||||||
| chr16:48290715 | A | T | 63 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(60): Show |
64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.1384-5300A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48290715 | |||||||
| chr16:48290753 | C | T | 1 | a0001c0001t0029g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1384-5262C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48290753 | |||||||
| chr16:48290904 | C | T | 1 | a0001c0001t0082g0026 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1384-5111C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48290904 | |||||||
| chr16:48291182 | TTCTGTGG others(2): Show |
T | 5 | a0001c0001t0022g0117 a0001c0001t0023g0115 a0001c0001t0024g0118 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1384-4830_1384-482 others(13): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr16 | 48291182 | ||||||
| chr16:48291590 | C | G | 1 | a0001c0001t0011g0056 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1384-4425C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48291590 | |||||||
| chr16:48291609 | T | A | 4 | a0001c0003t0058g0123 a0001c0003t0059g0121 a0001c0003t0060g0122 others(1): Show |
4 | HG02486.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1384-4406T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48291609 | |||||||
| chr16:48291751 | G | A | 1 | a0001c0006t0038g0144 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1384-4264G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48291751 | |||||||
| chr16:48292682 | A | C | 1 | a0001c0001t0008g0090 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1384-3333A>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48292682 | |||||||
| chr16:48292838 | C | CT | 6 | a0001c0001t0032g0124 a0001c0001t0033g0147 a0001c0001t0034g0125 others(3): Show |
6 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1384-3176dupT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr16 | 48292838 | ||||||
| chr16:48292893 | C | T | 1 | a0002c0005t0052g0138 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1384-3122C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48292893 | |||||||
| chr16:48292926 | T | C | 1 | a0001c0002t0045g0012 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1384-3089T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48292926 | |||||||
| chr16:48292965 | A | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1384-3050A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48292965 | |||||||
| chr16:48292966 | A | G | 1 | a0001c0001t0073g0022 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1384-3049A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48292966 | |||||||
| chr16:48292970 | C | A | 1 | a0001c0002t0042g0009 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1384-3045C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48292970 | |||||||
| chr16:48293024 | G | A | 3 | a0001c0001t0030g0143 a0001c0001t0062g0142 a0001c0006t0038g0144 |
3 | HG02896.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1384-2991G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48293024 | |||||||
| chr16:48293177 | C | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1384-2838C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48293177 | |||||||
| chr16:48293225 | G | A | 10 | a0001c0001t0003g0024 a0001c0001t0003g0028 a0001c0001t0003g0029 others(7): Show |
10 | HG00323.hp1 HG00621.hp2 HG00642.hp2 others(7): Show |
intron_variant | MODIFIER | c.1384-2790G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48293225 | |||||||
| chr16:48293301 | G | A | 1 | a0001c0001t0089g0067 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1384-2714G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48293301 | |||||||
| chr16:48293324 | A | T | 1 | a0001c0001t0029g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1384-2691A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48293324 | |||||||
| chr16:48293374 | G | A | 6 | a0001c0001t0032g0124 a0001c0001t0033g0147 a0001c0001t0034g0125 others(3): Show |
6 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1384-2641G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48293374 | |||||||
| chr16:48293384 | C | T | 6 | a0001c0001t0032g0124 a0001c0001t0033g0147 a0001c0001t0034g0125 others(3): Show |
6 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1384-2631C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48293384 | |||||||
| chr16:48293425 | CA | C | 11 | a0001c0001t0003g0031 a0001c0002t0041g0015 a0001c0002t0042g0009 others(8): Show |
11 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.1384-2578delA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr16 | 48293425 | ||||||
| chr16:48293595 | G | A | 8 | a0001c0001t0029g0113 a0001c0001t0030g0143 a0001c0001t0062g0142 others(5): Show |
8 | HG02280.hp1 HG02486.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1384-2420G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48293595 | |||||||
| chr16:48293614 | G | A | 63 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(60): Show |
64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.1384-2401G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48293614 | |||||||
| chr16:48293731 | A | G | 2 | a0001c0001t0030g0143 a0001c0006t0038g0144 |
2 | HG02896.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1384-2284A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48293731 | |||||||
| chr16:48293877 | A | G | 1 | a0001c0001t0002g0043 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1384-2138A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48293877 | |||||||
| chr16:48293926 | A | C | 1 | a0001c0001t0005g0128 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1384-2089A>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48293926 | |||||||
| chr16:48293926 | AG | A | 8 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(5): Show |
8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1384-2088delG | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48293926 | |||||||
| chr16:48293981 | C | A | 63 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(60): Show |
64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.1384-2034C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48293981 | |||||||
| chr16:48294290 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1384-1725A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48294290 | |||||||
| chr16:48294636 | C | T | 2 | a0001c0002t0049g0017 a0001c0002t0050g0007 |
2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1384-1379C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48294636 | |||||||
| chr16:48294733 | C | CAAACA | 5 | a0001c0001t0032g0124 a0001c0001t0034g0125 a0001c0001t0035g0127 others(2): Show |
5 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1384-1258_1384-125 others(9): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr16 | 48294733 | ||||||
| chr16:48294733 | C | CAAACAAA others(3): Show |
1 | a0001c0001t0033g0147 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1384-1263_1384-125 others(14): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr16 | 48294733 | ||||||
| chr16:48294768 | C | T | 8 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(5): Show |
8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1384-1247C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48294768 | |||||||
| chr16:48295197 | C | T | 1 | a0001c0001t0003g0031 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1384-818C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | chr16 | 48295197 | |||||||
| chr16:48296007 | TC | T | 53 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(50): Show |
54 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(51): Show |
splice_region_variant&intron_variant | LOW | c.1384-4delC | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr16 | 48296007 | ||||||
| chr16:48296334 | A | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1534+169A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48296334 | |||||||
| chr16:48296343 | C | A | 1 | a0001c0001t0033g0147 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1534+178C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48296343 | |||||||
| chr16:48296542 | A | G | 1 | a0001c0002t0050g0007 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1534+377A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48296542 | |||||||
| chr16:48296620 | G | A | 1 | a0001c0001t0051g0146 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1534+455G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48296620 | |||||||
| chr16:48296722 | C | CA | 5 | a0001c0001t0006g0136 a0001c0001t0013g0099 a0001c0001t0022g0117 others(2): Show |
5 | HG02055.hp1 HG02572.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1534+576dupA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 48296722 | ||||||
| chr16:48296722 | CAAAAAAA others(1): Show |
C | 5 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0034 others(2): Show |
5 | HG01175.hp2 HG01496.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1534+569_1534+576d others(10): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 48296722 | ||||||
| chr16:48296797 | C | T | 1 | a0001c0003t0058g0123 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1534+632C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48296797 | |||||||
| chr16:48296958 | A | G | 1 | a0001c0001t0004g0107 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1534+793A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48296958 | |||||||
| chr16:48297029 | G | A | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1534+864G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48297029 | |||||||
| chr16:48297217 | C | G | 1 | a0001c0001t0029g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1534+1052C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48297217 | |||||||
| chr16:48297533 | C | A | 5 | a0001c0001t0032g0124 a0001c0001t0033g0147 a0001c0001t0034g0125 others(2): Show |
5 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1534+1368C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48297533 | |||||||
| chr16:48297630 | A | G | 6 | a0001c0001t0022g0117 a0001c0001t0023g0115 a0001c0001t0024g0118 others(3): Show |
6 | HG01884.hp2 HG02145.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1534+1465A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48297630 | |||||||
| chr16:48297641 | A | G | 3 | a0001c0001t0030g0143 a0001c0001t0062g0142 a0001c0006t0038g0144 |
3 | HG02896.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1534+1476A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48297641 | |||||||
| chr16:48297785 | T | C | 1 | a0001c0001t0001g0046 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1534+1620T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48297785 | |||||||
| chr16:48297837 | C | T | 1 | a0001c0001t0030g0143 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1534+1672C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48297837 | |||||||
| chr16:48298293 | A | G | 1 | a0001c0001t0008g0093 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1535-1369A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48298293 | |||||||
| chr16:48298460 | TAC | T | 4 | a0001c0003t0058g0123 a0001c0003t0059g0121 a0001c0003t0060g0122 others(1): Show |
4 | HG02486.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1535-1186_1535-118 others(6): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 48298460 | ||||||
| chr16:48298478 | T | C | 1 | a0001c0001t0016g0131 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1535-1184T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48298478 | |||||||
| chr16:48298506 | A | G | 4 | a0001c0003t0058g0123 a0001c0003t0059g0121 a0001c0003t0060g0122 others(1): Show |
4 | HG02486.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1535-1156A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48298506 | |||||||
| chr16:48298626 | G | GGGGT | 3 | a0001c0001t0007g0130 a0001c0001t0016g0001 a0003c0007t0007g0135 |
3 | HG01099.hp2 HG01106.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1535-1035_1535-103 others(8): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 48298626 | ||||||
| chr16:48298626 | G | GGGGTGTG others(1): Show |
5 | a0001c0001t0005g0111 a0001c0001t0005g0128 a0001c0001t0006g0133 others(2): Show |
5 | HG00323.hp2 HG01109.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.1535-1035_1535-103 others(12): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 48298626 | ||||||
| chr16:48298626 | G | GGGGTGTG others(3): Show |
3 | a0001c0001t0005g0132 a0001c0001t0006g0136 a0001c0001t0056g0001 |
3 | HG00733.hp2 HG01081.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1535-1035_1535-103 others(14): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 48298626 | ||||||
| chr16:48298626 | G | GGGGTGTG others(5): Show |
1 | a0002c0005t0052g0138 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1535-1035_1535-103 others(16): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 48298626 | ||||||
| chr16:48298626 | G | GGT | 23 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0046 others(20): Show |
24 | HG01071.hp2 HG01106.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.1535-993_1535-992d others(4): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 48298626 | ||||||
| chr16:48298626 | G | GGTGT | 22 | a0001c0001t0001g0034 a0001c0001t0001g0058 a0001c0001t0001g0059 others(19): Show |
22 | HG00621.hp2 HG00642.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.1535-995_1535-992d others(6): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 48298626 | ||||||
| chr16:48298626 | G | GGTGTGT | 12 | a0001c0001t0001g0047 a0001c0001t0001g0050 a0001c0001t0002g0075 others(9): Show |
12 | HG00558.hp1 HG00621.hp1 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.1535-997_1535-992d others(8): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 48298626 | ||||||
| chr16:48298626 | G | GGTGTGTG others(1): Show |
13 | a0001c0001t0001g0052 a0001c0001t0001g0072 a0001c0001t0002g0095 others(10): Show |
13 | HG00323.hp1 HG00733.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1535-999_1535-992d others(10): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 48298626 | ||||||
| chr16:48298626 | G | GGTGTGTG others(3): Show |
1 | a0001c0001t0082g0026 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1535-1001_1535-992 others(13): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 48298626 | ||||||
| chr16:48298626 | G | GGTGTGTG others(5): Show |
1 | a0001c0001t0001g0084 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1535-1003_1535-992 others(15): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 48298626 | ||||||
| chr16:48298626 | G | GGTGTGTG others(7): Show |
1 | a0001c0001t0001g0004 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1535-1005_1535-992 others(17): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 48298626 | ||||||
| chr16:48298626 | GGT | G | 8 | a0001c0001t0014g0005 a0001c0001t0014g0101 a0001c0001t0027g0102 others(5): Show |
8 | HG01891.hp1 HG01891.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1535-993_1535-992d others(4): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 48298626 | ||||||
| chr16:48298626 | GGTGT | G | 3 | a0001c0001t0002g0065 a0001c0001t0069g0066 a0001c0001t0089g0067 |
3 | HG01070.hp1 HG01515.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1535-995_1535-992d others(6): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 48298626 | ||||||
| chr16:48298626 | GGTGTGT | G | 7 | a0001c0001t0001g0073 a0001c0001t0002g0074 a0001c0001t0022g0117 others(4): Show |
7 | HG01081.hp1 HG01099.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.1535-997_1535-992d others(8): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 48298626 | ||||||
| chr16:48298626 | GGTGTGTG others(1): Show |
G | 2 | a0001c0001t0001g0091 a0001c0001t0064g0088 |
2 | HG00558.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.1535-999_1535-992d others(10): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 48298626 | ||||||
| chr16:48298626 | GGTGTGTG others(3): Show |
G | 7 | a0001c0001t0051g0146 a0001c0002t0049g0017 a0001c0002t0050g0007 others(4): Show |
7 | HG02486.hp2 HG02622.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1535-1001_1535-992 others(13): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 48298626 | ||||||
| chr16:48298626 | GGTGTGTG others(9): Show |
G | 1 | a0001c0001t0040g0119 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1535-1007_1535-992 others(19): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 48298626 | ||||||
| chr16:48298626 | GGTGTGTG others(19): Show |
G | 1 | a0001c0001t0007g0137 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1535-1017_1535-992 others(29): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr16 | 48298626 | ||||||
| chr16:48298628 | T | G | 3 | a0001c0001t0054g0139 a0001c0001t0055g0141 a0001c0001t0057g0140 |
3 | HG01175.hp1 HG02074.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.1535-1034T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48298628 | |||||||
| chr16:48298654 | T | G | 1 | a0001c0001t0007g0137 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1535-1008T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48298654 | |||||||
| chr16:48298670 | T | TGTG | 2 | a0001c0001t0070g0061 a0001c0001t0071g0098 |
2 | HG04199.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1535-992_1535-991i others(5): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48298670 | |||||||
| chr16:48298670 | T | TGTGTG | 2 | a0001c0001t0002g0043 a0001c0001t0076g0064 |
2 | HG01109.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1535-992_1535-991i others(7): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48298670 | |||||||
| chr16:48298670 | T | TGTGTGTG | 2 | a0001c0001t0003g0016 a0001c0001t0009g0019 |
2 | HG02922.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1535-992_1535-991i others(9): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48298670 | |||||||
| chr16:48298670 | T | TGTGTGTG others(2): Show |
2 | a0001c0001t0010g0021 a0001c0001t0020g0036 |
2 | HG02055.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1535-992_1535-991i others(11): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48298670 | |||||||
| chr16:48298670 | T | TGTGTGTG others(4): Show |
1 | a0001c0001t0021g0039 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1535-992_1535-991i others(13): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48298670 | |||||||
| chr16:48298683 | T | A | 1 | a0001c0001t0002g0075 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1535-979T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48298683 | |||||||
| chr16:48298874 | A | G | 2 | a0001c0001t0002g0003 a0001c0001t0008g0093 |
3 | HG02559.hp2 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1535-788A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48298874 | |||||||
| chr16:48299181 | C | T | 1 | a0001c0001t0084g0032 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1535-481C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48299181 | |||||||
| chr16:48299193 | G | T | 13 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0034 others(10): Show |
13 | HG01106.hp1 HG01175.hp2 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.1535-469G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48299193 | |||||||
| chr16:48299401 | T | C | 1 | a0001c0001t0083g0112 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1535-261T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48299401 | |||||||
| chr16:48299624 | A | G | 7 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(4): Show |
8 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.1535-38A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 9/14 | chr16 | 48299624 | |||||||
| chr16:48300007 | G | A | 1 | a0002c0005t0052g0138 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1661+219G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 10/14 | chr16 | 48300007 | |||||||
| chr16:48300198 | G | C | 1 | a0001c0001t0001g0091 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1661+410G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 10/14 | chr16 | 48300198 | |||||||
| chr16:48300250 | T | A | 2 | a0001c0002t0049g0017 a0001c0002t0050g0007 |
2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1661+462T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 10/14 | chr16 | 48300250 | |||||||
| chr16:48300403 | A | G | 8 | a0001c0001t0029g0113 a0001c0001t0030g0143 a0001c0001t0062g0142 others(5): Show |
8 | HG02280.hp1 HG02486.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1661+615A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 10/14 | chr16 | 48300403 | |||||||
| chr16:48300525 | C | A | 1 | a0001c0001t0006g0136 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1661+737C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 10/14 | chr16 | 48300525 | |||||||
| chr16:48300689 | C | CT | 48 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(45): Show |
49 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.1661+902dupT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr16 | 48300689 | ||||||
| chr16:48300942 | A | T | 3 | a0001c0001t0030g0143 a0001c0001t0062g0142 a0001c0006t0038g0144 |
3 | HG02896.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1661+1154A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 10/14 | chr16 | 48300942 | |||||||
| chr16:48300962 | G | C | 1 | a0001c0001t0008g0090 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1661+1174G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 10/14 | chr16 | 48300962 | |||||||
| chr16:48301070 | T | C | 2 | a0001c0001t0002g0003 a0001c0001t0008g0093 |
3 | HG02559.hp2 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1661+1282T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 10/14 | chr16 | 48301070 | |||||||
| chr16:48301570 | G | A | 1 | a0001c0001t0087g0027 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1662-1602G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 10/14 | chr16 | 48301570 | |||||||
| chr16:48301679 | C | G | 13 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0034 others(10): Show |
13 | HG01106.hp1 HG01175.hp2 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.1662-1493C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 10/14 | chr16 | 48301679 | |||||||
| chr16:48301705 | G | C | 2 | a0001c0002t0049g0017 a0001c0002t0050g0007 |
2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1662-1467G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 10/14 | chr16 | 48301705 | |||||||
| chr16:48302108 | A | G | 1 | a0001c0002t0049g0017 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1662-1064A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 10/14 | chr16 | 48302108 | |||||||
| chr16:48302419 | A | G | 1 | a0001c0001t0035g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1662-753A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 10/14 | chr16 | 48302419 | |||||||
| chr16:48302509 | G | A | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1662-663G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 10/14 | chr16 | 48302509 | |||||||
| chr16:48302571 | TA | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1662-598delA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr16 | 48302571 | ||||||
| chr16:48302586 | A | G | 63 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(60): Show |
64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.1662-586A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 10/14 | chr16 | 48302586 | |||||||
| chr16:48302869 | G | T | 12 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0034 others(9): Show |
12 | HG01106.hp1 HG01175.hp2 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.1662-303G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 10/14 | chr16 | 48302869 | |||||||
| chr16:48303647 | C | A | 43 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(40): Show |
44 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1795+342C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48303647 | |||||||
| chr16:48303673 | G | C | 4 | a0001c0003t0058g0123 a0001c0003t0059g0121 a0001c0003t0060g0122 others(1): Show |
4 | HG02486.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1795+368G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48303673 | |||||||
| chr16:48303824 | C | T | 1 | a0001c0001t0003g0029 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1795+519C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48303824 | |||||||
| chr16:48303845 | A | G | 1 | a0001c0001t0040g0119 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1795+540A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48303845 | |||||||
| chr16:48303946 | C | G | 18 | a0001c0001t0005g0001 a0001c0001t0005g0111 a0001c0001t0005g0128 others(15): Show |
18 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.1795+641C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48303946 | |||||||
| chr16:48303983 | C | A | 4 | a0001c0001t0032g0124 a0001c0001t0034g0125 a0001c0001t0035g0127 others(1): Show |
4 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1795+678C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48303983 | |||||||
| chr16:48304215 | C | A | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1795+910C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48304215 | |||||||
| chr16:48304589 | C | T | 2 | a0001c0002t0049g0017 a0001c0002t0050g0007 |
2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1795+1284C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48304589 | |||||||
| chr16:48304684 | A | G | 1 | a0001c0001t0002g0075 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1795+1379A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48304684 | |||||||
| chr16:48304845 | T | A | 2 | a0001c0002t0049g0017 a0001c0002t0050g0007 |
2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1795+1540T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48304845 | |||||||
| chr16:48305232 | T | G | 1 | a0001c0002t0041g0015 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1795+1927T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48305232 | |||||||
| chr16:48305251 | T | G | 6 | a0001c0001t0013g0099 a0001c0001t0013g0100 a0001c0001t0014g0005 others(3): Show |
6 | HG01891.hp2 HG02258.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1795+1946T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48305251 | |||||||
| chr16:48305411 | C | T | 15 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(12): Show |
16 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.1795+2106C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48305411 | |||||||
| chr16:48305426 | T | C | 1 | a0001c0001t0074g0081 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1795+2121T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48305426 | |||||||
| chr16:48305478 | C | G | 1 | a0001c0004t0063g0094 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1795+2173C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48305478 | |||||||
| chr16:48305577 | C | T | 1 | a0001c0001t0007g0137 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1795+2272C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48305577 | |||||||
| chr16:48305857 | A | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1795+2552A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48305857 | |||||||
| chr16:48305886 | A | G | 1 | a0001c0001t0029g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1795+2581A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48305886 | |||||||
| chr16:48305947 | T | A | 4 | a0001c0003t0058g0123 a0001c0003t0059g0121 a0001c0003t0060g0122 others(1): Show |
4 | HG02486.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1795+2642T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48305947 | |||||||
| chr16:48306104 | C | T | 4 | a0001c0001t0032g0124 a0001c0001t0034g0125 a0001c0001t0035g0127 others(1): Show |
4 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1795+2799C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48306104 | |||||||
| chr16:48306222 | A | G | 40 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(37): Show |
41 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.1795+2917A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48306222 | |||||||
| chr16:48306307 | T | G | 3 | a0001c0001t0030g0143 a0001c0001t0062g0142 a0001c0006t0038g0144 |
3 | HG02896.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1795+3002T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48306307 | |||||||
| chr16:48306318 | T | G | 1 | a0001c0001t0034g0125 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1795+3013T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48306318 | |||||||
| chr16:48306359 | T | C | 63 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(60): Show |
64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.1795+3054T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48306359 | |||||||
| chr16:48306434 | G | A | 1 | a0001c0001t0062g0142 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1795+3129G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48306434 | |||||||
| chr16:48306574 | C | T | 2 | a0001c0002t0049g0017 a0001c0002t0050g0007 |
2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1795+3269C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48306574 | |||||||
| chr16:48306727 | A | G | 3 | a0001c0001t0009g0019 a0001c0001t0009g0020 a0001c0001t0068g0077 |
3 | HG02258.hp2 HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1795+3422A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48306727 | |||||||
| chr16:48307056 | G | T | 1 | a0001c0001t0002g0062 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1795+3751G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48307056 | |||||||
| chr16:48307138 | G | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1795+3833G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48307138 | |||||||
| chr16:48307164 | G | T | 2 | a0001c0001t0030g0143 a0001c0006t0038g0144 |
2 | HG02896.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1795+3859G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48307164 | |||||||
| chr16:48307516 | T | C | 1 | a0001c0001t0064g0088 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1795+4211T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48307516 | |||||||
| chr16:48307561 | G | C | 1 | a0001c0001t0040g0119 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1795+4256G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48307561 | |||||||
| chr16:48307653 | T | TA | 7 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(4): Show |
8 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.1795+4349dupA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 48307653 | ||||||
| chr16:48307833 | G | A | 5 | a0001c0001t0032g0124 a0001c0001t0033g0147 a0001c0001t0034g0125 others(2): Show |
5 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1795+4528G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48307833 | |||||||
| chr16:48308069 | T | C | 1 | a0001c0002t0049g0017 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1795+4764T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48308069 | |||||||
| chr16:48308367 | C | T | 6 | a0001c0001t0032g0124 a0001c0001t0033g0147 a0001c0001t0034g0125 others(3): Show |
6 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1795+5062C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48308367 | |||||||
| chr16:48308628 | C | CA | 44 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(41): Show |
45 | HG00738.hp1 HG00738.hp2 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.1795+5341dupA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 48308628 | ||||||
| chr16:48308825 | C | T | 4 | a0001c0001t0032g0124 a0001c0001t0034g0125 a0001c0001t0035g0127 others(1): Show |
4 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1795+5520C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48308825 | |||||||
| chr16:48308847 | A | G | 7 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(4): Show |
8 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.1795+5542A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48308847 | |||||||
| chr16:48309251 | C | T | 1 | a0001c0001t0082g0026 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1795+5946C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48309251 | |||||||
| chr16:48309286 | A | C | 6 | a0001c0001t0032g0124 a0001c0001t0033g0147 a0001c0001t0034g0125 others(3): Show |
6 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1795+5981A>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48309286 | |||||||
| chr16:48309537 | C | T | 4 | a0001c0003t0058g0123 a0001c0003t0059g0121 a0001c0003t0060g0122 others(1): Show |
4 | HG02486.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1795+6232C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48309537 | |||||||
| chr16:48309694 | T | C | 1 | a0001c0001t0001g0079 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1795+6389T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48309694 | |||||||
| chr16:48309731 | A | T | 88 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0034 others(85): Show |
90 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(87): Show |
intron_variant | MODIFIER | c.1795+6426A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48309731 | |||||||
| chr16:48309964 | G | A | 1 | a0001c0001t0033g0147 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1795+6659G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48309964 | |||||||
| chr16:48309977 | G | C | 5 | a0001c0001t0022g0117 a0001c0001t0023g0115 a0001c0001t0024g0118 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1795+6672G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48309977 | |||||||
| chr16:48310414 | C | T | 8 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(5): Show |
8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1795+7109C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48310414 | |||||||
| chr16:48310445 | A | G | 64 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(61): Show |
65 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(62): Show |
intron_variant | MODIFIER | c.1795+7140A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48310445 | |||||||
| chr16:48310799 | C | CA | 64 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(61): Show |
65 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(62): Show |
intron_variant | MODIFIER | c.1795+7495dupA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 48310799 | ||||||
| chr16:48310802 | C | T | 6 | a0001c0001t0019g0018 a0001c0001t0022g0117 a0001c0001t0023g0115 others(3): Show |
6 | HG01884.hp2 HG02145.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1795+7497C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48310802 | |||||||
| chr16:48310946 | T | C | 1 | a0001c0001t0029g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1795+7641T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48310946 | |||||||
| chr16:48311049 | A | G | 18 | a0001c0001t0005g0001 a0001c0001t0005g0111 a0001c0001t0005g0128 others(15): Show |
18 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.1795+7744A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48311049 | |||||||
| chr16:48311235 | C | T | 1 | a0001c0001t0027g0102 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1795+7930C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48311235 | |||||||
| chr16:48311280 | T | C | 8 | a0001c0001t0013g0099 a0001c0001t0013g0100 a0001c0001t0014g0005 others(5): Show |
8 | HG01891.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1795+7975T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48311280 | |||||||
| chr16:48311666 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1795+8361G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48311666 | |||||||
| chr16:48311944 | T | C | 1 | a0001c0001t0040g0119 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1795+8639T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48311944 | |||||||
| chr16:48312104 | C | A | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1795+8799C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48312104 | |||||||
| chr16:48312156 | A | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1795+8851A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48312156 | |||||||
| chr16:48312325 | G | A | 2 | a0001c0002t0049g0017 a0001c0002t0050g0007 |
2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1795+9020G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48312325 | |||||||
| chr16:48312531 | A | G | 1 | a0001c0001t0003g0078 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1795+9226A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48312531 | |||||||
| chr16:48312623 | G | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1795+9318G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48312623 | |||||||
| chr16:48313035 | A | G | 1 | a0001c0001t0029g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1795+9730A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48313035 | |||||||
| chr16:48313064 | A | T | 4 | a0001c0001t0005g0111 a0001c0001t0005g0128 a0001c0001t0006g0133 others(1): Show |
4 | HG01109.hp1 HG02145.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1795+9759A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48313064 | |||||||
| chr16:48313222 | T | C | 1 | a0001c0001t0004g0006 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1795+9917T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48313222 | |||||||
| chr16:48313286 | C | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1795+9981C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48313286 | |||||||
| chr16:48313438 | C | G | 5 | a0001c0001t0032g0124 a0001c0001t0033g0147 a0001c0001t0034g0125 others(2): Show |
5 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1795+10133C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48313438 | |||||||
| chr16:48313501 | C | A | 5 | a0001c0001t0032g0124 a0001c0001t0033g0147 a0001c0001t0034g0125 others(2): Show |
5 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1795+10196C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48313501 | |||||||
| chr16:48313617 | T | C | 2 | a0001c0001t0067g0068 a0001c0001t0080g0025 |
2 | HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1795+10312T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48313617 | |||||||
| chr16:48313734 | C | T | 5 | a0001c0001t0032g0124 a0001c0001t0033g0147 a0001c0001t0034g0125 others(2): Show |
5 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1795+10429C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48313734 | |||||||
| chr16:48313953 | A | G | 1 | a0001c0001t0051g0146 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1795+10648A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48313953 | |||||||
| chr16:48313990 | A | G | 15 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(12): Show |
16 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.1795+10685A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48313990 | |||||||
| chr16:48314023 | A | C | 1 | a0001c0001t0029g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1795+10718A>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48314023 | |||||||
| chr16:48314080 | T | A | 5 | a0001c0001t0032g0124 a0001c0001t0033g0147 a0001c0001t0034g0125 others(2): Show |
5 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1795+10775T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48314080 | |||||||
| chr16:48314377 | C | T | 3 | a0001c0001t0001g0046 a0001c0001t0001g0050 a0001c0001t0011g0051 |
3 | HG00621.hp1 HG01071.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.1795+11072C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48314377 | |||||||
| chr16:48314741 | C | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1795+11436C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48314741 | |||||||
| chr16:48314757 | T | C | 1 | a0001c0001t0002g0043 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1795+11452T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48314757 | |||||||
| chr16:48314862 | G | T | 4 | a0001c0003t0058g0123 a0001c0003t0059g0121 a0001c0003t0060g0122 others(1): Show |
4 | HG02486.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1795+11557G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48314862 | |||||||
| chr16:48314988 | A | C | 63 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(60): Show |
64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.1795+11683A>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48314988 | |||||||
| chr16:48315062 | G | A | 2 | a0001c0002t0043g0011 a0001c0002t0047g0010 |
2 | HG01884.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1795+11757G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48315062 | |||||||
| chr16:48315214 | C | T | 5 | a0001c0001t0032g0124 a0001c0001t0033g0147 a0001c0001t0034g0125 others(2): Show |
5 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1795+11909C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48315214 | |||||||
| chr16:48315263 | G | A | 1 | a0001c0001t0017g0054 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1795+11958G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48315263 | |||||||
| chr16:48315398 | C | T | 8 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(5): Show |
8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1795+12093C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48315398 | |||||||
| chr16:48315425 | G | C | 2 | a0001c0002t0049g0017 a0001c0002t0050g0007 |
2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1795+12120G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48315425 | |||||||
| chr16:48315518 | A | C | 1 | a0001c0001t0070g0061 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1795+12213A>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48315518 | |||||||
| chr16:48315765 | C | G | 1 | a0001c0001t0090g0106 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1795+12460C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48315765 | |||||||
| chr16:48315795 | C | T | 64 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(61): Show |
65 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(62): Show |
intron_variant | MODIFIER | c.1795+12490C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48315795 | |||||||
| chr16:48315822 | A | AT | 15 | a0001c0001t0022g0117 a0001c0001t0023g0115 a0001c0001t0024g0118 others(12): Show |
15 | HG01884.hp1 HG01884.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1795+12527dupT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 48315822 | ||||||
| chr16:48315963 | A | AT | 37 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(34): Show |
38 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.1795+12679dupT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 48315963 | ||||||
| chr16:48315963 | A | ATT | 13 | a0001c0001t0029g0113 a0001c0001t0030g0143 a0001c0001t0032g0124 others(10): Show |
13 | HG01891.hp1 HG02280.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1795+12678_1795+12 others(8): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 48315963 | ||||||
| chr16:48315963 | ATT | A | 7 | a0001c0002t0042g0009 a0001c0002t0043g0011 a0001c0002t0044g0014 others(4): Show |
7 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1795+12678_1795+12 others(8): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 48315963 | ||||||
| chr16:48315984 | T | A | 1 | a0001c0002t0047g0010 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1795+12679T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48315984 | |||||||
| chr16:48316070 | C | T | 8 | a0001c0001t0013g0099 a0001c0001t0013g0100 a0001c0001t0014g0005 others(5): Show |
8 | HG01891.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1795+12765C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48316070 | |||||||
| chr16:48316272 | G | A | 18 | a0001c0001t0005g0001 a0001c0001t0005g0111 a0001c0001t0005g0128 others(15): Show |
18 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.1795+12967G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48316272 | |||||||
| chr16:48316305 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1795+13000C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48316305 | |||||||
| chr16:48316323 | C | CT | 36 | a0001c0001t0005g0001 a0001c0001t0005g0111 a0001c0001t0005g0128 others(33): Show |
36 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(33): Show |
intron_variant | MODIFIER | c.1795+13039dupT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 48316323 | ||||||
| chr16:48316323 | C | CTT | 11 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(8): Show |
12 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.1795+13038_1795+13 others(8): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 48316323 | ||||||
| chr16:48316475 | C | T | 1 | a0001c0001t0017g0054 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1795+13170C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48316475 | |||||||
| chr16:48316507 | A | T | 1 | a0001c0001t0002g0075 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1795+13202A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48316507 | |||||||
| chr16:48316655 | A | G | 1 | a0001c0001t0003g0024 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1795+13350A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48316655 | |||||||
| chr16:48316977 | T | C | 1 | a0001c0001t0051g0146 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1795+13672T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48316977 | |||||||
| chr16:48317016 | G | A | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1795+13711G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48317016 | |||||||
| chr16:48317576 | A | G | 6 | a0001c0001t0013g0099 a0001c0001t0013g0100 a0001c0001t0014g0005 others(3): Show |
6 | HG01891.hp2 HG02258.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1795+14271A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48317576 | |||||||
| chr16:48317988 | G | A | 1 | a0001c0001t0006g0136 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1795+14683G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48317988 | |||||||
| chr16:48318227 | A | G | 53 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(50): Show |
54 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.1795+14922A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48318227 | |||||||
| chr16:48318597 | T | G | 1 | a0001c0006t0038g0144 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1795+15292T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48318597 | |||||||
| chr16:48318978 | C | CT | 9 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(6): Show |
10 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.1796-15225dupT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 48318978 | ||||||
| chr16:48319078 | G | GTT | 63 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(60): Show |
64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.1796-15136_1796-15 others(8): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 48319078 | ||||||
| chr16:48319183 | C | T | 1 | a0001c0001t0030g0143 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1796-15033C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48319183 | |||||||
| chr16:48319342 | A | T | 2 | a0001c0001t0065g0030 a0001c0001t0080g0025 |
2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1796-14874A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48319342 | |||||||
| chr16:48319536 | A | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1796-14680A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48319536 | |||||||
| chr16:48319609 | G | A | 63 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(60): Show |
64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.1796-14607G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48319609 | |||||||
| chr16:48319687 | G | T | 3 | a0001c0001t0030g0143 a0001c0001t0062g0142 a0001c0006t0038g0144 |
3 | HG02896.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1796-14529G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48319687 | |||||||
| chr16:48319751 | C | T | 2 | a0001c0002t0049g0017 a0001c0002t0050g0007 |
2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1796-14465C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48319751 | |||||||
| chr16:48319972 | C | T | 4 | a0001c0003t0058g0123 a0001c0003t0059g0121 a0001c0003t0060g0122 others(1): Show |
4 | HG02486.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1796-14244C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48319972 | |||||||
| chr16:48320159 | C | CA | 15 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(12): Show |
16 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.1796-14037dupA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 48320159 | ||||||
| chr16:48320159 | CA | C | 5 | a0001c0001t0001g0084 a0001c0001t0002g0074 a0001c0001t0029g0113 others(2): Show |
5 | HG01099.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1796-14037delA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 48320159 | ||||||
| chr16:48320180 | G | A | 4 | a0001c0003t0058g0123 a0001c0003t0059g0121 a0001c0003t0060g0122 others(1): Show |
4 | HG02486.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1796-14036G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48320180 | |||||||
| chr16:48320250 | A | G | 1 | a0001c0001t0062g0142 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1796-13966A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48320250 | |||||||
| chr16:48320452 | G | A | 5 | a0001c0001t0022g0117 a0001c0001t0023g0115 a0001c0001t0024g0118 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1796-13764G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48320452 | |||||||
| chr16:48320529 | A | T | 5 | a0001c0001t0032g0124 a0001c0001t0033g0147 a0001c0001t0034g0125 others(2): Show |
5 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1796-13687A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48320529 | |||||||
| chr16:48321022 | C | T | 1 | a0001c0001t0029g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1796-13194C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48321022 | |||||||
| chr16:48321034 | A | C | 1 | a0001c0001t0004g0006 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1796-13182A>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48321034 | |||||||
| chr16:48321177 | G | A | 1 | a0001c0001t0009g0019 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1796-13039G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48321177 | |||||||
| chr16:48321180 | C | T | 1 | a0001c0001t0033g0147 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1796-13036C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48321180 | |||||||
| chr16:48321356 | A | G | 4 | a0001c0003t0058g0123 a0001c0003t0059g0121 a0001c0003t0060g0122 others(1): Show |
4 | HG02486.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1796-12860A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48321356 | |||||||
| chr16:48321372 | C | T | 4 | a0001c0001t0012g0055 a0001c0001t0012g0092 a0001c0001t0075g0082 others(1): Show |
4 | HG02129.hp2 HG03927.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.1796-12844C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48321372 | |||||||
| chr16:48321378 | A | G | 1 | a0001c0001t0029g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1796-12838A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48321378 | |||||||
| chr16:48321393 | G | A | 5 | a0001c0001t0032g0124 a0001c0001t0033g0147 a0001c0001t0034g0125 others(2): Show |
5 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1796-12823G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48321393 | |||||||
| chr16:48321419 | A | G | 1 | a0001c0001t0040g0119 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1796-12797A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48321419 | |||||||
| chr16:48321499 | C | T | 5 | a0001c0001t0029g0113 a0001c0003t0058g0123 a0001c0003t0059g0121 others(2): Show |
5 | HG02280.hp1 HG02486.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1796-12717C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48321499 | |||||||
| chr16:48321509 | G | A | 2 | a0001c0001t0002g0003 a0001c0001t0008g0093 |
3 | HG02559.hp2 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1796-12707G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48321509 | |||||||
| chr16:48321573 | T | A | 7 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(4): Show |
8 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.1796-12643T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48321573 | |||||||
| chr16:48321578 | G | A | 2 | a0001c0002t0049g0017 a0001c0002t0050g0007 |
2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1796-12638G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48321578 | |||||||
| chr16:48321625 | G | C | 3 | a0001c0001t0030g0143 a0001c0001t0062g0142 a0001c0006t0038g0144 |
3 | HG02896.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1796-12591G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48321625 | |||||||
| chr16:48321633 | GTA | G | 2 | a0001c0002t0049g0017 a0001c0002t0050g0007 |
2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1796-12580_1796-12 others(8): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 48321633 | ||||||
| chr16:48321823 | G | T | 1 | a0001c0001t0030g0143 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1796-12393G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48321823 | |||||||
| chr16:48321944 | CT | C | 8 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(5): Show |
8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1796-12259delT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 48321944 | ||||||
| chr16:48322028 | C | T | 5 | a0001c0001t0022g0117 a0001c0001t0023g0115 a0001c0001t0024g0118 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1796-12188C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48322028 | |||||||
| chr16:48322079 | C | T | 7 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(4): Show |
8 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.1796-12137C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48322079 | |||||||
| chr16:48322694 | G | A | 3 | a0001c0001t0030g0143 a0001c0001t0062g0142 a0001c0006t0038g0144 |
3 | HG02896.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1796-11522G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48322694 | |||||||
| chr16:48322703 | C | T | 2 | a0001c0001t0065g0030 a0001c0001t0080g0025 |
2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1796-11513C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48322703 | |||||||
| chr16:48322734 | T | A | 11 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(8): Show |
11 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.1796-11482T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48322734 | |||||||
| chr16:48323036 | C | G | 1 | a0001c0001t0081g0070 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1796-11180C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48323036 | |||||||
| chr16:48323247 | T | A | 1 | a0001c0001t0029g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1796-10969T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48323247 | |||||||
| chr16:48323369 | G | A | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1796-10847G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48323369 | |||||||
| chr16:48323425 | C | T | 6 | a0001c0001t0005g0001 a0001c0001t0005g0132 a0001c0001t0006g0129 others(3): Show |
6 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.1796-10791C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48323425 | |||||||
| chr16:48323477 | A | G | 4 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0017g0004 others(1): Show |
4 | HG01496.hp2 HG01975.hp1 HG02074.hp2 others(1): Show |
intron_variant | MODIFIER | c.1796-10739A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48323477 | |||||||
| chr16:48323484 | G | A | 5 | a0001c0001t0022g0117 a0001c0001t0023g0115 a0001c0001t0024g0118 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1796-10732G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48323484 | |||||||
| chr16:48323528 | C | T | 5 | a0001c0001t0022g0117 a0001c0001t0023g0115 a0001c0001t0024g0118 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1796-10688C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48323528 | |||||||
| chr16:48323657 | C | CA | 5 | a0001c0001t0020g0063 a0001c0001t0022g0117 a0001c0001t0034g0125 others(2): Show |
5 | HG00741.hp2 HG01106.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.1796-10544dupA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 48323657 | ||||||
| chr16:48323657 | CA | C | 8 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(5): Show |
8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1796-10544delA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 48323657 | ||||||
| chr16:48323781 | C | T | 2 | a0001c0001t0001g0038 a0001c0001t0002g0037 |
2 | HG02572.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1796-10435C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48323781 | |||||||
| chr16:48324457 | A | G | 108 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0034 others(105): Show |
110 | HG00323.hp2 HG00558.hp2 HG00733.hp2 others(107): Show |
intron_variant | MODIFIER | c.1796-9759A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48324457 | |||||||
| chr16:48324664 | C | T | 2 | a0001c0001t0055g0141 a0001c0001t0057g0140 |
2 | HG02074.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.1796-9552C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48324664 | |||||||
| chr16:48324665 | G | A | 1 | a0001c0002t0041g0015 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1796-9551G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48324665 | |||||||
| chr16:48324773 | C | A | 63 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(60): Show |
64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.1796-9443C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48324773 | |||||||
| chr16:48325628 | A | G | 2 | a0001c0002t0049g0017 a0001c0002t0050g0007 |
2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1796-8588A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48325628 | |||||||
| chr16:48325664 | A | G | 2 | a0001c0001t0033g0147 a0001c0001t0051g0146 |
2 | NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1796-8552A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48325664 | |||||||
| chr16:48325721 | T | C | 1 | a0001c0001t0006g0136 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1796-8495T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48325721 | |||||||
| chr16:48326342 | C | T | 5 | a0001c0001t0032g0124 a0001c0001t0033g0147 a0001c0001t0034g0125 others(2): Show |
5 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1796-7874C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48326342 | |||||||
| chr16:48326948 | A | C | 1 | a0001c0001t0006g0133 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1796-7268A>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48326948 | |||||||
| chr16:48327039 | C | A | 4 | a0001c0003t0058g0123 a0001c0003t0059g0121 a0001c0003t0060g0122 others(1): Show |
4 | HG02486.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1796-7177C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48327039 | |||||||
| chr16:48327129 | G | A | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1796-7087G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48327129 | |||||||
| chr16:48327271 | T | G | 64 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(61): Show |
65 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(62): Show |
intron_variant | MODIFIER | c.1796-6945T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48327271 | |||||||
| chr16:48327467 | T | G | 1 | a0001c0001t0032g0124 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1796-6749T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48327467 | |||||||
| chr16:48328076 | G | A | 8 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(5): Show |
8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1796-6140G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48328076 | |||||||
| chr16:48328214 | A | T | 1 | a0001c0001t0070g0061 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1796-6002A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48328214 | |||||||
| chr16:48328221 | C | T | 5 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0050 others(2): Show |
5 | HG00558.hp1 HG00621.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1796-5995C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48328221 | |||||||
| chr16:48328222 | C | T | 5 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0050 others(2): Show |
5 | HG00558.hp1 HG00621.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1796-5994C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48328222 | |||||||
| chr16:48328224 | A | G | 3 | a0001c0001t0030g0143 a0001c0001t0062g0142 a0001c0006t0038g0144 |
3 | HG02896.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1796-5992A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48328224 | |||||||
| chr16:48328322 | A | T | 5 | a0001c0001t0022g0117 a0001c0001t0023g0115 a0001c0001t0024g0118 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1796-5894A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48328322 | |||||||
| chr16:48328504 | C | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1796-5712C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48328504 | |||||||
| chr16:48328670 | C | T | 1 | a0001c0002t0050g0007 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1796-5546C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48328670 | |||||||
| chr16:48328675 | C | CA | 5 | a0001c0001t0032g0124 a0001c0001t0034g0125 a0001c0001t0035g0127 others(2): Show |
5 | HG00642.hp2 HG01891.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1796-5521dupA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 48328675 | ||||||
| chr16:48328787 | G | A | 2 | a0001c0002t0043g0011 a0001c0002t0047g0010 |
2 | HG01884.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1796-5429G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48328787 | |||||||
| chr16:48328836 | A | G | 6 | a0001c0002t0049g0017 a0001c0002t0050g0007 a0001c0003t0058g0123 others(3): Show |
6 | HG02486.hp2 HG02622.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1796-5380A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48328836 | |||||||
| chr16:48329160 | C | A | 8 | a0001c0001t0029g0113 a0001c0001t0030g0143 a0001c0001t0062g0142 others(5): Show |
8 | HG02280.hp1 HG02486.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1796-5056C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48329160 | |||||||
| chr16:48329257 | G | C | 3 | a0001c0001t0001g0059 a0001c0001t0002g0060 a0001c0001t0002g0062 |
3 | HG02109.hp1 HG03130.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1796-4959G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48329257 | |||||||
| chr16:48329608 | A | G | 18 | a0001c0001t0005g0001 a0001c0001t0005g0111 a0001c0001t0005g0128 others(15): Show |
18 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.1796-4608A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48329608 | |||||||
| chr16:48329643 | C | T | 1 | a0001c0001t0051g0146 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1796-4573C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48329643 | |||||||
| chr16:48329661 | T | C | 3 | a0001c0001t0030g0143 a0001c0001t0062g0142 a0001c0006t0038g0144 |
3 | HG02896.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1796-4555T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48329661 | |||||||
| chr16:48329772 | A | G | 1 | a0001c0001t0062g0142 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1796-4444A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48329772 | |||||||
| chr16:48329971 | G | C | 6 | a0001c0001t0013g0099 a0001c0001t0013g0100 a0001c0001t0014g0005 others(3): Show |
6 | HG01891.hp2 HG02258.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1796-4245G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48329971 | |||||||
| chr16:48329978 | AG | A | 8 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(5): Show |
8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1796-4237delG | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48329978 | |||||||
| chr16:48329999 | G | A | 15 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(12): Show |
16 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.1796-4217G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48329999 | |||||||
| chr16:48330334 | G | A | 8 | a0001c0001t0013g0099 a0001c0001t0013g0100 a0001c0001t0014g0005 others(5): Show |
8 | HG01891.hp2 HG02109.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1796-3882G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48330334 | |||||||
| chr16:48331140 | C | T | 2 | a0001c0001t0008g0089 a0001c0001t0008g0090 |
2 | HG02083.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.1796-3076C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48331140 | |||||||
| chr16:48331151 | T | TAG | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1796-3064_1796-306 others(6): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 48331151 | ||||||
| chr16:48331403 | A | T | 1 | a0001c0001t0002g0075 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1796-2813A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48331403 | |||||||
| chr16:48331566 | C | CTT | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1796-2635_1796-263 others(6): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 48331566 | ||||||
| chr16:48331642 | G | A | 4 | a0001c0001t0009g0019 a0001c0001t0009g0020 a0001c0001t0009g0076 others(1): Show |
4 | HG02258.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1796-2574G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48331642 | |||||||
| chr16:48331665 | C | T | 8 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(5): Show |
8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1796-2551C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48331665 | |||||||
| chr16:48331839 | C | T | 18 | a0001c0001t0005g0001 a0001c0001t0005g0111 a0001c0001t0005g0128 others(15): Show |
18 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.1796-2377C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48331839 | |||||||
| chr16:48331846 | G | A | 2 | a0001c0002t0049g0017 a0001c0002t0050g0007 |
2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1796-2370G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48331846 | |||||||
| chr16:48332370 | G | A | 1 | a0001c0001t0087g0027 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1796-1846G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48332370 | |||||||
| chr16:48332607 | A | T | 1 | a0001c0001t0030g0143 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1796-1609A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48332607 | |||||||
| chr16:48332698 | G | A | 4 | a0001c0001t0009g0019 a0001c0001t0009g0020 a0001c0001t0009g0076 others(1): Show |
4 | HG02258.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1796-1518G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48332698 | |||||||
| chr16:48332924 | T | TAGAC | 63 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(60): Show |
64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.1796-1290_1796-128 others(8): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 48332924 | ||||||
| chr16:48333124 | G | T | 1 | a0001c0001t0086g0080 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1796-1092G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48333124 | |||||||
| chr16:48333647 | CA | C | 12 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(9): Show |
13 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.1796-555delA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 48333647 | ||||||
| chr16:48333647 | CAAAA | C | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1796-558_1796-555d others(6): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 48333647 | ||||||
| chr16:48333801 | TAGATC | T | 7 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(4): Show |
8 | HG00738.hp2 HG00741.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.1796-411_1796-407d others(7): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 48333801 | ||||||
| chr16:48333961 | A | G | 1 | a0001c0001t0015g0108 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1796-255A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48333961 | |||||||
| chr16:48334037 | G | A | 1 | a0001c0001t0033g0147 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1796-179G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 11/14 | chr16 | 48334037 | |||||||
| chr16:48334579 | C | G | 63 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(60): Show |
64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.1938+221C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48334579 | |||||||
| chr16:48334635 | A | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1938+277A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48334635 | |||||||
| chr16:48334741 | A | C | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1938+383A>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48334741 | |||||||
| chr16:48334804 | G | A | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1938+446G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48334804 | |||||||
| chr16:48335054 | G | A | 1 | a0001c0006t0038g0144 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1938+696G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48335054 | |||||||
| chr16:48335216 | G | A | 3 | a0001c0001t0030g0143 a0001c0001t0062g0142 a0001c0006t0038g0144 |
3 | HG02896.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1938+858G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48335216 | |||||||
| chr16:48335914 | T | C | 3 | a0001c0001t0030g0143 a0001c0001t0062g0142 a0001c0006t0038g0144 |
3 | HG02896.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1938+1556T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48335914 | |||||||
| chr16:48336435 | G | A | 1 | a0001c0001t0062g0142 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1938+2077G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48336435 | |||||||
| chr16:48336819 | G | T | 1 | a0001c0001t0033g0147 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1938+2461G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48336819 | |||||||
| chr16:48336828 | G | T | 5 | a0001c0001t0029g0113 a0001c0003t0058g0123 a0001c0003t0059g0121 others(2): Show |
5 | HG02280.hp1 HG02486.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1938+2470G>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48336828 | |||||||
| chr16:48337594 | A | G | 1 | a0001c0001t0074g0081 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1938+3236A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48337594 | |||||||
| chr16:48337794 | G | A | 5 | a0001c0001t0022g0117 a0001c0001t0023g0115 a0001c0001t0024g0118 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1938+3436G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48337794 | |||||||
| chr16:48337876 | T | C | 1 | a0001c0001t0083g0112 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1938+3518T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48337876 | |||||||
| chr16:48337922 | C | T | 18 | a0001c0001t0005g0001 a0001c0001t0005g0111 a0001c0001t0005g0128 others(15): Show |
18 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.1938+3564C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48337922 | |||||||
| chr16:48338113 | C | CT | 5 | a0001c0001t0022g0117 a0001c0001t0023g0115 a0001c0001t0024g0118 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1938+3763dupT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr16 | 48338113 | ||||||
| chr16:48338155 | T | C | 2 | a0001c0001t0001g0059 a0001c0001t0002g0062 |
2 | HG03130.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1938+3797T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48338155 | |||||||
| chr16:48338157 | C | A | 2 | a0001c0001t0001g0059 a0001c0001t0002g0062 |
2 | HG03130.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1938+3799C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48338157 | |||||||
| chr16:48338158 | AGTCTAGG others(11): Show |
A | 2 | a0001c0001t0001g0059 a0001c0001t0002g0062 |
2 | HG03130.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1938+3801_1938+381 others(22): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48338158 | |||||||
| chr16:48338440 | T | C | 1 | a0001c0001t0027g0102 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1938+4082T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48338440 | |||||||
| chr16:48338545 | A | T | 1 | a0001c0001t0003g0078 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1938+4187A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48338545 | |||||||
| chr16:48338550 | T | C | 63 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(60): Show |
64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.1938+4192T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48338550 | |||||||
| chr16:48338551 | G | C | 1 | a0001c0001t0002g0095 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1938+4193G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48338551 | |||||||
| chr16:48338635 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1938+4277C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48338635 | |||||||
| chr16:48338748 | A | C | 1 | a0001c0001t0001g0079 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1938+4390A>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48338748 | |||||||
| chr16:48338915 | TAAAATA | T | 2 | a0001c0001t0055g0141 a0001c0001t0057g0140 |
2 | HG02074.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.1938+4561_1938+456 others(10): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr16 | 48338915 | ||||||
| chr16:48339237 | T | C | 2 | a0001c0001t0033g0147 a0001c0001t0051g0146 |
2 | NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1938+4879T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48339237 | |||||||
| chr16:48339376 | G | A | 8 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(5): Show |
8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1938+5018G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48339376 | |||||||
| chr16:48339432 | T | C | 1 | a0001c0001t0012g0044 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1938+5074T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48339432 | |||||||
| chr16:48339453 | C | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1938+5095C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48339453 | |||||||
| chr16:48339529 | G | C | 1 | a0001c0001t0032g0124 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1938+5171G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48339529 | |||||||
| chr16:48339582 | G | A | 1 | a0002c0005t0052g0138 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1938+5224G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48339582 | |||||||
| chr16:48339753 | G | A | 1 | a0001c0002t0041g0015 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1938+5395G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48339753 | |||||||
| chr16:48339756 | T | C | 1 | a0001c0004t0063g0094 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1938+5398T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48339756 | |||||||
| chr16:48340384 | C | G | 2 | a0001c0001t0031g0103 a0001c0001t0036g0104 |
2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1938+6026C>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48340384 | |||||||
| chr16:48340396 | A | T | 2 | a0001c0001t0031g0103 a0001c0001t0036g0104 |
2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1938+6038A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48340396 | |||||||
| chr16:48340401 | C | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1938+6043C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48340401 | |||||||
| chr16:48340407 | A | G | 1 | a0001c0001t0030g0143 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1938+6049A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48340407 | |||||||
| chr16:48340714 | G | A | 2 | a0001c0002t0049g0017 a0001c0002t0050g0007 |
2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1938+6356G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48340714 | |||||||
| chr16:48340811 | G | A | 1 | a0001c0001t0027g0102 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1938+6453G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48340811 | |||||||
| chr16:48340963 | G | C | 1 | a0001c0001t0029g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1939-6544G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48340963 | |||||||
| chr16:48340969 | T | A | 1 | a0001c0001t0029g0113 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1939-6538T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48340969 | |||||||
| chr16:48340979 | A | T | 1 | a0001c0001t0006g0136 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1939-6528A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48340979 | |||||||
| chr16:48341214 | C | T | 3 | a0001c0001t0030g0143 a0001c0001t0062g0142 a0001c0006t0038g0144 |
3 | HG02896.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1939-6293C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48341214 | |||||||
| chr16:48341301 | AAAATAAA others(1): Show |
A | 13 | a0001c0001t0001g0004 a0001c0001t0001g0072 a0001c0001t0017g0004 others(10): Show |
13 | HG01496.hp2 HG01884.hp1 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.1939-6184_1939-617 others(12): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr16 | 48341301 | ||||||
| chr16:48341305 | T | C | 8 | a0001c0001t0029g0113 a0001c0001t0030g0143 a0001c0001t0062g0142 others(5): Show |
8 | HG02280.hp1 HG02486.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1939-6202T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48341305 | |||||||
| chr16:48341329 | T | C | 2 | a0001c0001t0065g0030 a0001c0001t0080g0025 |
2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1939-6178T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48341329 | |||||||
| chr16:48341499 | GGAC | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1939-6004_1939-600 others(7): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr16 | 48341499 | ||||||
| chr16:48341552 | G | A | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1939-5955G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48341552 | |||||||
| chr16:48341649 | G | A | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1939-5858G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48341649 | |||||||
| chr16:48341866 | A | G | 129 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0034 others(126): Show |
131 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(128): Show |
intron_variant | MODIFIER | c.1939-5641A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48341866 | |||||||
| chr16:48341942 | G | A | 2 | a0001c0002t0049g0017 a0001c0002t0050g0007 |
2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1939-5565G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48341942 | |||||||
| chr16:48342016 | G | A | 1 | a0001c0001t0003g0016 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1939-5491G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48342016 | |||||||
| chr16:48342025 | G | A | 2 | a0001c0002t0049g0017 a0001c0002t0050g0007 |
2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1939-5482G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48342025 | |||||||
| chr16:48342199 | T | G | 8 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(5): Show |
8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1939-5308T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48342199 | |||||||
| chr16:48342251 | A | C | 4 | a0001c0001t0032g0124 a0001c0001t0034g0125 a0001c0001t0035g0127 others(1): Show |
4 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1939-5256A>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48342251 | |||||||
| chr16:48342308 | C | T | 1 | a0001c0006t0038g0144 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1939-5199C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48342308 | |||||||
| chr16:48342877 | A | T | 8 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(5): Show |
8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1939-4630A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48342877 | |||||||
| chr16:48342905 | C | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1939-4602C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48342905 | |||||||
| chr16:48342939 | C | T | 5 | a0001c0001t0022g0117 a0001c0001t0023g0115 a0001c0001t0024g0118 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1939-4568C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48342939 | |||||||
| chr16:48343146 | T | G | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1939-4361T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48343146 | |||||||
| chr16:48343300 | T | G | 1 | a0001c0001t0002g0065 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1939-4207T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48343300 | |||||||
| chr16:48343420 | C | T | 5 | a0001c0001t0022g0117 a0001c0001t0023g0115 a0001c0001t0024g0118 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1939-4087C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48343420 | |||||||
| chr16:48343467 | G | A | 8 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(5): Show |
8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1939-4040G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48343467 | |||||||
| chr16:48343486 | C | T | 1 | a0001c0001t0006g0136 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1939-4021C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48343486 | |||||||
| chr16:48343505 | T | G | 1 | a0001c0001t0011g0096 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1939-4002T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48343505 | |||||||
| chr16:48343695 | TA | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1939-3801delA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr16 | 48343695 | ||||||
| chr16:48343785 | A | G | 2 | a0001c0002t0043g0011 a0001c0002t0047g0010 |
2 | HG01884.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1939-3722A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48343785 | |||||||
| chr16:48343990 | C | T | 18 | a0001c0001t0005g0001 a0001c0001t0005g0111 a0001c0001t0005g0128 others(15): Show |
18 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.1939-3517C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48343990 | |||||||
| chr16:48344203 | A | C | 53 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(50): Show |
54 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(51): Show |
intron_variant | MODIFIER | c.1939-3304A>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48344203 | |||||||
| chr16:48344823 | T | G | 1 | a0001c0001t0088g0071 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1939-2684T>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48344823 | |||||||
| chr16:48345019 | C | T | 3 | a0001c0001t0001g0038 a0001c0001t0001g0145 a0001c0001t0002g0037 |
3 | HG02572.hp2 HG02818.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1939-2488C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48345019 | |||||||
| chr16:48345371 | G | A | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.1939-2136G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48345371 | |||||||
| chr16:48345511 | A | G | 63 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(60): Show |
64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.1939-1996A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48345511 | |||||||
| chr16:48345628 | C | T | 8 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(5): Show |
8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1939-1879C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48345628 | |||||||
| chr16:48345892 | A | G | 2 | a0001c0001t0012g0092 a0001c0001t0085g0045 |
2 | NA18986.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1939-1615A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48345892 | |||||||
| chr16:48345913 | T | C | 63 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(60): Show |
64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.1939-1594T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48345913 | |||||||
| chr16:48345996 | A | G | 1 | a0001c0001t0004g0006 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1939-1511A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48345996 | |||||||
| chr16:48346044 | C | CA | 9 | a0001c0001t0001g0084 a0001c0001t0002g0060 a0001c0001t0011g0096 others(6): Show |
9 | HG00621.hp2 HG00642.hp1 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.1939-1443dupA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr16 | 48346044 | ||||||
| chr16:48346044 | CA | C | 18 | a0001c0001t0001g0047 a0001c0001t0004g0006 a0001c0001t0004g0107 others(15): Show |
19 | HG00558.hp1 HG00738.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.1939-1443delA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr16 | 48346044 | ||||||
| chr16:48346071 | A | G | 4 | a0001c0001t0032g0124 a0001c0001t0034g0125 a0001c0001t0035g0127 others(1): Show |
4 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1939-1436A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48346071 | |||||||
| chr16:48346071 | A | T | 2 | a0001c0002t0049g0017 a0001c0002t0050g0007 |
2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1939-1436A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48346071 | |||||||
| chr16:48346130 | G | A | 1 | a0001c0001t0014g0101 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1939-1377G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48346130 | |||||||
| chr16:48346132 | A | G | 1 | a0001c0001t0021g0039 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1939-1375A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48346132 | |||||||
| chr16:48346254 | A | T | 17 | a0001c0001t0005g0001 a0001c0001t0005g0111 a0001c0001t0005g0128 others(14): Show |
17 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.1939-1253A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48346254 | |||||||
| chr16:48346276 | G | C | 2 | a0001c0002t0049g0017 a0001c0002t0050g0007 |
2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1939-1231G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48346276 | |||||||
| chr16:48346421 | A | G | 38 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(35): Show |
39 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.1939-1086A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48346421 | |||||||
| chr16:48346935 | G | A | 3 | a0001c0001t0010g0041 a0001c0001t0018g0040 a0001c0001t0018g0042 |
3 | HG02615.hp1 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1939-572G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48346935 | |||||||
| chr16:48346968 | T | C | 5 | a0001c0001t0022g0117 a0001c0001t0023g0115 a0001c0001t0024g0118 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1939-539T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48346968 | |||||||
| chr16:48347007 | G | A | 2 | a0001c0001t0001g0084 a0001c0001t0002g0085 |
2 | HG02622.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1939-500G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48347007 | |||||||
| chr16:48347184 | A | ATACT | 4 | a0001c0001t0032g0124 a0001c0001t0034g0125 a0001c0001t0035g0127 others(1): Show |
4 | HG01891.hp1 HG02965.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1939-320_1939-317d others(6): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr16 | 48347184 | ||||||
| chr16:48347226 | G | A | 1 | a0001c0001t0062g0142 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1939-281G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48347226 | |||||||
| chr16:48347296 | G | C | 1 | a0001c0001t0078g0048 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1939-211G>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 12/14 | chr16 | 48347296 | |||||||
| chr16:48347963 | C | T | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.2147-137C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 13/14 | chr16 | 48347963 | |||||||
| chr16:48348371 | CTTCT | C | 2 | a0001c0001t0002g0060 a0001c0001t0016g0131 |
2 | HG00323.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.2337+86_2337+89del others(4): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr16 | 48348371 | ||||||
| chr16:48348409 | T | A | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.2337+119T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | chr16 | 48348409 | |||||||
| chr16:48348487 | CT | C | 32 | a0001c0001t0001g0059 a0001c0001t0001g0073 a0001c0001t0001g0079 others(29): Show |
32 | HG00558.hp2 HG01070.hp1 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.2337+219delT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr16 | 48348487 | ||||||
| chr16:48348487 | CTT | C | 41 | a0001c0001t0002g0086 a0001c0001t0004g0006 a0001c0001t0004g0107 others(38): Show |
42 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.2337+218_2337+219d others(4): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr16 | 48348487 | ||||||
| chr16:48348487 | CTTT | C | 9 | a0001c0001t0027g0102 a0001c0002t0041g0015 a0001c0002t0042g0009 others(6): Show |
9 | HG01884.hp1 HG02258.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.2337+217_2337+219d others(5): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr16 | 48348487 | ||||||
| chr16:48348539 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2337+249G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | chr16 | 48348539 | |||||||
| chr16:48348611 | A | G | 128 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0034 others(125): Show |
130 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.2337+321A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | chr16 | 48348611 | |||||||
| chr16:48349061 | A | G | 1 | a0001c0001t0027g0102 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2337+771A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | chr16 | 48349061 | |||||||
| chr16:48349204 | AT | A | 87 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0034 others(84): Show |
89 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(86): Show |
intron_variant | MODIFIER | c.2337+918delT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr16 | 48349204 | ||||||
| chr16:48349250 | A | G | 8 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(5): Show |
8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.2337+960A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | chr16 | 48349250 | |||||||
| chr16:48349265 | T | C | 2 | a0001c0001t0002g0083 a0001c0001t0002g0095 |
2 | HG03139.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2337+975T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | chr16 | 48349265 | |||||||
| chr16:48349269 | CT | C | 63 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(60): Show |
64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.2337+986delT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr16 | 48349269 | ||||||
| chr16:48349463 | A | G | 2 | a0001c0001t0055g0141 a0001c0001t0057g0140 |
2 | HG02074.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.2337+1173A>G | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | chr16 | 48349463 | |||||||
| chr16:48349584 | T | C | 19 | a0001c0001t0005g0001 a0001c0001t0005g0111 a0001c0001t0005g0128 others(16): Show |
19 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.2337+1294T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | chr16 | 48349584 | |||||||
| chr16:48349672 | G | A | 8 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(5): Show |
8 | HG01884.hp1 HG02647.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.2337+1382G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | chr16 | 48349672 | |||||||
| chr16:48349917 | G | A | 4 | a0001c0001t0022g0117 a0001c0001t0023g0115 a0001c0001t0025g0116 others(1): Show |
4 | HG02145.hp2 HG02886.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2337+1627G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | chr16 | 48349917 | |||||||
| chr16:48349968 | A | T | 1 | a0001c0001t0009g0020 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2338-1613A>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | chr16 | 48349968 | |||||||
| chr16:48349978 | C | T | 1 | a0001c0001t0078g0048 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2338-1603C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | chr16 | 48349978 | |||||||
| chr16:48349986 | CT | C | 19 | a0001c0001t0005g0001 a0001c0001t0005g0111 a0001c0001t0005g0128 others(16): Show |
19 | HG00323.hp2 HG00733.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.2338-1594delT | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | chr16 | 48349986 | |||||||
| chr16:48350088 | T | C | 3 | a0001c0001t0029g0113 a0001c0001t0030g0143 a0001c0006t0038g0144 |
3 | HG02280.hp1 HG02896.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2338-1493T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | chr16 | 48350088 | |||||||
| chr16:48350175 | T | C | 4 | a0001c0003t0058g0123 a0001c0003t0059g0121 a0001c0003t0060g0122 others(1): Show |
4 | HG02486.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.2338-1406T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | chr16 | 48350175 | |||||||
| chr16:48350258 | C | T | 2 | a0001c0001t0002g0003 a0001c0001t0008g0093 |
3 | HG02559.hp2 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2338-1323C>T | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | chr16 | 48350258 | |||||||
| chr16:48350321 | GA | G | 63 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(60): Show |
64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.2338-1257delA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr16 | 48350321 | ||||||
| chr16:48350386 | C | CA | 32 | a0001c0001t0002g0043 a0001c0001t0003g0024 a0001c0001t0003g0028 others(29): Show |
32 | HG00323.hp1 HG00323.hp2 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.2338-1181dupA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr16 | 48350386 | ||||||
| chr16:48350386 | C | CAA | 7 | a0001c0001t0005g0132 a0001c0001t0007g0130 a0001c0001t0007g0137 others(4): Show |
7 | HG01081.hp2 HG01099.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.2338-1182_2338-118 others(6): Show |
LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr16 | 48350386 | ||||||
| chr16:48350386 | CA | C | 11 | a0001c0001t0001g0073 a0001c0002t0041g0015 a0001c0002t0042g0009 others(8): Show |
11 | HG01081.hp1 HG01884.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.2338-1181delA | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr16 | 48350386 | ||||||
| chr16:48350401 | T | A | 4 | a0001c0003t0058g0123 a0001c0003t0059g0121 a0001c0003t0060g0122 others(1): Show |
4 | HG02486.hp2 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.2338-1180T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | chr16 | 48350401 | |||||||
| chr16:48350433 | C | A | 66 | a0001c0001t0001g0084 a0001c0001t0002g0085 a0001c0001t0004g0006 others(63): Show |
67 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(64): Show |
intron_variant | MODIFIER | c.2338-1148C>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | chr16 | 48350433 | |||||||
| chr16:48350459 | G | A | 63 | a0001c0001t0004g0006 a0001c0001t0004g0107 a0001c0001t0004g0110 others(60): Show |
64 | HG00323.hp2 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.2338-1122G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | chr16 | 48350459 | |||||||
| chr16:48350472 | G | A | 3 | a0001c0001t0001g0038 a0001c0001t0001g0145 a0001c0001t0002g0037 |
3 | HG02572.hp2 HG02818.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.2338-1109G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | chr16 | 48350472 | |||||||
| chr16:48350693 | G | A | 1 | a0001c0001t0054g0139 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2338-888G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | chr16 | 48350693 | |||||||
| chr16:48351021 | T | A | 10 | a0001c0002t0041g0015 a0001c0002t0042g0009 a0001c0002t0043g0011 others(7): Show |
10 | HG01884.hp1 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.2338-560T>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | chr16 | 48351021 | |||||||
| chr16:48351074 | T | C | 1 | a0001c0001t0003g0078 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2338-507T>C | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | chr16 | 48351074 | |||||||
| chr16:48351325 | G | A | 1 | a0001c0001t0051g0146 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2338-256G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | chr16 | 48351325 | |||||||
| chr16:48351460 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2338-121G>A | LONP2 | ENSG00000102910.14 | transcript | ENST00000285737.9 | protein_coding | 14/14 | chr16 | 48351460 |