Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5073 |
| ensemblid | ENSG00000140694.18 |
| hgncid | 8609 |
| symbol | PARN |
| name | poly(A)-specific ribonuclease |
| refseq_nuc | NM_002582.4 |
| refseq_prot | NP_002573.1 |
| ensembl_nuc | ENST00000437198.7 |
| ensembl_prot | ENSP00000387911.2 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 14435701 |
| end | 14630260 |
| strand | - |
| ver | v1.2 |
| region | chr16:14435701-14630260 |
| region5000 | chr16:14430701-14635260 |
| regionname0 | PARN_chr16_14435701_14630260 |
| regionname5000 | PARN_chr16_14430701_14635260 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 639 | 166 | 58 | 31 | 45 | 9 | 22 | 27 | PARN_chr16_14430701_14635260 | PARN | MEIIR others(634): Show |
chr16 | 14430701 | 14635260 |
| a0002 | 0/0 | 639 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | MEIIR others(634): Show |
chr16 | 14430701 | 14635260 |
| a0003 | 0/0 | 639 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | MEIIR others(634): Show |
chr16 | 14430701 | 14635260 |
| a0004 | 0/0 | 639 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PARN_chr16_14430701_14635260 | PARN | MEIIR others(634): Show |
chr16 | 14430701 | 14635260 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1917 | 160 | 53 | 31 | 45 | 9 | 22 | PARN_chr16_14430701_14635260 | PARN | ATGGA others(1912): Show |
chr16 | 14430701 | 14635260 | ||
| a0001c0002 | 0/0 | 1917 | 4 | 4 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | ATGGA others(1912): Show |
chr16 | 14430701 | 14635260 | ||
| a0001c0003 | 0/0 | 1917 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | ATGGA others(1912): Show |
chr16 | 14430701 | 14635260 | ||
| a0001c0007 | 0/1 | 1917 | 1 | 0 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | ATGGA others(1912): Show |
chr16 | 14430701 | 14635260 | ||
| a0002c0005 | 0/0 | 1917 | 1 | 0 | 1 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | ATGGA others(1912): Show |
chr16 | 14430701 | 14635260 | ||
| a0003c0006 | 0/0 | 1917 | 1 | 0 | 0 | 0 | 1 | 0 | PARN_chr16_14430701_14635260 | PARN | ATGGA others(1912): Show |
chr16 | 14430701 | 14635260 | ||
| a0004c0004 | 0/0 | 1917 | 1 | 0 | 0 | 1 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | ATGGA others(1912): Show |
chr16 | 14430701 | 14635260 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3071 | 28 | 9 | 11 | 5 | 2 | 1 | PARN_chr16_14430701_14635260 | PARN | GTTTC others(3066): Show |
chr16 | 14430701 | 14635260 |
| a0001c0001t0002 | 0/0 | 3069 | 24 | 12 | 7 | 5 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | GTTTC others(3064): Show |
chr16 | 14430701 | 14635260 |
| a0001c0001t0003 | 0/0 | 3063 | 17 | 4 | 5 | 0 | 2 | 6 | PARN_chr16_14430701_14635260 | PARN | GTTTC others(3058): Show |
chr16 | 14430701 | 14635260 |
| a0001c0001t0004 | 0/0 | 3073 | 19 | 4 | 3 | 4 | 3 | 5 | PARN_chr16_14430701_14635260 | PARN | GTTTC others(3068): Show |
chr16 | 14430701 | 14635260 |
| a0001c0001t0005 | 0/0 | 3075 | 18 | 1 | 0 | 13 | 1 | 3 | PARN_chr16_14430701_14635260 | PARN | GTTTC others(3070): Show |
chr16 | 14430701 | 14635260 |
| a0001c0001t0006 | 0/0 | 3067 | 15 | 7 | 0 | 6 | 0 | 2 | PARN_chr16_14430701_14635260 | PARN | GTTTC others(3062): Show |
chr16 | 14430701 | 14635260 |
| a0001c0001t0007 | 0/0 | 3065 | 15 | 6 | 4 | 4 | 1 | 0 | PARN_chr16_14430701_14635260 | PARN | GTTTC others(3060): Show |
chr16 | 14430701 | 14635260 |
| a0001c0001t0008 | 0/0 | 3077 | 4 | 1 | 0 | 3 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | GTTTC others(3072): Show |
chr16 | 14430701 | 14635260 |
| a0001c0001t0009 | 0/0 | 3069 | 4 | 0 | 0 | 3 | 0 | 1 | PARN_chr16_14430701_14635260 | PARN | GTTTC others(3064): Show |
chr16 | 14430701 | 14635260 |
| a0001c0001t0010 | 0/0 | 3059 | 3 | 1 | 0 | 0 | 0 | 2 | PARN_chr16_14430701_14635260 | PARN | GTTTC others(3054): Show |
chr16 | 14430701 | 14635260 |
| a0001c0001t0011 | 0/0 | 3073 | 2 | 2 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | GTTTC others(3068): Show |
chr16 | 14430701 | 14635260 |
| a0001c0001t0012 | 0/0 | 3061 | 2 | 0 | 1 | 1 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | GTTTC others(3056): Show |
chr16 | 14430701 | 14635260 |
| a0001c0001t0013 | 0/0 | 3079 | 1 | 0 | 0 | 0 | 0 | 1 | PARN_chr16_14430701_14635260 | PARN | GTTTC others(3074): Show |
chr16 | 14430701 | 14635260 |
| a0001c0001t0014 | 0/0 | 3077 | 1 | 0 | 0 | 0 | 0 | 1 | PARN_chr16_14430701_14635260 | PARN | GTTTC others(3072): Show |
chr16 | 14430701 | 14635260 |
| a0001c0001t0015 | 0/0 | 3039 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | GTTTC others(3034): Show |
chr16 | 14430701 | 14635260 |
| a0001c0001t0016 | 0/0 | 3069 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | GTTTC others(3064): Show |
chr16 | 14430701 | 14635260 |
| a0001c0001t0017 | 0/0 | 3071 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | GTTTC others(3066): Show |
chr16 | 14430701 | 14635260 |
| a0001c0001t0018 | 0/0 | 3081 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | GTTTC others(3076): Show |
chr16 | 14430701 | 14635260 |
| a0001c0001t0019 | 0/0 | 3071 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | GTTTC others(3066): Show |
chr16 | 14430701 | 14635260 |
| a0001c0001t0020 | 0/0 | 3073 | 1 | 0 | 0 | 1 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | GTTTC others(3068): Show |
chr16 | 14430701 | 14635260 |
| a0001c0001t0021 | 0/0 | 3077 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | GTTTC others(3072): Show |
chr16 | 14430701 | 14635260 |
| a0001c0002t0003 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | GTTTC others(3058): Show |
chr16 | 14430701 | 14635260 |
| a0001c0002t0004 | 0/0 | 3073 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | GTTTC others(3068): Show |
chr16 | 14430701 | 14635260 |
| a0001c0002t0006 | 0/0 | 3067 | 2 | 2 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | GTTTC others(3062): Show |
chr16 | 14430701 | 14635260 |
| a0001c0003t0001 | 0/0 | 3071 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | GTTTC others(3066): Show |
chr16 | 14430701 | 14635260 |
| a0001c0007t0003 | 0/1 | 3063 | 1 | 0 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | GTTTC others(3058): Show |
chr16 | 14430701 | 14635260 |
| a0002c0005t0003 | 0/0 | 3063 | 1 | 0 | 1 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | GTTTC others(3058): Show |
chr16 | 14430701 | 14635260 |
| a0003c0006t0013 | 0/0 | 3079 | 1 | 0 | 0 | 0 | 1 | 0 | PARN_chr16_14430701_14635260 | PARN | GTTTC others(3074): Show |
chr16 | 14430701 | 14635260 |
| a0004c0004t0002 | 0/0 | 3069 | 1 | 0 | 0 | 1 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | GTTTC others(3064): Show |
chr16 | 14430701 | 14635260 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0003g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0003g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0004g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0004g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0004g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0004g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0004g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0004g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0004g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0004g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0004g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0004g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0004g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0005g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0005g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0005g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0005g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0005g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0005g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0005g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0005g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0005g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0005g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0005g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0005g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0005g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0005g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0005g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0005g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0005g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0005g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0006g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0006g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0006g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0006g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0006g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0006g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0006g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0006g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0006g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0006g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0006g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0006g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0006g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0006g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0006g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0007g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0007g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0007g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0007g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0007g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0007g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0007g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0007g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0007g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0007g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0007g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0007g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0007g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0007g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0007g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0008g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0008g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0008g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0008g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0009g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0009g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0009g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0009g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0010g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0010g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0010g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0011g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0011g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0012g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0012g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0013g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0014g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0015g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0016g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0017g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0018g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0019g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0020g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0001t0021g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0002t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0002t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0002t0006g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0002t0006g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0003t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0001c0007t0003g0098 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0002c0005t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0003c0006t0013g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| a0004c0004t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0005 | g0025 | EUR | GBR | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0027 | EUR | GBR | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG00280 | hp1 | a0001 | c0001 | t0004 | g0006 | EUR | FIN | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0092 | EUR | FIN | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0088 | EUR | FIN | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | FIN | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG00438 | hp1 | a0001 | c0001 | t0005 | g0074 | EAS | CHS | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | CHS | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG00597 | hp1 | a0001 | c0001 | t0005 | g0054 | EAS | CHS | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG00597 | hp2 | a0001 | c0001 | t0007 | g0052 | EAS | CHS | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG00639 | hp2 | a0001 | c0001 | t0007 | g0166 | AMR | PUR | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG00673 | hp1 | a0001 | c0001 | t0005 | g0077 | EAS | CHS | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG00673 | hp2 | a0001 | c0001 | t0012 | g0034 | EAS | CHS | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG00741 | hp1 | a0002 | c0005 | t0003 | g0125 | AMR | PUR | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG00741 | hp2 | a0001 | c0001 | t0012 | g0078 | AMR | PUR | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0136 | AMR | PUR | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0104 | AMR | PUR | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG01175 | hp1 | a0001 | c0001 | t0007 | g0008 | AMR | PUR | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG01192 | hp2 | a0001 | c0001 | t0007 | g0053 | AMR | PUR | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0133 | AMR | CLM | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0154 | AMR | CLM | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0099 | AMR | CLM | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0113 | AMR | CLM | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | CLM | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG01433 | hp1 | a0001 | c0001 | t0004 | g0124 | AMR | CLM | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG01496 | hp1 | a0001 | c0001 | t0007 | g0003 | AMR | CLM | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0135 | AMR | CLM | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0100 | EUR | IBS | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0017 | EUR | IBS | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG01516 | hp1 | a0001 | c0001 | t0007 | g0002 | EUR | IBS | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG01516 | hp2 | a0003 | c0006 | t0013 | g0061 | EUR | IBS | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0168 | AFR | ACB | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG01891 | hp1 | a0001 | c0001 | t0006 | g0164 | AFR | ACB | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG01891 | hp2 | a0001 | c0001 | t0021 | g0117 | AFR | ACB | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0041 | AMR | PEL | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0042 | AMR | PEL | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG02027 | hp1 | a0001 | c0001 | t0005 | g0140 | EAS | KHV | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG02027 | hp2 | a0001 | c0001 | t0005 | g0045 | EAS | KHV | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG02040 | hp1 | a0001 | c0001 | t0009 | g0049 | EAS | KHV | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG02040 | hp2 | a0001 | c0001 | t0004 | g0038 | EAS | KHV | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | KHV | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | KHV | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG02132 | hp1 | a0001 | c0001 | t0006 | g0012 | EAS | KHV | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG02132 | hp2 | a0001 | c0001 | t0005 | g0014 | EAS | KHV | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0131 | AFR | ACB | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0128 | AFR | ACB | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG02165 | hp1 | a0001 | c0001 | t0020 | g0161 | EAS | CDX | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG02165 | hp2 | a0001 | c0001 | t0005 | g0156 | EAS | CDX | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG02451 | hp1 | a0001 | c0001 | t0016 | g0146 | AFR | ACB | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG02451 | hp2 | a0001 | c0001 | t0019 | g0169 | AFR | ACB | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0069 | AFR | GWD | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG02602 | hp1 | a0001 | c0001 | t0005 | g0083 | SAS | PJL | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0102 | SAS | PJL | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG02615 | hp2 | a0001 | c0002 | t0006 | g0150 | AFR | GWD | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0068 | AFR | GWD | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0044 | AFR | GWD | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG02683 | hp1 | a0001 | c0001 | t0005 | g0035 | SAS | PJL | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG02683 | hp2 | a0001 | c0001 | t0014 | g0001 | SAS | PJL | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG02717 | hp1 | a0001 | c0001 | t0017 | g0046 | AFR | GWD | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG02717 | hp2 | a0001 | c0001 | t0011 | g0090 | AFR | GWD | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG02809 | hp1 | a0001 | c0001 | t0008 | g0020 | AFR | GWD | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0093 | AFR | GWD | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG02886 | hp1 | a0001 | c0001 | t0006 | g0080 | AFR | GWD | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG02886 | hp2 | a0001 | c0002 | t0003 | g0151 | AFR | GWD | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0023 | AFR | GWD | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | GWD | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0070 | AFR | ESN | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG02922 | hp2 | a0001 | c0001 | t0006 | g0163 | AFR | ESN | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG02970 | hp1 | a0001 | c0001 | t0006 | g0144 | AFR | ESN | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0132 | AFR | ESN | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | ESN | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG03017 | hp1 | a0001 | c0001 | t0004 | g0029 | SAS | PJL | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0097 | SAS | PJL | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0115 | AFR | MSL | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG03098 | hp2 | a0001 | c0001 | t0007 | g0123 | AFR | MSL | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG03130 | hp1 | a0001 | c0003 | t0001 | g0116 | AFR | ESN | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG03130 | hp2 | a0001 | c0001 | t0007 | g0109 | AFR | ESN | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | ESN | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0071 | AFR | ESN | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG03195 | hp2 | a0001 | c0001 | t0007 | g0066 | AFR | ESN | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG03209 | hp1 | a0001 | c0001 | t0015 | g0110 | AFR | MSL | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0118 | AFR | MSL | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG03486 | hp1 | a0001 | c0001 | t0011 | g0158 | AFR | MSL | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG03486 | hp2 | a0001 | c0001 | t0010 | g0064 | AFR | MSL | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG03516 | hp1 | a0001 | c0001 | t0007 | g0094 | AFR | ESN | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0126 | AFR | ESN | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0159 | AFR | GWD | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG03710 | hp1 | a0001 | c0001 | t0004 | g0062 | SAS | PJL | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG03710 | hp2 | a0001 | c0001 | t0009 | g0031 | SAS | PJL | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0101 | SAS | BEB | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG03831 | hp2 | a0001 | c0001 | t0013 | g0056 | SAS | BEB | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG03834 | hp1 | a0001 | c0001 | t0010 | g0103 | SAS | BEB | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG03834 | hp2 | a0001 | c0001 | t0005 | g0138 | SAS | BEB | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0067 | SAS | BEB | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG03942 | hp2 | a0001 | c0001 | t0004 | g0039 | SAS | BEB | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0107 | SAS | STU | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | STU | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0007 | SAS | STU | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG04199 | hp2 | a0001 | c0001 | t0006 | g0086 | SAS | STU | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG04204 | hp1 | a0001 | c0001 | t0010 | g0106 | SAS | STU | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG04204 | hp2 | a0001 | c0001 | t0006 | g0087 | SAS | STU | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0095 | AFR | YRI | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | YRI | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | CHB | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| NA18612 | hp2 | a0001 | c0001 | t0006 | g0011 | EAS | CHB | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| NA18906 | hp1 | a0001 | c0001 | t0006 | g0058 | AFR | YRI | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0072 | AFR | YRI | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| NA18950 | hp2 | a0001 | c0001 | t0005 | g0082 | EAS | JPT | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| NA18957 | hp1 | a0001 | c0001 | t0005 | g0075 | EAS | JPT | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| NA18957 | hp2 | a0004 | c0004 | t0002 | g0130 | EAS | JPT | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| NA18959 | hp1 | a0001 | c0001 | t0005 | g0141 | EAS | JPT | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| NA18959 | hp2 | a0001 | c0001 | t0006 | g0040 | EAS | JPT | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| NA18964 | hp1 | a0001 | c0001 | t0005 | g0055 | EAS | JPT | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| NA18964 | hp2 | a0001 | c0001 | t0009 | g0048 | EAS | JPT | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| NA18966 | hp1 | a0001 | c0001 | t0008 | g0129 | EAS | JPT | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| NA18966 | hp2 | a0001 | c0001 | t0009 | g0081 | EAS | JPT | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| NA18968 | hp1 | a0001 | c0001 | t0008 | g0155 | EAS | JPT | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| NA18968 | hp2 | a0001 | c0001 | t0008 | g0162 | EAS | JPT | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| NA18973 | hp1 | a0001 | c0001 | t0007 | g0010 | EAS | JPT | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| NA18973 | hp2 | a0001 | c0001 | t0006 | g0016 | EAS | JPT | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| NA18979 | hp1 | a0001 | c0001 | t0007 | g0142 | EAS | JPT | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| NA18979 | hp2 | a0001 | c0001 | t0005 | g0120 | EAS | JPT | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| NA18986 | hp1 | a0001 | c0001 | t0004 | g0167 | EAS | JPT | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| NA18986 | hp2 | a0001 | c0001 | t0007 | g0160 | EAS | JPT | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| NA18999 | hp1 | a0001 | c0001 | t0004 | g0076 | EAS | JPT | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| NA19002 | hp1 | a0001 | c0001 | t0004 | g0137 | EAS | JPT | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| NA19002 | hp2 | a0001 | c0001 | t0006 | g0157 | EAS | JPT | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| NA19005 | hp1 | a0001 | c0001 | t0005 | g0112 | EAS | JPT | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| NA19030 | hp1 | a0001 | c0001 | t0006 | g0152 | AFR | LWK | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| NA19030 | hp2 | a0001 | c0002 | t0004 | g0148 | AFR | LWK | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| NA19043 | hp1 | a0001 | c0002 | t0006 | g0149 | AFR | LWK | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0096 | AFR | LWK | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| NA19066 | hp1 | a0001 | c0001 | t0006 | g0013 | EAS | JPT | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0105 | SAS | GIH | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| NA20905 | hp2 | a0001 | c0001 | t0004 | g0085 | SAS | GIH | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG03471 | hp1 | a0001 | c0001 | t0007 | g0063 | AFR | MSL | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | USA | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| HG06807 | hp2 | a0001 | c0001 | t0007 | g0127 | AFR | USA | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| NA20300 | hp1 | a0001 | c0001 | t0018 | g0065 | AFR | USA | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| NA20300 | hp2 | a0001 | c0001 | t0006 | g0165 | AFR | USA | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| homoSapiens | chm13v2 | a0001 | c0007 | t0003 | g0098 | REF | REF | PARN_chr16_14430701_14635260 | PARN | chr16 | 14430701 | 14635260 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:14436746 | T | C | 1 | a0002 | 1 | HG00741.hp1 | missense_variant | MODERATE | c.1891A>G | p.Thr631Ala | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 24/24 | 2026/3071 | 1891/1920 | 631/639 | chr16 | 14436746 | |||
| chr16:14447011 | C | T | 1 | a0004 | 1 | NA18957.hp2 | missense_variant | MODERATE | c.1741G>A | p.Gly581Arg | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 23/24 | 1876/3071 | 1741/1920 | 581/639 | chr16 | 14447011 | |||
| chr16:14584353 | T | C | 1 | a0003 | 1 | HG01516.hp2 | missense_variant | MODERATE | c.1075A>G | p.Lys359Glu | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 16/24 | 1210/3071 | 1075/1920 | 359/639 | chr16 | 14584353 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:14552067 | G | A | 1 | a0001c0003 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.1434C>T | p.Asp478Asp | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/24 | 1569/3071 | 1434/1920 | 478/639 | chr16 | 14552067 | |||
| chr16:14552088 | A | G | 1 | a0001c0003 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.1413T>C | p.Ile471Ile | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/24 | 1548/3071 | 1413/1920 | 471/639 | chr16 | 14552088 | |||
| chr16:14554087 | A | G | 1 | a0001c0002 | 4 | HG02615.hp2 HG02886.hp2 NA19030.hp2 others(1): Show |
synonymous_variant | LOW | c.1383T>C | p.Leu461Leu | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 20/24 | 1518/3071 | 1383/1920 | 461/639 | chr16 | 14554087 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:14435896 | T | A | 1 | a0001c0001t0017 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*821A>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 24/24 | 821 | chr16 | 14435896 | ||||||
| chr16:14435896 | T | TCA | 3 | a0001c0001t0004 a0001c0001t0020 a0001c0002t0004 |
21 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*819_*820dupTG | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 24/24 | 820 | chr16 | 14435896 | ||||||
| chr16:14435896 | T | TCACA | 1 | a0001c0001t0005 | 18 | HG00099.hp1 HG00438.hp1 HG00597.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*817_*820dupTGTG | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 24/24 | 820 | chr16 | 14435896 | ||||||
| chr16:14435896 | T | TCACACA | 3 | a0001c0001t0008 a0001c0001t0014 a0001c0001t0021 |
6 | HG01891.hp2 HG02683.hp2 HG02809.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*815_*820dupTGTGTG | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 24/24 | 820 | chr16 | 14435896 | ||||||
| chr16:14435896 | T | TCACACAC others(1): Show |
2 | a0001c0001t0013 a0003c0006t0013 |
2 | HG01516.hp2 HG03831.hp2 |
3_prime_UTR_variant | MODIFIER | c.*813_*820dupTGTGTG others(2): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 24/24 | 820 | chr16 | 14435896 | ||||||
| chr16:14435896 | T | TCACACAC others(3): Show |
1 | a0001c0001t0018 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*811_*820dupTGTGTG others(4): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 24/24 | 820 | chr16 | 14435896 | ||||||
| chr16:14435896 | TCA | T | 3 | a0001c0001t0002 a0001c0001t0016 a0004c0004t0002 |
26 | HG00438.hp2 HG00735.hp2 HG01081.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*819_*820delTG | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 24/24 | 819 | chr16 | 14435896 | ||||||
| chr16:14435896 | TCACA | T | 2 | a0001c0001t0006 a0001c0002t0006 |
17 | HG01891.hp1 HG02132.hp1 HG02615.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*817_*820delTGTG | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 24/24 | 817 | chr16 | 14435896 | ||||||
| chr16:14435896 | TCACACA | T | 1 | a0001c0001t0007 | 15 | HG00597.hp2 HG00639.hp2 HG01175.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*815_*820delTGTGTG | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 24/24 | 815 | chr16 | 14435896 | ||||||
| chr16:14435896 | TCACACAC others(1): Show |
T | 3 | a0001c0001t0003 a0001c0002t0003 a0002c0005t0003 |
19 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*813_*820delTGTGTG others(2): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 24/24 | 813 | chr16 | 14435896 | ||||||
| chr16:14435896 | TCACACAC others(3): Show |
T | 1 | a0001c0001t0012 | 2 | HG00673.hp2 HG00741.hp2 |
3_prime_UTR_variant | MODIFIER | c.*811_*820delTGTGTG others(4): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 24/24 | 811 | chr16 | 14435896 | ||||||
| chr16:14435896 | TCACACAC others(5): Show |
T | 1 | a0001c0001t0010 | 3 | HG03486.hp2 HG03834.hp1 HG04204.hp1 |
3_prime_UTR_variant | MODIFIER | c.*809_*820delTGTGTG others(6): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 24/24 | 809 | chr16 | 14435896 | ||||||
| chr16:14435896 | TCACACAC others(25): Show |
T | 1 | a0001c0001t0015 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*789_*820delTGTGTG others(26): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 24/24 | 789 | chr16 | 14435896 | ||||||
| chr16:14435900 | A | T | 1 | a0001c0001t0016 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*817T>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 24/24 | 817 | chr16 | 14435900 | ||||||
| chr16:14435943 | C | CAG | 1 | a0001c0001t0011 | 2 | HG02717.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*772_*773dupCT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 24/24 | 773 | chr16 | 14435943 | ||||||
| chr16:14435943 | CAG | C | 1 | a0001c0001t0009 | 4 | HG02040.hp1 HG03710.hp2 NA18964.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*772_*773delCT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 24/24 | 772 | chr16 | 14435943 | ||||||
| chr16:14435945 | G | C | 2 | a0001c0001t0001 a0001c0001t0005 |
2 | HG02027.hp2 NA18999.hp2 |
3_prime_UTR_variant | MODIFIER | c.*772C>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 24/24 | 772 | chr16 | 14435945 | ||||||
| chr16:14436160 | G | C | 1 | a0001c0001t0019 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*557C>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 24/24 | 557 | chr16 | 14436160 | ||||||
| chr16:14436375 | T | C | 1 | a0001c0001t0020 | 1 | HG02165.hp1 | 3_prime_UTR_variant | MODIFIER | c.*342A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 24/24 | 342 | chr16 | 14436375 | ||||||
| chr16:14436638 | T | C | 1 | a0001c0001t0021 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*79A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 24/24 | 79 | chr16 | 14436638 | ||||||
| chr16:14630192 | A | G | 1 | a0001c0001t0014 | 1 | HG02683.hp2 | 5_prime_UTR_variant | MODIFIER | c.-67T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 1/24 | 67 | chr16 | 14630192 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:14436869 | G | A | 21 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0097 others(18): Show |
21 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.1865-97C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 23/23 | chr16 | 14436869 | |||||||
| chr16:14437289 | T | C | 51 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0022 others(48): Show |
51 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.1865-517A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 23/23 | chr16 | 14437289 | |||||||
| chr16:14437315 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1865-543G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 23/23 | chr16 | 14437315 | |||||||
| chr16:14437587 | C | T | 51 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0022 others(48): Show |
51 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.1865-815G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 23/23 | chr16 | 14437587 | |||||||
| chr16:14437638 | C | T | 1 | a0001c0001t0007g0123 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1865-866G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 23/23 | chr16 | 14437638 | |||||||
| chr16:14437647 | G | A | 10 | a0001c0001t0002g0036 a0001c0001t0002g0068 a0001c0001t0002g0070 others(7): Show |
10 | HG01496.hp2 HG01884.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1865-875C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 23/23 | chr16 | 14437647 | |||||||
| chr16:14438293 | C | G | 15 | a0001c0001t0001g0009 a0001c0001t0002g0036 a0001c0001t0002g0068 others(12): Show |
15 | HG01496.hp2 HG01884.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.1865-1521G>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 23/23 | chr16 | 14438293 | |||||||
| chr16:14438441 | T | TG | 21 | a0001c0001t0001g0030 a0001c0001t0001g0050 a0001c0001t0001g0079 others(18): Show |
21 | HG00597.hp1 HG00673.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.1865-1670dupC | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 23/23 | chr16 | 14438441 | |||||||
| chr16:14438441 | T | TGG | 30 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0047 others(27): Show |
30 | HG00323.hp2 HG00438.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.1865-1671_1865-167 others(6): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 23/23 | chr16 | 14438441 | |||||||
| chr16:14438441 | T | TGGG | 18 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0057 others(15): Show |
18 | HG00597.hp2 HG00735.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.1865-1672_1865-167 others(7): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 23/23 | chr16 | 14438441 | |||||||
| chr16:14438441 | T | TGGGG | 15 | a0001c0001t0002g0032 a0001c0001t0002g0070 a0001c0001t0002g0071 others(12): Show |
15 | HG00280.hp2 HG01081.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.1865-1673_1865-167 others(8): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 23/23 | chr16 | 14438441 | |||||||
| chr16:14438453 | T | G | 11 | a0001c0001t0002g0036 a0001c0001t0002g0068 a0001c0001t0002g0070 others(8): Show |
11 | HG01496.hp2 HG01884.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1865-1681A>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 23/23 | chr16 | 14438453 | |||||||
| chr16:14438560 | G | A | 3 | a0001c0001t0006g0016 a0001c0001t0006g0040 a0001c0001t0006g0157 |
3 | NA18959.hp2 NA18973.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1865-1788C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 23/23 | chr16 | 14438560 | |||||||
| chr16:14438791 | T | C | 1 | a0001c0001t0006g0163 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1865-2019A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 23/23 | chr16 | 14438791 | |||||||
| chr16:14439161 | C | A | 1 | a0001c0001t0001g0089 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1865-2389G>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 23/23 | chr16 | 14439161 | |||||||
| chr16:14439271 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1865-2499G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 23/23 | chr16 | 14439271 | |||||||
| chr16:14439375 | CA | C | 63 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0028 others(60): Show |
63 | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.1865-2604delT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 23/23 | chr16 | 14439375 | |||||||
| chr16:14439375 | CAA | C | 52 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(49): Show |
52 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.1865-2605_1865-260 others(6): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 23/23 | chr16 | 14439375 | |||||||
| chr16:14439753 | C | T | 1 | a0001c0001t0001g0009 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1865-2981G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 23/23 | chr16 | 14439753 | |||||||
| chr16:14441148 | T | C | 1 | a0001c0001t0002g0111 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1865-4376A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 23/23 | chr16 | 14441148 | |||||||
| chr16:14441332 | G | A | 16 | a0001c0001t0001g0051 a0001c0001t0002g0153 a0001c0001t0004g0076 others(13): Show |
16 | HG00673.hp1 HG01257.hp1 HG02056.hp2 others(13): Show |
intron_variant | MODIFIER | c.1865-4560C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 23/23 | chr16 | 14441332 | |||||||
| chr16:14441448 | A | G | 1 | a0001c0001t0011g0090 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1865-4676T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 23/23 | chr16 | 14441448 | |||||||
| chr16:14441466 | T | C | 3 | a0001c0002t0003g0151 a0001c0002t0006g0149 a0001c0002t0006g0150 |
3 | HG02615.hp2 HG02886.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1865-4694A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 23/23 | chr16 | 14441466 | |||||||
| chr16:14441622 | T | C | 35 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(32): Show |
35 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(32): Show |
intron_variant | MODIFIER | c.1865-4850A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 23/23 | chr16 | 14441622 | |||||||
| chr16:14441837 | A | T | 1 | a0001c0001t0001g0028 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1864+5051T>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 23/23 | chr16 | 14441837 | |||||||
| chr16:14442448 | A | G | 3 | a0001c0002t0003g0151 a0001c0002t0006g0149 a0001c0002t0006g0150 |
3 | HG02615.hp2 HG02886.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1864+4440T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 23/23 | chr16 | 14442448 | |||||||
| chr16:14442543 | C | T | 1 | a0001c0001t0002g0019 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1864+4345G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 23/23 | chr16 | 14442543 | |||||||
| chr16:14442964 | T | C | 119 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0021 others(116): Show |
119 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.1864+3924A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 23/23 | chr16 | 14442964 | |||||||
| chr16:14443096 | T | C | 1 | a0001c0001t0005g0131 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1864+3792A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 23/23 | chr16 | 14443096 | |||||||
| chr16:14443338 | T | C | 3 | a0001c0001t0006g0163 a0001c0001t0006g0164 a0001c0001t0006g0165 |
3 | HG01891.hp1 HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1864+3550A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 23/23 | chr16 | 14443338 | |||||||
| chr16:14443340 | C | CT | 20 | a0001c0001t0001g0009 a0001c0001t0001g0050 a0001c0001t0002g0036 others(17): Show |
20 | HG01433.hp2 HG01496.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1864+3547dupA | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 23/23 | chr16 | 14443340 | |||||||
| chr16:14443474 | G | A | 18 | a0001c0001t0001g0009 a0001c0001t0002g0036 a0001c0001t0002g0068 others(15): Show |
18 | HG01496.hp2 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.1864+3414C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 23/23 | chr16 | 14443474 | |||||||
| chr16:14444032 | G | A | 17 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0097 others(14): Show |
17 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.1864+2856C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 23/23 | chr16 | 14444032 | |||||||
| chr16:14444234 | T | C | 1 | a0001c0001t0004g0062 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1864+2654A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 23/23 | chr16 | 14444234 | |||||||
| chr16:14444307 | C | CT | 80 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0022 others(77): Show |
80 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.1864+2580dupA | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 23/23 | chr16 | 14444307 | |||||||
| chr16:14444983 | A | AT | 23 | a0001c0001t0001g0022 a0001c0001t0001g0084 a0001c0001t0002g0041 others(20): Show |
23 | HG00323.hp2 HG00438.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.1864+1904dupA | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 23/23 | chr16 | 14444983 | |||||||
| chr16:14445143 | G | T | 7 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(4): Show |
7 | HG01891.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1864+1745C>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 23/23 | chr16 | 14445143 | |||||||
| chr16:14445492 | G | A | 7 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(4): Show |
7 | HG01891.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1864+1396C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 23/23 | chr16 | 14445492 | |||||||
| chr16:14445623 | G | A | 1 | a0001c0001t0004g0092 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1864+1265C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 23/23 | chr16 | 14445623 | |||||||
| chr16:14445675 | A | G | 8 | a0001c0001t0004g0076 a0001c0001t0005g0014 a0001c0001t0005g0055 others(5): Show |
8 | HG00673.hp1 HG02132.hp2 NA18957.hp1 others(5): Show |
intron_variant | MODIFIER | c.1864+1213T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 23/23 | chr16 | 14445675 | |||||||
| chr16:14445752 | C | T | 1 | a0001c0001t0009g0081 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1864+1136G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 23/23 | chr16 | 14445752 | |||||||
| chr16:14445813 | C | A | 1 | a0001c0001t0001g0005 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1864+1075G>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 23/23 | chr16 | 14445813 | |||||||
| chr16:14445829 | G | T | 1 | a0001c0001t0001g0139 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1864+1059C>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 23/23 | chr16 | 14445829 | |||||||
| chr16:14446086 | T | G | 1 | a0001c0001t0008g0020 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1864+802A>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 23/23 | chr16 | 14446086 | |||||||
| chr16:14446183 | T | C | 41 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0022 others(38): Show |
41 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.1864+705A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 23/23 | chr16 | 14446183 | |||||||
| chr16:14446260 | G | A | 1 | a0001c0001t0004g0027 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1864+628C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 23/23 | chr16 | 14446260 | |||||||
| chr16:14446479 | G | A | 1 | a0001c0001t0001g0009 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1864+409C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 23/23 | chr16 | 14446479 | |||||||
| chr16:14446571 | T | C | 1 | a0001c0001t0006g0040 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1864+317A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 23/23 | chr16 | 14446571 | |||||||
| chr16:14446702 | G | A | 1 | a0001c0001t0001g0009 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1864+186C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 23/23 | chr16 | 14446702 | |||||||
| chr16:14446724 | C | T | 4 | a0001c0001t0001g0134 a0001c0001t0002g0041 a0001c0001t0002g0042 others(1): Show |
4 | HG01192.hp1 HG01255.hp2 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.1864+164G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 23/23 | chr16 | 14446724 | |||||||
| chr16:14446833 | C | A | 1 | a0001c0001t0005g0131 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1864+55G>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 23/23 | chr16 | 14446833 | |||||||
| chr16:14447239 | T | C | 1 | a0001c0001t0005g0083 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1671-158A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14447239 | |||||||
| chr16:14447467 | A | T | 1 | a0001c0001t0006g0012 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1671-386T>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14447467 | |||||||
| chr16:14447496 | G | C | 41 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0022 others(38): Show |
41 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.1671-415C>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14447496 | |||||||
| chr16:14447698 | C | T | 3 | a0001c0002t0003g0151 a0001c0002t0006g0149 a0001c0002t0006g0150 |
3 | HG02615.hp2 HG02886.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1671-617G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14447698 | |||||||
| chr16:14447870 | G | T | 34 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(31): Show |
34 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.1671-789C>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14447870 | |||||||
| chr16:14447927 | A | G | 41 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0022 others(38): Show |
41 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.1671-846T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14447927 | |||||||
| chr16:14447938 | T | TTATC | 20 | a0001c0001t0001g0028 a0001c0001t0001g0121 a0001c0001t0001g0139 others(17): Show |
20 | HG00673.hp2 HG00741.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.1671-861_1671-858d others(6): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14447938 | |||||||
| chr16:14447938 | T | TTATCTAT others(1): Show |
3 | a0001c0001t0002g0072 a0001c0001t0003g0107 a0001c0001t0009g0049 |
3 | HG02040.hp1 HG04115.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1671-865_1671-858d others(10): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14447938 | |||||||
| chr16:14447938 | TTATC | T | 47 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0051 others(44): Show |
47 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.1671-861_1671-858d others(6): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14447938 | |||||||
| chr16:14447938 | TTATCTAT others(1): Show |
T | 21 | a0001c0001t0001g0024 a0001c0001t0001g0047 a0001c0001t0001g0050 others(18): Show |
21 | HG00099.hp2 HG00438.hp1 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.1671-865_1671-858d others(10): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14447938 | |||||||
| chr16:14447938 | TTATCTAT others(5): Show |
T | 5 | a0001c0001t0001g0030 a0001c0001t0001g0057 a0001c0001t0003g0044 others(2): Show |
5 | HG02622.hp2 HG02717.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1671-869_1671-858d others(14): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14447938 | |||||||
| chr16:14447938 | TTATCTAT others(9): Show |
T | 2 | a0001c0001t0006g0164 a0001c0001t0006g0165 |
2 | HG01891.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1671-873_1671-858d others(18): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14447938 | |||||||
| chr16:14448151 | A | AT | 5 | a0001c0001t0002g0026 a0001c0001t0006g0016 a0001c0001t0006g0040 others(2): Show |
5 | HG01175.hp1 NA18612.hp1 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.1671-1071dupA | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14448151 | |||||||
| chr16:14448195 | C | A | 1 | a0001c0001t0001g0122 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1671-1114G>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14448195 | |||||||
| chr16:14448794 | C | T | 1 | a0001c0001t0002g0037 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1671-1713G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14448794 | |||||||
| chr16:14448849 | G | A | 1 | a0001c0001t0003g0102 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1671-1768C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14448849 | |||||||
| chr16:14448965 | G | T | 4 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(1): Show |
4 | HG01891.hp1 HG02922.hp2 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.1671-1884C>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14448965 | |||||||
| chr16:14449551 | G | A | 5 | a0001c0001t0001g0114 a0001c0001t0001g0143 a0001c0001t0001g0145 others(2): Show |
5 | HG01884.hp1 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1671-2470C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14449551 | |||||||
| chr16:14449919 | G | A | 40 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0022 others(37): Show |
40 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.1671-2838C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14449919 | |||||||
| chr16:14449947 | T | C | 3 | a0001c0002t0003g0151 a0001c0002t0006g0149 a0001c0002t0006g0150 |
3 | HG02615.hp2 HG02886.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1671-2866A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14449947 | |||||||
| chr16:14449956 | T | C | 1 | a0001c0001t0005g0035 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1671-2875A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14449956 | |||||||
| chr16:14450039 | A | G | 41 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0022 others(38): Show |
41 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.1671-2958T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14450039 | |||||||
| chr16:14450704 | T | C | 42 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0022 others(39): Show |
42 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.1671-3623A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14450704 | |||||||
| chr16:14450996 | C | G | 1 | a0001c0001t0006g0163 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1671-3915G>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14450996 | |||||||
| chr16:14451203 | T | C | 1 | a0001c0001t0002g0096 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1671-4122A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14451203 | |||||||
| chr16:14451208 | C | A | 4 | a0001c0002t0003g0151 a0001c0002t0004g0148 a0001c0002t0006g0149 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1671-4127G>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14451208 | |||||||
| chr16:14451407 | T | C | 53 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0022 others(50): Show |
53 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.1671-4326A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14451407 | |||||||
| chr16:14451510 | G | C | 1 | a0001c0001t0002g0118 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1671-4429C>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14451510 | |||||||
| chr16:14451796 | C | A | 2 | a0001c0001t0001g0119 a0001c0001t0004g0067 |
2 | HG01175.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1671-4715G>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14451796 | |||||||
| chr16:14451843 | T | TA | 7 | a0001c0001t0002g0060 a0001c0001t0003g0126 a0001c0001t0003g0128 others(4): Show |
7 | HG02056.hp1 HG02145.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1671-4763dupT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14451843 | |||||||
| chr16:14451843 | TA | T | 13 | a0001c0001t0001g0139 a0001c0001t0003g0004 a0001c0001t0003g0007 others(10): Show |
13 | HG01081.hp1 HG01168.hp2 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1671-4763delT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14451843 | |||||||
| chr16:14451843 | TAAAAAAA others(19): Show |
T | 9 | a0001c0001t0001g0015 a0001c0001t0001g0073 a0001c0001t0002g0070 others(6): Show |
9 | HG01496.hp2 HG01884.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.1671-4788_1671-476 others(30): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14451843 | |||||||
| chr16:14451843 | TAAAAAAA others(20): Show |
T | 1 | a0001c0001t0002g0036 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1671-4789_1671-476 others(31): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14451843 | |||||||
| chr16:14451843 | TAAAAAAA others(21): Show |
T | 7 | a0001c0001t0001g0024 a0001c0001t0001g0030 a0001c0001t0001g0057 others(4): Show |
7 | HG01168.hp1 HG01255.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1671-4790_1671-476 others(32): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14451843 | |||||||
| chr16:14451843 | TAAAAAAA others(22): Show |
T | 31 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0022 others(28): Show |
31 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.1671-4791_1671-476 others(33): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14451843 | |||||||
| chr16:14451844 | AAAAAAAA others(18): Show |
A | 6 | a0001c0001t0004g0069 a0001c0002t0003g0151 a0001c0002t0004g0148 others(3): Show |
6 | HG00741.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1671-4788_1671-476 others(29): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14451844 | |||||||
| chr16:14451845 | AAAAAAAA others(17): Show |
A | 1 | a0001c0001t0004g0039 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1671-4788_1671-476 others(28): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14451845 | |||||||
| chr16:14451867 | T | A | 1 | a0001c0001t0006g0080 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1671-4786A>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14451867 | |||||||
| chr16:14451869 | C | T | 1 | a0001c0001t0006g0080 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1671-4788G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14451869 | |||||||
| chr16:14451869 | CA | C | 30 | a0001c0001t0001g0114 a0001c0001t0001g0143 a0001c0001t0002g0060 others(27): Show |
30 | HG00099.hp2 HG00597.hp2 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.1671-4789delT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14451869 | |||||||
| chr16:14451869 | CAA | C | 23 | a0001c0001t0001g0084 a0001c0001t0001g0088 a0001c0001t0001g0108 others(20): Show |
23 | HG00323.hp1 HG00735.hp1 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.1671-4790_1671-478 others(6): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14451869 | |||||||
| chr16:14451871 | A | C | 1 | a0001c0001t0006g0080 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1671-4790T>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14451871 | |||||||
| chr16:14451885 | AAAAAAAA others(1): Show |
A | 6 | a0001c0001t0002g0153 a0001c0001t0004g0154 a0001c0001t0004g0167 others(3): Show |
6 | HG01257.hp1 HG02056.hp2 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.1671-4812_1671-480 others(12): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14451885 | |||||||
| chr16:14451886 | AAAAAAAT | A | 9 | a0001c0001t0004g0076 a0001c0001t0005g0014 a0001c0001t0005g0055 others(6): Show |
9 | HG00438.hp1 HG00673.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.1671-4812_1671-480 others(11): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14451886 | |||||||
| chr16:14452307 | T | C | 1 | a0001c0001t0007g0010 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1671-5226A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14452307 | |||||||
| chr16:14452563 | C | T | 1 | a0001c0001t0005g0140 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1671-5482G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14452563 | |||||||
| chr16:14452970 | G | GT | 3 | a0001c0001t0005g0054 a0001c0001t0005g0082 a0001c0001t0005g0112 |
3 | HG00597.hp1 NA18950.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1671-5890dupA | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14452970 | |||||||
| chr16:14452991 | G | C | 2 | a0001c0001t0003g0101 a0001c0001t0003g0113 |
2 | HG01346.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1671-5910C>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14452991 | |||||||
| chr16:14453143 | A | G | 3 | a0001c0002t0003g0151 a0001c0002t0006g0149 a0001c0002t0006g0150 |
3 | HG02615.hp2 HG02886.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1671-6062T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14453143 | |||||||
| chr16:14453201 | G | T | 33 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(30): Show |
33 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.1671-6120C>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14453201 | |||||||
| chr16:14453265 | C | G | 3 | a0001c0002t0003g0151 a0001c0002t0006g0149 a0001c0002t0006g0150 |
3 | HG02615.hp2 HG02886.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1671-6184G>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14453265 | |||||||
| chr16:14453272 | G | A | 1 | a0001c0001t0002g0072 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1671-6191C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14453272 | |||||||
| chr16:14453362 | G | A | 8 | a0001c0001t0004g0076 a0001c0001t0005g0014 a0001c0001t0005g0055 others(5): Show |
8 | HG00438.hp1 HG00673.hp1 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.1671-6281C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14453362 | |||||||
| chr16:14453757 | G | T | 1 | a0001c0001t0002g0071 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1671-6676C>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14453757 | |||||||
| chr16:14454153 | T | A | 1 | a0001c0001t0005g0156 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1671-7072A>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14454153 | |||||||
| chr16:14454249 | G | C | 37 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0022 others(34): Show |
37 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.1671-7168C>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14454249 | |||||||
| chr16:14454255 | C | T | 1 | a0001c0001t0002g0041 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1671-7174G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14454255 | |||||||
| chr16:14454993 | C | T | 1 | a0001c0001t0006g0152 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1671-7912G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14454993 | |||||||
| chr16:14455198 | T | C | 4 | a0001c0001t0002g0096 a0001c0001t0002g0132 a0001c0001t0004g0095 others(1): Show |
4 | HG02976.hp1 HG03516.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1671-8117A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14455198 | |||||||
| chr16:14455613 | AAAACTTA others(1133): Show |
A | 1 | a0001c0001t0005g0156 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1671-9672_1671-853 others(4): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14455613 | |||||||
| chr16:14455827 | C | G | 2 | a0001c0001t0003g0007 a0001c0001t0003g0105 |
2 | HG04199.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1671-8746G>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14455827 | |||||||
| chr16:14456058 | C | T | 21 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0097 others(18): Show |
21 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.1671-8977G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14456058 | |||||||
| chr16:14456229 | G | A | 1 | a0001c0001t0002g0060 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1671-9148C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14456229 | |||||||
| chr16:14456570 | T | C | 1 | a0001c0001t0002g0118 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1671-9489A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14456570 | |||||||
| chr16:14456758 | T | A | 1 | a0001c0001t0004g0027 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1671-9677A>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14456758 | |||||||
| chr16:14456830 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1671-9749G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14456830 | |||||||
| chr16:14456961 | G | C | 1 | a0001c0001t0004g0027 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1671-9880C>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14456961 | |||||||
| chr16:14457182 | T | G | 52 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0022 others(49): Show |
52 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.1671-10101A>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14457182 | |||||||
| chr16:14457184 | T | C | 1 | a0001c0001t0003g0007 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1671-10103A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14457184 | |||||||
| chr16:14457313 | G | A | 1 | a0001c0001t0001g0009 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1671-10232C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14457313 | |||||||
| chr16:14457398 | G | C | 3 | a0001c0001t0006g0163 a0001c0001t0006g0164 a0001c0001t0006g0165 |
3 | HG01891.hp1 HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1671-10317C>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14457398 | |||||||
| chr16:14457637 | A | C | 1 | a0001c0001t0001g0134 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1671-10556T>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14457637 | |||||||
| chr16:14457790 | T | C | 2 | a0001c0001t0011g0090 a0001c0001t0011g0158 |
2 | HG02717.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1671-10709A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14457790 | |||||||
| chr16:14457797 | C | CA | 28 | a0001c0001t0001g0028 a0001c0001t0001g0073 a0001c0001t0001g0089 others(25): Show |
28 | HG00099.hp2 HG00673.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.1671-10717dupT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14457797 | |||||||
| chr16:14457797 | CA | C | 34 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0050 others(31): Show |
34 | HG00323.hp1 HG00323.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.1671-10717delT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14457797 | |||||||
| chr16:14457797 | CAA | C | 5 | a0001c0001t0001g0139 a0001c0001t0003g0126 a0001c0001t0003g0128 others(2): Show |
5 | HG00280.hp2 HG01168.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.1671-10718_1671-10 others(8): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14457797 | |||||||
| chr16:14457797 | CAAA | C | 7 | a0001c0001t0001g0009 a0001c0001t0003g0115 a0001c0001t0006g0163 others(4): Show |
7 | HG01891.hp1 HG02922.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1671-10719_1671-10 others(9): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14457797 | |||||||
| chr16:14457797 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0006g0012 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1671-10727_1671-10 others(17): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14457797 | |||||||
| chr16:14457902 | AGGGGTGT others(7): Show |
A | 6 | a0001c0001t0001g0084 a0001c0001t0001g0088 a0001c0001t0001g0108 others(3): Show |
6 | HG00323.hp1 HG00735.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.1671-10835_1671-10 others(20): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14457902 | |||||||
| chr16:14457907 | TGTGTGTG others(5): Show |
T | 3 | a0001c0001t0002g0026 a0001c0001t0006g0016 a0001c0001t0006g0040 |
3 | NA18612.hp1 NA18959.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.1671-10838_1671-10 others(18): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14457907 | |||||||
| chr16:14457947 | T | A | 3 | a0001c0001t0002g0091 a0001c0001t0002g0111 a0001c0001t0006g0011 |
3 | HG00438.hp2 NA18612.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1671-10866A>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14457947 | |||||||
| chr16:14457978 | A | C | 8 | a0001c0001t0001g0084 a0001c0001t0001g0088 a0001c0001t0001g0108 others(5): Show |
8 | HG00323.hp1 HG00735.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.1671-10897T>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14457978 | |||||||
| chr16:14458116 | A | C | 2 | a0001c0001t0005g0045 a0001c0001t0009g0048 |
2 | HG02027.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.1671-11035T>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14458116 | |||||||
| chr16:14458202 | T | G | 3 | a0001c0001t0005g0054 a0001c0001t0005g0082 a0001c0001t0005g0112 |
3 | HG00597.hp1 NA18950.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1671-11121A>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14458202 | |||||||
| chr16:14458346 | T | G | 1 | a0001c0001t0003g0100 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1671-11265A>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14458346 | |||||||
| chr16:14458857 | C | T | 3 | a0001c0001t0001g0088 a0001c0001t0004g0085 a0001c0001t0006g0086 |
3 | HG00323.hp1 HG04199.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1671-11776G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14458857 | |||||||
| chr16:14458913 | G | A | 2 | a0001c0001t0002g0019 a0001c0001t0002g0093 |
2 | HG02809.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1671-11832C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14458913 | |||||||
| chr16:14459020 | A | C | 1 | a0001c0001t0001g0114 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1671-11939T>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14459020 | |||||||
| chr16:14459032 | TA | T | 42 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0022 others(39): Show |
42 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.1671-11952delT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14459032 | |||||||
| chr16:14459072 | T | C | 1 | a0001c0001t0001g0073 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1671-11991A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14459072 | |||||||
| chr16:14459262 | A | G | 1 | a0001c0001t0018g0065 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1671-12181T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14459262 | |||||||
| chr16:14459295 | T | G | 1 | a0001c0001t0005g0074 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1671-12214A>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14459295 | |||||||
| chr16:14459932 | A | G | 5 | a0001c0001t0015g0110 a0001c0002t0003g0151 a0001c0002t0004g0148 others(2): Show |
5 | HG02615.hp2 HG02886.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1671-12851T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14459932 | |||||||
| chr16:14460019 | G | T | 1 | a0001c0001t0007g0008 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1671-12938C>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14460019 | |||||||
| chr16:14460126 | C | T | 1 | a0001c0001t0005g0025 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1671-13045G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14460126 | |||||||
| chr16:14460298 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1671-13217G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14460298 | |||||||
| chr16:14460760 | T | C | 1 | a0001c0001t0007g0166 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1671-13679A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14460760 | |||||||
| chr16:14460950 | A | C | 5 | a0001c0001t0004g0038 a0001c0001t0005g0074 a0001c0001t0005g0075 others(2): Show |
5 | HG00438.hp1 HG02040.hp2 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.1671-13869T>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14460950 | |||||||
| chr16:14461404 | A | G | 4 | a0001c0002t0003g0151 a0001c0002t0004g0148 a0001c0002t0006g0149 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1671-14323T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14461404 | |||||||
| chr16:14461694 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1671-14613G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14461694 | |||||||
| chr16:14462310 | A | G | 1 | a0001c0001t0003g0104 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1671-15229T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14462310 | |||||||
| chr16:14462650 | G | GAGA | 57 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0022 others(54): Show |
57 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.1671-15572_1671-15 others(9): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14462650 | |||||||
| chr16:14463027 | G | A | 1 | a0001c0001t0002g0133 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1671-15946C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14463027 | |||||||
| chr16:14463115 | C | T | 1 | a0001c0001t0004g0006 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1671-16034G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14463115 | |||||||
| chr16:14463329 | AGGTAAAA others(12): Show |
A | 1 | a0001c0001t0006g0152 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1671-16267_1671-16 others(25): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14463329 | |||||||
| chr16:14463838 | T | G | 3 | a0001c0002t0003g0151 a0001c0002t0006g0149 a0001c0003t0001g0116 |
3 | HG02886.hp2 HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1671-16757A>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14463838 | |||||||
| chr16:14463838 | T | TG | 33 | a0001c0001t0001g0047 a0001c0001t0001g0073 a0001c0001t0001g0114 others(30): Show |
33 | HG00099.hp1 HG00280.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.1671-16758dupC | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14463838 | |||||||
| chr16:14463838 | T | TGG | 12 | a0001c0001t0001g0119 a0001c0001t0002g0019 a0001c0001t0003g0101 others(9): Show |
12 | HG00741.hp1 HG01106.hp1 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.1671-16759_1671-16 others(8): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14463838 | |||||||
| chr16:14463838 | TG | T | 12 | a0001c0001t0001g0089 a0001c0001t0004g0137 a0001c0001t0004g0154 others(9): Show |
12 | HG00438.hp1 HG00673.hp1 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1671-16758delC | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14463838 | |||||||
| chr16:14463841 | G | C | 1 | a0001c0001t0001g0084 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1671-16760C>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14463841 | |||||||
| chr16:14463851 | A | G | 16 | a0001c0001t0001g0009 a0001c0001t0002g0068 a0001c0001t0002g0070 others(13): Show |
16 | HG01496.hp2 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1671-16770T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14463851 | |||||||
| chr16:14463852 | C | G | 16 | a0001c0001t0001g0009 a0001c0001t0002g0068 a0001c0001t0002g0070 others(13): Show |
16 | HG01496.hp2 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1671-16771G>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14463852 | |||||||
| chr16:14463877 | G | A | 22 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0097 others(19): Show |
22 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.1671-16796C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14463877 | |||||||
| chr16:14464008 | G | T | 4 | a0001c0001t0004g0029 a0001c0001t0006g0163 a0001c0001t0006g0164 others(1): Show |
4 | HG01891.hp1 HG02922.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.1671-16927C>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14464008 | |||||||
| chr16:14464517 | A | C | 4 | a0001c0001t0002g0026 a0001c0001t0006g0016 a0001c0001t0006g0040 others(1): Show |
4 | NA18612.hp1 NA18959.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.1671-17436T>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14464517 | |||||||
| chr16:14464599 | A | G | 1 | a0001c0001t0006g0163 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1671-17518T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14464599 | |||||||
| chr16:14464625 | C | T | 5 | a0001c0001t0001g0024 a0001c0001t0001g0030 a0001c0001t0001g0057 others(2): Show |
5 | HG02622.hp2 HG02717.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1671-17544G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14464625 | |||||||
| chr16:14464678 | C | T | 4 | a0001c0002t0003g0151 a0001c0002t0004g0148 a0001c0002t0006g0149 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1671-17597G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14464678 | |||||||
| chr16:14464839 | T | C | 4 | a0001c0002t0003g0151 a0001c0002t0004g0148 a0001c0002t0006g0149 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1671-17758A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14464839 | |||||||
| chr16:14465091 | G | C | 1 | a0001c0001t0001g0084 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1670+17547C>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14465091 | |||||||
| chr16:14465445 | T | C | 2 | a0001c0001t0004g0039 a0001c0001t0013g0056 |
2 | HG03831.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1670+17193A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14465445 | |||||||
| chr16:14465818 | T | C | 1 | a0001c0001t0009g0031 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1670+16820A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14465818 | |||||||
| chr16:14466794 | A | G | 21 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0097 others(18): Show |
21 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.1670+15844T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14466794 | |||||||
| chr16:14466810 | T | TATAC | 38 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(35): Show |
38 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.1670+15827_1670+15 others(10): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14466810 | |||||||
| chr16:14466830 | C | T | 5 | a0001c0001t0001g0114 a0001c0001t0001g0143 a0001c0001t0001g0145 others(2): Show |
5 | HG01884.hp1 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1670+15808G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14466830 | |||||||
| chr16:14466992 | TG | T | 21 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0097 others(18): Show |
21 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.1670+15645delC | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14466992 | |||||||
| chr16:14467931 | T | G | 2 | a0001c0001t0002g0019 a0001c0001t0002g0093 |
2 | HG02809.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1670+14707A>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14467931 | |||||||
| chr16:14468107 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1670+14531G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14468107 | |||||||
| chr16:14468131 | A | G | 2 | a0001c0001t0007g0002 a0001c0001t0007g0003 |
2 | HG01496.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.1670+14507T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14468131 | |||||||
| chr16:14468420 | TCA | T | 2 | a0001c0001t0006g0058 a0001c0001t0006g0144 |
2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1670+14216_1670+14 others(8): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14468420 | |||||||
| chr16:14468463 | A | AAG | 21 | a0001c0001t0001g0009 a0001c0001t0001g0114 a0001c0001t0001g0145 others(18): Show |
21 | HG01496.hp2 HG01884.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.1670+14173_1670+14 others(8): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14468463 | |||||||
| chr16:14468527 | T | C | 4 | a0001c0002t0003g0151 a0001c0002t0004g0148 a0001c0002t0006g0149 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1670+14111A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14468527 | |||||||
| chr16:14468860 | A | C | 4 | a0001c0002t0003g0151 a0001c0002t0004g0148 a0001c0002t0006g0149 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1670+13778T>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14468860 | |||||||
| chr16:14468875 | C | CTATAGA | 2 | a0001c0001t0006g0013 a0001c0001t0009g0049 |
2 | HG02040.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1670+13762_1670+13 others(12): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14468875 | |||||||
| chr16:14468875 | CTAAA | C | 2 | a0001c0002t0004g0148 a0001c0002t0006g0150 |
2 | HG02615.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1670+13759_1670+13 others(10): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14468875 | |||||||
| chr16:14468878 | A | AATAG | 56 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0028 others(53): Show |
56 | HG00438.hp2 HG00597.hp2 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.1670+13756_1670+13 others(10): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14468878 | |||||||
| chr16:14468878 | A | AATAGATA others(1): Show |
40 | a0001c0001t0001g0015 a0001c0001t0001g0022 a0001c0001t0001g0050 others(37): Show |
40 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.1670+13752_1670+13 others(14): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14468878 | |||||||
| chr16:14468878 | A | G | 4 | a0001c0001t0006g0013 a0001c0001t0009g0049 a0001c0002t0003g0151 others(1): Show |
4 | HG02040.hp1 HG02886.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1670+13760T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14468878 | |||||||
| chr16:14468878 | AATAG | A | 5 | a0001c0001t0001g0021 a0001c0001t0001g0119 a0001c0001t0004g0039 others(2): Show |
5 | HG01175.hp2 HG01257.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.1670+13756_1670+13 others(10): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14468878 | |||||||
| chr16:14468878 | AATAGATA others(5): Show |
A | 2 | a0001c0001t0003g0097 a0001c0001t0006g0080 |
2 | HG02886.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1670+13748_1670+13 others(18): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14468878 | |||||||
| chr16:14468878 | AATAGATA others(9): Show |
A | 16 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0099 others(13): Show |
16 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.1670+13744_1670+13 others(22): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14468878 | |||||||
| chr16:14469555 | T | C | 1 | a0001c0001t0015g0110 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1670+13083A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14469555 | |||||||
| chr16:14469708 | C | CA | 41 | a0001c0001t0001g0015 a0001c0001t0001g0021 a0001c0001t0001g0024 others(38): Show |
41 | HG00280.hp2 HG00438.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.1670+12929dupT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14469708 | |||||||
| chr16:14469708 | CA | C | 25 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0097 others(22): Show |
25 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.1670+12929delT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14469708 | |||||||
| chr16:14469993 | T | C | 5 | a0001c0001t0003g0115 a0001c0001t0003g0126 a0001c0001t0003g0128 others(2): Show |
5 | HG02145.hp2 HG03098.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1670+12645A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14469993 | |||||||
| chr16:14470433 | G | GGATGATG others(2): Show |
12 | a0001c0001t0001g0009 a0001c0001t0002g0036 a0001c0001t0002g0068 others(9): Show |
12 | HG01496.hp2 HG01884.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1670+12204_1670+12 others(15): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14470433 | |||||||
| chr16:14470433 | G | GGATGATG others(8): Show |
3 | a0001c0002t0003g0151 a0001c0002t0006g0149 a0001c0002t0006g0150 |
3 | HG02615.hp2 HG02886.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1670+12204_1670+12 others(21): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14470433 | |||||||
| chr16:14470433 | G | GGATGATG others(11): Show |
1 | a0001c0002t0004g0148 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1670+12204_1670+12 others(24): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14470433 | |||||||
| chr16:14470437 | G | GATT | 22 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0089 others(19): Show |
22 | HG01106.hp2 HG01168.hp2 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.1670+12198_1670+12 others(9): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14470437 | |||||||
| chr16:14470437 | G | GATTATT | 6 | a0001c0001t0001g0084 a0001c0001t0002g0091 a0001c0001t0002g0153 others(3): Show |
6 | HG00099.hp1 HG00438.hp2 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.1670+12195_1670+12 others(12): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14470437 | |||||||
| chr16:14470437 | G | GATTATTA others(2): Show |
3 | a0001c0001t0001g0024 a0001c0001t0001g0057 a0001c0001t0003g0044 |
3 | HG02622.hp2 HG03471.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1670+12192_1670+12 others(15): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14470437 | |||||||
| chr16:14470437 | G | GATTATTA others(5): Show |
1 | a0001c0001t0001g0030 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1670+12189_1670+12 others(18): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14470437 | |||||||
| chr16:14470437 | G | T | 1 | a0001c0001t0003g0017 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1670+12201C>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14470437 | |||||||
| chr16:14470437 | GATTATTA others(2): Show |
G | 3 | a0001c0001t0004g0062 a0001c0001t0005g0045 a0001c0001t0005g0140 |
3 | HG02027.hp1 HG02027.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1670+12192_1670+12 others(15): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14470437 | |||||||
| chr16:14470437 | GATTATTA others(8): Show |
G | 21 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0097 others(18): Show |
21 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.1670+12186_1670+12 others(21): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14470437 | |||||||
| chr16:14470440 | T | G | 19 | a0001c0001t0001g0009 a0001c0001t0002g0036 a0001c0001t0002g0068 others(16): Show |
19 | HG01496.hp2 HG01884.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.1670+12198A>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14470440 | |||||||
| chr16:14470443 | T | G | 19 | a0001c0001t0001g0009 a0001c0001t0002g0036 a0001c0001t0002g0068 others(16): Show |
19 | HG01496.hp2 HG01884.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.1670+12195A>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14470443 | |||||||
| chr16:14470446 | T | G | 18 | a0001c0001t0001g0009 a0001c0001t0002g0036 a0001c0001t0002g0068 others(15): Show |
18 | HG01496.hp2 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.1670+12192A>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14470446 | |||||||
| chr16:14470449 | T | G | 14 | a0001c0001t0001g0009 a0001c0001t0002g0036 a0001c0001t0002g0068 others(11): Show |
14 | HG01496.hp2 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.1670+12189A>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14470449 | |||||||
| chr16:14470452 | T | G | 3 | a0001c0001t0002g0068 a0001c0001t0002g0071 a0001c0001t0002g0118 |
3 | HG02622.hp1 HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1670+12186A>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14470452 | |||||||
| chr16:14470776 | A | T | 17 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0097 others(14): Show |
17 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.1670+11862T>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14470776 | |||||||
| chr16:14471530 | G | A | 1 | a0001c0001t0001g0009 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1670+11108C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14471530 | |||||||
| chr16:14471531 | C | T | 17 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0097 others(14): Show |
17 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.1670+11107G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14471531 | |||||||
| chr16:14471634 | G | C | 1 | a0001c0001t0006g0152 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1670+11004C>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14471634 | |||||||
| chr16:14471651 | T | G | 2 | a0001c0001t0001g0047 a0001c0001t0005g0035 |
2 | HG01978.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.1670+10987A>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14471651 | |||||||
| chr16:14471805 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1670+10833C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14471805 | |||||||
| chr16:14471880 | G | A | 17 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0097 others(14): Show |
17 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.1670+10758C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14471880 | |||||||
| chr16:14472068 | G | C | 2 | a0001c0001t0011g0090 a0001c0001t0011g0158 |
2 | HG02717.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1670+10570C>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14472068 | |||||||
| chr16:14472327 | A | G | 1 | a0001c0001t0010g0064 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1670+10311T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14472327 | |||||||
| chr16:14472450 | G | A | 41 | a0001c0001t0001g0009 a0001c0001t0002g0036 a0001c0001t0002g0068 others(38): Show |
41 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.1670+10188C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14472450 | |||||||
| chr16:14472575 | T | C | 116 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0021 others(113): Show |
116 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.1670+10063A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14472575 | |||||||
| chr16:14472624 | C | T | 4 | a0001c0001t0003g0115 a0001c0001t0003g0126 a0001c0001t0003g0128 others(1): Show |
4 | HG02145.hp2 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1670+10014G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14472624 | |||||||
| chr16:14472655 | CTAGTAAT others(10): Show |
C | 1 | a0001c0001t0004g0076 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1670+9966_1670+998 others(21): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14472655 | |||||||
| chr16:14472740 | A | T | 1 | a0001c0001t0007g0094 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1670+9898T>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14472740 | |||||||
| chr16:14472870 | C | T | 1 | a0001c0001t0004g0069 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1670+9768G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14472870 | |||||||
| chr16:14473136 | T | C | 1 | a0001c0001t0007g0010 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1670+9502A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14473136 | |||||||
| chr16:14473232 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1670+9406G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14473232 | |||||||
| chr16:14473782 | G | A | 1 | a0001c0001t0008g0020 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1670+8856C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14473782 | |||||||
| chr16:14473976 | G | T | 4 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(1): Show |
4 | HG01891.hp1 HG02922.hp2 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.1670+8662C>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14473976 | |||||||
| chr16:14474161 | T | TTTTG | 28 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0047 others(25): Show |
28 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.1670+8473_1670+847 others(8): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14474161 | |||||||
| chr16:14474426 | A | G | 5 | a0001c0001t0002g0026 a0001c0001t0006g0016 a0001c0001t0006g0040 others(2): Show |
5 | HG01175.hp1 NA18612.hp1 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.1670+8212T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14474426 | |||||||
| chr16:14474751 | C | G | 1 | a0001c0001t0008g0129 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1670+7887G>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14474751 | |||||||
| chr16:14474913 | A | G | 4 | a0001c0002t0003g0151 a0001c0002t0004g0148 a0001c0002t0006g0149 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1670+7725T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14474913 | |||||||
| chr16:14475049 | T | A | 2 | a0001c0001t0002g0019 a0001c0001t0002g0093 |
2 | HG02809.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1670+7589A>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14475049 | |||||||
| chr16:14475311 | G | A | 4 | a0001c0001t0001g0134 a0001c0001t0002g0041 a0001c0001t0002g0042 others(1): Show |
4 | HG01192.hp1 HG01255.hp2 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.1670+7327C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14475311 | |||||||
| chr16:14475322 | T | C | 4 | a0001c0002t0003g0151 a0001c0002t0004g0148 a0001c0002t0006g0149 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1670+7316A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14475322 | |||||||
| chr16:14475611 | C | T | 1 | a0001c0001t0010g0106 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1670+7027G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14475611 | |||||||
| chr16:14475752 | C | T | 3 | a0001c0001t0001g0088 a0001c0001t0004g0085 a0001c0001t0006g0086 |
3 | HG00323.hp1 HG04199.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1670+6886G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14475752 | |||||||
| chr16:14476032 | T | A | 1 | a0001c0001t0002g0060 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1670+6606A>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14476032 | |||||||
| chr16:14476168 | A | T | 5 | a0001c0001t0001g0024 a0001c0001t0001g0030 a0001c0001t0001g0057 others(2): Show |
5 | HG02622.hp2 HG02717.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1670+6470T>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14476168 | |||||||
| chr16:14476365 | A | G | 1 | a0001c0001t0002g0060 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1670+6273T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14476365 | |||||||
| chr16:14476643 | A | G | 1 | a0001c0001t0004g0038 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1670+5995T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14476643 | |||||||
| chr16:14477084 | T | C | 1 | a0001c0001t0008g0162 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1670+5554A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14477084 | |||||||
| chr16:14477439 | C | CA | 21 | a0001c0001t0001g0009 a0001c0001t0001g0057 a0001c0001t0002g0036 others(18): Show |
21 | HG01496.hp2 HG01884.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.1670+5198dupT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14477439 | |||||||
| chr16:14477751 | C | T | 1 | a0001c0001t0005g0035 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1670+4887G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14477751 | |||||||
| chr16:14477914 | C | T | 18 | a0001c0001t0001g0009 a0001c0001t0002g0036 a0001c0001t0002g0068 others(15): Show |
18 | HG01496.hp2 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.1670+4724G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14477914 | |||||||
| chr16:14478078 | T | C | 1 | a0001c0001t0018g0065 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1670+4560A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14478078 | |||||||
| chr16:14478257 | C | T | 1 | a0001c0001t0001g0073 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1670+4381G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14478257 | |||||||
| chr16:14478330 | A | C | 1 | a0001c0001t0002g0093 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1670+4308T>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14478330 | |||||||
| chr16:14478426 | G | A | 1 | a0001c0001t0004g0023 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1670+4212C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14478426 | |||||||
| chr16:14478620 | A | T | 5 | a0001c0001t0001g0024 a0001c0001t0001g0030 a0001c0001t0001g0057 others(2): Show |
5 | HG02622.hp2 HG02717.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1670+4018T>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14478620 | |||||||
| chr16:14478724 | G | C | 2 | a0001c0001t0006g0164 a0001c0001t0006g0165 |
2 | HG01891.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1670+3914C>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14478724 | |||||||
| chr16:14478974 | T | C | 1 | a0001c0001t0006g0080 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1670+3664A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14478974 | |||||||
| chr16:14479066 | G | A | 1 | a0001c0001t0006g0087 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1670+3572C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14479066 | |||||||
| chr16:14479084 | T | A | 19 | a0001c0001t0001g0009 a0001c0001t0002g0036 a0001c0001t0002g0068 others(16): Show |
19 | HG01496.hp2 HG01884.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.1670+3554A>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14479084 | |||||||
| chr16:14479300 | T | C | 3 | a0001c0001t0006g0016 a0001c0001t0006g0040 a0001c0001t0006g0157 |
3 | NA18959.hp2 NA18973.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1670+3338A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14479300 | |||||||
| chr16:14479317 | G | A | 12 | a0001c0001t0001g0009 a0001c0001t0002g0036 a0001c0001t0002g0068 others(9): Show |
12 | HG01496.hp2 HG01884.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1670+3321C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14479317 | |||||||
| chr16:14479535 | T | C | 1 | a0001c0001t0004g0023 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1670+3103A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14479535 | |||||||
| chr16:14479920 | CA | C | 20 | a0001c0001t0001g0009 a0001c0001t0001g0088 a0001c0001t0002g0036 others(17): Show |
20 | HG00323.hp1 HG01496.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1670+2717delT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14479920 | |||||||
| chr16:14480041 | A | G | 1 | a0001c0001t0002g0037 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1670+2597T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14480041 | |||||||
| chr16:14480059 | C | G | 18 | a0001c0001t0001g0009 a0001c0001t0002g0036 a0001c0001t0002g0068 others(15): Show |
18 | HG01496.hp2 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.1670+2579G>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14480059 | |||||||
| chr16:14480127 | G | GTTCGAGG others(7): Show |
1 | a0001c0001t0003g0102 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1670+2510_1670+251 others(18): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14480127 | |||||||
| chr16:14480206 | A | G | 1 | a0001c0001t0003g0105 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1670+2432T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14480206 | |||||||
| chr16:14480271 | T | C | 1 | a0001c0001t0011g0158 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1670+2367A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14480271 | |||||||
| chr16:14480641 | T | C | 1 | a0001c0001t0002g0072 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1670+1997A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14480641 | |||||||
| chr16:14480798 | G | A | 1 | a0001c0001t0006g0080 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1670+1840C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14480798 | |||||||
| chr16:14480823 | C | G | 1 | a0001c0001t0001g0089 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1670+1815G>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14480823 | |||||||
| chr16:14480841 | G | A | 1 | a0001c0001t0007g0142 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1670+1797C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14480841 | |||||||
| chr16:14480940 | A | AAAAT | 64 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0021 others(61): Show |
64 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.1670+1694_1670+169 others(8): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14480940 | |||||||
| chr16:14480940 | A | AAAATAAA others(5): Show |
2 | a0001c0001t0001g0022 a0001c0001t0017g0046 |
2 | HG00323.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1670+1686_1670+169 others(16): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14480940 | |||||||
| chr16:14480988 | C | T | 1 | a0001c0001t0005g0131 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1670+1650G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14480988 | |||||||
| chr16:14481062 | A | G | 1 | a0001c0002t0006g0149 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1670+1576T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14481062 | |||||||
| chr16:14481408 | G | A | 1 | a0001c0001t0009g0081 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1670+1230C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14481408 | |||||||
| chr16:14481927 | T | C | 3 | a0001c0001t0006g0163 a0001c0001t0006g0164 a0001c0001t0006g0165 |
3 | HG01891.hp1 HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1670+711A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14481927 | |||||||
| chr16:14482072 | C | CCTCCAT | 2 | a0001c0001t0001g0079 a0001c0001t0019g0169 |
2 | HG02451.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1670+560_1670+565d others(8): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14482072 | |||||||
| chr16:14482145 | C | A | 2 | a0001c0001t0002g0032 a0001c0001t0002g0033 |
2 | HG00735.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.1670+493G>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14482145 | |||||||
| chr16:14482621 | C | A | 2 | a0001c0001t0001g0079 a0001c0001t0019g0169 |
2 | HG02451.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1670+17G>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 22/23 | chr16 | 14482621 | |||||||
| chr16:14483070 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1481-243A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14483070 | |||||||
| chr16:14483186 | A | G | 18 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0097 others(15): Show |
18 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.1481-359T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14483186 | |||||||
| chr16:14483299 | G | A | 6 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0007g0010 others(3): Show |
6 | HG00597.hp2 HG02132.hp1 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.1481-472C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14483299 | |||||||
| chr16:14483321 | T | C | 2 | a0001c0001t0011g0090 a0001c0001t0011g0158 |
2 | HG02717.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1481-494A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14483321 | |||||||
| chr16:14483629 | A | T | 1 | a0001c0001t0009g0049 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1481-802T>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14483629 | |||||||
| chr16:14483727 | T | C | 1 | a0001c0001t0002g0133 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1481-900A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14483727 | |||||||
| chr16:14483830 | T | C | 1 | a0001c0001t0004g0124 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1481-1003A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14483830 | |||||||
| chr16:14483939 | C | A | 1 | a0001c0001t0003g0017 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1481-1112G>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14483939 | |||||||
| chr16:14483958 | G | A | 4 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(1): Show |
4 | HG01891.hp1 HG02922.hp2 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.1481-1131C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14483958 | |||||||
| chr16:14484148 | G | A | 1 | a0001c0001t0012g0078 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1481-1321C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14484148 | |||||||
| chr16:14484294 | C | T | 19 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0097 others(16): Show |
19 | HG00673.hp2 HG00741.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.1481-1467G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14484294 | |||||||
| chr16:14484314 | A | G | 12 | a0001c0001t0001g0028 a0001c0001t0001g0084 a0001c0001t0001g0088 others(9): Show |
12 | HG00323.hp1 HG00735.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.1481-1487T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14484314 | |||||||
| chr16:14484439 | G | A | 18 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0097 others(15): Show |
18 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.1481-1612C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14484439 | |||||||
| chr16:14484947 | A | T | 1 | a0001c0001t0003g0017 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1481-2120T>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14484947 | |||||||
| chr16:14485199 | AT | A | 5 | a0001c0001t0002g0026 a0001c0001t0006g0016 a0001c0001t0006g0040 others(2): Show |
5 | HG01175.hp1 NA18612.hp1 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.1481-2373delA | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14485199 | |||||||
| chr16:14485402 | T | C | 1 | a0001c0001t0007g0066 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1481-2575A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14485402 | |||||||
| chr16:14485601 | T | C | 2 | a0001c0001t0002g0041 a0001c0001t0002g0042 |
2 | HG01928.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.1481-2774A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14485601 | |||||||
| chr16:14485968 | G | A | 8 | a0001c0001t0001g0084 a0001c0001t0001g0088 a0001c0001t0001g0108 others(5): Show |
8 | HG00323.hp1 HG00735.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.1481-3141C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14485968 | |||||||
| chr16:14485977 | C | T | 6 | a0001c0001t0002g0036 a0001c0001t0002g0070 a0001c0001t0002g0072 others(3): Show |
6 | HG01496.hp2 HG01884.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1481-3150G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14485977 | |||||||
| chr16:14485996 | G | T | 3 | a0001c0001t0006g0163 a0001c0001t0006g0164 a0001c0001t0006g0165 |
3 | HG01891.hp1 HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1481-3169C>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14485996 | |||||||
| chr16:14486054 | T | C | 4 | a0001c0002t0003g0151 a0001c0002t0004g0148 a0001c0002t0006g0149 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1481-3227A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14486054 | |||||||
| chr16:14486472 | C | T | 1 | a0001c0001t0018g0065 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1481-3645G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14486472 | |||||||
| chr16:14487037 | C | T | 1 | a0001c0001t0002g0037 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1481-4210G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14487037 | |||||||
| chr16:14487598 | A | G | 18 | a0001c0001t0001g0015 a0001c0001t0002g0153 a0001c0001t0004g0076 others(15): Show |
18 | HG00438.hp1 HG00673.hp1 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.1481-4771T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14487598 | |||||||
| chr16:14487710 | G | C | 1 | a0001c0001t0002g0018 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1481-4883C>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14487710 | |||||||
| chr16:14487872 | G | A | 1 | a0001c0001t0002g0037 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1481-5045C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14487872 | |||||||
| chr16:14488196 | A | G | 5 | a0001c0001t0001g0114 a0001c0001t0001g0143 a0001c0001t0001g0145 others(2): Show |
5 | HG01884.hp1 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1481-5369T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14488196 | |||||||
| chr16:14488229 | G | A | 5 | a0001c0001t0002g0026 a0001c0001t0006g0016 a0001c0001t0006g0040 others(2): Show |
5 | HG01175.hp1 NA18612.hp1 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.1481-5402C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14488229 | |||||||
| chr16:14488872 | C | CA | 7 | a0001c0001t0001g0088 a0001c0001t0002g0019 a0001c0001t0002g0093 others(4): Show |
7 | HG00323.hp1 HG01192.hp2 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.1481-6046dupT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14488872 | |||||||
| chr16:14488882 | A | G | 1 | a0001c0001t0004g0027 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1481-6055T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14488882 | |||||||
| chr16:14489161 | A | T | 1 | a0001c0001t0001g0009 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1481-6334T>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14489161 | |||||||
| chr16:14489173 | T | A | 3 | a0001c0001t0006g0163 a0001c0001t0006g0164 a0001c0001t0006g0165 |
3 | HG01891.hp1 HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1481-6346A>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14489173 | |||||||
| chr16:14489271 | G | A | 1 | a0001c0001t0004g0039 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1481-6444C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14489271 | |||||||
| chr16:14489437 | C | CA | 16 | a0001c0001t0001g0028 a0001c0001t0001g0073 a0001c0001t0001g0114 others(13): Show |
16 | HG00099.hp1 HG01106.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.1481-6611dupT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14489437 | |||||||
| chr16:14489437 | CAA | C | 15 | a0001c0001t0001g0009 a0001c0001t0001g0084 a0001c0001t0001g0088 others(12): Show |
15 | HG00323.hp1 HG00735.hp1 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.1481-6612_1481-661 others(6): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14489437 | |||||||
| chr16:14489581 | C | T | 1 | a0001c0001t0003g0017 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1481-6754G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14489581 | |||||||
| chr16:14490555 | TACTTCAC | T | 4 | a0001c0002t0003g0151 a0001c0002t0004g0148 a0001c0002t0006g0149 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1481-7735_1481-772 others(11): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14490555 | |||||||
| chr16:14490600 | T | C | 2 | a0001c0002t0006g0149 a0001c0002t0006g0150 |
2 | HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1481-7773A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14490600 | |||||||
| chr16:14490913 | C | T | 12 | a0001c0001t0001g0009 a0001c0001t0001g0084 a0001c0001t0001g0088 others(9): Show |
12 | HG00323.hp1 HG00735.hp1 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.1481-8086G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14490913 | |||||||
| chr16:14491025 | C | T | 1 | a0001c0001t0021g0117 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1481-8198G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14491025 | |||||||
| chr16:14491530 | C | A | 1 | a0001c0001t0005g0141 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1481-8703G>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14491530 | |||||||
| chr16:14491750 | C | A | 1 | a0001c0002t0006g0149 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1481-8923G>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14491750 | |||||||
| chr16:14491792 | A | C | 2 | a0001c0001t0011g0090 a0001c0001t0011g0158 |
2 | HG02717.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1481-8965T>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14491792 | |||||||
| chr16:14491975 | G | A | 2 | a0001c0001t0004g0023 a0001c0001t0005g0035 |
2 | HG02683.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1481-9148C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14491975 | |||||||
| chr16:14491976 | C | T | 12 | a0001c0001t0001g0009 a0001c0001t0001g0084 a0001c0001t0001g0088 others(9): Show |
12 | HG00323.hp1 HG00735.hp1 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.1481-9149G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14491976 | |||||||
| chr16:14492283 | T | C | 2 | a0001c0001t0006g0058 a0001c0001t0006g0144 |
2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1481-9456A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14492283 | |||||||
| chr16:14492549 | T | A | 1 | a0001c0001t0004g0167 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1481-9722A>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14492549 | |||||||
| chr16:14492964 | G | A | 40 | a0001c0001t0001g0009 a0001c0001t0002g0036 a0001c0001t0002g0068 others(37): Show |
40 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.1481-10137C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14492964 | |||||||
| chr16:14493081 | T | TA | 4 | a0001c0002t0003g0151 a0001c0002t0004g0148 a0001c0002t0006g0149 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1481-10255dupT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14493081 | |||||||
| chr16:14493285 | G | A | 2 | a0001c0001t0006g0164 a0001c0001t0006g0165 |
2 | HG01891.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1481-10458C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14493285 | |||||||
| chr16:14493301 | G | A | 1 | a0001c0001t0005g0131 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1481-10474C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14493301 | |||||||
| chr16:14493517 | T | A | 1 | a0001c0001t0015g0110 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1481-10690A>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14493517 | |||||||
| chr16:14494159 | T | C | 8 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(5): Show |
8 | HG01891.hp1 HG02615.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1481-11332A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14494159 | |||||||
| chr16:14494185 | G | A | 8 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(5): Show |
8 | HG01891.hp1 HG02615.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1481-11358C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14494185 | |||||||
| chr16:14494332 | A | T | 1 | a0001c0001t0006g0152 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1481-11505T>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14494332 | |||||||
| chr16:14494825 | C | T | 4 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(1): Show |
4 | HG01891.hp1 HG02922.hp2 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.1481-11998G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14494825 | |||||||
| chr16:14495208 | A | G | 1 | a0001c0001t0015g0110 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1481-12381T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14495208 | |||||||
| chr16:14495223 | T | C | 8 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(5): Show |
8 | HG01891.hp1 HG02615.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1481-12396A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14495223 | |||||||
| chr16:14495311 | C | G | 35 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(32): Show |
35 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.1481-12484G>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14495311 | |||||||
| chr16:14495494 | G | A | 1 | a0001c0001t0002g0037 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1481-12667C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14495494 | |||||||
| chr16:14495786 | A | G | 1 | a0001c0001t0004g0023 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1481-12959T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14495786 | |||||||
| chr16:14495788 | C | A | 1 | a0001c0001t0001g0009 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1481-12961G>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14495788 | |||||||
| chr16:14495823 | A | G | 5 | a0001c0001t0007g0063 a0001c0001t0007g0066 a0001c0001t0007g0123 others(2): Show |
5 | HG03098.hp2 HG03195.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1481-12996T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14495823 | |||||||
| chr16:14495997 | G | A | 1 | a0001c0001t0005g0131 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1481-13170C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14495997 | |||||||
| chr16:14496175 | C | A | 2 | a0001c0001t0006g0164 a0001c0001t0006g0165 |
2 | HG01891.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1481-13348G>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14496175 | |||||||
| chr16:14496204 | T | A | 4 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(1): Show |
4 | HG01891.hp1 HG02922.hp2 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.1481-13377A>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14496204 | |||||||
| chr16:14496207 | C | A | 1 | a0001c0001t0005g0075 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1481-13380G>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14496207 | |||||||
| chr16:14496240 | T | A | 1 | a0001c0001t0004g0038 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1481-13413A>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14496240 | |||||||
| chr16:14496274 | C | G | 4 | a0001c0001t0003g0115 a0001c0001t0003g0126 a0001c0001t0003g0128 others(1): Show |
4 | HG02145.hp2 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1481-13447G>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14496274 | |||||||
| chr16:14496318 | C | T | 3 | a0001c0001t0006g0163 a0001c0001t0006g0164 a0001c0001t0006g0165 |
3 | HG01891.hp1 HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1481-13491G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14496318 | |||||||
| chr16:14496402 | C | A | 8 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(5): Show |
8 | HG01891.hp1 HG02615.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1481-13575G>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14496402 | |||||||
| chr16:14496446 | C | T | 1 | a0001c0001t0005g0140 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1481-13619G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14496446 | |||||||
| chr16:14497111 | C | T | 1 | a0001c0001t0015g0110 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1481-14284G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14497111 | |||||||
| chr16:14497340 | G | A | 1 | a0001c0001t0003g0017 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1481-14513C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14497340 | |||||||
| chr16:14497492 | A | G | 27 | a0001c0001t0001g0009 a0001c0001t0001g0084 a0001c0001t0001g0088 others(24): Show |
27 | HG00323.hp1 HG00735.hp1 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.1481-14665T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14497492 | |||||||
| chr16:14497734 | TGGGCTGC others(20): Show |
T | 4 | a0001c0001t0001g0024 a0001c0001t0001g0030 a0001c0001t0001g0057 others(1): Show |
4 | HG02717.hp1 HG03471.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1481-14934_1481-14 others(33): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14497734 | |||||||
| chr16:14498122 | C | CA | 10 | a0001c0001t0001g0047 a0001c0001t0002g0133 a0001c0001t0004g0023 others(7): Show |
10 | HG01192.hp2 HG01255.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1481-15296dupT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14498122 | |||||||
| chr16:14498292 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1481-15465C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14498292 | |||||||
| chr16:14498577 | A | G | 27 | a0001c0001t0001g0009 a0001c0001t0001g0084 a0001c0001t0001g0088 others(24): Show |
27 | HG00323.hp1 HG00735.hp1 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.1481-15750T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14498577 | |||||||
| chr16:14499011 | G | A | 158 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0021 others(155): Show |
158 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.1481-16184C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14499011 | |||||||
| chr16:14499318 | T | C | 1 | a0001c0001t0015g0110 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1481-16491A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14499318 | |||||||
| chr16:14499569 | G | T | 1 | a0001c0001t0005g0131 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1481-16742C>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14499569 | |||||||
| chr16:14499998 | G | A | 1 | a0001c0002t0006g0149 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1481-17171C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14499998 | |||||||
| chr16:14500113 | T | C | 1 | a0001c0001t0003g0104 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1481-17286A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14500113 | |||||||
| chr16:14500125 | G | A | 1 | a0001c0001t0003g0101 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1481-17298C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14500125 | |||||||
| chr16:14500198 | G | A | 21 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0097 others(18): Show |
21 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.1481-17371C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14500198 | |||||||
| chr16:14501128 | A | G | 5 | a0001c0001t0001g0079 a0001c0001t0004g0069 a0001c0001t0006g0152 others(2): Show |
5 | HG01891.hp2 HG02451.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1481-18301T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501128 | |||||||
| chr16:14501207 | T | C | 1 | a0001c0001t0002g0068 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1481-18380A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501207 | |||||||
| chr16:14501265 | C | CA | 11 | a0001c0001t0001g0084 a0001c0001t0001g0088 a0001c0001t0001g0108 others(8): Show |
11 | HG00323.hp1 HG00735.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.1481-18439dupT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501265 | |||||||
| chr16:14501285 | AC | A | 19 | a0001c0001t0001g0009 a0001c0001t0002g0036 a0001c0001t0002g0068 others(16): Show |
19 | HG01496.hp2 HG01884.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.1481-18459delG | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501285 | |||||||
| chr16:14501290 | A | C | 19 | a0001c0001t0001g0009 a0001c0001t0002g0036 a0001c0001t0002g0068 others(16): Show |
19 | HG01496.hp2 HG01884.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.1481-18463T>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501290 | |||||||
| chr16:14501294 | C | CAAT | 7 | a0001c0001t0001g0022 a0001c0001t0002g0060 a0001c0001t0002g0153 others(4): Show |
7 | HG00099.hp2 HG00323.hp2 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.1481-18470_1481-18 others(9): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501294 | |||||||
| chr16:14501294 | CAATAAT | C | 24 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0017 others(21): Show |
24 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.1481-18473_1481-18 others(12): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501294 | |||||||
| chr16:14501296 | AT | A | 19 | a0001c0001t0001g0009 a0001c0001t0002g0036 a0001c0001t0002g0068 others(16): Show |
19 | HG01496.hp2 HG01884.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.1481-18470delA | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501296 | |||||||
| chr16:14501300 | T | A | 19 | a0001c0001t0001g0009 a0001c0001t0002g0036 a0001c0001t0002g0068 others(16): Show |
19 | HG01496.hp2 HG01884.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.1481-18473A>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501300 | |||||||
| chr16:14501303 | T | C | 19 | a0001c0001t0001g0009 a0001c0001t0002g0036 a0001c0001t0002g0068 others(16): Show |
19 | HG01496.hp2 HG01884.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.1481-18476A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501303 | |||||||
| chr16:14501329 | C | T | 1 | a0001c0001t0007g0052 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1481-18502G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501329 | |||||||
| chr16:14501338 | T | C | 1 | a0001c0001t0005g0075 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1481-18511A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501338 | |||||||
| chr16:14501345 | C | T | 1 | a0001c0001t0008g0020 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1481-18518G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501345 | |||||||
| chr16:14501371 | G | A | 1 | a0001c0001t0004g0038 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1481-18544C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501371 | |||||||
| chr16:14501435 | C | CA | 11 | a0001c0001t0001g0051 a0001c0001t0001g0088 a0001c0001t0002g0026 others(8): Show |
11 | HG00323.hp1 HG00597.hp1 HG02602.hp2 others(8): Show |
intron_variant | MODIFIER | c.1481-18609dupT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501435 | |||||||
| chr16:14501435 | C | CAA | 11 | a0001c0001t0003g0007 a0001c0001t0003g0099 a0001c0001t0003g0100 others(8): Show |
11 | HG00741.hp1 HG01106.hp1 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1481-18610_1481-18 others(8): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501435 | |||||||
| chr16:14501435 | C | CAAA | 7 | a0001c0001t0002g0042 a0001c0001t0003g0004 a0001c0001t0003g0097 others(4): Show |
7 | HG01081.hp1 HG01168.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.1481-18611_1481-18 others(9): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501435 | |||||||
| chr16:14501435 | C | CAAAAAAA others(3): Show |
3 | a0001c0001t0001g0024 a0001c0001t0003g0044 a0001c0001t0009g0031 |
3 | HG02622.hp2 HG03710.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1481-18618_1481-18 others(16): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501435 | |||||||
| chr16:14501435 | C | CAAAAAAA others(4): Show |
5 | a0001c0001t0001g0057 a0001c0001t0001g0147 a0001c0001t0004g0095 others(2): Show |
5 | HG02572.hp1 HG02717.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1481-18619_1481-18 others(17): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501435 | |||||||
| chr16:14501435 | C | CAAAAAAA others(5): Show |
4 | a0001c0001t0001g0108 a0001c0001t0001g0143 a0001c0001t0001g0145 others(1): Show |
4 | HG01346.hp1 HG01884.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1481-18620_1481-18 others(18): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501435 | |||||||
| chr16:14501435 | C | CAAAAAAA others(6): Show |
12 | a0001c0001t0001g0030 a0001c0001t0001g0139 a0001c0001t0002g0096 others(9): Show |
12 | HG00639.hp2 HG01168.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1481-18621_1481-18 others(19): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501435 | |||||||
| chr16:14501435 | C | CAAAAAAA others(7): Show |
7 | a0001c0001t0001g0021 a0001c0001t0001g0079 a0001c0001t0001g0114 others(4): Show |
7 | HG01175.hp2 HG01255.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1481-18622_1481-18 others(20): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501435 | |||||||
| chr16:14501435 | C | CAAAAAAA others(8): Show |
8 | a0001c0001t0002g0037 a0001c0001t0004g0137 a0001c0001t0006g0016 others(5): Show |
8 | HG01175.hp1 HG02976.hp2 HG03516.hp1 others(5): Show |
intron_variant | MODIFIER | c.1481-18623_1481-18 others(21): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501435 | |||||||
| chr16:14501435 | C | CAAAAAAA others(9): Show |
6 | a0001c0001t0001g0050 a0001c0001t0002g0033 a0001c0001t0004g0069 others(3): Show |
6 | HG00735.hp2 HG01433.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.1481-18624_1481-18 others(22): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501435 | |||||||
| chr16:14501435 | C | CAAAAAAA others(10): Show |
3 | a0001c0001t0004g0038 a0001c0001t0005g0055 a0001c0001t0005g0083 |
3 | HG02040.hp2 HG02602.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.1481-18625_1481-18 others(23): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501435 | |||||||
| chr16:14501435 | C | CAAAAAAA others(11): Show |
8 | a0001c0001t0001g0028 a0001c0001t0001g0121 a0001c0001t0002g0093 others(5): Show |
8 | HG01106.hp2 HG01361.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1481-18626_1481-18 others(24): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501435 | |||||||
| chr16:14501435 | C | CAAAAAAA others(12): Show |
4 | a0001c0001t0002g0019 a0001c0001t0004g0023 a0001c0001t0007g0052 others(1): Show |
4 | HG00597.hp2 HG02895.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1481-18627_1481-18 others(25): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501435 | |||||||
| chr16:14501435 | C | CAAAAAAA others(13): Show |
3 | a0001c0001t0004g0006 a0001c0001t0004g0039 a0001c0001t0013g0056 |
3 | HG00280.hp1 HG03831.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1481-18628_1481-18 others(26): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501435 | |||||||
| chr16:14501435 | C | CAAAAAAA others(14): Show |
1 | a0001c0001t0002g0018 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1481-18629_1481-18 others(27): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501435 | |||||||
| chr16:14501435 | C | CAAAAAAA others(15): Show |
2 | a0001c0001t0002g0133 a0001c0001t0005g0045 |
2 | HG01255.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.1481-18630_1481-18 others(28): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501435 | |||||||
| chr16:14501435 | C | CAAAAAAA others(16): Show |
4 | a0001c0001t0001g0047 a0001c0001t0005g0075 a0001c0001t0007g0142 others(1): Show |
4 | HG01978.hp2 NA18957.hp1 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.1481-18631_1481-18 others(29): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501435 | |||||||
| chr16:14501435 | C | CAAAAAAA others(17): Show |
3 | a0001c0001t0001g0022 a0001c0001t0002g0032 a0001c0001t0005g0120 |
3 | HG00323.hp2 HG01081.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.1481-18632_1481-18 others(30): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501435 | |||||||
| chr16:14501435 | C | CAAAAAAA others(18): Show |
5 | a0001c0001t0001g0015 a0001c0001t0002g0043 a0001c0001t0004g0027 others(2): Show |
5 | HG00099.hp2 HG01192.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.1481-18633_1481-18 others(31): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501435 | |||||||
| chr16:14501435 | C | CAAAAAAA others(19): Show |
3 | a0001c0001t0002g0060 a0001c0001t0002g0153 a0001c0001t0006g0058 |
3 | HG02056.hp1 HG02056.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1481-18609_1481-18 others(32): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501435 | |||||||
| chr16:14501435 | C | CAAAAAAA others(20): Show |
4 | a0001c0001t0002g0041 a0001c0001t0002g0111 a0001c0001t0004g0062 others(1): Show |
4 | HG01928.hp1 HG03710.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.1481-18609_1481-18 others(33): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501435 | |||||||
| chr16:14501435 | C | CAAAAAAA others(22): Show |
2 | a0001c0001t0006g0013 a0001c0001t0008g0162 |
2 | NA18968.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1481-18609_1481-18 others(35): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501435 | |||||||
| chr16:14501435 | C | CAAAAAAA others(23): Show |
2 | a0001c0001t0005g0074 a0001c0001t0005g0140 |
2 | HG00438.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.1481-18609_1481-18 others(36): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501435 | |||||||
| chr16:14501435 | C | CAAAAAAA others(24): Show |
3 | a0001c0001t0001g0073 a0001c0001t0005g0156 a0001c0001t0006g0012 |
3 | HG02132.hp1 HG02165.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1481-18609_1481-18 others(37): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501435 | |||||||
| chr16:14501435 | C | CAAAAAAA others(26): Show |
2 | a0001c0001t0004g0154 a0001c0001t0006g0080 |
2 | HG01257.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1481-18609_1481-18 others(39): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501435 | |||||||
| chr16:14501435 | C | CAAAAAAA others(27): Show |
1 | a0001c0001t0005g0025 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1481-18609_1481-18 others(40): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501435 | |||||||
| chr16:14501435 | C | CAAAAAAA others(32): Show |
1 | a0001c0001t0004g0092 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1481-18609_1481-18 others(45): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501435 | |||||||
| chr16:14501435 | C | CAAAAAAA others(36): Show |
1 | a0001c0001t0001g0059 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1481-18609_1481-18 others(49): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501435 | |||||||
| chr16:14501435 | C | CAAAAAAA others(49): Show |
1 | a0001c0001t0005g0035 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1481-18609_1481-18 others(62): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501435 | |||||||
| chr16:14501435 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0002g0071 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1481-18620_1481-18 others(18): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501435 | |||||||
| chr16:14501435 | CAAAAAAA others(6): Show |
C | 15 | a0001c0001t0001g0009 a0001c0001t0002g0036 a0001c0001t0002g0068 others(12): Show |
15 | HG01496.hp2 HG01515.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1481-18621_1481-18 others(19): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501435 | |||||||
| chr16:14501453 | A | AAAAAAAA others(3): Show |
1 | a0001c0001t0014g0001 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1481-18627_1481-18 others(16): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501453 | |||||||
| chr16:14501460 | A | AAAAAAAA others(8): Show |
1 | a0001c0001t0001g0089 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1481-18634_1481-18 others(21): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501460 | |||||||
| chr16:14501461 | C | A | 5 | a0001c0001t0001g0021 a0001c0001t0005g0045 a0001c0001t0009g0048 others(2): Show |
5 | HG02027.hp2 HG02040.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.1481-18634G>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501461 | |||||||
| chr16:14501462 | A | C | 2 | a0001c0001t0001g0119 a0001c0001t0004g0067 |
2 | HG01175.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1481-18635T>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501462 | |||||||
| chr16:14501463 | G | A | 1 | a0001c0001t0007g0053 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1481-18636C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501463 | |||||||
| chr16:14501463 | G | C | 5 | a0001c0001t0001g0021 a0001c0001t0005g0045 a0001c0001t0009g0048 others(2): Show |
5 | HG02027.hp2 HG02040.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.1481-18636C>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501463 | |||||||
| chr16:14501467 | G | A | 1 | a0001c0001t0007g0053 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1481-18640C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501467 | |||||||
| chr16:14501473 | G | A | 1 | a0001c0001t0007g0053 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1481-18646C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501473 | |||||||
| chr16:14501475 | G | A | 1 | a0001c0001t0007g0053 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1481-18648C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501475 | |||||||
| chr16:14501478 | T | A | 1 | a0001c0001t0007g0053 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1481-18651A>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501478 | |||||||
| chr16:14501479 | G | A | 1 | a0001c0001t0007g0053 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1481-18652C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501479 | |||||||
| chr16:14501482 | T | A | 1 | a0001c0001t0007g0053 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1481-18655A>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501482 | |||||||
| chr16:14501483 | G | A | 1 | a0001c0001t0007g0053 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1481-18656C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501483 | |||||||
| chr16:14501484 | T | A | 1 | a0001c0001t0007g0053 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1481-18657A>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501484 | |||||||
| chr16:14501485 | T | A | 1 | a0001c0001t0007g0053 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1481-18658A>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501485 | |||||||
| chr16:14501627 | C | T | 8 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(5): Show |
8 | HG01891.hp1 HG02615.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1481-18800G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14501627 | |||||||
| chr16:14502208 | A | G | 41 | a0001c0001t0001g0009 a0001c0001t0002g0036 a0001c0001t0002g0068 others(38): Show |
41 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.1481-19381T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14502208 | |||||||
| chr16:14502475 | G | A | 3 | a0001c0001t0006g0163 a0001c0001t0006g0164 a0001c0001t0006g0165 |
3 | HG01891.hp1 HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1481-19648C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14502475 | |||||||
| chr16:14503020 | T | C | 1 | a0001c0002t0003g0151 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1481-20193A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14503020 | |||||||
| chr16:14503042 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1481-20215C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14503042 | |||||||
| chr16:14503179 | G | A | 1 | a0001c0001t0008g0020 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1481-20352C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14503179 | |||||||
| chr16:14503256 | A | C | 1 | a0001c0001t0001g0009 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1481-20429T>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14503256 | |||||||
| chr16:14503430 | A | ATC | 11 | a0001c0001t0002g0036 a0001c0001t0002g0068 a0001c0001t0002g0070 others(8): Show |
11 | HG01496.hp2 HG01884.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1481-20604_1481-20 others(8): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14503430 | |||||||
| chr16:14503531 | A | T | 4 | a0001c0002t0003g0151 a0001c0002t0004g0148 a0001c0002t0006g0149 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1481-20704T>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14503531 | |||||||
| chr16:14503555 | G | A | 1 | a0001c0001t0002g0133 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1481-20728C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14503555 | |||||||
| chr16:14503965 | A | G | 3 | a0001c0001t0006g0163 a0001c0001t0006g0164 a0001c0001t0006g0165 |
3 | HG01891.hp1 HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1481-21138T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14503965 | |||||||
| chr16:14504459 | T | C | 2 | a0001c0001t0001g0051 a0001c0001t0005g0082 |
2 | NA18950.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.1481-21632A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14504459 | |||||||
| chr16:14504883 | T | TAAA | 19 | a0001c0001t0001g0009 a0001c0001t0002g0036 a0001c0001t0002g0068 others(16): Show |
19 | HG01496.hp2 HG01884.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.1481-22059_1481-22 others(9): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14504883 | |||||||
| chr16:14505020 | G | A | 11 | a0001c0001t0002g0036 a0001c0001t0002g0068 a0001c0001t0002g0070 others(8): Show |
11 | HG01496.hp2 HG01884.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1481-22193C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14505020 | |||||||
| chr16:14505258 | A | G | 4 | a0001c0002t0003g0151 a0001c0002t0004g0148 a0001c0002t0006g0149 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1481-22431T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14505258 | |||||||
| chr16:14505480 | A | AAC | 9 | a0001c0001t0001g0050 a0001c0001t0002g0072 a0001c0001t0004g0027 others(6): Show |
9 | HG00099.hp2 HG00639.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.1481-22655_1481-22 others(8): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14505480 | |||||||
| chr16:14505613 | C | T | 4 | a0001c0002t0003g0151 a0001c0002t0004g0148 a0001c0002t0006g0149 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1481-22786G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14505613 | |||||||
| chr16:14505670 | T | C | 1 | a0001c0001t0007g0166 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1481-22843A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14505670 | |||||||
| chr16:14505940 | T | C | 1 | a0001c0001t0002g0037 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1481-23113A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14505940 | |||||||
| chr16:14505951 | C | T | 1 | a0001c0001t0001g0021 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1481-23124G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14505951 | |||||||
| chr16:14506476 | T | G | 1 | a0001c0001t0014g0001 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1481-23649A>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14506476 | |||||||
| chr16:14506921 | T | C | 18 | a0001c0001t0001g0009 a0001c0001t0002g0036 a0001c0001t0002g0068 others(15): Show |
18 | HG01496.hp2 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.1481-24094A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14506921 | |||||||
| chr16:14506966 | GA | G | 39 | a0001c0001t0001g0009 a0001c0001t0002g0036 a0001c0001t0002g0068 others(36): Show |
39 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.1481-24140delT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14506966 | |||||||
| chr16:14507064 | T | C | 39 | a0001c0001t0001g0009 a0001c0001t0002g0036 a0001c0001t0002g0068 others(36): Show |
39 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.1481-24237A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14507064 | |||||||
| chr16:14507131 | A | G | 9 | a0001c0001t0001g0022 a0001c0001t0001g0047 a0001c0001t0001g0121 others(6): Show |
9 | HG00323.hp2 HG00735.hp2 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.1481-24304T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14507131 | |||||||
| chr16:14507502 | A | T | 34 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(31): Show |
34 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.1481-24675T>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14507502 | |||||||
| chr16:14507676 | G | GA | 5 | a0001c0001t0003g0115 a0001c0001t0003g0126 a0001c0001t0003g0128 others(2): Show |
5 | HG02145.hp2 HG03098.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1481-24850dupT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14507676 | |||||||
| chr16:14507676 | GA | G | 4 | a0001c0001t0002g0068 a0001c0001t0003g0107 a0001c0001t0011g0090 others(1): Show |
4 | HG02622.hp1 HG02717.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1481-24850delT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14507676 | |||||||
| chr16:14507932 | T | C | 1 | a0001c0001t0005g0074 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1481-25105A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14507932 | |||||||
| chr16:14508066 | T | A | 15 | a0001c0001t0001g0009 a0001c0001t0002g0036 a0001c0001t0002g0068 others(12): Show |
15 | HG01496.hp2 HG01884.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.1481-25239A>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14508066 | |||||||
| chr16:14508169 | T | TAGGCAGG others(5): Show |
4 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(1): Show |
4 | HG01891.hp1 HG02922.hp2 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.1481-25354_1481-25 others(18): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14508169 | |||||||
| chr16:14508347 | G | A | 1 | a0001c0001t0009g0031 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1481-25520C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14508347 | |||||||
| chr16:14508424 | A | C | 1 | a0001c0001t0018g0065 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1481-25597T>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14508424 | |||||||
| chr16:14508740 | G | GA | 40 | a0001c0001t0001g0009 a0001c0001t0002g0036 a0001c0001t0002g0068 others(37): Show |
40 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.1481-25914dupT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14508740 | |||||||
| chr16:14508903 | A | AAT | 5 | a0001c0001t0004g0062 a0001c0001t0005g0025 a0001c0001t0012g0078 others(2): Show |
5 | HG00099.hp1 HG00741.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1481-26078_1481-26 others(8): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14508903 | |||||||
| chr16:14509067 | C | T | 1 | a0001c0002t0006g0149 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1481-26240G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14509067 | |||||||
| chr16:14509190 | T | A | 16 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0097 others(13): Show |
16 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.1481-26363A>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14509190 | |||||||
| chr16:14509282 | T | C | 4 | a0001c0002t0003g0151 a0001c0002t0004g0148 a0001c0002t0006g0149 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1481-26455A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14509282 | |||||||
| chr16:14509762 | T | A | 3 | a0001c0001t0006g0163 a0001c0001t0006g0164 a0001c0001t0006g0165 |
3 | HG01891.hp1 HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1481-26935A>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14509762 | |||||||
| chr16:14509793 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1481-26966T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14509793 | |||||||
| chr16:14510400 | C | T | 1 | a0001c0001t0007g0166 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1481-27573G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14510400 | |||||||
| chr16:14510405 | T | A | 3 | a0001c0001t0006g0163 a0001c0001t0006g0164 a0001c0001t0006g0165 |
3 | HG01891.hp1 HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1481-27578A>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14510405 | |||||||
| chr16:14510542 | A | G | 2 | a0001c0001t0011g0090 a0001c0001t0011g0158 |
2 | HG02717.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1481-27715T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14510542 | |||||||
| chr16:14511447 | TA | T | 8 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(5): Show |
8 | HG01891.hp1 HG02615.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1481-28621delT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14511447 | |||||||
| chr16:14511541 | T | C | 1 | a0001c0001t0003g0128 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1481-28714A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14511541 | |||||||
| chr16:14511689 | G | GTATGT | 2 | a0001c0001t0002g0133 a0001c0001t0004g0023 |
2 | HG01255.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1481-28867_1481-28 others(11): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14511689 | |||||||
| chr16:14512003 | T | C | 1 | a0001c0001t0002g0037 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1481-29176A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14512003 | |||||||
| chr16:14512258 | T | G | 1 | a0001c0001t0006g0012 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1481-29431A>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14512258 | |||||||
| chr16:14512379 | T | C | 1 | a0001c0001t0004g0092 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1481-29552A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14512379 | |||||||
| chr16:14512381 | T | C | 1 | a0001c0001t0001g0015 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1481-29554A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14512381 | |||||||
| chr16:14512387 | C | T | 1 | a0001c0001t0006g0163 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1481-29560G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14512387 | |||||||
| chr16:14512471 | C | A | 17 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0143 others(14): Show |
17 | HG01192.hp1 HG01255.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.1481-29644G>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14512471 | |||||||
| chr16:14512953 | G | C | 1 | a0001c0001t0001g0009 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1481-30126C>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14512953 | |||||||
| chr16:14513057 | TG | T | 4 | a0001c0002t0003g0151 a0001c0002t0004g0148 a0001c0002t0006g0149 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1481-30231delC | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14513057 | |||||||
| chr16:14513131 | G | T | 2 | a0001c0001t0007g0002 a0001c0001t0007g0003 |
2 | HG01496.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.1481-30304C>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14513131 | |||||||
| chr16:14513387 | G | A | 4 | a0001c0001t0003g0115 a0001c0001t0003g0126 a0001c0001t0003g0128 others(1): Show |
4 | HG02145.hp2 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1481-30560C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14513387 | |||||||
| chr16:14513572 | C | A | 1 | a0001c0001t0004g0092 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1481-30745G>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14513572 | |||||||
| chr16:14513677 | C | G | 1 | a0001c0001t0002g0033 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1481-30850G>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14513677 | |||||||
| chr16:14513766 | C | G | 5 | a0001c0001t0003g0115 a0001c0001t0003g0126 a0001c0001t0003g0128 others(2): Show |
5 | HG02145.hp2 HG03098.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1481-30939G>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14513766 | |||||||
| chr16:14513826 | G | A | 5 | a0001c0001t0003g0115 a0001c0001t0003g0126 a0001c0001t0003g0128 others(2): Show |
5 | HG02145.hp2 HG03098.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1481-30999C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14513826 | |||||||
| chr16:14514170 | T | G | 4 | a0001c0002t0003g0151 a0001c0002t0004g0148 a0001c0002t0006g0149 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1481-31343A>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14514170 | |||||||
| chr16:14514243 | G | A | 1 | a0001c0001t0003g0007 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1481-31416C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14514243 | |||||||
| chr16:14514648 | A | G | 1 | a0001c0001t0003g0007 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1481-31821T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14514648 | |||||||
| chr16:14514716 | T | C | 1 | a0001c0001t0001g0134 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1481-31889A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14514716 | |||||||
| chr16:14514833 | G | A | 5 | a0001c0001t0001g0143 a0001c0001t0001g0145 a0001c0001t0001g0147 others(2): Show |
5 | HG01884.hp1 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1481-32006C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14514833 | |||||||
| chr16:14514933 | T | G | 1 | a0001c0001t0007g0052 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1481-32106A>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14514933 | |||||||
| chr16:14515272 | GGCT | G | 4 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(1): Show |
4 | HG01891.hp1 HG02922.hp2 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.1481-32448_1481-32 others(9): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14515272 | |||||||
| chr16:14515299 | C | A | 4 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(1): Show |
4 | HG01891.hp1 HG02922.hp2 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.1481-32472G>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14515299 | |||||||
| chr16:14515336 | T | C | 2 | a0001c0001t0004g0154 a0001c0001t0008g0155 |
2 | HG01257.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.1481-32509A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14515336 | |||||||
| chr16:14515402 | T | C | 26 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0097 others(23): Show |
26 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.1481-32575A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14515402 | |||||||
| chr16:14515853 | T | C | 1 | a0001c0001t0001g0073 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1481-33026A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14515853 | |||||||
| chr16:14515885 | A | G | 1 | a0001c0001t0018g0065 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1481-33058T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14515885 | |||||||
| chr16:14515931 | A | G | 5 | a0001c0001t0003g0115 a0001c0001t0003g0126 a0001c0001t0003g0128 others(2): Show |
5 | HG02145.hp2 HG03098.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1481-33104T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14515931 | |||||||
| chr16:14516180 | G | C | 1 | a0001c0001t0018g0065 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1481-33353C>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14516180 | |||||||
| chr16:14516524 | T | C | 1 | a0001c0001t0012g0034 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1481-33697A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14516524 | |||||||
| chr16:14516884 | T | A | 5 | a0001c0001t0003g0115 a0001c0001t0003g0126 a0001c0001t0003g0128 others(2): Show |
5 | HG02145.hp2 HG03098.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1481-34057A>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14516884 | |||||||
| chr16:14516980 | A | C | 2 | a0001c0001t0002g0072 a0001c0001t0002g0132 |
2 | HG02976.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1481-34153T>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14516980 | |||||||
| chr16:14517274 | A | G | 1 | a0001c0001t0007g0160 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1481-34447T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14517274 | |||||||
| chr16:14517558 | G | A | 1 | a0001c0001t0002g0118 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1480+34463C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14517558 | |||||||
| chr16:14517567 | A | G | 1 | a0001c0001t0003g0004 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1480+34454T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14517567 | |||||||
| chr16:14517676 | A | C | 1 | a0001c0001t0005g0083 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1480+34345T>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14517676 | |||||||
| chr16:14517681 | A | C | 30 | a0001c0001t0001g0009 a0001c0001t0003g0004 a0001c0001t0003g0007 others(27): Show |
30 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.1480+34340T>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14517681 | |||||||
| chr16:14517788 | C | T | 1 | a0001c0001t0005g0035 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1480+34233G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14517788 | |||||||
| chr16:14517827 | C | T | 1 | a0001c0001t0004g0038 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1480+34194G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14517827 | |||||||
| chr16:14517999 | G | A | 1 | a0001c0001t0007g0094 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1480+34022C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14517999 | |||||||
| chr16:14518291 | C | CA | 5 | a0001c0001t0001g0119 a0001c0001t0004g0067 a0001c0001t0004g0069 others(2): Show |
5 | HG00673.hp1 HG01175.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.1480+33729dupT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14518291 | |||||||
| chr16:14518291 | CA | C | 92 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0022 others(89): Show |
92 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.1480+33729delT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14518291 | |||||||
| chr16:14518291 | CAA | C | 10 | a0001c0001t0001g0009 a0001c0001t0001g0088 a0001c0001t0001g0139 others(7): Show |
10 | HG00323.hp1 HG01168.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1480+33728_1480+33 others(8): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14518291 | |||||||
| chr16:14518591 | GAAACAGA others(1923): Show |
G | 1 | a0001c0001t0001g0089 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1480+31500_1480+33 others(6): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14518591 | |||||||
| chr16:14518627 | T | C | 2 | a0001c0001t0006g0164 a0001c0001t0006g0165 |
2 | HG01891.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1480+33394A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14518627 | |||||||
| chr16:14519114 | T | C | 1 | a0001c0001t0008g0020 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1480+32907A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14519114 | |||||||
| chr16:14519116 | GA | G | 2 | a0001c0001t0001g0114 a0001c0001t0006g0058 |
2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1480+32904delT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14519116 | |||||||
| chr16:14519435 | T | C | 5 | a0001c0001t0003g0115 a0001c0001t0003g0126 a0001c0001t0003g0128 others(2): Show |
5 | HG02145.hp2 HG03098.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1480+32586A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14519435 | |||||||
| chr16:14519564 | G | A | 9 | a0001c0001t0004g0076 a0001c0001t0005g0014 a0001c0001t0005g0055 others(6): Show |
9 | HG00438.hp1 HG00673.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.1480+32457C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14519564 | |||||||
| chr16:14519787 | T | C | 26 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0097 others(23): Show |
26 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.1480+32234A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14519787 | |||||||
| chr16:14519816 | TAA | T | 4 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(1): Show |
4 | HG01891.hp1 HG02922.hp2 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.1480+32203_1480+32 others(8): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14519816 | |||||||
| chr16:14520122 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1480+31899C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14520122 | |||||||
| chr16:14520477 | C | A | 2 | a0001c0001t0006g0164 a0001c0001t0006g0165 |
2 | HG01891.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1480+31544G>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14520477 | |||||||
| chr16:14520536 | G | A | 4 | a0001c0001t0005g0074 a0001c0001t0005g0075 a0001c0001t0005g0120 others(1): Show |
4 | HG00438.hp1 NA18957.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.1480+31485C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14520536 | |||||||
| chr16:14520699 | C | CA | 22 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0097 others(19): Show |
22 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.1480+31321dupT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14520699 | |||||||
| chr16:14521095 | T | C | 1 | a0001c0001t0005g0035 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1480+30926A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14521095 | |||||||
| chr16:14521330 | G | A | 19 | a0001c0001t0001g0009 a0001c0001t0002g0036 a0001c0001t0002g0068 others(16): Show |
19 | HG01496.hp2 HG01884.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.1480+30691C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14521330 | |||||||
| chr16:14521338 | G | C | 1 | a0001c0001t0005g0156 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1480+30683C>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14521338 | |||||||
| chr16:14521707 | C | G | 1 | a0001c0001t0003g0104 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1480+30314G>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14521707 | |||||||
| chr16:14521854 | T | C | 3 | a0001c0001t0001g0088 a0001c0001t0004g0085 a0001c0001t0006g0086 |
3 | HG00323.hp1 HG04199.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1480+30167A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14521854 | |||||||
| chr16:14521870 | TG | T | 2 | a0001c0001t0006g0164 a0001c0001t0006g0165 |
2 | HG01891.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1480+30150delC | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14521870 | |||||||
| chr16:14522818 | G | C | 2 | a0001c0001t0007g0002 a0001c0001t0007g0003 |
2 | HG01496.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.1480+29203C>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14522818 | |||||||
| chr16:14523224 | T | TAC | 36 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0047 others(33): Show |
36 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(33): Show |
intron_variant | MODIFIER | c.1480+28795_1480+28 others(8): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14523224 | |||||||
| chr16:14523224 | T | TACAC | 5 | a0001c0001t0001g0022 a0001c0001t0004g0095 a0001c0001t0004g0159 others(2): Show |
5 | HG00323.hp2 HG03540.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.1480+28793_1480+28 others(10): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14523224 | |||||||
| chr16:14523224 | T | TACACAC | 9 | a0001c0001t0002g0036 a0001c0001t0002g0068 a0001c0001t0002g0070 others(6): Show |
9 | HG01496.hp2 HG01884.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1480+28791_1480+28 others(12): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14523224 | |||||||
| chr16:14523224 | TAC | T | 8 | a0001c0001t0002g0026 a0001c0001t0002g0033 a0001c0001t0002g0091 others(5): Show |
8 | HG00438.hp2 HG00735.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1480+28795_1480+28 others(8): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14523224 | |||||||
| chr16:14523224 | TACAC | T | 5 | a0001c0001t0010g0103 a0001c0002t0003g0151 a0001c0002t0004g0148 others(2): Show |
5 | HG02615.hp2 HG02886.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.1480+28793_1480+28 others(10): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14523224 | |||||||
| chr16:14523224 | TACACAC | T | 16 | a0001c0001t0003g0004 a0001c0001t0003g0007 a0001c0001t0003g0099 others(13): Show |
16 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.1480+28791_1480+28 others(12): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14523224 | |||||||
| chr16:14523224 | TACACACA others(1): Show |
T | 5 | a0001c0001t0003g0115 a0001c0001t0003g0126 a0001c0001t0003g0128 others(2): Show |
5 | HG02145.hp2 HG03098.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1480+28789_1480+28 others(14): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14523224 | |||||||
| chr16:14523345 | C | A | 1 | a0001c0001t0001g0114 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1480+28676G>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14523345 | |||||||
| chr16:14523884 | C | G | 1 | a0001c0001t0004g0023 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1480+28137G>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14523884 | |||||||
| chr16:14524368 | C | G | 1 | a0001c0001t0007g0166 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1480+27653G>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14524368 | |||||||
| chr16:14524403 | T | A | 9 | a0001c0001t0004g0076 a0001c0001t0005g0014 a0001c0001t0005g0055 others(6): Show |
9 | HG00438.hp1 HG00673.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.1480+27618A>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14524403 | |||||||
| chr16:14524454 | T | G | 25 | a0001c0001t0003g0004 a0001c0001t0003g0097 a0001c0001t0003g0099 others(22): Show |
25 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.1480+27567A>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14524454 | |||||||
| chr16:14524456 | T | G | 1 | a0001c0001t0007g0166 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1480+27565A>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14524456 | |||||||
| chr16:14524477 | G | C | 25 | a0001c0001t0003g0004 a0001c0001t0003g0097 a0001c0001t0003g0099 others(22): Show |
25 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.1480+27544C>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14524477 | |||||||
| chr16:14524534 | G | A | 1 | a0001c0001t0007g0166 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1480+27487C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14524534 | |||||||
| chr16:14524667 | A | G | 1 | a0001c0001t0007g0008 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1480+27354T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14524667 | |||||||
| chr16:14524698 | A | G | 5 | a0001c0001t0007g0063 a0001c0001t0007g0066 a0001c0001t0007g0123 others(2): Show |
5 | HG03098.hp2 HG03195.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1480+27323T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14524698 | |||||||
| chr16:14524957 | T | C | 29 | a0001c0001t0001g0009 a0001c0001t0003g0004 a0001c0001t0003g0097 others(26): Show |
29 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.1480+27064A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14524957 | |||||||
| chr16:14525195 | A | G | 1 | a0001c0001t0008g0020 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1480+26826T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14525195 | |||||||
| chr16:14525653 | G | T | 1 | a0001c0001t0001g0022 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1480+26368C>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14525653 | |||||||
| chr16:14525842 | T | C | 5 | a0001c0001t0001g0024 a0001c0001t0001g0030 a0001c0001t0001g0057 others(2): Show |
5 | HG02622.hp2 HG02717.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1480+26179A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14525842 | |||||||
| chr16:14525881 | C | A | 1 | a0001c0001t0008g0020 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1480+26140G>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14525881 | |||||||
| chr16:14526106 | C | A | 3 | a0001c0001t0003g0107 a0001c0001t0010g0103 a0001c0001t0010g0106 |
3 | HG03834.hp1 HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1480+25915G>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14526106 | |||||||
| chr16:14526265 | C | T | 2 | a0001c0001t0002g0041 a0001c0001t0002g0042 |
2 | HG01928.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.1480+25756G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14526265 | |||||||
| chr16:14526563 | C | T | 2 | a0001c0001t0002g0019 a0001c0001t0002g0093 |
2 | HG02809.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1480+25458G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14526563 | |||||||
| chr16:14526750 | G | A | 29 | a0001c0001t0001g0009 a0001c0001t0003g0004 a0001c0001t0003g0097 others(26): Show |
29 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.1480+25271C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14526750 | |||||||
| chr16:14526795 | G | A | 1 | a0001c0001t0004g0067 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1480+25226C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14526795 | |||||||
| chr16:14526965 | T | C | 4 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(1): Show |
4 | HG01891.hp1 HG02922.hp2 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.1480+25056A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14526965 | |||||||
| chr16:14527239 | C | G | 2 | a0001c0002t0006g0149 a0001c0002t0006g0150 |
2 | HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1480+24782G>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14527239 | |||||||
| chr16:14527240 | G | T | 1 | a0001c0001t0001g0057 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1480+24781C>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14527240 | |||||||
| chr16:14527489 | C | T | 1 | a0001c0001t0004g0067 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1480+24532G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14527489 | |||||||
| chr16:14527692 | G | A | 2 | a0001c0001t0001g0114 a0001c0001t0006g0058 |
2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1480+24329C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14527692 | |||||||
| chr16:14527864 | G | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0073 a0001c0001t0005g0138 |
3 | HG03834.hp2 NA19066.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1480+24157C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14527864 | |||||||
| chr16:14527939 | A | G | 25 | a0001c0001t0003g0004 a0001c0001t0003g0097 a0001c0001t0003g0099 others(22): Show |
25 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.1480+24082T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14527939 | |||||||
| chr16:14528004 | C | T | 2 | a0001c0001t0001g0015 a0001c0001t0005g0138 |
2 | HG03834.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1480+24017G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14528004 | |||||||
| chr16:14529540 | T | C | 1 | a0001c0001t0007g0160 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1480+22481A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14529540 | |||||||
| chr16:14529780 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1480+22241G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14529780 | |||||||
| chr16:14529983 | C | CAA | 29 | a0001c0001t0001g0009 a0001c0001t0003g0004 a0001c0001t0003g0097 others(26): Show |
29 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.1480+22036_1480+22 others(8): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14529983 | |||||||
| chr16:14530104 | T | C | 1 | a0001c0001t0004g0029 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1480+21917A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14530104 | |||||||
| chr16:14530275 | A | G | 1 | a0001c0001t0001g0021 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1480+21746T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14530275 | |||||||
| chr16:14530375 | C | G | 2 | a0001c0001t0006g0164 a0001c0001t0006g0165 |
2 | HG01891.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1480+21646G>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14530375 | |||||||
| chr16:14530444 | ACT | A | 2 | a0001c0001t0003g0044 a0001c0001t0006g0163 |
2 | HG02622.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1480+21575_1480+21 others(8): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14530444 | |||||||
| chr16:14530448 | T | C | 1 | a0001c0001t0004g0038 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1480+21573A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14530448 | |||||||
| chr16:14530479 | G | A | 25 | a0001c0001t0003g0004 a0001c0001t0003g0097 a0001c0001t0003g0099 others(22): Show |
25 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.1480+21542C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14530479 | |||||||
| chr16:14530544 | T | TA | 48 | a0001c0001t0001g0009 a0001c0001t0001g0028 a0001c0001t0001g0079 others(45): Show |
48 | HG00597.hp1 HG00741.hp1 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.1480+21476dupT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14530544 | |||||||
| chr16:14530555 | A | C | 1 | a0001c0001t0001g0005 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1480+21466T>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14530555 | |||||||
| chr16:14530557 | C | A | 2 | a0001c0001t0002g0019 a0001c0001t0002g0093 |
2 | HG02809.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1480+21464G>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14530557 | |||||||
| chr16:14530858 | T | C | 1 | a0001c0001t0004g0038 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1480+21163A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14530858 | |||||||
| chr16:14530975 | T | TCATC | 5 | a0001c0001t0003g0136 a0001c0001t0004g0023 a0001c0001t0004g0167 others(2): Show |
5 | HG01106.hp1 HG02809.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1480+21042_1480+21 others(10): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14530975 | |||||||
| chr16:14530975 | T | TCATCCAT others(1): Show |
16 | a0001c0001t0003g0004 a0001c0001t0003g0097 a0001c0001t0003g0099 others(13): Show |
16 | HG00597.hp2 HG00741.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.1480+21038_1480+21 others(14): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14530975 | |||||||
| chr16:14530975 | T | TCATCCAT others(5): Show |
5 | a0001c0001t0003g0115 a0001c0001t0003g0126 a0001c0001t0003g0128 others(2): Show |
5 | HG02145.hp2 HG03098.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1480+21034_1480+21 others(18): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14530975 | |||||||
| chr16:14530975 | TCATC | T | 4 | a0001c0001t0001g0009 a0001c0001t0001g0119 a0001c0001t0002g0037 others(1): Show |
4 | HG01175.hp2 HG02976.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.1480+21042_1480+21 others(10): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14530975 | |||||||
| chr16:14531076 | C | T | 6 | a0001c0001t0001g0084 a0001c0001t0001g0088 a0001c0001t0001g0108 others(3): Show |
6 | HG00323.hp1 HG00735.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.1480+20945G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14531076 | |||||||
| chr16:14531206 | G | A | 2 | a0001c0001t0011g0090 a0001c0001t0011g0158 |
2 | HG02717.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1480+20815C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14531206 | |||||||
| chr16:14531209 | G | A | 1 | a0001c0001t0011g0158 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1480+20812C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14531209 | |||||||
| chr16:14531297 | G | A | 25 | a0001c0001t0003g0004 a0001c0001t0003g0097 a0001c0001t0003g0099 others(22): Show |
25 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.1480+20724C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14531297 | |||||||
| chr16:14531309 | G | C | 4 | a0001c0001t0001g0134 a0001c0001t0002g0041 a0001c0001t0002g0042 others(1): Show |
4 | HG01192.hp1 HG01255.hp2 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.1480+20712C>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14531309 | |||||||
| chr16:14531361 | C | CA | 25 | a0001c0001t0003g0004 a0001c0001t0003g0097 a0001c0001t0003g0099 others(22): Show |
25 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.1480+20659dupT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14531361 | |||||||
| chr16:14531450 | G | A | 1 | a0001c0001t0018g0065 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1480+20571C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14531450 | |||||||
| chr16:14531807 | G | A | 25 | a0001c0001t0003g0004 a0001c0001t0003g0097 a0001c0001t0003g0099 others(22): Show |
25 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.1480+20214C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14531807 | |||||||
| chr16:14531896 | CT | C | 25 | a0001c0001t0003g0004 a0001c0001t0003g0097 a0001c0001t0003g0099 others(22): Show |
25 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.1480+20124delA | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14531896 | |||||||
| chr16:14531898 | T | G | 1 | a0001c0001t0001g0114 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1480+20123A>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14531898 | |||||||
| chr16:14531899 | TA | T | 5 | a0001c0001t0001g0050 a0001c0001t0004g0039 a0001c0001t0004g0159 others(2): Show |
5 | HG01192.hp2 HG01433.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1480+20121delT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14531899 | |||||||
| chr16:14531900 | A | C | 23 | a0001c0001t0003g0004 a0001c0001t0003g0097 a0001c0001t0003g0099 others(20): Show |
23 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.1480+20121T>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14531900 | |||||||
| chr16:14531916 | A | AG | 3 | a0001c0001t0006g0163 a0001c0001t0006g0164 a0001c0001t0006g0165 |
3 | HG01891.hp1 HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1480+20104dupC | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14531916 | |||||||
| chr16:14531916 | A | G | 1 | a0001c0001t0001g0009 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1480+20105T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14531916 | |||||||
| chr16:14532133 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1480+19888T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14532133 | |||||||
| chr16:14532174 | A | AT | 6 | a0001c0001t0001g0028 a0001c0001t0001g0121 a0001c0001t0002g0018 others(3): Show |
6 | HG01106.hp2 HG01361.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.1480+19846dupA | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14532174 | |||||||
| chr16:14532174 | AT | A | 9 | a0001c0001t0001g0089 a0001c0001t0002g0133 a0001c0001t0005g0075 others(6): Show |
9 | HG00639.hp2 HG00673.hp2 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.1480+19846delA | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14532174 | |||||||
| chr16:14532195 | A | T | 28 | a0001c0001t0001g0009 a0001c0001t0003g0004 a0001c0001t0003g0099 others(25): Show |
28 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.1480+19826T>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14532195 | |||||||
| chr16:14532196 | A | T | 1 | a0001c0001t0001g0009 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1480+19825T>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14532196 | |||||||
| chr16:14532287 | G | A | 29 | a0001c0001t0001g0009 a0001c0001t0003g0004 a0001c0001t0003g0097 others(26): Show |
29 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.1480+19734C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14532287 | |||||||
| chr16:14532291 | T | G | 152 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0021 others(149): Show |
152 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.1480+19730A>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14532291 | |||||||
| chr16:14532383 | G | C | 1 | a0001c0001t0001g0009 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1480+19638C>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14532383 | |||||||
| chr16:14532530 | GT | G | 33 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0084 others(30): Show |
33 | HG00099.hp2 HG00323.hp1 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.1480+19490delA | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14532530 | |||||||
| chr16:14532565 | T | G | 1 | a0001c0001t0005g0082 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1480+19456A>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14532565 | |||||||
| chr16:14532695 | C | CG | 25 | a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0001t0001g0108 others(22): Show |
25 | HG00597.hp1 HG01192.hp2 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.1480+19325dupC | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14532695 | |||||||
| chr16:14532708 | G | A | 4 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(1): Show |
4 | HG01891.hp1 HG02922.hp2 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.1480+19313C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14532708 | |||||||
| chr16:14532735 | A | C | 29 | a0001c0001t0001g0009 a0001c0001t0003g0004 a0001c0001t0003g0097 others(26): Show |
29 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.1480+19286T>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14532735 | |||||||
| chr16:14532883 | A | G | 25 | a0001c0001t0003g0004 a0001c0001t0003g0097 a0001c0001t0003g0099 others(22): Show |
25 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.1480+19138T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14532883 | |||||||
| chr16:14532982 | T | C | 29 | a0001c0001t0001g0009 a0001c0001t0003g0004 a0001c0001t0003g0097 others(26): Show |
29 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.1480+19039A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14532982 | |||||||
| chr16:14533158 | C | A | 1 | a0001c0001t0002g0018 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1480+18863G>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14533158 | |||||||
| chr16:14533233 | G | T | 25 | a0001c0001t0003g0004 a0001c0001t0003g0097 a0001c0001t0003g0099 others(22): Show |
25 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.1480+18788C>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14533233 | |||||||
| chr16:14533273 | G | C | 21 | a0001c0001t0003g0004 a0001c0001t0003g0097 a0001c0001t0003g0099 others(18): Show |
21 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.1480+18748C>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14533273 | |||||||
| chr16:14533311 | C | T | 1 | a0001c0002t0004g0148 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1480+18710G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14533311 | |||||||
| chr16:14533415 | G | T | 1 | a0001c0001t0009g0081 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1480+18606C>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14533415 | |||||||
| chr16:14533421 | C | CGGAGAG | 8 | a0001c0001t0001g0024 a0001c0001t0001g0088 a0001c0001t0001g0108 others(5): Show |
8 | HG00323.hp1 HG01192.hp1 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.1480+18594_1480+18 others(12): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14533421 | |||||||
| chr16:14533421 | C | CGGAGAGG others(5): Show |
3 | a0001c0001t0002g0042 a0001c0001t0007g0166 a0001c0001t0013g0056 |
3 | HG00639.hp2 HG01978.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1480+18588_1480+18 others(18): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14533421 | |||||||
| chr16:14533421 | C | CGGAGAGG others(17): Show |
1 | a0001c0001t0001g0114 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1480+18576_1480+18 others(30): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14533421 | |||||||
| chr16:14533421 | CGGAGAG | C | 82 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0047 others(79): Show |
82 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.1480+18594_1480+18 others(12): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14533421 | |||||||
| chr16:14533421 | CGGAGAGG others(5): Show |
C | 31 | a0001c0001t0001g0021 a0001c0001t0002g0018 a0001c0001t0002g0026 others(28): Show |
31 | HG00438.hp2 HG00597.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.1480+18588_1480+18 others(18): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14533421 | |||||||
| chr16:14533421 | CGGAGAGG others(11): Show |
C | 9 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0079 others(6): Show |
9 | HG00323.hp2 HG00673.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1480+18582_1480+18 others(24): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14533421 | |||||||
| chr16:14533421 | CGGAGAGG others(17): Show |
C | 20 | a0001c0001t0001g0015 a0001c0001t0001g0145 a0001c0001t0002g0096 others(17): Show |
20 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.1480+18576_1480+18 others(30): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14533421 | |||||||
| chr16:14533421 | CGGAGAGG others(23): Show |
C | 1 | a0001c0002t0003g0151 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1480+18570_1480+18 others(36): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14533421 | |||||||
| chr16:14533580 | C | T | 1 | a0001c0001t0004g0069 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1480+18441G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14533580 | |||||||
| chr16:14533753 | G | A | 1 | a0004c0004t0002g0130 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1480+18268C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14533753 | |||||||
| chr16:14533837 | C | T | 29 | a0001c0001t0001g0009 a0001c0001t0003g0004 a0001c0001t0003g0097 others(26): Show |
29 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.1480+18184G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14533837 | |||||||
| chr16:14533938 | T | C | 3 | a0001c0001t0002g0096 a0001c0001t0004g0095 a0001c0001t0007g0094 |
3 | HG03516.hp1 NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1480+18083A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14533938 | |||||||
| chr16:14534019 | T | C | 29 | a0001c0001t0001g0009 a0001c0001t0003g0004 a0001c0001t0003g0097 others(26): Show |
29 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.1480+18002A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14534019 | |||||||
| chr16:14534191 | C | A | 4 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(1): Show |
4 | HG01891.hp1 HG02922.hp2 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.1480+17830G>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14534191 | |||||||
| chr16:14534260 | A | G | 1 | a0001c0001t0005g0075 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1480+17761T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14534260 | |||||||
| chr16:14534341 | C | T | 16 | a0001c0001t0003g0004 a0001c0001t0003g0097 a0001c0001t0003g0099 others(13): Show |
16 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.1480+17680G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14534341 | |||||||
| chr16:14534833 | A | AT | 26 | a0001c0001t0003g0004 a0001c0001t0003g0097 a0001c0001t0003g0099 others(23): Show |
26 | HG00280.hp1 HG00741.hp1 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.1480+17187dupA | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14534833 | |||||||
| chr16:14534970 | A | G | 4 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(1): Show |
4 | HG01891.hp1 HG02922.hp2 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.1480+17051T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14534970 | |||||||
| chr16:14535598 | A | T | 36 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0084 others(33): Show |
36 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.1480+16423T>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14535598 | |||||||
| chr16:14535631 | A | G | 29 | a0001c0001t0001g0009 a0001c0001t0003g0004 a0001c0001t0003g0097 others(26): Show |
29 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.1480+16390T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14535631 | |||||||
| chr16:14535895 | C | A | 4 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(1): Show |
4 | HG01891.hp1 HG02922.hp2 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.1480+16126G>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14535895 | |||||||
| chr16:14536260 | G | C | 4 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(1): Show |
4 | HG01891.hp1 HG02922.hp2 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.1480+15761C>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14536260 | |||||||
| chr16:14536582 | G | A | 25 | a0001c0001t0003g0004 a0001c0001t0003g0097 a0001c0001t0003g0099 others(22): Show |
25 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.1480+15439C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14536582 | |||||||
| chr16:14537743 | G | A | 3 | a0001c0001t0006g0163 a0001c0001t0006g0164 a0001c0001t0006g0165 |
3 | HG01891.hp1 HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1480+14278C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14537743 | |||||||
| chr16:14537775 | A | C | 1 | a0001c0001t0009g0048 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1480+14246T>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14537775 | |||||||
| chr16:14537791 | G | A | 1 | a0001c0001t0002g0068 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1480+14230C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14537791 | |||||||
| chr16:14538022 | C | T | 2 | a0001c0001t0002g0019 a0001c0001t0002g0093 |
2 | HG02809.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1480+13999G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14538022 | |||||||
| chr16:14538058 | G | T | 5 | a0001c0001t0001g0021 a0001c0001t0005g0045 a0001c0001t0008g0129 others(2): Show |
5 | HG02027.hp2 HG02040.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.1480+13963C>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14538058 | |||||||
| chr16:14538074 | T | C | 21 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0143 others(18): Show |
21 | HG00099.hp2 HG00597.hp1 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.1480+13947A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14538074 | |||||||
| chr16:14538084 | A | G | 26 | a0001c0001t0003g0004 a0001c0001t0003g0097 a0001c0001t0003g0099 others(23): Show |
26 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.1480+13937T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14538084 | |||||||
| chr16:14538219 | C | CT | 8 | a0001c0001t0001g0047 a0001c0001t0002g0091 a0001c0001t0003g0044 others(5): Show |
8 | HG00438.hp2 HG00639.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.1480+13801dupA | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14538219 | |||||||
| chr16:14538219 | CT | C | 5 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(2): Show |
5 | HG01891.hp1 HG01891.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1480+13801delA | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14538219 | |||||||
| chr16:14538649 | C | T | 26 | a0001c0001t0003g0004 a0001c0001t0003g0097 a0001c0001t0003g0099 others(23): Show |
26 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.1480+13372G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14538649 | |||||||
| chr16:14538675 | G | A | 1 | a0001c0001t0002g0091 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1480+13346C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14538675 | |||||||
| chr16:14538897 | T | C | 1 | a0001c0001t0002g0041 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1480+13124A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14538897 | |||||||
| chr16:14538904 | T | C | 4 | a0001c0002t0003g0151 a0001c0002t0004g0148 a0001c0002t0006g0149 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1480+13117A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14538904 | |||||||
| chr16:14539085 | G | A | 25 | a0001c0001t0003g0004 a0001c0001t0003g0097 a0001c0001t0003g0099 others(22): Show |
25 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.1480+12936C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14539085 | |||||||
| chr16:14539836 | T | C | 31 | a0001c0001t0001g0009 a0001c0001t0002g0037 a0001c0001t0003g0004 others(28): Show |
31 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.1480+12185A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14539836 | |||||||
| chr16:14539937 | G | A | 17 | a0001c0001t0003g0004 a0001c0001t0003g0097 a0001c0001t0003g0099 others(14): Show |
17 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.1480+12084C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14539937 | |||||||
| chr16:14540003 | G | C | 2 | a0001c0001t0011g0090 a0001c0001t0011g0158 |
2 | HG02717.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1480+12018C>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14540003 | |||||||
| chr16:14540014 | A | G | 1 | a0001c0001t0001g0022 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1480+12007T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14540014 | |||||||
| chr16:14540043 | G | C | 4 | a0001c0002t0003g0151 a0001c0002t0004g0148 a0001c0002t0006g0149 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1480+11978C>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14540043 | |||||||
| chr16:14540866 | G | A | 1 | a0001c0003t0001g0116 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1480+11155C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14540866 | |||||||
| chr16:14541071 | G | A | 25 | a0001c0001t0003g0004 a0001c0001t0003g0097 a0001c0001t0003g0099 others(22): Show |
25 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.1480+10950C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14541071 | |||||||
| chr16:14541108 | T | C | 31 | a0001c0001t0001g0009 a0001c0001t0002g0037 a0001c0001t0003g0004 others(28): Show |
31 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.1480+10913A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14541108 | |||||||
| chr16:14541111 | C | T | 18 | a0001c0001t0002g0060 a0001c0001t0002g0153 a0001c0001t0004g0076 others(15): Show |
18 | HG00438.hp1 HG00673.hp1 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.1480+10910G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14541111 | |||||||
| chr16:14541119 | CT | C | 8 | a0001c0001t0001g0088 a0001c0001t0003g0017 a0001c0001t0004g0023 others(5): Show |
8 | HG00323.hp1 HG01175.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.1480+10901delA | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14541119 | |||||||
| chr16:14541139 | A | T | 26 | a0001c0001t0003g0004 a0001c0001t0003g0097 a0001c0001t0003g0099 others(23): Show |
26 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.1480+10882T>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14541139 | |||||||
| chr16:14541142 | G | A | 26 | a0001c0001t0003g0004 a0001c0001t0003g0097 a0001c0001t0003g0099 others(23): Show |
26 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.1480+10879C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14541142 | |||||||
| chr16:14541405 | C | T | 36 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0084 others(33): Show |
36 | HG00099.hp2 HG00323.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.1480+10616G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14541405 | |||||||
| chr16:14541792 | T | G | 26 | a0001c0001t0003g0004 a0001c0001t0003g0097 a0001c0001t0003g0099 others(23): Show |
26 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.1480+10229A>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14541792 | |||||||
| chr16:14541879 | A | G | 5 | a0001c0001t0001g0009 a0001c0001t0002g0037 a0001c0001t0006g0163 others(2): Show |
5 | HG01891.hp1 HG02922.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1480+10142T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14541879 | |||||||
| chr16:14542014 | T | C | 108 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0021 others(105): Show |
108 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.1480+10007A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14542014 | |||||||
| chr16:14542132 | G | A | 1 | a0001c0001t0009g0031 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1480+9889C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14542132 | |||||||
| chr16:14542243 | T | C | 1 | a0001c0001t0009g0081 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1480+9778A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14542243 | |||||||
| chr16:14542344 | C | T | 2 | a0001c0001t0007g0063 a0001c0001t0010g0064 |
2 | HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1480+9677G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14542344 | |||||||
| chr16:14542410 | C | A | 3 | a0001c0001t0003g0107 a0001c0001t0010g0103 a0001c0001t0010g0106 |
3 | HG03834.hp1 HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1480+9611G>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14542410 | |||||||
| chr16:14542567 | TA | T | 32 | a0001c0001t0001g0009 a0001c0001t0001g0059 a0001c0001t0002g0037 others(29): Show |
32 | HG00639.hp1 HG00741.hp1 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.1480+9453delT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14542567 | |||||||
| chr16:14542568 | A | T | 136 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0021 others(133): Show |
136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.1480+9453T>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14542568 | |||||||
| chr16:14542569 | A | T | 31 | a0001c0001t0001g0009 a0001c0001t0002g0037 a0001c0001t0003g0004 others(28): Show |
31 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.1480+9452T>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14542569 | |||||||
| chr16:14542673 | G | A | 108 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0021 others(105): Show |
108 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.1480+9348C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14542673 | |||||||
| chr16:14543013 | C | G | 3 | a0001c0001t0002g0096 a0001c0001t0004g0095 a0001c0001t0007g0094 |
3 | HG03516.hp1 NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1480+9008G>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14543013 | |||||||
| chr16:14543049 | T | C | 2 | a0001c0001t0004g0039 a0001c0001t0013g0056 |
2 | HG03831.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1480+8972A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14543049 | |||||||
| chr16:14543446 | TAG | T | 25 | a0001c0001t0003g0004 a0001c0001t0003g0097 a0001c0001t0003g0099 others(22): Show |
25 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.1480+8573_1480+857 others(6): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14543446 | |||||||
| chr16:14543800 | C | T | 3 | a0001c0001t0003g0102 a0001c0001t0007g0002 a0001c0001t0007g0003 |
3 | HG01496.hp1 HG01516.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.1480+8221G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14543800 | |||||||
| chr16:14543922 | C | T | 1 | a0001c0001t0003g0104 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1480+8099G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14543922 | |||||||
| chr16:14544021 | C | T | 1 | a0001c0001t0001g0028 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1480+8000G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14544021 | |||||||
| chr16:14544107 | G | A | 25 | a0001c0001t0003g0004 a0001c0001t0003g0097 a0001c0001t0003g0099 others(22): Show |
25 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.1480+7914C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14544107 | |||||||
| chr16:14544171 | G | A | 1 | a0002c0005t0003g0125 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1480+7850C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14544171 | |||||||
| chr16:14544483 | G | A | 1 | a0001c0001t0007g0166 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1480+7538C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14544483 | |||||||
| chr16:14544528 | C | T | 25 | a0001c0001t0003g0004 a0001c0001t0003g0097 a0001c0001t0003g0099 others(22): Show |
25 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.1480+7493G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14544528 | |||||||
| chr16:14544539 | C | T | 1 | a0001c0001t0003g0105 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1480+7482G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14544539 | |||||||
| chr16:14544836 | C | T | 21 | a0001c0001t0003g0004 a0001c0001t0003g0097 a0001c0001t0003g0099 others(18): Show |
21 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.1480+7185G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14544836 | |||||||
| chr16:14544847 | C | G | 36 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0084 others(33): Show |
36 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(33): Show |
intron_variant | MODIFIER | c.1480+7174G>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14544847 | |||||||
| chr16:14545390 | A | C | 28 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0047 others(25): Show |
28 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.1480+6631T>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14545390 | |||||||
| chr16:14545497 | TAAAC | T | 25 | a0001c0001t0003g0004 a0001c0001t0003g0097 a0001c0001t0003g0099 others(22): Show |
25 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.1480+6520_1480+652 others(8): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14545497 | |||||||
| chr16:14545685 | A | C | 1 | a0001c0002t0004g0148 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1480+6336T>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14545685 | |||||||
| chr16:14545904 | G | A | 14 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0002g0041 others(11): Show |
14 | HG00099.hp2 HG01192.hp1 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.1480+6117C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14545904 | |||||||
| chr16:14545925 | G | A | 30 | a0001c0001t0001g0009 a0001c0001t0002g0037 a0001c0001t0003g0004 others(27): Show |
30 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.1480+6096C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14545925 | |||||||
| chr16:14545945 | C | G | 2 | a0001c0001t0007g0063 a0001c0001t0010g0064 |
2 | HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1480+6076G>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14545945 | |||||||
| chr16:14546291 | T | C | 4 | a0001c0002t0003g0151 a0001c0002t0004g0148 a0001c0002t0006g0149 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1480+5730A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14546291 | |||||||
| chr16:14546354 | C | T | 1 | a0001c0001t0002g0133 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1480+5667G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14546354 | |||||||
| chr16:14546451 | T | C | 1 | a0001c0001t0004g0027 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1480+5570A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14546451 | |||||||
| chr16:14546687 | G | C | 5 | a0001c0001t0001g0009 a0001c0001t0002g0037 a0001c0001t0006g0163 others(2): Show |
5 | HG01891.hp1 HG02922.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1480+5334C>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14546687 | |||||||
| chr16:14546859 | G | C | 2 | a0001c0001t0002g0072 a0001c0001t0002g0132 |
2 | HG02976.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1480+5162C>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14546859 | |||||||
| chr16:14547092 | CA | C | 9 | a0001c0001t0001g0009 a0001c0001t0002g0037 a0001c0001t0006g0163 others(6): Show |
9 | HG01891.hp1 HG02615.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.1480+4928delT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14547092 | |||||||
| chr16:14547106 | A | G | 21 | a0001c0001t0003g0004 a0001c0001t0003g0097 a0001c0001t0003g0099 others(18): Show |
21 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.1480+4915T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14547106 | |||||||
| chr16:14547107 | G | A | 21 | a0001c0001t0003g0004 a0001c0001t0003g0097 a0001c0001t0003g0099 others(18): Show |
21 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.1480+4914C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14547107 | |||||||
| chr16:14547268 | C | T | 1 | a0001c0001t0015g0110 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1480+4753G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14547268 | |||||||
| chr16:14547498 | G | GGAGAGAG others(3): Show |
1 | a0001c0001t0007g0166 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1480+4522_1480+452 others(14): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14547498 | |||||||
| chr16:14547499 | A | G | 1 | a0001c0001t0007g0166 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1480+4522T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14547499 | |||||||
| chr16:14547863 | T | C | 12 | a0001c0001t0001g0028 a0001c0001t0001g0084 a0001c0001t0001g0088 others(9): Show |
12 | HG00323.hp1 HG00735.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.1480+4158A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14547863 | |||||||
| chr16:14548021 | G | C | 1 | a0001c0001t0001g0009 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1480+4000C>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14548021 | |||||||
| chr16:14548184 | G | A | 1 | a0001c0001t0001g0009 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1480+3837C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14548184 | |||||||
| chr16:14548185 | T | C | 1 | a0001c0001t0005g0025 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1480+3836A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14548185 | |||||||
| chr16:14548264 | T | G | 1 | a0001c0001t0001g0147 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1480+3757A>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14548264 | |||||||
| chr16:14548677 | G | A | 1 | a0001c0001t0004g0124 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1480+3344C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14548677 | |||||||
| chr16:14548729 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1480+3292G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14548729 | |||||||
| chr16:14548763 | T | C | 3 | a0001c0001t0006g0163 a0001c0001t0006g0164 a0001c0001t0006g0165 |
3 | HG01891.hp1 HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1480+3258A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14548763 | |||||||
| chr16:14548780 | C | A | 1 | a0001c0001t0002g0037 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1480+3241G>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14548780 | |||||||
| chr16:14548866 | A | G | 1 | a0001c0001t0021g0117 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1480+3155T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14548866 | |||||||
| chr16:14548925 | G | A | 2 | a0001c0001t0006g0164 a0001c0001t0006g0165 |
2 | HG01891.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1480+3096C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14548925 | |||||||
| chr16:14549409 | C | T | 4 | a0001c0002t0003g0151 a0001c0002t0004g0148 a0001c0002t0006g0149 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1480+2612G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14549409 | |||||||
| chr16:14549441 | G | C | 2 | a0001c0001t0002g0072 a0001c0001t0002g0132 |
2 | HG02976.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1480+2580C>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14549441 | |||||||
| chr16:14549814 | C | A | 4 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(1): Show |
4 | HG01891.hp1 HG02922.hp2 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.1480+2207G>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14549814 | |||||||
| chr16:14550464 | T | C | 5 | a0001c0001t0003g0115 a0001c0001t0003g0126 a0001c0001t0003g0128 others(2): Show |
5 | HG02145.hp2 HG03098.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1480+1557A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14550464 | |||||||
| chr16:14550531 | T | G | 1 | a0001c0001t0001g0030 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1480+1490A>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14550531 | |||||||
| chr16:14550582 | G | A | 4 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(1): Show |
4 | HG01891.hp1 HG02922.hp2 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.1480+1439C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14550582 | |||||||
| chr16:14550844 | T | C | 2 | a0001c0001t0003g0101 a0001c0001t0003g0113 |
2 | HG01346.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1480+1177A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14550844 | |||||||
| chr16:14551156 | T | G | 5 | a0001c0001t0003g0115 a0001c0001t0003g0126 a0001c0001t0003g0128 others(2): Show |
5 | HG02145.hp2 HG03098.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1480+865A>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14551156 | |||||||
| chr16:14551342 | G | A | 1 | a0001c0001t0004g0067 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1480+679C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14551342 | |||||||
| chr16:14551648 | G | C | 1 | a0001c0001t0006g0163 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1480+373C>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14551648 | |||||||
| chr16:14551659 | TG | T | 29 | a0001c0001t0001g0009 a0001c0001t0003g0004 a0001c0001t0003g0097 others(26): Show |
29 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.1480+361delC | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14551659 | |||||||
| chr16:14551992 | T | C | 1 | a0004c0004t0002g0130 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1480+29A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 21/23 | chr16 | 14551992 | |||||||
| chr16:14552239 | C | A | 8 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(5): Show |
8 | HG01891.hp1 HG02615.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1406-144G>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 20/23 | chr16 | 14552239 | |||||||
| chr16:14552345 | C | T | 3 | a0001c0001t0001g0051 a0001c0001t0005g0054 a0001c0001t0005g0112 |
3 | HG00597.hp1 NA18950.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1406-250G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 20/23 | chr16 | 14552345 | |||||||
| chr16:14552715 | G | A | 1 | a0001c0001t0002g0132 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1406-620C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 20/23 | chr16 | 14552715 | |||||||
| chr16:14552782 | C | A | 1 | a0001c0001t0005g0045 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1406-687G>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 20/23 | chr16 | 14552782 | |||||||
| chr16:14553011 | C | A | 1 | a0001c0001t0001g0009 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1406-916G>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 20/23 | chr16 | 14553011 | |||||||
| chr16:14553094 | A | C | 1 | a0001c0001t0001g0009 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1405+971T>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 20/23 | chr16 | 14553094 | |||||||
| chr16:14553112 | A | G | 1 | a0001c0001t0020g0161 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1405+953T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 20/23 | chr16 | 14553112 | |||||||
| chr16:14553255 | T | TA | 3 | a0001c0002t0003g0151 a0001c0002t0006g0149 a0001c0002t0006g0150 |
3 | HG02615.hp2 HG02886.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1405+809_1405+810i others(3): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 20/23 | chr16 | 14553255 | |||||||
| chr16:14553256 | T | A | 3 | a0001c0002t0003g0151 a0001c0002t0006g0149 a0001c0002t0006g0150 |
3 | HG02615.hp2 HG02886.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1405+809A>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 20/23 | chr16 | 14553256 | |||||||
| chr16:14553256 | TA | T | 82 | a0001c0001t0001g0015 a0001c0001t0001g0073 a0001c0001t0001g0079 others(79): Show |
82 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.1405+808delT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 20/23 | chr16 | 14553256 | |||||||
| chr16:14553256 | TAA | T | 77 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0024 others(74): Show |
77 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.1405+807_1405+808d others(4): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 20/23 | chr16 | 14553256 | |||||||
| chr16:14553259 | A | T | 1 | a0001c0001t0002g0026 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1405+806T>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 20/23 | chr16 | 14553259 | |||||||
| chr16:14553275 | A | G | 1 | a0001c0001t0004g0006 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1405+790T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 20/23 | chr16 | 14553275 | |||||||
| chr16:14553702 | T | A | 2 | a0001c0001t0002g0036 a0001c0001t0004g0135 |
2 | HG01496.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1405+363A>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 20/23 | chr16 | 14553702 | |||||||
| chr16:14553804 | C | G | 4 | a0001c0002t0003g0151 a0001c0002t0004g0148 a0001c0002t0006g0149 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1405+261G>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 20/23 | chr16 | 14553804 | |||||||
| chr16:14554194 | G | A | 4 | a0001c0001t0003g0115 a0001c0001t0003g0126 a0001c0001t0003g0128 others(1): Show |
4 | HG02145.hp2 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1319-43C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 19/23 | chr16 | 14554194 | |||||||
| chr16:14554304 | G | C | 2 | a0001c0001t0006g0164 a0001c0001t0006g0165 |
2 | HG01891.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1319-153C>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 19/23 | chr16 | 14554304 | |||||||
| chr16:14554434 | A | AT | 7 | a0001c0001t0001g0021 a0001c0001t0004g0076 a0001c0001t0005g0045 others(4): Show |
7 | HG00597.hp2 HG02027.hp2 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.1319-284dupA | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 19/23 | chr16 | 14554434 | |||||||
| chr16:14554434 | AT | A | 26 | a0001c0001t0003g0004 a0001c0001t0003g0097 a0001c0001t0003g0099 others(23): Show |
26 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.1319-284delA | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 19/23 | chr16 | 14554434 | |||||||
| chr16:14554695 | C | T | 3 | a0001c0001t0002g0091 a0001c0001t0002g0111 a0001c0001t0006g0011 |
3 | HG00438.hp2 NA18612.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1319-544G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 19/23 | chr16 | 14554695 | |||||||
| chr16:14554719 | C | T | 5 | a0001c0001t0001g0024 a0001c0001t0001g0030 a0001c0001t0001g0057 others(2): Show |
5 | HG02622.hp2 HG02717.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1319-568G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 19/23 | chr16 | 14554719 | |||||||
| chr16:14554745 | T | C | 5 | a0001c0001t0001g0024 a0001c0001t0001g0030 a0001c0001t0001g0057 others(2): Show |
5 | HG02622.hp2 HG02717.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1319-594A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 19/23 | chr16 | 14554745 | |||||||
| chr16:14554761 | G | GA | 5 | a0001c0001t0002g0032 a0001c0001t0006g0163 a0001c0001t0006g0164 others(2): Show |
5 | HG01081.hp2 HG01891.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1319-611dupT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 19/23 | chr16 | 14554761 | |||||||
| chr16:14554934 | T | C | 30 | a0001c0001t0001g0009 a0001c0001t0003g0004 a0001c0001t0003g0097 others(27): Show |
30 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.1318+720A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 19/23 | chr16 | 14554934 | |||||||
| chr16:14555393 | T | A | 3 | a0001c0001t0006g0163 a0001c0001t0006g0164 a0001c0001t0006g0165 |
3 | HG01891.hp1 HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1318+261A>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 19/23 | chr16 | 14555393 | |||||||
| chr16:14555411 | T | C | 1 | a0001c0001t0005g0140 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1318+243A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 19/23 | chr16 | 14555411 | |||||||
| chr16:14555769 | C | T | 4 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(1): Show |
4 | HG01891.hp1 HG02922.hp2 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.1263-60G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14555769 | |||||||
| chr16:14556284 | G | A | 24 | a0001c0001t0003g0004 a0001c0001t0003g0097 a0001c0001t0003g0099 others(21): Show |
24 | HG00741.hp1 HG01081.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.1263-575C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14556284 | |||||||
| chr16:14556507 | C | T | 4 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(1): Show |
4 | HG01891.hp1 HG02922.hp2 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.1263-798G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14556507 | |||||||
| chr16:14556519 | A | G | 1 | a0001c0001t0001g0009 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1263-810T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14556519 | |||||||
| chr16:14556536 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1263-827T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14556536 | |||||||
| chr16:14556568 | C | T | 1 | a0001c0001t0001g0009 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1263-859G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14556568 | |||||||
| chr16:14556788 | A | G | 2 | a0001c0001t0001g0084 a0001c0001t0001g0122 |
2 | HG00735.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.1263-1079T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14556788 | |||||||
| chr16:14556962 | T | C | 4 | a0001c0002t0003g0151 a0001c0002t0004g0148 a0001c0002t0006g0149 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1263-1253A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14556962 | |||||||
| chr16:14557284 | G | A | 25 | a0001c0001t0003g0004 a0001c0001t0003g0097 a0001c0001t0003g0099 others(22): Show |
25 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.1263-1575C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14557284 | |||||||
| chr16:14557557 | C | CA | 7 | a0001c0001t0001g0005 a0001c0001t0001g0047 a0001c0001t0002g0033 others(4): Show |
7 | HG00735.hp2 HG01978.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.1263-1849dupT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14557557 | |||||||
| chr16:14557920 | C | T | 1 | a0001c0001t0002g0096 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1263-2211G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14557920 | |||||||
| chr16:14558104 | T | C | 4 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(1): Show |
4 | HG01891.hp1 HG02922.hp2 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.1263-2395A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14558104 | |||||||
| chr16:14558310 | C | T | 36 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0084 others(33): Show |
36 | HG00099.hp2 HG00323.hp1 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.1263-2601G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14558310 | |||||||
| chr16:14558413 | AC | A | 3 | a0001c0001t0004g0137 a0001c0001t0006g0040 a0001c0001t0007g0010 |
3 | NA18959.hp2 NA18973.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1263-2705delG | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14558413 | |||||||
| chr16:14558431 | G | A | 1 | a0001c0001t0001g0009 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1263-2722C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14558431 | |||||||
| chr16:14558454 | C | T | 4 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(1): Show |
4 | HG01891.hp1 HG02922.hp2 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.1263-2745G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14558454 | |||||||
| chr16:14558496 | C | CA | 8 | a0001c0001t0002g0036 a0001c0001t0002g0070 a0001c0001t0002g0072 others(5): Show |
8 | HG01496.hp2 HG01884.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1263-2788dupT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14558496 | |||||||
| chr16:14558520 | G | C | 1 | a0001c0001t0011g0158 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1263-2811C>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14558520 | |||||||
| chr16:14558730 | A | C | 4 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(1): Show |
4 | HG01891.hp1 HG02922.hp2 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.1263-3021T>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14558730 | |||||||
| chr16:14558934 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1263-3225C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14558934 | |||||||
| chr16:14558982 | C | T | 3 | a0001c0001t0002g0096 a0001c0001t0004g0095 a0001c0001t0007g0094 |
3 | HG03516.hp1 NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1263-3273G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14558982 | |||||||
| chr16:14559003 | C | A | 1 | a0001c0001t0004g0167 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1263-3294G>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14559003 | |||||||
| chr16:14559229 | T | G | 5 | a0001c0001t0003g0115 a0001c0001t0003g0126 a0001c0001t0003g0128 others(2): Show |
5 | HG02145.hp2 HG03098.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1263-3520A>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14559229 | |||||||
| chr16:14559337 | C | T | 21 | a0001c0001t0003g0004 a0001c0001t0003g0097 a0001c0001t0003g0099 others(18): Show |
21 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.1263-3628G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14559337 | |||||||
| chr16:14559350 | T | A | 1 | a0001c0001t0004g0167 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1263-3641A>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14559350 | |||||||
| chr16:14559382 | T | C | 1 | a0001c0001t0001g0009 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1263-3673A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14559382 | |||||||
| chr16:14559409 | GT | G | 21 | a0001c0001t0003g0004 a0001c0001t0003g0097 a0001c0001t0003g0099 others(18): Show |
21 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.1263-3701delA | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14559409 | |||||||
| chr16:14559575 | CTA | C | 4 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(1): Show |
4 | HG01891.hp1 HG02922.hp2 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.1263-3868_1263-386 others(6): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14559575 | |||||||
| chr16:14560210 | A | G | 1 | a0001c0001t0005g0156 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1263-4501T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14560210 | |||||||
| chr16:14560737 | C | A | 21 | a0001c0001t0003g0004 a0001c0001t0003g0097 a0001c0001t0003g0099 others(18): Show |
21 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.1263-5028G>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14560737 | |||||||
| chr16:14561157 | C | CA | 5 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0006g0163 others(2): Show |
5 | HG01891.hp1 HG02922.hp2 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.1263-5449dupT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14561157 | |||||||
| chr16:14561206 | C | T | 1 | a0001c0001t0002g0026 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1263-5497G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14561206 | |||||||
| chr16:14561327 | A | G | 4 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(1): Show |
4 | HG01891.hp1 HG02922.hp2 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.1263-5618T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14561327 | |||||||
| chr16:14561399 | C | G | 1 | a0001c0001t0001g0108 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1263-5690G>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14561399 | |||||||
| chr16:14561591 | T | A | 1 | a0001c0001t0004g0029 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1263-5882A>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14561591 | |||||||
| chr16:14561657 | A | C | 22 | a0001c0001t0003g0004 a0001c0001t0003g0097 a0001c0001t0003g0099 others(19): Show |
22 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.1263-5948T>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14561657 | |||||||
| chr16:14562021 | G | A | 1 | a0001c0001t0007g0094 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1263-6312C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14562021 | |||||||
| chr16:14562025 | G | A | 1 | a0001c0001t0001g0009 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1263-6316C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14562025 | |||||||
| chr16:14562067 | G | A | 9 | a0001c0001t0002g0036 a0001c0001t0002g0068 a0001c0001t0002g0070 others(6): Show |
9 | HG01496.hp2 HG01884.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1263-6358C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14562067 | |||||||
| chr16:14562207 | T | C | 17 | a0001c0001t0003g0004 a0001c0001t0003g0097 a0001c0001t0003g0099 others(14): Show |
17 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.1263-6498A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14562207 | |||||||
| chr16:14562894 | G | C | 1 | a0001c0001t0002g0043 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1263-7185C>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14562894 | |||||||
| chr16:14563475 | TTTG | T | 2 | a0001c0001t0001g0119 a0001c0001t0002g0153 |
2 | HG01175.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.1263-7769_1263-776 others(7): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14563475 | |||||||
| chr16:14563476 | TTG | T | 20 | a0001c0001t0001g0015 a0001c0001t0001g0051 a0001c0001t0001g0073 others(17): Show |
20 | HG00597.hp1 HG01081.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.1263-7769_1263-776 others(6): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14563476 | |||||||
| chr16:14563476 | TTGTG | T | 23 | a0001c0001t0001g0079 a0001c0001t0002g0026 a0001c0001t0002g0036 others(20): Show |
23 | HG00099.hp1 HG00099.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.1263-7771_1263-776 others(8): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14563476 | |||||||
| chr16:14563476 | TTGTGTG | T | 53 | a0001c0001t0001g0005 a0001c0001t0001g0114 a0001c0001t0001g0134 others(50): Show |
53 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.1263-7773_1263-776 others(10): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14563476 | |||||||
| chr16:14563476 | TTGTGTGT others(1): Show |
T | 19 | a0001c0001t0001g0021 a0001c0001t0001g0028 a0001c0001t0001g0050 others(16): Show |
19 | HG00323.hp1 HG00735.hp1 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.1263-7775_1263-776 others(12): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14563476 | |||||||
| chr16:14563476 | TTGTGTGT others(3): Show |
T | 29 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0030 others(26): Show |
29 | HG00323.hp2 HG00438.hp2 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.1263-7777_1263-776 others(14): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14563476 | |||||||
| chr16:14563476 | TTGTGTGT others(5): Show |
T | 2 | a0001c0001t0002g0033 a0001c0001t0003g0044 |
2 | HG00735.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1263-7779_1263-776 others(16): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14563476 | |||||||
| chr16:14563520 | G | A | 6 | a0001c0001t0001g0084 a0001c0001t0001g0108 a0001c0001t0001g0122 others(3): Show |
6 | HG00735.hp1 HG01346.hp1 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.1263-7811C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14563520 | |||||||
| chr16:14563520 | G | GTA | 4 | a0001c0001t0003g0115 a0001c0001t0003g0126 a0001c0001t0003g0128 others(1): Show |
4 | HG02145.hp2 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1263-7812_1263-781 others(6): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14563520 | |||||||
| chr16:14563522 | G | A | 153 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0021 others(150): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.1263-7813C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14563522 | |||||||
| chr16:14563522 | G | GTATATAT others(1): Show |
4 | a0001c0001t0006g0164 a0001c0001t0006g0165 a0001c0002t0003g0151 others(1): Show |
4 | HG01891.hp1 HG02886.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1263-7814_1263-781 others(12): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14563522 | |||||||
| chr16:14563522 | G | GTGTGTGT others(7): Show |
1 | a0001c0001t0001g0009 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1263-7814_1263-781 others(18): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14563522 | |||||||
| chr16:14563577 | G | A | 2 | a0001c0001t0006g0164 a0001c0001t0006g0165 |
2 | HG01891.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1263-7868C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14563577 | |||||||
| chr16:14563679 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1263-7970C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14563679 | |||||||
| chr16:14563699 | C | CT | 7 | a0001c0001t0002g0096 a0001c0001t0003g0107 a0001c0001t0004g0095 others(4): Show |
7 | HG02145.hp1 HG03516.hp1 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.1263-7991dupA | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14563699 | |||||||
| chr16:14563759 | G | A | 25 | a0001c0001t0003g0004 a0001c0001t0003g0097 a0001c0001t0003g0099 others(22): Show |
25 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.1263-8050C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14563759 | |||||||
| chr16:14563874 | T | C | 3 | a0001c0001t0005g0140 a0001c0001t0008g0162 a0001c0001t0020g0161 |
3 | HG02027.hp1 HG02165.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.1263-8165A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14563874 | |||||||
| chr16:14563978 | G | A | 1 | a0004c0004t0002g0130 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1263-8269C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14563978 | |||||||
| chr16:14564106 | C | T | 1 | a0001c0001t0007g0008 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1263-8397G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14564106 | |||||||
| chr16:14564415 | C | G | 109 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0021 others(106): Show |
109 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.1263-8706G>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14564415 | |||||||
| chr16:14564460 | C | T | 4 | a0001c0001t0001g0024 a0001c0001t0001g0030 a0001c0001t0001g0057 others(1): Show |
4 | HG02717.hp1 HG03471.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1263-8751G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14564460 | |||||||
| chr16:14564472 | G | A | 4 | a0001c0002t0003g0151 a0001c0002t0004g0148 a0001c0002t0006g0149 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1263-8763C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14564472 | |||||||
| chr16:14564596 | G | T | 29 | a0001c0001t0001g0009 a0001c0001t0003g0004 a0001c0001t0003g0097 others(26): Show |
29 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.1263-8887C>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14564596 | |||||||
| chr16:14564606 | G | T | 1 | a0001c0001t0006g0080 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1263-8897C>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14564606 | |||||||
| chr16:14564669 | G | A | 4 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(1): Show |
4 | HG01891.hp1 HG02922.hp2 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.1263-8960C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14564669 | |||||||
| chr16:14564975 | C | G | 1 | a0001c0001t0007g0008 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1263-9266G>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14564975 | |||||||
| chr16:14565115 | T | C | 1 | a0001c0001t0006g0080 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1263-9406A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14565115 | |||||||
| chr16:14565230 | T | C | 1 | a0001c0001t0006g0011 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1263-9521A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14565230 | |||||||
| chr16:14565410 | C | CA | 14 | a0001c0001t0001g0009 a0001c0001t0001g0143 a0001c0001t0001g0145 others(11): Show |
14 | HG01884.hp1 HG02451.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.1263-9702dupT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14565410 | |||||||
| chr16:14566515 | T | C | 16 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0002g0041 others(13): Show |
16 | HG00099.hp2 HG00280.hp2 HG00597.hp2 others(13): Show |
intron_variant | MODIFIER | c.1263-10806A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14566515 | |||||||
| chr16:14566762 | T | G | 1 | a0001c0001t0004g0006 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1263-11053A>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14566762 | |||||||
| chr16:14566881 | T | C | 8 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(5): Show |
8 | HG01891.hp1 HG02615.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1263-11172A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14566881 | |||||||
| chr16:14567193 | T | C | 1 | a0001c0001t0009g0081 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1263-11484A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14567193 | |||||||
| chr16:14567302 | T | C | 3 | a0001c0001t0004g0137 a0001c0001t0006g0040 a0001c0001t0007g0010 |
3 | NA18959.hp2 NA18973.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1263-11593A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14567302 | |||||||
| chr16:14567338 | C | A | 5 | a0001c0001t0001g0024 a0001c0001t0001g0030 a0001c0001t0001g0057 others(2): Show |
5 | HG02622.hp2 HG02717.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1263-11629G>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14567338 | |||||||
| chr16:14567379 | C | A | 2 | a0001c0001t0008g0162 a0001c0001t0020g0161 |
2 | HG02165.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.1263-11670G>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14567379 | |||||||
| chr16:14567853 | G | A | 1 | a0001c0001t0005g0156 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1263-12144C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14567853 | |||||||
| chr16:14568098 | C | T | 4 | a0001c0002t0003g0151 a0001c0002t0004g0148 a0001c0002t0006g0149 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1263-12389G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14568098 | |||||||
| chr16:14568196 | T | A | 1 | a0001c0001t0005g0141 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1263-12487A>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14568196 | |||||||
| chr16:14568197 | A | T | 1 | a0001c0001t0005g0141 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1263-12488T>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14568197 | |||||||
| chr16:14568214 | CT | C | 24 | a0001c0001t0003g0004 a0001c0001t0003g0097 a0001c0001t0003g0099 others(21): Show |
24 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.1263-12506delA | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14568214 | |||||||
| chr16:14568338 | G | A | 2 | a0001c0001t0003g0136 a0002c0005t0003g0125 |
2 | HG00741.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.1262+12536C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14568338 | |||||||
| chr16:14568442 | T | TA | 8 | a0001c0001t0001g0119 a0001c0001t0003g0007 a0001c0001t0004g0062 others(5): Show |
8 | HG00099.hp1 HG00741.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.1262+12431dupT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14568442 | |||||||
| chr16:14568767 | C | T | 1 | a0001c0001t0004g0069 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1262+12107G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14568767 | |||||||
| chr16:14568844 | G | C | 1 | a0001c0001t0002g0033 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1262+12030C>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14568844 | |||||||
| chr16:14568866 | G | A | 1 | a0004c0004t0002g0130 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1262+12008C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14568866 | |||||||
| chr16:14569101 | A | G | 1 | a0001c0001t0002g0037 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1262+11773T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14569101 | |||||||
| chr16:14569226 | T | A | 1 | a0001c0001t0002g0037 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1262+11648A>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14569226 | |||||||
| chr16:14569378 | C | T | 4 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(1): Show |
4 | HG01891.hp1 HG02922.hp2 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.1262+11496G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14569378 | |||||||
| chr16:14569664 | T | C | 1 | a0001c0001t0001g0022 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1262+11210A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14569664 | |||||||
| chr16:14570043 | G | C | 2 | a0001c0001t0001g0051 a0001c0001t0005g0054 |
2 | HG00597.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.1262+10831C>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14570043 | |||||||
| chr16:14570321 | CA | C | 116 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0022 others(113): Show |
116 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.1262+10552delT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14570321 | |||||||
| chr16:14570321 | CAA | C | 10 | a0001c0001t0001g0009 a0001c0001t0002g0072 a0001c0001t0002g0118 others(7): Show |
10 | HG01515.hp2 HG01516.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1262+10551_1262+10 others(8): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14570321 | |||||||
| chr16:14570321 | CAAA | C | 24 | a0001c0001t0003g0004 a0001c0001t0003g0097 a0001c0001t0003g0099 others(21): Show |
24 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.1262+10550_1262+10 others(9): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14570321 | |||||||
| chr16:14570426 | C | T | 4 | a0001c0001t0002g0036 a0001c0001t0002g0168 a0001c0001t0004g0135 others(1): Show |
4 | HG01496.hp2 HG01884.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1262+10448G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14570426 | |||||||
| chr16:14570513 | G | A | 3 | a0001c0001t0006g0163 a0001c0001t0006g0164 a0001c0001t0006g0165 |
3 | HG01891.hp1 HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1262+10361C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14570513 | |||||||
| chr16:14570815 | C | CA | 13 | a0001c0001t0001g0005 a0001c0001t0001g0122 a0001c0001t0002g0060 others(10): Show |
13 | HG00735.hp1 HG01106.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.1262+10058dupT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14570815 | |||||||
| chr16:14570815 | CA | C | 9 | a0001c0001t0004g0092 a0001c0001t0008g0162 a0001c0001t0009g0081 others(6): Show |
9 | HG00280.hp2 HG02165.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1262+10058delT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14570815 | |||||||
| chr16:14571064 | A | G | 1 | a0001c0001t0001g0015 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1262+9810T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14571064 | |||||||
| chr16:14571082 | TTCCCAAT others(13): Show |
T | 4 | a0001c0002t0003g0151 a0001c0002t0004g0148 a0001c0002t0006g0149 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1262+9772_1262+979 others(24): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14571082 | |||||||
| chr16:14571357 | C | CA | 24 | a0001c0001t0001g0005 a0001c0001t0001g0134 a0001c0001t0001g0143 others(21): Show |
24 | HG00099.hp2 HG00280.hp2 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.1262+9516dupT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14571357 | |||||||
| chr16:14571418 | C | T | 4 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(1): Show |
4 | HG01891.hp1 HG02922.hp2 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.1262+9456G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14571418 | |||||||
| chr16:14571487 | A | G | 22 | a0001c0001t0003g0004 a0001c0001t0003g0097 a0001c0001t0003g0099 others(19): Show |
22 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.1262+9387T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14571487 | |||||||
| chr16:14571622 | C | T | 30 | a0001c0001t0001g0009 a0001c0001t0003g0004 a0001c0001t0003g0097 others(27): Show |
30 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.1262+9252G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14571622 | |||||||
| chr16:14572065 | T | C | 1 | a0001c0001t0001g0047 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1262+8809A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14572065 | |||||||
| chr16:14572737 | G | A | 8 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(5): Show |
8 | HG01891.hp1 HG02615.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1262+8137C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14572737 | |||||||
| chr16:14573100 | T | C | 4 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(1): Show |
4 | HG01891.hp1 HG02922.hp2 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.1262+7774A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14573100 | |||||||
| chr16:14573145 | T | G | 16 | a0001c0001t0001g0079 a0001c0001t0002g0036 a0001c0001t0002g0068 others(13): Show |
16 | HG01496.hp2 HG01884.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.1262+7729A>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14573145 | |||||||
| chr16:14573318 | A | G | 3 | a0001c0002t0003g0151 a0001c0002t0006g0149 a0001c0002t0006g0150 |
3 | HG02615.hp2 HG02886.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1262+7556T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14573318 | |||||||
| chr16:14573691 | C | T | 1 | a0001c0001t0006g0152 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1262+7183G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14573691 | |||||||
| chr16:14573833 | C | T | 2 | a0001c0001t0003g0099 a0001c0001t0003g0100 |
2 | HG01257.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.1262+7041G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14573833 | |||||||
| chr16:14573951 | G | A | 5 | a0001c0001t0003g0115 a0001c0001t0003g0126 a0001c0001t0003g0128 others(2): Show |
5 | HG02145.hp2 HG03098.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1262+6923C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14573951 | |||||||
| chr16:14574146 | C | CTGAGATG others(26): Show |
1 | a0001c0001t0002g0032 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1262+6695_1262+672 others(37): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14574146 | |||||||
| chr16:14574298 | A | G | 2 | a0001c0001t0003g0004 a0001c0001t0003g0104 |
2 | HG01081.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.1262+6576T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14574298 | |||||||
| chr16:14574375 | T | C | 1 | a0001c0001t0005g0077 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1262+6499A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14574375 | |||||||
| chr16:14574581 | C | T | 1 | a0001c0001t0002g0168 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1262+6293G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14574581 | |||||||
| chr16:14574582 | G | A | 1 | a0001c0001t0006g0087 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1262+6292C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14574582 | |||||||
| chr16:14574696 | G | C | 1 | a0001c0001t0007g0160 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1262+6178C>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14574696 | |||||||
| chr16:14574735 | C | G | 1 | a0001c0001t0007g0160 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1262+6139G>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14574735 | |||||||
| chr16:14574821 | G | A | 4 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(1): Show |
4 | HG01891.hp1 HG02922.hp2 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.1262+6053C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14574821 | |||||||
| chr16:14575163 | A | C | 1 | a0001c0001t0006g0080 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1262+5711T>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14575163 | |||||||
| chr16:14575556 | T | C | 1 | a0001c0001t0004g0023 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1262+5318A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14575556 | |||||||
| chr16:14575584 | C | G | 5 | a0001c0001t0003g0115 a0001c0001t0003g0126 a0001c0001t0003g0128 others(2): Show |
5 | HG02145.hp2 HG03098.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1262+5290G>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14575584 | |||||||
| chr16:14575597 | G | A | 1 | a0001c0001t0002g0093 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1262+5277C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14575597 | |||||||
| chr16:14575686 | T | C | 3 | a0001c0001t0006g0163 a0001c0001t0006g0164 a0001c0001t0006g0165 |
3 | HG01891.hp1 HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1262+5188A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14575686 | |||||||
| chr16:14576474 | G | T | 1 | a0001c0001t0001g0009 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1262+4400C>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14576474 | |||||||
| chr16:14576910 | T | C | 35 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(32): Show |
35 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.1262+3964A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14576910 | |||||||
| chr16:14577011 | G | T | 1 | a0001c0001t0001g0047 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1262+3863C>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14577011 | |||||||
| chr16:14577273 | T | C | 1 | a0001c0001t0001g0009 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1262+3601A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14577273 | |||||||
| chr16:14577396 | C | T | 1 | a0001c0001t0002g0060 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1262+3478G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14577396 | |||||||
| chr16:14577419 | C | T | 1 | a0001c0001t0002g0037 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1262+3455G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14577419 | |||||||
| chr16:14577459 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1262+3415C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14577459 | |||||||
| chr16:14577652 | T | C | 26 | a0001c0001t0003g0004 a0001c0001t0003g0097 a0001c0001t0003g0099 others(23): Show |
26 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.1262+3222A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14577652 | |||||||
| chr16:14577728 | C | T | 1 | a0001c0001t0005g0141 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1262+3146G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14577728 | |||||||
| chr16:14577823 | A | G | 1 | a0001c0001t0004g0038 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1262+3051T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14577823 | |||||||
| chr16:14578200 | G | A | 1 | a0001c0002t0004g0148 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1262+2674C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14578200 | |||||||
| chr16:14578203 | C | T | 1 | a0001c0001t0001g0009 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1262+2671G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14578203 | |||||||
| chr16:14578319 | ACT | A | 33 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(30): Show |
33 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.1262+2553_1262+255 others(6): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14578319 | |||||||
| chr16:14578331 | C | CAA | 24 | a0001c0001t0001g0009 a0001c0001t0002g0037 a0001c0001t0003g0004 others(21): Show |
24 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.1262+2541_1262+254 others(6): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14578331 | |||||||
| chr16:14578331 | C | CAAA | 5 | a0001c0001t0003g0097 a0001c0001t0003g0113 a0001c0001t0003g0115 others(2): Show |
5 | HG01346.hp2 HG03017.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1262+2540_1262+254 others(7): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14578331 | |||||||
| chr16:14578394 | T | C | 30 | a0001c0001t0001g0009 a0001c0001t0003g0004 a0001c0001t0003g0097 others(27): Show |
30 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.1262+2480A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14578394 | |||||||
| chr16:14578426 | G | C | 3 | a0001c0001t0006g0163 a0001c0001t0006g0164 a0001c0001t0006g0165 |
3 | HG01891.hp1 HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1262+2448C>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14578426 | |||||||
| chr16:14578453 | G | A | 38 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0084 others(35): Show |
38 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.1262+2421C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14578453 | |||||||
| chr16:14578630 | T | C | 27 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0047 others(24): Show |
27 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.1262+2244A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14578630 | |||||||
| chr16:14579112 | G | A | 1 | a0001c0001t0005g0156 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1262+1762C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14579112 | |||||||
| chr16:14579628 | G | C | 4 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(1): Show |
4 | HG01891.hp1 HG02922.hp2 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.1262+1246C>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14579628 | |||||||
| chr16:14579723 | C | G | 1 | a0001c0001t0005g0054 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1262+1151G>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14579723 | |||||||
| chr16:14579959 | G | C | 4 | a0001c0001t0001g0028 a0001c0001t0002g0018 a0001c0001t0003g0017 others(1): Show |
4 | HG01106.hp2 HG01361.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.1262+915C>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14579959 | |||||||
| chr16:14579982 | CA | C | 29 | a0001c0001t0001g0009 a0001c0001t0003g0004 a0001c0001t0003g0097 others(26): Show |
29 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.1262+891delT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14579982 | |||||||
| chr16:14580160 | T | C | 22 | a0001c0001t0003g0004 a0001c0001t0003g0097 a0001c0001t0003g0099 others(19): Show |
22 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.1262+714A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14580160 | |||||||
| chr16:14580347 | G | A | 25 | a0001c0001t0003g0004 a0001c0001t0003g0097 a0001c0001t0003g0099 others(22): Show |
25 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.1262+527C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14580347 | |||||||
| chr16:14580476 | C | T | 1 | a0001c0001t0005g0141 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1262+398G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14580476 | |||||||
| chr16:14580485 | T | C | 29 | a0001c0001t0001g0009 a0001c0001t0003g0004 a0001c0001t0003g0097 others(26): Show |
29 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.1262+389A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14580485 | |||||||
| chr16:14580502 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1262+372C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14580502 | |||||||
| chr16:14580507 | G | A | 1 | a0001c0001t0015g0110 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1262+367C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 18/23 | chr16 | 14580507 | |||||||
| chr16:14581327 | C | A | 3 | a0001c0001t0006g0163 a0001c0001t0006g0164 a0001c0001t0006g0165 |
3 | HG01891.hp1 HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1193-384G>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 17/23 | chr16 | 14581327 | |||||||
| chr16:14581917 | G | A | 5 | a0001c0001t0001g0024 a0001c0001t0001g0030 a0001c0001t0001g0057 others(2): Show |
5 | HG02622.hp2 HG02717.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1192+264C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 17/23 | chr16 | 14581917 | |||||||
| chr16:14582086 | C | G | 30 | a0001c0001t0001g0009 a0001c0001t0003g0004 a0001c0001t0003g0097 others(27): Show |
30 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.1192+95G>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 17/23 | chr16 | 14582086 | |||||||
| chr16:14582508 | T | G | 5 | a0001c0001t0003g0115 a0001c0001t0003g0126 a0001c0001t0003g0128 others(2): Show |
5 | HG02145.hp2 HG03098.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1082-217A>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 16/23 | chr16 | 14582508 | |||||||
| chr16:14582723 | G | A | 1 | a0001c0001t0004g0092 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1082-432C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 16/23 | chr16 | 14582723 | |||||||
| chr16:14582732 | T | A | 1 | a0001c0001t0004g0154 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1082-441A>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 16/23 | chr16 | 14582732 | |||||||
| chr16:14582919 | A | G | 3 | a0001c0001t0001g0050 a0001c0001t0005g0025 a0001c0001t0007g0053 |
3 | HG00099.hp1 HG01192.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1082-628T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 16/23 | chr16 | 14582919 | |||||||
| chr16:14583060 | C | T | 1 | a0001c0001t0002g0041 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1082-769G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 16/23 | chr16 | 14583060 | |||||||
| chr16:14583113 | C | A | 1 | a0001c0001t0002g0118 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1082-822G>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 16/23 | chr16 | 14583113 | |||||||
| chr16:14583273 | C | T | 1 | a0001c0001t0012g0034 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1082-982G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 16/23 | chr16 | 14583273 | |||||||
| chr16:14583505 | C | T | 1 | a0001c0001t0002g0060 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1081+842G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 16/23 | chr16 | 14583505 | |||||||
| chr16:14583720 | C | T | 8 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(5): Show |
8 | HG01891.hp1 HG02615.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1081+627G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 16/23 | chr16 | 14583720 | |||||||
| chr16:14583821 | C | A | 2 | a0001c0001t0003g0101 a0001c0001t0003g0113 |
2 | HG01346.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1081+526G>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 16/23 | chr16 | 14583821 | |||||||
| chr16:14583827 | G | T | 1 | a0001c0001t0004g0039 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1081+520C>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 16/23 | chr16 | 14583827 | |||||||
| chr16:14584300 | A | G | 1 | a0001c0001t0004g0062 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1081+47T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 16/23 | chr16 | 14584300 | |||||||
| chr16:14584492 | A | AC | 40 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0050 others(37): Show |
40 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.1006-71dupG | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 15/23 | chr16 | 14584492 | |||||||
| chr16:14584931 | TA | T | 4 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(1): Show |
4 | HG01891.hp1 HG02922.hp2 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.963-141delT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 14/23 | chr16 | 14584931 | |||||||
| chr16:14585170 | C | G | 4 | a0001c0001t0001g0028 a0001c0001t0002g0018 a0001c0001t0003g0017 others(1): Show |
4 | HG01106.hp2 HG01361.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.963-379G>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 14/23 | chr16 | 14585170 | |||||||
| chr16:14585364 | GT | G | 82 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0028 others(79): Show |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.963-574delA | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 14/23 | chr16 | 14585364 | |||||||
| chr16:14585370 | T | G | 1 | a0001c0001t0001g0009 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.963-579A>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 14/23 | chr16 | 14585370 | |||||||
| chr16:14585374 | T | G | 1 | a0001c0001t0003g0101 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.963-583A>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 14/23 | chr16 | 14585374 | |||||||
| chr16:14585375 | T | G | 5 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0016 others(2): Show |
5 | HG02132.hp1 NA18973.hp2 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.963-584A>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 14/23 | chr16 | 14585375 | |||||||
| chr16:14585501 | G | A | 1 | a0001c0001t0002g0060 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.963-710C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 14/23 | chr16 | 14585501 | |||||||
| chr16:14585509 | C | G | 2 | a0001c0001t0002g0019 a0001c0001t0008g0020 |
2 | HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.963-718G>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 14/23 | chr16 | 14585509 | |||||||
| chr16:14585510 | C | A | 2 | a0001c0001t0002g0019 a0001c0001t0008g0020 |
2 | HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.963-719G>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 14/23 | chr16 | 14585510 | |||||||
| chr16:14585511 | A | C | 2 | a0001c0001t0002g0019 a0001c0001t0008g0020 |
2 | HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.963-720T>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 14/23 | chr16 | 14585511 | |||||||
| chr16:14585512 | C | CTATGATG | 2 | a0001c0001t0002g0019 a0001c0001t0008g0020 |
2 | HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.963-722_963-721ins others(7): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 14/23 | chr16 | 14585512 | |||||||
| chr16:14585976 | G | A | 16 | a0001c0001t0003g0004 a0001c0001t0003g0097 a0001c0001t0003g0099 others(13): Show |
16 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.962+342C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 14/23 | chr16 | 14585976 | |||||||
| chr16:14585980 | C | CT | 6 | a0001c0001t0001g0024 a0001c0001t0001g0030 a0001c0001t0001g0057 others(3): Show |
6 | HG02056.hp1 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.962+337dupA | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 14/23 | chr16 | 14585980 | |||||||
| chr16:14586032 | G | C | 2 | a0001c0001t0006g0164 a0001c0001t0006g0165 |
2 | HG01891.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.962+286C>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 14/23 | chr16 | 14586032 | |||||||
| chr16:14586828 | A | G | 1 | a0001c0001t0005g0075 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.919-467T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 13/23 | chr16 | 14586828 | |||||||
| chr16:14586854 | A | T | 4 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(1): Show |
4 | HG01891.hp1 HG02922.hp2 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.919-493T>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 13/23 | chr16 | 14586854 | |||||||
| chr16:14587405 | A | C | 1 | a0001c0001t0007g0166 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.919-1044T>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 13/23 | chr16 | 14587405 | |||||||
| chr16:14587817 | T | C | 1 | a0001c0001t0002g0068 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.919-1456A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 13/23 | chr16 | 14587817 | |||||||
| chr16:14588153 | C | T | 1 | a0001c0001t0005g0045 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.919-1792G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 13/23 | chr16 | 14588153 | |||||||
| chr16:14588258 | C | CA | 2 | a0001c0001t0002g0019 a0001c0001t0008g0020 |
2 | HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.919-1898dupT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 13/23 | chr16 | 14588258 | |||||||
| chr16:14588408 | G | A | 5 | a0001c0001t0001g0143 a0001c0001t0001g0145 a0001c0001t0001g0147 others(2): Show |
5 | HG01884.hp1 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.919-2047C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 13/23 | chr16 | 14588408 | |||||||
| chr16:14588413 | G | T | 1 | a0001c0001t0001g0047 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.919-2052C>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 13/23 | chr16 | 14588413 | |||||||
| chr16:14588874 | C | A | 1 | a0001c0001t0003g0104 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.919-2513G>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 13/23 | chr16 | 14588874 | |||||||
| chr16:14588930 | A | T | 4 | a0001c0002t0003g0151 a0001c0002t0004g0148 a0001c0002t0006g0149 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.919-2569T>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 13/23 | chr16 | 14588930 | |||||||
| chr16:14589094 | C | T | 1 | a0001c0001t0007g0166 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.919-2733G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 13/23 | chr16 | 14589094 | |||||||
| chr16:14589105 | G | A | 1 | a0001c0001t0002g0111 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.919-2744C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 13/23 | chr16 | 14589105 | |||||||
| chr16:14589181 | A | AAAAT | 18 | a0001c0001t0001g0021 a0001c0001t0003g0004 a0001c0001t0003g0017 others(15): Show |
18 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.919-2824_919-2821d others(6): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 13/23 | chr16 | 14589181 | |||||||
| chr16:14589181 | A | AAAATAAA others(1): Show |
4 | a0001c0001t0003g0101 a0001c0001t0003g0102 a0001c0001t0003g0113 others(1): Show |
4 | HG01346.hp2 HG01433.hp1 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.919-2828_919-2821d others(10): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 13/23 | chr16 | 14589181 | |||||||
| chr16:14589436 | G | A | 1 | a0002c0005t0003g0125 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.919-3075C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 13/23 | chr16 | 14589436 | |||||||
| chr16:14589582 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.919-3221T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 13/23 | chr16 | 14589582 | |||||||
| chr16:14589628 | G | T | 2 | a0001c0001t0002g0068 a0001c0001t0002g0071 |
2 | HG02622.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.919-3267C>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 13/23 | chr16 | 14589628 | |||||||
| chr16:14589722 | C | T | 1 | a0001c0002t0003g0151 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.919-3361G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 13/23 | chr16 | 14589722 | |||||||
| chr16:14589781 | C | T | 17 | a0001c0001t0001g0028 a0001c0001t0001g0084 a0001c0001t0001g0088 others(14): Show |
17 | HG00323.hp1 HG00735.hp1 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.919-3420G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 13/23 | chr16 | 14589781 | |||||||
| chr16:14590234 | CA | C | 92 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0024 others(89): Show |
92 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.918+3066delT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 13/23 | chr16 | 14590234 | |||||||
| chr16:14590234 | CAA | C | 10 | a0001c0001t0001g0009 a0001c0001t0004g0027 a0001c0001t0004g0029 others(7): Show |
10 | HG00099.hp1 HG00099.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.918+3065_918+3066d others(4): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 13/23 | chr16 | 14590234 | |||||||
| chr16:14590234 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0003g0115 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.918+3056_918+3066d others(13): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 13/23 | chr16 | 14590234 | |||||||
| chr16:14590234 | CAAAAAAA others(5): Show |
C | 4 | a0001c0001t0003g0126 a0001c0001t0003g0128 a0001c0001t0007g0109 others(1): Show |
4 | HG02145.hp2 HG03130.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.918+3055_918+3066d others(14): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 13/23 | chr16 | 14590234 | |||||||
| chr16:14590386 | G | A | 1 | a0001c0001t0003g0097 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.918+2915C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 13/23 | chr16 | 14590386 | |||||||
| chr16:14590634 | CA | C | 7 | a0001c0001t0003g0017 a0001c0001t0003g0126 a0001c0001t0006g0163 others(4): Show |
7 | HG01515.hp2 HG01891.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.918+2666delT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 13/23 | chr16 | 14590634 | |||||||
| chr16:14590634 | CAA | C | 5 | a0001c0001t0001g0009 a0001c0002t0003g0151 a0001c0002t0004g0148 others(2): Show |
5 | HG02615.hp2 HG02886.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.918+2665_918+2666d others(4): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 13/23 | chr16 | 14590634 | |||||||
| chr16:14590653 | A | G | 1 | a0001c0001t0005g0075 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.918+2648T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 13/23 | chr16 | 14590653 | |||||||
| chr16:14590660 | C | T | 1 | a0001c0001t0006g0087 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.918+2641G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 13/23 | chr16 | 14590660 | |||||||
| chr16:14591390 | TA | T | 80 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(77): Show |
80 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.918+1910delT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 13/23 | chr16 | 14591390 | |||||||
| chr16:14592154 | T | C | 4 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(1): Show |
4 | HG01891.hp1 HG02922.hp2 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.918+1147A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 13/23 | chr16 | 14592154 | |||||||
| chr16:14592903 | T | C | 152 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0021 others(149): Show |
152 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.918+398A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 13/23 | chr16 | 14592903 | |||||||
| chr16:14593287 | A | G | 4 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(1): Show |
4 | HG01891.hp1 HG02922.hp2 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.918+14T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 13/23 | chr16 | 14593287 | |||||||
| chr16:14593490 | CT | C | 2 | a0001c0001t0006g0163 a0001c0001t0006g0165 |
2 | HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.841-113delA | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 12/23 | chr16 | 14593490 | |||||||
| chr16:14593492 | T | A | 1 | a0001c0001t0001g0009 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.841-114A>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 12/23 | chr16 | 14593492 | |||||||
| chr16:14593492 | T | TA | 88 | a0001c0001t0001g0015 a0001c0001t0001g0021 a0001c0001t0001g0022 others(85): Show |
88 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.841-115dupT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 12/23 | chr16 | 14593492 | |||||||
| chr16:14593492 | T | TAA | 34 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0030 others(31): Show |
34 | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(31): Show |
intron_variant | MODIFIER | c.841-116_841-115dup others(2): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 12/23 | chr16 | 14593492 | |||||||
| chr16:14593492 | T | TAAA | 8 | a0001c0001t0002g0060 a0001c0001t0002g0096 a0001c0001t0003g0101 others(5): Show |
8 | HG00741.hp1 HG01106.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.841-117_841-115dup others(3): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 12/23 | chr16 | 14593492 | |||||||
| chr16:14593492 | TAAAAAAA others(4): Show |
T | 2 | a0001c0001t0011g0090 a0001c0001t0011g0158 |
2 | HG02717.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.841-125_841-115del others(11): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 12/23 | chr16 | 14593492 | |||||||
| chr16:14593818 | G | A | 1 | a0001c0001t0006g0087 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.841-440C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 12/23 | chr16 | 14593818 | |||||||
| chr16:14593963 | C | T | 3 | a0001c0001t0006g0163 a0001c0001t0006g0164 a0001c0001t0006g0165 |
3 | HG01891.hp1 HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.841-585G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 12/23 | chr16 | 14593963 | |||||||
| chr16:14594272 | A | G | 4 | a0001c0002t0003g0151 a0001c0002t0004g0148 a0001c0002t0006g0149 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.841-894T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 12/23 | chr16 | 14594272 | |||||||
| chr16:14594347 | T | C | 1 | a0001c0001t0003g0004 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.841-969A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 12/23 | chr16 | 14594347 | |||||||
| chr16:14594504 | C | T | 1 | a0001c0001t0001g0009 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.841-1126G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 12/23 | chr16 | 14594504 | |||||||
| chr16:14594648 | G | A | 1 | a0001c0001t0004g0167 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.841-1270C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 12/23 | chr16 | 14594648 | |||||||
| chr16:14594736 | C | T | 17 | a0001c0001t0002g0153 a0001c0001t0004g0076 a0001c0001t0004g0154 others(14): Show |
17 | HG00438.hp1 HG00673.hp1 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.841-1358G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 12/23 | chr16 | 14594736 | |||||||
| chr16:14595143 | G | A | 1 | a0001c0001t0009g0049 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.841-1765C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 12/23 | chr16 | 14595143 | |||||||
| chr16:14595440 | A | G | 1 | a0001c0001t0002g0168 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.841-2062T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 12/23 | chr16 | 14595440 | |||||||
| chr16:14595840 | A | G | 5 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(2): Show |
5 | HG00639.hp2 HG01891.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.841-2462T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 12/23 | chr16 | 14595840 | |||||||
| chr16:14595984 | C | A | 1 | a0001c0001t0013g0056 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.841-2606G>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 12/23 | chr16 | 14595984 | |||||||
| chr16:14596155 | T | A | 5 | a0001c0001t0002g0026 a0001c0001t0004g0137 a0001c0001t0006g0040 others(2): Show |
5 | HG01175.hp1 NA18612.hp1 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.841-2777A>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 12/23 | chr16 | 14596155 | |||||||
| chr16:14596395 | A | T | 2 | a0001c0001t0005g0074 a0001c0001t0005g0120 |
2 | HG00438.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.841-3017T>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 12/23 | chr16 | 14596395 | |||||||
| chr16:14596505 | C | T | 3 | a0001c0001t0006g0163 a0001c0001t0006g0164 a0001c0001t0006g0165 |
3 | HG01891.hp1 HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.841-3127G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 12/23 | chr16 | 14596505 | |||||||
| chr16:14596581 | T | A | 2 | a0001c0001t0015g0110 a0001c0001t0018g0065 |
2 | HG03209.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.841-3203A>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 12/23 | chr16 | 14596581 | |||||||
| chr16:14596671 | G | A | 16 | a0001c0001t0003g0004 a0001c0001t0003g0097 a0001c0001t0003g0099 others(13): Show |
16 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.840+3233C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 12/23 | chr16 | 14596671 | |||||||
| chr16:14596805 | G | A | 2 | a0001c0001t0011g0090 a0001c0001t0011g0158 |
2 | HG02717.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.840+3099C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 12/23 | chr16 | 14596805 | |||||||
| chr16:14596839 | T | G | 1 | a0001c0001t0005g0083 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.840+3065A>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 12/23 | chr16 | 14596839 | |||||||
| chr16:14596936 | G | A | 1 | a0001c0001t0021g0117 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.840+2968C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 12/23 | chr16 | 14596936 | |||||||
| chr16:14596944 | G | A | 1 | a0001c0001t0003g0104 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.840+2960C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 12/23 | chr16 | 14596944 | |||||||
| chr16:14597030 | G | A | 2 | a0001c0001t0006g0164 a0001c0001t0006g0165 |
2 | HG01891.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.840+2874C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 12/23 | chr16 | 14597030 | |||||||
| chr16:14597295 | T | C | 2 | a0001c0001t0007g0066 a0001c0001t0007g0123 |
2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.840+2609A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 12/23 | chr16 | 14597295 | |||||||
| chr16:14597385 | C | G | 4 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(1): Show |
4 | HG01891.hp1 HG02922.hp2 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.840+2519G>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 12/23 | chr16 | 14597385 | |||||||
| chr16:14597413 | C | T | 4 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(1): Show |
4 | HG01891.hp1 HG02922.hp2 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.840+2491G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 12/23 | chr16 | 14597413 | |||||||
| chr16:14597524 | G | A | 1 | a0001c0001t0002g0026 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.840+2380C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 12/23 | chr16 | 14597524 | |||||||
| chr16:14597713 | T | G | 5 | a0001c0001t0001g0024 a0001c0001t0001g0030 a0001c0001t0001g0057 others(2): Show |
5 | HG02622.hp2 HG02717.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.840+2191A>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 12/23 | chr16 | 14597713 | |||||||
| chr16:14597719 | G | A | 1 | a0001c0001t0006g0012 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.840+2185C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 12/23 | chr16 | 14597719 | |||||||
| chr16:14597731 | C | T | 1 | a0001c0001t0004g0006 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.840+2173G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 12/23 | chr16 | 14597731 | |||||||
| chr16:14597866 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.840+2038C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 12/23 | chr16 | 14597866 | |||||||
| chr16:14597914 | A | G | 8 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(5): Show |
8 | HG01891.hp1 HG02615.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.840+1990T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 12/23 | chr16 | 14597914 | |||||||
| chr16:14598147 | AAT | A | 4 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(1): Show |
4 | HG01891.hp1 HG02922.hp2 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.840+1755_840+1756d others(4): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 12/23 | chr16 | 14598147 | |||||||
| chr16:14598149 | T | A | 4 | a0001c0002t0003g0151 a0001c0002t0004g0148 a0001c0002t0006g0149 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.840+1755A>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 12/23 | chr16 | 14598149 | |||||||
| chr16:14598398 | G | C | 4 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(1): Show |
4 | HG01891.hp1 HG02922.hp2 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.840+1506C>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 12/23 | chr16 | 14598398 | |||||||
| chr16:14598434 | G | A | 1 | a0001c0001t0002g0036 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.840+1470C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 12/23 | chr16 | 14598434 | |||||||
| chr16:14599003 | G | T | 3 | a0001c0001t0001g0015 a0001c0001t0001g0073 a0001c0001t0005g0138 |
3 | HG03834.hp2 NA19066.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.840+901C>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 12/23 | chr16 | 14599003 | |||||||
| chr16:14599037 | C | CT | 49 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0028 others(46): Show |
49 | HG00280.hp1 HG00639.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.840+866dupA | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 12/23 | chr16 | 14599037 | |||||||
| chr16:14599037 | C | CTT | 6 | a0001c0001t0001g0009 a0001c0001t0003g0101 a0001c0001t0003g0113 others(3): Show |
6 | HG01106.hp1 HG01346.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.840+865_840+866dup others(2): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 12/23 | chr16 | 14599037 | |||||||
| chr16:14599037 | CT | C | 31 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0047 others(28): Show |
31 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.840+866delA | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 12/23 | chr16 | 14599037 | |||||||
| chr16:14599087 | G | T | 4 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(1): Show |
4 | HG01891.hp1 HG02922.hp2 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.840+817C>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 12/23 | chr16 | 14599087 | |||||||
| chr16:14599186 | G | A | 3 | a0001c0001t0006g0163 a0001c0001t0006g0164 a0001c0001t0006g0165 |
3 | HG01891.hp1 HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.840+718C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 12/23 | chr16 | 14599186 | |||||||
| chr16:14599736 | T | C | 1 | a0001c0001t0002g0133 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.840+168A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 12/23 | chr16 | 14599736 | |||||||
| chr16:14599898 | A | G | 1 | a0001c0001t0001g0009 | 1 | NA19090.hp1 | splice_region_variant&intron_variant | LOW | c.840+6T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 12/23 | chr16 | 14599898 | |||||||
| chr16:14600072 | T | C | 1 | a0001c0001t0008g0155 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.784-112A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 11/23 | chr16 | 14600072 | |||||||
| chr16:14600129 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.784-169G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 11/23 | chr16 | 14600129 | |||||||
| chr16:14600250 | A | G | 5 | a0001c0001t0003g0115 a0001c0001t0003g0126 a0001c0001t0003g0128 others(2): Show |
5 | HG02145.hp2 HG03098.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.784-290T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 11/23 | chr16 | 14600250 | |||||||
| chr16:14600385 | T | C | 4 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(1): Show |
4 | HG01891.hp1 HG02922.hp2 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.784-425A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 11/23 | chr16 | 14600385 | |||||||
| chr16:14600544 | C | T | 3 | a0001c0001t0006g0163 a0001c0001t0006g0164 a0001c0001t0006g0165 |
3 | HG01891.hp1 HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.784-584G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 11/23 | chr16 | 14600544 | |||||||
| chr16:14600624 | C | T | 4 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(1): Show |
4 | HG01891.hp1 HG02922.hp2 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.784-664G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 11/23 | chr16 | 14600624 | |||||||
| chr16:14600790 | C | T | 8 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(5): Show |
8 | HG01891.hp1 HG02615.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.784-830G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 11/23 | chr16 | 14600790 | |||||||
| chr16:14600989 | G | C | 1 | a0001c0001t0005g0014 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.784-1029C>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 11/23 | chr16 | 14600989 | |||||||
| chr16:14601449 | G | A | 4 | a0001c0002t0003g0151 a0001c0002t0004g0148 a0001c0002t0006g0149 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.784-1489C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 11/23 | chr16 | 14601449 | |||||||
| chr16:14601744 | G | A | 3 | a0001c0001t0004g0137 a0001c0001t0006g0040 a0001c0001t0007g0010 |
3 | NA18959.hp2 NA18973.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.784-1784C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 11/23 | chr16 | 14601744 | |||||||
| chr16:14601968 | T | C | 1 | a0001c0001t0001g0028 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.784-2008A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 11/23 | chr16 | 14601968 | |||||||
| chr16:14602017 | G | A | 1 | a0001c0001t0012g0034 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.784-2057C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 11/23 | chr16 | 14602017 | |||||||
| chr16:14602124 | G | A | 1 | a0001c0001t0003g0004 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.783+2022C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 11/23 | chr16 | 14602124 | |||||||
| chr16:14602285 | G | A | 1 | a0001c0001t0009g0081 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.783+1861C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 11/23 | chr16 | 14602285 | |||||||
| chr16:14602385 | G | T | 1 | a0001c0001t0001g0121 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.783+1761C>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 11/23 | chr16 | 14602385 | |||||||
| chr16:14602491 | G | A | 2 | a0001c0001t0001g0021 a0001c0001t0008g0129 |
2 | NA18966.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.783+1655C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 11/23 | chr16 | 14602491 | |||||||
| chr16:14602714 | T | C | 4 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(1): Show |
4 | HG01891.hp1 HG02922.hp2 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.783+1432A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 11/23 | chr16 | 14602714 | |||||||
| chr16:14602776 | T | C | 1 | a0001c0001t0011g0158 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.783+1370A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 11/23 | chr16 | 14602776 | |||||||
| chr16:14602803 | G | A | 3 | a0001c0001t0006g0163 a0001c0001t0006g0164 a0001c0001t0006g0165 |
3 | HG01891.hp1 HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.783+1343C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 11/23 | chr16 | 14602803 | |||||||
| chr16:14602905 | C | T | 1 | a0001c0001t0003g0128 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.783+1241G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 11/23 | chr16 | 14602905 | |||||||
| chr16:14603013 | C | T | 1 | a0001c0001t0002g0118 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.783+1133G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 11/23 | chr16 | 14603013 | |||||||
| chr16:14603192 | T | A | 1 | a0001c0001t0002g0093 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.783+954A>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 11/23 | chr16 | 14603192 | |||||||
| chr16:14603331 | T | C | 1 | a0001c0002t0004g0148 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.783+815A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 11/23 | chr16 | 14603331 | |||||||
| chr16:14603442 | T | C | 7 | a0001c0001t0006g0163 a0001c0001t0006g0164 a0001c0001t0006g0165 others(4): Show |
7 | HG01891.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.783+704A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 11/23 | chr16 | 14603442 | |||||||
| chr16:14603500 | C | T | 16 | a0001c0001t0003g0004 a0001c0001t0003g0097 a0001c0001t0003g0099 others(13): Show |
16 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.783+646G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 11/23 | chr16 | 14603500 | |||||||
| chr16:14603595 | A | G | 1 | a0001c0001t0004g0038 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.783+551T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 11/23 | chr16 | 14603595 | |||||||
| chr16:14603636 | C | T | 1 | a0001c0001t0003g0004 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.783+510G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 11/23 | chr16 | 14603636 | |||||||
| chr16:14603841 | G | A | 34 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(31): Show |
34 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.783+305C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 11/23 | chr16 | 14603841 | |||||||
| chr16:14604386 | G | A | 4 | a0001c0002t0003g0151 a0001c0002t0004g0148 a0001c0002t0006g0149 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.703-160C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 10/23 | chr16 | 14604386 | |||||||
| chr16:14604434 | T | C | 4 | a0001c0002t0003g0151 a0001c0002t0004g0148 a0001c0002t0006g0149 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.703-208A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 10/23 | chr16 | 14604434 | |||||||
| chr16:14604442 | G | C | 2 | a0001c0001t0002g0036 a0001c0001t0005g0035 |
2 | HG02683.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.703-216C>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 10/23 | chr16 | 14604442 | |||||||
| chr16:14604449 | C | T | 4 | a0001c0002t0003g0151 a0001c0002t0004g0148 a0001c0002t0006g0149 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.703-223G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 10/23 | chr16 | 14604449 | |||||||
| chr16:14604615 | T | C | 5 | a0001c0001t0001g0009 a0001c0001t0003g0104 a0001c0001t0006g0163 others(2): Show |
5 | HG01168.hp1 HG01891.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.703-389A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 10/23 | chr16 | 14604615 | |||||||
| chr16:14604629 | T | C | 38 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0084 others(35): Show |
38 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.703-403A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 10/23 | chr16 | 14604629 | |||||||
| chr16:14604848 | T | C | 1 | a0001c0001t0003g0017 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.703-622A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 10/23 | chr16 | 14604848 | |||||||
| chr16:14605020 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.703-794C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 10/23 | chr16 | 14605020 | |||||||
| chr16:14605328 | T | C | 3 | a0001c0001t0001g0050 a0001c0001t0005g0025 a0001c0001t0007g0053 |
3 | HG00099.hp1 HG01192.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.703-1102A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 10/23 | chr16 | 14605328 | |||||||
| chr16:14605496 | A | G | 5 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0016 others(2): Show |
5 | HG02132.hp1 NA18973.hp2 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.702+988T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 10/23 | chr16 | 14605496 | |||||||
| chr16:14605528 | A | ATATGT | 8 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(5): Show |
8 | HG01891.hp1 HG02615.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.702+955_702+956ins others(5): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 10/23 | chr16 | 14605528 | |||||||
| chr16:14605822 | T | G | 4 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(1): Show |
4 | HG01891.hp1 HG02922.hp2 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.702+662A>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 10/23 | chr16 | 14605822 | |||||||
| chr16:14605827 | T | C | 1 | a0001c0001t0002g0132 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.702+657A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 10/23 | chr16 | 14605827 | |||||||
| chr16:14606030 | G | A | 4 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(1): Show |
4 | HG01891.hp1 HG02922.hp2 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.702+454C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 10/23 | chr16 | 14606030 | |||||||
| chr16:14606166 | G | A | 36 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0084 others(33): Show |
36 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.702+318C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 10/23 | chr16 | 14606166 | |||||||
| chr16:14606397 | G | A | 167 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0015 others(164): Show |
167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.702+87C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 10/23 | chr16 | 14606397 | |||||||
| chr16:14606781 | A | AT | 6 | a0001c0001t0001g0134 a0001c0001t0002g0041 a0001c0001t0002g0042 others(3): Show |
6 | HG00597.hp2 HG01175.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.660-256dupA | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 9/23 | chr16 | 14606781 | |||||||
| chr16:14606972 | G | A | 1 | a0001c0001t0003g0017 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.660-446C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 9/23 | chr16 | 14606972 | |||||||
| chr16:14607068 | A | G | 1 | a0001c0002t0004g0148 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.660-542T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 9/23 | chr16 | 14607068 | |||||||
| chr16:14607178 | A | G | 5 | a0001c0001t0001g0143 a0001c0001t0001g0145 a0001c0001t0001g0147 others(2): Show |
5 | HG01884.hp1 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.660-652T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 9/23 | chr16 | 14607178 | |||||||
| chr16:14607483 | C | A | 3 | a0001c0001t0006g0163 a0001c0001t0006g0164 a0001c0001t0006g0165 |
3 | HG01891.hp1 HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.659+798G>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 9/23 | chr16 | 14607483 | |||||||
| chr16:14608490 | C | A | 2 | a0001c0001t0011g0090 a0001c0001t0011g0158 |
2 | HG02717.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.621-171G>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 8/23 | chr16 | 14608490 | |||||||
| chr16:14608572 | T | C | 1 | a0001c0001t0007g0053 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.621-253A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 8/23 | chr16 | 14608572 | |||||||
| chr16:14608941 | T | C | 1 | a0001c0001t0010g0103 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.620+117A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 8/23 | chr16 | 14608941 | |||||||
| chr16:14609548 | G | C | 1 | a0001c0001t0005g0120 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.555-425C>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 7/23 | chr16 | 14609548 | |||||||
| chr16:14609669 | C | T | 1 | a0001c0001t0009g0081 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.555-546G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 7/23 | chr16 | 14609669 | |||||||
| chr16:14609816 | C | A | 4 | a0001c0001t0001g0134 a0001c0001t0002g0041 a0001c0001t0002g0042 others(1): Show |
4 | HG01192.hp1 HG01255.hp2 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.555-693G>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 7/23 | chr16 | 14609816 | |||||||
| chr16:14609949 | C | T | 1 | a0001c0001t0008g0129 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.554+695G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 7/23 | chr16 | 14609949 | |||||||
| chr16:14610079 | G | A | 2 | a0001c0001t0011g0090 a0001c0001t0011g0158 |
2 | HG02717.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.554+565C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 7/23 | chr16 | 14610079 | |||||||
| chr16:14610082 | G | A | 3 | a0001c0001t0006g0163 a0001c0001t0006g0164 a0001c0001t0006g0165 |
3 | HG01891.hp1 HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.554+562C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 7/23 | chr16 | 14610082 | |||||||
| chr16:14610141 | C | A | 1 | a0001c0002t0006g0150 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.554+503G>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 7/23 | chr16 | 14610141 | |||||||
| chr16:14610244 | G | A | 1 | a0001c0001t0002g0118 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.554+400C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 7/23 | chr16 | 14610244 | |||||||
| chr16:14610265 | G | A | 16 | a0001c0001t0003g0004 a0001c0001t0003g0097 a0001c0001t0003g0099 others(13): Show |
16 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.554+379C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 7/23 | chr16 | 14610265 | |||||||
| chr16:14610434 | A | G | 1 | a0001c0001t0002g0132 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.554+210T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 7/23 | chr16 | 14610434 | |||||||
| chr16:14610470 | C | CA | 17 | a0001c0001t0003g0097 a0001c0001t0003g0099 a0001c0001t0003g0101 others(14): Show |
17 | HG01106.hp1 HG01168.hp1 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.554+173dupT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 7/23 | chr16 | 14610470 | |||||||
| chr16:14610504 | T | C | 1 | a0001c0002t0003g0151 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.554+140A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 7/23 | chr16 | 14610504 | |||||||
| chr16:14610977 | CCATT | C | 5 | a0001c0001t0006g0012 a0001c0001t0006g0013 a0001c0001t0006g0016 others(2): Show |
5 | HG02132.hp1 NA18973.hp2 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.389-172_389-169del others(4): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 6/23 | chr16 | 14610977 | |||||||
| chr16:14611144 | G | C | 37 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0084 others(34): Show |
37 | HG00099.hp2 HG00323.hp1 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.389-335C>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 6/23 | chr16 | 14611144 | |||||||
| chr16:14611216 | C | T | 2 | a0001c0001t0006g0164 a0001c0001t0006g0165 |
2 | HG01891.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.389-407G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 6/23 | chr16 | 14611216 | |||||||
| chr16:14611354 | T | C | 1 | a0001c0001t0003g0104 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.389-545A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 6/23 | chr16 | 14611354 | |||||||
| chr16:14611842 | G | A | 3 | a0001c0001t0006g0163 a0001c0001t0006g0164 a0001c0001t0006g0165 |
3 | HG01891.hp1 HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.389-1033C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 6/23 | chr16 | 14611842 | |||||||
| chr16:14612050 | G | A | 4 | a0001c0002t0003g0151 a0001c0002t0004g0148 a0001c0002t0006g0149 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.389-1241C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 6/23 | chr16 | 14612050 | |||||||
| chr16:14612388 | G | T | 1 | a0004c0004t0002g0130 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.389-1579C>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 6/23 | chr16 | 14612388 | |||||||
| chr16:14612546 | C | T | 3 | a0001c0001t0006g0163 a0001c0001t0006g0164 a0001c0001t0006g0165 |
3 | HG01891.hp1 HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.389-1737G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 6/23 | chr16 | 14612546 | |||||||
| chr16:14612742 | C | T | 2 | a0001c0001t0006g0164 a0001c0001t0006g0165 |
2 | HG01891.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.389-1933G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 6/23 | chr16 | 14612742 | |||||||
| chr16:14612875 | G | A | 2 | a0001c0001t0011g0090 a0001c0001t0011g0158 |
2 | HG02717.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.389-2066C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 6/23 | chr16 | 14612875 | |||||||
| chr16:14613031 | G | A | 6 | a0001c0001t0002g0153 a0001c0001t0004g0154 a0001c0001t0004g0167 others(3): Show |
6 | HG01257.hp1 HG02056.hp2 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.389-2222C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 6/23 | chr16 | 14613031 | |||||||
| chr16:14613035 | C | T | 4 | a0001c0002t0003g0151 a0001c0002t0004g0148 a0001c0002t0006g0149 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.389-2226G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 6/23 | chr16 | 14613035 | |||||||
| chr16:14613326 | C | A | 7 | a0001c0001t0006g0163 a0001c0001t0006g0164 a0001c0001t0006g0165 others(4): Show |
7 | HG01891.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.389-2517G>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 6/23 | chr16 | 14613326 | |||||||
| chr16:14613490 | C | G | 108 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0021 others(105): Show |
108 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.389-2681G>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 6/23 | chr16 | 14613490 | |||||||
| chr16:14613495 | C | T | 1 | a0001c0001t0003g0017 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.389-2686G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 6/23 | chr16 | 14613495 | |||||||
| chr16:14613712 | C | T | 1 | a0001c0001t0001g0009 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.389-2903G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 6/23 | chr16 | 14613712 | |||||||
| chr16:14613903 | T | C | 1 | a0001c0001t0007g0127 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.389-3094A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 6/23 | chr16 | 14613903 | |||||||
| chr16:14613909 | C | G | 2 | a0001c0001t0007g0002 a0001c0001t0007g0003 |
2 | HG01496.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.389-3100G>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 6/23 | chr16 | 14613909 | |||||||
| chr16:14614117 | C | T | 1 | a0001c0002t0004g0148 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.389-3308G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 6/23 | chr16 | 14614117 | |||||||
| chr16:14614154 | G | T | 1 | a0001c0001t0003g0044 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.389-3345C>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 6/23 | chr16 | 14614154 | |||||||
| chr16:14614174 | T | C | 5 | a0001c0001t0001g0143 a0001c0001t0001g0145 a0001c0001t0001g0147 others(2): Show |
5 | HG01884.hp1 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.389-3365A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 6/23 | chr16 | 14614174 | |||||||
| chr16:14614434 | G | A | 2 | a0001c0001t0002g0019 a0001c0001t0008g0020 |
2 | HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.388+3156C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 6/23 | chr16 | 14614434 | |||||||
| chr16:14614668 | T | G | 39 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0028 others(36): Show |
39 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.388+2922A>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 6/23 | chr16 | 14614668 | |||||||
| chr16:14614731 | C | T | 2 | a0001c0001t0001g0119 a0001c0001t0004g0067 |
2 | HG01175.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.388+2859G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 6/23 | chr16 | 14614731 | |||||||
| chr16:14614846 | C | CA | 8 | a0001c0001t0001g0121 a0001c0001t0003g0097 a0001c0001t0003g0100 others(5): Show |
8 | HG01106.hp1 HG01346.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.388+2743dupT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 6/23 | chr16 | 14614846 | |||||||
| chr16:14614846 | CA | C | 42 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0021 others(39): Show |
42 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(39): Show |
intron_variant | MODIFIER | c.388+2743delT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 6/23 | chr16 | 14614846 | |||||||
| chr16:14614846 | CAA | C | 74 | a0001c0001t0001g0009 a0001c0001t0001g0022 a0001c0001t0001g0024 others(71): Show |
74 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.388+2742_388+2743d others(4): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 6/23 | chr16 | 14614846 | |||||||
| chr16:14614846 | CAAA | C | 6 | a0001c0001t0002g0019 a0001c0001t0003g0017 a0001c0001t0004g0029 others(3): Show |
6 | HG01515.hp2 HG02809.hp1 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.388+2741_388+2743d others(5): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 6/23 | chr16 | 14614846 | |||||||
| chr16:14614846 | CAAAAAAA others(8): Show |
C | 5 | a0001c0001t0001g0028 a0001c0002t0003g0151 a0001c0002t0004g0148 others(2): Show |
5 | HG01106.hp2 HG02615.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.388+2729_388+2743d others(17): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 6/23 | chr16 | 14614846 | |||||||
| chr16:14614846 | CAAAAAAA others(9): Show |
C | 2 | a0001c0001t0007g0002 a0001c0001t0007g0003 |
2 | HG01496.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.388+2728_388+2743d others(18): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 6/23 | chr16 | 14614846 | |||||||
| chr16:14614914 | G | A | 2 | a0001c0001t0006g0013 a0001c0001t0007g0142 |
2 | NA18979.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.388+2676C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 6/23 | chr16 | 14614914 | |||||||
| chr16:14615039 | G | A | 1 | a0001c0001t0007g0166 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.388+2551C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 6/23 | chr16 | 14615039 | |||||||
| chr16:14615051 | A | G | 2 | a0001c0001t0003g0099 a0001c0001t0003g0100 |
2 | HG01257.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.388+2539T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 6/23 | chr16 | 14615051 | |||||||
| chr16:14615303 | G | GA | 5 | a0001c0001t0002g0026 a0001c0001t0005g0140 a0001c0001t0006g0163 others(2): Show |
5 | HG01891.hp1 HG02027.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.388+2286dupT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 6/23 | chr16 | 14615303 | |||||||
| chr16:14616001 | T | G | 3 | a0001c0001t0006g0163 a0001c0001t0006g0164 a0001c0001t0006g0165 |
3 | HG01891.hp1 HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.388+1589A>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 6/23 | chr16 | 14616001 | |||||||
| chr16:14616097 | T | C | 17 | a0001c0001t0001g0084 a0001c0001t0001g0088 a0001c0001t0001g0108 others(14): Show |
17 | HG00323.hp1 HG00735.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.388+1493A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 6/23 | chr16 | 14616097 | |||||||
| chr16:14616331 | C | A | 1 | a0001c0001t0001g0147 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.388+1259G>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 6/23 | chr16 | 14616331 | |||||||
| chr16:14616346 | G | T | 3 | a0001c0001t0006g0163 a0001c0001t0006g0164 a0001c0001t0006g0165 |
3 | HG01891.hp1 HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.388+1244C>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 6/23 | chr16 | 14616346 | |||||||
| chr16:14616447 | T | C | 1 | a0001c0001t0004g0027 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.388+1143A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 6/23 | chr16 | 14616447 | |||||||
| chr16:14616565 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.388+1025C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 6/23 | chr16 | 14616565 | |||||||
| chr16:14616590 | G | A | 3 | a0001c0001t0006g0163 a0001c0001t0006g0164 a0001c0001t0006g0165 |
3 | HG01891.hp1 HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.388+1000C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 6/23 | chr16 | 14616590 | |||||||
| chr16:14616954 | C | T | 2 | a0001c0001t0003g0136 a0002c0005t0003g0125 |
2 | HG00741.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.388+636G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 6/23 | chr16 | 14616954 | |||||||
| chr16:14617076 | T | A | 16 | a0001c0001t0003g0099 a0001c0001t0003g0100 a0001c0001t0003g0101 others(13): Show |
16 | HG00280.hp1 HG00741.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.388+514A>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 6/23 | chr16 | 14617076 | |||||||
| chr16:14617076 | TA | T | 8 | a0001c0001t0001g0024 a0001c0001t0001g0059 a0001c0001t0002g0026 others(5): Show |
8 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(5): Show |
intron_variant | MODIFIER | c.388+513delT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 6/23 | chr16 | 14617076 | |||||||
| chr16:14617077 | A | T | 8 | a0001c0001t0004g0023 a0001c0001t0004g0135 a0001c0001t0006g0163 others(5): Show |
8 | HG01496.hp2 HG01891.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.388+513T>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 6/23 | chr16 | 14617077 | |||||||
| chr16:14617078 | A | T | 1 | a0001c0002t0006g0149 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.388+512T>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 6/23 | chr16 | 14617078 | |||||||
| chr16:14617124 | C | G | 1 | a0001c0001t0001g0021 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.388+466G>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 6/23 | chr16 | 14617124 | |||||||
| chr16:14617166 | C | T | 2 | a0001c0001t0001g0114 a0001c0001t0006g0058 |
2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.388+424G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 6/23 | chr16 | 14617166 | |||||||
| chr16:14617339 | A | G | 2 | a0001c0001t0008g0162 a0001c0001t0020g0161 |
2 | HG02165.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.388+251T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 6/23 | chr16 | 14617339 | |||||||
| chr16:14617371 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.388+219C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 6/23 | chr16 | 14617371 | |||||||
| chr16:14617382 | CA | C | 92 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0001c0001t0001g0030 others(89): Show |
92 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.388+207delT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 6/23 | chr16 | 14617382 | |||||||
| chr16:14617382 | CAA | C | 6 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0022 others(3): Show |
6 | HG00323.hp2 HG01891.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.388+206_388+207del others(2): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 6/23 | chr16 | 14617382 | |||||||
| chr16:14617441 | A | G | 2 | a0001c0001t0002g0019 a0001c0001t0008g0020 |
2 | HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.388+149T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 6/23 | chr16 | 14617441 | |||||||
| chr16:14617788 | A | G | 4 | a0001c0002t0003g0151 a0001c0002t0004g0148 a0001c0002t0006g0149 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-138T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14617788 | |||||||
| chr16:14618000 | T | C | 7 | a0001c0001t0006g0163 a0001c0001t0006g0164 a0001c0001t0006g0165 others(4): Show |
7 | HG01891.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.328-350A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14618000 | |||||||
| chr16:14618106 | G | C | 3 | a0001c0001t0006g0163 a0001c0001t0006g0164 a0001c0001t0006g0165 |
3 | HG01891.hp1 HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.328-456C>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14618106 | |||||||
| chr16:14618230 | G | C | 3 | a0001c0001t0006g0163 a0001c0001t0006g0164 a0001c0001t0006g0165 |
3 | HG01891.hp1 HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.328-580C>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14618230 | |||||||
| chr16:14618258 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.328-608G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14618258 | |||||||
| chr16:14618279 | A | G | 1 | a0001c0001t0002g0018 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.328-629T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14618279 | |||||||
| chr16:14618413 | G | A | 1 | a0001c0001t0002g0091 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.328-763C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14618413 | |||||||
| chr16:14618493 | C | CA | 5 | a0001c0001t0002g0091 a0001c0001t0005g0131 a0001c0001t0007g0123 others(2): Show |
5 | HG00438.hp2 HG02145.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.328-844dupT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14618493 | |||||||
| chr16:14618519 | G | A | 1 | a0001c0001t0002g0132 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.328-869C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14618519 | |||||||
| chr16:14618564 | G | A | 3 | a0001c0001t0006g0163 a0001c0001t0006g0164 a0001c0001t0006g0165 |
3 | HG01891.hp1 HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.328-914C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14618564 | |||||||
| chr16:14618656 | C | CA | 7 | a0001c0001t0001g0015 a0001c0001t0002g0093 a0001c0001t0004g0092 others(4): Show |
7 | HG00280.hp2 HG02615.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.328-1007dupT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14618656 | |||||||
| chr16:14618931 | C | G | 16 | a0001c0001t0003g0004 a0001c0001t0003g0097 a0001c0001t0003g0099 others(13): Show |
16 | HG00741.hp1 HG01081.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.328-1281G>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14618931 | |||||||
| chr16:14619113 | T | G | 3 | a0001c0002t0003g0151 a0001c0002t0006g0149 a0001c0002t0006g0150 |
3 | HG02615.hp2 HG02886.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.328-1463A>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14619113 | |||||||
| chr16:14619147 | G | A | 1 | a0001c0001t0004g0124 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.328-1497C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14619147 | |||||||
| chr16:14619309 | A | T | 3 | a0001c0001t0006g0163 a0001c0001t0006g0164 a0001c0001t0006g0165 |
3 | HG01891.hp1 HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.328-1659T>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14619309 | |||||||
| chr16:14619327 | T | C | 3 | a0001c0001t0002g0096 a0001c0001t0004g0095 a0001c0001t0007g0094 |
3 | HG03516.hp1 NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.328-1677A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14619327 | |||||||
| chr16:14619504 | C | A | 1 | a0001c0001t0007g0166 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.328-1854G>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14619504 | |||||||
| chr16:14619760 | C | G | 1 | a0001c0001t0004g0006 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.328-2110G>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14619760 | |||||||
| chr16:14620018 | C | T | 3 | a0001c0001t0006g0163 a0001c0001t0006g0164 a0001c0001t0006g0165 |
3 | HG01891.hp1 HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.328-2368G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14620018 | |||||||
| chr16:14620069 | C | CA | 41 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0108 others(38): Show |
41 | HG00639.hp2 HG00735.hp1 HG01106.hp1 others(38): Show |
intron_variant | MODIFIER | c.328-2420dupT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14620069 | |||||||
| chr16:14620069 | C | CAA | 5 | a0001c0001t0003g0004 a0001c0001t0003g0126 a0001c0001t0003g0128 others(2): Show |
5 | HG00741.hp1 HG01081.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.328-2421_328-2420d others(4): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14620069 | |||||||
| chr16:14620226 | A | C | 3 | a0001c0001t0006g0163 a0001c0001t0006g0164 a0001c0001t0006g0165 |
3 | HG01891.hp1 HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.328-2576T>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14620226 | |||||||
| chr16:14620287 | G | A | 1 | a0001c0001t0007g0127 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.328-2637C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14620287 | |||||||
| chr16:14620303 | G | A | 1 | a0001c0001t0006g0016 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.328-2653C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14620303 | |||||||
| chr16:14620579 | A | T | 1 | a0001c0001t0003g0017 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.328-2929T>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14620579 | |||||||
| chr16:14620792 | C | T | 1 | a0001c0001t0007g0166 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.328-3142G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14620792 | |||||||
| chr16:14620893 | G | A | 1 | a0001c0001t0003g0128 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.328-3243C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14620893 | |||||||
| chr16:14621285 | G | A | 1 | a0001c0001t0008g0129 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.328-3635C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14621285 | |||||||
| chr16:14621328 | T | C | 1 | a0004c0004t0002g0130 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.328-3678A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14621328 | |||||||
| chr16:14621467 | G | A | 1 | a0001c0001t0005g0131 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.328-3817C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14621467 | |||||||
| chr16:14621562 | G | A | 1 | a0001c0001t0002g0132 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.328-3912C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14621562 | |||||||
| chr16:14621806 | C | CA | 7 | a0001c0001t0001g0134 a0001c0001t0002g0133 a0001c0001t0003g0136 others(4): Show |
7 | HG01106.hp1 HG01255.hp1 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.328-4157dupT | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14621806 | |||||||
| chr16:14621979 | G | A | 4 | a0001c0002t0003g0151 a0001c0002t0004g0148 a0001c0002t0006g0149 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-4329C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14621979 | |||||||
| chr16:14622035 | A | G | 1 | a0001c0001t0006g0163 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.328-4385T>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14622035 | |||||||
| chr16:14622201 | TAAA | T | 7 | a0001c0001t0001g0015 a0001c0001t0005g0014 a0001c0001t0006g0012 others(4): Show |
7 | HG02132.hp1 HG02132.hp2 NA18973.hp2 others(4): Show |
intron_variant | MODIFIER | c.328-4554_328-4552d others(5): Show |
PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14622201 | |||||||
| chr16:14622433 | G | A | 1 | a0001c0001t0005g0138 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.327+4673C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14622433 | |||||||
| chr16:14622527 | C | T | 1 | a0001c0001t0006g0011 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.327+4579G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14622527 | |||||||
| chr16:14622557 | C | T | 1 | a0001c0002t0004g0148 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.327+4549G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14622557 | |||||||
| chr16:14622568 | G | C | 1 | a0001c0001t0001g0139 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.327+4538C>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14622568 | |||||||
| chr16:14622651 | C | T | 1 | a0001c0001t0001g0005 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.327+4455G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14622651 | |||||||
| chr16:14623066 | TG | T | 5 | a0001c0001t0001g0143 a0001c0001t0001g0145 a0001c0001t0001g0147 others(2): Show |
5 | HG01884.hp1 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.327+4039delC | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14623066 | |||||||
| chr16:14623138 | C | T | 3 | a0001c0001t0006g0163 a0001c0001t0006g0164 a0001c0001t0006g0165 |
3 | HG01891.hp1 HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.327+3968G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14623138 | |||||||
| chr16:14623446 | G | A | 1 | a0001c0001t0005g0140 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.327+3660C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14623446 | |||||||
| chr16:14624657 | G | A | 1 | a0001c0001t0005g0141 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.327+2449C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14624657 | |||||||
| chr16:14624773 | C | G | 1 | a0001c0001t0007g0142 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.327+2333G>C | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14624773 | |||||||
| chr16:14624884 | T | C | 1 | a0001c0001t0007g0142 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.327+2222A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14624884 | |||||||
| chr16:14624937 | C | T | 1 | a0001c0001t0007g0010 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.327+2169G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14624937 | |||||||
| chr16:14625208 | A | C | 4 | a0001c0001t0001g0009 a0001c0001t0006g0163 a0001c0001t0006g0164 others(1): Show |
4 | HG01891.hp1 HG02922.hp2 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+1898T>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14625208 | |||||||
| chr16:14625240 | G | A | 5 | a0001c0001t0001g0143 a0001c0001t0001g0145 a0001c0001t0001g0147 others(2): Show |
5 | HG01884.hp1 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.327+1866C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14625240 | |||||||
| chr16:14625296 | G | A | 4 | a0001c0002t0003g0151 a0001c0002t0004g0148 a0001c0002t0006g0149 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+1810C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14625296 | |||||||
| chr16:14625500 | G | A | 3 | a0001c0001t0006g0163 a0001c0001t0006g0164 a0001c0001t0006g0165 |
3 | HG01891.hp1 HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.327+1606C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14625500 | |||||||
| chr16:14625881 | G | A | 1 | a0001c0001t0006g0152 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.327+1225C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14625881 | |||||||
| chr16:14626596 | T | C | 6 | a0001c0001t0002g0153 a0001c0001t0004g0154 a0001c0001t0004g0167 others(3): Show |
6 | HG01257.hp1 HG02056.hp2 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.327+510A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14626596 | |||||||
| chr16:14626681 | G | A | 1 | a0001c0001t0011g0158 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.327+425C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14626681 | |||||||
| chr16:14626766 | C | T | 1 | a0001c0001t0007g0008 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.327+340G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 5/23 | chr16 | 14626766 | |||||||
| chr16:14628028 | A | C | 1 | a0001c0001t0003g0007 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.177+144T>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 3/23 | chr16 | 14628028 | |||||||
| chr16:14628273 | T | C | 1 | a0001c0001t0004g0159 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.98-22A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 2/23 | chr16 | 14628273 | |||||||
| chr16:14628345 | C | A | 1 | a0001c0001t0007g0160 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.98-94G>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 2/23 | chr16 | 14628345 | |||||||
| chr16:14628345 | C | T | 1 | a0001c0001t0004g0006 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.98-94G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 2/23 | chr16 | 14628345 | |||||||
| chr16:14628449 | G | A | 2 | a0001c0001t0008g0162 a0001c0001t0020g0161 |
2 | HG02165.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.98-198C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 2/23 | chr16 | 14628449 | |||||||
| chr16:14628562 | T | C | 3 | a0001c0001t0006g0163 a0001c0001t0006g0164 a0001c0001t0006g0165 |
3 | HG01891.hp1 HG02922.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.98-311A>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 2/23 | chr16 | 14628562 | |||||||
| chr16:14628912 | G | A | 1 | a0001c0001t0007g0166 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.98-661C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 2/23 | chr16 | 14628912 | |||||||
| chr16:14629051 | G | C | 1 | a0001c0001t0004g0167 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.97+546C>G | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 2/23 | chr16 | 14629051 | |||||||
| chr16:14629082 | C | T | 1 | a0001c0001t0001g0005 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.97+515G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 2/23 | chr16 | 14629082 | |||||||
| chr16:14629858 | G | T | 1 | a0001c0001t0003g0004 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.20-184C>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 1/23 | chr16 | 14629858 | |||||||
| chr16:14629861 | G | A | 1 | a0001c0001t0002g0168 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.20-187C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 1/23 | chr16 | 14629861 | |||||||
| chr16:14629927 | C | T | 2 | a0001c0001t0007g0002 a0001c0001t0007g0003 |
2 | HG01496.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.19+180G>A | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 1/23 | chr16 | 14629927 | |||||||
| chr16:14630015 | G | A | 1 | a0001c0001t0019g0169 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.19+92C>T | PARN | ENSG00000140694.18 | transcript | ENST00000437198.7 | protein_coding | 1/23 | chr16 | 14630015 |