Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 53373 |
| ensemblid | ENSG00000186815.13 |
| hgncid | 18182 |
| symbol | TPCN1 |
| name | two pore segment channel 1 |
| refseq_nuc | NM_017901.6 |
| refseq_prot | NP_060371.2 |
| ensembl_nuc | ENST00000335509.11 |
| ensembl_prot | ENSP00000335300.6 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 113221464 |
| end | 113298585 |
| strand | + |
| ver | v1.2 |
| region | chr12:113221464-113298585 |
| region5000 | chr12:113216464-113303585 |
| regionname0 | TPCN1_chr12_113221464_113298585 |
| regionname5000 | TPCN1_chr12_113216464_113303585 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 816 | 249 | 84 | 22 | 112 | 10 | 19 | 92 | TPCN1_chr12_113216464_113303585 | TPCN1 | MAVSL others(811): Show |
chr12 | 113216464 | 113303585 |
| a0002 | 0/0 | 816 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | MAVSS others(811): Show |
chr12 | 113216464 | 113303585 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2448 | 228 | 74 | 17 | 107 | 9 | 19 | TPCN1_chr12_113216464_113303585 | TPCN1 | ATGGC others(2443): Show |
chr12 | 113216464 | 113303585 | ||
| a0001c0002 | 0/0 | 2448 | 3 | 3 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | ATGGC others(2443): Show |
chr12 | 113216464 | 113303585 | ||
| a0001c0003 | 0/0 | 2448 | 3 | 1 | 1 | 0 | 1 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | ATGGC others(2443): Show |
chr12 | 113216464 | 113303585 | ||
| a0001c0004 | 0/0 | 2448 | 3 | 0 | 0 | 3 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | ATGGC others(2443): Show |
chr12 | 113216464 | 113303585 | ||
| a0001c0005 | 0/0 | 2448 | 2 | 0 | 2 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | ATGGC others(2443): Show |
chr12 | 113216464 | 113303585 | ||
| a0001c0006 | 0/0 | 2448 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | ATGGC others(2443): Show |
chr12 | 113216464 | 113303585 | ||
| a0001c0007 | 0/0 | 2448 | 2 | 2 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | ATGGC others(2443): Show |
chr12 | 113216464 | 113303585 | ||
| a0001c0008 | 0/0 | 2448 | 2 | 2 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | ATGGC others(2443): Show |
chr12 | 113216464 | 113303585 | ||
| a0001c0010 | 0/0 | 2448 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | ATGGC others(2443): Show |
chr12 | 113216464 | 113303585 | ||
| a0001c0011 | 0/0 | 2448 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | ATGGC others(2443): Show |
chr12 | 113216464 | 113303585 | ||
| a0001c0012 | 0/0 | 2448 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | ATGGC others(2443): Show |
chr12 | 113216464 | 113303585 | ||
| a0001c0013 | 0/0 | 2448 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | ATGGC others(2443): Show |
chr12 | 113216464 | 113303585 | ||
| a0002c0009 | 0/0 | 2448 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN1_chr12_113216464_113303585 | TPCN1 | ATGGC others(2443): Show |
chr12 | 113216464 | 113303585 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 5248 | 94 | 33 | 10 | 41 | 2 | 7 | TPCN1_chr12_113216464_113303585 | TPCN1 | GAGCT others(5243): Show |
chr12 | 113216464 | 113303585 |
| a0001c0001t0002 | 0/0 | 5248 | 53 | 2 | 1 | 45 | 0 | 5 | TPCN1_chr12_113216464_113303585 | TPCN1 | GAGCT others(5243): Show |
chr12 | 113216464 | 113303585 |
| a0001c0001t0003 | 0/0 | 5248 | 31 | 25 | 1 | 1 | 2 | 2 | TPCN1_chr12_113216464_113303585 | TPCN1 | GAGCT others(5243): Show |
chr12 | 113216464 | 113303585 |
| a0001c0001t0004 | 0/1 | 5248 | 21 | 2 | 3 | 8 | 4 | 3 | TPCN1_chr12_113216464_113303585 | TPCN1 | GAGCT others(5243): Show |
chr12 | 113216464 | 113303585 |
| a0001c0001t0005 | 0/0 | 5248 | 7 | 1 | 0 | 6 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | GAGCT others(5243): Show |
chr12 | 113216464 | 113303585 |
| a0001c0001t0006 | 0/0 | 5248 | 3 | 3 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | GAGCT others(5243): Show |
chr12 | 113216464 | 113303585 |
| a0001c0001t0007 | 0/0 | 5248 | 4 | 0 | 1 | 0 | 1 | 2 | TPCN1_chr12_113216464_113303585 | TPCN1 | GAGCT others(5243): Show |
chr12 | 113216464 | 113303585 |
| a0001c0001t0010 | 0/0 | 5248 | 2 | 2 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | GAGCT others(5243): Show |
chr12 | 113216464 | 113303585 |
| a0001c0001t0012 | 0/0 | 5248 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | GAGCT others(5243): Show |
chr12 | 113216464 | 113303585 |
| a0001c0001t0013 | 0/0 | 5248 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | GAGCT others(5243): Show |
chr12 | 113216464 | 113303585 |
| a0001c0001t0014 | 0/0 | 5248 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | GAGCT others(5243): Show |
chr12 | 113216464 | 113303585 |
| a0001c0001t0015 | 0/0 | 5292 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | GAGCT others(5287): Show |
chr12 | 113216464 | 113303585 |
| a0001c0001t0016 | 0/0 | 5248 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | GAGCT others(5243): Show |
chr12 | 113216464 | 113303585 |
| a0001c0001t0017 | 0/0 | 5248 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | GAGCT others(5243): Show |
chr12 | 113216464 | 113303585 |
| a0001c0001t0018 | 0/0 | 5248 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | GAGCT others(5243): Show |
chr12 | 113216464 | 113303585 |
| a0001c0001t0019 | 0/0 | 5248 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | GAGCT others(5243): Show |
chr12 | 113216464 | 113303585 |
| a0001c0001t0020 | 0/0 | 5248 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | GAGCT others(5243): Show |
chr12 | 113216464 | 113303585 |
| a0001c0001t0021 | 0/0 | 5248 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | GAGCT others(5243): Show |
chr12 | 113216464 | 113303585 |
| a0001c0001t0022 | 0/0 | 5248 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | GAGCT others(5243): Show |
chr12 | 113216464 | 113303585 |
| a0001c0001t0023 | 0/0 | 5248 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | GAGCT others(5243): Show |
chr12 | 113216464 | 113303585 |
| a0001c0001t0024 | 0/0 | 5248 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | GAGCT others(5243): Show |
chr12 | 113216464 | 113303585 |
| a0001c0002t0009 | 0/0 | 5248 | 3 | 3 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | GAGCT others(5243): Show |
chr12 | 113216464 | 113303585 |
| a0001c0003t0008 | 0/0 | 5248 | 3 | 1 | 1 | 0 | 1 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | GAGCT others(5243): Show |
chr12 | 113216464 | 113303585 |
| a0001c0004t0002 | 0/0 | 5248 | 3 | 0 | 0 | 3 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | GAGCT others(5243): Show |
chr12 | 113216464 | 113303585 |
| a0001c0005t0001 | 0/0 | 5248 | 2 | 0 | 2 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | GAGCT others(5243): Show |
chr12 | 113216464 | 113303585 |
| a0001c0006t0001 | 0/0 | 5248 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | GAGCT others(5243): Show |
chr12 | 113216464 | 113303585 |
| a0001c0007t0002 | 0/0 | 5248 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | GAGCT others(5243): Show |
chr12 | 113216464 | 113303585 |
| a0001c0007t0011 | 0/0 | 5248 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | GAGCT others(5243): Show |
chr12 | 113216464 | 113303585 |
| a0001c0008t0006 | 0/0 | 5248 | 2 | 2 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | GAGCT others(5243): Show |
chr12 | 113216464 | 113303585 |
| a0001c0010t0004 | 0/0 | 5248 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | GAGCT others(5243): Show |
chr12 | 113216464 | 113303585 |
| a0001c0011t0001 | 0/0 | 5248 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | GAGCT others(5243): Show |
chr12 | 113216464 | 113303585 |
| a0001c0012t0001 | 0/0 | 5248 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | GAGCT others(5243): Show |
chr12 | 113216464 | 113303585 |
| a0001c0013t0011 | 0/0 | 5248 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | GAGCT others(5243): Show |
chr12 | 113216464 | 113303585 |
| a0002c0009t0001 | 0/0 | 5248 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN1_chr12_113216464_113303585 | TPCN1 | GAGCT others(5243): Show |
chr12 | 113216464 | 113303585 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0004 | 1/0 | 3 | 0 | 0 | 2 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0003g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0003g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0004g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0004g0012 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0004g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0004g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0004g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0004g0101 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0004g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0004g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0004g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0004g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0004g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0005g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0005g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0005g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0005g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0005g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0005g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0005g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0006g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0006g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0006g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0007g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0007g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0007g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0007g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0010g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0010g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0012g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0013g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0014g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0015g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0016g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0017g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0018g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0019g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0020g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0021g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0022g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0023g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0001t0024g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0002t0009g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0002t0009g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0002t0009g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0003t0008g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0003t0008g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0003t0008g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0004t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0004t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0004t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0005t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0005t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0006t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0006t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0007t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0007t0011g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0008t0006g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0008t0006g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0010t0004g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0011t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0012t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0001c0013t0011g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| a0002c0009t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0007 | g0072 | EUR | GBR | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0074 | EUR | GBR | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0179 | EUR | GBR | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0012 | EUR | GBR | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG00280 | hp1 | a0001 | c0001 | t0004 | g0125 | EUR | FIN | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG00280 | hp2 | a0001 | c0003 | t0008 | g0227 | EUR | FIN | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0142 | EUR | FIN | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0181 | EUR | FIN | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | CHS | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG00408 | hp2 | a0001 | c0001 | t0004 | g0145 | EAS | CHS | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | CHS | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | CHS | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0077 | AMR | PUR | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0076 | AMR | PUR | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG00738 | hp1 | a0001 | c0010 | t0004 | g0141 | AMR | PUR | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0014 | AMR | PUR | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG01168 | hp1 | a0001 | c0005 | t0001 | g0120 | AMR | PUR | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG01168 | hp2 | a0001 | c0003 | t0008 | g0226 | AMR | PUR | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG01169 | hp2 | a0001 | c0005 | t0001 | g0079 | AMR | PUR | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG01358 | hp2 | a0001 | c0001 | t0007 | g0064 | AMR | CLM | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG01361 | hp2 | a0001 | c0001 | t0014 | g0100 | AMR | CLM | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG01517 | hp1 | a0001 | c0001 | t0004 | g0081 | EUR | IBS | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0066 | EUR | IBS | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0171 | AFR | ACB | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG01891 | hp1 | a0001 | c0001 | t0006 | g0205 | AFR | ACB | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG01978 | hp1 | a0001 | c0011 | t0001 | g0109 | AMR | PEL | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | KHV | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02055 | hp1 | a0001 | c0008 | t0006 | g0204 | AFR | ACB | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0193 | AFR | ACB | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02071 | hp2 | a0001 | c0001 | t0013 | g0030 | EAS | KHV | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | KHV | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | KHV | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02135 | hp1 | a0001 | c0006 | t0001 | g0163 | EAS | KHV | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0199 | AFR | ACB | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | CDX | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | CDX | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CDX | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02165 | hp2 | a0001 | c0001 | t0004 | g0098 | EAS | CDX | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0188 | AFR | ACB | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | ACB | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02293 | hp2 | a0001 | c0001 | t0004 | g0063 | AMR | PEL | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0220 | AMR | PEL | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | ACB | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0183 | AFR | ACB | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02572 | hp1 | a0001 | c0013 | t0011 | g0173 | AFR | GWD | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0192 | AFR | GWD | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02615 | hp2 | a0001 | c0012 | t0001 | g0201 | AFR | GWD | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02622 | hp2 | a0001 | c0001 | t0020 | g0075 | AFR | GWD | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02630 | hp1 | a0001 | c0001 | t0010 | g0149 | AFR | GWD | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0012 | AFR | GWD | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02647 | hp1 | a0001 | c0001 | t0018 | g0124 | AFR | GWD | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02647 | hp2 | a0001 | c0007 | t0011 | g0174 | AFR | GWD | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0212 | SAS | PJL | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0197 | AFR | GWD | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02717 | hp2 | a0001 | c0002 | t0009 | g0054 | AFR | GWD | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02723 | hp1 | a0001 | c0001 | t0017 | g0138 | AFR | GWD | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0198 | AFR | GWD | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0182 | SAS | PJL | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0196 | AFR | GWD | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02886 | hp2 | a0001 | c0001 | t0010 | g0150 | AFR | GWD | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0187 | AFR | GWD | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0194 | AFR | GWD | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | ESN | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ESN | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02965 | hp2 | a0001 | c0001 | t0012 | g0175 | AFR | ESN | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02976 | hp1 | a0001 | c0001 | t0019 | g0151 | AFR | ESN | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ESN | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | MSL | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0195 | AFR | MSL | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0191 | AFR | ESN | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0016 | AFR | ESN | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG03195 | hp1 | a0001 | c0002 | t0009 | g0056 | AFR | ESN | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0113 | AFR | ESN | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG03209 | hp1 | a0001 | c0001 | t0006 | g0202 | AFR | MSL | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0136 | AFR | MSL | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | MSL | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG03225 | hp2 | a0001 | c0007 | t0002 | g0058 | AFR | MSL | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | MSL | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | MSL | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG03486 | hp1 | a0001 | c0002 | t0009 | g0055 | AFR | MSL | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0177 | AFR | MSL | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0021 | AFR | GWD | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0014 | AFR | GWD | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | MSL | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0185 | AFR | MSL | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG03654 | hp1 | a0001 | c0001 | t0007 | g0112 | SAS | PJL | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG03654 | hp2 | a0001 | c0001 | t0004 | g0118 | SAS | PJL | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0209 | SAS | PJL | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0090 | SAS | BEB | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0221 | SAS | BEB | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG03942 | hp1 | a0002 | c0009 | t0001 | g0115 | SAS | BEB | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG03942 | hp2 | a0001 | c0001 | t0007 | g0083 | SAS | BEB | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0050 | SAS | STU | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG04115 | hp2 | a0001 | c0001 | t0004 | g0137 | SAS | STU | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | BEB | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0180 | SAS | BEB | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | STU | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0106 | SAS | STU | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | YRI | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0059 | AFR | YRI | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0189 | AFR | YRI | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | YRI | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18942 | hp2 | a0001 | c0001 | t0005 | g0067 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18950 | hp1 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18950 | hp2 | a0001 | c0001 | t0005 | g0097 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18960 | hp1 | a0001 | c0001 | t0004 | g0009 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18969 | hp2 | a0001 | c0001 | t0022 | g0005 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18971 | hp1 | a0001 | c0001 | t0004 | g0104 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18974 | hp1 | a0001 | c0004 | t0002 | g0033 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18977 | hp2 | a0001 | c0001 | t0015 | g0211 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18979 | hp2 | a0001 | c0001 | t0005 | g0095 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18990 | hp1 | a0001 | c0001 | t0005 | g0099 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18991 | hp2 | a0001 | c0001 | t0023 | g0088 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18998 | hp1 | a0001 | c0001 | t0016 | g0003 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | LWK | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | LWK | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA19067 | hp1 | a0001 | c0001 | t0004 | g0105 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA19072 | hp2 | a0001 | c0001 | t0004 | g0153 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA19074 | hp1 | a0001 | c0004 | t0002 | g0022 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA19074 | hp2 | a0001 | c0001 | t0005 | g0094 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA19081 | hp2 | a0001 | c0006 | t0001 | g0165 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA19083 | hp1 | a0001 | c0001 | t0004 | g0170 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA19084 | hp1 | a0001 | c0001 | t0005 | g0093 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA19085 | hp2 | a0001 | c0004 | t0002 | g0034 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA19089 | hp1 | a0001 | c0001 | t0024 | g0042 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA19089 | hp2 | a0001 | c0001 | t0004 | g0108 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | ASW | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ASW | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0190 | AFR | ACB | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02559 | hp1 | a0001 | c0008 | t0006 | g0203 | AFR | ACB | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG02559 | hp2 | a0001 | c0001 | t0021 | g0053 | AFR | ACB | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG03471 | hp1 | a0001 | c0001 | t0006 | g0176 | AFR | MSL | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | MSL | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | USA | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| HG06807 | hp2 | a0001 | c0003 | t0008 | g0200 | AFR | USA | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0089 | AFR | USA | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0091 | AFR | USA | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0004 | g0101 | REF | REF | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0004 | REF | REF | TPCN1_chr12_113216464_113303585 | TPCN1 | chr12 | 113216464 | 113303585 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:113226866 | T | C | 1 | a0002 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.14T>C | p.Leu5Ser | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/28 | 302/5248 | 14/2451 | 5/816 | chr12 | 113226866 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:113266287 | G | A | 1 | a0001c0005 | 2 | HG01168.hp1 HG01169.hp2 |
synonymous_variant | LOW | c.345G>A | p.Thr115Thr | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 4/28 | 633/5248 | 345/2451 | 115/816 | chr12 | 113266287 | |||
| chr12:113267845 | C | T | 1 | a0001c0008 | 2 | HG02055.hp1 HG02559.hp1 |
splice_region_variant&synonymous_variant | LOW | c.417C>T | p.Val139Val | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 5/28 | 705/5248 | 417/2451 | 139/816 | chr12 | 113267845 | |||
| chr12:113269781 | C | T | 2 | a0001c0007 a0001c0013 |
3 | HG02572.hp1 HG02647.hp2 HG03225.hp2 |
synonymous_variant | LOW | c.684C>T | p.Ser228Ser | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 7/28 | 972/5248 | 684/2451 | 228/816 | chr12 | 113269781 | |||
| chr12:113277314 | G | A | 1 | a0001c0013 | 1 | HG02572.hp1 | synonymous_variant | LOW | c.1134G>A | p.Glu378Glu | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 12/28 | 1422/5248 | 1134/2451 | 378/816 | chr12 | 113277314 | |||
| chr12:113278816 | G | A | 1 | a0001c0002 | 3 | HG02717.hp2 HG03195.hp1 HG03486.hp1 |
synonymous_variant | LOW | c.1278G>A | p.Thr426Thr | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/28 | 1566/5248 | 1278/2451 | 426/816 | chr12 | 113278816 | |||
| chr12:113285908 | C | T | 1 | a0001c0013 | 1 | HG02572.hp1 | synonymous_variant | LOW | c.1473C>T | p.Phe491Phe | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 18/28 | 1761/5248 | 1473/2451 | 491/816 | chr12 | 113285908 | |||
| chr12:113287065 | C | T | 1 | a0001c0004 | 3 | NA18974.hp1 NA19074.hp1 NA19085.hp2 |
synonymous_variant | LOW | c.1605C>T | p.Ile535Ile | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 19/28 | 1893/5248 | 1605/2451 | 535/816 | chr12 | 113287065 | |||
| chr12:113288839 | C | T | 1 | a0001c0012 | 1 | HG02615.hp2 | synonymous_variant | LOW | c.1788C>T | p.Asn596Asn | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 21/28 | 2076/5248 | 1788/2451 | 596/816 | chr12 | 113288839 | |||
| chr12:113290155 | C | T | 1 | a0001c0011 | 1 | HG01978.hp1 | synonymous_variant | LOW | c.1824C>T | p.Arg608Arg | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 22/28 | 2112/5248 | 1824/2451 | 608/816 | chr12 | 113290155 | |||
| chr12:113293025 | G | A | 1 | a0001c0010 | 1 | HG00738.hp1 | synonymous_variant | LOW | c.2205G>A | p.Ser735Ser | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 26/28 | 2493/5248 | 2205/2451 | 735/816 | chr12 | 113293025 | |||
| chr12:113296025 | C | T | 1 | a0001c0003 | 3 | HG00280.hp2 HG01168.hp2 HG06807.hp2 |
synonymous_variant | LOW | c.2400C>T | p.Pro800Pro | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 28/28 | 2688/5248 | 2400/2451 | 800/816 | chr12 | 113296025 | |||
| chr12:113296067 | C | T | 1 | a0001c0006 | 2 | HG02135.hp1 NA19081.hp2 |
synonymous_variant | LOW | c.2442C>T | p.Thr814Thr | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 28/28 | 2730/5248 | 2442/2451 | 814/816 | chr12 | 113296067 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:113221542 | G | T | 1 | a0001c0001t0024 | 1 | NA19089.hp1 | 5_prime_UTR_variant | MODIFIER | c.-210G>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/28 | 5311 | chr12 | 113221542 | ||||||
| chr12:113221568 | C | G | 1 | a0001c0001t0023 | 1 | NA18991.hp2 | 5_prime_UTR_variant | MODIFIER | c.-184C>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/28 | 5285 | chr12 | 113221568 | ||||||
| chr12:113221569 | G | C | 1 | a0001c0001t0023 | 1 | NA18991.hp2 | 5_prime_UTR_variant | MODIFIER | c.-183G>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/28 | 5284 | chr12 | 113221569 | ||||||
| chr12:113226819 | A | C | 1 | a0001c0001t0005 | 7 | NA18942.hp2 NA18950.hp2 NA18979.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-34A>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/28 | 34 | chr12 | 113226819 | ||||||
| chr12:113296354 | C | T | 1 | a0001c0002t0009 | 3 | HG02717.hp2 HG03195.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*278C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 28/28 | 278 | chr12 | 113296354 | ||||||
| chr12:113296542 | G | A | 1 | a0001c0003t0008 | 3 | HG00280.hp2 HG01168.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*466G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 28/28 | 466 | chr12 | 113296542 | ||||||
| chr12:113296554 | C | T | 2 | a0001c0007t0011 a0001c0013t0011 |
2 | HG02572.hp1 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*478C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 28/28 | 478 | chr12 | 113296554 | ||||||
| chr12:113296608 | G | A | 2 | a0001c0001t0003 a0001c0001t0012 |
32 | HG00140.hp1 HG00323.hp2 HG01109.hp2 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*532G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 28/28 | 532 | chr12 | 113296608 | ||||||
| chr12:113296659 | A | G | 1 | a0001c0003t0008 | 3 | HG00280.hp2 HG01168.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*583A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 28/28 | 583 | chr12 | 113296659 | ||||||
| chr12:113296772 | G | T | 1 | a0001c0001t0022 | 1 | NA18969.hp2 | 3_prime_UTR_variant | MODIFIER | c.*696G>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 28/28 | 696 | chr12 | 113296772 | ||||||
| chr12:113296914 | C | A | 1 | a0001c0001t0013 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*838C>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 28/28 | 838 | chr12 | 113296914 | ||||||
| chr12:113297022 | C | T | 1 | a0001c0001t0021 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*946C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 28/28 | 946 | chr12 | 113297022 | ||||||
| chr12:113297127 | T | G | 2 | a0001c0001t0007 a0001c0001t0014 |
5 | HG00099.hp1 HG01358.hp2 HG01361.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1051T>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 28/28 | 1051 | chr12 | 113297127 | ||||||
| chr12:113297199 | A | ACATCTGA others(37): Show |
1 | a0001c0001t0015 | 1 | NA18977.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1125_*1168dupATCT others(40): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 28/28 | 1169 | INFO_REALIGN_3_PRIME | chr12 | 113297199 | |||||
| chr12:113297287 | G | A | 1 | a0001c0001t0010 | 2 | HG02630.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1211G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 28/28 | 1211 | chr12 | 113297287 | ||||||
| chr12:113297344 | G | A | 1 | a0001c0001t0012 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1268G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 28/28 | 1268 | chr12 | 113297344 | ||||||
| chr12:113297606 | C | G | 2 | a0001c0007t0011 a0001c0013t0011 |
2 | HG02572.hp1 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1530C>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 28/28 | 1530 | chr12 | 113297606 | ||||||
| chr12:113297905 | G | A | 1 | a0001c0001t0014 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1829G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 28/28 | 1829 | chr12 | 113297905 | ||||||
| chr12:113297933 | G | A | 1 | a0001c0001t0016 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1857G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 28/28 | 1857 | chr12 | 113297933 | ||||||
| chr12:113297937 | G | C | 16 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0012 others(13): Show |
102 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*1861G>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 28/28 | 1861 | chr12 | 113297937 | ||||||
| chr12:113298084 | T | A | 1 | a0001c0001t0017 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2008T>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 28/28 | 2008 | chr12 | 113298084 | ||||||
| chr12:113298085 | C | A | 1 | a0001c0001t0017 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2009C>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 28/28 | 2009 | chr12 | 113298085 | ||||||
| chr12:113298292 | G | A | 4 | a0001c0001t0003 a0001c0001t0012 a0001c0001t0018 others(1): Show |
34 | HG00140.hp1 HG00323.hp2 HG01109.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*2216G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 28/28 | 2216 | chr12 | 113298292 | ||||||
| chr12:113298311 | C | T | 2 | a0001c0001t0004 a0001c0010t0004 |
21 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2235C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 28/28 | 2235 | chr12 | 113298311 | ||||||
| chr12:113298316 | A | G | 16 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0012 others(13): Show |
102 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*2240A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 28/28 | 2240 | chr12 | 113298316 | ||||||
| chr12:113298496 | C | T | 1 | a0001c0001t0020 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2420C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 28/28 | 2420 | chr12 | 113298496 | ||||||
| chr12:113298535 | T | C | 2 | a0001c0001t0006 a0001c0008t0006 |
5 | HG01891.hp1 HG02055.hp1 HG02559.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2459T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 28/28 | 2459 | chr12 | 113298535 | ||||||
| chr12:113298536 | T | C | 1 | a0001c0001t0019 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2460T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 28/28 | 2460 | chr12 | 113298536 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:113221816 | C | G | 32 | a0001c0001t0002g0005 a0001c0001t0002g0206 a0001c0001t0002g0207 others(29): Show |
33 | HG00280.hp2 HG01168.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.-126+190C>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/27 | chr12 | 113221816 | |||||||
| chr12:113221910 | T | G | 1 | a0001c0003t0008g0200 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-126+284T>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/27 | chr12 | 113221910 | |||||||
| chr12:113221947 | T | C | 79 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(76): Show |
84 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.-126+321T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/27 | chr12 | 113221947 | |||||||
| chr12:113222000 | G | A | 1 | a0001c0001t0001g0015 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-126+374G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/27 | chr12 | 113222000 | |||||||
| chr12:113222019 | T | C | 1 | a0001c0007t0002g0058 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-126+393T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/27 | chr12 | 113222019 | |||||||
| chr12:113222495 | C | T | 1 | a0001c0001t0001g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-126+869C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/27 | chr12 | 113222495 | |||||||
| chr12:113222514 | C | T | 27 | a0001c0001t0002g0005 a0001c0001t0002g0206 a0001c0001t0002g0207 others(24): Show |
28 | HG00280.hp2 HG01168.hp2 HG02080.hp2 others(25): Show |
intron_variant | MODIFIER | c.-126+888C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/27 | chr12 | 113222514 | |||||||
| chr12:113222558 | A | C | 7 | a0001c0001t0006g0202 a0001c0001t0006g0205 a0001c0002t0009g0054 others(4): Show |
7 | HG01891.hp1 HG02055.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-126+932A>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/27 | chr12 | 113222558 | |||||||
| chr12:113223087 | C | T | 13 | a0001c0001t0003g0187 a0001c0001t0003g0188 a0001c0001t0003g0189 others(10): Show |
13 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.-126+1461C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/27 | chr12 | 113223087 | |||||||
| chr12:113223188 | C | T | 27 | a0001c0001t0002g0005 a0001c0001t0002g0206 a0001c0001t0002g0207 others(24): Show |
28 | HG00280.hp2 HG01168.hp2 HG02080.hp2 others(25): Show |
intron_variant | MODIFIER | c.-126+1562C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/27 | chr12 | 113223188 | |||||||
| chr12:113223223 | G | T | 1 | a0001c0001t0006g0205 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-126+1597G>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/27 | chr12 | 113223223 | |||||||
| chr12:113223341 | G | A | 1 | a0001c0001t0003g0016 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-126+1715G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/27 | chr12 | 113223341 | |||||||
| chr12:113223358 | AGCCCAGA others(24): Show |
A | 1 | a0001c0001t0021g0053 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-126+1735_-126+176 others(35): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 113223358 | ||||||
| chr12:113223404 | G | A | 1 | a0001c0001t0003g0059 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-126+1778G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/27 | chr12 | 113223404 | |||||||
| chr12:113223435 | C | CT | 12 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0164 others(9): Show |
12 | HG01884.hp1 HG01891.hp2 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.-126+1826dupT | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 113223435 | ||||||
| chr12:113223435 | C | CTTTTT | 21 | a0001c0001t0002g0005 a0001c0001t0002g0207 a0001c0001t0002g0208 others(18): Show |
22 | HG02080.hp2 HG02083.hp2 HG02155.hp2 others(19): Show |
intron_variant | MODIFIER | c.-126+1822_-126+182 others(9): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 113223435 | ||||||
| chr12:113223435 | C | CTTTTTT | 5 | a0001c0001t0002g0228 a0001c0001t0002g0229 a0001c0003t0008g0200 others(2): Show |
5 | HG00280.hp2 HG01168.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.-126+1821_-126+182 others(10): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 113223435 | ||||||
| chr12:113223435 | C | CTTTTTTT | 6 | a0001c0001t0001g0017 a0001c0001t0003g0018 a0001c0001t0006g0202 others(3): Show |
6 | HG01891.hp1 HG02559.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-126+1820_-126+182 others(11): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 113223435 | ||||||
| chr12:113223435 | C | CTTTTTTT others(1): Show |
5 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0003g0002 others(2): Show |
7 | HG02055.hp1 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-126+1819_-126+182 others(12): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 113223435 | ||||||
| chr12:113223435 | C | CTTTTTTT others(2): Show |
7 | a0001c0001t0001g0015 a0001c0001t0002g0023 a0001c0001t0003g0016 others(4): Show |
7 | HG02027.hp2 HG02717.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.-126+1818_-126+182 others(13): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 113223435 | ||||||
| chr12:113223435 | C | CTTTTTTT others(3): Show |
31 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(28): Show |
33 | HG00408.hp1 HG00438.hp1 HG02027.hp1 others(30): Show |
intron_variant | MODIFIER | c.-126+1817_-126+182 others(14): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 113223435 | ||||||
| chr12:113223435 | C | CTTTTTTT others(4): Show |
10 | a0001c0001t0001g0057 a0001c0001t0001g0178 a0001c0001t0002g0051 others(7): Show |
10 | HG00423.hp1 HG02572.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.-126+1816_-126+182 others(15): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 113223435 | ||||||
| chr12:113223435 | C | CTTTTTTT others(5): Show |
19 | a0001c0001t0001g0184 a0001c0001t0003g0179 a0001c0001t0003g0180 others(16): Show |
19 | HG00140.hp1 HG00323.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.-126+1815_-126+182 others(16): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 113223435 | ||||||
| chr12:113223435 | C | CTTTTTTT others(6): Show |
2 | a0001c0001t0003g0186 a0001c0001t0003g0199 |
2 | HG02145.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.-126+1814_-126+182 others(17): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 113223435 | ||||||
| chr12:113223453 | G | T | 27 | a0001c0001t0002g0005 a0001c0001t0002g0206 a0001c0001t0002g0207 others(24): Show |
28 | HG00280.hp2 HG01168.hp2 HG02080.hp2 others(25): Show |
intron_variant | MODIFIER | c.-126+1827G>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/27 | chr12 | 113223453 | |||||||
| chr12:113223547 | G | A | 1 | a0001c0012t0001g0201 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-126+1921G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/27 | chr12 | 113223547 | |||||||
| chr12:113223824 | A | C | 4 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(1): Show |
4 | HG02572.hp2 HG02897.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-126+2198A>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/27 | chr12 | 113223824 | |||||||
| chr12:113223924 | T | G | 2 | a0001c0007t0011g0174 a0001c0013t0011g0173 |
2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-126+2298T>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/27 | chr12 | 113223924 | |||||||
| chr12:113224078 | A | G | 79 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(76): Show |
84 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.-126+2452A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/27 | chr12 | 113224078 | |||||||
| chr12:113224093 | A | G | 87 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(84): Show |
92 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.-126+2467A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/27 | chr12 | 113224093 | |||||||
| chr12:113224258 | C | A | 27 | a0001c0001t0002g0005 a0001c0001t0002g0206 a0001c0001t0002g0207 others(24): Show |
28 | HG00280.hp2 HG01168.hp2 HG02080.hp2 others(25): Show |
intron_variant | MODIFIER | c.-125-2470C>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/27 | chr12 | 113224258 | |||||||
| chr12:113224315 | T | A | 27 | a0001c0001t0002g0005 a0001c0001t0002g0206 a0001c0001t0002g0207 others(24): Show |
28 | HG00280.hp2 HG01168.hp2 HG02080.hp2 others(25): Show |
intron_variant | MODIFIER | c.-125-2413T>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/27 | chr12 | 113224315 | |||||||
| chr12:113224369 | A | G | 1 | a0001c0001t0002g0225 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-125-2359A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/27 | chr12 | 113224369 | |||||||
| chr12:113224470 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-125-2258C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/27 | chr12 | 113224470 | |||||||
| chr12:113224473 | T | G | 1 | a0001c0001t0003g0016 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-125-2255T>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/27 | chr12 | 113224473 | |||||||
| chr12:113224697 | C | A | 34 | a0001c0001t0002g0005 a0001c0001t0002g0206 a0001c0001t0002g0207 others(31): Show |
35 | HG00280.hp2 HG01168.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.-125-2031C>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/27 | chr12 | 113224697 | |||||||
| chr12:113224757 | T | A | 44 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(41): Show |
46 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(43): Show |
intron_variant | MODIFIER | c.-125-1971T>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/27 | chr12 | 113224757 | |||||||
| chr12:113224819 | C | T | 1 | a0001c0001t0003g0198 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-125-1909C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/27 | chr12 | 113224819 | |||||||
| chr12:113224942 | G | A | 4 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0061 others(1): Show |
6 | NA18943.hp1 NA18951.hp2 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.-125-1786G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/27 | chr12 | 113224942 | |||||||
| chr12:113225066 | T | A | 3 | a0001c0003t0008g0200 a0001c0003t0008g0226 a0001c0003t0008g0227 |
3 | HG00280.hp2 HG01168.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-125-1662T>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/27 | chr12 | 113225066 | |||||||
| chr12:113225181 | A | G | 6 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(3): Show |
8 | HG02280.hp1 HG02451.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-125-1547A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/27 | chr12 | 113225181 | |||||||
| chr12:113225426 | T | C | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | NA18968.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.-125-1302T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/27 | chr12 | 113225426 | |||||||
| chr12:113225515 | A | G | 8 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0178 others(5): Show |
8 | HG02572.hp1 HG02647.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-125-1213A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/27 | chr12 | 113225515 | |||||||
| chr12:113225657 | C | T | 6 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(3): Show |
8 | HG02280.hp1 HG02451.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-125-1071C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/27 | chr12 | 113225657 | |||||||
| chr12:113225659 | A | C | 1 | a0001c0001t0004g0153 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.-125-1069A>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/27 | chr12 | 113225659 | |||||||
| chr12:113225800 | C | T | 6 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(3): Show |
8 | HG02280.hp1 HG02451.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-125-928C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/27 | chr12 | 113225800 | |||||||
| chr12:113225801 | G | A | 27 | a0001c0001t0002g0005 a0001c0001t0002g0206 a0001c0001t0002g0207 others(24): Show |
28 | HG00280.hp2 HG01168.hp2 HG02080.hp2 others(25): Show |
intron_variant | MODIFIER | c.-125-927G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/27 | chr12 | 113225801 | |||||||
| chr12:113226093 | T | TAATTTTT others(10): Show |
1 | a0001c0001t0004g0153 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.-125-633_-125-617d others(19): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr12 | 113226093 | ||||||
| chr12:113226098 | T | C | 3 | a0001c0007t0002g0058 a0001c0007t0011g0174 a0001c0013t0011g0173 |
3 | HG02572.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-125-630T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/27 | chr12 | 113226098 | |||||||
| chr12:113226251 | A | G | 2 | a0001c0001t0002g0223 a0001c0001t0002g0224 |
2 | NA18953.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.-125-477A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/27 | chr12 | 113226251 | |||||||
| chr12:113226255 | T | C | 2 | a0001c0001t0006g0202 a0001c0001t0006g0205 |
2 | HG01891.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-125-473T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/27 | chr12 | 113226255 | |||||||
| chr12:113226456 | A | G | 3 | a0001c0003t0008g0200 a0001c0003t0008g0226 a0001c0003t0008g0227 |
3 | HG00280.hp2 HG01168.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-125-272A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/27 | chr12 | 113226456 | |||||||
| chr12:113226581 | CT | C | 7 | a0001c0001t0006g0202 a0001c0001t0006g0205 a0001c0002t0009g0054 others(4): Show |
7 | HG01891.hp1 HG02055.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-125-146delT | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/27 | chr12 | 113226581 | |||||||
| chr12:113226639 | C | T | 6 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(3): Show |
8 | HG02280.hp1 HG02451.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-125-89C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 1/27 | chr12 | 113226639 | |||||||
| chr12:113227013 | G | A | 38 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(35): Show |
40 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.112+49G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113227013 | |||||||
| chr12:113227021 | G | A | 1 | a0001c0007t0002g0058 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.112+57G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113227021 | |||||||
| chr12:113227030 | C | T | 3 | a0001c0002t0009g0054 a0001c0002t0009g0055 a0001c0002t0009g0056 |
3 | HG02717.hp2 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.112+66C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113227030 | |||||||
| chr12:113227193 | C | T | 2 | a0001c0001t0001g0172 a0001c0001t0003g0171 |
2 | HG01884.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.112+229C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113227193 | |||||||
| chr12:113227197 | A | C | 79 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(76): Show |
84 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.112+233A>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113227197 | |||||||
| chr12:113227247 | A | T | 3 | a0001c0002t0009g0054 a0001c0002t0009g0055 a0001c0002t0009g0056 |
3 | HG02717.hp2 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.112+283A>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113227247 | |||||||
| chr12:113227342 | C | G | 1 | a0001c0012t0001g0201 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.112+378C>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113227342 | |||||||
| chr12:113227386 | G | A | 1 | a0001c0001t0004g0063 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.112+422G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113227386 | |||||||
| chr12:113227419 | A | C | 3 | a0001c0002t0009g0054 a0001c0002t0009g0055 a0001c0002t0009g0056 |
3 | HG02717.hp2 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.112+455A>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113227419 | |||||||
| chr12:113227470 | G | A | 6 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(3): Show |
8 | HG02280.hp1 HG02451.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.112+506G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113227470 | |||||||
| chr12:113227534 | A | T | 1 | a0001c0001t0004g0153 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.112+570A>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113227534 | |||||||
| chr12:113227614 | G | A | 2 | a0001c0001t0001g0065 a0001c0001t0007g0064 |
2 | HG01358.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.112+650G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113227614 | |||||||
| chr12:113227687 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.112+723C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113227687 | |||||||
| chr12:113227795 | G | A | 3 | a0001c0002t0009g0054 a0001c0002t0009g0055 a0001c0002t0009g0056 |
3 | HG02717.hp2 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.112+831G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113227795 | |||||||
| chr12:113228040 | A | T | 1 | a0001c0001t0003g0186 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.112+1076A>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113228040 | |||||||
| chr12:113228434 | C | T | 1 | a0001c0001t0019g0151 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.112+1470C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113228434 | |||||||
| chr12:113228601 | C | T | 6 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(3): Show |
8 | HG02280.hp1 HG02451.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.112+1637C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113228601 | |||||||
| chr12:113228668 | C | T | 38 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(35): Show |
40 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.112+1704C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113228668 | |||||||
| chr12:113228983 | C | T | 3 | a0001c0001t0001g0008 a0001c0001t0001g0062 a0001c0012t0001g0201 |
4 | HG02615.hp2 NA18981.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.112+2019C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113228983 | |||||||
| chr12:113229106 | A | C | 1 | a0001c0001t0001g0069 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.112+2142A>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113229106 | |||||||
| chr12:113229133 | A | T | 3 | a0001c0001t0001g0148 a0001c0001t0010g0149 a0001c0001t0010g0150 |
3 | HG02630.hp1 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.112+2169A>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113229133 | |||||||
| chr12:113229315 | G | A | 1 | a0001c0001t0001g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.112+2351G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113229315 | |||||||
| chr12:113229396 | G | T | 1 | a0001c0012t0001g0201 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.112+2432G>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113229396 | |||||||
| chr12:113229679 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.112+2715C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113229679 | |||||||
| chr12:113229680 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.112+2716G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113229680 | |||||||
| chr12:113229739 | G | A | 1 | a0001c0001t0003g0016 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.112+2775G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113229739 | |||||||
| chr12:113229743 | C | T | 4 | a0001c0001t0006g0202 a0001c0001t0006g0205 a0001c0008t0006g0203 others(1): Show |
4 | HG01891.hp1 HG02055.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+2779C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113229743 | |||||||
| chr12:113229907 | C | T | 38 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(35): Show |
40 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.112+2943C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113229907 | |||||||
| chr12:113229911 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.112+2947G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113229911 | |||||||
| chr12:113229917 | C | T | 1 | a0001c0001t0002g0050 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.112+2953C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113229917 | |||||||
| chr12:113229918 | G | A | 1 | a0001c0001t0002g0225 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.112+2954G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113229918 | |||||||
| chr12:113230144 | C | G | 3 | a0001c0001t0001g0146 a0001c0001t0004g0145 a0001c0001t0004g0170 |
3 | HG00408.hp2 NA18982.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.112+3180C>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113230144 | |||||||
| chr12:113230144 | C | T | 1 | a0001c0001t0002g0049 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.112+3180C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113230144 | |||||||
| chr12:113230283 | C | CT | 33 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0142 others(30): Show |
34 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.112+3342dupT | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 113230283 | ||||||
| chr12:113230283 | C | CTTT | 25 | a0001c0001t0002g0005 a0001c0001t0002g0206 a0001c0001t0002g0207 others(22): Show |
26 | HG02055.hp1 HG02080.hp2 HG02083.hp2 others(23): Show |
intron_variant | MODIFIER | c.112+3340_112+3342d others(5): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 113230283 | ||||||
| chr12:113230283 | CT | C | 9 | a0001c0001t0001g0009 a0001c0001t0001g0024 a0001c0001t0001g0066 others(6): Show |
9 | HG00438.hp2 HG01517.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.112+3342delT | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 113230283 | ||||||
| chr12:113230302 | T | C | 6 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(3): Show |
8 | HG02280.hp1 HG02451.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.112+3338T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113230302 | |||||||
| chr12:113230327 | C | CA | 27 | a0001c0001t0002g0005 a0001c0001t0002g0206 a0001c0001t0002g0207 others(24): Show |
28 | HG00280.hp2 HG01168.hp2 HG02080.hp2 others(25): Show |
intron_variant | MODIFIER | c.112+3364dupA | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 113230327 | ||||||
| chr12:113230398 | C | T | 1 | a0001c0001t0017g0138 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.112+3434C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113230398 | |||||||
| chr12:113230455 | A | G | 38 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(35): Show |
40 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.112+3491A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113230455 | |||||||
| chr12:113230690 | G | A | 1 | a0001c0001t0003g0188 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.112+3726G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113230690 | |||||||
| chr12:113230866 | A | G | 24 | a0001c0001t0002g0005 a0001c0001t0002g0206 a0001c0001t0002g0207 others(21): Show |
25 | HG02080.hp2 HG02083.hp2 HG02155.hp2 others(22): Show |
intron_variant | MODIFIER | c.112+3902A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113230866 | |||||||
| chr12:113231057 | G | A | 3 | a0001c0002t0009g0054 a0001c0002t0009g0055 a0001c0002t0009g0056 |
3 | HG02717.hp2 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.112+4093G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113231057 | |||||||
| chr12:113231058 | C | T | 6 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(3): Show |
8 | HG02280.hp1 HG02451.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.112+4094C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113231058 | |||||||
| chr12:113231103 | G | A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 |
3 | NA18960.hp2 NA18968.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.112+4139G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113231103 | |||||||
| chr12:113231218 | A | G | 1 | a0001c0001t0003g0016 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.112+4254A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113231218 | |||||||
| chr12:113231262 | C | G | 1 | a0001c0001t0004g0153 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.112+4298C>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113231262 | |||||||
| chr12:113231409 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.112+4445G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113231409 | |||||||
| chr12:113231532 | T | C | 5 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0178 others(2): Show |
5 | HG02809.hp2 HG02886.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.112+4568T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113231532 | |||||||
| chr12:113231712 | A | T | 1 | a0001c0002t0009g0056 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.112+4748A>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113231712 | |||||||
| chr12:113231731 | C | G | 37 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(34): Show |
39 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.112+4767C>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113231731 | |||||||
| chr12:113231823 | G | C | 2 | a0001c0001t0002g0207 a0001c0001t0002g0208 |
2 | NA18946.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.112+4859G>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113231823 | |||||||
| chr12:113231877 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.112+4913G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113231877 | |||||||
| chr12:113231910 | C | T | 1 | a0001c0001t0003g0016 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.112+4946C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113231910 | |||||||
| chr12:113232097 | G | A | 27 | a0001c0001t0002g0005 a0001c0001t0002g0206 a0001c0001t0002g0207 others(24): Show |
28 | HG00280.hp2 HG01168.hp2 HG02080.hp2 others(25): Show |
intron_variant | MODIFIER | c.112+5133G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113232097 | |||||||
| chr12:113232150 | G | A | 1 | a0001c0001t0003g0016 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.112+5186G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113232150 | |||||||
| chr12:113232231 | C | T | 3 | a0001c0001t0001g0178 a0001c0001t0003g0016 a0001c0002t0009g0055 |
3 | HG03139.hp2 HG03486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.112+5267C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113232231 | |||||||
| chr12:113232451 | G | A | 2 | a0001c0001t0002g0177 a0001c0001t0006g0176 |
2 | HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.112+5487G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113232451 | |||||||
| chr12:113232900 | C | T | 1 | a0001c0001t0002g0048 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.112+5936C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113232900 | |||||||
| chr12:113232966 | C | T | 1 | a0001c0001t0017g0138 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.112+6002C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113232966 | |||||||
| chr12:113232985 | C | T | 1 | a0001c0001t0003g0016 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.112+6021C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113232985 | |||||||
| chr12:113232998 | T | C | 6 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(3): Show |
8 | HG02280.hp1 HG02451.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.112+6034T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113232998 | |||||||
| chr12:113233065 | G | A | 6 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(3): Show |
8 | HG02280.hp1 HG02451.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.112+6101G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113233065 | |||||||
| chr12:113233083 | G | A | 2 | a0001c0001t0001g0073 a0001c0001t0007g0072 |
2 | HG00099.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.112+6119G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113233083 | |||||||
| chr12:113233336 | C | G | 27 | a0001c0001t0002g0005 a0001c0001t0002g0206 a0001c0001t0002g0207 others(24): Show |
28 | HG00280.hp2 HG01168.hp2 HG02080.hp2 others(25): Show |
intron_variant | MODIFIER | c.112+6372C>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113233336 | |||||||
| chr12:113233372 | C | T | 1 | a0001c0012t0001g0201 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.112+6408C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113233372 | |||||||
| chr12:113233384 | A | G | 27 | a0001c0001t0002g0005 a0001c0001t0002g0206 a0001c0001t0002g0207 others(24): Show |
28 | HG00280.hp2 HG01168.hp2 HG02080.hp2 others(25): Show |
intron_variant | MODIFIER | c.112+6420A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113233384 | |||||||
| chr12:113233413 | G | C | 4 | a0001c0001t0006g0202 a0001c0001t0006g0205 a0001c0008t0006g0203 others(1): Show |
4 | HG01891.hp1 HG02055.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+6449G>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113233413 | |||||||
| chr12:113233418 | G | A | 1 | a0001c0001t0002g0209 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.112+6454G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113233418 | |||||||
| chr12:113233480 | A | T | 3 | a0001c0007t0002g0058 a0001c0007t0011g0174 a0001c0013t0011g0173 |
3 | HG02572.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.112+6516A>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113233480 | |||||||
| chr12:113233606 | G | T | 1 | a0001c0001t0003g0016 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.112+6642G>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113233606 | |||||||
| chr12:113233689 | C | T | 27 | a0001c0001t0002g0005 a0001c0001t0002g0206 a0001c0001t0002g0207 others(24): Show |
28 | HG00280.hp2 HG01168.hp2 HG02080.hp2 others(25): Show |
intron_variant | MODIFIER | c.112+6725C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113233689 | |||||||
| chr12:113233707 | C | T | 6 | a0001c0001t0003g0179 a0001c0001t0003g0180 a0001c0001t0003g0181 others(3): Show |
6 | HG00140.hp1 HG00323.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.112+6743C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113233707 | |||||||
| chr12:113233722 | G | A | 37 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(34): Show |
39 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.112+6758G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113233722 | |||||||
| chr12:113233926 | C | T | 1 | a0001c0001t0002g0047 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.112+6962C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113233926 | |||||||
| chr12:113233995 | T | C | 1 | a0001c0001t0004g0074 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.112+7031T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113233995 | |||||||
| chr12:113234129 | G | A | 2 | a0001c0001t0001g0172 a0001c0001t0003g0171 |
2 | HG01884.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.112+7165G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113234129 | |||||||
| chr12:113234209 | T | C | 3 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 |
3 | NA18960.hp2 NA18968.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.112+7245T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113234209 | |||||||
| chr12:113234420 | G | A | 3 | a0001c0007t0002g0058 a0001c0007t0011g0174 a0001c0013t0011g0173 |
3 | HG02572.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.112+7456G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113234420 | |||||||
| chr12:113234564 | C | T | 3 | a0001c0007t0002g0058 a0001c0007t0011g0174 a0001c0013t0011g0173 |
3 | HG02572.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.112+7600C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113234564 | |||||||
| chr12:113234707 | C | T | 1 | a0001c0001t0003g0016 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.112+7743C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113234707 | |||||||
| chr12:113234721 | G | T | 1 | a0001c0001t0004g0137 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.112+7757G>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113234721 | |||||||
| chr12:113234772 | T | C | 111 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(108): Show |
116 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.112+7808T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113234772 | |||||||
| chr12:113234975 | G | A | 4 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(1): Show |
4 | HG02559.hp2 NA18960.hp2 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.112+8011G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113234975 | |||||||
| chr12:113235059 | C | T | 4 | a0001c0001t0001g0135 a0001c0001t0003g0014 a0001c0001t0003g0059 others(1): Show |
5 | HG01109.hp2 HG03209.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.112+8095C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113235059 | |||||||
| chr12:113235329 | G | A | 32 | a0001c0001t0001g0015 a0001c0001t0002g0003 a0001c0001t0002g0006 others(29): Show |
34 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(31): Show |
intron_variant | MODIFIER | c.112+8365G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113235329 | |||||||
| chr12:113235351 | G | A | 32 | a0001c0001t0001g0015 a0001c0001t0002g0003 a0001c0001t0002g0006 others(29): Show |
34 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(31): Show |
intron_variant | MODIFIER | c.112+8387G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113235351 | |||||||
| chr12:113235382 | C | T | 6 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(3): Show |
8 | HG02280.hp1 HG02451.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.112+8418C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113235382 | |||||||
| chr12:113235470 | C | G | 6 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(3): Show |
8 | HG02280.hp1 HG02451.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.112+8506C>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113235470 | |||||||
| chr12:113235507 | T | TA | 22 | a0001c0001t0002g0005 a0001c0001t0002g0206 a0001c0001t0002g0207 others(19): Show |
23 | HG01168.hp2 HG02080.hp2 HG02083.hp2 others(20): Show |
intron_variant | MODIFIER | c.112+8557dupA | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 113235507 | ||||||
| chr12:113235507 | TA | T | 21 | a0001c0001t0001g0169 a0001c0001t0001g0184 a0001c0001t0002g0023 others(18): Show |
21 | HG00280.hp2 HG02055.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.112+8557delA | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 113235507 | ||||||
| chr12:113235749 | G | C | 4 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(1): Show |
4 | HG02559.hp2 NA18960.hp2 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.112+8785G>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113235749 | |||||||
| chr12:113236012 | G | C | 1 | a0001c0001t0001g0178 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.112+9048G>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113236012 | |||||||
| chr12:113236157 | G | A | 2 | a0001c0001t0001g0066 a0001c0001t0004g0076 |
2 | HG00639.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.112+9193G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113236157 | |||||||
| chr12:113236241 | A | G | 3 | a0001c0002t0009g0054 a0001c0002t0009g0055 a0001c0002t0009g0056 |
3 | HG02717.hp2 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.112+9277A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113236241 | |||||||
| chr12:113236407 | C | G | 82 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(79): Show |
87 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.112+9443C>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113236407 | |||||||
| chr12:113236620 | G | T | 3 | a0001c0007t0002g0058 a0001c0007t0011g0174 a0001c0013t0011g0173 |
3 | HG02572.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.112+9656G>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113236620 | |||||||
| chr12:113236656 | C | T | 109 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(106): Show |
114 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.112+9692C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113236656 | |||||||
| chr12:113236668 | C | T | 1 | a0001c0001t0002g0220 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.112+9704C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113236668 | |||||||
| chr12:113236711 | G | C | 1 | a0001c0001t0004g0077 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.112+9747G>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113236711 | |||||||
| chr12:113236932 | T | C | 1 | a0001c0001t0001g0026 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.112+9968T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113236932 | |||||||
| chr12:113237359 | CT | C | 44 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(41): Show |
48 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.112+10407delT | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 113237359 | ||||||
| chr12:113237511 | C | T | 1 | a0001c0001t0003g0197 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.112+10547C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113237511 | |||||||
| chr12:113237512 | G | A | 82 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(79): Show |
87 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.112+10548G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113237512 | |||||||
| chr12:113237699 | A | G | 1 | a0001c0003t0008g0227 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.112+10735A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113237699 | |||||||
| chr12:113237911 | C | T | 5 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0178 others(2): Show |
5 | HG02809.hp2 HG02886.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.112+10947C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113237911 | |||||||
| chr12:113238063 | C | T | 1 | a0001c0001t0001g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.112+11099C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113238063 | |||||||
| chr12:113238150 | C | G | 1 | a0001c0001t0003g0186 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.112+11186C>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113238150 | |||||||
| chr12:113238153 | A | G | 38 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(35): Show |
40 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.112+11189A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113238153 | |||||||
| chr12:113238371 | T | C | 1 | a0001c0013t0011g0173 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.112+11407T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113238371 | |||||||
| chr12:113238467 | TAG | T | 3 | a0001c0003t0008g0200 a0001c0003t0008g0226 a0001c0003t0008g0227 |
3 | HG00280.hp2 HG01168.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.112+11506_112+1150 others(6): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 113238467 | ||||||
| chr12:113238546 | C | T | 3 | a0001c0007t0002g0058 a0001c0007t0011g0174 a0001c0013t0011g0173 |
3 | HG02572.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.112+11582C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113238546 | |||||||
| chr12:113238637 | C | G | 1 | a0001c0007t0011g0174 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.112+11673C>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113238637 | |||||||
| chr12:113238858 | G | A | 3 | a0001c0007t0002g0058 a0001c0007t0011g0174 a0001c0013t0011g0173 |
3 | HG02572.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.112+11894G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113238858 | |||||||
| chr12:113239001 | G | A | 1 | a0001c0013t0011g0173 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.112+12037G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113239001 | |||||||
| chr12:113239073 | G | A | 1 | a0001c0001t0002g0210 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.112+12109G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113239073 | |||||||
| chr12:113239198 | G | C | 2 | a0001c0001t0003g0185 a0001c0001t0012g0175 |
2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.112+12234G>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113239198 | |||||||
| chr12:113239274 | C | T | 37 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(34): Show |
39 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.112+12310C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113239274 | |||||||
| chr12:113239512 | A | G | 1 | a0001c0001t0017g0138 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.112+12548A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113239512 | |||||||
| chr12:113239646 | C | T | 76 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(73): Show |
79 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.112+12682C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113239646 | |||||||
| chr12:113239657 | C | T | 1 | a0001c0001t0006g0205 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.112+12693C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113239657 | |||||||
| chr12:113239729 | C | T | 1 | a0001c0007t0002g0058 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.112+12765C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113239729 | |||||||
| chr12:113239738 | C | G | 3 | a0001c0002t0009g0054 a0001c0002t0009g0055 a0001c0002t0009g0056 |
3 | HG02717.hp2 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.112+12774C>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113239738 | |||||||
| chr12:113239750 | C | T | 5 | a0001c0001t0001g0071 a0001c0001t0001g0133 a0001c0001t0001g0134 others(2): Show |
5 | HG02071.hp1 HG02080.hp1 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.112+12786C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113239750 | |||||||
| chr12:113239794 | C | T | 3 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 |
3 | NA18961.hp1 NA18971.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.112+12830C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113239794 | |||||||
| chr12:113239803 | A | G | 1 | a0001c0008t0006g0203 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.112+12839A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113239803 | |||||||
| chr12:113239865 | T | A | 6 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(3): Show |
8 | HG02280.hp1 HG02451.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.112+12901T>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113239865 | |||||||
| chr12:113240006 | A | G | 4 | a0001c0001t0006g0202 a0001c0001t0006g0205 a0001c0008t0006g0203 others(1): Show |
4 | HG01891.hp1 HG02055.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+13042A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113240006 | |||||||
| chr12:113240011 | T | C | 2 | a0001c0001t0002g0177 a0001c0001t0006g0176 |
2 | HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.112+13047T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113240011 | |||||||
| chr12:113240028 | G | C | 2 | a0001c0001t0004g0145 a0001c0001t0004g0170 |
2 | HG00408.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.112+13064G>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113240028 | |||||||
| chr12:113240247 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.112+13283G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113240247 | |||||||
| chr12:113240318 | G | A | 1 | a0001c0001t0001g0146 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.112+13354G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113240318 | |||||||
| chr12:113240325 | T | C | 1 | a0001c0001t0006g0205 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.112+13361T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113240325 | |||||||
| chr12:113240326 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.112+13362A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113240326 | |||||||
| chr12:113240383 | G | A | 32 | a0001c0001t0001g0015 a0001c0001t0002g0003 a0001c0001t0002g0006 others(29): Show |
34 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(31): Show |
intron_variant | MODIFIER | c.112+13419G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113240383 | |||||||
| chr12:113240384 | C | T | 16 | a0001c0001t0001g0184 a0001c0001t0003g0185 a0001c0001t0003g0187 others(13): Show |
16 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.112+13420C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113240384 | |||||||
| chr12:113240385 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.112+13421G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113240385 | |||||||
| chr12:113240586 | G | A | 27 | a0001c0001t0002g0005 a0001c0001t0002g0206 a0001c0001t0002g0207 others(24): Show |
28 | HG00280.hp2 HG01168.hp2 HG02080.hp2 others(25): Show |
intron_variant | MODIFIER | c.112+13622G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113240586 | |||||||
| chr12:113240699 | G | T | 3 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 |
3 | NA18960.hp2 NA18968.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.112+13735G>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113240699 | |||||||
| chr12:113240747 | CT | C | 53 | a0001c0001t0001g0015 a0001c0001t0001g0078 a0001c0001t0001g0080 others(50): Show |
55 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.112+13801delT | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 113240747 | ||||||
| chr12:113240747 | CTT | C | 21 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(18): Show |
22 | HG01891.hp1 HG02055.hp1 HG02071.hp2 others(19): Show |
intron_variant | MODIFIER | c.112+13800_112+1380 others(6): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 113240747 | ||||||
| chr12:113240934 | T | TG | 3 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0061 |
5 | NA18943.hp1 NA18951.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.112+13974dupG | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 113240934 | ||||||
| chr12:113240948 | G | A | 1 | a0001c0001t0006g0202 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.112+13984G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113240948 | |||||||
| chr12:113240986 | A | T | 76 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(73): Show |
79 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.112+14022A>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113240986 | |||||||
| chr12:113241269 | C | T | 6 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(3): Show |
8 | HG02280.hp1 HG02451.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.112+14305C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113241269 | |||||||
| chr12:113241290 | T | C | 87 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(84): Show |
92 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.112+14326T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113241290 | |||||||
| chr12:113241338 | C | T | 4 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 others(1): Show |
4 | HG01081.hp2 HG01978.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+14374C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113241338 | |||||||
| chr12:113241347 | G | A | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.112+14383G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113241347 | |||||||
| chr12:113241352 | C | T | 1 | a0001c0001t0003g0186 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.112+14388C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113241352 | |||||||
| chr12:113241353 | TGCA | T | 75 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(72): Show |
78 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.112+14406_112+1440 others(7): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 113241353 | ||||||
| chr12:113241508 | A | G | 4 | a0001c0001t0001g0135 a0001c0001t0003g0014 a0001c0001t0003g0059 others(1): Show |
5 | HG01109.hp2 HG03209.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.112+14544A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113241508 | |||||||
| chr12:113241709 | G | A | 38 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(35): Show |
40 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.112+14745G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113241709 | |||||||
| chr12:113241731 | T | C | 3 | a0001c0004t0002g0022 a0001c0004t0002g0033 a0001c0004t0002g0034 |
3 | NA18974.hp1 NA19074.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.112+14767T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113241731 | |||||||
| chr12:113241751 | C | T | 3 | a0001c0007t0002g0058 a0001c0007t0011g0174 a0001c0013t0011g0173 |
3 | HG02572.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.112+14787C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113241751 | |||||||
| chr12:113241761 | C | CGT | 46 | a0001c0001t0001g0060 a0001c0001t0001g0065 a0001c0001t0001g0066 others(43): Show |
47 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(44): Show |
intron_variant | MODIFIER | c.112+14829_112+1483 others(6): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 113241761 | ||||||
| chr12:113241761 | C | CGTGT | 22 | a0001c0001t0001g0013 a0001c0001t0001g0070 a0001c0001t0001g0080 others(19): Show |
23 | HG00408.hp2 HG01168.hp1 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.112+14827_112+1483 others(8): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 113241761 | ||||||
| chr12:113241761 | C | CGTGTGT | 14 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(11): Show |
14 | HG00280.hp1 HG02083.hp2 HG02155.hp2 others(11): Show |
intron_variant | MODIFIER | c.112+14825_112+1483 others(10): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 113241761 | ||||||
| chr12:113241761 | C | CGTGTGTG others(1): Show |
15 | a0001c0001t0002g0005 a0001c0001t0002g0206 a0001c0001t0002g0210 others(12): Show |
16 | HG02080.hp2 HG03195.hp1 HG03486.hp1 others(13): Show |
intron_variant | MODIFIER | c.112+14823_112+1483 others(12): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 113241761 | ||||||
| chr12:113241761 | C | CGTGTGTG others(3): Show |
2 | a0001c0001t0003g0002 a0001c0001t0003g0018 |
4 | HG02280.hp1 HG02451.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+14821_112+1483 others(14): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 113241761 | ||||||
| chr12:113241761 | C | CGTGTGTG others(5): Show |
1 | a0001c0001t0003g0021 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.112+14819_112+1483 others(16): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 113241761 | ||||||
| chr12:113241761 | C | T | 3 | a0001c0007t0002g0058 a0001c0007t0011g0174 a0001c0013t0011g0173 |
3 | HG02572.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.112+14797C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113241761 | |||||||
| chr12:113241761 | CGT | C | 22 | a0001c0001t0001g0015 a0001c0001t0001g0135 a0001c0001t0001g0152 others(19): Show |
23 | HG00408.hp1 HG02027.hp1 HG02027.hp2 others(20): Show |
intron_variant | MODIFIER | c.112+14829_112+1483 others(6): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 113241761 | ||||||
| chr12:113241761 | CGTGT | C | 20 | a0001c0001t0001g0010 a0001c0001t0001g0024 a0001c0001t0001g0025 others(17): Show |
22 | HG02071.hp2 HG02155.hp1 HG02809.hp2 others(19): Show |
intron_variant | MODIFIER | c.112+14827_112+1483 others(8): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 113241761 | ||||||
| chr12:113241761 | CGTGTGT | C | 6 | a0001c0001t0002g0047 a0001c0001t0002g0049 a0001c0001t0006g0202 others(3): Show |
6 | HG00438.hp1 HG01891.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.112+14825_112+1483 others(10): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 113241761 | ||||||
| chr12:113241793 | T | TGTGTGTG others(5): Show |
1 | a0001c0003t0008g0227 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.112+14830_112+1483 others(16): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 113241793 | ||||||
| chr12:113241793 | T | TGTGTGTG others(9): Show |
1 | a0001c0003t0008g0226 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.112+14830_112+1483 others(20): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 113241793 | ||||||
| chr12:113241793 | T | TGTGTGTG others(11): Show |
1 | a0001c0003t0008g0200 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.112+14830_112+1483 others(22): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 113241793 | ||||||
| chr12:113241880 | C | A | 1 | a0001c0001t0007g0064 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.112+14916C>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113241880 | |||||||
| chr12:113242175 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.112+15211C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113242175 | |||||||
| chr12:113242211 | A | G | 24 | a0001c0001t0002g0005 a0001c0001t0002g0206 a0001c0001t0002g0207 others(21): Show |
25 | HG02080.hp2 HG02083.hp2 HG02155.hp2 others(22): Show |
intron_variant | MODIFIER | c.112+15247A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113242211 | |||||||
| chr12:113242216 | G | T | 1 | a0001c0001t0001g0117 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.112+15252G>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113242216 | |||||||
| chr12:113242365 | C | A | 32 | a0001c0001t0001g0015 a0001c0001t0002g0003 a0001c0001t0002g0006 others(29): Show |
34 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(31): Show |
intron_variant | MODIFIER | c.112+15401C>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113242365 | |||||||
| chr12:113242395 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.112+15431A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113242395 | |||||||
| chr12:113242462 | G | T | 32 | a0001c0001t0001g0015 a0001c0001t0002g0003 a0001c0001t0002g0006 others(29): Show |
34 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(31): Show |
intron_variant | MODIFIER | c.112+15498G>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113242462 | |||||||
| chr12:113242699 | C | CT | 45 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(42): Show |
47 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.112+15736dupT | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 113242699 | ||||||
| chr12:113242721 | T | G | 1 | a0001c0001t0002g0223 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.112+15757T>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113242721 | |||||||
| chr12:113242742 | A | G | 76 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(73): Show |
79 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.112+15778A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113242742 | |||||||
| chr12:113242790 | A | G | 3 | a0001c0002t0009g0054 a0001c0002t0009g0055 a0001c0002t0009g0056 |
3 | HG02717.hp2 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.112+15826A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113242790 | |||||||
| chr12:113242939 | A | C | 1 | a0001c0001t0021g0053 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.112+15975A>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113242939 | |||||||
| chr12:113243081 | T | A | 1 | a0001c0001t0004g0076 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.112+16117T>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113243081 | |||||||
| chr12:113243324 | C | T | 28 | a0001c0001t0002g0005 a0001c0001t0002g0206 a0001c0001t0002g0207 others(25): Show |
29 | HG00280.hp2 HG01168.hp2 HG02080.hp2 others(26): Show |
intron_variant | MODIFIER | c.112+16360C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113243324 | |||||||
| chr12:113243362 | C | T | 82 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(79): Show |
87 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.112+16398C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113243362 | |||||||
| chr12:113243369 | C | CA | 28 | a0001c0001t0002g0005 a0001c0001t0002g0206 a0001c0001t0002g0207 others(25): Show |
29 | HG00280.hp2 HG01168.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.112+16418dupA | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 113243369 | ||||||
| chr12:113243369 | C | CAA | 49 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(46): Show |
53 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.112+16417_112+1641 others(6): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 113243369 | ||||||
| chr12:113243400 | T | G | 3 | a0001c0007t0002g0058 a0001c0007t0011g0174 a0001c0013t0011g0173 |
3 | HG02572.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.112+16436T>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113243400 | |||||||
| chr12:113243428 | T | C | 1 | a0001c0007t0002g0058 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.112+16464T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113243428 | |||||||
| chr12:113243454 | A | C | 38 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(35): Show |
40 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.112+16490A>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113243454 | |||||||
| chr12:113243483 | A | G | 82 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(79): Show |
87 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.112+16519A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113243483 | |||||||
| chr12:113243520 | G | A | 2 | a0001c0001t0004g0118 a0001c0001t0014g0100 |
2 | HG01361.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.112+16556G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113243520 | |||||||
| chr12:113243769 | AAAAATAA others(4): Show |
A | 28 | a0001c0001t0002g0005 a0001c0001t0002g0206 a0001c0001t0002g0207 others(25): Show |
29 | HG00280.hp2 HG01168.hp2 HG02080.hp2 others(26): Show |
intron_variant | MODIFIER | c.113-16588_113-1657 others(15): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 113243769 | ||||||
| chr12:113243794 | T | A | 82 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(79): Show |
87 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.113-16574T>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113243794 | |||||||
| chr12:113243806 | T | G | 1 | a0001c0001t0001g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.113-16562T>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113243806 | |||||||
| chr12:113243836 | G | A | 32 | a0001c0001t0001g0015 a0001c0001t0002g0003 a0001c0001t0002g0006 others(29): Show |
34 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(31): Show |
intron_variant | MODIFIER | c.113-16532G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113243836 | |||||||
| chr12:113243933 | T | C | 1 | a0001c0001t0004g0081 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.113-16435T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113243933 | |||||||
| chr12:113244039 | C | G | 47 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(44): Show |
49 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.113-16329C>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113244039 | |||||||
| chr12:113244083 | G | A | 1 | a0001c0012t0001g0201 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.113-16285G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113244083 | |||||||
| chr12:113244147 | C | T | 13 | a0001c0001t0003g0187 a0001c0001t0003g0188 a0001c0001t0003g0189 others(10): Show |
13 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.113-16221C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113244147 | |||||||
| chr12:113244225 | T | C | 89 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(86): Show |
94 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.113-16143T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113244225 | |||||||
| chr12:113244243 | C | T | 1 | a0001c0001t0001g0020 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.113-16125C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113244243 | |||||||
| chr12:113244244 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.113-16124G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113244244 | |||||||
| chr12:113244427 | G | A | 2 | a0001c0001t0001g0082 a0001c0001t0007g0083 |
2 | HG03942.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.113-15941G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113244427 | |||||||
| chr12:113244484 | G | A | 1 | a0001c0001t0002g0220 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.113-15884G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113244484 | |||||||
| chr12:113244581 | C | T | 4 | a0001c0001t0006g0202 a0001c0001t0006g0205 a0001c0008t0006g0203 others(1): Show |
4 | HG01891.hp1 HG02055.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-15787C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113244581 | |||||||
| chr12:113244665 | G | A | 6 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(3): Show |
8 | HG02280.hp1 HG02451.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.113-15703G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113244665 | |||||||
| chr12:113244725 | G | A | 2 | a0001c0007t0011g0174 a0001c0013t0011g0173 |
2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.113-15643G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113244725 | |||||||
| chr12:113245061 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.113-15307C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113245061 | |||||||
| chr12:113245103 | C | T | 3 | a0001c0007t0002g0058 a0001c0007t0011g0174 a0001c0013t0011g0173 |
3 | HG02572.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.113-15265C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113245103 | |||||||
| chr12:113245205 | G | C | 2 | a0001c0001t0002g0177 a0001c0001t0006g0176 |
2 | HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.113-15163G>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113245205 | |||||||
| chr12:113245223 | C | T | 38 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(35): Show |
40 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.113-15145C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113245223 | |||||||
| chr12:113245306 | TAGAAAAG others(312): Show |
T | 82 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(79): Show |
87 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.113-15051_113-1473 others(4): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 113245306 | ||||||
| chr12:113245312 | A | G | 22 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0069 others(19): Show |
23 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(20): Show |
intron_variant | MODIFIER | c.113-15056A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113245312 | |||||||
| chr12:113245336 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.113-15032G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113245336 | |||||||
| chr12:113245379 | C | T | 1 | a0001c0001t0001g0069 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.113-14989C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113245379 | |||||||
| chr12:113245425 | G | A | 5 | a0001c0001t0005g0067 a0001c0001t0005g0093 a0001c0001t0005g0095 others(2): Show |
5 | NA18942.hp2 NA18950.hp2 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.113-14943G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113245425 | |||||||
| chr12:113245493 | C | T | 1 | a0001c0001t0003g0180 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.113-14875C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113245493 | |||||||
| chr12:113245506 | C | T | 1 | a0001c0001t0003g0196 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.113-14862C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113245506 | |||||||
| chr12:113245600 | C | CA | 11 | a0001c0001t0001g0060 a0001c0001t0001g0068 a0001c0001t0001g0069 others(8): Show |
11 | HG00099.hp1 HG01358.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.113-14747dupA | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 113245600 | ||||||
| chr12:113245622 | G | A | 5 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0178 others(2): Show |
5 | HG02809.hp2 HG02886.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.113-14746G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113245622 | |||||||
| chr12:113245660 | T | C | 2 | a0001c0007t0011g0174 a0001c0013t0011g0173 |
2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.113-14708T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113245660 | |||||||
| chr12:113245674 | C | A | 1 | a0001c0001t0017g0138 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.113-14694C>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113245674 | |||||||
| chr12:113245681 | T | C | 1 | a0001c0001t0021g0053 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.113-14687T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113245681 | |||||||
| chr12:113245699 | C | T | 1 | a0001c0001t0003g0183 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.113-14669C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113245699 | |||||||
| chr12:113246012 | G | A | 1 | a0001c0001t0001g0161 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.113-14356G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113246012 | |||||||
| chr12:113246039 | G | A | 1 | a0001c0001t0002g0220 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.113-14329G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113246039 | |||||||
| chr12:113246050 | G | T | 1 | a0001c0001t0003g0016 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.113-14318G>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113246050 | |||||||
| chr12:113246088 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.113-14280C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113246088 | |||||||
| chr12:113246217 | C | T | 1 | a0001c0007t0002g0058 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.113-14151C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113246217 | |||||||
| chr12:113246585 | G | C | 1 | a0001c0001t0001g0084 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.113-13783G>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113246585 | |||||||
| chr12:113246677 | C | T | 1 | a0001c0001t0002g0222 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.113-13691C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113246677 | |||||||
| chr12:113246838 | G | A | 1 | a0001c0012t0001g0201 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.113-13530G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113246838 | |||||||
| chr12:113246887 | G | A | 1 | a0001c0001t0001g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.113-13481G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113246887 | |||||||
| chr12:113246906 | C | T | 5 | a0001c0001t0001g0071 a0001c0001t0001g0133 a0001c0001t0001g0134 others(2): Show |
5 | HG02071.hp1 HG02080.hp1 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.113-13462C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113246906 | |||||||
| chr12:113246966 | G | C | 1 | a0001c0001t0001g0178 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.113-13402G>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113246966 | |||||||
| chr12:113247072 | A | G | 24 | a0001c0001t0002g0005 a0001c0001t0002g0206 a0001c0001t0002g0207 others(21): Show |
25 | HG02080.hp2 HG02083.hp2 HG02155.hp2 others(22): Show |
intron_variant | MODIFIER | c.113-13296A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113247072 | |||||||
| chr12:113247214 | C | T | 3 | a0001c0001t0001g0102 a0001c0001t0001g0116 a0001c0001t0018g0124 |
3 | HG02280.hp2 HG02647.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.113-13154C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113247214 | |||||||
| chr12:113247215 | G | A | 4 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(1): Show |
4 | HG02572.hp2 HG02897.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.113-13153G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113247215 | |||||||
| chr12:113247309 | C | T | 38 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(35): Show |
40 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.113-13059C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113247309 | |||||||
| chr12:113247561 | G | A | 3 | a0001c0003t0008g0200 a0001c0003t0008g0226 a0001c0003t0008g0227 |
3 | HG00280.hp2 HG01168.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.113-12807G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113247561 | |||||||
| chr12:113247611 | G | A | 1 | a0001c0012t0001g0201 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.113-12757G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113247611 | |||||||
| chr12:113247618 | C | T | 4 | a0001c0001t0006g0202 a0001c0001t0006g0205 a0001c0008t0006g0203 others(1): Show |
4 | HG01891.hp1 HG02055.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-12750C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113247618 | |||||||
| chr12:113247658 | G | A | 1 | a0001c0001t0004g0077 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.113-12710G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113247658 | |||||||
| chr12:113247976 | C | G | 10 | a0001c0001t0006g0202 a0001c0001t0006g0205 a0001c0002t0009g0054 others(7): Show |
10 | HG01891.hp1 HG02055.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.113-12392C>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113247976 | |||||||
| chr12:113248170 | C | T | 1 | a0001c0001t0003g0183 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.113-12198C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113248170 | |||||||
| chr12:113248485 | G | A | 1 | a0001c0007t0002g0058 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.113-11883G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113248485 | |||||||
| chr12:113248523 | A | G | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.113-11845A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113248523 | |||||||
| chr12:113248736 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.113-11632G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113248736 | |||||||
| chr12:113248739 | C | T | 3 | a0001c0002t0009g0054 a0001c0002t0009g0055 a0001c0002t0009g0056 |
3 | HG02717.hp2 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.113-11629C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113248739 | |||||||
| chr12:113248788 | T | A | 76 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(73): Show |
79 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.113-11580T>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113248788 | |||||||
| chr12:113248801 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.113-11567A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113248801 | |||||||
| chr12:113249096 | T | C | 1 | a0001c0008t0006g0204 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.113-11272T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113249096 | |||||||
| chr12:113249233 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.113-11135G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113249233 | |||||||
| chr12:113249545 | G | C | 3 | a0001c0007t0002g0058 a0001c0007t0011g0174 a0001c0013t0011g0173 |
3 | HG02572.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.113-10823G>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113249545 | |||||||
| chr12:113249689 | C | T | 3 | a0001c0002t0009g0054 a0001c0002t0009g0055 a0001c0002t0009g0056 |
3 | HG02717.hp2 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.113-10679C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113249689 | |||||||
| chr12:113249722 | C | T | 1 | a0002c0009t0001g0115 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.113-10646C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113249722 | |||||||
| chr12:113249747 | C | G | 37 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(34): Show |
39 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.113-10621C>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113249747 | |||||||
| chr12:113249872 | C | T | 3 | a0001c0007t0002g0058 a0001c0007t0011g0174 a0001c0013t0011g0173 |
3 | HG02572.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.113-10496C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113249872 | |||||||
| chr12:113249899 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.113-10469G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113249899 | |||||||
| chr12:113249931 | C | T | 1 | a0001c0001t0002g0044 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.113-10437C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113249931 | |||||||
| chr12:113249984 | A | T | 76 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(73): Show |
79 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.113-10384A>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113249984 | |||||||
| chr12:113250054 | A | G | 29 | a0001c0001t0001g0135 a0001c0001t0002g0005 a0001c0001t0002g0206 others(26): Show |
30 | HG00280.hp2 HG01168.hp2 HG02080.hp2 others(27): Show |
intron_variant | MODIFIER | c.113-10314A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113250054 | |||||||
| chr12:113250145 | C | A | 2 | a0001c0001t0002g0207 a0001c0001t0002g0208 |
2 | NA18946.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.113-10223C>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113250145 | |||||||
| chr12:113250183 | C | T | 24 | a0001c0001t0002g0005 a0001c0001t0002g0206 a0001c0001t0002g0207 others(21): Show |
25 | HG02080.hp2 HG02083.hp2 HG02155.hp2 others(22): Show |
intron_variant | MODIFIER | c.113-10185C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113250183 | |||||||
| chr12:113250692 | C | T | 1 | a0001c0001t0002g0050 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.113-9676C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113250692 | |||||||
| chr12:113250783 | C | T | 1 | a0001c0001t0005g0099 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.113-9585C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113250783 | |||||||
| chr12:113250829 | G | A | 1 | a0001c0012t0001g0201 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.113-9539G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113250829 | |||||||
| chr12:113250863 | G | A | 4 | a0001c0001t0006g0202 a0001c0001t0006g0205 a0001c0008t0006g0203 others(1): Show |
4 | HG01891.hp1 HG02055.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-9505G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113250863 | |||||||
| chr12:113250963 | CA | C | 77 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(74): Show |
80 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.113-9395delA | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 113250963 | ||||||
| chr12:113251139 | C | CA | 24 | a0001c0001t0001g0152 a0001c0001t0001g0184 a0001c0001t0003g0179 others(21): Show |
24 | HG00140.hp1 HG00323.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.113-9217dupA | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 113251139 | ||||||
| chr12:113251282 | A | T | 1 | a0001c0001t0003g0186 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.113-9086A>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113251282 | |||||||
| chr12:113251325 | C | T | 1 | a0001c0001t0001g0026 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.113-9043C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113251325 | |||||||
| chr12:113251326 | G | A | 2 | a0001c0001t0002g0177 a0001c0001t0006g0176 |
2 | HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.113-9042G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113251326 | |||||||
| chr12:113251401 | C | T | 4 | a0001c0001t0006g0202 a0001c0001t0006g0205 a0001c0008t0006g0203 others(1): Show |
4 | HG01891.hp1 HG02055.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-8967C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113251401 | |||||||
| chr12:113251438 | A | G | 1 | a0001c0001t0001g0178 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.113-8930A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113251438 | |||||||
| chr12:113251478 | C | T | 4 | a0001c0001t0006g0202 a0001c0001t0006g0205 a0001c0008t0006g0203 others(1): Show |
4 | HG01891.hp1 HG02055.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-8890C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113251478 | |||||||
| chr12:113251642 | C | T | 1 | a0001c0001t0004g0098 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.113-8726C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113251642 | |||||||
| chr12:113251655 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.113-8713G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113251655 | |||||||
| chr12:113251785 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.113-8583C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113251785 | |||||||
| chr12:113251860 | G | T | 4 | a0001c0001t0006g0202 a0001c0001t0006g0205 a0001c0008t0006g0203 others(1): Show |
4 | HG01891.hp1 HG02055.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-8508G>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113251860 | |||||||
| chr12:113251903 | G | A | 1 | a0001c0001t0002g0221 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.113-8465G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113251903 | |||||||
| chr12:113251944 | A | G | 3 | a0001c0007t0002g0058 a0001c0007t0011g0174 a0001c0013t0011g0173 |
3 | HG02572.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.113-8424A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113251944 | |||||||
| chr12:113251985 | C | T | 1 | a0001c0001t0002g0223 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.113-8383C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113251985 | |||||||
| chr12:113252087 | AG | A | 28 | a0001c0001t0002g0005 a0001c0001t0002g0206 a0001c0001t0002g0207 others(25): Show |
29 | HG00280.hp2 HG01168.hp2 HG02080.hp2 others(26): Show |
intron_variant | MODIFIER | c.113-8280delG | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113252087 | |||||||
| chr12:113252367 | G | A | 1 | a0001c0012t0001g0201 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.113-8001G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113252367 | |||||||
| chr12:113252397 | C | T | 1 | a0001c0001t0005g0097 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.113-7971C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113252397 | |||||||
| chr12:113252456 | T | C | 3 | a0001c0002t0009g0054 a0001c0002t0009g0055 a0001c0002t0009g0056 |
3 | HG02717.hp2 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.113-7912T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113252456 | |||||||
| chr12:113252564 | C | T | 1 | a0001c0001t0021g0053 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.113-7804C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113252564 | |||||||
| chr12:113252591 | T | C | 82 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(79): Show |
87 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.113-7777T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113252591 | |||||||
| chr12:113252593 | C | T | 1 | a0001c0001t0003g0186 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.113-7775C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113252593 | |||||||
| chr12:113252624 | A | T | 1 | a0001c0012t0001g0201 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.113-7744A>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113252624 | |||||||
| chr12:113252680 | C | T | 2 | a0001c0001t0004g0145 a0001c0001t0004g0170 |
2 | HG00408.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.113-7688C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113252680 | |||||||
| chr12:113252703 | C | A | 2 | a0001c0003t0008g0200 a0001c0003t0008g0226 |
2 | HG01168.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.113-7665C>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113252703 | |||||||
| chr12:113252738 | G | T | 48 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(45): Show |
50 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.113-7630G>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113252738 | |||||||
| chr12:113252794 | C | A | 87 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(84): Show |
92 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.113-7574C>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113252794 | |||||||
| chr12:113252799 | G | A | 3 | a0001c0007t0002g0058 a0001c0007t0011g0174 a0001c0013t0011g0173 |
3 | HG02572.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.113-7569G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113252799 | |||||||
| chr12:113253336 | A | G | 6 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(3): Show |
8 | HG02280.hp1 HG02451.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.113-7032A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113253336 | |||||||
| chr12:113253569 | C | A | 3 | a0001c0002t0009g0054 a0001c0002t0009g0055 a0001c0002t0009g0056 |
3 | HG02717.hp2 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.113-6799C>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113253569 | |||||||
| chr12:113254149 | G | C | 2 | a0001c0008t0006g0203 a0001c0008t0006g0204 |
2 | HG02055.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.113-6219G>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113254149 | |||||||
| chr12:113254196 | T | A | 1 | a0001c0001t0003g0016 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.113-6172T>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113254196 | |||||||
| chr12:113254779 | C | T | 1 | a0001c0001t0003g0171 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.113-5589C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113254779 | |||||||
| chr12:113254789 | A | T | 27 | a0001c0001t0002g0005 a0001c0001t0002g0206 a0001c0001t0002g0207 others(24): Show |
28 | HG00280.hp2 HG01168.hp2 HG02080.hp2 others(25): Show |
intron_variant | MODIFIER | c.113-5579A>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113254789 | |||||||
| chr12:113254919 | C | T | 48 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(45): Show |
50 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.113-5449C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113254919 | |||||||
| chr12:113255439 | A | G | 2 | a0001c0007t0011g0174 a0001c0013t0011g0173 |
2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.113-4929A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113255439 | |||||||
| chr12:113255467 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.113-4901T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113255467 | |||||||
| chr12:113255487 | CT | C | 42 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0057 others(39): Show |
45 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.113-4871delT | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 113255487 | ||||||
| chr12:113255586 | C | T | 1 | a0001c0001t0001g0178 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.113-4782C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113255586 | |||||||
| chr12:113255597 | C | T | 48 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(45): Show |
50 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.113-4771C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113255597 | |||||||
| chr12:113255602 | C | T | 1 | a0001c0001t0020g0075 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.113-4766C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113255602 | |||||||
| chr12:113255746 | T | C | 48 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(45): Show |
50 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.113-4622T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113255746 | |||||||
| chr12:113255858 | T | G | 1 | a0001c0001t0018g0124 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.113-4510T>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113255858 | |||||||
| chr12:113256123 | A | T | 1 | a0001c0001t0003g0181 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.113-4245A>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113256123 | |||||||
| chr12:113256144 | T | A | 4 | a0001c0001t0006g0202 a0001c0001t0006g0205 a0001c0008t0006g0203 others(1): Show |
4 | HG01891.hp1 HG02055.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-4224T>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113256144 | |||||||
| chr12:113256196 | T | A | 1 | a0001c0012t0001g0201 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.113-4172T>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113256196 | |||||||
| chr12:113256290 | A | AT | 38 | a0001c0001t0001g0015 a0001c0001t0001g0025 a0001c0001t0001g0026 others(35): Show |
40 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.113-4066dupT | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 113256290 | ||||||
| chr12:113256290 | A | T | 1 | a0001c0001t0001g0068 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.113-4078A>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113256290 | |||||||
| chr12:113256346 | G | A | 1 | a0001c0001t0002g0228 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.113-4022G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113256346 | |||||||
| chr12:113256517 | G | C | 1 | a0001c0001t0003g0016 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.113-3851G>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113256517 | |||||||
| chr12:113256531 | G | A | 1 | a0001c0001t0001g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.113-3837G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113256531 | |||||||
| chr12:113256618 | G | A | 1 | a0001c0001t0021g0053 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.113-3750G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113256618 | |||||||
| chr12:113256751 | C | A | 1 | a0001c0001t0001g0178 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.113-3617C>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113256751 | |||||||
| chr12:113256786 | T | C | 1 | a0001c0001t0001g0061 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.113-3582T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113256786 | |||||||
| chr12:113256856 | A | T | 28 | a0001c0001t0002g0005 a0001c0001t0002g0206 a0001c0001t0002g0207 others(25): Show |
29 | HG00280.hp2 HG01168.hp2 HG02080.hp2 others(26): Show |
intron_variant | MODIFIER | c.113-3512A>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113256856 | |||||||
| chr12:113257034 | CAATTT | C | 24 | a0001c0001t0002g0005 a0001c0001t0002g0206 a0001c0001t0002g0207 others(21): Show |
25 | HG02080.hp2 HG02083.hp2 HG02155.hp2 others(22): Show |
intron_variant | MODIFIER | c.113-3330_113-3326d others(7): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 113257034 | ||||||
| chr12:113257217 | C | T | 1 | a0001c0001t0003g0016 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.113-3151C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113257217 | |||||||
| chr12:113257257 | C | T | 3 | a0001c0007t0002g0058 a0001c0007t0011g0174 a0001c0013t0011g0173 |
3 | HG02572.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.113-3111C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113257257 | |||||||
| chr12:113257488 | C | CA | 22 | a0001c0001t0001g0068 a0001c0001t0001g0071 a0001c0001t0001g0084 others(19): Show |
22 | HG02055.hp1 HG02071.hp1 HG02080.hp1 others(19): Show |
intron_variant | MODIFIER | c.113-2865dupA | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 113257488 | ||||||
| chr12:113257488 | C | CAAA | 35 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(32): Show |
37 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.113-2867_113-2865d others(5): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 113257488 | ||||||
| chr12:113257518 | G | A | 1 | a0001c0012t0001g0201 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.113-2850G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113257518 | |||||||
| chr12:113257716 | T | C | 28 | a0001c0001t0002g0005 a0001c0001t0002g0206 a0001c0001t0002g0207 others(25): Show |
29 | HG00280.hp2 HG01168.hp2 HG02080.hp2 others(26): Show |
intron_variant | MODIFIER | c.113-2652T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113257716 | |||||||
| chr12:113257871 | C | T | 3 | a0001c0002t0009g0054 a0001c0002t0009g0055 a0001c0002t0009g0056 |
3 | HG02717.hp2 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.113-2497C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113257871 | |||||||
| chr12:113258115 | G | A | 32 | a0001c0001t0001g0015 a0001c0001t0002g0003 a0001c0001t0002g0006 others(29): Show |
34 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(31): Show |
intron_variant | MODIFIER | c.113-2253G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113258115 | |||||||
| chr12:113258195 | G | A | 2 | a0001c0001t0001g0078 a0001c0001t0001g0080 |
2 | HG01169.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.113-2173G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113258195 | |||||||
| chr12:113258264 | T | C | 82 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(79): Show |
87 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.113-2104T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113258264 | |||||||
| chr12:113258330 | G | T | 1 | a0001c0001t0003g0016 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.113-2038G>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113258330 | |||||||
| chr12:113258391 | C | G | 82 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(79): Show |
87 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.113-1977C>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113258391 | |||||||
| chr12:113258478 | A | G | 1 | a0001c0001t0002g0224 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.113-1890A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113258478 | |||||||
| chr12:113258557 | G | T | 48 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(45): Show |
50 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.113-1811G>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113258557 | |||||||
| chr12:113258815 | A | T | 1 | a0001c0001t0001g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.113-1553A>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113258815 | |||||||
| chr12:113258979 | AT | A | 7 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(4): Show |
9 | HG02280.hp1 HG02451.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.113-1372delT | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 113258979 | ||||||
| chr12:113258979 | ATT | A | 75 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(72): Show |
78 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.113-1373_113-1372d others(4): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr12 | 113258979 | ||||||
| chr12:113259040 | G | A | 1 | a0001c0012t0001g0201 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.113-1328G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113259040 | |||||||
| chr12:113259123 | C | T | 28 | a0001c0001t0002g0005 a0001c0001t0002g0206 a0001c0001t0002g0207 others(25): Show |
29 | HG00280.hp2 HG01168.hp2 HG02080.hp2 others(26): Show |
intron_variant | MODIFIER | c.113-1245C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113259123 | |||||||
| chr12:113259186 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.113-1182A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113259186 | |||||||
| chr12:113259219 | C | T | 6 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(3): Show |
8 | HG02280.hp1 HG02451.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.113-1149C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113259219 | |||||||
| chr12:113259266 | C | T | 37 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(34): Show |
39 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.113-1102C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113259266 | |||||||
| chr12:113259312 | T | C | 4 | a0001c0001t0006g0202 a0001c0001t0006g0205 a0001c0008t0006g0203 others(1): Show |
4 | HG01891.hp1 HG02055.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-1056T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113259312 | |||||||
| chr12:113259448 | A | G | 27 | a0001c0001t0002g0005 a0001c0001t0002g0206 a0001c0001t0002g0207 others(24): Show |
28 | HG00280.hp2 HG01168.hp2 HG02080.hp2 others(25): Show |
intron_variant | MODIFIER | c.113-920A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113259448 | |||||||
| chr12:113259747 | G | A | 37 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(34): Show |
39 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.113-621G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113259747 | |||||||
| chr12:113259923 | T | A | 2 | a0001c0001t0001g0066 a0001c0001t0004g0076 |
2 | HG00639.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.113-445T>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113259923 | |||||||
| chr12:113260009 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.113-359T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113260009 | |||||||
| chr12:113260106 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.113-262C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113260106 | |||||||
| chr12:113260202 | G | A | 2 | a0001c0001t0002g0177 a0001c0001t0006g0176 |
2 | HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.113-166G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 2/27 | chr12 | 113260202 | |||||||
| chr12:113260717 | C | T | 4 | a0001c0001t0006g0202 a0001c0001t0006g0205 a0001c0008t0006g0203 others(1): Show |
4 | HG01891.hp1 HG02055.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.237+225C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | chr12 | 113260717 | |||||||
| chr12:113260745 | C | T | 13 | a0001c0001t0003g0187 a0001c0001t0003g0188 a0001c0001t0003g0189 others(10): Show |
13 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.237+253C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | chr12 | 113260745 | |||||||
| chr12:113260827 | C | T | 1 | a0001c0001t0004g0113 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.237+335C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | chr12 | 113260827 | |||||||
| chr12:113260882 | A | AT | 33 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(30): Show |
34 | HG00280.hp2 HG01168.hp2 HG02080.hp2 others(31): Show |
intron_variant | MODIFIER | c.237+403dupT | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr12 | 113260882 | ||||||
| chr12:113261043 | A | G | 3 | a0001c0002t0009g0054 a0001c0002t0009g0055 a0001c0002t0009g0056 |
3 | HG02717.hp2 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.237+551A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | chr12 | 113261043 | |||||||
| chr12:113261064 | C | T | 3 | a0001c0002t0009g0054 a0001c0002t0009g0055 a0001c0002t0009g0056 |
3 | HG02717.hp2 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.237+572C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | chr12 | 113261064 | |||||||
| chr12:113261353 | C | T | 1 | a0001c0001t0010g0150 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.237+861C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | chr12 | 113261353 | |||||||
| chr12:113261368 | G | A | 6 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(3): Show |
8 | HG02280.hp1 HG02451.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.237+876G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | chr12 | 113261368 | |||||||
| chr12:113261412 | C | CT | 100 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0017 others(97): Show |
107 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.237+941dupT | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr12 | 113261412 | ||||||
| chr12:113261412 | C | CTT | 8 | a0001c0001t0002g0221 a0001c0001t0002g0223 a0001c0001t0013g0030 others(5): Show |
8 | HG00280.hp2 HG01168.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.237+940_237+941dup others(2): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr12 | 113261412 | ||||||
| chr12:113261509 | A | G | 1 | a0001c0001t0021g0053 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.237+1017A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | chr12 | 113261509 | |||||||
| chr12:113261531 | C | T | 2 | a0001c0001t0001g0066 a0001c0001t0004g0076 |
2 | HG00639.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.237+1039C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | chr12 | 113261531 | |||||||
| chr12:113261552 | C | T | 48 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(45): Show |
50 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.237+1060C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | chr12 | 113261552 | |||||||
| chr12:113261916 | C | A | 1 | a0001c0001t0019g0151 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.237+1424C>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | chr12 | 113261916 | |||||||
| chr12:113262069 | G | A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 |
3 | NA18960.hp2 NA18968.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.237+1577G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | chr12 | 113262069 | |||||||
| chr12:113262270 | C | T | 5 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0178 others(2): Show |
5 | HG02809.hp2 HG02886.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.237+1778C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | chr12 | 113262270 | |||||||
| chr12:113262333 | C | T | 1 | a0001c0001t0001g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.237+1841C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | chr12 | 113262333 | |||||||
| chr12:113262408 | TA | T | 49 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0024 others(46): Show |
56 | HG00423.hp2 HG01168.hp1 HG01168.hp2 others(53): Show |
intron_variant | MODIFIER | c.237+1935delA | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr12 | 113262408 | ||||||
| chr12:113262576 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.237+2084A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | chr12 | 113262576 | |||||||
| chr12:113262586 | A | G | 1 | a0001c0001t0002g0213 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.237+2094A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | chr12 | 113262586 | |||||||
| chr12:113262733 | T | C | 1 | a0001c0006t0001g0163 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.237+2241T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | chr12 | 113262733 | |||||||
| chr12:113262933 | A | G | 76 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(73): Show |
79 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.237+2441A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | chr12 | 113262933 | |||||||
| chr12:113262945 | A | G | 3 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 |
3 | NA18960.hp2 NA18968.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.237+2453A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | chr12 | 113262945 | |||||||
| chr12:113263062 | A | C | 4 | a0001c0002t0009g0054 a0001c0002t0009g0055 a0001c0002t0009g0056 others(1): Show |
4 | HG02615.hp2 HG02717.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.237+2570A>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | chr12 | 113263062 | |||||||
| chr12:113263413 | G | A | 7 | a0001c0001t0001g0110 a0001c0001t0001g0148 a0001c0001t0005g0089 others(4): Show |
7 | HG01978.hp1 HG02630.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.238-2767G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | chr12 | 113263413 | |||||||
| chr12:113263448 | A | T | 3 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 |
3 | NA18961.hp1 NA18971.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.238-2732A>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | chr12 | 113263448 | |||||||
| chr12:113263768 | T | G | 4 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(1): Show |
4 | HG02559.hp2 NA18960.hp2 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.238-2412T>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | chr12 | 113263768 | |||||||
| chr12:113263816 | C | T | 3 | a0001c0002t0009g0054 a0001c0002t0009g0055 a0001c0002t0009g0056 |
3 | HG02717.hp2 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.238-2364C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | chr12 | 113263816 | |||||||
| chr12:113263877 | C | A | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.238-2303C>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | chr12 | 113263877 | |||||||
| chr12:113263994 | C | A | 1 | a0001c0001t0004g0104 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.238-2186C>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | chr12 | 113263994 | |||||||
| chr12:113264001 | C | G | 1 | a0001c0001t0002g0043 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.238-2179C>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | chr12 | 113264001 | |||||||
| chr12:113264022 | C | T | 3 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 |
3 | NA18960.hp2 NA18968.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.238-2158C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | chr12 | 113264022 | |||||||
| chr12:113264023 | G | A | 1 | a0001c0001t0004g0063 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.238-2157G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | chr12 | 113264023 | |||||||
| chr12:113264071 | C | CT | 6 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(3): Show |
8 | HG02280.hp1 HG02451.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.238-2109_238-2108i others(3): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | chr12 | 113264071 | |||||||
| chr12:113264072 | A | T | 6 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(3): Show |
8 | HG02280.hp1 HG02451.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.238-2108A>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | chr12 | 113264072 | |||||||
| chr12:113264072 | AT | A | 76 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(73): Show |
79 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.238-2097delT | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr12 | 113264072 | ||||||
| chr12:113264126 | C | A | 1 | a0001c0012t0001g0201 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.238-2054C>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | chr12 | 113264126 | |||||||
| chr12:113264194 | G | A | 2 | a0001c0001t0003g0185 a0001c0001t0012g0175 |
2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.238-1986G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | chr12 | 113264194 | |||||||
| chr12:113264305 | G | A | 1 | a0001c0001t0001g0121 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.238-1875G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | chr12 | 113264305 | |||||||
| chr12:113264401 | G | A | 3 | a0001c0003t0008g0200 a0001c0003t0008g0226 a0001c0003t0008g0227 |
3 | HG00280.hp2 HG01168.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.238-1779G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | chr12 | 113264401 | |||||||
| chr12:113264506 | C | G | 1 | a0001c0001t0001g0103 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.238-1674C>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | chr12 | 113264506 | |||||||
| chr12:113264537 | G | C | 3 | a0001c0003t0008g0200 a0001c0003t0008g0226 a0001c0003t0008g0227 |
3 | HG00280.hp2 HG01168.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.238-1643G>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | chr12 | 113264537 | |||||||
| chr12:113264571 | C | T | 32 | a0001c0001t0001g0015 a0001c0001t0002g0003 a0001c0001t0002g0006 others(29): Show |
34 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(31): Show |
intron_variant | MODIFIER | c.238-1609C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | chr12 | 113264571 | |||||||
| chr12:113264612 | G | A | 1 | a0001c0001t0007g0064 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.238-1568G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | chr12 | 113264612 | |||||||
| chr12:113264678 | CA | C | 76 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(73): Show |
79 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.238-1493delA | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr12 | 113264678 | ||||||
| chr12:113264827 | A | G | 6 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(3): Show |
8 | HG02280.hp1 HG02451.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.238-1353A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | chr12 | 113264827 | |||||||
| chr12:113264970 | C | T | 28 | a0001c0001t0002g0005 a0001c0001t0002g0206 a0001c0001t0002g0207 others(25): Show |
29 | HG00280.hp2 HG01168.hp2 HG02080.hp2 others(26): Show |
intron_variant | MODIFIER | c.238-1210C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | chr12 | 113264970 | |||||||
| chr12:113265016 | A | G | 6 | a0001c0001t0002g0206 a0001c0001t0002g0217 a0001c0001t0002g0218 others(3): Show |
6 | NA18942.hp1 NA18991.hp1 NA19002.hp1 others(3): Show |
intron_variant | MODIFIER | c.238-1164A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | chr12 | 113265016 | |||||||
| chr12:113265158 | A | G | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.238-1022A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | chr12 | 113265158 | |||||||
| chr12:113265224 | C | A | 1 | a0001c0012t0001g0201 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.238-956C>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | chr12 | 113265224 | |||||||
| chr12:113265309 | G | A | 1 | a0001c0001t0001g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.238-871G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | chr12 | 113265309 | |||||||
| chr12:113265548 | C | CT | 23 | a0001c0001t0002g0005 a0001c0001t0002g0206 a0001c0001t0002g0207 others(20): Show |
24 | HG02080.hp2 HG02083.hp2 HG02155.hp2 others(21): Show |
intron_variant | MODIFIER | c.238-616dupT | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr12 | 113265548 | ||||||
| chr12:113265548 | CT | C | 7 | a0001c0001t0001g0121 a0001c0001t0001g0131 a0001c0001t0002g0023 others(4): Show |
7 | HG02257.hp2 NA18951.hp1 NA18962.hp2 others(4): Show |
intron_variant | MODIFIER | c.238-616delT | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr12 | 113265548 | ||||||
| chr12:113265580 | T | C | 1 | a0001c0001t0002g0217 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.238-600T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | chr12 | 113265580 | |||||||
| chr12:113265628 | C | G | 2 | a0001c0001t0006g0202 a0001c0001t0006g0205 |
2 | HG01891.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.238-552C>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | chr12 | 113265628 | |||||||
| chr12:113265634 | C | G | 28 | a0001c0001t0002g0005 a0001c0001t0002g0206 a0001c0001t0002g0207 others(25): Show |
29 | HG00280.hp2 HG01168.hp2 HG02080.hp2 others(26): Show |
intron_variant | MODIFIER | c.238-546C>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | chr12 | 113265634 | |||||||
| chr12:113265796 | C | A | 3 | a0001c0007t0002g0058 a0001c0007t0011g0174 a0001c0013t0011g0173 |
3 | HG02572.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.238-384C>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | chr12 | 113265796 | |||||||
| chr12:113265877 | G | A | 1 | a0001c0001t0003g0016 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.238-303G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | chr12 | 113265877 | |||||||
| chr12:113266015 | CCGTGAGT others(2): Show |
C | 3 | a0001c0002t0009g0054 a0001c0002t0009g0055 a0001c0002t0009g0056 |
3 | HG02717.hp2 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.238-162_238-154del others(9): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | INFO_REALIGN_3_PRIME | chr12 | 113266015 | ||||||
| chr12:113266031 | G | A | 2 | a0001c0001t0002g0214 a0001c0001t0015g0211 |
2 | HG02083.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.238-149G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | chr12 | 113266031 | |||||||
| chr12:113266130 | G | A | 1 | a0001c0001t0003g0016 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.238-50G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 3/27 | chr12 | 113266130 | |||||||
| chr12:113266490 | A | G | 1 | a0001c0001t0021g0053 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.414+134A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 4/27 | chr12 | 113266490 | |||||||
| chr12:113266507 | G | A | 1 | a0001c0001t0002g0216 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.414+151G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 4/27 | chr12 | 113266507 | |||||||
| chr12:113266671 | T | C | 3 | a0001c0007t0002g0058 a0001c0007t0011g0174 a0001c0013t0011g0173 |
3 | HG02572.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.414+315T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 4/27 | chr12 | 113266671 | |||||||
| chr12:113266896 | C | T | 24 | a0001c0001t0002g0005 a0001c0001t0002g0206 a0001c0001t0002g0207 others(21): Show |
25 | HG02080.hp2 HG02083.hp2 HG02155.hp2 others(22): Show |
intron_variant | MODIFIER | c.414+540C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 4/27 | chr12 | 113266896 | |||||||
| chr12:113266946 | T | C | 28 | a0001c0001t0002g0005 a0001c0001t0002g0206 a0001c0001t0002g0207 others(25): Show |
29 | HG00280.hp2 HG01168.hp2 HG02080.hp2 others(26): Show |
intron_variant | MODIFIER | c.414+590T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 4/27 | chr12 | 113266946 | |||||||
| chr12:113266954 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.414+598C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 4/27 | chr12 | 113266954 | |||||||
| chr12:113267277 | G | A | 1 | a0001c0001t0005g0097 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.415-566G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 4/27 | chr12 | 113267277 | |||||||
| chr12:113267403 | C | CT | 5 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0178 others(2): Show |
5 | HG02809.hp2 HG02886.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.415-427dupT | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 4/27 | INFO_REALIGN_3_PRIME | chr12 | 113267403 | ||||||
| chr12:113267422 | T | G | 1 | a0001c0001t0001g0069 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.415-421T>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 4/27 | chr12 | 113267422 | |||||||
| chr12:113267548 | G | A | 28 | a0001c0001t0002g0005 a0001c0001t0002g0206 a0001c0001t0002g0207 others(25): Show |
29 | HG00280.hp2 HG01168.hp2 HG02080.hp2 others(26): Show |
intron_variant | MODIFIER | c.415-295G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 4/27 | chr12 | 113267548 | |||||||
| chr12:113267596 | C | T | 32 | a0001c0001t0001g0015 a0001c0001t0002g0003 a0001c0001t0002g0006 others(29): Show |
34 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(31): Show |
intron_variant | MODIFIER | c.415-247C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 4/27 | chr12 | 113267596 | |||||||
| chr12:113267643 | A | C | 1 | a0001c0001t0001g0172 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.415-200A>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 4/27 | chr12 | 113267643 | |||||||
| chr12:113267724 | A | C | 38 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(35): Show |
40 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.415-119A>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 4/27 | chr12 | 113267724 | |||||||
| chr12:113268130 | C | T | 48 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(45): Show |
50 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.528+174C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 5/27 | chr12 | 113268130 | |||||||
| chr12:113268157 | T | G | 83 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(80): Show |
88 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.528+201T>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 5/27 | chr12 | 113268157 | |||||||
| chr12:113268336 | A | G | 3 | a0001c0002t0009g0054 a0001c0002t0009g0055 a0001c0002t0009g0056 |
3 | HG02717.hp2 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.528+380A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 5/27 | chr12 | 113268336 | |||||||
| chr12:113268366 | G | A | 3 | a0001c0003t0008g0200 a0001c0003t0008g0226 a0001c0003t0008g0227 |
3 | HG00280.hp2 HG01168.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.529-376G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 5/27 | chr12 | 113268366 | |||||||
| chr12:113268433 | C | A | 48 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(45): Show |
50 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.529-309C>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 5/27 | chr12 | 113268433 | |||||||
| chr12:113268467 | G | A | 1 | a0001c0001t0003g0136 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.529-275G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 5/27 | chr12 | 113268467 | |||||||
| chr12:113268488 | G | A | 3 | a0001c0003t0008g0200 a0001c0003t0008g0226 a0001c0003t0008g0227 |
3 | HG00280.hp2 HG01168.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.529-254G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 5/27 | chr12 | 113268488 | |||||||
| chr12:113268541 | G | T | 48 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(45): Show |
50 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.529-201G>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 5/27 | chr12 | 113268541 | |||||||
| chr12:113268554 | G | A | 1 | a0001c0001t0001g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.529-188G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 5/27 | chr12 | 113268554 | |||||||
| chr12:113268640 | C | T | 1 | a0001c0001t0003g0185 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.529-102C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 5/27 | chr12 | 113268640 | |||||||
| chr12:113268711 | G | T | 1 | a0001c0001t0002g0052 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.529-31G>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 5/27 | chr12 | 113268711 | |||||||
| chr12:113269042 | C | T | 28 | a0001c0001t0001g0013 a0001c0001t0001g0070 a0001c0001t0001g0103 others(25): Show |
30 | HG00099.hp1 HG01081.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.659+170C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 6/27 | chr12 | 113269042 | |||||||
| chr12:113269104 | C | T | 28 | a0001c0001t0002g0005 a0001c0001t0002g0206 a0001c0001t0002g0207 others(25): Show |
29 | HG00280.hp2 HG01168.hp2 HG02080.hp2 others(26): Show |
intron_variant | MODIFIER | c.659+232C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 6/27 | chr12 | 113269104 | |||||||
| chr12:113269211 | G | A | 4 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0005t0001g0079 others(1): Show |
4 | HG01168.hp1 HG01169.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.659+339G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 6/27 | chr12 | 113269211 | |||||||
| chr12:113269432 | T | A | 1 | a0001c0008t0006g0204 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.660-325T>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 6/27 | chr12 | 113269432 | |||||||
| chr12:113269583 | G | A | 77 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(74): Show |
80 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.660-174G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 6/27 | chr12 | 113269583 | |||||||
| chr12:113269588 | G | A | 1 | a0001c0001t0001g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.660-169G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 6/27 | chr12 | 113269588 | |||||||
| chr12:113269615 | A | G | 25 | a0001c0001t0002g0005 a0001c0001t0002g0090 a0001c0001t0002g0206 others(22): Show |
26 | HG02080.hp2 HG02083.hp2 HG02155.hp2 others(23): Show |
intron_variant | MODIFIER | c.660-142A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 6/27 | chr12 | 113269615 | |||||||
| chr12:113269713 | C | T | 3 | a0001c0001t0003g0014 a0001c0001t0003g0059 a0001c0001t0003g0136 |
4 | HG01109.hp2 HG03209.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.660-44C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 6/27 | chr12 | 113269713 | |||||||
| chr12:113269874 | C | T | 38 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(35): Show |
40 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.748+29C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 7/27 | chr12 | 113269874 | |||||||
| chr12:113270209 | A | G | 2 | a0001c0008t0006g0203 a0001c0008t0006g0204 |
2 | HG02055.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.748+364A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 7/27 | chr12 | 113270209 | |||||||
| chr12:113270210 | A | T | 3 | a0001c0001t0001g0102 a0001c0001t0001g0116 a0001c0001t0018g0124 |
3 | HG02280.hp2 HG02647.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.748+365A>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 7/27 | chr12 | 113270210 | |||||||
| chr12:113270242 | T | A | 4 | a0001c0001t0001g0135 a0001c0001t0003g0014 a0001c0001t0003g0059 others(1): Show |
5 | HG01109.hp2 HG03209.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.748+397T>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 7/27 | chr12 | 113270242 | |||||||
| chr12:113270389 | T | G | 5 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0178 others(2): Show |
5 | HG02809.hp2 HG02886.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.748+544T>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 7/27 | chr12 | 113270389 | |||||||
| chr12:113270485 | G | GT | 46 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(43): Show |
48 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.748+653dupT | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 7/27 | INFO_REALIGN_3_PRIME | chr12 | 113270485 | ||||||
| chr12:113270485 | G | T | 6 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(3): Show |
8 | HG02280.hp1 HG02451.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.748+640G>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 7/27 | chr12 | 113270485 | |||||||
| chr12:113270566 | T | C | 1 | a0001c0001t0001g0085 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.748+721T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 7/27 | chr12 | 113270566 | |||||||
| chr12:113270775 | G | A | 3 | a0001c0007t0002g0058 a0001c0007t0011g0174 a0001c0013t0011g0173 |
3 | HG02572.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.748+930G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 7/27 | chr12 | 113270775 | |||||||
| chr12:113270785 | A | G | 111 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(108): Show |
116 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.748+940A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 7/27 | chr12 | 113270785 | |||||||
| chr12:113271022 | A | C | 77 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(74): Show |
80 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.748+1177A>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 7/27 | chr12 | 113271022 | |||||||
| chr12:113271023 | G | T | 77 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(74): Show |
80 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.748+1178G>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 7/27 | chr12 | 113271023 | |||||||
| chr12:113271102 | C | A | 42 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(39): Show |
45 | HG00280.hp2 HG01168.hp2 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.748+1257C>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 7/27 | chr12 | 113271102 | |||||||
| chr12:113271132 | T | C | 1 | a0001c0001t0001g0117 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.748+1287T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 7/27 | chr12 | 113271132 | |||||||
| chr12:113271189 | T | A | 25 | a0001c0001t0002g0005 a0001c0001t0002g0090 a0001c0001t0002g0206 others(22): Show |
26 | HG02080.hp2 HG02083.hp2 HG02155.hp2 others(23): Show |
intron_variant | MODIFIER | c.748+1344T>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 7/27 | chr12 | 113271189 | |||||||
| chr12:113271417 | T | C | 6 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(3): Show |
8 | HG02280.hp1 HG02451.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.749-1241T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 7/27 | chr12 | 113271417 | |||||||
| chr12:113271518 | C | A | 48 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(45): Show |
50 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.749-1140C>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 7/27 | chr12 | 113271518 | |||||||
| chr12:113271591 | T | G | 1 | a0001c0001t0001g0140 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.749-1067T>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 7/27 | chr12 | 113271591 | |||||||
| chr12:113271693 | A | G | 1 | a0001c0001t0001g0117 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.749-965A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 7/27 | chr12 | 113271693 | |||||||
| chr12:113271707 | C | T | 37 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(34): Show |
39 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.749-951C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 7/27 | chr12 | 113271707 | |||||||
| chr12:113272029 | G | A | 1 | a0001c0001t0002g0216 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.749-629G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 7/27 | chr12 | 113272029 | |||||||
| chr12:113272087 | G | C | 1 | a0001c0001t0005g0089 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.749-571G>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 7/27 | chr12 | 113272087 | |||||||
| chr12:113272122 | G | A | 37 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(34): Show |
39 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.749-536G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 7/27 | chr12 | 113272122 | |||||||
| chr12:113272252 | C | T | 24 | a0001c0001t0002g0005 a0001c0001t0002g0206 a0001c0001t0002g0207 others(21): Show |
25 | HG02080.hp2 HG02083.hp2 HG02155.hp2 others(22): Show |
intron_variant | MODIFIER | c.749-406C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 7/27 | chr12 | 113272252 | |||||||
| chr12:113272303 | C | T | 3 | a0001c0002t0009g0054 a0001c0002t0009g0055 a0001c0002t0009g0056 |
3 | HG02717.hp2 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.749-355C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 7/27 | chr12 | 113272303 | |||||||
| chr12:113272515 | C | T | 3 | a0001c0001t0001g0148 a0001c0001t0010g0149 a0001c0001t0010g0150 |
3 | HG02630.hp1 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.749-143C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 7/27 | chr12 | 113272515 | |||||||
| chr12:113272541 | C | T | 1 | a0001c0001t0001g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.749-117C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 7/27 | chr12 | 113272541 | |||||||
| chr12:113272735 | G | C | 1 | a0001c0002t0009g0054 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.783+43G>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 8/27 | chr12 | 113272735 | |||||||
| chr12:113272783 | G | C | 1 | a0001c0001t0002g0049 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.783+91G>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 8/27 | chr12 | 113272783 | |||||||
| chr12:113272899 | T | C | 83 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(80): Show |
88 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.783+207T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 8/27 | chr12 | 113272899 | |||||||
| chr12:113272936 | T | C | 3 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0002g0215 |
3 | NA18946.hp2 NA18981.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.783+244T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 8/27 | chr12 | 113272936 | |||||||
| chr12:113273143 | G | A | 3 | a0001c0007t0002g0058 a0001c0007t0011g0174 a0001c0013t0011g0173 |
3 | HG02572.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.784-89G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 8/27 | chr12 | 113273143 | |||||||
| chr12:113273186 | G | T | 1 | a0001c0001t0001g0135 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.784-46G>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 8/27 | chr12 | 113273186 | |||||||
| chr12:113273198 | G | A | 1 | a0001c0001t0004g0077 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.784-34G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 8/27 | chr12 | 113273198 | |||||||
| chr12:113273201 | C | G | 6 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0029 others(3): Show |
6 | HG02071.hp2 NA18946.hp1 NA18951.hp1 others(3): Show |
intron_variant | MODIFIER | c.784-31C>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 8/27 | chr12 | 113273201 | |||||||
| chr12:113273331 | G | A | 1 | a0001c0012t0001g0201 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.842+41G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 9/27 | chr12 | 113273331 | |||||||
| chr12:113273458 | C | T | 3 | a0001c0002t0009g0054 a0001c0002t0009g0055 a0001c0002t0009g0056 |
3 | HG02717.hp2 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.843-111C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 9/27 | chr12 | 113273458 | |||||||
| chr12:113273459 | A | G | 77 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(74): Show |
80 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.843-110A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 9/27 | chr12 | 113273459 | |||||||
| chr12:113273504 | G | A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 |
3 | NA18960.hp2 NA18968.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.843-65G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 9/27 | chr12 | 113273504 | |||||||
| chr12:113273759 | T | G | 1 | a0001c0013t0011g0173 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.942+91T>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 10/27 | chr12 | 113273759 | |||||||
| chr12:113273816 | G | A | 1 | a0001c0001t0003g0183 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.942+148G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 10/27 | chr12 | 113273816 | |||||||
| chr12:113274115 | G | A | 48 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(45): Show |
50 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.942+447G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 10/27 | chr12 | 113274115 | |||||||
| chr12:113274296 | A | G | 16 | a0001c0001t0001g0184 a0001c0001t0003g0185 a0001c0001t0003g0187 others(13): Show |
16 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.942+628A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 10/27 | chr12 | 113274296 | |||||||
| chr12:113274308 | C | T | 2 | a0001c0001t0003g0185 a0001c0001t0012g0175 |
2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.942+640C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 10/27 | chr12 | 113274308 | |||||||
| chr12:113274676 | C | G | 1 | a0001c0001t0012g0175 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.942+1008C>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 10/27 | chr12 | 113274676 | |||||||
| chr12:113274745 | T | C | 1 | a0001c0001t0004g0063 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.942+1077T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 10/27 | chr12 | 113274745 | |||||||
| chr12:113274830 | C | G | 1 | a0001c0001t0017g0138 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.942+1162C>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 10/27 | chr12 | 113274830 | |||||||
| chr12:113274870 | C | T | 4 | a0001c0001t0006g0202 a0001c0001t0006g0205 a0001c0008t0006g0203 others(1): Show |
4 | HG01891.hp1 HG02055.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.942+1202C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 10/27 | chr12 | 113274870 | |||||||
| chr12:113274957 | G | A | 24 | a0001c0001t0002g0005 a0001c0001t0002g0206 a0001c0001t0002g0207 others(21): Show |
25 | HG02080.hp2 HG02083.hp2 HG02155.hp2 others(22): Show |
intron_variant | MODIFIER | c.942+1289G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 10/27 | chr12 | 113274957 | |||||||
| chr12:113275046 | G | C | 37 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(34): Show |
39 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.942+1378G>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 10/27 | chr12 | 113275046 | |||||||
| chr12:113275065 | G | A | 1 | a0001c0012t0001g0201 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.942+1397G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 10/27 | chr12 | 113275065 | |||||||
| chr12:113275257 | A | C | 3 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0004g0108 |
8 | HG00423.hp2 NA18962.hp1 NA19003.hp1 others(5): Show |
intron_variant | MODIFIER | c.942+1589A>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 10/27 | chr12 | 113275257 | |||||||
| chr12:113275265 | T | G | 1 | a0001c0007t0002g0058 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.942+1597T>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 10/27 | chr12 | 113275265 | |||||||
| chr12:113275268 | C | T | 6 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(3): Show |
8 | HG02280.hp1 HG02451.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.942+1600C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 10/27 | chr12 | 113275268 | |||||||
| chr12:113275307 | A | G | 88 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(85): Show |
93 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.943-1612A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 10/27 | chr12 | 113275307 | |||||||
| chr12:113275321 | G | T | 82 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(79): Show |
87 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.943-1598G>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 10/27 | chr12 | 113275321 | |||||||
| chr12:113275404 | C | T | 48 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(45): Show |
50 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.943-1515C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 10/27 | chr12 | 113275404 | |||||||
| chr12:113275422 | T | C | 28 | a0001c0001t0002g0005 a0001c0001t0002g0090 a0001c0001t0002g0206 others(25): Show |
29 | HG00280.hp2 HG01168.hp2 HG02080.hp2 others(26): Show |
intron_variant | MODIFIER | c.943-1497T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 10/27 | chr12 | 113275422 | |||||||
| chr12:113275488 | T | C | 82 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(79): Show |
87 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.943-1431T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 10/27 | chr12 | 113275488 | |||||||
| chr12:113275600 | A | G | 1 | a0001c0001t0002g0209 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.943-1319A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 10/27 | chr12 | 113275600 | |||||||
| chr12:113275636 | G | A | 14 | a0001c0001t0001g0103 a0001c0001t0001g0110 a0001c0001t0001g0111 others(11): Show |
15 | HG01081.hp1 HG01109.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.943-1283G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 10/27 | chr12 | 113275636 | |||||||
| chr12:113275716 | G | C | 48 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(45): Show |
50 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.943-1203G>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 10/27 | chr12 | 113275716 | |||||||
| chr12:113275778 | T | G | 82 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(79): Show |
87 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.943-1141T>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 10/27 | chr12 | 113275778 | |||||||
| chr12:113275827 | C | T | 1 | a0001c0011t0001g0109 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.943-1092C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 10/27 | chr12 | 113275827 | |||||||
| chr12:113275880 | T | G | 1 | a0001c0001t0001g0134 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.943-1039T>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 10/27 | chr12 | 113275880 | |||||||
| chr12:113276380 | C | T | 1 | a0001c0001t0020g0075 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.943-539C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 10/27 | chr12 | 113276380 | |||||||
| chr12:113276540 | G | A | 1 | a0001c0001t0001g0071 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.943-379G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 10/27 | chr12 | 113276540 | |||||||
| chr12:113276565 | C | A | 2 | a0001c0001t0001g0085 a0001c0001t0001g0086 |
2 | HG02300.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.943-354C>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 10/27 | chr12 | 113276565 | |||||||
| chr12:113276603 | C | G | 1 | a0001c0001t0017g0138 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.943-316C>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 10/27 | chr12 | 113276603 | |||||||
| chr12:113276628 | G | A | 1 | a0001c0001t0002g0038 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.943-291G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 10/27 | chr12 | 113276628 | |||||||
| chr12:113276836 | A | G | 1 | a0001c0001t0004g0076 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.943-83A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 10/27 | chr12 | 113276836 | |||||||
| chr12:113277426 | C | T | 6 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(3): Show |
8 | HG02280.hp1 HG02451.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1184+62C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 12/27 | chr12 | 113277426 | |||||||
| chr12:113277446 | T | G | 110 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(107): Show |
115 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.1184+82T>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 12/27 | chr12 | 113277446 | |||||||
| chr12:113277567 | A | G | 29 | a0001c0001t0002g0005 a0001c0001t0002g0090 a0001c0001t0002g0206 others(26): Show |
30 | HG00280.hp2 HG01168.hp2 HG02080.hp2 others(27): Show |
intron_variant | MODIFIER | c.1184+203A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 12/27 | chr12 | 113277567 | |||||||
| chr12:113277752 | T | C | 83 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(80): Show |
88 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.1184+388T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 12/27 | chr12 | 113277752 | |||||||
| chr12:113277892 | C | T | 3 | a0001c0001t0001g0162 a0001c0001t0001g0164 a0001c0001t0001g0167 |
3 | HG01891.hp2 HG02976.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1185-297C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 12/27 | chr12 | 113277892 | |||||||
| chr12:113278086 | T | TCCCA | 77 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(74): Show |
80 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.1185-100_1185-99in others(5): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr12 | 113278086 | ||||||
| chr12:113278172 | T | C | 1 | a0001c0001t0003g0016 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1185-17T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 12/27 | chr12 | 113278172 | |||||||
| chr12:113278314 | C | T | 2 | a0001c0001t0001g0166 a0001c0001t0001g0169 |
2 | NA18977.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.1233+77C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 13/27 | chr12 | 113278314 | |||||||
| chr12:113278433 | C | T | 50 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(47): Show |
52 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.1233+196C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 13/27 | chr12 | 113278433 | |||||||
| chr12:113278434 | G | T | 1 | a0001c0001t0001g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1233+197G>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 13/27 | chr12 | 113278434 | |||||||
| chr12:113278908 | G | A | 25 | a0001c0001t0002g0005 a0001c0001t0002g0091 a0001c0001t0002g0206 others(22): Show |
26 | HG02080.hp2 HG02083.hp2 HG02155.hp2 others(23): Show |
intron_variant | MODIFIER | c.1297+73G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | chr12 | 113278908 | |||||||
| chr12:113278933 | T | G | 8 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(5): Show |
10 | HG02280.hp1 HG02451.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1297+98T>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | chr12 | 113278933 | |||||||
| chr12:113279210 | G | A | 3 | a0001c0002t0009g0054 a0001c0002t0009g0055 a0001c0002t0009g0056 |
3 | HG02717.hp2 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1297+375G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | chr12 | 113279210 | |||||||
| chr12:113279295 | A | G | 1 | a0001c0012t0001g0201 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1297+460A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | chr12 | 113279295 | |||||||
| chr12:113279307 | G | A | 1 | a0001c0012t0001g0201 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1297+472G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | chr12 | 113279307 | |||||||
| chr12:113279317 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1297+482A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | chr12 | 113279317 | |||||||
| chr12:113279317 | ATG | A | 4 | a0001c0001t0001g0158 a0001c0001t0001g0184 a0001c0001t0003g0186 others(1): Show |
4 | HG02897.hp2 HG03139.hp1 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.1297+502_1297+503d others(4): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279317 | ||||||
| chr12:113279319 | G | A | 77 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(74): Show |
82 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.1297+484G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | chr12 | 113279319 | |||||||
| chr12:113279335 | G | A | 8 | a0001c0001t0001g0057 a0001c0001t0002g0023 a0001c0001t0002g0045 others(5): Show |
8 | HG02572.hp1 HG02615.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1297+500G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | chr12 | 113279335 | |||||||
| chr12:113279337 | G | A | 81 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(78): Show |
86 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.1297+502G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | chr12 | 113279337 | |||||||
| chr12:113279339 | A | G | 3 | a0001c0001t0001g0154 a0001c0001t0003g0182 a0001c0001t0020g0075 |
3 | HG02622.hp2 HG02698.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1297+504A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | chr12 | 113279339 | |||||||
| chr12:113279345 | A | ATG | 4 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0157 others(1): Show |
4 | HG02165.hp2 HG02572.hp2 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.1297+524_1297+525d others(4): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279345 | ||||||
| chr12:113279345 | A | G | 12 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(9): Show |
14 | HG01358.hp1 HG01361.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1297+510A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | chr12 | 113279345 | |||||||
| chr12:113279345 | ATG | A | 3 | a0001c0001t0003g0179 a0001c0001t0003g0183 a0001c0001t0003g0199 |
3 | HG00140.hp1 HG02145.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1297+524_1297+525d others(4): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279345 | ||||||
| chr12:113279347 | G | A | 35 | a0001c0001t0002g0005 a0001c0001t0002g0091 a0001c0001t0002g0206 others(32): Show |
36 | HG01891.hp1 HG02055.hp1 HG02080.hp2 others(33): Show |
intron_variant | MODIFIER | c.1297+512G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | chr12 | 113279347 | |||||||
| chr12:113279355 | GTGTGTAT others(3): Show |
G | 1 | a0001c0002t0009g0055 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1297+522_1297+531d others(12): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279355 | ||||||
| chr12:113279355 | GTGTGTAT others(15): Show |
G | 1 | a0001c0012t0001g0201 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1297+522_1297+543d others(24): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279355 | ||||||
| chr12:113279359 | G | A | 26 | a0001c0001t0001g0065 a0001c0001t0001g0073 a0001c0001t0001g0184 others(23): Show |
26 | HG00280.hp2 HG00323.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.1297+524G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | chr12 | 113279359 | |||||||
| chr12:113279359 | GTATATAT others(5): Show |
G | 1 | a0001c0001t0002g0051 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1297+546_1297+557d others(14): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279359 | ||||||
| chr12:113279361 | A | G | 46 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0017 others(43): Show |
50 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(47): Show |
intron_variant | MODIFIER | c.1297+526A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | chr12 | 113279361 | |||||||
| chr12:113279363 | A | G | 6 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(3): Show |
8 | HG02280.hp1 HG02451.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1297+528A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | chr12 | 113279363 | |||||||
| chr12:113279365 | A | G | 7 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(4): Show |
9 | HG02280.hp1 HG02451.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1297+530A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | chr12 | 113279365 | |||||||
| chr12:113279367 | A | G | 1 | a0001c0004t0002g0022 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1297+532A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | chr12 | 113279367 | |||||||
| chr12:113279371 | ATATATAT others(14): Show |
A | 1 | a0001c0001t0002g0091 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1297+538_1297+558d others(23): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279371 | ||||||
| chr12:113279373 | A | G | 1 | a0001c0001t0002g0051 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1297+538A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | chr12 | 113279373 | |||||||
| chr12:113279373 | ATATATAT others(14): Show |
A | 17 | a0001c0001t0002g0005 a0001c0001t0002g0206 a0001c0001t0002g0207 others(14): Show |
18 | HG02080.hp2 HG02083.hp2 HG02698.hp1 others(15): Show |
intron_variant | MODIFIER | c.1297+540_1297+560d others(23): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279373 | ||||||
| chr12:113279373 | ATATATAT others(15): Show |
A | 5 | a0001c0001t0002g0213 a0001c0001t0002g0217 a0001c0001t0002g0219 others(2): Show |
5 | HG02155.hp2 NA18942.hp1 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.1297+540_1297+561d others(24): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279373 | ||||||
| chr12:113279373 | ATATATAT others(16): Show |
A | 1 | a0001c0001t0002g0218 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1297+540_1297+562d others(25): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279373 | ||||||
| chr12:113279375 | ATATATAT others(14): Show |
A | 3 | a0001c0001t0002g0220 a0001c0003t0008g0200 a0001c0003t0008g0226 |
3 | HG01168.hp2 HG02300.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1297+542_1297+562d others(23): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279375 | ||||||
| chr12:113279375 | ATATATAT others(15): Show |
A | 1 | a0001c0003t0008g0227 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1297+542_1297+563d others(24): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279375 | ||||||
| chr12:113279378 | TATA | T | 3 | a0001c0001t0003g0191 a0001c0001t0003g0192 a0001c0001t0003g0197 |
3 | HG02615.hp1 HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1297+544_1297+546d others(5): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | chr12 | 113279378 | |||||||
| chr12:113279378 | TATATATA others(4): Show |
T | 6 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(3): Show |
7 | HG02280.hp1 HG02451.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1297+544_1297+554d others(13): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | chr12 | 113279378 | |||||||
| chr12:113279380 | TATA | T | 6 | a0001c0001t0003g0187 a0001c0001t0003g0188 a0001c0001t0003g0189 others(3): Show |
6 | HG02109.hp2 HG02257.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1297+546_1297+548d others(5): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | chr12 | 113279380 | |||||||
| chr12:113279380 | TATATATA others(4): Show |
T | 3 | a0001c0001t0003g0002 a0001c0007t0011g0174 a0001c0013t0011g0173 |
3 | HG02572.hp1 HG02647.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1297+546_1297+556d others(13): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | chr12 | 113279380 | |||||||
| chr12:113279381 | A | T | 1 | a0001c0001t0003g0199 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1297+546A>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | chr12 | 113279381 | |||||||
| chr12:113279383 | A | T | 5 | a0001c0001t0001g0184 a0001c0001t0003g0191 a0001c0001t0003g0192 others(2): Show |
5 | HG02145.hp2 HG02615.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1297+548A>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | chr12 | 113279383 | |||||||
| chr12:113279383 | ATATATAT others(4): Show |
A | 1 | a0001c0001t0006g0205 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1297+550_1297+560d others(13): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279383 | ||||||
| chr12:113279385 | A | AT | 3 | a0001c0001t0001g0010 a0001c0001t0001g0092 a0001c0001t0001g0167 |
3 | HG01891.hp2 HG03710.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1297+551dupT | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279385 | ||||||
| chr12:113279385 | A | ATT | 3 | a0001c0001t0001g0007 a0001c0001t0004g0113 a0001c0010t0004g0141 |
3 | HG00738.hp1 HG03195.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.1297+551_1297+552i others(4): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279385 | ||||||
| chr12:113279385 | A | ATTT | 3 | a0001c0001t0001g0007 a0001c0001t0004g0118 a0001c0001t0019g0151 |
3 | HG02976.hp1 HG03654.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.1297+551_1297+552i others(5): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279385 | ||||||
| chr12:113279385 | A | T | 15 | a0001c0001t0001g0154 a0001c0001t0001g0184 a0001c0001t0002g0051 others(12): Show |
15 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1297+550A>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | chr12 | 113279385 | |||||||
| chr12:113279385 | ATATATAT others(3): Show |
A | 1 | a0001c0001t0006g0202 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1297+552_1297+561d others(12): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279385 | ||||||
| chr12:113279385 | ATATATAT others(4): Show |
A | 1 | a0001c0007t0002g0058 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1297+552_1297+562d others(13): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279385 | ||||||
| chr12:113279385 | ATATATAT others(10): Show |
A | 2 | a0001c0001t0002g0177 a0001c0001t0006g0176 |
2 | HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1297+552_1297+568d others(19): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279385 | ||||||
| chr12:113279386 | TA | T | 3 | a0001c0001t0001g0146 a0001c0001t0003g0180 a0001c0001t0017g0138 |
3 | HG02723.hp1 HG04184.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.1297+552delA | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | chr12 | 113279386 | |||||||
| chr12:113279387 | A | AT | 8 | a0001c0001t0001g0070 a0001c0001t0001g0084 a0001c0001t0001g0143 others(5): Show |
8 | HG00639.hp1 HG01169.hp2 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.1297+553dupT | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279387 | ||||||
| chr12:113279387 | A | ATT | 17 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0062 others(14): Show |
18 | HG00408.hp2 HG00639.hp2 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.1297+553_1297+554i others(4): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279387 | ||||||
| chr12:113279387 | A | ATTT | 7 | a0001c0001t0001g0069 a0001c0001t0001g0122 a0001c0001t0001g0132 others(4): Show |
7 | HG01884.hp1 HG02257.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1297+553_1297+554i others(5): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279387 | ||||||
| chr12:113279387 | A | T | 39 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0065 others(36): Show |
40 | HG00140.hp1 HG00140.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.1297+552A>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | chr12 | 113279387 | |||||||
| chr12:113279389 | A | AT | 8 | a0001c0001t0001g0068 a0001c0001t0001g0071 a0001c0001t0001g0085 others(5): Show |
9 | HG00323.hp1 HG01109.hp2 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.1297+555dupT | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279389 | ||||||
| chr12:113279389 | A | ATT | 13 | a0001c0001t0001g0004 a0001c0001t0001g0096 a0001c0001t0001g0107 others(10): Show |
13 | HG00280.hp1 HG01109.hp1 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.1297+555_1297+556i others(4): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279389 | ||||||
| chr12:113279389 | A | ATTT | 12 | a0001c0001t0001g0010 a0001c0001t0001g0061 a0001c0001t0001g0103 others(9): Show |
12 | HG01081.hp1 HG01081.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1297+555_1297+556i others(5): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279389 | ||||||
| chr12:113279389 | A | T | 85 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(82): Show |
89 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.1297+554A>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | chr12 | 113279389 | |||||||
| chr12:113279391 | A | ATATATAT others(24): Show |
1 | a0001c0001t0002g0050 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1297+557_1297+558i others(33): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279391 | ||||||
| chr12:113279391 | A | ATATATAT others(23): Show |
1 | a0001c0001t0002g0036 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1297+557_1297+558i others(32): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279391 | ||||||
| chr12:113279391 | A | ATATATAT others(17): Show |
1 | a0001c0001t0012g0175 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1297+557_1297+558i others(26): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279391 | ||||||
| chr12:113279391 | A | ATATATAT others(19): Show |
1 | a0001c0001t0002g0027 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1297+557_1297+558i others(28): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279391 | ||||||
| chr12:113279391 | A | ATATATAT others(22): Show |
1 | a0001c0001t0002g0037 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1297+557_1297+558i others(31): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279391 | ||||||
| chr12:113279391 | A | ATATATAT others(17): Show |
1 | a0001c0001t0002g0035 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1297+557_1297+558i others(26): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279391 | ||||||
| chr12:113279391 | A | ATATATAT others(19): Show |
1 | a0001c0001t0002g0032 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1297+557_1297+558i others(28): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279391 | ||||||
| chr12:113279391 | A | ATATATAT others(22): Show |
1 | a0001c0001t0002g0044 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1297+557_1297+558i others(31): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279391 | ||||||
| chr12:113279391 | A | ATATATAT others(23): Show |
1 | a0001c0001t0002g0045 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1297+557_1297+558i others(32): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279391 | ||||||
| chr12:113279391 | A | ATATATAT others(13): Show |
1 | a0001c0004t0002g0033 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1297+557_1297+558i others(22): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279391 | ||||||
| chr12:113279391 | A | ATATATAT others(15): Show |
1 | a0001c0001t0001g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1297+557_1297+558i others(24): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279391 | ||||||
| chr12:113279391 | A | ATATATAT others(17): Show |
1 | a0001c0001t0002g0039 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1297+557_1297+558i others(26): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279391 | ||||||
| chr12:113279391 | A | ATATATAT others(20): Show |
2 | a0001c0001t0002g0043 a0001c0001t0016g0003 |
2 | NA18948.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.1297+557_1297+558i others(29): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279391 | ||||||
| chr12:113279391 | A | ATATATAT others(12): Show |
2 | a0001c0001t0002g0006 a0001c0001t0002g0028 |
3 | NA18969.hp1 NA19065.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1297+557_1297+558i others(21): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279391 | ||||||
| chr12:113279391 | A | ATATATAT others(13): Show |
4 | a0001c0001t0001g0015 a0001c0001t0002g0029 a0001c0001t0002g0048 others(1): Show |
4 | HG02027.hp1 HG02027.hp2 HG02071.hp2 others(1): Show |
intron_variant | MODIFIER | c.1297+557_1297+558i others(22): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279391 | ||||||
| chr12:113279391 | A | ATATATAT others(15): Show |
1 | a0001c0001t0002g0038 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1297+557_1297+558i others(24): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279391 | ||||||
| chr12:113279391 | A | ATATATAT others(16): Show |
1 | a0001c0001t0002g0052 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1297+557_1297+558i others(25): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279391 | ||||||
| chr12:113279391 | A | ATATATAT others(17): Show |
1 | a0001c0001t0002g0047 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1297+557_1297+558i others(26): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279391 | ||||||
| chr12:113279391 | A | ATATATAT others(18): Show |
1 | a0001c0001t0002g0049 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1297+557_1297+558i others(27): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279391 | ||||||
| chr12:113279391 | A | ATATATAT others(20): Show |
1 | a0001c0001t0002g0003 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1297+557_1297+558i others(29): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279391 | ||||||
| chr12:113279391 | A | ATATATAT others(11): Show |
2 | a0001c0001t0002g0031 a0001c0004t0002g0034 |
2 | NA18982.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1297+557_1297+558i others(20): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279391 | ||||||
| chr12:113279391 | A | ATATATAT others(13): Show |
1 | a0001c0001t0002g0046 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1297+557_1297+558i others(22): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279391 | ||||||
| chr12:113279391 | A | ATATATAT others(14): Show |
1 | a0001c0001t0024g0042 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1297+557_1297+558i others(23): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279391 | ||||||
| chr12:113279391 | A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0026 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1297+557_1297+558i others(25): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279391 | ||||||
| chr12:113279391 | A | ATATATAT others(13): Show |
1 | a0001c0001t0021g0053 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1297+557_1297+558i others(22): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279391 | ||||||
| chr12:113279391 | A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0087 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1297+557_1297+558i others(13): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279391 | ||||||
| chr12:113279391 | A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0024 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1297+557_1297+558i others(28): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279391 | ||||||
| chr12:113279391 | A | ATATATAT others(3): Show |
1 | a0001c0001t0001g0001 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1297+557_1297+558i others(12): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279391 | ||||||
| chr12:113279391 | A | ATATATTT others(12): Show |
1 | a0001c0001t0002g0023 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1297+557_1297+558i others(21): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279391 | ||||||
| chr12:113279391 | A | ATATTTT | 3 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0004g0108 |
5 | HG00423.hp2 NA19003.hp1 NA19060.hp2 others(2): Show |
intron_variant | MODIFIER | c.1297+557_1297+558i others(8): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279391 | ||||||
| chr12:113279391 | A | ATATTTTT others(12): Show |
1 | a0001c0001t0001g0025 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1297+557_1297+558i others(21): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279391 | ||||||
| chr12:113279391 | A | ATT | 6 | a0001c0001t0001g0060 a0001c0001t0001g0080 a0001c0001t0001g0134 others(3): Show |
6 | HG01169.hp1 HG01361.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.1297+581_1297+582d others(4): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr12 | 113279391 | ||||||
| chr12:113279391 | A | T | 128 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(125): Show |
136 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.1297+556A>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | chr12 | 113279391 | |||||||
| chr12:113279393 | T | A | 1 | a0001c0012t0001g0201 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1297+558T>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | chr12 | 113279393 | |||||||
| chr12:113279471 | T | C | 28 | a0001c0001t0002g0005 a0001c0001t0002g0091 a0001c0001t0002g0206 others(25): Show |
29 | HG00280.hp2 HG01168.hp2 HG02080.hp2 others(26): Show |
intron_variant | MODIFIER | c.1297+636T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | chr12 | 113279471 | |||||||
| chr12:113279478 | A | C | 3 | a0001c0001t0001g0148 a0001c0001t0010g0149 a0001c0001t0010g0150 |
3 | HG02630.hp1 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1297+643A>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | chr12 | 113279478 | |||||||
| chr12:113279484 | C | T | 3 | a0001c0002t0009g0054 a0001c0002t0009g0055 a0001c0002t0009g0056 |
3 | HG02717.hp2 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1297+649C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | chr12 | 113279484 | |||||||
| chr12:113279844 | A | C | 3 | a0001c0003t0008g0200 a0001c0003t0008g0226 a0001c0003t0008g0227 |
3 | HG00280.hp2 HG01168.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1298-307A>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | chr12 | 113279844 | |||||||
| chr12:113280022 | G | C | 25 | a0001c0001t0002g0005 a0001c0001t0002g0091 a0001c0001t0002g0206 others(22): Show |
26 | HG02080.hp2 HG02083.hp2 HG02155.hp2 others(23): Show |
intron_variant | MODIFIER | c.1298-129G>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | chr12 | 113280022 | |||||||
| chr12:113280096 | A | G | 84 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(81): Show |
89 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.1298-55A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 14/27 | chr12 | 113280096 | |||||||
| chr12:113280412 | C | T | 1 | a0001c0012t0001g0201 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1342+217C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 15/27 | chr12 | 113280412 | |||||||
| chr12:113280485 | C | T | 25 | a0001c0001t0002g0005 a0001c0001t0002g0091 a0001c0001t0002g0206 others(22): Show |
26 | HG02080.hp2 HG02083.hp2 HG02155.hp2 others(23): Show |
intron_variant | MODIFIER | c.1342+290C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 15/27 | chr12 | 113280485 | |||||||
| chr12:113280716 | A | G | 2 | a0001c0001t0007g0112 a0001c0001t0014g0100 |
2 | HG01361.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1342+521A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 15/27 | chr12 | 113280716 | |||||||
| chr12:113280778 | C | T | 29 | a0001c0001t0002g0005 a0001c0001t0002g0091 a0001c0001t0002g0206 others(26): Show |
30 | HG00280.hp2 HG01168.hp2 HG02080.hp2 others(27): Show |
intron_variant | MODIFIER | c.1342+583C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 15/27 | chr12 | 113280778 | |||||||
| chr12:113280908 | T | C | 2 | a0001c0001t0005g0067 a0001c0001t0005g0095 |
2 | NA18942.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.1342+713T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 15/27 | chr12 | 113280908 | |||||||
| chr12:113280966 | A | G | 1 | a0001c0001t0003g0016 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1342+771A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 15/27 | chr12 | 113280966 | |||||||
| chr12:113280983 | A | G | 54 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(51): Show |
58 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.1342+788A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 15/27 | chr12 | 113280983 | |||||||
| chr12:113281405 | T | A | 2 | a0001c0001t0001g0015 a0001c0001t0002g0048 |
2 | HG02027.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.1342+1210T>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 15/27 | chr12 | 113281405 | |||||||
| chr12:113281817 | G | T | 54 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(51): Show |
58 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.1342+1622G>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 15/27 | chr12 | 113281817 | |||||||
| chr12:113281855 | T | C | 15 | a0001c0001t0001g0184 a0001c0001t0003g0185 a0001c0001t0003g0187 others(12): Show |
15 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1342+1660T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 15/27 | chr12 | 113281855 | |||||||
| chr12:113281912 | C | CT | 41 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(38): Show |
42 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(39): Show |
intron_variant | MODIFIER | c.1342+1737dupT | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr12 | 113281912 | ||||||
| chr12:113281912 | C | CTT | 13 | a0001c0001t0001g0015 a0001c0001t0002g0006 a0001c0001t0002g0027 others(10): Show |
14 | HG02027.hp1 HG02027.hp2 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1342+1736_1342+173 others(6): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr12 | 113281912 | ||||||
| chr12:113281912 | CT | C | 18 | a0001c0001t0002g0207 a0001c0001t0002g0209 a0001c0001t0002g0222 others(15): Show |
18 | HG02109.hp2 HG02145.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.1342+1737delT | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr12 | 113281912 | ||||||
| chr12:113281969 | G | A | 1 | a0001c0008t0006g0204 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1342+1774G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 15/27 | chr12 | 113281969 | |||||||
| chr12:113281983 | T | C | 84 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(81): Show |
89 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.1342+1788T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 15/27 | chr12 | 113281983 | |||||||
| chr12:113281987 | C | G | 3 | a0001c0001t0001g0148 a0001c0001t0010g0149 a0001c0001t0010g0150 |
3 | HG02630.hp1 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1342+1792C>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 15/27 | chr12 | 113281987 | |||||||
| chr12:113282016 | G | T | 4 | a0001c0001t0006g0202 a0001c0001t0006g0205 a0001c0008t0006g0203 others(1): Show |
4 | HG01891.hp1 HG02055.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1342+1821G>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 15/27 | chr12 | 113282016 | |||||||
| chr12:113282072 | C | G | 30 | a0001c0001t0002g0005 a0001c0001t0002g0090 a0001c0001t0002g0091 others(27): Show |
31 | HG00280.hp2 HG01168.hp2 HG02080.hp2 others(28): Show |
intron_variant | MODIFIER | c.1342+1877C>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 15/27 | chr12 | 113282072 | |||||||
| chr12:113282087 | A | AT | 8 | a0001c0001t0001g0156 a0001c0001t0003g0196 a0001c0001t0004g0074 others(5): Show |
8 | HG00099.hp1 HG00099.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1342+1913dupT | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr12 | 113282087 | ||||||
| chr12:113282087 | A | ATT | 40 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(37): Show |
42 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.1342+1912_1342+191 others(6): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr12 | 113282087 | ||||||
| chr12:113282087 | A | ATTT | 27 | a0001c0001t0001g0015 a0001c0001t0002g0005 a0001c0001t0002g0036 others(24): Show |
28 | HG00280.hp2 HG01168.hp2 HG02027.hp1 others(25): Show |
intron_variant | MODIFIER | c.1342+1911_1342+191 others(7): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr12 | 113282087 | ||||||
| chr12:113282087 | A | ATTTT | 5 | a0001c0001t0002g0209 a0001c0001t0002g0221 a0001c0001t0006g0202 others(2): Show |
5 | HG01891.hp1 HG02055.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1342+1910_1342+191 others(8): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr12 | 113282087 | ||||||
| chr12:113282087 | A | ATTTTT | 6 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(3): Show |
8 | HG02280.hp1 HG02451.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1342+1909_1342+191 others(9): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr12 | 113282087 | ||||||
| chr12:113282313 | G | A | 3 | a0001c0007t0002g0058 a0001c0007t0011g0174 a0001c0013t0011g0173 |
3 | HG02572.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1342+2118G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 15/27 | chr12 | 113282313 | |||||||
| chr12:113282332 | A | G | 1 | a0001c0012t0001g0201 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1342+2137A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 15/27 | chr12 | 113282332 | |||||||
| chr12:113282388 | C | T | 1 | a0001c0001t0002g0046 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1342+2193C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 15/27 | chr12 | 113282388 | |||||||
| chr12:113282472 | G | A | 2 | a0001c0001t0002g0177 a0001c0001t0006g0176 |
2 | HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1343-2109G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 15/27 | chr12 | 113282472 | |||||||
| chr12:113282693 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1343-1888G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 15/27 | chr12 | 113282693 | |||||||
| chr12:113282712 | G | A | 30 | a0001c0001t0002g0005 a0001c0001t0002g0090 a0001c0001t0002g0091 others(27): Show |
31 | HG00280.hp2 HG01168.hp2 HG02080.hp2 others(28): Show |
intron_variant | MODIFIER | c.1343-1869G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 15/27 | chr12 | 113282712 | |||||||
| chr12:113282714 | G | A | 1 | a0001c0001t0003g0016 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1343-1867G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 15/27 | chr12 | 113282714 | |||||||
| chr12:113282749 | C | T | 3 | a0001c0007t0002g0058 a0001c0007t0011g0174 a0001c0013t0011g0173 |
3 | HG02572.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1343-1832C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 15/27 | chr12 | 113282749 | |||||||
| chr12:113282949 | C | T | 1 | a0001c0012t0001g0201 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1343-1632C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 15/27 | chr12 | 113282949 | |||||||
| chr12:113283012 | G | A | 54 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(51): Show |
58 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.1343-1569G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 15/27 | chr12 | 113283012 | |||||||
| chr12:113283086 | C | CA | 4 | a0001c0001t0001g0135 a0001c0001t0003g0014 a0001c0001t0003g0059 others(1): Show |
5 | HG01109.hp2 HG03209.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1343-1486dupA | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr12 | 113283086 | ||||||
| chr12:113283232 | G | A | 3 | a0001c0002t0009g0054 a0001c0002t0009g0055 a0001c0002t0009g0056 |
3 | HG02717.hp2 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1343-1349G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 15/27 | chr12 | 113283232 | |||||||
| chr12:113283244 | C | A | 1 | a0001c0001t0001g0148 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1343-1337C>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 15/27 | chr12 | 113283244 | |||||||
| chr12:113283305 | T | G | 1 | a0001c0001t0024g0042 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1343-1276T>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 15/27 | chr12 | 113283305 | |||||||
| chr12:113283547 | T | C | 1 | a0001c0001t0003g0196 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1343-1034T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 15/27 | chr12 | 113283547 | |||||||
| chr12:113283617 | T | C | 89 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(86): Show |
94 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.1343-964T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 15/27 | chr12 | 113283617 | |||||||
| chr12:113283718 | A | G | 3 | a0001c0007t0002g0058 a0001c0007t0011g0174 a0001c0013t0011g0173 |
3 | HG02572.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1343-863A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 15/27 | chr12 | 113283718 | |||||||
| chr12:113283861 | G | T | 1 | a0001c0001t0002g0050 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1343-720G>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 15/27 | chr12 | 113283861 | |||||||
| chr12:113283993 | T | C | 1 | a0001c0001t0001g0128 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1343-588T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 15/27 | chr12 | 113283993 | |||||||
| chr12:113284026 | T | A | 1 | a0001c0001t0003g0016 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1343-555T>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 15/27 | chr12 | 113284026 | |||||||
| chr12:113284068 | A | G | 30 | a0001c0001t0002g0005 a0001c0001t0002g0090 a0001c0001t0002g0091 others(27): Show |
31 | HG00280.hp2 HG01168.hp2 HG02080.hp2 others(28): Show |
intron_variant | MODIFIER | c.1343-513A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 15/27 | chr12 | 113284068 | |||||||
| chr12:113284251 | A | C | 1 | a0001c0001t0001g0117 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1343-330A>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 15/27 | chr12 | 113284251 | |||||||
| chr12:113284274 | C | T | 1 | a0001c0001t0012g0175 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1343-307C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 15/27 | chr12 | 113284274 | |||||||
| chr12:113284667 | C | G | 50 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(47): Show |
54 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.1399+30C>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 16/27 | chr12 | 113284667 | |||||||
| chr12:113284680 | C | G | 1 | a0001c0001t0001g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1400-38C>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 16/27 | chr12 | 113284680 | |||||||
| chr12:113284699 | C | T | 2 | a0001c0001t0002g0207 a0001c0001t0002g0208 |
2 | NA18946.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.1400-19C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 16/27 | chr12 | 113284699 | |||||||
| chr12:113284836 | A | G | 6 | a0001c0001t0005g0067 a0001c0001t0005g0093 a0001c0001t0005g0094 others(3): Show |
6 | NA18942.hp2 NA18950.hp2 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.1453+65A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 17/27 | chr12 | 113284836 | |||||||
| chr12:113284953 | A | G | 55 | a0001c0001t0001g0184 a0001c0001t0002g0005 a0001c0001t0002g0090 others(52): Show |
56 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.1453+182A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 17/27 | chr12 | 113284953 | |||||||
| chr12:113284967 | C | T | 29 | a0001c0001t0002g0005 a0001c0001t0002g0090 a0001c0001t0002g0091 others(26): Show |
30 | HG00280.hp2 HG01168.hp2 HG02080.hp2 others(27): Show |
intron_variant | MODIFIER | c.1453+196C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 17/27 | chr12 | 113284967 | |||||||
| chr12:113284972 | C | T | 1 | a0001c0012t0001g0201 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1453+201C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 17/27 | chr12 | 113284972 | |||||||
| chr12:113285126 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1453+355T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 17/27 | chr12 | 113285126 | |||||||
| chr12:113285130 | C | T | 2 | a0001c0005t0001g0079 a0001c0005t0001g0120 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1453+359C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 17/27 | chr12 | 113285130 | |||||||
| chr12:113285381 | CT | C | 85 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(82): Show |
90 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.1454-501delT | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr12 | 113285381 | ||||||
| chr12:113285411 | C | T | 16 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(13): Show |
18 | HG01891.hp1 HG02055.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.1454-478C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 17/27 | chr12 | 113285411 | |||||||
| chr12:113285493 | C | T | 39 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(36): Show |
41 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.1454-396C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 17/27 | chr12 | 113285493 | |||||||
| chr12:113285697 | C | G | 1 | a0001c0001t0001g0019 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1454-192C>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 17/27 | chr12 | 113285697 | |||||||
| chr12:113285825 | G | A | 1 | a0001c0001t0002g0039 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1454-64G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 17/27 | chr12 | 113285825 | |||||||
| chr12:113285884 | C | T | 1 | a0001c0001t0003g0190 | 1 | HG02109.hp2 | splice_region_variant&intron_variant | LOW | c.1454-5C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 17/27 | chr12 | 113285884 | |||||||
| chr12:113286417 | T | TTGGGCCG others(94): Show |
1 | a0001c0001t0024g0042 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1526+472_1526+473i others(103): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 18/27 | INFO_REALIGN_3_PRIME | chr12 | 113286417 | ||||||
| chr12:113286417 | T | TTGGGCCG others(95): Show |
66 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(63): Show |
69 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.1526+490_1526+491i others(104): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 18/27 | INFO_REALIGN_3_PRIME | chr12 | 113286417 | ||||||
| chr12:113286417 | T | TTGGGCCG others(129): Show |
3 | a0001c0007t0002g0058 a0001c0007t0011g0174 a0001c0013t0011g0173 |
3 | HG02572.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1526+490_1526+491i others(138): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 18/27 | INFO_REALIGN_3_PRIME | chr12 | 113286417 | ||||||
| chr12:113286417 | T | TTGGGCCG others(95): Show |
1 | a0001c0001t0003g0016 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1526+490_1526+491i others(104): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 18/27 | INFO_REALIGN_3_PRIME | chr12 | 113286417 | ||||||
| chr12:113286709 | C | T | 14 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0010 others(11): Show |
17 | HG03704.hp1 HG03710.hp2 NA18942.hp2 others(14): Show |
intron_variant | MODIFIER | c.1527-278C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 18/27 | chr12 | 113286709 | |||||||
| chr12:113286741 | TC | T | 3 | a0001c0002t0009g0054 a0001c0002t0009g0055 a0001c0002t0009g0056 |
3 | HG02717.hp2 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1527-243delC | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 18/27 | INFO_REALIGN_3_PRIME | chr12 | 113286741 | ||||||
| chr12:113287140 | A | G | 105 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(102): Show |
108 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.1634+46A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 19/27 | chr12 | 113287140 | |||||||
| chr12:113287530 | G | C | 4 | a0001c0001t0001g0135 a0001c0001t0003g0014 a0001c0001t0003g0059 others(1): Show |
5 | HG01109.hp2 HG03209.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1634+436G>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 19/27 | chr12 | 113287530 | |||||||
| chr12:113287652 | C | T | 2 | a0001c0001t0002g0177 a0001c0001t0006g0176 |
2 | HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1635-511C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 19/27 | chr12 | 113287652 | |||||||
| chr12:113287801 | A | G | 1 | a0001c0001t0001g0178 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1635-362A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 19/27 | chr12 | 113287801 | |||||||
| chr12:113287803 | C | T | 28 | a0001c0001t0002g0005 a0001c0001t0002g0090 a0001c0001t0002g0091 others(25): Show |
29 | HG00280.hp2 HG01168.hp2 HG02080.hp2 others(26): Show |
intron_variant | MODIFIER | c.1635-360C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 19/27 | chr12 | 113287803 | |||||||
| chr12:113287816 | G | A | 1 | a0001c0001t0002g0046 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1635-347G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 19/27 | chr12 | 113287816 | |||||||
| chr12:113287972 | C | G | 1 | a0001c0001t0004g0113 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1635-191C>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 19/27 | chr12 | 113287972 | |||||||
| chr12:113288000 | C | G | 2 | a0001c0001t0002g0177 a0001c0001t0006g0176 |
2 | HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1635-163C>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 19/27 | chr12 | 113288000 | |||||||
| chr12:113288347 | C | T | 28 | a0001c0001t0001g0140 a0001c0001t0001g0147 a0001c0001t0002g0005 others(25): Show |
29 | HG00280.hp2 HG00738.hp2 HG01168.hp2 others(26): Show |
intron_variant | MODIFIER | c.1706+113C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 20/27 | chr12 | 113288347 | |||||||
| chr12:113288614 | C | G | 1 | a0001c0013t0011g0173 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1707-144C>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 20/27 | chr12 | 113288614 | |||||||
| chr12:113288693 | C | T | 2 | a0001c0001t0001g0057 a0001c0001t0018g0124 |
2 | HG02647.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1707-65C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 20/27 | chr12 | 113288693 | |||||||
| chr12:113288724 | G | A | 1 | a0001c0001t0003g0016 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1707-34G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 20/27 | chr12 | 113288724 | |||||||
| chr12:113288977 | G | A | 3 | a0001c0001t0001g0148 a0001c0001t0010g0149 a0001c0001t0010g0150 |
3 | HG02630.hp1 HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1796+130G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 21/27 | chr12 | 113288977 | |||||||
| chr12:113288997 | T | A | 13 | a0001c0001t0003g0187 a0001c0001t0003g0188 a0001c0001t0003g0189 others(10): Show |
13 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1796+150T>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 21/27 | chr12 | 113288997 | |||||||
| chr12:113289186 | C | T | 3 | a0001c0002t0009g0054 a0001c0002t0009g0055 a0001c0002t0009g0056 |
3 | HG02717.hp2 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1796+339C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 21/27 | chr12 | 113289186 | |||||||
| chr12:113289206 | T | C | 3 | a0001c0007t0002g0058 a0001c0007t0011g0174 a0001c0013t0011g0173 |
3 | HG02572.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1796+359T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 21/27 | chr12 | 113289206 | |||||||
| chr12:113289223 | C | T | 4 | a0001c0001t0006g0202 a0001c0001t0006g0205 a0001c0008t0006g0203 others(1): Show |
4 | HG01891.hp1 HG02055.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1796+376C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 21/27 | chr12 | 113289223 | |||||||
| chr12:113289229 | C | T | 1 | a0001c0001t0012g0175 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1796+382C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 21/27 | chr12 | 113289229 | |||||||
| chr12:113289305 | C | A | 6 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(3): Show |
8 | HG02280.hp1 HG02451.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1796+458C>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 21/27 | chr12 | 113289305 | |||||||
| chr12:113289413 | A | G | 4 | a0001c0001t0006g0202 a0001c0001t0006g0205 a0001c0008t0006g0203 others(1): Show |
4 | HG01891.hp1 HG02055.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1796+566A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 21/27 | chr12 | 113289413 | |||||||
| chr12:113289565 | G | A | 3 | a0001c0007t0002g0058 a0001c0007t0011g0174 a0001c0013t0011g0173 |
3 | HG02572.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1797-563G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 21/27 | chr12 | 113289565 | |||||||
| chr12:113289622 | G | A | 1 | a0001c0001t0003g0182 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1797-506G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 21/27 | chr12 | 113289622 | |||||||
| chr12:113289631 | A | C | 5 | a0001c0001t0007g0064 a0001c0001t0007g0072 a0001c0001t0007g0083 others(2): Show |
5 | HG00099.hp1 HG01358.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.1797-497A>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 21/27 | chr12 | 113289631 | |||||||
| chr12:113289721 | T | C | 1 | a0001c0008t0006g0204 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1797-407T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 21/27 | chr12 | 113289721 | |||||||
| chr12:113289833 | C | T | 6 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(3): Show |
8 | HG02280.hp1 HG02451.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1797-295C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 21/27 | chr12 | 113289833 | |||||||
| chr12:113289891 | C | A | 1 | a0001c0001t0001g0024 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1797-237C>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 21/27 | chr12 | 113289891 | |||||||
| chr12:113289892 | A | G | 1 | a0001c0001t0001g0024 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1797-236A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 21/27 | chr12 | 113289892 | |||||||
| chr12:113289893 | G | C | 1 | a0001c0001t0001g0024 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1797-235G>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 21/27 | chr12 | 113289893 | |||||||
| chr12:113289904 | G | GGTGGCAG others(3): Show |
1 | a0001c0001t0001g0024 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1797-223_1797-222i others(12): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 113289904 | ||||||
| chr12:113289907 | T | A | 1 | a0001c0001t0001g0024 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1797-221T>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 21/27 | chr12 | 113289907 | |||||||
| chr12:113289917 | A | C | 1 | a0001c0001t0001g0024 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1797-211A>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 21/27 | chr12 | 113289917 | |||||||
| chr12:113289918 | T | A | 1 | a0001c0001t0001g0024 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1797-210T>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 21/27 | chr12 | 113289918 | |||||||
| chr12:113289919 | C | T | 1 | a0001c0001t0001g0024 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1797-209C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 21/27 | chr12 | 113289919 | |||||||
| chr12:113289949 | AGGGCATT others(18): Show |
A | 1 | a0001c0001t0001g0024 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1797-177_1797-153d others(27): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr12 | 113289949 | ||||||
| chr12:113289980 | A | C | 1 | a0001c0001t0001g0024 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1797-148A>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 21/27 | chr12 | 113289980 | |||||||
| chr12:113289981 | G | T | 1 | a0001c0001t0001g0024 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1797-147G>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 21/27 | chr12 | 113289981 | |||||||
| chr12:113289982 | G | T | 1 | a0001c0001t0001g0024 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1797-146G>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 21/27 | chr12 | 113289982 | |||||||
| chr12:113289983 | T | A | 1 | a0001c0001t0001g0024 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1797-145T>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 21/27 | chr12 | 113289983 | |||||||
| chr12:113289994 | A | G | 1 | a0001c0001t0001g0024 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1797-134A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 21/27 | chr12 | 113289994 | |||||||
| chr12:113289996 | G | A | 1 | a0001c0001t0001g0024 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1797-132G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 21/27 | chr12 | 113289996 | |||||||
| chr12:113289998 | A | C | 1 | a0001c0001t0001g0024 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1797-130A>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 21/27 | chr12 | 113289998 | |||||||
| chr12:113289999 | G | T | 1 | a0001c0001t0001g0024 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1797-129G>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 21/27 | chr12 | 113289999 | |||||||
| chr12:113290004 | C | G | 1 | a0001c0001t0001g0024 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1797-124C>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 21/27 | chr12 | 113290004 | |||||||
| chr12:113290005 | C | A | 1 | a0001c0001t0001g0024 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1797-123C>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 21/27 | chr12 | 113290005 | |||||||
| chr12:113290006 | A | G | 1 | a0001c0001t0001g0024 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1797-122A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 21/27 | chr12 | 113290006 | |||||||
| chr12:113290007 | G | A | 1 | a0001c0001t0001g0024 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1797-121G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 21/27 | chr12 | 113290007 | |||||||
| chr12:113290009 | C | G | 1 | a0001c0001t0001g0024 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1797-119C>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 21/27 | chr12 | 113290009 | |||||||
| chr12:113290013 | G | A | 1 | a0001c0001t0001g0024 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1797-115G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 21/27 | chr12 | 113290013 | |||||||
| chr12:113290020 | A | G | 1 | a0001c0001t0001g0024 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1797-108A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 21/27 | chr12 | 113290020 | |||||||
| chr12:113290021 | C | G | 1 | a0001c0001t0001g0024 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1797-107C>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 21/27 | chr12 | 113290021 | |||||||
| chr12:113290024 | A | G | 1 | a0001c0001t0001g0024 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1797-104A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 21/27 | chr12 | 113290024 | |||||||
| chr12:113290029 | T | A | 1 | a0001c0001t0001g0024 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1797-99T>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 21/27 | chr12 | 113290029 | |||||||
| chr12:113290037 | C | A | 1 | a0001c0001t0001g0024 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1797-91C>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 21/27 | chr12 | 113290037 | |||||||
| chr12:113290045 | G | A | 1 | a0001c0001t0001g0024 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1797-83G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 21/27 | chr12 | 113290045 | |||||||
| chr12:113290047 | T | C | 1 | a0001c0001t0001g0024 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1797-81T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 21/27 | chr12 | 113290047 | |||||||
| chr12:113290057 | A | G | 1 | a0001c0001t0001g0024 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1797-71A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 21/27 | chr12 | 113290057 | |||||||
| chr12:113290058 | C | A | 1 | a0001c0001t0001g0024 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1797-70C>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 21/27 | chr12 | 113290058 | |||||||
| chr12:113290059 | T | C | 1 | a0001c0001t0001g0024 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1797-69T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 21/27 | chr12 | 113290059 | |||||||
| chr12:113290121 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG01978.hp2 | splice_region_variant&intron_variant | LOW | c.1797-7C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 21/27 | chr12 | 113290121 | |||||||
| chr12:113290250 | G | A | 1 | a0001c0001t0003g0016 | 1 | HG03139.hp2 | splice_region_variant&intron_variant | LOW | c.1912+7G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 22/27 | chr12 | 113290250 | |||||||
| chr12:113290259 | C | A | 1 | a0001c0001t0002g0220 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1912+16C>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 22/27 | chr12 | 113290259 | |||||||
| chr12:113290272 | T | C | 1 | a0001c0001t0004g0077 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1912+29T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 22/27 | chr12 | 113290272 | |||||||
| chr12:113290447 | C | A | 1 | a0001c0001t0001g0024 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1912+204C>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 22/27 | chr12 | 113290447 | |||||||
| chr12:113290448 | A | C | 1 | a0001c0001t0001g0024 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1912+205A>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 22/27 | chr12 | 113290448 | |||||||
| chr12:113290603 | C | A | 1 | a0001c0001t0001g0024 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1913-349C>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 22/27 | chr12 | 113290603 | |||||||
| chr12:113290687 | C | T | 3 | a0001c0007t0002g0058 a0001c0007t0011g0174 a0001c0013t0011g0173 |
3 | HG02572.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1913-265C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 22/27 | chr12 | 113290687 | |||||||
| chr12:113290762 | A | G | 1 | a0001c0001t0001g0178 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1913-190A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 22/27 | chr12 | 113290762 | |||||||
| chr12:113290817 | C | T | 1 | a0001c0001t0004g0125 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1913-135C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 22/27 | chr12 | 113290817 | |||||||
| chr12:113290819 | C | T | 6 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(3): Show |
8 | HG02280.hp1 HG02451.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1913-133C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 22/27 | chr12 | 113290819 | |||||||
| chr12:113290827 | A | T | 1 | a0001c0001t0001g0024 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1913-125A>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 22/27 | chr12 | 113290827 | |||||||
| chr12:113290941 | T | C | 1 | a0001c0001t0001g0024 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1913-11T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 22/27 | chr12 | 113290941 | |||||||
| chr12:113290942 | C | T | 1 | a0001c0001t0001g0024 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1913-10C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 22/27 | chr12 | 113290942 | |||||||
| chr12:113291183 | T | C | 86 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(83): Show |
92 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.1959+185T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 23/27 | chr12 | 113291183 | |||||||
| chr12:113291349 | A | C | 1 | a0001c0001t0004g0153 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1960-260A>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 23/27 | chr12 | 113291349 | |||||||
| chr12:113291350 | C | T | 1 | a0001c0001t0004g0153 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1960-259C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 23/27 | chr12 | 113291350 | |||||||
| chr12:113291519 | G | A | 3 | a0001c0007t0002g0058 a0001c0007t0011g0174 a0001c0013t0011g0173 |
3 | HG02572.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1960-90G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 23/27 | chr12 | 113291519 | |||||||
| chr12:113291570 | A | C | 6 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(3): Show |
8 | HG02280.hp1 HG02451.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1960-39A>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 23/27 | chr12 | 113291570 | |||||||
| chr12:113291695 | G | C | 3 | a0001c0003t0008g0200 a0001c0003t0008g0226 a0001c0003t0008g0227 |
3 | HG00280.hp2 HG01168.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2028+18G>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 24/27 | chr12 | 113291695 | |||||||
| chr12:113291738 | G | C | 6 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(3): Show |
8 | HG02280.hp1 HG02451.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.2028+61G>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 24/27 | chr12 | 113291738 | |||||||
| chr12:113291763 | G | A | 2 | a0001c0001t0002g0177 a0001c0001t0006g0176 |
2 | HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2028+86G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 24/27 | chr12 | 113291763 | |||||||
| chr12:113291974 | A | G | 1 | a0001c0001t0005g0097 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2113+16A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 25/27 | chr12 | 113291974 | |||||||
| chr12:113292151 | G | A | 76 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(73): Show |
81 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.2113+193G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 25/27 | chr12 | 113292151 | |||||||
| chr12:113292242 | C | G | 2 | a0001c0001t0003g0179 a0001c0001t0003g0181 |
2 | HG00140.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.2113+284C>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 25/27 | chr12 | 113292242 | |||||||
| chr12:113292453 | C | A | 1 | a0001c0001t0001g0119 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2114-481C>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 25/27 | chr12 | 113292453 | |||||||
| chr12:113292459 | G | A | 81 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(78): Show |
86 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.2114-475G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 25/27 | chr12 | 113292459 | |||||||
| chr12:113292516 | A | G | 1 | a0001c0001t0003g0016 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2114-418A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 25/27 | chr12 | 113292516 | |||||||
| chr12:113292550 | C | G | 6 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(3): Show |
8 | HG02280.hp1 HG02451.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.2114-384C>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 25/27 | chr12 | 113292550 | |||||||
| chr12:113292647 | A | G | 2 | a0001c0001t0002g0214 a0001c0001t0015g0211 |
2 | HG02083.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.2114-287A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 25/27 | chr12 | 113292647 | |||||||
| chr12:113292788 | A | G | 1 | a0001c0004t0002g0022 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2114-146A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 25/27 | chr12 | 113292788 | |||||||
| chr12:113292899 | C | T | 2 | a0001c0007t0011g0174 a0001c0013t0011g0173 |
2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.2114-35C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 25/27 | chr12 | 113292899 | |||||||
| chr12:113292900 | G | A | 1 | a0001c0001t0018g0124 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2114-34G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 25/27 | chr12 | 113292900 | |||||||
| chr12:113292931 | C | T | 15 | a0001c0001t0003g0185 a0001c0001t0003g0187 a0001c0001t0003g0188 others(12): Show |
15 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(12): Show |
splice_region_variant&intron_variant | LOW | c.2114-3C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 25/27 | chr12 | 113292931 | |||||||
| chr12:113293484 | C | G | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.2334+135C>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 27/27 | chr12 | 113293484 | |||||||
| chr12:113293507 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2334+158G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 27/27 | chr12 | 113293507 | |||||||
| chr12:113293521 | C | T | 3 | a0001c0001t0001g0057 a0001c0001t0001g0178 a0001c0001t0002g0177 |
3 | HG03486.hp2 NA19043.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2334+172C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 27/27 | chr12 | 113293521 | |||||||
| chr12:113293570 | C | T | 5 | a0001c0001t0006g0176 a0001c0001t0006g0202 a0001c0001t0006g0205 others(2): Show |
5 | HG01891.hp1 HG02055.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.2334+221C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 27/27 | chr12 | 113293570 | |||||||
| chr12:113293576 | T | C | 3 | a0001c0001t0003g0002 a0001c0001t0003g0018 a0001c0001t0003g0021 |
5 | HG02280.hp1 HG02451.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2334+227T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 27/27 | chr12 | 113293576 | |||||||
| chr12:113293588 | C | G | 3 | a0001c0002t0009g0054 a0001c0002t0009g0055 a0001c0002t0009g0056 |
3 | HG02717.hp2 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2334+239C>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 27/27 | chr12 | 113293588 | |||||||
| chr12:113293649 | CAT | C | 3 | a0001c0002t0009g0054 a0001c0002t0009g0055 a0001c0002t0009g0056 |
3 | HG02717.hp2 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2334+301_2334+302d others(4): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 27/27 | chr12 | 113293649 | |||||||
| chr12:113293717 | C | G | 52 | a0001c0001t0002g0003 a0001c0001t0002g0006 a0001c0001t0002g0023 others(49): Show |
56 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.2334+368C>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 27/27 | chr12 | 113293717 | |||||||
| chr12:113293869 | G | A | 1 | a0001c0001t0002g0177 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2334+520G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 27/27 | chr12 | 113293869 | |||||||
| chr12:113293962 | C | T | 2 | a0001c0001t0002g0223 a0001c0001t0002g0224 |
2 | NA18953.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.2334+613C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 27/27 | chr12 | 113293962 | |||||||
| chr12:113293996 | C | T | 3 | a0001c0007t0002g0058 a0001c0007t0011g0174 a0001c0013t0011g0173 |
3 | HG02572.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2334+647C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 27/27 | chr12 | 113293996 | |||||||
| chr12:113294058 | G | A | 2 | a0001c0001t0001g0166 a0001c0001t0001g0169 |
2 | NA18977.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.2334+709G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 27/27 | chr12 | 113294058 | |||||||
| chr12:113294084 | T | TTTTTG | 3 | a0001c0007t0002g0058 a0001c0007t0011g0174 a0001c0013t0011g0173 |
3 | HG02572.hp1 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2334+750_2334+754d others(7): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr12 | 113294084 | ||||||
| chr12:113294121 | G | T | 6 | a0001c0003t0008g0200 a0001c0003t0008g0226 a0001c0003t0008g0227 others(3): Show |
6 | HG00280.hp2 HG01168.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.2334+772G>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 27/27 | chr12 | 113294121 | |||||||
| chr12:113294282 | G | C | 1 | a0001c0001t0002g0223 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.2334+933G>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 27/27 | chr12 | 113294282 | |||||||
| chr12:113294389 | G | A | 1 | a0001c0001t0002g0046 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2334+1040G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 27/27 | chr12 | 113294389 | |||||||
| chr12:113294469 | T | A | 37 | a0001c0001t0003g0002 a0001c0001t0003g0014 a0001c0001t0003g0016 others(34): Show |
40 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.2334+1120T>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 27/27 | chr12 | 113294469 | |||||||
| chr12:113294483 | C | T | 1 | a0001c0001t0004g0077 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2334+1134C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 27/27 | chr12 | 113294483 | |||||||
| chr12:113294490 | G | T | 37 | a0001c0001t0003g0002 a0001c0001t0003g0014 a0001c0001t0003g0016 others(34): Show |
40 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.2334+1141G>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 27/27 | chr12 | 113294490 | |||||||
| chr12:113294496 | G | A | 1 | a0001c0001t0021g0053 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2334+1147G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 27/27 | chr12 | 113294496 | |||||||
| chr12:113294519 | G | A | 54 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(51): Show |
57 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.2334+1170G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 27/27 | chr12 | 113294519 | |||||||
| chr12:113294621 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2334+1272T>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 27/27 | chr12 | 113294621 | |||||||
| chr12:113294626 | CA | C | 10 | a0001c0001t0004g0108 a0001c0001t0006g0176 a0001c0001t0006g0202 others(7): Show |
10 | HG01891.hp1 HG02055.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.2334+1293delA | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr12 | 113294626 | ||||||
| chr12:113294626 | CAAAAA | C | 31 | a0001c0001t0003g0002 a0001c0001t0003g0014 a0001c0001t0003g0016 others(28): Show |
34 | HG00140.hp1 HG00323.hp2 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.2334+1289_2334+129 others(9): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr12 | 113294626 | ||||||
| chr12:113294676 | C | T | 1 | a0001c0001t0004g0153 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2335-1284C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 27/27 | chr12 | 113294676 | |||||||
| chr12:113294749 | G | A | 3 | a0001c0002t0009g0054 a0001c0002t0009g0055 a0001c0002t0009g0056 |
3 | HG02717.hp2 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2335-1211G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 27/27 | chr12 | 113294749 | |||||||
| chr12:113294819 | G | C | 1 | a0001c0001t0017g0138 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2335-1141G>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 27/27 | chr12 | 113294819 | |||||||
| chr12:113294941 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2335-1019C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 27/27 | chr12 | 113294941 | |||||||
| chr12:113295181 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2335-779C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 27/27 | chr12 | 113295181 | |||||||
| chr12:113295210 | C | G | 2 | a0001c0001t0002g0023 a0001c0001t0002g0045 |
2 | NA18962.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.2335-750C>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 27/27 | chr12 | 113295210 | |||||||
| chr12:113295348 | C | T | 3 | a0001c0003t0008g0200 a0001c0003t0008g0226 a0001c0003t0008g0227 |
3 | HG00280.hp2 HG01168.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2335-612C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 27/27 | chr12 | 113295348 | |||||||
| chr12:113295443 | T | TA | 77 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(74): Show |
80 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.2335-497dupA | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr12 | 113295443 | ||||||
| chr12:113295443 | T | TAA | 31 | a0001c0001t0002g0037 a0001c0001t0003g0014 a0001c0001t0003g0059 others(28): Show |
32 | HG00140.hp1 HG00323.hp2 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.2335-498_2335-497d others(4): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr12 | 113295443 | ||||||
| chr12:113295443 | T | TAAA | 5 | a0001c0001t0003g0002 a0001c0001t0003g0016 a0001c0001t0003g0018 others(2): Show |
7 | HG02280.hp1 HG02451.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.2335-499_2335-497d others(5): Show |
TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr12 | 113295443 | ||||||
| chr12:113295443 | TA | T | 6 | a0001c0001t0001g0096 a0001c0001t0001g0103 a0001c0001t0001g0110 others(3): Show |
6 | HG01109.hp1 HG01168.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.2335-497delA | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr12 | 113295443 | ||||||
| chr12:113295570 | A | G | 3 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 |
3 | HG02809.hp1 HG02970.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2335-390A>G | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 27/27 | chr12 | 113295570 | |||||||
| chr12:113295579 | A | T | 1 | a0001c0001t0021g0053 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2335-381A>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 27/27 | chr12 | 113295579 | |||||||
| chr12:113295599 | G | A | 1 | a0001c0001t0020g0075 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2335-361G>A | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 27/27 | chr12 | 113295599 | |||||||
| chr12:113295731 | C | T | 1 | a0001c0001t0004g0098 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2335-229C>T | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 27/27 | chr12 | 113295731 | |||||||
| chr12:113295836 | A | C | 2 | a0001c0001t0018g0124 a0001c0001t0021g0053 |
2 | HG02559.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.2335-124A>C | TPCN1 | ENSG00000186815.13 | transcript | ENST00000335509.11 | protein_coding | 27/27 | chr12 | 113295836 |