Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 160419 |
| ensemblid | ENSG00000165805.10 |
| hgncid | 26665 |
| symbol | C12orf50 |
| name | chromosome 12 open reading frame 50 |
| refseq_nuc | NM_152589.3 |
| refseq_prot | NP_689802.1 |
| ensembl_nuc | ENST00000298699.7 |
| ensembl_prot | ENSP00000298699.2 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 87980035 |
| end | 88029401 |
| strand | - |
| ver | v1.2 |
| region | chr12:87980035-88029401 |
| region5000 | chr12:87975035-88034401 |
| regionname0 | C12orf50_chr12_87980035_88029401 |
| regionname5000 | C12orf50_chr12_87975035_88034401 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 414 | 166 | 15 | 43 | 80 | 9 | 17 | 61 | C12orf50_chr12_87975035_88034401 | C12orf50 | MEMQQ others(409): Show |
chr12 | 87975035 | 88034401 |
| a0002 | 0/0 | 414 | 87 | 58 | 8 | 15 | 0 | 6 | 12 | C12orf50_chr12_87975035_88034401 | C12orf50 | MEMQQ others(409): Show |
chr12 | 87975035 | 88034401 |
| a0003 | 0/0 | 414 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | MEMQQ others(409): Show |
chr12 | 87975035 | 88034401 |
| a0004 | 0/0 | 414 | 4 | 1 | 2 | 0 | 0 | 1 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | MEMQQ others(409): Show |
chr12 | 87975035 | 88034401 |
| a0005 | 0/0 | 414 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | MEMQQ others(409): Show |
chr12 | 87975035 | 88034401 |
| a0006 | 0/0 | 414 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | MEMQQ others(409): Show |
chr12 | 87975035 | 88034401 |
| a0007 | 0/0 | 414 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | MEMQQ others(409): Show |
chr12 | 87975035 | 88034401 |
| a0008 | 0/0 | 414 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | C12orf50_chr12_87975035_88034401 | C12orf50 | MEMQQ others(409): Show |
chr12 | 87975035 | 88034401 |
| a0009 | 0/0 | 414 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | MEMQQ others(409): Show |
chr12 | 87975035 | 88034401 |
| a0010 | 0/0 | 414 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | MEMQQ others(409): Show |
chr12 | 87975035 | 88034401 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1242 | 166 | 15 | 43 | 80 | 9 | 17 | C12orf50_chr12_87975035_88034401 | C12orf50 | ATGGA others(1237): Show |
chr12 | 87975035 | 88034401 | ||
| a0002c0002 | 0/0 | 1242 | 78 | 49 | 8 | 15 | 0 | 6 | C12orf50_chr12_87975035_88034401 | C12orf50 | ATGGA others(1237): Show |
chr12 | 87975035 | 88034401 | ||
| a0002c0003 | 0/0 | 1242 | 9 | 9 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | ATGGA others(1237): Show |
chr12 | 87975035 | 88034401 | ||
| a0003c0004 | 0/0 | 1242 | 6 | 6 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | ATGGA others(1237): Show |
chr12 | 87975035 | 88034401 | ||
| a0004c0005 | 0/0 | 1242 | 4 | 1 | 2 | 0 | 0 | 1 | C12orf50_chr12_87975035_88034401 | C12orf50 | ATGGA others(1237): Show |
chr12 | 87975035 | 88034401 | ||
| a0005c0006 | 0/0 | 1242 | 4 | 4 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | ATGGA others(1237): Show |
chr12 | 87975035 | 88034401 | ||
| a0006c0009 | 0/0 | 1242 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | ATGGA others(1237): Show |
chr12 | 87975035 | 88034401 | ||
| a0007c0007 | 0/0 | 1242 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | ATGGA others(1237): Show |
chr12 | 87975035 | 88034401 | ||
| a0008c0011 | 0/0 | 1242 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | ATGGA others(1237): Show |
chr12 | 87975035 | 88034401 | ||
| a0009c0010 | 0/0 | 1242 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | ATGGA others(1237): Show |
chr12 | 87975035 | 88034401 | ||
| a0010c0008 | 0/0 | 1242 | 1 | 0 | 0 | 0 | 1 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | ATGGA others(1237): Show |
chr12 | 87975035 | 88034401 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1711 | 165 | 15 | 42 | 80 | 9 | 17 | C12orf50_chr12_87975035_88034401 | C12orf50 | AGAAG others(1706): Show |
chr12 | 87975035 | 88034401 |
| a0001c0001t0004 | 0/0 | 1649 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | GGTTC others(1644): Show |
chr12 | 87975035 | 88034401 |
| a0002c0002t0001 | 0/0 | 1711 | 68 | 40 | 7 | 15 | 0 | 6 | C12orf50_chr12_87975035_88034401 | C12orf50 | AGAAG others(1706): Show |
chr12 | 87975035 | 88034401 |
| a0002c0002t0002 | 0/0 | 1712 | 7 | 7 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | AGAAG others(1707): Show |
chr12 | 87975035 | 88034401 |
| a0002c0002t0003 | 0/0 | 1711 | 3 | 2 | 1 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | AGAAG others(1706): Show |
chr12 | 87975035 | 88034401 |
| a0002c0003t0001 | 0/0 | 1711 | 9 | 9 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | AGAAG others(1706): Show |
chr12 | 87975035 | 88034401 |
| a0003c0004t0002 | 0/0 | 1712 | 6 | 6 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | AGAAG others(1707): Show |
chr12 | 87975035 | 88034401 |
| a0004c0005t0001 | 0/0 | 1711 | 4 | 1 | 2 | 0 | 0 | 1 | C12orf50_chr12_87975035_88034401 | C12orf50 | AGAAG others(1706): Show |
chr12 | 87975035 | 88034401 |
| a0005c0006t0001 | 0/0 | 1711 | 4 | 4 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | AGAAG others(1706): Show |
chr12 | 87975035 | 88034401 |
| a0006c0009t0001 | 0/0 | 1711 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | AGAAG others(1706): Show |
chr12 | 87975035 | 88034401 |
| a0007c0007t0001 | 0/0 | 1711 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | AGAAG others(1706): Show |
chr12 | 87975035 | 88034401 |
| a0008c0011t0001 | 0/0 | 1711 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | AGAAG others(1706): Show |
chr12 | 87975035 | 88034401 |
| a0009c0010t0001 | 0/0 | 1711 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | AGAAG others(1706): Show |
chr12 | 87975035 | 88034401 |
| a0010c0008t0001 | 0/0 | 1711 | 1 | 0 | 0 | 0 | 1 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | AGAAG others(1706): Show |
chr12 | 87975035 | 88034401 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 10 | 3 | 6 | 0 | 1 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0002 | 0/0 | 6 | 0 | 5 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0004 | 0/0 | 5 | 0 | 2 | 0 | 1 | 2 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0024 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0042 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0181 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0001c0001t0004g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0001g0003 | 0/0 | 5 | 3 | 2 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0001g0007 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0001g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0002t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0003t0001g0006 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0003t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0003t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0003t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0002c0003t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0003c0004t0002g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0003c0004t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0003c0004t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0003c0004t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0004c0005t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0004c0005t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0004c0005t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0004c0005t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0005c0006t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0005c0006t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0005c0006t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0005c0006t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0006c0009t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0007c0007t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0008c0011t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0009c0010t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| a0010c0008t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0068 | EUR | GBR | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | FIN | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | FIN | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | CHS | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG00639 | hp1 | a0002 | c0002 | t0003 | g0044 | AMR | PUR | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0142 | AMR | PUR | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG00741 | hp2 | a0004 | c0005 | t0001 | g0037 | AMR | PUR | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0190 | AMR | PUR | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0032 | AMR | PUR | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0013 | AMR | PUR | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0059 | AMR | CLM | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0088 | AMR | CLM | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG01496 | hp2 | a0004 | c0005 | t0001 | g0048 | AMR | CLM | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0103 | EUR | IBS | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG01884 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | ACB | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG01884 | hp2 | a0005 | c0006 | t0001 | g0204 | AFR | ACB | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG01943 | hp1 | a0006 | c0009 | t0001 | g0106 | AMR | PEL | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0090 | EAS | KHV | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0013 | AFR | ACB | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0031 | AFR | ACB | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02145 | hp1 | a0002 | c0002 | t0002 | g0123 | AFR | ACB | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02145 | hp2 | a0002 | c0002 | t0001 | g0073 | AFR | ACB | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | CDX | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0055 | EAS | CDX | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0164 | AFR | ACB | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | ACB | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02258 | hp2 | a0002 | c0002 | t0001 | g0191 | AFR | ACB | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02280 | hp2 | a0003 | c0004 | t0002 | g0185 | AFR | ACB | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02451 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | ACB | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0031 | AFR | GWD | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02572 | hp2 | a0002 | c0003 | t0001 | g0176 | AFR | GWD | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02615 | hp2 | a0003 | c0004 | t0002 | g0011 | AFR | GWD | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02622 | hp2 | a0002 | c0002 | t0002 | g0040 | AFR | GWD | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02630 | hp1 | a0002 | c0003 | t0001 | g0006 | AFR | GWD | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02647 | hp1 | a0005 | c0006 | t0001 | g0207 | AFR | GWD | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02647 | hp2 | a0002 | c0002 | t0001 | g0069 | AFR | GWD | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0118 | SAS | PJL | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02717 | hp1 | a0002 | c0003 | t0001 | g0177 | AFR | GWD | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02717 | hp2 | a0002 | c0002 | t0001 | g0074 | AFR | GWD | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0186 | AFR | GWD | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0026 | AFR | GWD | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0193 | AFR | GWD | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02886 | hp1 | a0002 | c0002 | t0001 | g0056 | AFR | GWD | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0141 | AFR | GWD | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02895 | hp1 | a0005 | c0006 | t0001 | g0206 | AFR | GWD | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02895 | hp2 | a0003 | c0004 | t0002 | g0183 | AFR | GWD | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02896 | hp1 | a0002 | c0002 | t0001 | g0064 | AFR | GWD | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02896 | hp2 | a0003 | c0004 | t0002 | g0182 | AFR | GWD | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | ESN | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0188 | AFR | ESN | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02976 | hp1 | a0003 | c0004 | t0002 | g0011 | AFR | ESN | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ESN | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG03041 | hp1 | a0007 | c0007 | t0001 | g0184 | AFR | GWD | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0165 | AFR | GWD | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | MSL | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG03098 | hp2 | a0002 | c0002 | t0001 | g0054 | AFR | MSL | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | ESN | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG03130 | hp2 | a0002 | c0002 | t0002 | g0061 | AFR | ESN | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG03139 | hp2 | a0002 | c0003 | t0001 | g0006 | AFR | ESN | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG03195 | hp1 | a0002 | c0002 | t0001 | g0076 | AFR | ESN | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0195 | AFR | ESN | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG03209 | hp1 | a0002 | c0002 | t0001 | g0196 | AFR | MSL | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG03209 | hp2 | a0002 | c0002 | t0002 | g0060 | AFR | MSL | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG03225 | hp1 | a0003 | c0004 | t0002 | g0011 | AFR | MSL | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG03225 | hp2 | a0005 | c0006 | t0001 | g0205 | AFR | MSL | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG03453 | hp1 | a0002 | c0003 | t0001 | g0006 | AFR | MSL | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG03453 | hp2 | a0002 | c0002 | t0002 | g0035 | AFR | MSL | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0014 | SAS | PJL | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0014 | SAS | PJL | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG03516 | hp1 | a0002 | c0002 | t0003 | g0045 | AFR | ESN | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0052 | AFR | ESN | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG03540 | hp1 | a0002 | c0002 | t0001 | g0197 | AFR | GWD | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG03540 | hp2 | a0002 | c0003 | t0001 | g0166 | AFR | GWD | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | STU | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0066 | SAS | STU | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | BEB | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | BEB | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG03834 | hp1 | a0004 | c0005 | t0001 | g0143 | SAS | BEB | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | STU | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | STU | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | STU | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0192 | SAS | STU | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA18522 | hp1 | a0002 | c0003 | t0001 | g0006 | AFR | YRI | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA18522 | hp2 | a0002 | c0002 | t0001 | g0077 | AFR | YRI | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA18906 | hp1 | a0002 | c0002 | t0001 | g0175 | AFR | YRI | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA18906 | hp2 | a0002 | c0002 | t0001 | g0189 | AFR | YRI | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0203 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA18949 | hp1 | a0002 | c0002 | t0001 | g0168 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA18962 | hp2 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA18994 | hp1 | a0008 | c0011 | t0001 | g0163 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA18994 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA19030 | hp1 | a0002 | c0002 | t0001 | g0194 | AFR | LWK | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | LWK | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA19043 | hp1 | a0004 | c0005 | t0001 | g0075 | AFR | LWK | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA19043 | hp2 | a0002 | c0003 | t0001 | g0006 | AFR | LWK | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA19058 | hp1 | a0002 | c0002 | t0001 | g0169 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA19059 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA19075 | hp1 | a0002 | c0002 | t0001 | g0087 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA19075 | hp2 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA19083 | hp1 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA19240 | hp1 | a0002 | c0002 | t0001 | g0180 | AFR | YRI | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA19240 | hp2 | a0009 | c0010 | t0001 | g0179 | AFR | YRI | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0174 | AFR | ASW | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA20129 | hp2 | a0002 | c0002 | t0002 | g0062 | AFR | ASW | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0210 | EUR | TSI | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0102 | EUR | TSI | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA20805 | hp1 | a0010 | c0008 | t0001 | g0120 | EUR | TSI | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | GIH | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0187 | SAS | GIH | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0063 | AFR | ACB | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0026 | AFR | ACB | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02486 | hp2 | a0002 | c0002 | t0001 | g0053 | AFR | ACB | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG02559 | hp2 | a0002 | c0002 | t0002 | g0034 | AFR | ACB | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG03471 | hp1 | a0002 | c0002 | t0001 | g0198 | AFR | MSL | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| HG03471 | hp2 | a0002 | c0002 | t0003 | g0046 | AFR | MSL | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0065 | AFR | USA | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | LWK | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| NA21309 | hp2 | a0002 | c0003 | t0001 | g0199 | AFR | LWK | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0042 | REF | REF | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0181 | REF | REF | C12orf50_chr12_87975035_88034401 | C12orf50 | chr12 | 87975035 | 88034401 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:87985975 | T | C | 1 | a0010 | 1 | NA20805.hp1 | missense_variant | MODERATE | c.1001A>G | p.Tyr334Cys | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 11/13 | 1171/1711 | 1001/1245 | 334/414 | chr12 | 87985975 | |||
| chr12:87985996 | C | T | 1 | a0005 | 4 | HG01884.hp2 HG02647.hp1 HG02895.hp1 others(1): Show |
missense_variant | MODERATE | c.980G>A | p.Arg327Gln | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 11/13 | 1150/1711 | 980/1245 | 327/414 | chr12 | 87985996 | |||
| chr12:87986011 | C | T | 1 | a0004 | 4 | HG00741.hp2 HG01496.hp2 HG03834.hp1 others(1): Show |
missense_variant | MODERATE | c.965G>A | p.Arg322His | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 11/13 | 1135/1711 | 965/1245 | 322/414 | chr12 | 87986011 | |||
| chr12:87986317 | T | C | 4 | a0002 a0003 a0004 others(1): Show |
101 | HG00621.hp1 HG00639.hp1 HG00738.hp2 others(98): Show |
missense_variant | MODERATE | c.917A>G | p.Gln306Arg | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 10/13 | 1087/1711 | 917/1245 | 306/414 | chr12 | 87986317 | |||
| chr12:87987875 | C | A | 1 | a0006 | 1 | HG01943.hp1 | missense_variant | MODERATE | c.792G>T | p.Met264Ile | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 9/13 | 962/1711 | 792/1245 | 264/414 | chr12 | 87987875 | |||
| chr12:87996391 | C | A | 1 | a0009 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.464G>T | p.Gly155Val | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 6/13 | 634/1711 | 464/1245 | 155/414 | chr12 | 87996391 | |||
| chr12:87996412 | A | G | 2 | a0003 a0007 |
7 | HG02280.hp2 HG02615.hp2 HG02895.hp2 others(4): Show |
missense_variant | MODERATE | c.443T>C | p.Leu148Ser | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 6/13 | 613/1711 | 443/1245 | 148/414 | chr12 | 87996412 | |||
| chr12:88026536 | G | A | 1 | a0008 | 1 | NA18994.hp1 | missense_variant | MODERATE | c.85C>T | p.His29Tyr | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/13 | 255/1711 | 85/1245 | 29/414 | chr12 | 88026536 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:87985938 | C | T | 1 | a0002c0003 | 9 | HG02572.hp2 HG02630.hp1 HG02717.hp1 others(6): Show |
synonymous_variant | LOW | c.1038G>A | p.Ala346Ala | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 11/13 | 1208/1711 | 1038/1245 | 346/414 | chr12 | 87985938 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:87980105 | A | C | 1 | a0002c0002t0003 | 3 | HG00639.hp1 HG03471.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*226T>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 13/13 | 226 | chr12 | 87980105 | ||||||
| chr12:87980295 | A | AT | 2 | a0002c0002t0002 a0003c0004t0002 |
13 | HG02145.hp1 HG02280.hp2 HG02559.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*35dupA | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 13/13 | 35 | chr12 | 87980295 | ||||||
| chr12:88029312 | TCTTAAAG others(192): Show |
T | 1 | a0001c0001t0004 | 1 | HG01169.hp2 | splice_donor_variant&5_prime_UTR_truncation&exon_loss_variant&splice_region_variant&intron_variant | HIGH | c.-280_-109+27del | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 1/13 | chr12 | 88029312 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:87980482 | C | T | 46 | a0001c0001t0001g0116 a0002c0002t0001g0013 a0002c0002t0001g0014 others(43): Show |
54 | HG00639.hp1 HG01069.hp1 HG01081.hp2 others(51): Show |
intron_variant | MODIFIER | c.1220-126G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 12/12 | chr12 | 87980482 | |||||||
| chr12:87980503 | A | G | 9 | a0002c0002t0001g0003 a0002c0002t0001g0052 a0002c0002t0001g0053 others(6): Show |
13 | HG01109.hp1 HG01243.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1220-147T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 12/12 | chr12 | 87980503 | |||||||
| chr12:87980515 | C | T | 1 | a0007c0007t0001g0184 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1220-159G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 12/12 | chr12 | 87980515 | |||||||
| chr12:87980624 | C | A | 10 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0060 others(7): Show |
12 | HG02145.hp1 HG02280.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1220-268G>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 12/12 | chr12 | 87980624 | |||||||
| chr12:87980624 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1220-268G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 12/12 | chr12 | 87980624 | |||||||
| chr12:87980959 | A | G | 3 | a0002c0002t0001g0052 a0002c0002t0001g0053 a0002c0002t0001g0164 |
3 | HG02257.hp2 HG02486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1220-603T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 12/12 | chr12 | 87980959 | |||||||
| chr12:87981331 | G | A | 1 | a0001c0001t0001g0099 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1220-975C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 12/12 | chr12 | 87981331 | |||||||
| chr12:87981485 | T | C | 34 | a0002c0002t0001g0013 a0002c0002t0001g0014 a0002c0002t0001g0054 others(31): Show |
40 | HG00639.hp1 HG01069.hp1 HG01192.hp1 others(37): Show |
intron_variant | MODIFIER | c.1220-1129A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 12/12 | chr12 | 87981485 | |||||||
| chr12:87981583 | C | G | 1 | a0001c0001t0001g0012 | 2 | HG02622.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1220-1227G>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 12/12 | chr12 | 87981583 | |||||||
| chr12:87981711 | T | G | 45 | a0002c0002t0001g0013 a0002c0002t0001g0014 a0002c0002t0001g0054 others(42): Show |
53 | HG00639.hp1 HG01069.hp1 HG01192.hp1 others(50): Show |
intron_variant | MODIFIER | c.1220-1355A>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 12/12 | chr12 | 87981711 | |||||||
| chr12:87981926 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1219+1177G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 12/12 | chr12 | 87981926 | |||||||
| chr12:87982114 | A | G | 4 | a0005c0006t0001g0204 a0005c0006t0001g0205 a0005c0006t0001g0206 others(1): Show |
4 | HG01884.hp2 HG02647.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1219+989T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 12/12 | chr12 | 87982114 | |||||||
| chr12:87982156 | A | G | 1 | a0001c0001t0001g0012 | 2 | HG02622.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1219+947T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 12/12 | chr12 | 87982156 | |||||||
| chr12:87982376 | A | T | 6 | a0002c0002t0001g0016 a0002c0002t0001g0017 a0002c0002t0001g0066 others(3): Show |
8 | HG00621.hp1 HG01433.hp2 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.1219+727T>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 12/12 | chr12 | 87982376 | |||||||
| chr12:87982421 | C | T | 1 | a0002c0002t0001g0195 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1219+682G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 12/12 | chr12 | 87982421 | |||||||
| chr12:87982756 | T | C | 19 | a0002c0002t0001g0013 a0002c0002t0001g0014 a0002c0002t0001g0054 others(16): Show |
21 | HG01069.hp1 HG01192.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.1219+347A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 12/12 | chr12 | 87982756 | |||||||
| chr12:87982798 | C | CA | 19 | a0001c0001t0001g0082 a0001c0001t0001g0105 a0001c0001t0001g0135 others(16): Show |
21 | HG00558.hp1 HG00639.hp1 HG02071.hp2 others(18): Show |
intron_variant | MODIFIER | c.1219+304dupT | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 12/12 | chr12 | 87982798 | |||||||
| chr12:87982825 | G | A | 42 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0016 others(39): Show |
54 | HG00621.hp1 HG00738.hp2 HG00741.hp2 others(51): Show |
intron_variant | MODIFIER | c.1219+278C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 12/12 | chr12 | 87982825 | |||||||
| chr12:87982894 | C | A | 29 | a0002c0002t0001g0013 a0002c0002t0001g0014 a0002c0002t0001g0054 others(26): Show |
35 | HG00639.hp1 HG01069.hp1 HG01192.hp1 others(32): Show |
intron_variant | MODIFIER | c.1219+209G>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 12/12 | chr12 | 87982894 | |||||||
| chr12:87982912 | G | A | 1 | a0007c0007t0001g0184 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1219+191C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 12/12 | chr12 | 87982912 | |||||||
| chr12:87982961 | T | C | 1 | a0002c0002t0001g0063 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1219+142A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 12/12 | chr12 | 87982961 | |||||||
| chr12:87983018 | A | G | 9 | a0002c0002t0002g0040 a0002c0002t0002g0060 a0002c0002t0002g0061 others(6): Show |
11 | HG02145.hp1 HG02280.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1219+85T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 12/12 | chr12 | 87983018 | |||||||
| chr12:87983254 | T | C | 1 | a0001c0001t0001g0137 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1127-59A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 11/12 | chr12 | 87983254 | |||||||
| chr12:87983335 | G | A | 4 | a0002c0002t0001g0003 a0002c0002t0001g0063 a0002c0002t0001g0064 others(1): Show |
8 | HG01109.hp1 HG01243.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1127-140C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 11/12 | chr12 | 87983335 | |||||||
| chr12:87983383 | T | C | 2 | a0002c0002t0002g0034 a0002c0002t0002g0035 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1127-188A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 11/12 | chr12 | 87983383 | |||||||
| chr12:87983390 | G | GT | 9 | a0002c0002t0002g0040 a0002c0002t0002g0060 a0002c0002t0002g0061 others(6): Show |
11 | HG02145.hp1 HG02280.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1127-196dupA | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 11/12 | chr12 | 87983390 | |||||||
| chr12:87983573 | G | A | 50 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0016 others(47): Show |
63 | HG00621.hp1 HG00738.hp2 HG00741.hp2 others(60): Show |
intron_variant | MODIFIER | c.1127-378C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 11/12 | chr12 | 87983573 | |||||||
| chr12:87983665 | T | G | 5 | a0001c0001t0001g0101 a0001c0001t0001g0171 a0001c0001t0001g0172 others(2): Show |
5 | NA18950.hp2 NA18979.hp1 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.1127-470A>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 11/12 | chr12 | 87983665 | |||||||
| chr12:87983791 | T | C | 35 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0016 others(32): Show |
46 | HG00621.hp1 HG00738.hp2 HG00741.hp2 others(43): Show |
intron_variant | MODIFIER | c.1127-596A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 11/12 | chr12 | 87983791 | |||||||
| chr12:87983835 | G | A | 65 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(62): Show |
85 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.1127-640C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 11/12 | chr12 | 87983835 | |||||||
| chr12:87983839 | C | T | 3 | a0001c0001t0001g0117 a0001c0001t0001g0148 a0008c0011t0001g0163 |
3 | NA18968.hp1 NA18994.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.1127-644G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 11/12 | chr12 | 87983839 | |||||||
| chr12:87983840 | A | G | 68 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(65): Show |
88 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.1127-645T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 11/12 | chr12 | 87983840 | |||||||
| chr12:87983843 | A | C | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1127-648T>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 11/12 | chr12 | 87983843 | |||||||
| chr12:87983853 | G | T | 10 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0060 others(7): Show |
12 | HG02145.hp1 HG02280.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1127-658C>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 11/12 | chr12 | 87983853 | |||||||
| chr12:87983865 | C | G | 65 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(62): Show |
85 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.1127-670G>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 11/12 | chr12 | 87983865 | |||||||
| chr12:87983872 | A | G | 65 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(62): Show |
85 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.1127-677T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 11/12 | chr12 | 87983872 | |||||||
| chr12:87983893 | T | TG | 65 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(62): Show |
85 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.1127-699dupC | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 11/12 | chr12 | 87983893 | |||||||
| chr12:87983960 | G | A | 1 | a0002c0003t0001g0176 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1127-765C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 11/12 | chr12 | 87983960 | |||||||
| chr12:87983973 | C | T | 66 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(63): Show |
86 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.1127-778G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 11/12 | chr12 | 87983973 | |||||||
| chr12:87983997 | G | A | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1127-802C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 11/12 | chr12 | 87983997 | |||||||
| chr12:87984087 | T | C | 4 | a0002c0002t0001g0013 a0002c0002t0001g0186 a0002c0002t0001g0188 others(1): Show |
5 | HG01192.hp1 HG02055.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1127-892A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 11/12 | chr12 | 87984087 | |||||||
| chr12:87984183 | G | A | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG02071.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.1127-988C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 11/12 | chr12 | 87984183 | |||||||
| chr12:87984212 | A | C | 1 | a0009c0010t0001g0179 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1127-1017T>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 11/12 | chr12 | 87984212 | |||||||
| chr12:87984269 | C | T | 11 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0040 others(8): Show |
13 | HG02145.hp1 HG02280.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1127-1074G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 11/12 | chr12 | 87984269 | |||||||
| chr12:87984271 | C | T | 35 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0016 others(32): Show |
46 | HG00621.hp1 HG00738.hp2 HG00741.hp2 others(43): Show |
intron_variant | MODIFIER | c.1127-1076G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 11/12 | chr12 | 87984271 | |||||||
| chr12:87984344 | A | G | 11 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0040 others(8): Show |
13 | HG02145.hp1 HG02280.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1127-1149T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 11/12 | chr12 | 87984344 | |||||||
| chr12:87984389 | G | T | 7 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0072 others(4): Show |
13 | NA18949.hp2 NA18953.hp1 NA18961.hp1 others(10): Show |
intron_variant | MODIFIER | c.1127-1194C>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 11/12 | chr12 | 87984389 | |||||||
| chr12:87984407 | G | A | 11 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0040 others(8): Show |
13 | HG02145.hp1 HG02280.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1127-1212C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 11/12 | chr12 | 87984407 | |||||||
| chr12:87984453 | G | A | 1 | a0002c0002t0001g0168 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1127-1258C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 11/12 | chr12 | 87984453 | |||||||
| chr12:87984569 | C | T | 1 | a0007c0007t0001g0184 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1126+1281G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 11/12 | chr12 | 87984569 | |||||||
| chr12:87984712 | G | A | 44 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0017 others(41): Show |
56 | HG00738.hp2 HG00741.hp2 HG01109.hp1 others(53): Show |
intron_variant | MODIFIER | c.1126+1138C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 11/12 | chr12 | 87984712 | |||||||
| chr12:87984833 | C | T | 1 | a0001c0001t0001g0108 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1126+1017G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 11/12 | chr12 | 87984833 | |||||||
| chr12:87984842 | C | T | 9 | a0002c0002t0002g0040 a0002c0002t0002g0060 a0002c0002t0002g0061 others(6): Show |
11 | HG02145.hp1 HG02280.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1126+1008G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 11/12 | chr12 | 87984842 | |||||||
| chr12:87984850 | A | C | 51 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0016 others(48): Show |
64 | HG00621.hp1 HG00738.hp2 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.1126+1000T>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 11/12 | chr12 | 87984850 | |||||||
| chr12:87985041 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1126+809T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 11/12 | chr12 | 87985041 | |||||||
| chr12:87985102 | T | A | 50 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0016 others(47): Show |
63 | HG00621.hp1 HG00738.hp2 HG00741.hp2 others(60): Show |
intron_variant | MODIFIER | c.1126+748A>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 11/12 | chr12 | 87985102 | |||||||
| chr12:87985198 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1126+652T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 11/12 | chr12 | 87985198 | |||||||
| chr12:87985246 | A | C | 4 | a0002c0002t0001g0003 a0002c0002t0001g0063 a0002c0002t0001g0064 others(1): Show |
8 | HG01109.hp1 HG01243.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1126+604T>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 11/12 | chr12 | 87985246 | |||||||
| chr12:87985264 | T | A | 1 | a0001c0001t0001g0095 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1126+586A>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 11/12 | chr12 | 87985264 | |||||||
| chr12:87985298 | G | C | 3 | a0002c0002t0003g0044 a0002c0002t0003g0045 a0002c0002t0003g0046 |
3 | HG00639.hp1 HG03471.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1126+552C>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 11/12 | chr12 | 87985298 | |||||||
| chr12:87985439 | C | T | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1126+411G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 11/12 | chr12 | 87985439 | |||||||
| chr12:87985619 | A | C | 1 | a0001c0001t0004g0032 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1126+231T>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 11/12 | chr12 | 87985619 | |||||||
| chr12:87985682 | T | C | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1126+168A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 11/12 | chr12 | 87985682 | |||||||
| chr12:87985743 | T | A | 80 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0013 others(77): Show |
100 | HG00621.hp1 HG00639.hp1 HG00738.hp2 others(97): Show |
intron_variant | MODIFIER | c.1126+107A>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 11/12 | chr12 | 87985743 | |||||||
| chr12:87985766 | A | C | 2 | a0001c0001t0001g0022 a0001c0001t0001g0036 |
3 | HG01109.hp2 HG01934.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.1126+84T>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 11/12 | chr12 | 87985766 | |||||||
| chr12:87985773 | T | A | 13 | a0002c0002t0001g0198 a0002c0002t0002g0034 a0002c0002t0002g0035 others(10): Show |
15 | HG01884.hp2 HG02145.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1126+77A>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 11/12 | chr12 | 87985773 | |||||||
| chr12:87985789 | A | G | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(203): Show |
268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.1126+61T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 11/12 | chr12 | 87985789 | |||||||
| chr12:87985838 | A | T | 1 | a0002c0002t0002g0034 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1126+12T>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 11/12 | chr12 | 87985838 | |||||||
| chr12:87986536 | C | A | 1 | a0001c0001t0001g0102 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.818-120G>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 9/12 | chr12 | 87986536 | |||||||
| chr12:87986695 | CA | C | 8 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0060 others(5): Show |
10 | HG02145.hp1 HG02280.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.818-280delT | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 9/12 | chr12 | 87986695 | |||||||
| chr12:87986741 | A | G | 4 | a0005c0006t0001g0204 a0005c0006t0001g0205 a0005c0006t0001g0206 others(1): Show |
4 | HG01884.hp2 HG02647.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.818-325T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 9/12 | chr12 | 87986741 | |||||||
| chr12:87987493 | A | G | 27 | a0002c0002t0001g0007 a0002c0002t0001g0017 a0002c0002t0001g0026 others(24): Show |
34 | HG00738.hp2 HG00741.hp2 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.817+357T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 9/12 | chr12 | 87987493 | |||||||
| chr12:87987523 | C | T | 1 | a0002c0002t0002g0060 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.817+327G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 9/12 | chr12 | 87987523 | |||||||
| chr12:87987729 | T | C | 26 | a0002c0002t0001g0007 a0002c0002t0001g0016 a0002c0002t0001g0017 others(23): Show |
33 | HG00621.hp1 HG00738.hp2 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.817+121A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 9/12 | chr12 | 87987729 | |||||||
| chr12:87987733 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.817+117C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 9/12 | chr12 | 87987733 | |||||||
| chr12:87988000 | T | C | 11 | a0002c0002t0001g0003 a0002c0002t0001g0052 a0002c0002t0001g0053 others(8): Show |
15 | HG01109.hp1 HG01243.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.701-34A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 8/12 | chr12 | 87988000 | |||||||
| chr12:87988170 | C | A | 6 | a0002c0002t0002g0060 a0002c0002t0002g0123 a0003c0004t0002g0011 others(3): Show |
8 | HG02145.hp1 HG02280.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.701-204G>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 8/12 | chr12 | 87988170 | |||||||
| chr12:87988345 | C | A | 1 | a0005c0006t0001g0204 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.701-379G>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 8/12 | chr12 | 87988345 | |||||||
| chr12:87988518 | A | C | 18 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(15): Show |
29 | HG01074.hp1 HG01081.hp1 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.701-552T>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 8/12 | chr12 | 87988518 | |||||||
| chr12:87988656 | C | T | 28 | a0002c0002t0001g0007 a0002c0002t0001g0017 a0002c0002t0001g0026 others(25): Show |
34 | HG00738.hp2 HG00741.hp2 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.700+608G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 8/12 | chr12 | 87988656 | |||||||
| chr12:87988742 | G | A | 4 | a0002c0002t0001g0026 a0002c0002t0001g0059 a0002c0002t0001g0141 others(1): Show |
5 | HG00738.hp2 HG01255.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.700+522C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 8/12 | chr12 | 87988742 | |||||||
| chr12:87988810 | G | C | 9 | a0002c0002t0001g0003 a0002c0002t0001g0052 a0002c0002t0001g0053 others(6): Show |
13 | HG01109.hp1 HG01243.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.700+454C>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 8/12 | chr12 | 87988810 | |||||||
| chr12:87988924 | C | G | 2 | a0002c0002t0001g0196 a0002c0002t0001g0197 |
2 | HG03209.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.700+340G>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 8/12 | chr12 | 87988924 | |||||||
| chr12:87989102 | G | A | 77 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0013 others(74): Show |
95 | HG00639.hp1 HG00738.hp2 HG00741.hp2 others(92): Show |
intron_variant | MODIFIER | c.700+162C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 8/12 | chr12 | 87989102 | |||||||
| chr12:87989113 | A | G | 3 | a0002c0002t0002g0061 a0002c0002t0002g0062 a0002c0002t0002g0123 |
3 | HG02145.hp1 HG03130.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.700+151T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 8/12 | chr12 | 87989113 | |||||||
| chr12:87989917 | T | C | 1 | a0002c0002t0001g0014 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.593-546A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 7/12 | chr12 | 87989917 | |||||||
| chr12:87990028 | G | A | 5 | a0002c0003t0001g0006 a0002c0003t0001g0166 a0002c0003t0001g0176 others(2): Show |
9 | HG02572.hp2 HG02630.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.593-657C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 7/12 | chr12 | 87990028 | |||||||
| chr12:87990110 | C | T | 8 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0060 others(5): Show |
10 | HG02145.hp1 HG02280.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.593-739G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 7/12 | chr12 | 87990110 | |||||||
| chr12:87990112 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.593-741G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 7/12 | chr12 | 87990112 | |||||||
| chr12:87990181 | T | C | 1 | a0002c0002t0001g0195 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.593-810A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 7/12 | chr12 | 87990181 | |||||||
| chr12:87990341 | T | G | 1 | a0001c0001t0001g0102 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.593-970A>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 7/12 | chr12 | 87990341 | |||||||
| chr12:87990363 | C | G | 8 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0060 others(5): Show |
10 | HG02145.hp1 HG02280.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.593-992G>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 7/12 | chr12 | 87990363 | |||||||
| chr12:87990410 | C | A | 8 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0060 others(5): Show |
10 | HG02145.hp1 HG02280.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.593-1039G>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 7/12 | chr12 | 87990410 | |||||||
| chr12:87990468 | C | G | 29 | a0002c0002t0001g0013 a0002c0002t0001g0014 a0002c0002t0001g0054 others(26): Show |
35 | HG00639.hp1 HG01069.hp1 HG01192.hp1 others(32): Show |
intron_variant | MODIFIER | c.593-1097G>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 7/12 | chr12 | 87990468 | |||||||
| chr12:87990527 | C | T | 8 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0060 others(5): Show |
10 | HG02145.hp1 HG02280.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.593-1156G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 7/12 | chr12 | 87990527 | |||||||
| chr12:87990663 | C | T | 31 | a0002c0002t0001g0007 a0002c0002t0001g0016 a0002c0002t0001g0017 others(28): Show |
38 | HG00621.hp1 HG00738.hp2 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.593-1292G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 7/12 | chr12 | 87990663 | |||||||
| chr12:87990673 | C | T | 19 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0021 others(16): Show |
27 | HG00099.hp2 HG00280.hp2 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.593-1302G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 7/12 | chr12 | 87990673 | |||||||
| chr12:87990696 | A | G | 2 | a0001c0001t0001g0030 a0001c0001t0001g0038 |
3 | HG01069.hp2 HG02293.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.593-1325T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 7/12 | chr12 | 87990696 | |||||||
| chr12:87990756 | T | G | 4 | a0005c0006t0001g0204 a0005c0006t0001g0205 a0005c0006t0001g0206 others(1): Show |
4 | HG01884.hp2 HG02647.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.593-1385A>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 7/12 | chr12 | 87990756 | |||||||
| chr12:87990845 | CT | C | 10 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0060 others(7): Show |
12 | HG02145.hp1 HG02280.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.593-1475delA | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 7/12 | chr12 | 87990845 | |||||||
| chr12:87990987 | G | A | 9 | a0002c0002t0001g0003 a0002c0002t0001g0052 a0002c0002t0001g0053 others(6): Show |
13 | HG01109.hp1 HG01243.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.593-1616C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 7/12 | chr12 | 87990987 | |||||||
| chr12:87991057 | T | C | 2 | a0001c0001t0001g0144 a0001c0001t0001g0145 |
2 | NA18970.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.593-1686A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 7/12 | chr12 | 87991057 | |||||||
| chr12:87991250 | A | G | 1 | a0002c0002t0001g0076 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.593-1879T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 7/12 | chr12 | 87991250 | |||||||
| chr12:87991441 | G | A | 2 | a0002c0002t0002g0034 a0002c0002t0002g0035 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.593-2070C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 7/12 | chr12 | 87991441 | |||||||
| chr12:87991471 | G | A | 1 | a0002c0002t0002g0060 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.593-2100C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 7/12 | chr12 | 87991471 | |||||||
| chr12:87991478 | A | G | 2 | a0002c0002t0002g0034 a0002c0002t0002g0035 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.593-2107T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 7/12 | chr12 | 87991478 | |||||||
| chr12:87991745 | T | C | 31 | a0002c0002t0001g0007 a0002c0002t0001g0016 a0002c0002t0001g0017 others(28): Show |
39 | HG00621.hp1 HG00738.hp2 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.593-2374A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 7/12 | chr12 | 87991745 | |||||||
| chr12:87991843 | G | A | 5 | a0002c0002t0002g0060 a0003c0004t0002g0011 a0003c0004t0002g0182 others(2): Show |
7 | HG02280.hp2 HG02615.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.593-2472C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 7/12 | chr12 | 87991843 | |||||||
| chr12:87991928 | C | T | 39 | a0002c0002t0001g0007 a0002c0002t0001g0016 a0002c0002t0001g0017 others(36): Show |
48 | HG00621.hp1 HG00738.hp2 HG00741.hp2 others(45): Show |
intron_variant | MODIFIER | c.593-2557G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 7/12 | chr12 | 87991928 | |||||||
| chr12:87992266 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.592+2367T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 7/12 | chr12 | 87992266 | |||||||
| chr12:87992292 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.592+2341C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 7/12 | chr12 | 87992292 | |||||||
| chr12:87992301 | T | C | 29 | a0002c0002t0001g0013 a0002c0002t0001g0014 a0002c0002t0001g0054 others(26): Show |
35 | HG00639.hp1 HG01069.hp1 HG01192.hp1 others(32): Show |
intron_variant | MODIFIER | c.592+2332A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 7/12 | chr12 | 87992301 | |||||||
| chr12:87992452 | C | T | 8 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0060 others(5): Show |
10 | HG02145.hp1 HG02280.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.592+2181G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 7/12 | chr12 | 87992452 | |||||||
| chr12:87992641 | CA | C | 11 | a0002c0002t0001g0003 a0002c0002t0001g0052 a0002c0002t0001g0053 others(8): Show |
15 | HG01109.hp1 HG01243.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.592+1991delT | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 7/12 | chr12 | 87992641 | |||||||
| chr12:87992666 | T | C | 1 | a0001c0001t0001g0167 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.592+1967A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 7/12 | chr12 | 87992666 | |||||||
| chr12:87992672 | C | T | 2 | a0002c0002t0001g0003 a0002c0002t0001g0065 |
6 | HG01109.hp1 HG01243.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.592+1961G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 7/12 | chr12 | 87992672 | |||||||
| chr12:87992855 | A | G | 8 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0060 others(5): Show |
10 | HG02145.hp1 HG02280.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.592+1778T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 7/12 | chr12 | 87992855 | |||||||
| chr12:87992917 | A | G | 2 | a0002c0002t0002g0061 a0002c0002t0002g0062 |
2 | HG03130.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.592+1716T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 7/12 | chr12 | 87992917 | |||||||
| chr12:87993153 | T | C | 8 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0060 others(5): Show |
10 | HG02145.hp1 HG02280.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.592+1480A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 7/12 | chr12 | 87993153 | |||||||
| chr12:87993231 | C | T | 1 | a0002c0002t0001g0195 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.592+1402G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 7/12 | chr12 | 87993231 | |||||||
| chr12:87993405 | G | A | 2 | a0002c0002t0002g0034 a0002c0002t0002g0035 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.592+1228C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 7/12 | chr12 | 87993405 | |||||||
| chr12:87993419 | C | A | 29 | a0001c0001t0001g0086 a0001c0001t0001g0089 a0002c0002t0001g0007 others(26): Show |
37 | HG00621.hp1 HG00738.hp2 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.592+1214G>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 7/12 | chr12 | 87993419 | |||||||
| chr12:87993438 | G | A | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.592+1195C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 7/12 | chr12 | 87993438 | |||||||
| chr12:87993726 | C | T | 10 | a0002c0002t0001g0003 a0002c0002t0001g0052 a0002c0002t0001g0053 others(7): Show |
14 | HG01109.hp1 HG01243.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.592+907G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 7/12 | chr12 | 87993726 | |||||||
| chr12:87993831 | A | G | 7 | a0002c0002t0002g0060 a0002c0002t0002g0123 a0003c0004t0002g0011 others(4): Show |
9 | HG02145.hp1 HG02280.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.592+802T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 7/12 | chr12 | 87993831 | |||||||
| chr12:87993912 | T | C | 1 | a0002c0002t0001g0056 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.592+721A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 7/12 | chr12 | 87993912 | |||||||
| chr12:87994028 | C | A | 3 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0150 |
3 | HG02074.hp2 HG02135.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.592+605G>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 7/12 | chr12 | 87994028 | |||||||
| chr12:87994070 | C | T | 19 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0043 others(16): Show |
22 | HG00621.hp2 HG02071.hp2 HG02080.hp1 others(19): Show |
intron_variant | MODIFIER | c.592+563G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 7/12 | chr12 | 87994070 | |||||||
| chr12:87994200 | C | CATAA | 4 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0102 others(1): Show |
4 | HG02074.hp2 HG02135.hp2 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.592+429_592+432dup others(4): Show |
C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 7/12 | chr12 | 87994200 | |||||||
| chr12:87994200 | CATAA | C | 28 | a0001c0001t0001g0138 a0002c0002t0001g0007 a0002c0002t0001g0028 others(25): Show |
34 | HG00738.hp2 HG00741.hp2 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.592+429_592+432del others(4): Show |
C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 7/12 | chr12 | 87994200 | |||||||
| chr12:87994251 | TAATC | T | 4 | a0005c0006t0001g0204 a0005c0006t0001g0205 a0005c0006t0001g0206 others(1): Show |
4 | HG01884.hp2 HG02647.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.592+378_592+381del others(4): Show |
C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 7/12 | chr12 | 87994251 | |||||||
| chr12:87994361 | G | GAC | 2 | a0001c0001t0001g0030 a0001c0001t0001g0038 |
3 | HG01069.hp2 HG02293.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.592+270_592+271dup others(2): Show |
C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 7/12 | chr12 | 87994361 | |||||||
| chr12:87994361 | GAC | G | 6 | a0002c0002t0002g0123 a0003c0004t0002g0011 a0003c0004t0002g0182 others(3): Show |
8 | HG02145.hp1 HG02280.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.592+270_592+271del others(2): Show |
C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 7/12 | chr12 | 87994361 | |||||||
| chr12:87994453 | G | T | 2 | a0002c0002t0002g0034 a0002c0002t0002g0035 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.592+180C>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 7/12 | chr12 | 87994453 | |||||||
| chr12:87994533 | G | A | 3 | a0001c0001t0001g0019 a0001c0001t0001g0095 a0001c0001t0001g0127 |
4 | HG00673.hp1 HG01934.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.592+100C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 7/12 | chr12 | 87994533 | |||||||
| chr12:87994541 | CA | C | 14 | a0002c0002t0001g0003 a0002c0002t0001g0052 a0002c0002t0001g0053 others(11): Show |
18 | HG01109.hp1 HG01243.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.592+91delT | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 7/12 | chr12 | 87994541 | |||||||
| chr12:87994815 | G | A | 23 | a0002c0002t0001g0003 a0002c0002t0001g0052 a0002c0002t0001g0053 others(20): Show |
29 | HG01109.hp1 HG01243.hp2 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.482-72C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 6/12 | chr12 | 87994815 | |||||||
| chr12:87995278 | G | GA | 9 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0040 others(6): Show |
11 | HG02145.hp1 HG02280.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.482-536dupT | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 6/12 | chr12 | 87995278 | |||||||
| chr12:87995690 | G | GT | 16 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0021 others(13): Show |
24 | HG00099.hp2 HG00280.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.481+683dupA | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 6/12 | chr12 | 87995690 | |||||||
| chr12:87995768 | G | A | 1 | a0004c0005t0001g0143 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.481+606C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 6/12 | chr12 | 87995768 | |||||||
| chr12:87996027 | G | T | 18 | a0002c0002t0001g0007 a0002c0002t0001g0028 a0002c0002t0001g0041 others(15): Show |
22 | HG00738.hp2 HG00741.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.481+347C>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 6/12 | chr12 | 87996027 | |||||||
| chr12:87996080 | G | T | 2 | a0005c0006t0001g0206 a0005c0006t0001g0207 |
2 | HG02647.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.481+294C>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 6/12 | chr12 | 87996080 | |||||||
| chr12:87996147 | A | G | 10 | a0002c0002t0001g0003 a0002c0002t0001g0052 a0002c0002t0001g0053 others(7): Show |
14 | HG01109.hp1 HG01243.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.481+227T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 6/12 | chr12 | 87996147 | |||||||
| chr12:87996279 | C | A | 8 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0123 others(5): Show |
10 | HG02145.hp1 HG02280.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.481+95G>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 6/12 | chr12 | 87996279 | |||||||
| chr12:87996303 | CTAAA | C | 4 | a0002c0002t0001g0187 a0002c0002t0001g0190 a0002c0002t0001g0192 others(1): Show |
4 | HG01069.hp1 HG04228.hp2 NA18947.hp1 others(1): Show |
intron_variant | MODIFIER | c.481+67_481+70delTT others(2): Show |
C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 6/12 | chr12 | 87996303 | |||||||
| chr12:87996363 | T | G | 1 | a0002c0002t0001g0118 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.481+11A>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 6/12 | chr12 | 87996363 | |||||||
| chr12:87996507 | G | C | 18 | a0002c0002t0001g0007 a0002c0002t0001g0028 a0002c0002t0001g0041 others(15): Show |
22 | HG00738.hp2 HG00741.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.368-20C>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 5/12 | chr12 | 87996507 | |||||||
| chr12:87996704 | T | C | 4 | a0005c0006t0001g0204 a0005c0006t0001g0205 a0005c0006t0001g0206 others(1): Show |
4 | HG01884.hp2 HG02647.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.290-58A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 4/12 | chr12 | 87996704 | |||||||
| chr12:87996838 | A | T | 6 | a0002c0002t0002g0123 a0003c0004t0002g0011 a0003c0004t0002g0182 others(3): Show |
8 | HG02145.hp1 HG02280.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.290-192T>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 4/12 | chr12 | 87996838 | |||||||
| chr12:87996876 | G | A | 1 | a0002c0002t0001g0087 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.290-230C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 4/12 | chr12 | 87996876 | |||||||
| chr12:87996877 | A | G | 1 | a0002c0002t0001g0087 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.290-231T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 4/12 | chr12 | 87996877 | |||||||
| chr12:87996878 | C | T | 4 | a0002c0002t0001g0003 a0002c0002t0001g0063 a0002c0002t0001g0064 others(1): Show |
8 | HG01109.hp1 HG01243.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.290-232G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 4/12 | chr12 | 87996878 | |||||||
| chr12:87996944 | G | A | 22 | a0002c0002t0001g0007 a0002c0002t0001g0028 a0002c0002t0001g0041 others(19): Show |
26 | HG00738.hp2 HG00741.hp2 HG01255.hp2 others(23): Show |
intron_variant | MODIFIER | c.290-298C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 4/12 | chr12 | 87996944 | |||||||
| chr12:87997150 | CA | C | 18 | a0002c0002t0001g0003 a0002c0002t0001g0052 a0002c0002t0001g0053 others(15): Show |
24 | HG01109.hp1 HG01243.hp2 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.290-505delT | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 4/12 | chr12 | 87997150 | |||||||
| chr12:87997163 | T | C | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.290-517A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 4/12 | chr12 | 87997163 | |||||||
| chr12:87997224 | T | C | 1 | a0001c0001t0001g0093 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.290-578A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 4/12 | chr12 | 87997224 | |||||||
| chr12:87997242 | A | G | 11 | a0002c0002t0001g0007 a0002c0002t0001g0031 a0002c0002t0001g0056 others(8): Show |
15 | HG00741.hp2 HG01496.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.290-596T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 4/12 | chr12 | 87997242 | |||||||
| chr12:87997398 | C | CTA | 8 | a0002c0002t0001g0003 a0002c0002t0001g0052 a0002c0002t0001g0053 others(5): Show |
12 | HG01109.hp1 HG01243.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.289+635_289+636dup others(2): Show |
C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 4/12 | chr12 | 87997398 | |||||||
| chr12:87997403 | T | C | 1 | a0001c0001t0001g0071 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.289+632A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 4/12 | chr12 | 87997403 | |||||||
| chr12:87997792 | A | T | 42 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0028 others(39): Show |
53 | HG00738.hp2 HG00741.hp2 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.289+243T>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 4/12 | chr12 | 87997792 | |||||||
| chr12:87997858 | C | G | 1 | a0002c0002t0001g0077 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.289+177G>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 4/12 | chr12 | 87997858 | |||||||
| chr12:87997861 | A | G | 20 | a0002c0002t0001g0007 a0002c0002t0001g0028 a0002c0002t0001g0031 others(17): Show |
25 | HG00738.hp2 HG00741.hp2 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.289+174T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 4/12 | chr12 | 87997861 | |||||||
| chr12:87997891 | T | G | 1 | a0001c0001t0001g0130 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.289+144A>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 4/12 | chr12 | 87997891 | |||||||
| chr12:87997981 | A | G | 42 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0028 others(39): Show |
53 | HG00738.hp2 HG00741.hp2 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.289+54T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 4/12 | chr12 | 87997981 | |||||||
| chr12:87997987 | G | A | 1 | a0001c0001t0001g0023 | 2 | NA18960.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.289+48C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 4/12 | chr12 | 87997987 | |||||||
| chr12:87998201 | A | C | 1 | a0002c0002t0001g0087 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.134-11T>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 87998201 | |||||||
| chr12:87998257 | A | C | 1 | a0002c0002t0001g0087 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.134-67T>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 87998257 | |||||||
| chr12:87998459 | G | T | 1 | a0001c0001t0001g0113 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.134-269C>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 87998459 | |||||||
| chr12:87998572 | C | T | 8 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0123 others(5): Show |
10 | HG02145.hp1 HG02280.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.134-382G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 87998572 | |||||||
| chr12:87998602 | C | T | 6 | a0002c0002t0002g0123 a0003c0004t0002g0011 a0003c0004t0002g0182 others(3): Show |
8 | HG02145.hp1 HG02280.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.134-412G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 87998602 | |||||||
| chr12:87998783 | C | T | 1 | a0001c0001t0004g0032 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.134-593G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 87998783 | |||||||
| chr12:87998788 | A | G | 1 | a0002c0002t0001g0186 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.134-598T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 87998788 | |||||||
| chr12:87998807 | C | A | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.134-617G>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 87998807 | |||||||
| chr12:87998863 | A | G | 33 | a0002c0002t0001g0007 a0002c0002t0001g0028 a0002c0002t0001g0031 others(30): Show |
40 | HG00738.hp2 HG00741.hp2 HG01255.hp2 others(37): Show |
intron_variant | MODIFIER | c.134-673T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 87998863 | |||||||
| chr12:87998888 | C | T | 41 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0028 others(38): Show |
51 | HG00738.hp2 HG00741.hp2 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.134-698G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 87998888 | |||||||
| chr12:87998894 | G | A | 8 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0123 others(5): Show |
10 | HG02145.hp1 HG02280.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.134-704C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 87998894 | |||||||
| chr12:87998896 | C | G | 8 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0123 others(5): Show |
10 | HG02145.hp1 HG02280.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.134-706G>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 87998896 | |||||||
| chr12:87999008 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.134-818T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 87999008 | |||||||
| chr12:87999018 | C | G | 3 | a0003c0004t0002g0011 a0003c0004t0002g0183 a0003c0004t0002g0185 |
5 | HG02280.hp2 HG02615.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.134-828G>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 87999018 | |||||||
| chr12:87999031 | A | T | 1 | a0002c0002t0001g0087 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.134-841T>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 87999031 | |||||||
| chr12:87999035 | T | A | 1 | a0002c0002t0001g0189 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.134-845A>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 87999035 | |||||||
| chr12:87999062 | A | G | 1 | a0002c0002t0002g0123 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.134-872T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 87999062 | |||||||
| chr12:87999400 | C | G | 27 | a0002c0002t0001g0007 a0002c0002t0001g0028 a0002c0002t0001g0041 others(24): Show |
33 | HG00738.hp2 HG00741.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.134-1210G>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 87999400 | |||||||
| chr12:87999575 | A | T | 1 | a0002c0002t0001g0087 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.134-1385T>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 87999575 | |||||||
| chr12:87999577 | A | G | 2 | a0002c0002t0002g0034 a0002c0002t0002g0035 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.134-1387T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 87999577 | |||||||
| chr12:87999584 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.134-1394G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 87999584 | |||||||
| chr12:87999850 | AAAGT | A | 6 | a0001c0001t0001g0022 a0001c0001t0001g0036 a0001c0001t0001g0049 others(3): Show |
7 | HG01109.hp2 HG01934.hp2 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.134-1664_134-1661d others(6): Show |
C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 87999850 | |||||||
| chr12:87999909 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.134-1719C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 87999909 | |||||||
| chr12:87999946 | T | A | 1 | a0001c0001t0001g0080 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.134-1756A>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 87999946 | |||||||
| chr12:88000025 | T | C | 10 | a0002c0002t0001g0003 a0002c0002t0001g0052 a0002c0002t0001g0053 others(7): Show |
14 | HG01109.hp1 HG01243.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.134-1835A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88000025 | |||||||
| chr12:88000056 | A | G | 34 | a0002c0002t0001g0007 a0002c0002t0001g0028 a0002c0002t0001g0031 others(31): Show |
41 | HG00738.hp2 HG00741.hp2 HG01255.hp2 others(38): Show |
intron_variant | MODIFIER | c.134-1866T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88000056 | |||||||
| chr12:88000083 | A | T | 4 | a0005c0006t0001g0204 a0005c0006t0001g0205 a0005c0006t0001g0206 others(1): Show |
4 | HG01884.hp2 HG02647.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.134-1893T>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88000083 | |||||||
| chr12:88000139 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.134-1949A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88000139 | |||||||
| chr12:88000237 | T | C | 4 | a0001c0001t0001g0049 a0001c0001t0001g0081 a0001c0001t0001g0082 others(1): Show |
4 | NA18944.hp2 NA18977.hp2 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.134-2047A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88000237 | |||||||
| chr12:88000245 | A | G | 9 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0040 others(6): Show |
11 | HG02145.hp1 HG02280.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.134-2055T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88000245 | |||||||
| chr12:88000274 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.134-2084C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88000274 | |||||||
| chr12:88000418 | A | G | 9 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0040 others(6): Show |
11 | HG02145.hp1 HG02280.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.134-2228T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88000418 | |||||||
| chr12:88000660 | G | A | 8 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0021 others(5): Show |
15 | HG00099.hp2 HG00280.hp2 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.134-2470C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88000660 | |||||||
| chr12:88000809 | T | C | 24 | a0002c0002t0001g0007 a0002c0002t0001g0028 a0002c0002t0001g0031 others(21): Show |
29 | HG00738.hp2 HG00741.hp2 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.134-2619A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88000809 | |||||||
| chr12:88000936 | C | A | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.134-2746G>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88000936 | |||||||
| chr12:88000994 | C | T | 44 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0028 others(41): Show |
55 | HG00738.hp2 HG00741.hp2 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.134-2804G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88000994 | |||||||
| chr12:88001014 | A | G | 1 | a0002c0003t0001g0176 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.134-2824T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88001014 | |||||||
| chr12:88001021 | A | G | 1 | a0001c0001t0001g0051 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.134-2831T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88001021 | |||||||
| chr12:88001033 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.134-2843C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88001033 | |||||||
| chr12:88001169 | C | A | 2 | a0002c0002t0001g0196 a0002c0002t0001g0197 |
2 | HG03209.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.134-2979G>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88001169 | |||||||
| chr12:88001182 | C | T | 44 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0028 others(41): Show |
55 | HG00738.hp2 HG00741.hp2 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.134-2992G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88001182 | |||||||
| chr12:88001210 | G | T | 4 | a0005c0006t0001g0204 a0005c0006t0001g0205 a0005c0006t0001g0206 others(1): Show |
4 | HG01884.hp2 HG02647.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.134-3020C>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88001210 | |||||||
| chr12:88001292 | A | ATAT | 60 | a0002c0002t0001g0007 a0002c0002t0001g0013 a0002c0002t0001g0014 others(57): Show |
74 | HG00639.hp1 HG00738.hp2 HG00741.hp2 others(71): Show |
intron_variant | MODIFIER | c.134-3105_134-3103d others(5): Show |
C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88001292 | |||||||
| chr12:88001486 | G | A | 1 | a0001c0001t0001g0012 | 2 | HG02622.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.134-3296C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88001486 | |||||||
| chr12:88001509 | G | A | 24 | a0002c0002t0001g0007 a0002c0002t0001g0028 a0002c0002t0001g0031 others(21): Show |
29 | HG00738.hp2 HG00741.hp2 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.134-3319C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88001509 | |||||||
| chr12:88001531 | CT | C | 43 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0051 others(40): Show |
53 | HG00558.hp1 HG00558.hp2 HG00741.hp2 others(50): Show |
intron_variant | MODIFIER | c.134-3342delA | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88001531 | |||||||
| chr12:88001555 | A | G | 44 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0028 others(41): Show |
55 | HG00738.hp2 HG00741.hp2 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.134-3365T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88001555 | |||||||
| chr12:88001687 | A | T | 11 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0040 others(8): Show |
13 | HG02145.hp1 HG02280.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.134-3497T>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88001687 | |||||||
| chr12:88001777 | T | G | 10 | a0002c0002t0001g0003 a0002c0002t0001g0052 a0002c0002t0001g0053 others(7): Show |
14 | HG01109.hp1 HG01243.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.134-3587A>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88001777 | |||||||
| chr12:88001884 | T | C | 1 | a0001c0001t0001g0015 | 2 | HG00280.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.134-3694A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88001884 | |||||||
| chr12:88001918 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.134-3728G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88001918 | |||||||
| chr12:88002095 | T | C | 1 | a0002c0002t0001g0077 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.134-3905A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88002095 | |||||||
| chr12:88002141 | T | G | 4 | a0005c0006t0001g0204 a0005c0006t0001g0205 a0005c0006t0001g0206 others(1): Show |
4 | HG01884.hp2 HG02647.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.134-3951A>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88002141 | |||||||
| chr12:88002184 | C | T | 1 | a0002c0002t0001g0118 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.134-3994G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88002184 | |||||||
| chr12:88002186 | A | G | 9 | a0002c0002t0002g0040 a0002c0002t0002g0061 a0002c0002t0002g0062 others(6): Show |
11 | HG02145.hp1 HG02280.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.134-3996T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88002186 | |||||||
| chr12:88002218 | C | T | 1 | a0005c0006t0001g0206 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.134-4028G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88002218 | |||||||
| chr12:88002326 | C | T | 1 | a0005c0006t0001g0205 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.134-4136G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88002326 | |||||||
| chr12:88002349 | A | G | 44 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0028 others(41): Show |
55 | HG00738.hp2 HG00741.hp2 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.134-4159T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88002349 | |||||||
| chr12:88002461 | T | C | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.134-4271A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88002461 | |||||||
| chr12:88002649 | T | C | 43 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0028 others(40): Show |
54 | HG00738.hp2 HG00741.hp2 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.134-4459A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88002649 | |||||||
| chr12:88002859 | A | G | 8 | a0002c0002t0001g0003 a0002c0002t0001g0052 a0002c0002t0001g0053 others(5): Show |
12 | HG01109.hp1 HG01243.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.134-4669T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88002859 | |||||||
| chr12:88002967 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.134-4777A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88002967 | |||||||
| chr12:88003039 | T | C | 5 | a0001c0001t0001g0033 a0001c0001t0001g0117 a0001c0001t0001g0148 others(2): Show |
5 | NA18943.hp1 NA18962.hp1 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.134-4849A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88003039 | |||||||
| chr12:88003103 | G | A | 20 | a0002c0002t0001g0007 a0002c0002t0001g0028 a0002c0002t0001g0031 others(17): Show |
25 | HG00738.hp2 HG00741.hp2 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.134-4913C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88003103 | |||||||
| chr12:88003126 | CAG | C | 10 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0061 others(7): Show |
12 | HG02145.hp1 HG02280.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.134-4938_134-4937d others(4): Show |
C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88003126 | |||||||
| chr12:88003141 | T | C | 1 | a0004c0005t0001g0075 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.134-4951A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88003141 | |||||||
| chr12:88003194 | T | C | 1 | a0001c0001t0001g0202 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.134-5004A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88003194 | |||||||
| chr12:88003217 | T | C | 1 | a0001c0001t0001g0132 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.134-5027A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88003217 | |||||||
| chr12:88003444 | C | T | 1 | a0002c0002t0001g0141 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.134-5254G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88003444 | |||||||
| chr12:88003487 | G | A | 20 | a0002c0002t0001g0007 a0002c0002t0001g0028 a0002c0002t0001g0031 others(17): Show |
25 | HG00738.hp2 HG00741.hp2 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.134-5297C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88003487 | |||||||
| chr12:88003507 | TTCTC | T | 3 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 |
3 | HG00558.hp2 NA18953.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.134-5321_134-5318d others(6): Show |
C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88003507 | |||||||
| chr12:88003645 | G | T | 2 | a0002c0002t0002g0034 a0002c0002t0002g0035 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.134-5455C>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88003645 | |||||||
| chr12:88003658 | C | T | 8 | a0002c0002t0001g0003 a0002c0002t0001g0052 a0002c0002t0001g0053 others(5): Show |
12 | HG01109.hp1 HG01243.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.134-5468G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88003658 | |||||||
| chr12:88003983 | C | T | 18 | a0002c0002t0001g0007 a0002c0002t0001g0028 a0002c0002t0001g0041 others(15): Show |
22 | HG00738.hp2 HG00741.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.134-5793G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88003983 | |||||||
| chr12:88004065 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.134-5875T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88004065 | |||||||
| chr12:88004118 | GTA | G | 8 | a0002c0002t0002g0061 a0002c0002t0002g0062 a0002c0002t0002g0123 others(5): Show |
10 | HG02145.hp1 HG02280.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.134-5930_134-5929d others(4): Show |
C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88004118 | |||||||
| chr12:88004185 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.134-5995A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88004185 | |||||||
| chr12:88004251 | T | G | 1 | a0001c0001t0001g0160 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.134-6061A>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88004251 | |||||||
| chr12:88004282 | A | T | 1 | a0002c0002t0001g0065 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.134-6092T>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88004282 | |||||||
| chr12:88004393 | A | G | 1 | a0002c0002t0001g0088 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.134-6203T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88004393 | |||||||
| chr12:88004422 | A | T | 1 | a0002c0002t0001g0087 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.134-6232T>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88004422 | |||||||
| chr12:88004954 | G | A | 8 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0123 others(5): Show |
10 | HG02145.hp1 HG02280.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.134-6764C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88004954 | |||||||
| chr12:88005199 | A | G | 2 | a0002c0002t0001g0059 a0002c0002t0001g0142 |
2 | HG00738.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.134-7009T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88005199 | |||||||
| chr12:88005576 | C | G | 29 | a0002c0002t0001g0007 a0002c0002t0001g0028 a0002c0002t0001g0041 others(26): Show |
35 | HG00738.hp2 HG00741.hp2 HG01255.hp2 others(32): Show |
intron_variant | MODIFIER | c.134-7386G>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88005576 | |||||||
| chr12:88005743 | G | A | 3 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 |
3 | HG00558.hp2 NA18953.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.134-7553C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88005743 | |||||||
| chr12:88005912 | G | GT | 40 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0022 others(37): Show |
47 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.134-7723dupA | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88005912 | |||||||
| chr12:88005912 | G | GTTTT | 6 | a0002c0002t0002g0034 a0003c0004t0002g0011 a0003c0004t0002g0182 others(3): Show |
8 | HG02280.hp2 HG02559.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.134-7726_134-7723d others(6): Show |
C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88005912 | |||||||
| chr12:88005912 | G | T | 4 | a0002c0003t0001g0006 a0002c0003t0001g0166 a0002c0003t0001g0176 others(1): Show |
8 | HG02572.hp2 HG02630.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.134-7722C>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88005912 | |||||||
| chr12:88005912 | GT | G | 27 | a0001c0001t0001g0156 a0002c0002t0001g0003 a0002c0002t0001g0007 others(24): Show |
35 | HG00741.hp2 HG01109.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.134-7723delA | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88005912 | |||||||
| chr12:88005918 | T | G | 1 | a0002c0003t0001g0166 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.134-7728A>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88005918 | |||||||
| chr12:88005920 | T | G | 9 | a0002c0002t0001g0007 a0002c0002t0001g0056 a0002c0002t0001g0076 others(6): Show |
12 | HG00741.hp2 HG01496.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.134-7730A>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88005920 | |||||||
| chr12:88005956 | G | A | 8 | a0002c0002t0001g0003 a0002c0002t0001g0052 a0002c0002t0001g0053 others(5): Show |
12 | HG01109.hp1 HG01243.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.134-7766C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88005956 | |||||||
| chr12:88005977 | C | T | 1 | a0009c0010t0001g0179 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.134-7787G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88005977 | |||||||
| chr12:88005986 | G | A | 1 | a0002c0002t0001g0090 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.134-7796C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88005986 | |||||||
| chr12:88006029 | G | C | 1 | a0006c0009t0001g0106 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.134-7839C>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88006029 | |||||||
| chr12:88006078 | C | T | 8 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0123 others(5): Show |
10 | HG02145.hp1 HG02280.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.134-7888G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88006078 | |||||||
| chr12:88006159 | G | A | 4 | a0005c0006t0001g0204 a0005c0006t0001g0205 a0005c0006t0001g0206 others(1): Show |
4 | HG01884.hp2 HG02647.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.134-7969C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88006159 | |||||||
| chr12:88006173 | C | T | 1 | a0001c0001t0001g0153 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.134-7983G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88006173 | |||||||
| chr12:88006247 | G | A | 2 | a0001c0001t0001g0200 a0001c0001t0001g0201 |
2 | HG01891.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.134-8057C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88006247 | |||||||
| chr12:88006249 | G | T | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.134-8059C>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88006249 | |||||||
| chr12:88006374 | C | T | 2 | a0002c0002t0002g0034 a0002c0002t0002g0035 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.134-8184G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88006374 | |||||||
| chr12:88006421 | G | C | 6 | a0002c0002t0002g0123 a0003c0004t0002g0011 a0003c0004t0002g0182 others(3): Show |
8 | HG02145.hp1 HG02280.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.134-8231C>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88006421 | |||||||
| chr12:88006524 | G | A | 41 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0028 others(38): Show |
51 | HG00738.hp2 HG00741.hp2 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.134-8334C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88006524 | |||||||
| chr12:88006644 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.134-8454C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88006644 | |||||||
| chr12:88006775 | C | A | 8 | a0002c0002t0001g0003 a0002c0002t0001g0052 a0002c0002t0001g0053 others(5): Show |
12 | HG01109.hp1 HG01243.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.134-8585G>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88006775 | |||||||
| chr12:88006878 | G | A | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.134-8688C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88006878 | |||||||
| chr12:88006988 | C | G | 10 | a0002c0002t0001g0003 a0002c0002t0001g0052 a0002c0002t0001g0053 others(7): Show |
14 | HG01109.hp1 HG01243.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.134-8798G>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88006988 | |||||||
| chr12:88007264 | A | G | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.134-9074T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88007264 | |||||||
| chr12:88007332 | A | G | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.134-9142T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88007332 | |||||||
| chr12:88007342 | C | T | 20 | a0002c0002t0001g0013 a0002c0002t0001g0014 a0002c0002t0001g0026 others(17): Show |
23 | HG01069.hp1 HG01192.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.134-9152G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88007342 | |||||||
| chr12:88007347 | TC | T | 14 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0061 others(11): Show |
16 | HG01884.hp2 HG02145.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.134-9158delG | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88007347 | |||||||
| chr12:88007349 | G | A | 14 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0002c0002t0002g0061 others(11): Show |
16 | HG01884.hp2 HG02145.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.134-9159C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88007349 | |||||||
| chr12:88007637 | A | G | 24 | a0002c0002t0001g0007 a0002c0002t0001g0028 a0002c0002t0001g0031 others(21): Show |
29 | HG00738.hp2 HG00741.hp2 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.134-9447T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88007637 | |||||||
| chr12:88007762 | G | T | 39 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0028 others(36): Show |
50 | HG00738.hp2 HG00741.hp2 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.134-9572C>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88007762 | |||||||
| chr12:88007902 | T | C | 1 | a0002c0002t0001g0014 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.134-9712A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88007902 | |||||||
| chr12:88007941 | G | A | 3 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 |
3 | HG00558.hp2 NA18953.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.134-9751C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88007941 | |||||||
| chr12:88008029 | G | A | 37 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0028 others(34): Show |
48 | HG00738.hp2 HG00741.hp2 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.134-9839C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88008029 | |||||||
| chr12:88008058 | CT | C | 20 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0025 others(17): Show |
30 | HG01074.hp1 HG01081.hp1 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.134-9869delA | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88008058 | |||||||
| chr12:88008353 | A | T | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.134-10163T>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88008353 | |||||||
| chr12:88008363 | A | G | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.134-10173T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88008363 | |||||||
| chr12:88008425 | A | G | 10 | a0002c0002t0001g0003 a0002c0002t0001g0013 a0002c0002t0001g0052 others(7): Show |
15 | HG01109.hp1 HG01192.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.134-10235T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88008425 | |||||||
| chr12:88008457 | T | C | 1 | a0005c0006t0001g0204 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.134-10267A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88008457 | |||||||
| chr12:88008486 | C | A | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.134-10296G>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88008486 | |||||||
| chr12:88008568 | T | C | 1 | a0002c0002t0001g0065 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.134-10378A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88008568 | |||||||
| chr12:88008720 | T | A | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.134-10530A>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88008720 | |||||||
| chr12:88008721 | C | T | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.134-10531G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88008721 | |||||||
| chr12:88008722 | A | T | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.134-10532T>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88008722 | |||||||
| chr12:88008725 | T | C | 3 | a0001c0001t0001g0117 a0001c0001t0001g0148 a0008c0011t0001g0163 |
3 | NA18968.hp1 NA18994.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.134-10535A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88008725 | |||||||
| chr12:88009033 | A | G | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.134-10843T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88009033 | |||||||
| chr12:88009037 | A | C | 3 | a0001c0001t0001g0117 a0001c0001t0001g0148 a0008c0011t0001g0163 |
3 | NA18968.hp1 NA18994.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.134-10847T>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88009037 | |||||||
| chr12:88009070 | G | A | 1 | a0001c0001t0001g0110 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.134-10880C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88009070 | |||||||
| chr12:88009466 | T | A | 2 | a0002c0002t0002g0034 a0002c0002t0002g0035 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.134-11276A>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88009466 | |||||||
| chr12:88009564 | C | T | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.134-11374G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88009564 | |||||||
| chr12:88010007 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.134-11817G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88010007 | |||||||
| chr12:88010147 | G | A | 4 | a0005c0006t0001g0204 a0005c0006t0001g0205 a0005c0006t0001g0206 others(1): Show |
4 | HG01884.hp2 HG02647.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.134-11957C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88010147 | |||||||
| chr12:88010202 | A | G | 1 | a0001c0001t0001g0202 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.134-12012T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88010202 | |||||||
| chr12:88010217 | A | G | 1 | a0001c0001t0001g0136 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.134-12027T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88010217 | |||||||
| chr12:88010254 | C | A | 8 | a0002c0002t0001g0007 a0002c0002t0001g0056 a0002c0002t0001g0076 others(5): Show |
11 | HG00741.hp2 HG01496.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.134-12064G>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88010254 | |||||||
| chr12:88010262 | T | C | 1 | a0002c0002t0001g0192 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.134-12072A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88010262 | |||||||
| chr12:88010370 | T | TAGATTAT others(29): Show |
6 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0050 others(3): Show |
9 | HG03239.hp2 HG04228.hp1 NA18961.hp1 others(6): Show |
intron_variant | MODIFIER | c.134-12216_134-1218 others(40): Show |
C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88010370 | |||||||
| chr12:88010370 | TAGATTAT others(29): Show |
T | 35 | a0001c0001t0001g0093 a0002c0002t0001g0003 a0002c0002t0001g0007 others(32): Show |
45 | HG00741.hp2 HG01109.hp1 HG01192.hp1 others(42): Show |
intron_variant | MODIFIER | c.134-12216_134-1218 others(40): Show |
C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88010370 | |||||||
| chr12:88010370 | TAGATTAT others(65): Show |
T | 29 | a0002c0002t0001g0014 a0002c0002t0001g0026 a0002c0002t0001g0141 others(26): Show |
35 | HG00639.hp1 HG01069.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.134-12252_134-1218 others(76): Show |
C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88010370 | |||||||
| chr12:88010398 | CTTATAAT others(57): Show |
C | 2 | a0002c0002t0001g0073 a0002c0002t0001g0074 |
2 | HG02145.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.134-12272_134-1220 others(68): Show |
C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88010398 | |||||||
| chr12:88010421 | A | T | 3 | a0002c0002t0001g0031 a0002c0002t0001g0069 a0002c0002t0001g0180 |
4 | HG02055.hp2 HG02572.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.134-12231T>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88010421 | |||||||
| chr12:88010428 | T | TATAATCT others(29): Show |
1 | a0001c0001t0001g0124 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.134-12239_134-1223 others(40): Show |
C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88010428 | |||||||
| chr12:88010439 | AATAAGAT others(1): Show |
A | 5 | a0003c0004t0002g0011 a0003c0004t0002g0182 a0003c0004t0002g0183 others(2): Show |
7 | HG02280.hp2 HG02615.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.134-12257_134-1225 others(12): Show |
C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88010439 | |||||||
| chr12:88010720 | A | G | 20 | a0002c0002t0001g0007 a0002c0002t0001g0028 a0002c0002t0001g0031 others(17): Show |
25 | HG00738.hp2 HG00741.hp2 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.134-12530T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88010720 | |||||||
| chr12:88010915 | A | T | 1 | a0003c0004t0002g0183 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.134-12725T>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88010915 | |||||||
| chr12:88010919 | C | G | 1 | a0003c0004t0002g0183 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.134-12729G>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88010919 | |||||||
| chr12:88011007 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.134-12817T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88011007 | |||||||
| chr12:88011221 | G | A | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.134-13031C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88011221 | |||||||
| chr12:88011271 | C | T | 2 | a0002c0002t0001g0052 a0002c0002t0001g0053 |
2 | HG02486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.134-13081G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88011271 | |||||||
| chr12:88011310 | A | G | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.134-13120T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88011310 | |||||||
| chr12:88011768 | T | C | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.134-13578A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88011768 | |||||||
| chr12:88011988 | T | C | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.134-13798A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88011988 | |||||||
| chr12:88012000 | C | T | 10 | a0002c0002t0001g0003 a0002c0002t0001g0013 a0002c0002t0001g0052 others(7): Show |
15 | HG01109.hp1 HG01192.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.134-13810G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88012000 | |||||||
| chr12:88012023 | A | G | 21 | a0002c0002t0001g0007 a0002c0002t0001g0028 a0002c0002t0001g0031 others(18): Show |
26 | HG00738.hp2 HG00741.hp2 HG01255.hp2 others(23): Show |
intron_variant | MODIFIER | c.134-13833T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88012023 | |||||||
| chr12:88012031 | A | G | 72 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0013 others(69): Show |
90 | HG00639.hp1 HG00738.hp2 HG00741.hp2 others(87): Show |
intron_variant | MODIFIER | c.134-13841T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88012031 | |||||||
| chr12:88012045 | A | C | 72 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0013 others(69): Show |
90 | HG00639.hp1 HG00738.hp2 HG00741.hp2 others(87): Show |
intron_variant | MODIFIER | c.134-13855T>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88012045 | |||||||
| chr12:88012056 | T | C | 2 | a0002c0002t0002g0034 a0002c0002t0002g0035 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.134-13866A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88012056 | |||||||
| chr12:88012164 | G | A | 1 | a0001c0001t0001g0135 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.134-13974C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88012164 | |||||||
| chr12:88012246 | A | G | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.134-14056T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88012246 | |||||||
| chr12:88012290 | A | G | 1 | a0002c0002t0001g0014 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.134-14100T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88012290 | |||||||
| chr12:88012387 | C | G | 1 | a0001c0001t0001g0036 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.133+14101G>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88012387 | |||||||
| chr12:88012430 | C | T | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.133+14058G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88012430 | |||||||
| chr12:88012448 | T | C | 1 | a0002c0002t0001g0193 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.133+14040A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88012448 | |||||||
| chr12:88012517 | A | G | 3 | a0004c0005t0001g0037 a0004c0005t0001g0048 a0004c0005t0001g0075 |
3 | HG00741.hp2 HG01496.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.133+13971T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88012517 | |||||||
| chr12:88012694 | T | C | 1 | a0001c0001t0001g0020 | 2 | HG00280.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.133+13794A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88012694 | |||||||
| chr12:88012729 | A | G | 20 | a0002c0002t0001g0007 a0002c0002t0001g0028 a0002c0002t0001g0031 others(17): Show |
25 | HG00738.hp2 HG00741.hp2 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.133+13759T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88012729 | |||||||
| chr12:88012757 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.133+13731T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88012757 | |||||||
| chr12:88012874 | C | G | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.133+13614G>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88012874 | |||||||
| chr12:88012996 | A | G | 1 | a0003c0004t0002g0182 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.133+13492T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88012996 | |||||||
| chr12:88013032 | C | G | 2 | a0002c0002t0001g0196 a0002c0002t0001g0197 |
2 | HG03209.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.133+13456G>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88013032 | |||||||
| chr12:88013209 | GA | G | 29 | a0002c0002t0001g0014 a0002c0002t0001g0026 a0002c0002t0001g0054 others(26): Show |
35 | HG00639.hp1 HG01069.hp1 HG02145.hp2 others(32): Show |
intron_variant | MODIFIER | c.133+13278delT | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88013209 | |||||||
| chr12:88013389 | A | G | 4 | a0005c0006t0001g0204 a0005c0006t0001g0205 a0005c0006t0001g0206 others(1): Show |
4 | HG01884.hp2 HG02647.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.133+13099T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88013389 | |||||||
| chr12:88014024 | C | G | 1 | a0001c0001t0001g0170 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.133+12464G>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88014024 | |||||||
| chr12:88014026 | T | G | 1 | a0001c0001t0001g0072 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.133+12462A>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88014026 | |||||||
| chr12:88014135 | T | G | 2 | a0001c0001t0001g0030 a0001c0001t0001g0038 |
3 | HG01069.hp2 HG02293.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.133+12353A>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88014135 | |||||||
| chr12:88014162 | G | A | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.133+12326C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88014162 | |||||||
| chr12:88014289 | T | A | 1 | a0001c0001t0001g0210 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.133+12199A>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88014289 | |||||||
| chr12:88014293 | T | TTTTA | 69 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0013 others(66): Show |
86 | HG00639.hp1 HG00738.hp2 HG00741.hp2 others(83): Show |
intron_variant | MODIFIER | c.133+12191_133+1219 others(8): Show |
C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88014293 | |||||||
| chr12:88014332 | C | T | 1 | a0001c0001t0001g0091 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.133+12156G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88014332 | |||||||
| chr12:88014336 | C | G | 17 | a0002c0002t0001g0007 a0002c0002t0001g0028 a0002c0002t0001g0041 others(14): Show |
21 | HG00738.hp2 HG00741.hp2 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.133+12152G>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88014336 | |||||||
| chr12:88014363 | G | A | 17 | a0002c0002t0001g0007 a0002c0002t0001g0028 a0002c0002t0001g0041 others(14): Show |
21 | HG00738.hp2 HG00741.hp2 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.133+12125C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88014363 | |||||||
| chr12:88014399 | T | G | 20 | a0002c0002t0001g0007 a0002c0002t0001g0028 a0002c0002t0001g0031 others(17): Show |
25 | HG00738.hp2 HG00741.hp2 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.133+12089A>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88014399 | |||||||
| chr12:88014469 | T | C | 10 | a0002c0002t0001g0003 a0002c0002t0001g0013 a0002c0002t0001g0052 others(7): Show |
15 | HG01109.hp1 HG01192.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.133+12019A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88014469 | |||||||
| chr12:88014505 | G | A | 1 | a0002c0002t0001g0017 | 2 | NA18994.hp2 NA19059.hp1 |
intron_variant | MODIFIER | c.133+11983C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88014505 | |||||||
| chr12:88014578 | C | T | 17 | a0002c0002t0001g0007 a0002c0002t0001g0028 a0002c0002t0001g0041 others(14): Show |
21 | HG00738.hp2 HG00741.hp2 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.133+11910G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88014578 | |||||||
| chr12:88014588 | C | A | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.133+11900G>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88014588 | |||||||
| chr12:88014629 | T | C | 7 | a0002c0002t0001g0003 a0002c0002t0001g0013 a0002c0002t0001g0052 others(4): Show |
12 | HG01109.hp1 HG01192.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.133+11859A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88014629 | |||||||
| chr12:88014696 | C | T | 6 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0113 others(3): Show |
11 | HG00099.hp2 HG00735.hp2 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.133+11792G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88014696 | |||||||
| chr12:88014702 | G | T | 69 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0013 others(66): Show |
86 | HG00639.hp1 HG00738.hp2 HG00741.hp2 others(83): Show |
intron_variant | MODIFIER | c.133+11786C>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88014702 | |||||||
| chr12:88014778 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.133+11710C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88014778 | |||||||
| chr12:88014796 | C | A | 2 | a0002c0002t0002g0034 a0002c0002t0002g0035 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.133+11692G>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88014796 | |||||||
| chr12:88014805 | A | C | 1 | a0002c0002t0001g0180 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.133+11683T>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88014805 | |||||||
| chr12:88014806 | C | T | 1 | a0001c0001t0001g0018 | 2 | HG01169.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.133+11682G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88014806 | |||||||
| chr12:88015092 | G | A | 2 | a0002c0002t0001g0052 a0002c0002t0001g0053 |
2 | HG02486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.133+11396C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88015092 | |||||||
| chr12:88015222 | C | T | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.133+11266G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88015222 | |||||||
| chr12:88015233 | T | C | 5 | a0002c0002t0001g0003 a0002c0002t0001g0013 a0002c0002t0001g0063 others(2): Show |
10 | HG01109.hp1 HG01192.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.133+11255A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88015233 | |||||||
| chr12:88015323 | T | C | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.133+11165A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88015323 | |||||||
| chr12:88015364 | A | G | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.133+11124T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88015364 | |||||||
| chr12:88015417 | A | G | 66 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(63): Show |
86 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.133+11071T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88015417 | |||||||
| chr12:88015590 | G | A | 10 | a0002c0002t0001g0003 a0002c0002t0001g0013 a0002c0002t0001g0052 others(7): Show |
15 | HG01109.hp1 HG01192.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.133+10898C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88015590 | |||||||
| chr12:88015596 | C | G | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.133+10892G>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88015596 | |||||||
| chr12:88015721 | A | T | 10 | a0002c0002t0001g0003 a0002c0002t0001g0013 a0002c0002t0001g0052 others(7): Show |
15 | HG01109.hp1 HG01192.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.133+10767T>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88015721 | |||||||
| chr12:88016317 | G | A | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.133+10171C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88016317 | |||||||
| chr12:88016346 | G | A | 1 | a0002c0002t0001g0164 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.133+10142C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88016346 | |||||||
| chr12:88016565 | A | G | 74 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(71): Show |
96 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.133+9923T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88016565 | |||||||
| chr12:88016760 | C | A | 6 | a0002c0002t0001g0165 a0002c0002t0001g0195 a0002c0003t0001g0006 others(3): Show |
10 | HG02572.hp2 HG02630.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.133+9728G>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88016760 | |||||||
| chr12:88016760 | C | G | 20 | a0002c0002t0001g0007 a0002c0002t0001g0028 a0002c0002t0001g0031 others(17): Show |
25 | HG00738.hp2 HG00741.hp2 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.133+9728G>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88016760 | |||||||
| chr12:88016786 | G | A | 1 | a0001c0001t0001g0173 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.133+9702C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88016786 | |||||||
| chr12:88016848 | G | A | 1 | a0001c0001t0001g0145 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.133+9640C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88016848 | |||||||
| chr12:88016869 | A | G | 2 | a0002c0002t0001g0059 a0002c0002t0001g0142 |
2 | HG00738.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.133+9619T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88016869 | |||||||
| chr12:88016908 | T | C | 72 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0013 others(69): Show |
90 | HG00639.hp1 HG00738.hp2 HG00741.hp2 others(87): Show |
intron_variant | MODIFIER | c.133+9580A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88016908 | |||||||
| chr12:88016918 | T | C | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.133+9570A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88016918 | |||||||
| chr12:88016951 | G | C | 21 | a0002c0002t0001g0007 a0002c0002t0001g0028 a0002c0002t0001g0031 others(18): Show |
26 | HG00738.hp2 HG00741.hp2 HG01255.hp2 others(23): Show |
intron_variant | MODIFIER | c.133+9537C>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88016951 | |||||||
| chr12:88016953 | T | A | 2 | a0002c0002t0001g0054 a0002c0002t0001g0175 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.133+9535A>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88016953 | |||||||
| chr12:88017004 | G | A | 20 | a0002c0002t0001g0007 a0002c0002t0001g0028 a0002c0002t0001g0031 others(17): Show |
25 | HG00738.hp2 HG00741.hp2 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.133+9484C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88017004 | |||||||
| chr12:88017092 | T | G | 1 | a0003c0004t0002g0185 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.133+9396A>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88017092 | |||||||
| chr12:88017198 | G | A | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.133+9290C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88017198 | |||||||
| chr12:88017209 | A | G | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.133+9279T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88017209 | |||||||
| chr12:88017247 | C | T | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.133+9241G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88017247 | |||||||
| chr12:88017248 | G | A | 10 | a0002c0002t0001g0003 a0002c0002t0001g0013 a0002c0002t0001g0052 others(7): Show |
15 | HG01109.hp1 HG01192.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.133+9240C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88017248 | |||||||
| chr12:88017427 | T | C | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.133+9061A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88017427 | |||||||
| chr12:88017519 | G | C | 1 | a0002c0002t0001g0057 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.133+8969C>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88017519 | |||||||
| chr12:88017533 | G | C | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.133+8955C>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88017533 | |||||||
| chr12:88017579 | C | A | 6 | a0002c0002t0001g0165 a0002c0002t0001g0195 a0002c0003t0001g0006 others(3): Show |
10 | HG02572.hp2 HG02630.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.133+8909G>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88017579 | |||||||
| chr12:88017840 | T | C | 5 | a0002c0002t0001g0028 a0002c0002t0001g0041 a0002c0002t0001g0058 others(2): Show |
6 | NA18949.hp1 NA18962.hp2 NA19058.hp1 others(3): Show |
intron_variant | MODIFIER | c.133+8648A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88017840 | |||||||
| chr12:88018026 | A | C | 2 | a0002c0002t0002g0034 a0002c0002t0002g0035 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.133+8462T>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88018026 | |||||||
| chr12:88018512 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.133+7976A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88018512 | |||||||
| chr12:88018603 | G | A | 1 | a0002c0002t0001g0164 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.133+7885C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88018603 | |||||||
| chr12:88018716 | C | T | 8 | a0001c0001t0001g0086 a0001c0001t0001g0089 a0002c0002t0001g0016 others(5): Show |
10 | HG00621.hp1 HG01433.hp2 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.133+7772G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88018716 | |||||||
| chr12:88018724 | C | T | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.133+7764G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88018724 | |||||||
| chr12:88018811 | C | T | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.133+7677G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88018811 | |||||||
| chr12:88018817 | G | T | 27 | a0002c0002t0001g0014 a0002c0002t0001g0026 a0002c0002t0001g0073 others(24): Show |
33 | HG00639.hp1 HG01069.hp1 HG02145.hp2 others(30): Show |
intron_variant | MODIFIER | c.133+7671C>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88018817 | |||||||
| chr12:88018838 | C | G | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.133+7650G>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88018838 | |||||||
| chr12:88018844 | T | A | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.133+7644A>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88018844 | |||||||
| chr12:88018871 | C | T | 8 | a0002c0002t0002g0060 a0002c0002t0002g0061 a0002c0002t0002g0062 others(5): Show |
10 | HG02280.hp2 HG02615.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.133+7617G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88018871 | |||||||
| chr12:88019011 | G | T | 1 | a0001c0001t0001g0086 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.133+7477C>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88019011 | |||||||
| chr12:88019200 | T | G | 10 | a0002c0002t0001g0003 a0002c0002t0001g0013 a0002c0002t0001g0052 others(7): Show |
15 | HG01109.hp1 HG01192.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.133+7288A>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88019200 | |||||||
| chr12:88019201 | ATTTC | A | 10 | a0002c0002t0001g0003 a0002c0002t0001g0013 a0002c0002t0001g0052 others(7): Show |
15 | HG01109.hp1 HG01192.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.133+7283_133+7286d others(6): Show |
C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88019201 | |||||||
| chr12:88019206 | C | A | 10 | a0002c0002t0001g0003 a0002c0002t0001g0013 a0002c0002t0001g0052 others(7): Show |
15 | HG01109.hp1 HG01192.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.133+7282G>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88019206 | |||||||
| chr12:88019297 | C | T | 2 | a0002c0002t0001g0054 a0002c0002t0001g0175 |
2 | HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.133+7191G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88019297 | |||||||
| chr12:88019314 | C | T | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.133+7174G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88019314 | |||||||
| chr12:88019559 | T | A | 4 | a0005c0006t0001g0204 a0005c0006t0001g0205 a0005c0006t0001g0206 others(1): Show |
4 | HG01884.hp2 HG02647.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.133+6929A>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88019559 | |||||||
| chr12:88019573 | C | T | 10 | a0002c0002t0001g0003 a0002c0002t0001g0013 a0002c0002t0001g0052 others(7): Show |
15 | HG01109.hp1 HG01192.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.133+6915G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88019573 | |||||||
| chr12:88019639 | A | G | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.133+6849T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88019639 | |||||||
| chr12:88019641 | A | C | 10 | a0002c0002t0001g0003 a0002c0002t0001g0013 a0002c0002t0001g0052 others(7): Show |
15 | HG01109.hp1 HG01192.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.133+6847T>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88019641 | |||||||
| chr12:88019690 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.133+6798G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88019690 | |||||||
| chr12:88019725 | G | C | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.133+6763C>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88019725 | |||||||
| chr12:88019770 | A | T | 1 | a0001c0001t0001g0084 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.133+6718T>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88019770 | |||||||
| chr12:88019801 | T | C | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.133+6687A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88019801 | |||||||
| chr12:88019812 | C | G | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.133+6676G>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88019812 | |||||||
| chr12:88020050 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.133+6438G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88020050 | |||||||
| chr12:88020411 | A | G | 72 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0013 others(69): Show |
90 | HG00639.hp1 HG00738.hp2 HG00741.hp2 others(87): Show |
intron_variant | MODIFIER | c.133+6077T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88020411 | |||||||
| chr12:88020611 | A | G | 1 | a0001c0001t0001g0167 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.133+5877T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88020611 | |||||||
| chr12:88020731 | A | G | 1 | a0002c0002t0001g0141 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.133+5757T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88020731 | |||||||
| chr12:88020759 | C | A | 69 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0013 others(66): Show |
86 | HG00639.hp1 HG00738.hp2 HG00741.hp2 others(83): Show |
intron_variant | MODIFIER | c.133+5729G>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88020759 | |||||||
| chr12:88020807 | T | TA | 23 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0002c0002t0001g0007 others(20): Show |
27 | HG00738.hp2 HG00741.hp2 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.133+5680dupT | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88020807 | |||||||
| chr12:88020820 | T | A | 27 | a0002c0002t0001g0014 a0002c0002t0001g0026 a0002c0002t0001g0073 others(24): Show |
33 | HG00639.hp1 HG01069.hp1 HG02145.hp2 others(30): Show |
intron_variant | MODIFIER | c.133+5668A>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88020820 | |||||||
| chr12:88020834 | C | G | 7 | a0002c0002t0001g0003 a0002c0002t0001g0013 a0002c0002t0001g0052 others(4): Show |
12 | HG01109.hp1 HG01192.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.133+5654G>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88020834 | |||||||
| chr12:88021301 | CA | C | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(175): Show |
236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.133+5186delT | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88021301 | |||||||
| chr12:88021343 | A | T | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.133+5145T>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88021343 | |||||||
| chr12:88021375 | G | A | 1 | a0001c0001t0001g0146 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.133+5113C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88021375 | |||||||
| chr12:88021531 | G | T | 1 | a0003c0004t0002g0183 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.133+4957C>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88021531 | |||||||
| chr12:88021593 | G | A | 3 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0002c0002t0001g0198 |
3 | HG03471.hp1 NA19060.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.133+4895C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88021593 | |||||||
| chr12:88021630 | T | C | 1 | a0002c0002t0001g0194 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.133+4858A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88021630 | |||||||
| chr12:88021637 | C | CA | 11 | a0002c0002t0001g0003 a0002c0002t0001g0013 a0002c0002t0001g0052 others(8): Show |
16 | HG01109.hp1 HG01192.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.133+4850dupT | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88021637 | |||||||
| chr12:88021822 | C | A | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.133+4666G>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88021822 | |||||||
| chr12:88021828 | T | C | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG02071.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.133+4660A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88021828 | |||||||
| chr12:88021863 | CA | C | 4 | a0001c0001t0001g0049 a0001c0001t0001g0081 a0001c0001t0001g0082 others(1): Show |
4 | NA18977.hp2 NA19064.hp1 NA19087.hp1 others(1): Show |
intron_variant | MODIFIER | c.133+4624delT | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88021863 | |||||||
| chr12:88021899 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.133+4589C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88021899 | |||||||
| chr12:88021966 | G | A | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.133+4522C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88021966 | |||||||
| chr12:88022050 | A | T | 1 | a0001c0001t0001g0080 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.133+4438T>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88022050 | |||||||
| chr12:88022068 | C | T | 27 | a0002c0002t0001g0014 a0002c0002t0001g0026 a0002c0002t0001g0073 others(24): Show |
33 | HG00639.hp1 HG01069.hp1 HG02145.hp2 others(30): Show |
intron_variant | MODIFIER | c.133+4420G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88022068 | |||||||
| chr12:88022147 | T | C | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.133+4341A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88022147 | |||||||
| chr12:88022372 | T | G | 1 | a0002c0002t0001g0197 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.133+4116A>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88022372 | |||||||
| chr12:88022510 | A | C | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.133+3978T>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88022510 | |||||||
| chr12:88022534 | A | G | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.133+3954T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88022534 | |||||||
| chr12:88022538 | C | T | 1 | a0001c0001t0001g0015 | 2 | HG00280.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.133+3950G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88022538 | |||||||
| chr12:88022543 | T | A | 1 | a0002c0002t0001g0164 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.133+3945A>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88022543 | |||||||
| chr12:88022702 | A | G | 17 | a0002c0002t0001g0007 a0002c0002t0001g0028 a0002c0002t0001g0041 others(14): Show |
21 | HG00738.hp2 HG00741.hp2 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.133+3786T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88022702 | |||||||
| chr12:88022715 | C | T | 17 | a0002c0002t0001g0007 a0002c0002t0001g0028 a0002c0002t0001g0041 others(14): Show |
21 | HG00738.hp2 HG00741.hp2 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.133+3773G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88022715 | |||||||
| chr12:88022852 | G | C | 10 | a0002c0002t0001g0003 a0002c0002t0001g0013 a0002c0002t0001g0052 others(7): Show |
15 | HG01109.hp1 HG01192.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.133+3636C>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88022852 | |||||||
| chr12:88022909 | C | T | 69 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0013 others(66): Show |
86 | HG00639.hp1 HG00738.hp2 HG00741.hp2 others(83): Show |
intron_variant | MODIFIER | c.133+3579G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88022909 | |||||||
| chr12:88023061 | C | G | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.133+3427G>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88023061 | |||||||
| chr12:88023234 | G | C | 1 | a0001c0001t0001g0050 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.133+3254C>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88023234 | |||||||
| chr12:88023245 | T | TAA | 26 | a0002c0002t0001g0014 a0002c0002t0001g0026 a0002c0002t0001g0073 others(23): Show |
32 | HG00639.hp1 HG01069.hp1 HG02145.hp2 others(29): Show |
intron_variant | MODIFIER | c.133+3241_133+3242d others(4): Show |
C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88023245 | |||||||
| chr12:88023248 | G | A | 27 | a0002c0002t0001g0014 a0002c0002t0001g0026 a0002c0002t0001g0073 others(24): Show |
33 | HG00639.hp1 HG01069.hp1 HG02145.hp2 others(30): Show |
intron_variant | MODIFIER | c.133+3240C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88023248 | |||||||
| chr12:88023252 | C | A | 27 | a0002c0002t0001g0014 a0002c0002t0001g0026 a0002c0002t0001g0073 others(24): Show |
33 | HG00639.hp1 HG01069.hp1 HG02145.hp2 others(30): Show |
intron_variant | MODIFIER | c.133+3236G>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88023252 | |||||||
| chr12:88023255 | G | A | 27 | a0002c0002t0001g0014 a0002c0002t0001g0026 a0002c0002t0001g0073 others(24): Show |
33 | HG00639.hp1 HG01069.hp1 HG02145.hp2 others(30): Show |
intron_variant | MODIFIER | c.133+3233C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88023255 | |||||||
| chr12:88023283 | G | A | 4 | a0005c0006t0001g0204 a0005c0006t0001g0205 a0005c0006t0001g0206 others(1): Show |
4 | HG01884.hp2 HG02647.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.133+3205C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88023283 | |||||||
| chr12:88023341 | A | C | 2 | a0002c0002t0002g0034 a0002c0002t0002g0035 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.133+3147T>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88023341 | |||||||
| chr12:88023491 | C | T | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.133+2997G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88023491 | |||||||
| chr12:88023500 | T | TA | 44 | a0002c0002t0001g0007 a0002c0002t0001g0014 a0002c0002t0001g0026 others(41): Show |
54 | HG00738.hp2 HG00741.hp2 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.133+2987dupT | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88023500 | |||||||
| chr12:88023500 | TA | T | 11 | a0001c0001t0001g0047 a0001c0001t0001g0147 a0002c0002t0002g0060 others(8): Show |
13 | HG00639.hp1 HG02040.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.133+2987delT | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88023500 | |||||||
| chr12:88023539 | G | A | 1 | a0002c0002t0001g0059 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.133+2949C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88023539 | |||||||
| chr12:88023666 | CA | C | 29 | a0001c0001t0001g0146 a0001c0001t0001g0160 a0002c0002t0001g0003 others(26): Show |
36 | HG01069.hp1 HG01109.hp1 HG01192.hp1 others(33): Show |
intron_variant | MODIFIER | c.133+2821delT | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88023666 | |||||||
| chr12:88023722 | C | G | 8 | a0002c0002t0002g0060 a0002c0002t0002g0061 a0002c0002t0002g0062 others(5): Show |
10 | HG02280.hp2 HG02615.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.133+2766G>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88023722 | |||||||
| chr12:88024069 | A | G | 1 | a0002c0002t0001g0198 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.133+2419T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88024069 | |||||||
| chr12:88024080 | C | G | 1 | a0001c0001t0001g0079 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.133+2408G>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88024080 | |||||||
| chr12:88024162 | A | T | 1 | a0002c0002t0002g0034 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.133+2326T>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88024162 | |||||||
| chr12:88024327 | C | A | 70 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0013 others(67): Show |
87 | HG00639.hp1 HG00738.hp2 HG00741.hp2 others(84): Show |
intron_variant | MODIFIER | c.133+2161G>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88024327 | |||||||
| chr12:88024448 | T | C | 1 | a0002c0002t0001g0197 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.133+2040A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88024448 | |||||||
| chr12:88024613 | T | A | 19 | a0002c0002t0001g0007 a0002c0002t0001g0028 a0002c0002t0001g0041 others(16): Show |
23 | HG00738.hp2 HG00741.hp2 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.133+1875A>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88024613 | |||||||
| chr12:88024668 | G | C | 70 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0013 others(67): Show |
87 | HG00639.hp1 HG00738.hp2 HG00741.hp2 others(84): Show |
intron_variant | MODIFIER | c.133+1820C>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88024668 | |||||||
| chr12:88024768 | A | T | 1 | a0001c0001t0001g0078 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.133+1720T>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88024768 | |||||||
| chr12:88025084 | G | C | 2 | a0001c0001t0001g0144 a0001c0001t0001g0145 |
2 | NA18970.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.133+1404C>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88025084 | |||||||
| chr12:88025213 | C | A | 17 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(14): Show |
28 | HG01074.hp1 HG01081.hp1 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.133+1275G>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88025213 | |||||||
| chr12:88025259 | T | C | 10 | a0002c0002t0001g0003 a0002c0002t0001g0013 a0002c0002t0001g0063 others(7): Show |
15 | HG01109.hp1 HG01192.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.133+1229A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88025259 | |||||||
| chr12:88025380 | G | A | 1 | a0001c0001t0001g0027 | 2 | HG03239.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.133+1108C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88025380 | |||||||
| chr12:88025418 | G | A | 8 | a0002c0002t0001g0003 a0002c0002t0001g0013 a0002c0002t0001g0063 others(5): Show |
13 | HG01109.hp1 HG01192.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.133+1070C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88025418 | |||||||
| chr12:88025609 | C | T | 4 | a0002c0002t0001g0175 a0002c0003t0001g0006 a0002c0003t0001g0176 others(1): Show |
8 | HG02572.hp2 HG02630.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.133+879G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88025609 | |||||||
| chr12:88025694 | G | A | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(130): Show |
178 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.133+794C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88025694 | |||||||
| chr12:88025722 | G | A | 1 | a0001c0001t0001g0157 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.133+766C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88025722 | |||||||
| chr12:88025741 | A | AAAAC | 3 | a0002c0002t0001g0164 a0002c0002t0001g0165 a0002c0003t0001g0166 |
3 | HG02257.hp2 HG03041.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.133+743_133+746dup others(4): Show |
C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88025741 | |||||||
| chr12:88025846 | C | A | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG00673.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.133+642G>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88025846 | |||||||
| chr12:88026184 | G | T | 21 | a0001c0001t0001g0051 a0002c0002t0001g0003 a0002c0002t0001g0013 others(18): Show |
27 | HG01109.hp1 HG01175.hp2 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.133+304C>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88026184 | |||||||
| chr12:88026215 | G | C | 3 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 |
3 | HG00558.hp2 NA18953.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.133+273C>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88026215 | |||||||
| chr12:88026226 | T | C | 6 | a0002c0002t0002g0034 a0002c0002t0002g0035 a0005c0006t0001g0204 others(3): Show |
6 | HG01884.hp2 HG02559.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.133+262A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88026226 | |||||||
| chr12:88026291 | T | C | 1 | a0002c0002t0001g0169 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.133+197A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88026291 | |||||||
| chr12:88026351 | A | T | 2 | a0001c0001t0001g0009 a0001c0001t0001g0050 |
4 | NA18966.hp2 NA18983.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.133+137T>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 3/12 | chr12 | 88026351 | |||||||
| chr12:88026931 | A | G | 2 | a0002c0002t0002g0034 a0002c0002t0002g0035 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.12+20T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 2/12 | chr12 | 88026931 | |||||||
| chr12:88027152 | C | T | 1 | a0001c0001t0001g0049 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-108-82G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 1/12 | chr12 | 88027152 | |||||||
| chr12:88027262 | A | G | 1 | a0004c0005t0001g0048 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-108-192T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 1/12 | chr12 | 88027262 | |||||||
| chr12:88027285 | C | A | 3 | a0002c0002t0001g0164 a0002c0002t0001g0165 a0002c0003t0001g0166 |
3 | HG02257.hp2 HG03041.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-108-215G>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 1/12 | chr12 | 88027285 | |||||||
| chr12:88027457 | C | T | 1 | a0002c0002t0001g0174 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-108-387G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 1/12 | chr12 | 88027457 | |||||||
| chr12:88027488 | C | A | 1 | a0001c0001t0001g0167 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-108-418G>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 1/12 | chr12 | 88027488 | |||||||
| chr12:88027718 | G | A | 4 | a0002c0002t0001g0028 a0002c0002t0001g0041 a0002c0002t0001g0168 others(1): Show |
5 | NA18949.hp1 NA19058.hp1 NA19075.hp2 others(2): Show |
intron_variant | MODIFIER | c.-108-648C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 1/12 | chr12 | 88027718 | |||||||
| chr12:88027759 | T | C | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(172): Show |
229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.-108-689A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 1/12 | chr12 | 88027759 | |||||||
| chr12:88027764 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-108-694T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 1/12 | chr12 | 88027764 | |||||||
| chr12:88027812 | A | G | 3 | a0002c0002t0003g0044 a0002c0002t0003g0045 a0002c0002t0003g0046 |
3 | HG00639.hp1 HG03471.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-108-742T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 1/12 | chr12 | 88027812 | |||||||
| chr12:88027969 | T | C | 6 | a0001c0001t0001g0029 a0001c0001t0001g0170 a0001c0001t0001g0171 others(3): Show |
7 | NA18950.hp1 NA18979.hp1 NA19002.hp2 others(4): Show |
intron_variant | MODIFIER | c.-108-899A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 1/12 | chr12 | 88027969 | |||||||
| chr12:88028179 | C | G | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(172): Show |
229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.-108-1109G>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 1/12 | chr12 | 88028179 | |||||||
| chr12:88028206 | G | A | 1 | a0002c0002t0001g0203 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-109+1134C>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 1/12 | chr12 | 88028206 | |||||||
| chr12:88028377 | T | C | 4 | a0005c0006t0001g0204 a0005c0006t0001g0205 a0005c0006t0001g0206 others(1): Show |
4 | HG01884.hp2 HG02647.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-109+963A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 1/12 | chr12 | 88028377 | |||||||
| chr12:88028605 | A | T | 1 | a0001c0001t0001g0043 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-109+735T>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 1/12 | chr12 | 88028605 | |||||||
| chr12:88028735 | C | A | 1 | a0001c0001t0001g0208 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-109+605G>T | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 1/12 | chr12 | 88028735 | |||||||
| chr12:88028760 | T | G | 1 | a0001c0001t0001g0209 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-109+580A>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 1/12 | chr12 | 88028760 | |||||||
| chr12:88028998 | T | C | 1 | a0001c0001t0001g0210 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-109+342A>G | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 1/12 | chr12 | 88028998 | |||||||
| chr12:88029149 | G | GT | 5 | a0001c0001t0001g0012 a0001c0001t0001g0038 a0001c0001t0001g0039 others(2): Show |
6 | HG01175.hp1 HG02622.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-109+190dupA | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 1/12 | chr12 | 88029149 | |||||||
| chr12:88029220 | A | G | 2 | a0001c0001t0001g0036 a0004c0005t0001g0037 |
2 | HG00741.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.-109+120T>C | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 1/12 | chr12 | 88029220 | |||||||
| chr12:88029299 | C | T | 2 | a0002c0002t0002g0034 a0002c0002t0002g0035 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-109+41G>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 1/12 | chr12 | 88029299 | |||||||
| chr12:88029300 | G | T | 1 | a0001c0001t0001g0033 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-109+40C>A | C12orf50 | ENSG00000165805.10 | transcript | ENST00000298699.7 | protein_coding | 1/12 | chr12 | 88029300 |