Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55749 |
| ensemblid | ENSG00000060339.14 |
| hgncid | 24236 |
| symbol | CCAR1 |
| name | cell division cycle and apoptosis regulator 1 |
| refseq_nuc | NM_018237.4 |
| refseq_prot | NP_060707.2 |
| ensembl_nuc | ENST00000265872.11 |
| ensembl_prot | ENSP00000265872.6 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 68721239 |
| end | 68792377 |
| strand | + |
| ver | v1.2 |
| region | chr10:68721239-68792377 |
| region5000 | chr10:68716239-68797377 |
| regionname0 | CCAR1_chr10_68721239_68792377 |
| regionname5000 | CCAR1_chr10_68716239_68797377 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1150 | 357 | 82 | 60 | 162 | 14 | 37 | 128 | CCAR1_chr10_68716239_68797377 | CCAR1 | MAQFG others(1145): Show |
chr10 | 68716239 | 68797377 |
| a0002 | 0/0 | 1150 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | MAQFG others(1145): Show |
chr10 | 68716239 | 68797377 |
| a0003 | 0/0 | 1150 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | MAQFG others(1145): Show |
chr10 | 68716239 | 68797377 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 3450 | 238 | 50 | 49 | 102 | 9 | 27 | CCAR1_chr10_68716239_68797377 | CCAR1 | ATGGC others(3445): Show |
chr10 | 68716239 | 68797377 | ||
| a0001c0002 | 1/0 | 3450 | 70 | 10 | 3 | 48 | 2 | 6 | CCAR1_chr10_68716239_68797377 | CCAR1 | ATGGC others(3445): Show |
chr10 | 68716239 | 68797377 | ||
| a0001c0003 | 0/0 | 3450 | 37 | 21 | 5 | 10 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | ATGGC others(3445): Show |
chr10 | 68716239 | 68797377 | ||
| a0001c0004 | 0/0 | 3450 | 8 | 0 | 2 | 0 | 3 | 3 | CCAR1_chr10_68716239_68797377 | CCAR1 | ATGGC others(3445): Show |
chr10 | 68716239 | 68797377 | ||
| a0001c0007 | 0/0 | 3450 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | ATGGC others(3445): Show |
chr10 | 68716239 | 68797377 | ||
| a0001c0008 | 0/0 | 3450 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | ATGGC others(3445): Show |
chr10 | 68716239 | 68797377 | ||
| a0001c0009 | 0/0 | 3450 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | ATGGC others(3445): Show |
chr10 | 68716239 | 68797377 | ||
| a0001c0010 | 0/0 | 3450 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | ATGGC others(3445): Show |
chr10 | 68716239 | 68797377 | ||
| a0002c0005 | 0/0 | 3450 | 2 | 2 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | ATGGC others(3445): Show |
chr10 | 68716239 | 68797377 | ||
| a0003c0006 | 0/0 | 3450 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | ATGGC others(3445): Show |
chr10 | 68716239 | 68797377 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4658 | 219 | 46 | 45 | 93 | 8 | 26 | CCAR1_chr10_68716239_68797377 | CCAR1 | GACGG others(4653): Show |
chr10 | 68716239 | 68797377 |
| a0001c0001t0003 | 0/0 | 4658 | 8 | 0 | 0 | 8 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | GACGG others(4653): Show |
chr10 | 68716239 | 68797377 |
| a0001c0001t0005 | 0/0 | 4658 | 3 | 0 | 2 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | GACGG others(4653): Show |
chr10 | 68716239 | 68797377 |
| a0001c0001t0007 | 0/0 | 4658 | 2 | 2 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | GACGG others(4653): Show |
chr10 | 68716239 | 68797377 |
| a0001c0001t0009 | 0/0 | 4658 | 2 | 0 | 1 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | GACGG others(4653): Show |
chr10 | 68716239 | 68797377 |
| a0001c0001t0010 | 0/0 | 4658 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | GACGG others(4653): Show |
chr10 | 68716239 | 68797377 |
| a0001c0001t0015 | 0/0 | 4658 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | GACGG others(4653): Show |
chr10 | 68716239 | 68797377 |
| a0001c0001t0016 | 0/0 | 4658 | 1 | 0 | 0 | 0 | 1 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | GACGG others(4653): Show |
chr10 | 68716239 | 68797377 |
| a0001c0001t0018 | 0/0 | 4658 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | GACGG others(4653): Show |
chr10 | 68716239 | 68797377 |
| a0001c0002t0001 | 1/0 | 4658 | 69 | 10 | 3 | 47 | 2 | 6 | CCAR1_chr10_68716239_68797377 | CCAR1 | GACGG others(4653): Show |
chr10 | 68716239 | 68797377 |
| a0001c0002t0011 | 0/0 | 4658 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | GACGG others(4653): Show |
chr10 | 68716239 | 68797377 |
| a0001c0003t0001 | 0/0 | 4658 | 3 | 3 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | GACGG others(4653): Show |
chr10 | 68716239 | 68797377 |
| a0001c0003t0002 | 0/0 | 4658 | 27 | 12 | 5 | 9 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | GACGG others(4653): Show |
chr10 | 68716239 | 68797377 |
| a0001c0003t0004 | 0/0 | 4656 | 5 | 5 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | GACGG others(4651): Show |
chr10 | 68716239 | 68797377 |
| a0001c0003t0014 | 0/0 | 4656 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | GACGG others(4651): Show |
chr10 | 68716239 | 68797377 |
| a0001c0003t0017 | 0/0 | 4658 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | GACGG others(4653): Show |
chr10 | 68716239 | 68797377 |
| a0001c0004t0001 | 0/0 | 4658 | 5 | 0 | 0 | 0 | 2 | 3 | CCAR1_chr10_68716239_68797377 | CCAR1 | GACGG others(4653): Show |
chr10 | 68716239 | 68797377 |
| a0001c0004t0006 | 0/0 | 4658 | 2 | 0 | 2 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | GACGG others(4653): Show |
chr10 | 68716239 | 68797377 |
| a0001c0004t0012 | 0/0 | 4658 | 1 | 0 | 0 | 0 | 1 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | GACGG others(4653): Show |
chr10 | 68716239 | 68797377 |
| a0001c0007t0001 | 0/0 | 4658 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | GACGG others(4653): Show |
chr10 | 68716239 | 68797377 |
| a0001c0008t0001 | 0/0 | 4658 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | GACGG others(4653): Show |
chr10 | 68716239 | 68797377 |
| a0001c0009t0001 | 0/0 | 4658 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | GACGG others(4653): Show |
chr10 | 68716239 | 68797377 |
| a0001c0010t0013 | 0/0 | 4658 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | GACGG others(4653): Show |
chr10 | 68716239 | 68797377 |
| a0002c0005t0008 | 0/0 | 4658 | 2 | 2 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | GACGG others(4653): Show |
chr10 | 68716239 | 68797377 |
| a0003c0006t0001 | 0/0 | 4658 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | GACGG others(4653): Show |
chr10 | 68716239 | 68797377 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0230 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0003g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0005g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0005g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0005g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0007g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0007g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0009g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0009g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0010g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0015g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0016g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0001t0018g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0090 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0002t0011g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0003t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0003t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0003t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0003t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0003t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0003t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0003t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0003t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0003t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0003t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0003t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0003t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0003t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0003t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0003t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0003t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0003t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0003t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0003t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0003t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0003t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0003t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0003t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0003t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0003t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0003t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0003t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0003t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0003t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0003t0002g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0003t0004g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0003t0004g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0003t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0003t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0003t0004g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0003t0014g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0003t0017g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0004t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0004t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0004t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0004t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0004t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0004t0006g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0004t0006g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0004t0012g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0007t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0008t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0009t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0001c0010t0013g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0002c0005t0008g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0002c0005t0008g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| a0003c0006t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0327 | EUR | GBR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0195 | EUR | GBR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG00140 | hp1 | a0001 | c0004 | t0012 | g0270 | EUR | GBR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0101 | EUR | GBR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0246 | EUR | FIN | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0325 | EUR | FIN | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | CHS | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0150 | EAS | CHS | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | CHS | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | CHS | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | CHS | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG00639 | hp1 | a0001 | c0003 | t0002 | g0352 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG00639 | hp2 | a0001 | c0003 | t0002 | g0047 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0104 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0323 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0329 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG01069 | hp2 | a0001 | c0001 | t0005 | g0225 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG01081 | hp1 | a0001 | c0003 | t0002 | g0065 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0346 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG01168 | hp1 | a0001 | c0010 | t0013 | g0267 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0349 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0345 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0103 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0096 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG01256 | hp2 | a0001 | c0004 | t0006 | g0269 | AMR | CLM | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG01257 | hp1 | a0001 | c0001 | t0015 | g0029 | AMR | CLM | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | CLM | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG01346 | hp1 | a0001 | c0004 | t0006 | g0268 | AMR | CLM | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG01346 | hp2 | a0001 | c0001 | t0009 | g0013 | AMR | CLM | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | CLM | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0331 | AMR | CLM | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG01433 | hp2 | a0001 | c0003 | t0002 | g0056 | AMR | CLM | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG01496 | hp1 | a0001 | c0001 | t0005 | g0240 | AMR | CLM | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG01496 | hp2 | a0001 | c0003 | t0002 | g0048 | AMR | CLM | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG01515 | hp1 | a0001 | c0004 | t0001 | g0265 | EUR | IBS | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0244 | EUR | IBS | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG01517 | hp1 | a0001 | c0004 | t0001 | g0266 | EUR | IBS | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0170 | EUR | IBS | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG01891 | hp2 | a0002 | c0005 | t0008 | g0050 | AFR | ACB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0289 | AMR | PEL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | KHV | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02015 | hp2 | a0001 | c0003 | t0002 | g0052 | EAS | KHV | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0136 | EAS | KHV | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | KHV | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | ACB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0091 | AFR | ACB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0160 | EAS | KHV | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0132 | EAS | KHV | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02074 | hp1 | a0001 | c0003 | t0002 | g0055 | EAS | KHV | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | KHV | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0158 | EAS | KHV | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | KHV | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02083 | hp2 | a0001 | c0003 | t0002 | g0053 | EAS | KHV | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0135 | EAS | KHV | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | KHV | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | KHV | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02135 | hp2 | a0001 | c0008 | t0001 | g0284 | EAS | KHV | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0106 | AFR | ACB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0111 | EAS | CDX | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | CDX | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02257 | hp1 | a0001 | c0003 | t0002 | g0058 | AFR | ACB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0348 | AFR | ACB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02280 | hp1 | a0001 | c0001 | t0007 | g0351 | AFR | ACB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0347 | AMR | PEL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0336 | AMR | PEL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02451 | hp1 | a0002 | c0005 | t0008 | g0049 | AFR | ACB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | ACB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02572 | hp1 | a0001 | c0003 | t0002 | g0059 | AFR | GWD | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02572 | hp2 | a0001 | c0003 | t0001 | g0339 | AFR | GWD | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0156 | SAS | PJL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02615 | hp1 | a0001 | c0001 | t0010 | g0353 | AFR | GWD | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | GWD | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | GWD | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02647 | hp1 | a0001 | c0003 | t0002 | g0075 | AFR | GWD | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02647 | hp2 | a0001 | c0003 | t0004 | g0068 | AFR | GWD | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02683 | hp2 | a0001 | c0003 | t0002 | g0054 | SAS | PJL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02698 | hp2 | a0003 | c0006 | t0001 | g0290 | SAS | PJL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02717 | hp1 | a0001 | c0001 | t0018 | g0088 | AFR | GWD | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | GWD | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02809 | hp1 | a0001 | c0003 | t0002 | g0076 | AFR | GWD | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0107 | AFR | GWD | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0093 | AFR | GWD | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02886 | hp1 | a0001 | c0003 | t0004 | g0072 | AFR | GWD | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02896 | hp1 | a0001 | c0003 | t0002 | g0066 | AFR | GWD | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | GWD | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02922 | hp1 | a0001 | c0003 | t0004 | g0067 | AFR | ESN | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02922 | hp2 | a0001 | c0007 | t0001 | g0280 | AFR | ESN | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0092 | AFR | ESN | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | ESN | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0108 | AFR | ESN | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02970 | hp2 | a0001 | c0003 | t0002 | g0073 | AFR | ESN | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ESN | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | ESN | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0328 | SAS | PJL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG03098 | hp1 | a0001 | c0003 | t0014 | g0069 | AFR | MSL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | MSL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG03130 | hp1 | a0001 | c0003 | t0002 | g0063 | AFR | ESN | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | ESN | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | ESN | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0094 | AFR | ESN | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | ESN | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | MSL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0095 | AFR | MSL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0305 | AFR | MSL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0341 | AFR | MSL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0123 | SAS | PJL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG03491 | hp2 | a0001 | c0004 | t0001 | g0271 | SAS | PJL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0139 | SAS | PJL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ESN | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | ESN | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | GWD | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG03540 | hp2 | a0001 | c0003 | t0002 | g0077 | AFR | GWD | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0340 | SAS | PJL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0134 | SAS | PJL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0321 | SAS | PJL | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0124 | SAS | STU | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0333 | SAS | STU | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0245 | SAS | BEB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0105 | SAS | BEB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | BEB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0282 | SAS | BEB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | STU | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG04115 | hp2 | a0001 | c0001 | t0009 | g0261 | SAS | STU | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | BEB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0310 | SAS | BEB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG04199 | hp1 | a0001 | c0004 | t0001 | g0322 | SAS | STU | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0277 | SAS | STU | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG04204 | hp1 | a0001 | c0004 | t0001 | g0272 | SAS | STU | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | STU | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0292 | SAS | STU | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | STU | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | YRI | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | YRI | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18612 | hp1 | a0001 | c0001 | t0005 | g0186 | EAS | CHB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | CHB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | CHB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CHB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | YRI | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | YRI | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18940 | hp2 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18946 | hp1 | a0001 | c0002 | t0001 | g0126 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18947 | hp1 | a0001 | c0003 | t0002 | g0080 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0161 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0131 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18949 | hp1 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0154 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0140 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0153 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18972 | hp2 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0127 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0122 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18985 | hp2 | a0001 | c0003 | t0017 | g0046 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0157 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18993 | hp2 | a0001 | c0003 | t0002 | g0079 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0143 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19001 | hp1 | a0001 | c0002 | t0001 | g0152 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0151 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19002 | hp2 | a0001 | c0003 | t0002 | g0078 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19005 | hp2 | a0001 | c0003 | t0002 | g0057 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0130 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0144 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0159 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19030 | hp1 | a0001 | c0003 | t0001 | g0338 | AFR | LWK | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19030 | hp2 | a0001 | c0003 | t0002 | g0062 | AFR | LWK | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | LWK | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19043 | hp2 | a0001 | c0003 | t0004 | g0071 | AFR | LWK | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0121 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0148 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19058 | hp1 | a0001 | c0002 | t0001 | g0147 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19064 | hp2 | a0001 | c0009 | t0001 | g0181 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0142 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19067 | hp1 | a0001 | c0003 | t0002 | g0060 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0155 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19079 | hp1 | a0001 | c0003 | t0002 | g0051 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0113 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19088 | hp1 | a0001 | c0002 | t0011 | g0146 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19089 | hp1 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19240 | hp1 | a0001 | c0003 | t0001 | g0337 | AFR | YRI | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0344 | AFR | YRI | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA20129 | hp1 | a0001 | c0003 | t0002 | g0061 | AFR | ASW | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ASW | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA20752 | hp1 | a0001 | c0001 | t0016 | g0028 | EUR | TSI | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0279 | EUR | TSI | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0190 | EUR | TSI | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0102 | EUR | TSI | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | GIH | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0293 | SAS | GIH | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0304 | AMR | CLM | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0006 | AFR | ACB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | ACB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02486 | hp2 | a0001 | c0003 | t0002 | g0074 | AFR | ACB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02559 | hp1 | a0001 | c0003 | t0004 | g0070 | AFR | ACB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG02559 | hp2 | a0001 | c0001 | t0007 | g0350 | AFR | ACB | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | USA | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | USA | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | USA | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | USA | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA21309 | hp1 | a0001 | c0003 | t0002 | g0064 | AFR | LWK | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0162 | AFR | LWK | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0230 | REF | REF | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0090 | REF | REF | CCAR1_chr10_68716239_68797377 | CCAR1 | chr10 | 68716239 | 68797377 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:68737865 | G | C | 1 | a0003 | 1 | HG02698.hp2 | missense_variant | MODERATE | c.267G>C | p.Gln89His | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/25 | 361/4658 | 267/3453 | 89/1150 | chr10 | 68737865 | |||
| chr10:68787948 | G | A | 1 | a0002 | 2 | HG01891.hp2 HG02451.hp1 |
missense_variant | MODERATE | c.2902G>A | p.Val968Ile | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 22/25 | 2996/4658 | 2902/3453 | 968/1150 | chr10 | 68787948 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:68742435 | A | T | 1 | a0001c0010 | 1 | HG01168.hp1 | synonymous_variant | LOW | c.384A>T | p.Ile128Ile | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/25 | 478/4658 | 384/3453 | 128/1150 | chr10 | 68742435 | |||
| chr10:68742522 | A | G | 1 | a0001c0009 | 1 | NA19064.hp2 | synonymous_variant | LOW | c.471A>G | p.Leu157Leu | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/25 | 565/4658 | 471/3453 | 157/1150 | chr10 | 68742522 | |||
| chr10:68742531 | G | A | 9 | a0001c0001 a0001c0003 a0001c0004 others(6): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
synonymous_variant | LOW | c.480G>A | p.Thr160Thr | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/25 | 574/4658 | 480/3453 | 160/1150 | chr10 | 68742531 | |||
| chr10:68749182 | G | A | 1 | a0001c0007 | 1 | HG02922.hp2 | synonymous_variant | LOW | c.873G>A | p.Pro291Pro | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 9/25 | 967/4658 | 873/3453 | 291/1150 | chr10 | 68749182 | |||
| chr10:68753927 | A | G | 2 | a0001c0003 a0002c0005 |
39 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(36): Show |
synonymous_variant | LOW | c.1194A>G | p.Gln398Gln | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 11/25 | 1288/4658 | 1194/3453 | 398/1150 | chr10 | 68753927 | |||
| chr10:68788318 | A | G | 1 | a0001c0008 | 1 | HG02135.hp2 | synonymous_variant | LOW | c.3177A>G | p.Glu1059Glu | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 23/25 | 3271/4658 | 3177/3453 | 1059/1150 | chr10 | 68788318 | |||
| chr10:68789822 | G | A | 2 | a0001c0004 a0001c0010 |
9 | HG00140.hp1 HG01168.hp1 HG01256.hp2 others(6): Show |
synonymous_variant | LOW | c.3300G>A | p.Ser1100Ser | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 24/25 | 3394/4658 | 3300/3453 | 1100/1150 | chr10 | 68789822 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:68721263 | T | G | 1 | a0001c0001t0010 | 1 | HG02615.hp1 | 5_prime_UTR_variant | MODIFIER | c.-70T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 1/25 | 1242 | chr10 | 68721263 | ||||||
| chr10:68721266 | G | C | 1 | a0001c0002t0011 | 1 | NA19088.hp1 | 5_prime_UTR_variant | MODIFIER | c.-67G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 1/25 | 1239 | chr10 | 68721266 | ||||||
| chr10:68721278 | C | T | 1 | a0001c0001t0018 | 1 | HG02717.hp1 | 5_prime_UTR_variant | MODIFIER | c.-55C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 1/25 | 1227 | chr10 | 68721278 | ||||||
| chr10:68722481 | G | A | 3 | a0001c0004t0006 a0001c0004t0012 a0001c0010t0013 |
4 | HG00140.hp1 HG01168.hp1 HG01256.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-24G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/25 | 24 | chr10 | 68722481 | ||||||
| chr10:68791291 | T | C | 1 | a0001c0001t0007 | 2 | HG02280.hp1 HG02559.hp2 |
3_prime_UTR_variant | MODIFIER | c.*25T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 25/25 | 25 | chr10 | 68791291 | ||||||
| chr10:68791475 | T | C | 1 | a0002c0005t0008 | 2 | HG01891.hp2 HG02451.hp1 |
3_prime_UTR_variant | MODIFIER | c.*209T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 25/25 | 209 | chr10 | 68791475 | ||||||
| chr10:68791520 | T | C | 1 | a0001c0003t0014 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*254T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 25/25 | 254 | chr10 | 68791520 | ||||||
| chr10:68791596 | C | G | 5 | a0001c0003t0002 a0001c0003t0004 a0001c0003t0014 others(2): Show |
36 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*330C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 25/25 | 330 | chr10 | 68791596 | ||||||
| chr10:68791663 | CAA | C | 2 | a0001c0003t0004 a0001c0003t0014 |
6 | HG02559.hp1 HG02647.hp2 HG02886.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*400_*401delAA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 25/25 | 400 | INFO_REALIGN_3_PRIME | chr10 | 68791663 | |||||
| chr10:68791836 | C | T | 1 | a0001c0001t0016 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*570C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 25/25 | 570 | chr10 | 68791836 | ||||||
| chr10:68791898 | C | T | 5 | a0001c0003t0002 a0001c0003t0004 a0001c0003t0014 others(2): Show |
36 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*632C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 25/25 | 632 | chr10 | 68791898 | ||||||
| chr10:68791985 | C | T | 1 | a0001c0001t0009 | 2 | HG01346.hp2 HG04115.hp2 |
3_prime_UTR_variant | MODIFIER | c.*719C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 25/25 | 719 | chr10 | 68791985 | ||||||
| chr10:68791986 | G | A | 1 | a0001c0001t0003 | 8 | NA18939.hp2 NA18941.hp1 NA18954.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*720G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 25/25 | 720 | chr10 | 68791986 | ||||||
| chr10:68792017 | C | T | 1 | a0001c0001t0015 | 1 | HG01257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*751C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 25/25 | 751 | chr10 | 68792017 | ||||||
| chr10:68792133 | A | G | 1 | a0001c0001t0005 | 3 | HG01069.hp2 HG01496.hp1 NA18612.hp1 |
3_prime_UTR_variant | MODIFIER | c.*867A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 25/25 | 867 | chr10 | 68792133 | ||||||
| chr10:68792144 | G | A | 2 | a0001c0004t0012 a0001c0010t0013 |
2 | HG00140.hp1 HG01168.hp1 |
3_prime_UTR_variant | MODIFIER | c.*878G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 25/25 | 878 | chr10 | 68792144 | ||||||
| chr10:68792196 | A | C | 1 | a0001c0003t0017 | 1 | NA18985.hp2 | 3_prime_UTR_variant | MODIFIER | c.*930A>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 25/25 | 930 | chr10 | 68792196 | ||||||
| chr10:68792281 | G | A | 1 | a0001c0004t0012 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1015G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 25/25 | 1015 | chr10 | 68792281 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:68721328 | G | T | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-51+46G>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 1/24 | chr10 | 68721328 | |||||||
| chr10:68721379 | G | A | 1 | a0001c0002t0001g0006 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-51+97G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 1/24 | chr10 | 68721379 | |||||||
| chr10:68721415 | C | T | 1 | a0001c0003t0002g0352 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-51+133C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 1/24 | chr10 | 68721415 | |||||||
| chr10:68721431 | G | C | 6 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(3): Show |
6 | HG01257.hp2 HG01952.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.-51+149G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 1/24 | chr10 | 68721431 | |||||||
| chr10:68721457 | G | A | 36 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(33): Show |
37 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.-51+175G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 1/24 | chr10 | 68721457 | |||||||
| chr10:68721497 | C | G | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.-51+215C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 1/24 | chr10 | 68721497 | |||||||
| chr10:68721632 | G | A | 36 | a0001c0003t0002g0047 a0001c0003t0002g0048 a0001c0003t0002g0051 others(33): Show |
36 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.-51+350G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 1/24 | chr10 | 68721632 | |||||||
| chr10:68721680 | C | T | 2 | a0001c0001t0003g0044 a0001c0001t0003g0045 |
2 | NA18939.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.-51+398C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 1/24 | chr10 | 68721680 | |||||||
| chr10:68721681 | C | G | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.-51+399C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 1/24 | chr10 | 68721681 | |||||||
| chr10:68721696 | G | T | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-51+414G>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 1/24 | chr10 | 68721696 | |||||||
| chr10:68721790 | C | T | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(192): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.-51+508C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 1/24 | chr10 | 68721790 | |||||||
| chr10:68721923 | C | T | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.-50-532C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 1/24 | chr10 | 68721923 | |||||||
| chr10:68722036 | T | A | 33 | a0001c0003t0002g0047 a0001c0003t0002g0048 a0001c0003t0002g0051 others(30): Show |
33 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.-50-419T>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 1/24 | chr10 | 68722036 | |||||||
| chr10:68722039 | C | A | 33 | a0001c0003t0002g0047 a0001c0003t0002g0048 a0001c0003t0002g0051 others(30): Show |
33 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.-50-416C>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 1/24 | chr10 | 68722039 | |||||||
| chr10:68722094 | A | T | 1 | a0001c0002t0001g0162 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-50-361A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 1/24 | chr10 | 68722094 | |||||||
| chr10:68722396 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-50-59T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 1/24 | chr10 | 68722396 | |||||||
| chr10:68722612 | G | T | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.73+35G>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68722612 | |||||||
| chr10:68722619 | A | T | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.73+42A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68722619 | |||||||
| chr10:68722647 | G | C | 7 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(4): Show |
7 | HG01109.hp1 HG02717.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.73+70G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68722647 | |||||||
| chr10:68722661 | A | G | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.73+84A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68722661 | |||||||
| chr10:68722772 | A | G | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.73+195A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68722772 | |||||||
| chr10:68722936 | A | C | 36 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(33): Show |
37 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.73+359A>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68722936 | |||||||
| chr10:68722980 | T | C | 43 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(40): Show |
44 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(41): Show |
intron_variant | MODIFIER | c.73+403T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68722980 | |||||||
| chr10:68723043 | C | G | 54 | a0001c0002t0001g0006 a0001c0002t0001g0109 a0001c0002t0001g0110 others(51): Show |
54 | HG00544.hp1 HG02040.hp1 HG02056.hp1 others(51): Show |
intron_variant | MODIFIER | c.73+466C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68723043 | |||||||
| chr10:68723057 | T | C | 6 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(3): Show |
6 | HG01109.hp1 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.73+480T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68723057 | |||||||
| chr10:68723078 | T | C | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.73+501T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68723078 | |||||||
| chr10:68723118 | A | G | 1 | a0001c0001t0001g0349 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.73+541A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68723118 | |||||||
| chr10:68723185 | A | G | 5 | a0001c0003t0002g0073 a0001c0003t0002g0074 a0001c0003t0002g0075 others(2): Show |
5 | HG02486.hp2 HG02647.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.73+608A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68723185 | |||||||
| chr10:68723223 | G | A | 2 | a0001c0001t0001g0081 a0001c0001t0001g0089 |
2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.73+646G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68723223 | |||||||
| chr10:68723288 | A | AT | 9 | a0001c0001t0001g0087 a0001c0001t0001g0342 a0001c0001t0001g0343 others(6): Show |
9 | HG01109.hp2 HG01175.hp2 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.73+725dupT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68723288 | ||||||
| chr10:68723288 | A | ATT | 71 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(68): Show |
71 | HG00140.hp2 HG00544.hp1 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.73+724_73+725dupTT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68723288 | ||||||
| chr10:68723317 | G | A | 60 | a0001c0002t0001g0006 a0001c0002t0001g0091 a0001c0002t0001g0092 others(57): Show |
60 | HG00544.hp1 HG02040.hp1 HG02055.hp2 others(57): Show |
intron_variant | MODIFIER | c.73+740G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68723317 | |||||||
| chr10:68723380 | C | T | 3 | a0001c0003t0002g0075 a0001c0003t0002g0076 a0001c0003t0002g0077 |
3 | HG02647.hp1 HG02809.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.73+803C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68723380 | |||||||
| chr10:68723389 | G | A | 1 | a0001c0002t0001g0096 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.73+812G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68723389 | |||||||
| chr10:68723413 | G | A | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(277): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.73+836G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68723413 | |||||||
| chr10:68723425 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.73+848G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68723425 | |||||||
| chr10:68723571 | G | A | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.73+994G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68723571 | |||||||
| chr10:68723581 | A | G | 2 | a0001c0001t0001g0341 a0001c0001t0001g0348 |
2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.73+1004A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68723581 | |||||||
| chr10:68723584 | C | T | 1 | a0001c0002t0001g0161 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.73+1007C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68723584 | |||||||
| chr10:68723586 | T | C | 2 | a0001c0001t0001g0341 a0001c0001t0001g0348 |
2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.73+1009T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68723586 | |||||||
| chr10:68723624 | A | G | 1 | a0001c0001t0001g0340 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.73+1047A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68723624 | |||||||
| chr10:68723658 | C | T | 3 | a0001c0003t0001g0337 a0001c0003t0001g0338 a0001c0003t0001g0339 |
3 | HG02572.hp2 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.73+1081C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68723658 | |||||||
| chr10:68723683 | C | T | 34 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(31): Show |
34 | HG00741.hp1 HG01123.hp2 HG01256.hp1 others(31): Show |
intron_variant | MODIFIER | c.73+1106C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68723683 | |||||||
| chr10:68723704 | C | T | 308 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(305): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.73+1127C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68723704 | |||||||
| chr10:68723758 | G | T | 1 | a0001c0001t0001g0336 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.73+1181G>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68723758 | |||||||
| chr10:68723853 | GA | G | 320 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(317): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.73+1289delA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68723853 | ||||||
| chr10:68723867 | G | A | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.73+1290G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68723867 | |||||||
| chr10:68723988 | GTC | G | 4 | a0001c0002t0001g0111 a0001c0002t0001g0112 a0001c0002t0001g0113 others(1): Show |
4 | HG02165.hp1 NA18940.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.73+1415_73+1416del others(2): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68723988 | ||||||
| chr10:68723990 | C | G | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.73+1413C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68723990 | |||||||
| chr10:68724049 | T | C | 1 | a0001c0002t0001g0096 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.73+1472T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68724049 | |||||||
| chr10:68724061 | A | G | 311 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(308): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.73+1484A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68724061 | |||||||
| chr10:68724081 | G | C | 347 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(344): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.73+1504G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68724081 | |||||||
| chr10:68724151 | T | C | 68 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(65): Show |
68 | HG00544.hp1 HG01243.hp1 HG02040.hp1 others(65): Show |
intron_variant | MODIFIER | c.73+1574T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68724151 | |||||||
| chr10:68724160 | GA | G | 311 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(308): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.73+1595delA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68724160 | ||||||
| chr10:68724435 | A | T | 66 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(63): Show |
66 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.73+1858A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68724435 | |||||||
| chr10:68724609 | T | C | 68 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(65): Show |
68 | HG00544.hp1 HG01243.hp1 HG02040.hp1 others(65): Show |
intron_variant | MODIFIER | c.73+2032T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68724609 | |||||||
| chr10:68724755 | A | G | 3 | a0001c0002t0001g0106 a0001c0002t0001g0107 a0001c0002t0001g0108 |
3 | HG02145.hp1 HG02818.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.73+2178A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68724755 | |||||||
| chr10:68724832 | A | G | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.73+2255A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68724832 | |||||||
| chr10:68724855 | G | C | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG01106.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.73+2278G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68724855 | |||||||
| chr10:68724988 | G | A | 311 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(308): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.73+2411G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68724988 | |||||||
| chr10:68724989 | G | T | 311 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(308): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.73+2412G>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68724989 | |||||||
| chr10:68725099 | G | A | 36 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(33): Show |
37 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.73+2522G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68725099 | |||||||
| chr10:68725269 | G | C | 1 | a0001c0001t0001g0087 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.73+2692G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68725269 | |||||||
| chr10:68725292 | C | T | 1 | a0001c0001t0001g0042 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.73+2715C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68725292 | |||||||
| chr10:68725315 | T | C | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.73+2738T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68725315 | |||||||
| chr10:68725320 | C | T | 1 | a0001c0001t0001g0281 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.73+2743C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68725320 | |||||||
| chr10:68725325 | G | A | 1 | a0001c0001t0001g0007 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.73+2748G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68725325 | |||||||
| chr10:68725397 | C | CA | 190 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(187): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.73+2828dupA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68725397 | ||||||
| chr10:68725430 | C | T | 1 | a0001c0001t0001g0335 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.73+2853C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68725430 | |||||||
| chr10:68725744 | C | T | 23 | a0001c0003t0002g0047 a0001c0003t0002g0048 a0001c0003t0002g0051 others(20): Show |
23 | HG00639.hp2 HG01433.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.73+3167C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68725744 | |||||||
| chr10:68725755 | T | G | 1 | a0001c0001t0001g0014 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.73+3178T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68725755 | |||||||
| chr10:68725945 | A | C | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.73+3368A>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68725945 | |||||||
| chr10:68725954 | A | C | 2 | a0001c0003t0004g0071 a0001c0003t0004g0072 |
2 | HG02886.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.73+3377A>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68725954 | |||||||
| chr10:68726113 | T | TA | 16 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0167 others(13): Show |
16 | HG00423.hp2 HG01361.hp2 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.73+3556dupA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68726113 | ||||||
| chr10:68726129 | A | G | 1 | a0001c0002t0001g0110 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.73+3552A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68726129 | |||||||
| chr10:68726130 | A | G | 1 | a0001c0003t0004g0070 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.73+3553A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68726130 | |||||||
| chr10:68726157 | A | AT | 307 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(304): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.73+3592dupT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68726157 | ||||||
| chr10:68726211 | G | T | 1 | a0001c0002t0001g0160 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.73+3634G>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68726211 | |||||||
| chr10:68726216 | A | G | 2 | a0001c0001t0001g0081 a0001c0001t0001g0089 |
2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.73+3639A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68726216 | |||||||
| chr10:68726456 | C | T | 1 | a0001c0001t0001g0279 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.73+3879C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68726456 | |||||||
| chr10:68726558 | A | G | 1 | a0001c0001t0018g0088 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.73+3981A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68726558 | |||||||
| chr10:68726568 | T | G | 108 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(105): Show |
113 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.73+3991T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68726568 | |||||||
| chr10:68726593 | A | G | 3 | a0001c0001t0007g0350 a0001c0001t0007g0351 a0001c0001t0010g0353 |
3 | HG02280.hp1 HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.73+4016A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68726593 | |||||||
| chr10:68726687 | CAT | C | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 |
3 | HG02056.hp2 NA19007.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.73+4112_73+4113del others(2): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68726687 | ||||||
| chr10:68726786 | A | C | 9 | a0001c0003t0002g0064 a0001c0003t0002g0065 a0001c0003t0002g0066 others(6): Show |
9 | HG01081.hp1 HG02559.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.73+4209A>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68726786 | |||||||
| chr10:68726793 | C | A | 36 | a0001c0003t0002g0047 a0001c0003t0002g0048 a0001c0003t0002g0051 others(33): Show |
36 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.73+4216C>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68726793 | |||||||
| chr10:68726825 | G | A | 36 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(33): Show |
37 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.73+4248G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68726825 | |||||||
| chr10:68726846 | A | G | 1 | a0001c0001t0003g0041 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.73+4269A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68726846 | |||||||
| chr10:68726853 | G | A | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.73+4276G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68726853 | |||||||
| chr10:68726853 | G | C | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.73+4276G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68726853 | |||||||
| chr10:68727062 | A | AT | 6 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(3): Show |
6 | HG02145.hp2 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.73+4496dupT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68727062 | ||||||
| chr10:68727073 | T | G | 2 | a0001c0001t0001g0175 a0001c0001t0010g0353 |
2 | HG01361.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.73+4496T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68727073 | |||||||
| chr10:68727074 | G | GT | 53 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0037 others(50): Show |
54 | HG00621.hp1 HG01106.hp2 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.73+4510dupT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68727074 | ||||||
| chr10:68727074 | G | T | 2 | a0001c0001t0001g0334 a0001c0001t0010g0353 |
2 | HG02074.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.73+4497G>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68727074 | |||||||
| chr10:68727131 | G | A | 34 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(31): Show |
34 | HG00741.hp1 HG01123.hp2 HG01256.hp1 others(31): Show |
intron_variant | MODIFIER | c.73+4554G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68727131 | |||||||
| chr10:68727147 | A | G | 3 | a0001c0003t0002g0061 a0001c0003t0002g0062 a0001c0003t0002g0063 |
3 | HG03130.hp1 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.73+4570A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68727147 | |||||||
| chr10:68727231 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.73+4654C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68727231 | |||||||
| chr10:68727355 | A | G | 1 | a0001c0001t0001g0264 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.73+4778A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68727355 | |||||||
| chr10:68727396 | A | G | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.73+4819A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68727396 | |||||||
| chr10:68727506 | G | A | 38 | a0001c0001t0007g0350 a0001c0001t0007g0351 a0001c0003t0002g0047 others(35): Show |
38 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.73+4929G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68727506 | |||||||
| chr10:68727605 | C | T | 36 | a0001c0003t0002g0047 a0001c0003t0002g0048 a0001c0003t0002g0051 others(33): Show |
36 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.73+5028C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68727605 | |||||||
| chr10:68727650 | A | G | 2 | a0001c0001t0001g0329 a0001c0001t0001g0333 |
2 | HG00741.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.73+5073A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68727650 | |||||||
| chr10:68727754 | A | G | 3 | a0001c0001t0007g0350 a0001c0001t0007g0351 a0001c0001t0010g0353 |
3 | HG02280.hp1 HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.73+5177A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68727754 | |||||||
| chr10:68727833 | A | G | 6 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0001g0275 others(3): Show |
6 | HG01109.hp2 HG02055.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.73+5256A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68727833 | |||||||
| chr10:68727997 | C | T | 2 | a0001c0001t0001g0327 a0001c0001t0001g0328 |
2 | HG00099.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.73+5420C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68727997 | |||||||
| chr10:68728024 | A | C | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.73+5447A>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68728024 | |||||||
| chr10:68728042 | G | T | 7 | a0001c0001t0001g0170 a0001c0001t0001g0241 a0001c0001t0001g0242 others(4): Show |
7 | HG00642.hp2 HG00738.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.73+5465G>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68728042 | |||||||
| chr10:68728184 | A | G | 1 | a0001c0001t0005g0240 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.73+5607A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68728184 | |||||||
| chr10:68728214 | T | A | 9 | a0001c0003t0002g0064 a0001c0003t0002g0065 a0001c0003t0002g0066 others(6): Show |
9 | HG01081.hp1 HG02559.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.73+5637T>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68728214 | |||||||
| chr10:68728300 | AT | A | 39 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(36): Show |
40 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.73+5735delT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68728300 | ||||||
| chr10:68728360 | T | G | 7 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(4): Show |
7 | HG01109.hp1 HG02717.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.73+5783T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68728360 | |||||||
| chr10:68728471 | G | A | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.73+5894G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68728471 | |||||||
| chr10:68728540 | G | C | 1 | a0001c0001t0001g0285 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.73+5963G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68728540 | |||||||
| chr10:68728603 | A | G | 1 | a0001c0001t0001g0239 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.73+6026A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68728603 | |||||||
| chr10:68728682 | C | T | 36 | a0001c0003t0002g0047 a0001c0003t0002g0048 a0001c0003t0002g0051 others(33): Show |
36 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.73+6105C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68728682 | |||||||
| chr10:68728866 | A | G | 1 | a0001c0001t0001g0326 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.73+6289A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68728866 | |||||||
| chr10:68728982 | G | A | 1 | a0001c0002t0001g0156 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.73+6405G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68728982 | |||||||
| chr10:68729057 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.73+6480A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68729057 | |||||||
| chr10:68729235 | G | T | 2 | a0001c0003t0002g0061 a0001c0003t0002g0063 |
2 | HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.73+6658G>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68729235 | |||||||
| chr10:68729274 | G | GT | 16 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0042 others(13): Show |
16 | HG00735.hp2 HG02293.hp2 HG02602.hp2 others(13): Show |
intron_variant | MODIFIER | c.73+6710dupT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68729274 | ||||||
| chr10:68729414 | C | T | 6 | a0001c0003t0004g0067 a0001c0003t0004g0068 a0001c0003t0004g0070 others(3): Show |
6 | HG02559.hp1 HG02647.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.73+6837C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68729414 | |||||||
| chr10:68729430 | C | T | 279 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(276): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.73+6853C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68729430 | |||||||
| chr10:68729610 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.73+7033C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68729610 | |||||||
| chr10:68729702 | TA | T | 201 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(198): Show |
206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.73+7141delA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68729702 | ||||||
| chr10:68729702 | TAA | T | 8 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0004t0001g0271 others(5): Show |
8 | HG00140.hp1 HG01168.hp1 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.73+7140_73+7141del others(2): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68729702 | ||||||
| chr10:68729784 | A | G | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.74-7092A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68729784 | |||||||
| chr10:68729820 | G | A | 4 | a0001c0001t0001g0081 a0001c0001t0001g0089 a0001c0001t0001g0287 others(1): Show |
4 | HG02074.hp2 HG02083.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.74-7056G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68729820 | |||||||
| chr10:68729889 | G | T | 2 | a0001c0001t0001g0081 a0001c0001t0001g0089 |
2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.74-6987G>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68729889 | |||||||
| chr10:68729922 | CT | C | 347 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(344): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.74-6943delT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68729922 | ||||||
| chr10:68729925 | T | C | 16 | a0001c0003t0002g0047 a0001c0003t0002g0048 a0001c0003t0002g0051 others(13): Show |
16 | HG00639.hp2 HG01433.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.74-6951T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68729925 | |||||||
| chr10:68730047 | G | C | 2 | a0001c0001t0001g0081 a0001c0001t0001g0089 |
2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.74-6829G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68730047 | |||||||
| chr10:68730199 | C | T | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.74-6677C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68730199 | |||||||
| chr10:68730262 | G | T | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.74-6614G>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68730262 | |||||||
| chr10:68730281 | A | T | 1 | a0001c0002t0001g0150 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.74-6595A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68730281 | |||||||
| chr10:68730326 | A | AAT | 16 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0177 others(13): Show |
16 | HG01106.hp2 HG01243.hp1 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.74-6531_74-6530dup others(2): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68730326 | ||||||
| chr10:68730326 | A | AATATAT | 5 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(2): Show |
5 | HG01109.hp1 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.74-6535_74-6530dup others(6): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68730326 | ||||||
| chr10:68730343 | A | T | 1 | a0001c0001t0001g0245 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.74-6533A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68730343 | |||||||
| chr10:68730347 | T | A | 1 | a0001c0002t0001g0150 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.74-6529T>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68730347 | |||||||
| chr10:68730349 | A | T | 54 | a0001c0002t0001g0006 a0001c0002t0001g0109 a0001c0002t0001g0110 others(51): Show |
54 | HG00544.hp1 HG02040.hp1 HG02056.hp1 others(51): Show |
intron_variant | MODIFIER | c.74-6527A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68730349 | |||||||
| chr10:68730414 | T | A | 1 | a0001c0001t0001g0087 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.74-6462T>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68730414 | |||||||
| chr10:68730578 | T | C | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.74-6298T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68730578 | |||||||
| chr10:68730594 | C | T | 2 | a0001c0002t0001g0148 a0001c0002t0001g0149 |
2 | NA18994.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.74-6282C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68730594 | |||||||
| chr10:68730692 | T | G | 3 | a0001c0003t0001g0337 a0001c0003t0001g0338 a0001c0003t0001g0339 |
3 | HG02572.hp2 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.74-6184T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68730692 | |||||||
| chr10:68730766 | C | T | 2 | a0001c0002t0001g0148 a0001c0002t0001g0149 |
2 | NA18994.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.74-6110C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68730766 | |||||||
| chr10:68730772 | C | T | 54 | a0001c0002t0001g0006 a0001c0002t0001g0109 a0001c0002t0001g0110 others(51): Show |
54 | HG00544.hp1 HG02040.hp1 HG02056.hp1 others(51): Show |
intron_variant | MODIFIER | c.74-6104C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68730772 | |||||||
| chr10:68730929 | G | A | 36 | a0001c0003t0002g0047 a0001c0003t0002g0048 a0001c0003t0002g0051 others(33): Show |
36 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.74-5947G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68730929 | |||||||
| chr10:68731074 | GTATC | G | 4 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(1): Show |
4 | HG02145.hp2 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.74-5798_74-5795del others(4): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68731074 | ||||||
| chr10:68731258 | T | A | 1 | a0001c0002t0001g0153 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.74-5618T>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68731258 | |||||||
| chr10:68731286 | C | T | 2 | a0001c0001t0001g0081 a0001c0001t0001g0089 |
2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.74-5590C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68731286 | |||||||
| chr10:68731354 | C | G | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.74-5522C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68731354 | |||||||
| chr10:68731425 | C | T | 1 | a0001c0001t0001g0325 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.74-5451C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68731425 | |||||||
| chr10:68731430 | A | T | 1 | a0001c0001t0001g0036 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.74-5446A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68731430 | |||||||
| chr10:68731509 | C | T | 1 | a0001c0001t0001g0234 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.74-5367C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68731509 | |||||||
| chr10:68731511 | C | G | 3 | a0001c0003t0001g0337 a0001c0003t0001g0338 a0001c0003t0001g0339 |
3 | HG02572.hp2 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.74-5365C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68731511 | |||||||
| chr10:68731559 | A | G | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.74-5317A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68731559 | |||||||
| chr10:68731591 | G | GT | 50 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0016 others(47): Show |
50 | HG00544.hp1 HG01123.hp2 HG01256.hp1 others(47): Show |
intron_variant | MODIFIER | c.74-5261dupT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68731591 | ||||||
| chr10:68731591 | G | GTT | 10 | a0001c0001t0001g0002 a0001c0001t0001g0032 a0001c0001t0001g0033 others(7): Show |
11 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.74-5262_74-5261dup others(2): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68731591 | ||||||
| chr10:68731591 | GT | G | 58 | a0001c0001t0001g0011 a0001c0001t0001g0164 a0001c0001t0001g0173 others(55): Show |
58 | HG00140.hp1 HG00639.hp2 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.74-5261delT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68731591 | ||||||
| chr10:68731591 | GTT | G | 167 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(164): Show |
172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.74-5262_74-5261del others(2): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68731591 | ||||||
| chr10:68731602 | T | G | 1 | a0001c0001t0001g0288 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.74-5274T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68731602 | |||||||
| chr10:68731683 | C | T | 1 | a0001c0004t0001g0272 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.74-5193C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68731683 | |||||||
| chr10:68731731 | C | A | 6 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(3): Show |
6 | HG01109.hp1 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.74-5145C>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68731731 | |||||||
| chr10:68732181 | T | C | 88 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(85): Show |
93 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.74-4695T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68732181 | |||||||
| chr10:68732190 | C | T | 2 | a0001c0001t0001g0217 a0001c0001t0001g0237 |
2 | HG00735.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.74-4686C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68732190 | |||||||
| chr10:68732312 | A | G | 6 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(3): Show |
6 | HG01109.hp1 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.74-4564A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68732312 | |||||||
| chr10:68732336 | T | TTTTG | 13 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(10): Show |
13 | HG01109.hp1 HG02572.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.74-4511_74-4508dup others(4): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68732336 | ||||||
| chr10:68732336 | TTTTG | T | 7 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(4): Show |
7 | HG00639.hp2 HG01496.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.74-4511_74-4508del others(4): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68732336 | ||||||
| chr10:68732348 | G | T | 1 | a0001c0002t0001g0096 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.74-4528G>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68732348 | |||||||
| chr10:68732470 | C | T | 2 | a0001c0003t0002g0057 a0001c0003t0017g0046 |
2 | NA18985.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.74-4406C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68732470 | |||||||
| chr10:68732543 | T | C | 7 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(4): Show |
7 | HG01109.hp1 HG02717.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.74-4333T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68732543 | |||||||
| chr10:68732545 | C | T | 7 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(4): Show |
7 | HG01109.hp1 HG02717.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.74-4331C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68732545 | |||||||
| chr10:68732546 | A | G | 7 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(4): Show |
7 | HG01109.hp1 HG02717.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.74-4330A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68732546 | |||||||
| chr10:68732548 | C | T | 7 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(4): Show |
7 | HG01109.hp1 HG02717.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.74-4328C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68732548 | |||||||
| chr10:68732549 | G | A | 7 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(4): Show |
7 | HG01109.hp1 HG02717.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.74-4327G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68732549 | |||||||
| chr10:68732551 | G | A | 7 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(4): Show |
7 | HG01109.hp1 HG02717.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.74-4325G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68732551 | |||||||
| chr10:68732555 | G | C | 7 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(4): Show |
7 | HG01109.hp1 HG02717.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.74-4321G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68732555 | |||||||
| chr10:68732595 | C | T | 2 | a0001c0001t0001g0081 a0001c0001t0001g0089 |
2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.74-4281C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68732595 | |||||||
| chr10:68732987 | G | T | 1 | a0001c0004t0001g0272 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.74-3889G>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68732987 | |||||||
| chr10:68733009 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.74-3867A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68733009 | |||||||
| chr10:68733057 | G | T | 1 | a0001c0001t0001g0229 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.74-3819G>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68733057 | |||||||
| chr10:68733058 | G | T | 36 | a0001c0003t0002g0047 a0001c0003t0002g0048 a0001c0003t0002g0051 others(33): Show |
36 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.74-3818G>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68733058 | |||||||
| chr10:68733125 | A | G | 1 | a0001c0001t0001g0031 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.74-3751A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68733125 | |||||||
| chr10:68733207 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.74-3669C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68733207 | |||||||
| chr10:68733282 | G | A | 43 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(40): Show |
44 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(41): Show |
intron_variant | MODIFIER | c.74-3594G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68733282 | |||||||
| chr10:68733286 | C | T | 5 | a0001c0002t0001g0091 a0001c0002t0001g0092 a0001c0002t0001g0093 others(2): Show |
5 | HG02055.hp2 HG02818.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.74-3590C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68733286 | |||||||
| chr10:68733366 | C | T | 36 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(33): Show |
37 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.74-3510C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68733366 | |||||||
| chr10:68733374 | G | C | 36 | a0001c0003t0002g0047 a0001c0003t0002g0048 a0001c0003t0002g0051 others(33): Show |
36 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.74-3502G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68733374 | |||||||
| chr10:68733495 | CA | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(190): Show |
198 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.74-3380delA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68733495 | |||||||
| chr10:68733532 | C | T | 4 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(1): Show |
4 | HG02145.hp2 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.74-3344C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68733532 | |||||||
| chr10:68733533 | T | C | 5 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0003t0001g0337 others(2): Show |
5 | HG01106.hp2 HG02572.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.74-3343T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68733533 | |||||||
| chr10:68733640 | T | C | 2 | a0002c0005t0008g0049 a0002c0005t0008g0050 |
2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.74-3236T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68733640 | |||||||
| chr10:68733780 | C | T | 243 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(240): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.74-3096C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68733780 | |||||||
| chr10:68733789 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.74-3087G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68733789 | |||||||
| chr10:68733877 | T | G | 36 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(33): Show |
37 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.74-2999T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68733877 | |||||||
| chr10:68734030 | A | G | 2 | a0001c0001t0001g0317 a0001c0001t0001g0318 |
2 | HG00558.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.74-2846A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68734030 | |||||||
| chr10:68734079 | T | A | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG01106.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.74-2797T>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68734079 | |||||||
| chr10:68734115 | G | A | 2 | a0001c0001t0001g0081 a0001c0001t0001g0089 |
2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.74-2761G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68734115 | |||||||
| chr10:68734488 | C | T | 3 | a0001c0003t0002g0047 a0001c0003t0002g0048 a0001c0003t0002g0056 |
3 | HG00639.hp2 HG01433.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.74-2388C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68734488 | |||||||
| chr10:68735109 | A | T | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.74-1767A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68735109 | |||||||
| chr10:68735158 | G | A | 1 | a0002c0005t0008g0049 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.74-1718G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68735158 | |||||||
| chr10:68735240 | C | G | 190 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(187): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.74-1636C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68735240 | |||||||
| chr10:68735287 | G | A | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.74-1589G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68735287 | |||||||
| chr10:68735371 | C | CT | 219 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(216): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.74-1485dupT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68735371 | ||||||
| chr10:68735371 | C | CTT | 41 | a0001c0001t0001g0030 a0001c0001t0001g0034 a0001c0001t0001g0036 others(38): Show |
41 | HG00639.hp1 HG00735.hp1 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.74-1486_74-1485dup others(2): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68735371 | ||||||
| chr10:68735371 | C | CTTT | 22 | a0001c0001t0007g0350 a0001c0001t0007g0351 a0001c0003t0002g0047 others(19): Show |
22 | HG00639.hp2 HG01081.hp1 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.74-1487_74-1485dup others(3): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68735371 | ||||||
| chr10:68735395 | A | G | 2 | a0001c0001t0001g0081 a0001c0001t0001g0089 |
2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.74-1481A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68735395 | |||||||
| chr10:68735402 | G | A | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.74-1474G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68735402 | |||||||
| chr10:68735420 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.74-1456G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68735420 | |||||||
| chr10:68735433 | A | G | 12 | a0001c0003t0002g0061 a0001c0003t0002g0062 a0001c0003t0002g0063 others(9): Show |
12 | HG01081.hp1 HG02559.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.74-1443A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68735433 | |||||||
| chr10:68735604 | C | G | 2 | a0001c0001t0001g0081 a0001c0001t0001g0089 |
2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.74-1272C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68735604 | |||||||
| chr10:68735652 | T | C | 279 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(276): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.74-1224T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68735652 | |||||||
| chr10:68735787 | T | C | 283 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(280): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.74-1089T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68735787 | |||||||
| chr10:68735789 | A | G | 2 | a0001c0001t0001g0097 a0001c0001t0001g0100 |
2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.74-1087A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68735789 | |||||||
| chr10:68735852 | A | G | 347 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(344): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.74-1024A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68735852 | |||||||
| chr10:68735897 | G | C | 279 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(276): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.74-979G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68735897 | |||||||
| chr10:68735955 | T | C | 279 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(276): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.74-921T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68735955 | |||||||
| chr10:68736041 | T | C | 39 | a0001c0001t0007g0350 a0001c0001t0007g0351 a0001c0001t0010g0353 others(36): Show |
39 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.74-835T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68736041 | |||||||
| chr10:68736260 | A | T | 1 | a0001c0001t0001g0228 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.74-616A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68736260 | |||||||
| chr10:68736335 | T | TACC | 9 | a0001c0003t0002g0051 a0001c0003t0002g0052 a0001c0003t0002g0053 others(6): Show |
9 | HG02015.hp2 HG02074.hp1 HG02083.hp2 others(6): Show |
intron_variant | MODIFIER | c.74-540_74-539insCC others(1): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68736335 | ||||||
| chr10:68736335 | T | TATC | 338 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(335): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.74-540_74-538dupAT others(1): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr10 | 68736335 | ||||||
| chr10:68736518 | A | G | 1 | a0001c0001t0001g0209 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.74-358A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68736518 | |||||||
| chr10:68736546 | T | C | 1 | a0001c0001t0001g0016 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.74-330T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68736546 | |||||||
| chr10:68736557 | C | T | 3 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0216 |
3 | HG03516.hp1 HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.74-319C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 2/24 | chr10 | 68736557 | |||||||
| chr10:68737210 | G | A | 4 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(1): Show |
4 | HG02145.hp2 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+162G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 3/24 | chr10 | 68737210 | |||||||
| chr10:68737285 | G | C | 2 | a0001c0004t0006g0268 a0001c0004t0006g0269 |
2 | HG01256.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.246+237G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 3/24 | chr10 | 68737285 | |||||||
| chr10:68737326 | G | C | 1 | a0001c0001t0018g0088 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.246+278G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 3/24 | chr10 | 68737326 | |||||||
| chr10:68737462 | C | T | 1 | a0001c0001t0018g0088 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.247-383C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 3/24 | chr10 | 68737462 | |||||||
| chr10:68737498 | C | CA | 11 | a0001c0001t0001g0034 a0001c0001t0001g0082 a0001c0001t0001g0083 others(8): Show |
11 | HG01109.hp1 HG02145.hp1 HG02976.hp1 others(8): Show |
intron_variant | MODIFIER | c.247-327dupA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr10 | 68737498 | ||||||
| chr10:68737498 | CA | C | 11 | a0001c0001t0001g0081 a0001c0001t0001g0089 a0001c0001t0001g0273 others(8): Show |
11 | HG02055.hp1 HG02486.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.247-327delA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr10 | 68737498 | ||||||
| chr10:68737498 | CAA | C | 35 | a0001c0003t0002g0047 a0001c0003t0002g0048 a0001c0003t0002g0051 others(32): Show |
35 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.247-328_247-327del others(2): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr10 | 68737498 | ||||||
| chr10:68737563 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.247-282C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 3/24 | chr10 | 68737563 | |||||||
| chr10:68737569 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.247-276C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 3/24 | chr10 | 68737569 | |||||||
| chr10:68737600 | T | C | 190 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(187): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.247-245T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 3/24 | chr10 | 68737600 | |||||||
| chr10:68737653 | A | T | 2 | a0001c0001t0001g0081 a0001c0001t0001g0089 |
2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.247-192A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 3/24 | chr10 | 68737653 | |||||||
| chr10:68737725 | A | G | 283 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(280): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.247-120A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 3/24 | chr10 | 68737725 | |||||||
| chr10:68737931 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.291+42G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/24 | chr10 | 68737931 | |||||||
| chr10:68737975 | C | G | 4 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(1): Show |
4 | HG02145.hp2 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.291+86C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/24 | chr10 | 68737975 | |||||||
| chr10:68737998 | A | G | 1 | a0001c0001t0001g0344 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.291+109A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/24 | chr10 | 68737998 | |||||||
| chr10:68738042 | C | T | 279 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(276): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.291+153C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/24 | chr10 | 68738042 | |||||||
| chr10:68738141 | G | A | 2 | a0001c0001t0001g0291 a0003c0006t0001g0290 |
2 | HG01074.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.291+252G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/24 | chr10 | 68738141 | |||||||
| chr10:68738283 | G | A | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.291+394G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/24 | chr10 | 68738283 | |||||||
| chr10:68738322 | G | A | 34 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(31): Show |
34 | HG00741.hp1 HG01123.hp2 HG01256.hp1 others(31): Show |
intron_variant | MODIFIER | c.291+433G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/24 | chr10 | 68738322 | |||||||
| chr10:68738592 | TTTTATTT others(7): Show |
T | 1 | a0001c0001t0001g0292 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.291+714_291+727del others(14): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr10 | 68738592 | ||||||
| chr10:68738596 | A | T | 3 | a0001c0001t0001g0081 a0001c0001t0001g0089 a0001c0001t0001g0306 |
3 | HG02886.hp2 HG03195.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.291+707A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/24 | chr10 | 68738596 | |||||||
| chr10:68738596 | AT | A | 6 | a0001c0001t0001g0221 a0001c0001t0001g0224 a0001c0001t0001g0229 others(3): Show |
6 | HG01069.hp2 HG01496.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.291+716delT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr10 | 68738596 | ||||||
| chr10:68738698 | C | T | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.291+809C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/24 | chr10 | 68738698 | |||||||
| chr10:68738775 | A | G | 1 | a0001c0001t0001g0328 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.291+886A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/24 | chr10 | 68738775 | |||||||
| chr10:68738791 | A | T | 1 | a0001c0001t0001g0011 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.291+902A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/24 | chr10 | 68738791 | |||||||
| chr10:68738822 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.291+933G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/24 | chr10 | 68738822 | |||||||
| chr10:68738897 | A | T | 1 | a0001c0001t0018g0088 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.291+1008A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/24 | chr10 | 68738897 | |||||||
| chr10:68738922 | C | T | 2 | a0001c0001t0001g0081 a0001c0001t0001g0089 |
2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.291+1033C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/24 | chr10 | 68738922 | |||||||
| chr10:68739257 | C | A | 2 | a0001c0003t0002g0058 a0001c0003t0002g0059 |
2 | HG02257.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.291+1368C>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/24 | chr10 | 68739257 | |||||||
| chr10:68739269 | C | T | 1 | a0001c0001t0005g0240 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.292-1360C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/24 | chr10 | 68739269 | |||||||
| chr10:68739460 | T | C | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG01106.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.292-1169T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/24 | chr10 | 68739460 | |||||||
| chr10:68739581 | G | A | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.292-1048G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/24 | chr10 | 68739581 | |||||||
| chr10:68739655 | C | G | 36 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(33): Show |
37 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.292-974C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/24 | chr10 | 68739655 | |||||||
| chr10:68739655 | C | T | 1 | a0001c0001t0001g0349 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.292-974C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/24 | chr10 | 68739655 | |||||||
| chr10:68739667 | C | T | 10 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(7): Show |
10 | HG01257.hp2 HG01952.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.292-962C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/24 | chr10 | 68739667 | |||||||
| chr10:68739782 | T | C | 196 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(193): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.292-847T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/24 | chr10 | 68739782 | |||||||
| chr10:68740047 | A | G | 2 | a0001c0002t0001g0106 a0001c0002t0001g0108 |
2 | HG02145.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.292-582A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/24 | chr10 | 68740047 | |||||||
| chr10:68740170 | G | A | 2 | a0001c0002t0001g0101 a0001c0002t0001g0105 |
2 | HG00140.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.292-459G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/24 | chr10 | 68740170 | |||||||
| chr10:68740414 | C | T | 2 | a0001c0001t0001g0081 a0001c0001t0001g0089 |
2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.292-215C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 4/24 | chr10 | 68740414 | |||||||
| chr10:68740713 | A | G | 2 | a0001c0001t0001g0275 a0001c0001t0001g0276 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.324+52A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 5/24 | chr10 | 68740713 | |||||||
| chr10:68740739 | C | G | 4 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(1): Show |
4 | HG02145.hp2 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.324+78C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 5/24 | chr10 | 68740739 | |||||||
| chr10:68740820 | A | G | 2 | a0001c0003t0002g0058 a0001c0003t0002g0059 |
2 | HG02257.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.324+159A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 5/24 | chr10 | 68740820 | |||||||
| chr10:68740871 | T | C | 1 | a0001c0001t0001g0239 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.324+210T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 5/24 | chr10 | 68740871 | |||||||
| chr10:68740883 | T | TTTTA | 10 | a0001c0001t0001g0017 a0001c0001t0001g0097 a0001c0001t0001g0178 others(7): Show |
10 | HG00621.hp1 HG01123.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.324+266_324+269dup others(4): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr10 | 68740883 | ||||||
| chr10:68740883 | TTTTA | T | 37 | a0001c0001t0001g0027 a0001c0001t0001g0081 a0001c0001t0001g0089 others(34): Show |
37 | HG00639.hp2 HG01433.hp1 HG01433.hp2 others(34): Show |
intron_variant | MODIFIER | c.324+266_324+269del others(4): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr10 | 68740883 | ||||||
| chr10:68740883 | TTTTATTT others(1): Show |
T | 8 | a0001c0001t0001g0033 a0001c0001t0001g0175 a0001c0001t0001g0205 others(5): Show |
8 | HG00741.hp1 HG01361.hp1 HG03516.hp1 others(5): Show |
intron_variant | MODIFIER | c.324+262_324+269del others(8): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr10 | 68740883 | ||||||
| chr10:68740883 | TTTTATTT others(5): Show |
T | 7 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(4): Show |
7 | HG01109.hp1 HG01257.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.324+258_324+269del others(12): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr10 | 68740883 | ||||||
| chr10:68740883 | TTTTATTT others(9): Show |
T | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.324+254_324+269del others(16): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr10 | 68740883 | ||||||
| chr10:68740884 | TTTATTTA others(8): Show |
T | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.324+226_324+240del others(15): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr10 | 68740884 | ||||||
| chr10:68740887 | A | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0170 |
2 | HG01517.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.324+226A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 5/24 | chr10 | 68740887 | |||||||
| chr10:68740953 | A | G | 279 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(276): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.324+292A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 5/24 | chr10 | 68740953 | |||||||
| chr10:68741066 | A | G | 1 | a0001c0001t0018g0088 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.324+405A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 5/24 | chr10 | 68741066 | |||||||
| chr10:68741141 | G | A | 2 | a0001c0001t0001g0081 a0001c0001t0001g0089 |
2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.324+480G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 5/24 | chr10 | 68741141 | |||||||
| chr10:68741145 | A | T | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.324+484A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 5/24 | chr10 | 68741145 | |||||||
| chr10:68741149 | C | G | 1 | a0001c0002t0001g0109 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.324+488C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 5/24 | chr10 | 68741149 | |||||||
| chr10:68741298 | G | A | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.324+637G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 5/24 | chr10 | 68741298 | |||||||
| chr10:68741392 | C | T | 2 | a0001c0004t0001g0271 a0001c0004t0001g0272 |
2 | HG03491.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.324+731C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 5/24 | chr10 | 68741392 | |||||||
| chr10:68741464 | G | A | 2 | a0001c0001t0001g0217 a0001c0001t0001g0237 |
2 | HG00735.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.324+803G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 5/24 | chr10 | 68741464 | |||||||
| chr10:68741520 | T | C | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.325-856T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 5/24 | chr10 | 68741520 | |||||||
| chr10:68741521 | G | A | 1 | a0001c0007t0001g0280 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.325-855G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 5/24 | chr10 | 68741521 | |||||||
| chr10:68741559 | G | A | 2 | a0001c0003t0004g0071 a0001c0003t0004g0072 |
2 | HG02886.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.325-817G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 5/24 | chr10 | 68741559 | |||||||
| chr10:68741591 | C | A | 347 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(344): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.325-785C>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 5/24 | chr10 | 68741591 | |||||||
| chr10:68741670 | T | C | 4 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(1): Show |
4 | HG02145.hp2 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.325-706T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 5/24 | chr10 | 68741670 | |||||||
| chr10:68741936 | A | G | 1 | a0001c0002t0001g0136 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.325-440A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 5/24 | chr10 | 68741936 | |||||||
| chr10:68742153 | G | A | 36 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(33): Show |
37 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.325-223G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 5/24 | chr10 | 68742153 | |||||||
| chr10:68742170 | G | C | 5 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0003t0001g0337 others(2): Show |
5 | HG01106.hp2 HG02572.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.325-206G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 5/24 | chr10 | 68742170 | |||||||
| chr10:68742669 | T | C | 346 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(343): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.518+100T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68742669 | |||||||
| chr10:68742851 | C | G | 4 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(1): Show |
4 | HG02145.hp2 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.518+282C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68742851 | |||||||
| chr10:68742909 | C | T | 1 | a0001c0001t0009g0013 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.518+340C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68742909 | |||||||
| chr10:68743035 | T | C | 3 | a0001c0001t0007g0350 a0001c0001t0007g0351 a0001c0001t0010g0353 |
3 | HG02280.hp1 HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.518+466T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68743035 | |||||||
| chr10:68743036 | G | A | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.518+467G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68743036 | |||||||
| chr10:68743082 | G | A | 1 | a0001c0003t0002g0352 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.518+513G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68743082 | |||||||
| chr10:68743200 | CTTT | C | 6 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(3): Show |
6 | HG01109.hp1 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.518+643_518+645del others(3): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr10 | 68743200 | ||||||
| chr10:68743223 | G | A | 1 | a0001c0003t0004g0068 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.518+654G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68743223 | |||||||
| chr10:68743393 | C | T | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.518+824C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68743393 | |||||||
| chr10:68743421 | C | T | 2 | a0001c0001t0001g0081 a0001c0001t0001g0089 |
2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.518+852C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68743421 | |||||||
| chr10:68743703 | C | T | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.518+1134C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68743703 | |||||||
| chr10:68743724 | ATTTG | A | 64 | a0001c0001t0001g0089 a0001c0002t0001g0006 a0001c0002t0001g0091 others(61): Show |
64 | HG00544.hp1 HG01243.hp1 HG02040.hp1 others(61): Show |
intron_variant | MODIFIER | c.518+1163_518+1166d others(6): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr10 | 68743724 | ||||||
| chr10:68743728 | GTTTGTTT others(1): Show |
G | 72 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(69): Show |
73 | HG00639.hp1 HG00639.hp2 HG00741.hp1 others(70): Show |
intron_variant | MODIFIER | c.518+1163_518+1170d others(10): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr10 | 68743728 | ||||||
| chr10:68743728 | GTTTGTTT others(5): Show |
G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(192): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.518+1163_518+1174d others(14): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr10 | 68743728 | ||||||
| chr10:68743732 | G | A | 7 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(4): Show |
7 | HG02145.hp1 HG02145.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.518+1163G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68743732 | |||||||
| chr10:68743732 | GTTTA | G | 9 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(6): Show |
9 | HG01109.hp1 HG02280.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.518+1192_518+1195d others(6): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr10 | 68743732 | ||||||
| chr10:68743767 | T | C | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.518+1198T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68743767 | |||||||
| chr10:68743773 | CAG | C | 36 | a0001c0003t0002g0047 a0001c0003t0002g0048 a0001c0003t0002g0051 others(33): Show |
36 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.518+1207_518+1208d others(4): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr10 | 68743773 | ||||||
| chr10:68744029 | G | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0011 |
2 | HG01257.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.518+1460G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68744029 | |||||||
| chr10:68744085 | A | G | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.518+1516A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68744085 | |||||||
| chr10:68744125 | T | C | 5 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0003t0001g0337 others(2): Show |
5 | HG01106.hp2 HG02572.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.518+1556T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68744125 | |||||||
| chr10:68744181 | A | G | 3 | a0001c0001t0007g0350 a0001c0001t0007g0351 a0001c0001t0010g0353 |
3 | HG02280.hp1 HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.518+1612A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68744181 | |||||||
| chr10:68744234 | A | G | 2 | a0001c0001t0001g0227 a0001c0001t0001g0238 |
2 | HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.518+1665A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68744234 | |||||||
| chr10:68744303 | C | T | 1 | a0001c0001t0001g0172 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.518+1734C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68744303 | |||||||
| chr10:68744420 | T | A | 14 | a0001c0003t0002g0047 a0001c0003t0002g0048 a0001c0003t0002g0051 others(11): Show |
14 | HG00639.hp2 HG01433.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.518+1851T>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68744420 | |||||||
| chr10:68744505 | G | A | 39 | a0001c0001t0007g0350 a0001c0001t0007g0351 a0001c0001t0010g0353 others(36): Show |
39 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.518+1936G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68744505 | |||||||
| chr10:68744522 | A | G | 1 | a0001c0001t0001g0204 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.518+1953A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68744522 | |||||||
| chr10:68744620 | G | C | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.518+2051G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68744620 | |||||||
| chr10:68744709 | T | C | 5 | a0001c0002t0001g0109 a0001c0002t0001g0126 a0001c0002t0001g0140 others(2): Show |
5 | NA18946.hp1 NA18960.hp1 NA18972.hp2 others(2): Show |
intron_variant | MODIFIER | c.518+2140T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68744709 | |||||||
| chr10:68744833 | CT | C | 6 | a0001c0001t0001g0180 a0001c0001t0001g0210 a0001c0001t0001g0317 others(3): Show |
6 | HG01168.hp2 NA18941.hp2 NA19060.hp1 others(3): Show |
intron_variant | MODIFIER | c.518+2278delT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr10 | 68744833 | ||||||
| chr10:68744916 | T | G | 3 | a0001c0003t0001g0337 a0001c0003t0001g0338 a0001c0003t0001g0339 |
3 | HG02572.hp2 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.519-2245T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68744916 | |||||||
| chr10:68744996 | AAATT | A | 66 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(63): Show |
66 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.519-2148_519-2145d others(6): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr10 | 68744996 | ||||||
| chr10:68745074 | T | C | 279 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(276): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.519-2087T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68745074 | |||||||
| chr10:68745075 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.519-2086G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68745075 | |||||||
| chr10:68745092 | G | A | 1 | a0001c0001t0018g0088 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.519-2069G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68745092 | |||||||
| chr10:68745167 | G | A | 1 | a0001c0002t0001g0109 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.519-1994G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68745167 | |||||||
| chr10:68745227 | C | T | 1 | a0001c0002t0001g0121 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.519-1934C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68745227 | |||||||
| chr10:68745325 | A | G | 4 | a0001c0001t0001g0169 a0001c0001t0001g0176 a0001c0001t0001g0203 others(1): Show |
4 | NA18984.hp1 NA18990.hp1 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.519-1836A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68745325 | |||||||
| chr10:68745458 | C | T | 5 | a0001c0001t0007g0350 a0001c0001t0007g0351 a0001c0002t0001g0106 others(2): Show |
5 | HG02145.hp1 HG02280.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.519-1703C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68745458 | |||||||
| chr10:68745465 | C | CT | 36 | a0001c0002t0001g0113 a0001c0003t0002g0047 a0001c0003t0002g0048 others(33): Show |
36 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.519-1682dupT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr10 | 68745465 | ||||||
| chr10:68745487 | G | A | 347 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(344): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.519-1674G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68745487 | |||||||
| chr10:68745513 | G | C | 1 | a0001c0001t0001g0257 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.519-1648G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68745513 | |||||||
| chr10:68745519 | A | C | 1 | a0001c0002t0001g0141 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.519-1642A>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68745519 | |||||||
| chr10:68745556 | C | T | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG01106.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.519-1605C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68745556 | |||||||
| chr10:68745620 | C | T | 7 | a0001c0003t0002g0066 a0001c0003t0004g0067 a0001c0003t0004g0068 others(4): Show |
7 | HG02559.hp1 HG02647.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.519-1541C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68745620 | |||||||
| chr10:68745646 | T | C | 2 | a0001c0003t0002g0058 a0001c0003t0002g0059 |
2 | HG02257.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.519-1515T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68745646 | |||||||
| chr10:68745743 | C | T | 3 | a0001c0004t0001g0265 a0001c0004t0001g0266 a0001c0004t0001g0322 |
3 | HG01515.hp1 HG01517.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.519-1418C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68745743 | |||||||
| chr10:68745847 | A | G | 2 | a0001c0001t0001g0002 a0001c0001t0009g0013 |
3 | HG01069.hp1 HG01071.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.519-1314A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68745847 | |||||||
| chr10:68745908 | G | A | 1 | a0001c0004t0006g0268 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.519-1253G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68745908 | |||||||
| chr10:68745970 | T | A | 5 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(2): Show |
5 | HG00544.hp1 HG02145.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.519-1191T>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68745970 | |||||||
| chr10:68745974 | A | G | 12 | a0001c0003t0002g0061 a0001c0003t0002g0062 a0001c0003t0002g0063 others(9): Show |
12 | HG01081.hp1 HG02559.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.519-1187A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68745974 | |||||||
| chr10:68746050 | A | G | 279 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(276): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.519-1111A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68746050 | |||||||
| chr10:68746065 | C | T | 2 | a0001c0001t0001g0081 a0001c0001t0001g0089 |
2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.519-1096C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68746065 | |||||||
| chr10:68746139 | ATTTTTGT others(6): Show |
A | 3 | a0001c0002t0001g0106 a0001c0002t0001g0107 a0001c0002t0001g0108 |
3 | HG02145.hp1 HG02818.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.519-1021_519-1009d others(15): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68746139 | |||||||
| chr10:68746232 | A | G | 63 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(60): Show |
63 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.519-929A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68746232 | |||||||
| chr10:68746262 | C | T | 1 | a0001c0001t0001g0213 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.519-899C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68746262 | |||||||
| chr10:68746333 | G | A | 36 | a0001c0003t0002g0047 a0001c0003t0002g0048 a0001c0003t0002g0051 others(33): Show |
36 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.519-828G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68746333 | |||||||
| chr10:68746371 | G | C | 2 | a0001c0001t0001g0081 a0001c0001t0001g0089 |
2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.519-790G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68746371 | |||||||
| chr10:68746384 | C | T | 1 | a0001c0001t0001g0321 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.519-777C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68746384 | |||||||
| chr10:68746491 | A | C | 1 | a0001c0003t0002g0055 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.519-670A>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68746491 | |||||||
| chr10:68746509 | A | G | 283 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(280): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.519-652A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68746509 | |||||||
| chr10:68746882 | C | G | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.519-279C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68746882 | |||||||
| chr10:68746890 | T | A | 1 | a0001c0001t0001g0228 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.519-271T>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68746890 | |||||||
| chr10:68747103 | G | T | 2 | a0001c0001t0001g0081 a0001c0001t0001g0089 |
2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.519-58G>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | chr10 | 68747103 | |||||||
| chr10:68747145 | C | CT | 39 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(36): Show |
40 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(37): Show |
splice_region_variant&intron_variant | LOW | c.519-5dupT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr10 | 68747145 | ||||||
| chr10:68747333 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.634-41A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 7/24 | chr10 | 68747333 | |||||||
| chr10:68747339 | A | AT | 15 | a0001c0001t0001g0005 a0001c0001t0001g0168 a0001c0001t0001g0172 others(12): Show |
16 | HG02056.hp2 NA18939.hp1 NA18940.hp1 others(13): Show |
intron_variant | MODIFIER | c.634-27dupT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr10 | 68747339 | ||||||
| chr10:68747695 | A | G | 1 | a0001c0001t0001g0320 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.826+129A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 8/24 | chr10 | 68747695 | |||||||
| chr10:68747725 | T | C | 1 | a0001c0003t0002g0058 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.826+159T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 8/24 | chr10 | 68747725 | |||||||
| chr10:68747747 | A | T | 1 | a0001c0003t0002g0080 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.826+181A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 8/24 | chr10 | 68747747 | |||||||
| chr10:68747869 | A | T | 1 | a0001c0003t0002g0064 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.826+303A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 8/24 | chr10 | 68747869 | |||||||
| chr10:68748140 | C | T | 2 | a0001c0001t0001g0081 a0001c0001t0001g0089 |
2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.826+574C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 8/24 | chr10 | 68748140 | |||||||
| chr10:68748218 | C | T | 2 | a0001c0001t0001g0081 a0001c0001t0001g0089 |
2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.826+652C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 8/24 | chr10 | 68748218 | |||||||
| chr10:68748261 | G | A | 190 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(187): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.826+695G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 8/24 | chr10 | 68748261 | |||||||
| chr10:68748485 | C | CT | 25 | a0001c0001t0001g0015 a0001c0001t0001g0097 a0001c0001t0001g0098 others(22): Show |
25 | HG00140.hp1 HG01168.hp1 HG01256.hp2 others(22): Show |
intron_variant | MODIFIER | c.827-630dupT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr10 | 68748485 | ||||||
| chr10:68748525 | A | G | 347 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(344): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.827-611A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 8/24 | chr10 | 68748525 | |||||||
| chr10:68748639 | G | A | 1 | a0001c0001t0001g0292 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.827-497G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 8/24 | chr10 | 68748639 | |||||||
| chr10:68748837 | C | A | 36 | a0001c0003t0002g0047 a0001c0003t0002g0048 a0001c0003t0002g0051 others(33): Show |
36 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.827-299C>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 8/24 | chr10 | 68748837 | |||||||
| chr10:68748925 | A | G | 1 | a0001c0001t0001g0026 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.827-211A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 8/24 | chr10 | 68748925 | |||||||
| chr10:68748982 | C | T | 36 | a0001c0003t0002g0047 a0001c0003t0002g0048 a0001c0003t0002g0051 others(33): Show |
36 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.827-154C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 8/24 | chr10 | 68748982 | |||||||
| chr10:68749058 | G | C | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG01106.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.827-78G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 8/24 | chr10 | 68749058 | |||||||
| chr10:68749117 | T | C | 43 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(40): Show |
44 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(41): Show |
intron_variant | MODIFIER | c.827-19T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 8/24 | chr10 | 68749117 | |||||||
| chr10:68749357 | A | C | 1 | a0001c0001t0001g0016 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.956+92A>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 9/24 | chr10 | 68749357 | |||||||
| chr10:68749384 | T | C | 1 | a0001c0001t0001g0182 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.956+119T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 9/24 | chr10 | 68749384 | |||||||
| chr10:68749723 | A | C | 1 | a0001c0001t0001g0033 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1118+38A>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68749723 | |||||||
| chr10:68749772 | G | C | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1118+87G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68749772 | |||||||
| chr10:68749845 | A | G | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1118+160A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68749845 | |||||||
| chr10:68749880 | C | T | 4 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(1): Show |
4 | HG02145.hp2 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1118+195C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68749880 | |||||||
| chr10:68749914 | AT | A | 3 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0031 |
3 | HG01934.hp1 NA18948.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.1118+231delT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr10 | 68749914 | ||||||
| chr10:68749936 | C | A | 3 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0216 |
3 | HG03516.hp1 HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1118+251C>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68749936 | |||||||
| chr10:68749995 | G | C | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG01106.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1118+310G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68749995 | |||||||
| chr10:68750021 | T | C | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1118+336T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68750021 | |||||||
| chr10:68750207 | CTTTTTTC others(1): Show |
C | 7 | a0001c0001t0001g0239 a0001c0001t0001g0273 a0001c0001t0001g0274 others(4): Show |
7 | HG01109.hp2 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1118+529_1118+536d others(10): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr10 | 68750207 | ||||||
| chr10:68750207 | CTTTTTTC others(2): Show |
C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(179): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.1118+529_1118+537d others(11): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr10 | 68750207 | ||||||
| chr10:68750207 | CTTTTTTC others(3): Show |
C | 1 | a0001c0001t0001g0012 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1118+529_1118+538d others(12): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr10 | 68750207 | ||||||
| chr10:68750214 | CT | C | 8 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0002t0001g0126 others(5): Show |
8 | HG00639.hp1 HG01106.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.1118+548delT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr10 | 68750214 | ||||||
| chr10:68750214 | CTT | C | 79 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(76): Show |
80 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(77): Show |
intron_variant | MODIFIER | c.1118+547_1118+548d others(4): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr10 | 68750214 | ||||||
| chr10:68750220 | T | G | 1 | a0001c0002t0001g0096 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1118+535T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68750220 | |||||||
| chr10:68750237 | A | G | 6 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(3): Show |
6 | HG01109.hp1 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1118+552A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68750237 | |||||||
| chr10:68750267 | G | C | 1 | a0001c0001t0001g0032 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1118+582G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68750267 | |||||||
| chr10:68750276 | C | T | 1 | a0001c0001t0001g0340 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1118+591C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68750276 | |||||||
| chr10:68750410 | C | T | 3 | a0001c0003t0002g0078 a0001c0003t0002g0079 a0001c0003t0002g0080 |
3 | NA18947.hp1 NA18993.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1118+725C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68750410 | |||||||
| chr10:68750455 | C | T | 1 | a0001c0001t0001g0239 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1118+770C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68750455 | |||||||
| chr10:68750780 | A | G | 3 | a0001c0001t0007g0350 a0001c0001t0007g0351 a0001c0001t0010g0353 |
3 | HG02280.hp1 HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1118+1095A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68750780 | |||||||
| chr10:68750864 | C | T | 279 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(276): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.1118+1179C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68750864 | |||||||
| chr10:68751021 | T | G | 3 | a0001c0001t0001g0328 a0001c0001t0007g0350 a0001c0001t0007g0351 |
3 | HG02280.hp1 HG02559.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1118+1336T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68751021 | |||||||
| chr10:68751027 | G | T | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1118+1342G>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68751027 | |||||||
| chr10:68751028 | T | G | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1118+1343T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68751028 | |||||||
| chr10:68751033 | G | GT | 19 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(16): Show |
19 | HG01081.hp1 HG01109.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.1118+1359dupT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr10 | 68751033 | ||||||
| chr10:68751033 | G | T | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1118+1348G>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68751033 | |||||||
| chr10:68751057 | C | T | 1 | a0001c0001t0001g0233 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1118+1372C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68751057 | |||||||
| chr10:68751153 | G | A | 190 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(187): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.1118+1468G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68751153 | |||||||
| chr10:68751153 | G | C | 1 | a0001c0003t0002g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1118+1468G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68751153 | |||||||
| chr10:68751297 | G | A | 7 | a0001c0001t0001g0170 a0001c0001t0001g0241 a0001c0001t0001g0242 others(4): Show |
7 | HG00642.hp2 HG00738.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.1118+1612G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68751297 | |||||||
| chr10:68751446 | C | G | 1 | a0001c0001t0001g0173 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1118+1761C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68751446 | |||||||
| chr10:68751673 | G | A | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG01106.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1118+1988G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68751673 | |||||||
| chr10:68751724 | C | T | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1118+2039C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68751724 | |||||||
| chr10:68751750 | G | C | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1118+2065G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68751750 | |||||||
| chr10:68751796 | A | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(192): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1119-2056A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68751796 | |||||||
| chr10:68751841 | G | A | 4 | a0001c0001t0001g0171 a0001c0001t0001g0183 a0001c0001t0001g0246 others(1): Show |
4 | HG00280.hp1 HG01261.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1119-2011G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68751841 | |||||||
| chr10:68751892 | C | G | 283 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(280): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.1119-1960C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68751892 | |||||||
| chr10:68751920 | G | GT | 78 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(75): Show |
79 | HG00639.hp1 HG00639.hp2 HG00741.hp1 others(76): Show |
intron_variant | MODIFIER | c.1119-1918dupT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr10 | 68751920 | ||||||
| chr10:68751925 | T | G | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG01106.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1119-1927T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68751925 | |||||||
| chr10:68751925 | T | TG | 7 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(4): Show |
7 | HG01109.hp1 HG01346.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1119-1927_1119-192 others(5): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68751925 | |||||||
| chr10:68751955 | C | T | 1 | a0001c0003t0004g0068 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1119-1897C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68751955 | |||||||
| chr10:68751956 | G | A | 1 | a0001c0003t0002g0051 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1119-1896G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68751956 | |||||||
| chr10:68752018 | G | A | 2 | a0001c0001t0001g0184 a0001c0001t0001g0232 |
2 | HG03017.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1119-1834G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68752018 | |||||||
| chr10:68752042 | G | C | 6 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(3): Show |
6 | HG01109.hp1 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1119-1810G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68752042 | |||||||
| chr10:68752105 | A | G | 3 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0031 |
3 | HG01934.hp1 NA18948.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.1119-1747A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68752105 | |||||||
| chr10:68752119 | C | T | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(192): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1119-1733C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68752119 | |||||||
| chr10:68752120 | G | A | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1119-1732G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68752120 | |||||||
| chr10:68752169 | C | T | 1 | a0001c0001t0001g0286 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1119-1683C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68752169 | |||||||
| chr10:68752222 | A | G | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1119-1630A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68752222 | |||||||
| chr10:68752259 | A | G | 1 | a0001c0001t0018g0088 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1119-1593A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68752259 | |||||||
| chr10:68752366 | C | T | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1119-1486C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68752366 | |||||||
| chr10:68752610 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1119-1242G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68752610 | |||||||
| chr10:68752628 | T | C | 1 | a0001c0004t0006g0268 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1119-1224T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68752628 | |||||||
| chr10:68752673 | C | T | 2 | a0001c0001t0001g0081 a0001c0001t0001g0089 |
2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1119-1179C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68752673 | |||||||
| chr10:68752871 | T | G | 1 | a0001c0001t0001g0087 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1119-981T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68752871 | |||||||
| chr10:68752883 | A | AATAG | 61 | a0001c0001t0001g0037 a0001c0001t0001g0089 a0001c0001t0001g0163 others(58): Show |
61 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.1119-914_1119-911d others(6): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr10 | 68752883 | ||||||
| chr10:68752883 | A | AATAGATA others(1): Show |
14 | a0001c0001t0001g0178 a0001c0001t0001g0185 a0001c0001t0001g0228 others(11): Show |
14 | HG00423.hp1 HG02055.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1119-918_1119-911d others(10): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr10 | 68752883 | ||||||
| chr10:68752883 | A | AATAGATA others(5): Show |
4 | a0001c0001t0001g0313 a0001c0001t0001g0326 a0001c0003t0002g0075 others(1): Show |
4 | HG02040.hp2 HG02647.hp1 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.1119-922_1119-911d others(14): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr10 | 68752883 | ||||||
| chr10:68752883 | A | AATAGATA others(9): Show |
1 | a0001c0001t0001g0294 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1119-926_1119-911d others(18): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr10 | 68752883 | ||||||
| chr10:68752883 | AATAG | A | 103 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(100): Show |
104 | HG00558.hp1 HG00642.hp1 HG00735.hp1 others(101): Show |
intron_variant | MODIFIER | c.1119-914_1119-911d others(6): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr10 | 68752883 | ||||||
| chr10:68752883 | AATAGATA others(1): Show |
A | 72 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(69): Show |
76 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.1119-918_1119-911d others(10): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr10 | 68752883 | ||||||
| chr10:68752883 | AATAGATA others(5): Show |
A | 13 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(10): Show |
13 | HG01168.hp2 HG01243.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1119-922_1119-911d others(14): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr10 | 68752883 | ||||||
| chr10:68752883 | AATAGATA others(9): Show |
A | 8 | a0001c0001t0001g0005 a0001c0001t0001g0085 a0001c0001t0001g0168 others(5): Show |
9 | HG01109.hp1 NA18939.hp1 NA18940.hp1 others(6): Show |
intron_variant | MODIFIER | c.1119-926_1119-911d others(18): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr10 | 68752883 | ||||||
| chr10:68752883 | AATAGATA others(13): Show |
A | 2 | a0001c0001t0001g0172 a0001c0001t0001g0325 |
2 | HG00280.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1119-930_1119-911d others(22): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr10 | 68752883 | ||||||
| chr10:68752928 | A | T | 1 | a0001c0001t0001g0309 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1119-924A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68752928 | |||||||
| chr10:68752938 | A | T | 7 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(4): Show |
7 | HG01109.hp1 HG02922.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1119-914A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68752938 | |||||||
| chr10:68752972 | A | G | 3 | a0001c0002t0001g0106 a0001c0002t0001g0107 a0001c0002t0001g0108 |
3 | HG02145.hp1 HG02818.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1119-880A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68752972 | |||||||
| chr10:68752978 | ATAGG | A | 3 | a0001c0003t0001g0337 a0001c0003t0001g0338 a0001c0003t0001g0339 |
3 | HG02572.hp2 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1119-869_1119-866d others(6): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr10 | 68752978 | ||||||
| chr10:68753094 | T | TTAGTTGT others(17): Show |
279 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(276): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.1119-747_1119-746i others(26): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr10 | 68753094 | ||||||
| chr10:68753353 | G | A | 1 | a0001c0002t0001g0128 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1119-499G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68753353 | |||||||
| chr10:68753383 | G | A | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1119-469G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68753383 | |||||||
| chr10:68753460 | G | A | 34 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(31): Show |
34 | HG00741.hp1 HG01123.hp2 HG01256.hp1 others(31): Show |
intron_variant | MODIFIER | c.1119-392G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68753460 | |||||||
| chr10:68753472 | T | C | 2 | a0001c0001t0001g0222 a0001c0001t0001g0231 |
2 | HG02486.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1119-380T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68753472 | |||||||
| chr10:68753669 | G | A | 1 | a0001c0002t0001g0159 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1119-183G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 10/24 | chr10 | 68753669 | |||||||
| chr10:68754163 | G | A | 1 | a0001c0002t0001g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1344+86G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 11/24 | chr10 | 68754163 | |||||||
| chr10:68754180 | G | A | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1344+103G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 11/24 | chr10 | 68754180 | |||||||
| chr10:68754188 | G | C | 10 | a0001c0001t0001g0163 a0001c0001t0001g0219 a0001c0001t0001g0220 others(7): Show |
10 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1344+111G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 11/24 | chr10 | 68754188 | |||||||
| chr10:68754240 | T | C | 1 | a0001c0001t0001g0170 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1344+163T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 11/24 | chr10 | 68754240 | |||||||
| chr10:68754521 | T | C | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1345-193T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 11/24 | chr10 | 68754521 | |||||||
| chr10:68754564 | T | A | 1 | a0001c0002t0001g0119 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1345-150T>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 11/24 | chr10 | 68754564 | |||||||
| chr10:68754870 | G | A | 1 | a0001c0001t0009g0261 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1458+43G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 12/24 | chr10 | 68754870 | |||||||
| chr10:68755133 | T | C | 1 | a0001c0003t0014g0069 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1459-237T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 12/24 | chr10 | 68755133 | |||||||
| chr10:68755317 | G | T | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1459-53G>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 12/24 | chr10 | 68755317 | |||||||
| chr10:68755584 | A | T | 1 | a0001c0001t0001g0218 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1625+48A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 13/24 | chr10 | 68755584 | |||||||
| chr10:68755671 | A | G | 1 | a0001c0004t0001g0272 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1625+135A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 13/24 | chr10 | 68755671 | |||||||
| chr10:68756627 | A | G | 1 | a0001c0003t0002g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1836+144A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 14/24 | chr10 | 68756627 | |||||||
| chr10:68756987 | A | G | 77 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(74): Show |
78 | HG00639.hp1 HG00639.hp2 HG00741.hp1 others(75): Show |
intron_variant | MODIFIER | c.1837-307A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 14/24 | chr10 | 68756987 | |||||||
| chr10:68757532 | A | G | 1 | a0001c0003t0002g0352 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1920+155A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68757532 | |||||||
| chr10:68757628 | T | C | 1 | a0001c0003t0002g0054 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1920+251T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68757628 | |||||||
| chr10:68757706 | G | A | 34 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(31): Show |
34 | HG00741.hp1 HG01123.hp2 HG01256.hp1 others(31): Show |
intron_variant | MODIFIER | c.1920+329G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68757706 | |||||||
| chr10:68757797 | G | C | 1 | a0001c0003t0002g0073 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1920+420G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68757797 | |||||||
| chr10:68757833 | TAAG | T | 196 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(193): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.1920+460_1920+462d others(5): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68757833 | ||||||
| chr10:68757845 | A | T | 3 | a0001c0004t0001g0265 a0001c0004t0001g0266 a0001c0004t0001g0322 |
3 | HG01515.hp1 HG01517.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1920+468A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68757845 | |||||||
| chr10:68757880 | A | G | 3 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0216 |
3 | HG03516.hp1 HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1920+503A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68757880 | |||||||
| chr10:68757886 | G | T | 6 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(3): Show |
6 | HG01257.hp2 HG01952.hp2 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1920+509G>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68757886 | |||||||
| chr10:68757901 | C | T | 36 | a0001c0003t0002g0047 a0001c0003t0002g0048 a0001c0003t0002g0051 others(33): Show |
36 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.1920+524C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68757901 | |||||||
| chr10:68758227 | G | C | 1 | a0001c0002t0001g0131 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1920+850G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68758227 | |||||||
| chr10:68758269 | G | A | 1 | a0001c0002t0001g0109 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1920+892G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68758269 | |||||||
| chr10:68758338 | A | T | 2 | a0001c0001t0001g0033 a0001c0001t0016g0028 |
2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1920+961A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68758338 | |||||||
| chr10:68758384 | T | A | 2 | a0002c0005t0008g0049 a0002c0005t0008g0050 |
2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1920+1007T>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68758384 | |||||||
| chr10:68758483 | A | G | 3 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0216 |
3 | HG03516.hp1 HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1920+1106A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68758483 | |||||||
| chr10:68758503 | A | AGT | 107 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(104): Show |
108 | HG00140.hp2 HG00558.hp2 HG00639.hp1 others(105): Show |
intron_variant | MODIFIER | c.1920+1167_1920+116 others(6): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68758503 | ||||||
| chr10:68758503 | A | AGTGT | 17 | a0001c0001t0001g0216 a0001c0001t0001g0244 a0001c0001t0001g0258 others(14): Show |
17 | HG01123.hp1 HG01515.hp2 HG02165.hp1 others(14): Show |
intron_variant | MODIFIER | c.1920+1165_1920+116 others(8): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68758503 | ||||||
| chr10:68758503 | A | AGTGTGT | 17 | a0001c0001t0001g0087 a0001c0001t0018g0088 a0001c0002t0001g0106 others(14): Show |
17 | HG00544.hp1 HG02145.hp1 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.1920+1163_1920+116 others(10): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68758503 | ||||||
| chr10:68758503 | A | AGTGTGTG others(3): Show |
1 | a0001c0002t0001g0108 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1920+1159_1920+116 others(14): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68758503 | ||||||
| chr10:68758503 | A | AGTGTGTG others(5): Show |
1 | a0001c0002t0001g0130 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1920+1157_1920+116 others(16): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68758503 | ||||||
| chr10:68758503 | AGT | A | 34 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0022 others(31): Show |
34 | HG00099.hp2 HG00140.hp1 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.1920+1167_1920+116 others(6): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68758503 | ||||||
| chr10:68758503 | AGTGT | A | 33 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(30): Show |
34 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.1920+1165_1920+116 others(8): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68758503 | ||||||
| chr10:68758503 | AGTGTGT | A | 18 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0089 others(15): Show |
18 | HG01346.hp2 HG01891.hp1 HG02165.hp2 others(15): Show |
intron_variant | MODIFIER | c.1920+1163_1920+116 others(10): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68758503 | ||||||
| chr10:68758503 | AGTGTGTG others(1): Show |
A | 5 | a0001c0001t0001g0081 a0001c0001t0001g0341 a0001c0001t0001g0348 others(2): Show |
5 | HG02257.hp2 HG02280.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1920+1161_1920+116 others(12): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68758503 | ||||||
| chr10:68758503 | AGTGTGTG others(5): Show |
A | 2 | a0001c0001t0001g0098 a0001c0001t0001g0099 |
2 | HG02145.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1920+1157_1920+116 others(16): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68758503 | ||||||
| chr10:68758503 | AGTGTGTG others(7): Show |
A | 9 | a0001c0003t0002g0064 a0001c0003t0002g0065 a0001c0003t0002g0066 others(6): Show |
9 | HG01081.hp1 HG02559.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1920+1155_1920+116 others(18): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68758503 | ||||||
| chr10:68758546 | A | G | 7 | a0001c0001t0001g0221 a0001c0001t0001g0224 a0001c0001t0001g0229 others(4): Show |
7 | HG01496.hp1 HG01952.hp1 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.1920+1169A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68758546 | |||||||
| chr10:68758555 | A | C | 190 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(187): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.1920+1178A>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68758555 | |||||||
| chr10:68758612 | T | TGTGTATA others(23): Show |
4 | a0001c0002t0001g0110 a0001c0002t0001g0122 a0001c0002t0001g0151 others(1): Show |
4 | NA18947.hp2 NA18961.hp1 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.1920+1251_1920+125 others(34): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68758612 | ||||||
| chr10:68758612 | TGTGTATA others(25): Show |
T | 1 | a0001c0002t0001g0104 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1920+1282_1920+131 others(36): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68758612 | ||||||
| chr10:68758614 | TGTATATA others(23): Show |
T | 36 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(33): Show |
37 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.1920+1240_1920+126 others(34): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68758614 | ||||||
| chr10:68758615 | GTA | G | 92 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(89): Show |
92 | HG00544.hp1 HG00639.hp2 HG01081.hp1 others(89): Show |
intron_variant | MODIFIER | c.1920+1252_1920+125 others(6): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68758615 | ||||||
| chr10:68758615 | GTATA | G | 3 | a0001c0002t0001g0134 a0001c0003t0002g0061 a0001c0003t0002g0063 |
3 | HG03130.hp1 HG03669.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1920+1250_1920+125 others(8): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68758615 | ||||||
| chr10:68758617 | A | G | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1920+1240A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68758617 | |||||||
| chr10:68758629 | ATGTATAT others(55): Show |
A | 1 | a0001c0001t0001g0293 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1920+1254_1920+131 others(66): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68758629 | ||||||
| chr10:68758647 | GTA | G | 36 | a0001c0003t0002g0047 a0001c0003t0002g0048 a0001c0003t0002g0051 others(33): Show |
36 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.1920+1284_1920+128 others(6): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68758647 | ||||||
| chr10:68758649 | A | G | 2 | a0001c0001t0001g0014 a0001c0001t0001g0035 |
2 | HG04184.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1920+1272A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68758649 | |||||||
| chr10:68758659 | ATATGTAT others(25): Show |
A | 191 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(188): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.1920+1284_1920+131 others(36): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68758659 | ||||||
| chr10:68758661 | ATGTATAT others(24): Show |
A | 10 | a0001c0001t0001g0163 a0001c0001t0001g0219 a0001c0001t0001g0220 others(7): Show |
10 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1920+1286_1920+131 others(35): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68758661 | ||||||
| chr10:68758661 | ATGTATAT others(25): Show |
A | 5 | a0001c0001t0001g0172 a0001c0001t0001g0205 a0001c0001t0001g0215 others(2): Show |
5 | HG02280.hp1 HG02559.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.1920+1286_1920+131 others(36): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68758661 | ||||||
| chr10:68758691 | T | A | 68 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(65): Show |
69 | HG00639.hp2 HG00741.hp1 HG01069.hp1 others(66): Show |
intron_variant | MODIFIER | c.1920+1314T>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68758691 | |||||||
| chr10:68758709 | G | GTCT | 7 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(4): Show |
7 | HG01109.hp1 HG02717.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1920+1334_1920+133 others(7): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68758709 | ||||||
| chr10:68758813 | C | T | 1 | a0001c0001t0018g0088 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1920+1436C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68758813 | |||||||
| chr10:68758858 | A | G | 190 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(187): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.1920+1481A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68758858 | |||||||
| chr10:68758957 | C | A | 54 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(51): Show |
54 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.1920+1580C>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68758957 | |||||||
| chr10:68759105 | ACAACAAC | A | 36 | a0001c0003t0002g0047 a0001c0003t0002g0048 a0001c0003t0002g0051 others(33): Show |
36 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.1920+1738_1920+174 others(11): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68759105 | ||||||
| chr10:68759238 | G | A | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1921-1769G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68759238 | |||||||
| chr10:68759321 | G | A | 1 | a0001c0002t0001g0128 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1921-1686G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68759321 | |||||||
| chr10:68759415 | AAAAT | A | 38 | a0001c0001t0007g0350 a0001c0001t0007g0351 a0001c0003t0002g0047 others(35): Show |
38 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.1921-1586_1921-158 others(8): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68759415 | ||||||
| chr10:68759457 | A | G | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1921-1550A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68759457 | |||||||
| chr10:68759561 | C | CA | 15 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0171 others(12): Show |
15 | HG00280.hp1 HG01081.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.1921-1433dupA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68759561 | ||||||
| chr10:68759807 | T | A | 1 | a0001c0001t0001g0313 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1921-1200T>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68759807 | |||||||
| chr10:68759815 | T | C | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1921-1192T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68759815 | |||||||
| chr10:68759846 | A | T | 283 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(280): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.1921-1161A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68759846 | |||||||
| chr10:68759923 | C | G | 3 | a0001c0003t0002g0047 a0001c0003t0002g0048 a0001c0003t0002g0056 |
3 | HG00639.hp2 HG01433.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.1921-1084C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68759923 | |||||||
| chr10:68759990 | A | G | 36 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(33): Show |
37 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.1921-1017A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68759990 | |||||||
| chr10:68760106 | ACAGGCAC others(4): Show |
A | 1 | a0001c0001t0001g0002 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1921-898_1921-888d others(13): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68760106 | ||||||
| chr10:68760169 | A | T | 1 | a0001c0002t0001g0125 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1921-838A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68760169 | |||||||
| chr10:68760204 | GAGTGCAG others(5): Show |
G | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1921-799_1921-788d others(14): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68760204 | ||||||
| chr10:68760235 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1921-772A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68760235 | |||||||
| chr10:68760382 | G | T | 5 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(2): Show |
5 | HG01109.hp1 HG02976.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1921-625G>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68760382 | |||||||
| chr10:68760475 | C | A | 1 | a0001c0001t0001g0226 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1921-532C>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68760475 | |||||||
| chr10:68760528 | A | T | 2 | a0001c0001t0001g0081 a0001c0001t0001g0089 |
2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1921-479A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68760528 | |||||||
| chr10:68760665 | G | A | 190 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(187): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.1921-342G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68760665 | |||||||
| chr10:68760714 | A | G | 7 | a0001c0003t0002g0066 a0001c0003t0004g0067 a0001c0003t0004g0068 others(4): Show |
7 | HG02559.hp1 HG02647.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1921-293A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68760714 | |||||||
| chr10:68760745 | T | A | 61 | a0001c0002t0001g0006 a0001c0002t0001g0091 a0001c0002t0001g0092 others(58): Show |
61 | HG00544.hp1 HG01243.hp1 HG02040.hp1 others(58): Show |
intron_variant | MODIFIER | c.1921-262T>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68760745 | |||||||
| chr10:68760832 | C | T | 1 | a0001c0001t0001g0027 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1921-175C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68760832 | |||||||
| chr10:68760872 | C | A | 1 | a0001c0001t0001g0286 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1921-135C>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68760872 | |||||||
| chr10:68760873 | A | C | 1 | a0001c0001t0001g0286 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1921-134A>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68760873 | |||||||
| chr10:68760879 | CA | C | 61 | a0001c0002t0001g0006 a0001c0002t0001g0091 a0001c0002t0001g0092 others(58): Show |
61 | HG00140.hp2 HG00642.hp1 HG01192.hp1 others(58): Show |
intron_variant | MODIFIER | c.1921-114delA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68760879 | ||||||
| chr10:68760879 | CAA | C | 38 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(35): Show |
39 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.1921-115_1921-114d others(4): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68760879 | ||||||
| chr10:68760879 | CAAA | C | 241 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(238): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.1921-116_1921-114d others(5): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr10 | 68760879 | ||||||
| chr10:68760883 | A | C | 3 | a0001c0002t0001g0134 a0001c0002t0001g0136 a0001c0002t0001g0150 |
3 | HG00544.hp1 HG02040.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1921-124A>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68760883 | |||||||
| chr10:68760884 | A | C | 1 | a0001c0002t0001g0119 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1921-123A>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68760884 | |||||||
| chr10:68760947 | G | A | 1 | a0001c0001t0001g0333 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1921-60G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68760947 | |||||||
| chr10:68760949 | T | C | 13 | a0001c0002t0001g0109 a0001c0002t0001g0116 a0001c0002t0001g0126 others(10): Show |
13 | NA18946.hp1 NA18960.hp1 NA18968.hp2 others(10): Show |
intron_variant | MODIFIER | c.1921-58T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68760949 | |||||||
| chr10:68760963 | C | T | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1921-44C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 15/24 | chr10 | 68760963 | |||||||
| chr10:68761272 | T | G | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2106+80T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68761272 | |||||||
| chr10:68761284 | A | T | 279 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(276): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.2106+92A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68761284 | |||||||
| chr10:68761312 | A | T | 1 | a0001c0001t0001g0245 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2106+120A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68761312 | |||||||
| chr10:68761312 | AATTT | A | 3 | a0001c0003t0002g0078 a0001c0003t0002g0079 a0001c0003t0002g0080 |
3 | NA18947.hp1 NA18993.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.2106+129_2106+132d others(6): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr10 | 68761312 | ||||||
| chr10:68761316 | T | A | 1 | a0001c0002t0001g0107 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2106+124T>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68761316 | |||||||
| chr10:68761367 | A | G | 43 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(40): Show |
44 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(41): Show |
intron_variant | MODIFIER | c.2106+175A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68761367 | |||||||
| chr10:68761375 | C | T | 36 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(33): Show |
37 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.2106+183C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68761375 | |||||||
| chr10:68761400 | A | G | 1 | a0001c0001t0001g0345 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2106+208A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68761400 | |||||||
| chr10:68761508 | A | G | 1 | a0001c0003t0002g0352 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2106+316A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68761508 | |||||||
| chr10:68761603 | C | G | 4 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(1): Show |
4 | HG02145.hp2 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2106+411C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68761603 | |||||||
| chr10:68761632 | C | T | 191 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(188): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.2106+440C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68761632 | |||||||
| chr10:68761665 | C | T | 7 | a0001c0001t0001g0012 a0001c0001t0001g0082 a0001c0001t0001g0083 others(4): Show |
7 | HG01109.hp1 HG01993.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.2106+473C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68761665 | |||||||
| chr10:68761728 | A | G | 1 | a0001c0002t0001g0162 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2106+536A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68761728 | |||||||
| chr10:68761787 | A | G | 1 | a0001c0002t0001g0156 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2106+595A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68761787 | |||||||
| chr10:68761790 | A | T | 279 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(276): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.2106+598A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68761790 | |||||||
| chr10:68761906 | A | G | 39 | a0001c0001t0007g0350 a0001c0001t0007g0351 a0001c0001t0010g0353 others(36): Show |
39 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.2106+714A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68761906 | |||||||
| chr10:68762051 | C | T | 1 | a0001c0003t0002g0059 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2106+859C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68762051 | |||||||
| chr10:68762099 | G | C | 1 | a0001c0007t0001g0280 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2106+907G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68762099 | |||||||
| chr10:68762111 | C | T | 3 | a0001c0004t0001g0265 a0001c0004t0001g0266 a0001c0004t0001g0322 |
3 | HG01515.hp1 HG01517.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.2106+919C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68762111 | |||||||
| chr10:68762144 | A | G | 39 | a0001c0001t0007g0350 a0001c0001t0007g0351 a0001c0001t0010g0353 others(36): Show |
39 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.2106+952A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68762144 | |||||||
| chr10:68762327 | TA | T | 274 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(271): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.2106+1146delA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr10 | 68762327 | ||||||
| chr10:68762344 | C | CA | 36 | a0001c0003t0002g0047 a0001c0003t0002g0048 a0001c0003t0002g0051 others(33): Show |
36 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.2106+1158dupA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr10 | 68762344 | ||||||
| chr10:68762355 | CA | C | 278 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(275): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.2106+1173delA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr10 | 68762355 | ||||||
| chr10:68762473 | A | C | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2106+1281A>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68762473 | |||||||
| chr10:68762619 | T | A | 1 | a0001c0001t0001g0014 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2106+1427T>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68762619 | |||||||
| chr10:68762679 | A | C | 2 | a0001c0003t0002g0058 a0001c0003t0002g0059 |
2 | HG02257.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.2106+1487A>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68762679 | |||||||
| chr10:68762745 | T | A | 1 | a0001c0001t0001g0286 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2106+1553T>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68762745 | |||||||
| chr10:68762748 | A | T | 1 | a0001c0001t0001g0286 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2106+1556A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68762748 | |||||||
| chr10:68762752 | T | C | 2 | a0001c0001t0001g0277 a0001c0001t0001g0282 |
2 | HG03942.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.2106+1560T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68762752 | |||||||
| chr10:68762907 | C | T | 1 | a0001c0001t0003g0045 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2106+1715C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68762907 | |||||||
| chr10:68762948 | AG | A | 14 | a0001c0003t0002g0047 a0001c0003t0002g0048 a0001c0003t0002g0051 others(11): Show |
14 | HG00639.hp2 HG01433.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.2106+1757delG | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68762948 | |||||||
| chr10:68762990 | A | G | 2 | a0001c0004t0006g0268 a0001c0004t0006g0269 |
2 | HG01256.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.2106+1798A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68762990 | |||||||
| chr10:68763112 | CT | C | 192 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(189): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.2106+1929delT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr10 | 68763112 | ||||||
| chr10:68763141 | CTTTA | C | 5 | a0001c0003t0002g0073 a0001c0003t0002g0074 a0001c0003t0002g0075 others(2): Show |
5 | HG02486.hp2 HG02647.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2106+1953_2106+195 others(8): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr10 | 68763141 | ||||||
| chr10:68763153 | A | G | 1 | a0001c0001t0018g0088 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2106+1961A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68763153 | |||||||
| chr10:68763174 | C | T | 36 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(33): Show |
37 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.2106+1982C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68763174 | |||||||
| chr10:68763304 | C | G | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2106+2112C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68763304 | |||||||
| chr10:68763316 | A | C | 5 | a0001c0003t0002g0073 a0001c0003t0002g0074 a0001c0003t0002g0075 others(2): Show |
5 | HG02486.hp2 HG02647.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2106+2124A>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68763316 | |||||||
| chr10:68763443 | G | A | 1 | a0001c0001t0009g0261 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2106+2251G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68763443 | |||||||
| chr10:68763497 | C | T | 1 | a0001c0002t0011g0146 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2106+2305C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68763497 | |||||||
| chr10:68763511 | G | A | 1 | a0001c0002t0001g0094 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2106+2319G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68763511 | |||||||
| chr10:68763573 | G | A | 1 | a0001c0001t0001g0004 | 2 | HG00738.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2107-2315G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68763573 | |||||||
| chr10:68763593 | G | A | 5 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(2): Show |
5 | HG01934.hp1 NA18747.hp2 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.2107-2295G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68763593 | |||||||
| chr10:68763739 | T | C | 1 | a0001c0002t0001g0135 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2107-2149T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68763739 | |||||||
| chr10:68763790 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2107-2098C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68763790 | |||||||
| chr10:68763989 | T | C | 1 | a0001c0001t0001g0010 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2107-1899T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68763989 | |||||||
| chr10:68764175 | A | G | 190 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(187): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.2107-1713A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68764175 | |||||||
| chr10:68764230 | A | T | 38 | a0001c0001t0007g0350 a0001c0001t0007g0351 a0001c0003t0002g0047 others(35): Show |
38 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.2107-1658A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68764230 | |||||||
| chr10:68764381 | C | CA | 30 | a0001c0001t0001g0042 a0001c0003t0002g0047 a0001c0003t0002g0048 others(27): Show |
30 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.2107-1492dupA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr10 | 68764381 | ||||||
| chr10:68764381 | C | CAA | 7 | a0001c0003t0002g0066 a0001c0003t0004g0067 a0001c0003t0004g0068 others(4): Show |
7 | HG02559.hp1 HG02647.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.2107-1493_2107-149 others(6): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr10 | 68764381 | ||||||
| chr10:68764539 | CA | C | 9 | a0001c0003t0002g0064 a0001c0003t0002g0065 a0001c0003t0002g0066 others(6): Show |
9 | HG01081.hp1 HG02559.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.2107-1337delA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | INFO_REALIGN_3_PRIME | chr10 | 68764539 | ||||||
| chr10:68764620 | T | G | 2 | a0002c0005t0008g0049 a0002c0005t0008g0050 |
2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2107-1268T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68764620 | |||||||
| chr10:68764719 | A | G | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2107-1169A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68764719 | |||||||
| chr10:68764881 | A | T | 1 | a0001c0001t0018g0088 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2107-1007A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68764881 | |||||||
| chr10:68764914 | T | C | 6 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(3): Show |
6 | HG01109.hp1 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2107-974T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68764914 | |||||||
| chr10:68764932 | A | G | 36 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(33): Show |
37 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.2107-956A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68764932 | |||||||
| chr10:68765048 | T | C | 1 | a0001c0001t0001g0307 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2107-840T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68765048 | |||||||
| chr10:68765376 | C | T | 2 | a0001c0001t0001g0081 a0001c0001t0001g0089 |
2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2107-512C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68765376 | |||||||
| chr10:68765420 | C | G | 1 | a0001c0001t0001g0325 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2107-468C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68765420 | |||||||
| chr10:68765665 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2107-223G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68765665 | |||||||
| chr10:68765679 | A | T | 2 | a0001c0001t0001g0341 a0001c0001t0001g0348 |
2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2107-209A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68765679 | |||||||
| chr10:68765728 | C | G | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2107-160C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68765728 | |||||||
| chr10:68765832 | A | G | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2107-56A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68765832 | |||||||
| chr10:68765834 | G | A | 190 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(187): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.2107-54G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 16/24 | chr10 | 68765834 | |||||||
| chr10:68766186 | G | GT | 14 | a0001c0001t0001g0197 a0001c0001t0018g0088 a0001c0003t0002g0061 others(11): Show |
14 | HG01081.hp1 HG02559.hp1 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.2298+115dupT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr10 | 68766186 | ||||||
| chr10:68766186 | G | T | 62 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0002t0001g0006 others(59): Show |
62 | HG00544.hp1 HG01106.hp2 HG02040.hp1 others(59): Show |
intron_variant | MODIFIER | c.2298+107G>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68766186 | |||||||
| chr10:68766187 | T | G | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2298+108T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68766187 | |||||||
| chr10:68766215 | T | A | 1 | a0001c0001t0001g0300 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2298+136T>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68766215 | |||||||
| chr10:68766217 | T | G | 1 | a0001c0001t0001g0022 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2298+138T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68766217 | |||||||
| chr10:68766563 | A | C | 5 | a0001c0003t0002g0073 a0001c0003t0002g0074 a0001c0003t0002g0075 others(2): Show |
5 | HG02486.hp2 HG02647.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2298+484A>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68766563 | |||||||
| chr10:68766612 | C | T | 1 | a0001c0001t0001g0235 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2298+533C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68766612 | |||||||
| chr10:68766652 | G | A | 1 | a0001c0001t0001g0250 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2298+573G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68766652 | |||||||
| chr10:68766775 | T | G | 4 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(1): Show |
4 | HG02145.hp2 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2298+696T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68766775 | |||||||
| chr10:68766839 | A | C | 1 | a0001c0003t0002g0352 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2298+760A>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68766839 | |||||||
| chr10:68767005 | T | G | 16 | a0001c0001t0001g0005 a0001c0001t0001g0168 a0001c0001t0001g0172 others(13): Show |
17 | HG02056.hp2 NA18939.hp1 NA18940.hp1 others(14): Show |
intron_variant | MODIFIER | c.2298+926T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68767005 | |||||||
| chr10:68767054 | C | T | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2298+975C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68767054 | |||||||
| chr10:68767250 | AT | A | 7 | a0001c0001t0001g0221 a0001c0001t0001g0224 a0001c0001t0001g0229 others(4): Show |
7 | HG01069.hp2 HG01496.hp1 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.2298+1177delT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr10 | 68767250 | ||||||
| chr10:68767308 | C | T | 1 | a0001c0002t0001g0103 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2298+1229C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68767308 | |||||||
| chr10:68767403 | G | C | 4 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(1): Show |
4 | HG02145.hp2 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2298+1324G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68767403 | |||||||
| chr10:68767413 | A | G | 4 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(1): Show |
4 | HG02145.hp2 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2298+1334A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68767413 | |||||||
| chr10:68767618 | C | T | 1 | a0001c0001t0001g0343 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.2298+1539C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68767618 | |||||||
| chr10:68767828 | A | AT | 3 | a0001c0001t0007g0350 a0001c0001t0007g0351 a0001c0001t0010g0353 |
3 | HG02280.hp1 HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.2298+1752dupT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr10 | 68767828 | ||||||
| chr10:68767904 | T | C | 2 | a0002c0005t0008g0049 a0002c0005t0008g0050 |
2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2298+1825T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68767904 | |||||||
| chr10:68768075 | T | C | 36 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(33): Show |
37 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.2298+1996T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68768075 | |||||||
| chr10:68768304 | CT | C | 36 | a0001c0003t0002g0047 a0001c0003t0002g0048 a0001c0003t0002g0051 others(33): Show |
36 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.2298+2236delT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr10 | 68768304 | ||||||
| chr10:68768428 | C | T | 1 | a0001c0001t0001g0212 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2298+2349C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68768428 | |||||||
| chr10:68768533 | C | T | 2 | a0001c0001t0001g0183 a0001c0002t0001g0096 |
2 | HG01243.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.2298+2454C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68768533 | |||||||
| chr10:68768577 | C | T | 3 | a0001c0003t0001g0337 a0001c0003t0001g0338 a0001c0003t0001g0339 |
3 | HG02572.hp2 NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2298+2498C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68768577 | |||||||
| chr10:68768638 | A | G | 9 | a0001c0003t0002g0051 a0001c0003t0002g0052 a0001c0003t0002g0053 others(6): Show |
9 | HG02015.hp2 HG02074.hp1 HG02083.hp2 others(6): Show |
intron_variant | MODIFIER | c.2298+2559A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68768638 | |||||||
| chr10:68768734 | C | T | 12 | a0001c0003t0002g0061 a0001c0003t0002g0062 a0001c0003t0002g0063 others(9): Show |
12 | HG01081.hp1 HG02559.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.2299-2472C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68768734 | |||||||
| chr10:68768787 | A | G | 9 | a0001c0003t0002g0064 a0001c0003t0002g0065 a0001c0003t0002g0066 others(6): Show |
9 | HG01081.hp1 HG02559.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.2299-2419A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68768787 | |||||||
| chr10:68768919 | A | G | 2 | a0001c0001t0001g0081 a0001c0001t0001g0089 |
2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2299-2287A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68768919 | |||||||
| chr10:68768968 | A | G | 1 | a0001c0002t0001g0096 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2299-2238A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68768968 | |||||||
| chr10:68769218 | C | A | 2 | a0001c0001t0001g0277 a0001c0001t0001g0282 |
2 | HG03942.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.2299-1988C>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68769218 | |||||||
| chr10:68769253 | C | T | 190 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(187): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.2299-1953C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68769253 | |||||||
| chr10:68769295 | T | G | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2299-1911T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68769295 | |||||||
| chr10:68769367 | T | A | 64 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(61): Show |
64 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.2299-1839T>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68769367 | |||||||
| chr10:68769379 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2299-1827G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68769379 | |||||||
| chr10:68769502 | C | A | 16 | a0001c0003t0002g0047 a0001c0003t0002g0048 a0001c0003t0002g0051 others(13): Show |
16 | HG00639.hp2 HG01433.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.2299-1704C>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68769502 | |||||||
| chr10:68769519 | C | G | 5 | a0001c0003t0002g0073 a0001c0003t0002g0074 a0001c0003t0002g0075 others(2): Show |
5 | HG02486.hp2 HG02647.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2299-1687C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68769519 | |||||||
| chr10:68769655 | A | G | 1 | a0001c0001t0001g0177 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.2299-1551A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68769655 | |||||||
| chr10:68769667 | C | T | 1 | a0001c0002t0001g0130 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2299-1539C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68769667 | |||||||
| chr10:68769758 | G | A | 15 | a0001c0001t0001g0293 a0001c0003t0002g0047 a0001c0003t0002g0048 others(12): Show |
15 | HG00639.hp2 HG01433.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.2299-1448G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68769758 | |||||||
| chr10:68769828 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2299-1378C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68769828 | |||||||
| chr10:68769940 | C | CA | 30 | a0001c0001t0001g0100 a0001c0001t0001g0169 a0001c0001t0001g0196 others(27): Show |
30 | HG00735.hp1 HG01109.hp2 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.2299-1244dupA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr10 | 68769940 | ||||||
| chr10:68769940 | CA | C | 55 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(52): Show |
55 | HG00639.hp1 HG00741.hp1 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.2299-1244delA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr10 | 68769940 | ||||||
| chr10:68770068 | G | A | 38 | a0001c0001t0007g0350 a0001c0001t0007g0351 a0001c0003t0002g0047 others(35): Show |
38 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.2299-1138G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68770068 | |||||||
| chr10:68770160 | A | G | 191 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(188): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.2299-1046A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68770160 | |||||||
| chr10:68770206 | A | G | 36 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(33): Show |
37 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.2299-1000A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68770206 | |||||||
| chr10:68770418 | T | A | 1 | a0001c0003t0002g0062 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2299-788T>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68770418 | |||||||
| chr10:68770423 | G | C | 1 | a0001c0003t0002g0062 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2299-783G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68770423 | |||||||
| chr10:68770635 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2299-571C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68770635 | |||||||
| chr10:68770762 | A | G | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG01106.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2299-444A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68770762 | |||||||
| chr10:68770805 | C | T | 7 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(4): Show |
7 | HG01109.hp1 HG02717.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.2299-401C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68770805 | |||||||
| chr10:68770816 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2299-390G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68770816 | |||||||
| chr10:68770880 | A | T | 36 | a0001c0003t0002g0047 a0001c0003t0002g0048 a0001c0003t0002g0051 others(33): Show |
36 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.2299-326A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68770880 | |||||||
| chr10:68770889 | G | A | 1 | a0001c0001t0001g0259 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2299-317G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68770889 | |||||||
| chr10:68770917 | A | T | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2299-289A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68770917 | |||||||
| chr10:68770947 | G | A | 2 | a0001c0002t0001g0106 a0001c0002t0001g0108 |
2 | HG02145.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2299-259G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68770947 | |||||||
| chr10:68770994 | C | T | 23 | a0001c0003t0002g0047 a0001c0003t0002g0048 a0001c0003t0002g0051 others(20): Show |
23 | HG00639.hp2 HG01433.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.2299-212C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68770994 | |||||||
| chr10:68771064 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2299-142C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68771064 | |||||||
| chr10:68771080 | A | G | 1 | a0001c0003t0002g0062 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2299-126A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68771080 | |||||||
| chr10:68771192 | A | G | 1 | a0001c0002t0001g0130 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2299-14A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 17/24 | chr10 | 68771192 | |||||||
| chr10:68771460 | C | T | 189 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(186): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.2538+15C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 18/24 | chr10 | 68771460 | |||||||
| chr10:68771642 | A | G | 2 | a0002c0005t0008g0049 a0002c0005t0008g0050 |
2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2538+197A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 18/24 | chr10 | 68771642 | |||||||
| chr10:68771643 | C | T | 2 | a0002c0005t0008g0049 a0002c0005t0008g0050 |
2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2538+198C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 18/24 | chr10 | 68771643 | |||||||
| chr10:68771644 | A | C | 2 | a0002c0005t0008g0049 a0002c0005t0008g0050 |
2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2538+199A>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 18/24 | chr10 | 68771644 | |||||||
| chr10:68771645 | T | A | 2 | a0002c0005t0008g0049 a0002c0005t0008g0050 |
2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2538+200T>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 18/24 | chr10 | 68771645 | |||||||
| chr10:68771826 | T | G | 4 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(1): Show |
4 | HG02145.hp2 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2538+381T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 18/24 | chr10 | 68771826 | |||||||
| chr10:68771835 | A | G | 1 | a0001c0001t0001g0014 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2538+390A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 18/24 | chr10 | 68771835 | |||||||
| chr10:68771852 | A | G | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG01106.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2538+407A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 18/24 | chr10 | 68771852 | |||||||
| chr10:68771866 | A | T | 1 | a0001c0001t0001g0302 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2538+421A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 18/24 | chr10 | 68771866 | |||||||
| chr10:68771887 | G | GA | 36 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(33): Show |
37 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.2538+443dupA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr10 | 68771887 | ||||||
| chr10:68771897 | T | C | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2538+452T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 18/24 | chr10 | 68771897 | |||||||
| chr10:68771923 | T | G | 1 | a0001c0001t0001g0037 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2538+478T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 18/24 | chr10 | 68771923 | |||||||
| chr10:68772308 | C | T | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2539-680C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 18/24 | chr10 | 68772308 | |||||||
| chr10:68772315 | T | A | 1 | a0001c0001t0001g0188 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.2539-673T>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 18/24 | chr10 | 68772315 | |||||||
| chr10:68772316 | C | A | 1 | a0001c0001t0001g0188 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.2539-672C>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 18/24 | chr10 | 68772316 | |||||||
| chr10:68772724 | C | G | 4 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(1): Show |
4 | HG02145.hp2 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2539-264C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 18/24 | chr10 | 68772724 | |||||||
| chr10:68772757 | C | CA | 8 | a0001c0001t0001g0197 a0001c0001t0001g0307 a0001c0001t0001g0310 others(5): Show |
8 | HG01109.hp2 HG01192.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.2539-218dupA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr10 | 68772757 | ||||||
| chr10:68772757 | CA | C | 74 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(71): Show |
74 | HG00639.hp1 HG00639.hp2 HG00741.hp1 others(71): Show |
intron_variant | MODIFIER | c.2539-218delA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr10 | 68772757 | ||||||
| chr10:68772915 | A | C | 3 | a0001c0004t0001g0265 a0001c0004t0001g0266 a0001c0004t0001g0322 |
3 | HG01515.hp1 HG01517.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.2539-73A>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 18/24 | chr10 | 68772915 | |||||||
| chr10:68773170 | C | A | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2650+71C>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68773170 | |||||||
| chr10:68773200 | T | G | 1 | a0001c0001t0001g0309 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2650+101T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68773200 | |||||||
| chr10:68773233 | G | A | 64 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(61): Show |
64 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.2650+134G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68773233 | |||||||
| chr10:68773342 | G | A | 4 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0036 others(1): Show |
4 | HG01123.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.2650+243G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68773342 | |||||||
| chr10:68773416 | A | T | 1 | a0001c0001t0001g0304 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2650+317A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68773416 | |||||||
| chr10:68773420 | T | C | 1 | a0001c0001t0001g0257 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2650+321T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68773420 | |||||||
| chr10:68773436 | G | A | 1 | a0001c0004t0001g0272 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2650+337G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68773436 | |||||||
| chr10:68773452 | A | G | 189 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(186): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.2650+353A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68773452 | |||||||
| chr10:68773535 | G | A | 2 | a0001c0001t0001g0184 a0001c0001t0001g0232 |
2 | HG03017.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.2650+436G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68773535 | |||||||
| chr10:68773546 | C | G | 2 | a0001c0001t0001g0164 a0001c0001t0001g0180 |
2 | NA18961.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.2650+447C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68773546 | |||||||
| chr10:68773665 | C | CA | 8 | a0001c0001t0001g0081 a0001c0001t0001g0089 a0001c0001t0001g0177 others(5): Show |
8 | HG02886.hp2 HG03453.hp1 NA18947.hp1 others(5): Show |
intron_variant | MODIFIER | c.2650+579dupA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr10 | 68773665 | ||||||
| chr10:68773678 | AT | A | 60 | a0001c0002t0001g0006 a0001c0002t0001g0091 a0001c0002t0001g0092 others(57): Show |
60 | HG00544.hp1 HG02040.hp1 HG02055.hp2 others(57): Show |
intron_variant | MODIFIER | c.2650+580delT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68773678 | |||||||
| chr10:68773707 | C | A | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2650+608C>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68773707 | |||||||
| chr10:68773822 | C | G | 1 | a0001c0002t0001g0128 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2650+723C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68773822 | |||||||
| chr10:68773884 | T | A | 1 | a0001c0001t0001g0197 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2650+785T>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68773884 | |||||||
| chr10:68773887 | A | T | 1 | a0001c0001t0001g0197 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2650+788A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68773887 | |||||||
| chr10:68773895 | T | G | 2 | a0001c0003t0002g0062 a0001c0008t0001g0284 |
2 | HG02135.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2650+796T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68773895 | |||||||
| chr10:68773904 | T | G | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2650+805T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68773904 | |||||||
| chr10:68774081 | G | C | 1 | a0001c0001t0001g0185 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2650+982G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68774081 | |||||||
| chr10:68774196 | T | C | 1 | a0001c0002t0001g0152 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2650+1097T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68774196 | |||||||
| chr10:68774320 | C | A | 2 | a0001c0001t0001g0082 a0001c0001t0001g0084 |
2 | HG03041.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2650+1221C>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68774320 | |||||||
| chr10:68774352 | T | C | 241 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(238): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.2650+1253T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68774352 | |||||||
| chr10:68774570 | G | T | 1 | a0001c0003t0002g0066 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2650+1471G>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68774570 | |||||||
| chr10:68774630 | C | CA | 8 | a0001c0001t0001g0081 a0001c0001t0001g0089 a0001c0001t0001g0311 others(5): Show |
8 | HG02145.hp1 HG02818.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.2650+1545dupA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr10 | 68774630 | ||||||
| chr10:68774713 | A | G | 1 | a0001c0001t0001g0344 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2650+1614A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68774713 | |||||||
| chr10:68774922 | T | A | 1 | a0001c0001t0001g0279 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2650+1823T>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68774922 | |||||||
| chr10:68774925 | G | A | 1 | a0001c0001t0001g0279 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2650+1826G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68774925 | |||||||
| chr10:68774954 | T | G | 14 | a0001c0003t0002g0047 a0001c0003t0002g0048 a0001c0003t0002g0051 others(11): Show |
14 | HG00639.hp2 HG01433.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.2650+1855T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68774954 | |||||||
| chr10:68774987 | A | C | 279 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(276): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.2650+1888A>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68774987 | |||||||
| chr10:68775194 | A | G | 36 | a0001c0003t0002g0047 a0001c0003t0002g0048 a0001c0003t0002g0051 others(33): Show |
36 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.2650+2095A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68775194 | |||||||
| chr10:68775497 | CT | C | 262 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(259): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.2650+2415delT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr10 | 68775497 | ||||||
| chr10:68775503 | T | C | 1 | a0001c0001t0018g0088 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2650+2404T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68775503 | |||||||
| chr10:68775508 | T | G | 13 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(10): Show |
13 | HG01106.hp2 HG01109.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.2650+2409T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68775508 | |||||||
| chr10:68775509 | T | G | 1 | a0001c0001t0001g0228 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2650+2410T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68775509 | |||||||
| chr10:68775511 | T | G | 1 | a0001c0003t0002g0352 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2650+2412T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68775511 | |||||||
| chr10:68775687 | C | CT | 30 | a0001c0002t0001g0006 a0001c0002t0001g0092 a0001c0002t0001g0094 others(27): Show |
30 | HG00639.hp2 HG01433.hp2 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.2650+2615dupT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr10 | 68775687 | ||||||
| chr10:68775687 | C | CTT | 13 | a0001c0002t0001g0091 a0001c0003t0002g0051 a0001c0003t0002g0060 others(10): Show |
13 | HG01081.hp1 HG01891.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.2650+2614_2650+261 others(6): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr10 | 68775687 | ||||||
| chr10:68775687 | CT | C | 49 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(46): Show |
50 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.2650+2615delT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr10 | 68775687 | ||||||
| chr10:68775687 | CTTT | C | 11 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0214 others(8): Show |
11 | HG01106.hp1 HG01175.hp1 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.2650+2613_2650+261 others(7): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr10 | 68775687 | ||||||
| chr10:68775687 | CTTTT | C | 169 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(166): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.2650+2612_2650+261 others(8): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr10 | 68775687 | ||||||
| chr10:68775687 | CTTTTT | C | 11 | a0001c0001t0001g0174 a0001c0001t0001g0183 a0001c0001t0001g0223 others(8): Show |
11 | HG01261.hp1 HG01261.hp2 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.2650+2611_2650+261 others(9): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr10 | 68775687 | ||||||
| chr10:68775687 | CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0007g0350 a0001c0001t0007g0351 a0001c0007t0001g0280 |
3 | HG02280.hp1 HG02559.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2650+2604_2650+261 others(16): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr10 | 68775687 | ||||||
| chr10:68775907 | G | T | 1 | a0001c0002t0001g0119 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2650+2808G>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68775907 | |||||||
| chr10:68775970 | T | C | 348 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(345): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.2650+2871T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68775970 | |||||||
| chr10:68776065 | G | A | 3 | a0001c0001t0007g0350 a0001c0001t0007g0351 a0001c0001t0010g0353 |
3 | HG02280.hp1 HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.2650+2966G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68776065 | |||||||
| chr10:68776141 | A | G | 84 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(81): Show |
89 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.2650+3042A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68776141 | |||||||
| chr10:68776186 | A | G | 23 | a0001c0003t0002g0047 a0001c0003t0002g0048 a0001c0003t0002g0051 others(20): Show |
23 | HG00639.hp2 HG01433.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.2650+3087A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68776186 | |||||||
| chr10:68776235 | TTTTTC | T | 11 | a0001c0001t0001g0163 a0001c0001t0001g0219 a0001c0001t0001g0220 others(8): Show |
11 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.2650+3156_2650+316 others(9): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr10 | 68776235 | ||||||
| chr10:68776235 | TTTTTCTT others(3): Show |
T | 1 | a0001c0001t0001g0250 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2650+3151_2650+316 others(14): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr10 | 68776235 | ||||||
| chr10:68776236 | T | G | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2650+3137T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68776236 | |||||||
| chr10:68776255 | C | CT | 8 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0003t0001g0337 others(5): Show |
8 | HG01106.hp2 HG01515.hp1 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.2650+3168dupT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr10 | 68776255 | ||||||
| chr10:68776433 | GCGGATGC others(9): Show |
G | 4 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0001g0316 others(1): Show |
4 | NA18942.hp1 NA18956.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.2650+3336_2650+335 others(20): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr10 | 68776433 | ||||||
| chr10:68776435 | G | A | 16 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(13): Show |
16 | HG01257.hp2 HG01934.hp2 HG01952.hp2 others(13): Show |
intron_variant | MODIFIER | c.2650+3336G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68776435 | |||||||
| chr10:68776515 | G | A | 1 | a0001c0001t0001g0345 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2650+3416G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68776515 | |||||||
| chr10:68776562 | G | A | 36 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(33): Show |
37 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.2650+3463G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68776562 | |||||||
| chr10:68776658 | GTCC | G | 3 | a0001c0002t0001g0137 a0001c0002t0001g0148 a0001c0002t0001g0149 |
3 | NA18980.hp1 NA18994.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.2650+3568_2650+357 others(7): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr10 | 68776658 | ||||||
| chr10:68776816 | C | G | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2650+3717C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68776816 | |||||||
| chr10:68776817 | T | C | 1 | a0001c0001t0001g0008 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2650+3718T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68776817 | |||||||
| chr10:68776937 | G | A | 279 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(276): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.2650+3838G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68776937 | |||||||
| chr10:68777060 | C | G | 2 | a0002c0005t0008g0049 a0002c0005t0008g0050 |
2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2650+3961C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68777060 | |||||||
| chr10:68777158 | G | C | 1 | a0001c0001t0001g0249 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.2650+4059G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68777158 | |||||||
| chr10:68777166 | C | G | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2650+4067C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68777166 | |||||||
| chr10:68777176 | C | G | 87 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(84): Show |
92 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.2650+4077C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68777176 | |||||||
| chr10:68777273 | C | A | 1 | a0001c0003t0002g0058 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2650+4174C>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68777273 | |||||||
| chr10:68777435 | C | T | 1 | a0001c0001t0001g0349 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2650+4336C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68777435 | |||||||
| chr10:68777544 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2650+4445C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68777544 | |||||||
| chr10:68777552 | C | T | 3 | a0001c0003t0002g0047 a0001c0003t0002g0048 a0001c0003t0002g0056 |
3 | HG00639.hp2 HG01433.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.2650+4453C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68777552 | |||||||
| chr10:68777683 | C | CA | 46 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(43): Show |
47 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.2650+4597dupA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr10 | 68777683 | ||||||
| chr10:68777699 | C | G | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2650+4600C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68777699 | |||||||
| chr10:68777789 | G | A | 1 | a0001c0001t0001g0341 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2650+4690G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68777789 | |||||||
| chr10:68777817 | A | T | 5 | a0001c0003t0002g0073 a0001c0003t0002g0074 a0001c0003t0002g0075 others(2): Show |
5 | HG02486.hp2 HG02647.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2650+4718A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68777817 | |||||||
| chr10:68777837 | T | A | 2 | a0001c0001t0003g0044 a0001c0001t0003g0045 |
2 | NA18939.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.2650+4738T>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68777837 | |||||||
| chr10:68777909 | A | G | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2650+4810A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68777909 | |||||||
| chr10:68777943 | G | A | 6 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(3): Show |
6 | HG01109.hp1 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2650+4844G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68777943 | |||||||
| chr10:68778214 | T | C | 5 | a0001c0003t0002g0073 a0001c0003t0002g0074 a0001c0003t0002g0075 others(2): Show |
5 | HG02486.hp2 HG02647.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2650+5115T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68778214 | |||||||
| chr10:68778310 | G | A | 1 | a0001c0001t0001g0301 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2650+5211G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68778310 | |||||||
| chr10:68778531 | C | CT | 6 | a0001c0002t0001g0125 a0001c0002t0001g0134 a0001c0002t0001g0136 others(3): Show |
6 | HG00544.hp1 HG02040.hp1 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.2650+5443dupT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr10 | 68778531 | ||||||
| chr10:68778532 | T | TA | 279 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(276): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.2650+5433_2650+543 others(5): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68778532 | |||||||
| chr10:68778773 | A | G | 13 | a0001c0001t0001g0005 a0001c0001t0001g0168 a0001c0001t0001g0196 others(10): Show |
14 | NA18939.hp1 NA18940.hp1 NA18946.hp2 others(11): Show |
intron_variant | MODIFIER | c.2650+5674A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68778773 | |||||||
| chr10:68778820 | C | T | 1 | a0001c0001t0001g0344 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2650+5721C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68778820 | |||||||
| chr10:68778874 | C | T | 4 | a0001c0001t0001g0021 a0001c0001t0001g0038 a0001c0001t0001g0081 others(1): Show |
4 | HG02886.hp2 HG03453.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.2650+5775C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68778874 | |||||||
| chr10:68778882 | C | T | 1 | a0001c0001t0001g0296 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2650+5783C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68778882 | |||||||
| chr10:68779146 | A | C | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2650+6047A>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68779146 | |||||||
| chr10:68779230 | A | G | 1 | a0001c0001t0001g0283 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2650+6131A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68779230 | |||||||
| chr10:68779261 | CT | C | 274 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(271): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.2650+6176delT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr10 | 68779261 | ||||||
| chr10:68779296 | C | T | 3 | a0001c0003t0002g0047 a0001c0003t0002g0048 a0001c0003t0002g0056 |
3 | HG00639.hp2 HG01433.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.2650+6197C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68779296 | |||||||
| chr10:68779367 | C | T | 1 | a0001c0003t0002g0052 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2650+6268C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68779367 | |||||||
| chr10:68779372 | C | G | 2 | a0001c0003t0002g0064 a0001c0003t0002g0065 |
2 | HG01081.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2650+6273C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68779372 | |||||||
| chr10:68779414 | A | T | 5 | a0001c0003t0002g0073 a0001c0003t0002g0074 a0001c0003t0002g0075 others(2): Show |
5 | HG02486.hp2 HG02647.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2650+6315A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68779414 | |||||||
| chr10:68779526 | C | T | 3 | a0001c0001t0007g0350 a0001c0001t0007g0351 a0001c0001t0009g0013 |
3 | HG01346.hp2 HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2650+6427C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68779526 | |||||||
| chr10:68779632 | G | A | 2 | a0001c0001t0001g0081 a0001c0001t0001g0089 |
2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2651-6504G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68779632 | |||||||
| chr10:68779772 | A | G | 6 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(3): Show |
6 | HG01109.hp1 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2651-6364A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68779772 | |||||||
| chr10:68779938 | T | C | 9 | a0001c0003t0002g0051 a0001c0003t0002g0052 a0001c0003t0002g0053 others(6): Show |
9 | HG02015.hp2 HG02074.hp1 HG02083.hp2 others(6): Show |
intron_variant | MODIFIER | c.2651-6198T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68779938 | |||||||
| chr10:68779987 | ACT | A | 3 | a0001c0002t0001g0137 a0001c0002t0001g0148 a0001c0002t0001g0149 |
3 | NA18980.hp1 NA18994.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.2651-6145_2651-614 others(6): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr10 | 68779987 | ||||||
| chr10:68780079 | G | A | 5 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0021 others(2): Show |
5 | HG01934.hp1 NA18747.hp2 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.2651-6057G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68780079 | |||||||
| chr10:68780172 | A | G | 2 | a0001c0001t0001g0081 a0001c0001t0001g0089 |
2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2651-5964A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68780172 | |||||||
| chr10:68780231 | T | C | 6 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(3): Show |
6 | HG01109.hp1 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2651-5905T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68780231 | |||||||
| chr10:68780297 | T | G | 1 | a0001c0001t0001g0245 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2651-5839T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68780297 | |||||||
| chr10:68780464 | A | G | 7 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(4): Show |
7 | HG01109.hp1 HG02717.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.2651-5672A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68780464 | |||||||
| chr10:68780503 | T | G | 2 | a0001c0001t0001g0097 a0001c0001t0001g0100 |
2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2651-5633T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68780503 | |||||||
| chr10:68780594 | G | T | 1 | a0001c0001t0001g0293 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2651-5542G>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68780594 | |||||||
| chr10:68780737 | A | G | 1 | a0001c0002t0001g0096 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2651-5399A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68780737 | |||||||
| chr10:68780867 | A | G | 1 | a0001c0001t0001g0246 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2651-5269A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68780867 | |||||||
| chr10:68780875 | G | A | 7 | a0001c0003t0002g0066 a0001c0003t0004g0067 a0001c0003t0004g0068 others(4): Show |
7 | HG02559.hp1 HG02647.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.2651-5261G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68780875 | |||||||
| chr10:68780901 | A | G | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2651-5235A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68780901 | |||||||
| chr10:68781105 | G | A | 10 | a0001c0001t0001g0163 a0001c0001t0001g0219 a0001c0001t0001g0220 others(7): Show |
10 | HG01891.hp1 HG02486.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.2651-5031G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68781105 | |||||||
| chr10:68781226 | C | T | 190 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(187): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.2651-4910C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68781226 | |||||||
| chr10:68781278 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2651-4858C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68781278 | |||||||
| chr10:68781400 | G | A | 1 | a0001c0001t0001g0286 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.2651-4736G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68781400 | |||||||
| chr10:68781436 | G | A | 2 | a0001c0001t0001g0345 a0001c0003t0001g0337 |
2 | HG01175.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2651-4700G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68781436 | |||||||
| chr10:68781505 | G | A | 2 | a0001c0001t0001g0081 a0001c0001t0001g0089 |
2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2651-4631G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68781505 | |||||||
| chr10:68781624 | C | A | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2651-4512C>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68781624 | |||||||
| chr10:68781657 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2651-4479C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68781657 | |||||||
| chr10:68781844 | C | CT | 196 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(193): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.2651-4291dupT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr10 | 68781844 | ||||||
| chr10:68781987 | C | G | 1 | a0001c0002t0001g0145 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2651-4149C>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68781987 | |||||||
| chr10:68782207 | A | G | 2 | a0001c0001t0001g0275 a0001c0001t0001g0276 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2651-3929A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68782207 | |||||||
| chr10:68782279 | A | G | 6 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(3): Show |
6 | HG01109.hp1 HG02976.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2651-3857A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68782279 | |||||||
| chr10:68782321 | G | A | 1 | a0001c0002t0001g0159 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.2651-3815G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68782321 | |||||||
| chr10:68782709 | T | C | 13 | a0001c0001t0001g0005 a0001c0001t0001g0168 a0001c0001t0001g0196 others(10): Show |
14 | NA18939.hp1 NA18940.hp1 NA18946.hp2 others(11): Show |
intron_variant | MODIFIER | c.2651-3427T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68782709 | |||||||
| chr10:68782821 | T | C | 2 | a0001c0001t0001g0283 a0001c0001t0001g0297 |
2 | HG01243.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.2651-3315T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68782821 | |||||||
| chr10:68782833 | G | A | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2651-3303G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68782833 | |||||||
| chr10:68782882 | T | G | 196 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(193): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.2651-3254T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68782882 | |||||||
| chr10:68783000 | CT | C | 261 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(258): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.2651-3116delT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr10 | 68783000 | ||||||
| chr10:68783114 | C | T | 36 | a0001c0003t0002g0047 a0001c0003t0002g0048 a0001c0003t0002g0051 others(33): Show |
36 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.2651-3022C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68783114 | |||||||
| chr10:68783212 | C | T | 8 | a0001c0003t0002g0051 a0001c0003t0002g0052 a0001c0003t0002g0053 others(5): Show |
8 | HG02015.hp2 HG02074.hp1 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.2651-2924C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68783212 | |||||||
| chr10:68783267 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2651-2869G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68783267 | |||||||
| chr10:68783322 | C | T | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2651-2814C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68783322 | |||||||
| chr10:68783323 | A | G | 39 | a0001c0001t0007g0350 a0001c0001t0007g0351 a0001c0001t0010g0353 others(36): Show |
39 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.2651-2813A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68783323 | |||||||
| chr10:68783371 | C | A | 1 | a0001c0001t0001g0287 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2651-2765C>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68783371 | |||||||
| chr10:68783482 | T | A | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2651-2654T>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68783482 | |||||||
| chr10:68783519 | A | C | 1 | a0001c0001t0001g0009 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2651-2617A>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68783519 | |||||||
| chr10:68783528 | A | T | 1 | a0001c0001t0001g0085 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2651-2608A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68783528 | |||||||
| chr10:68783588 | T | C | 1 | a0001c0001t0001g0014 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2651-2548T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68783588 | |||||||
| chr10:68783638 | A | G | 1 | a0001c0001t0001g0341 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2651-2498A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68783638 | |||||||
| chr10:68783696 | A | G | 3 | a0001c0001t0001g0188 a0001c0001t0001g0193 a0001c0001t0001g0336 |
3 | HG01071.hp2 HG02300.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.2651-2440A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68783696 | |||||||
| chr10:68783844 | G | A | 1 | a0001c0001t0001g0189 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2651-2292G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68783844 | |||||||
| chr10:68783899 | C | T | 1 | a0001c0001t0018g0088 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2651-2237C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68783899 | |||||||
| chr10:68783949 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2651-2187G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68783949 | |||||||
| chr10:68783999 | C | A | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2651-2137C>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68783999 | |||||||
| chr10:68784001 | G | A | 1 | a0001c0003t0002g0064 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2651-2135G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68784001 | |||||||
| chr10:68784271 | A | C | 1 | a0001c0007t0001g0280 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2651-1865A>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68784271 | |||||||
| chr10:68784286 | G | A | 1 | a0001c0002t0001g0096 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2651-1850G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68784286 | |||||||
| chr10:68784446 | T | C | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2651-1690T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68784446 | |||||||
| chr10:68784506 | T | C | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2651-1630T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68784506 | |||||||
| chr10:68784561 | A | G | 1 | a0001c0003t0002g0060 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.2651-1575A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68784561 | |||||||
| chr10:68784650 | G | A | 3 | a0001c0001t0001g0188 a0001c0001t0001g0193 a0001c0001t0001g0336 |
3 | HG01071.hp2 HG02300.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.2651-1486G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68784650 | |||||||
| chr10:68784690 | A | C | 1 | a0001c0001t0003g0041 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2651-1446A>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68784690 | |||||||
| chr10:68784703 | T | C | 1 | a0002c0005t0008g0050 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2651-1433T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68784703 | |||||||
| chr10:68784706 | G | A | 1 | a0001c0001t0001g0245 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2651-1430G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68784706 | |||||||
| chr10:68784714 | C | A | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2651-1422C>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68784714 | |||||||
| chr10:68784792 | G | T | 3 | a0001c0002t0001g0106 a0001c0002t0001g0107 a0001c0002t0001g0108 |
3 | HG02145.hp1 HG02818.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2651-1344G>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68784792 | |||||||
| chr10:68784821 | T | C | 6 | a0001c0001t0001g0273 a0001c0001t0001g0274 a0001c0001t0001g0275 others(3): Show |
6 | HG01109.hp2 HG02055.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.2651-1315T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68784821 | |||||||
| chr10:68784915 | C | CT | 9 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0276 others(6): Show |
9 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.2651-1201dupT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr10 | 68784915 | ||||||
| chr10:68784915 | CT | C | 90 | a0001c0001t0001g0034 a0001c0001t0001g0082 a0001c0001t0001g0083 others(87): Show |
90 | HG00544.hp1 HG01081.hp1 HG01109.hp1 others(87): Show |
intron_variant | MODIFIER | c.2651-1201delT | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr10 | 68784915 | ||||||
| chr10:68784915 | CTT | C | 37 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(34): Show |
38 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.2651-1202_2651-120 others(6): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr10 | 68784915 | ||||||
| chr10:68784921 | T | A | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2651-1215T>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68784921 | |||||||
| chr10:68784942 | G | A | 2 | a0001c0001t0001g0033 a0001c0001t0016g0028 |
2 | HG00741.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.2651-1194G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68784942 | |||||||
| chr10:68784961 | C | T | 36 | a0001c0003t0002g0047 a0001c0003t0002g0048 a0001c0003t0002g0051 others(33): Show |
36 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.2651-1175C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68784961 | |||||||
| chr10:68784962 | G | A | 64 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(61): Show |
64 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.2651-1174G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68784962 | |||||||
| chr10:68784991 | C | A | 36 | a0001c0003t0002g0047 a0001c0003t0002g0048 a0001c0003t0002g0051 others(33): Show |
36 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.2651-1145C>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68784991 | |||||||
| chr10:68785043 | G | A | 1 | a0001c0002t0001g0128 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2651-1093G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68785043 | |||||||
| chr10:68785044 | A | G | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG01106.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2651-1092A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68785044 | |||||||
| chr10:68785074 | T | C | 36 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(33): Show |
37 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.2651-1062T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68785074 | |||||||
| chr10:68785184 | T | C | 2 | a0001c0001t0001g0098 a0001c0001t0001g0099 |
2 | HG02145.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2651-952T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68785184 | |||||||
| chr10:68785192 | C | T | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2651-944C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68785192 | |||||||
| chr10:68785251 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2651-885C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68785251 | |||||||
| chr10:68785282 | A | G | 2 | a0001c0001t0001g0002 a0001c0001t0009g0013 |
3 | HG01069.hp1 HG01071.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.2651-854A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68785282 | |||||||
| chr10:68785365 | C | T | 1 | a0001c0002t0001g0111 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2651-771C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68785365 | |||||||
| chr10:68785522 | G | A | 36 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(33): Show |
37 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.2651-614G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68785522 | |||||||
| chr10:68785524 | A | G | 1 | a0001c0001t0018g0088 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2651-612A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68785524 | |||||||
| chr10:68785691 | A | G | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2651-445A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68785691 | |||||||
| chr10:68785862 | A | T | 2 | a0001c0001t0001g0285 a0001c0001t0001g0305 |
2 | HG02717.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2651-274A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | chr10 | 68785862 | |||||||
| chr10:68785943 | TTTG | T | 3 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0216 |
3 | HG03516.hp1 HG06807.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2651-181_2651-179d others(5): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr10 | 68785943 | ||||||
| chr10:68786297 | T | G | 6 | a0001c0001t0001g0301 a0001c0001t0001g0306 a0001c0001t0001g0307 others(3): Show |
6 | HG01433.hp1 HG02630.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.2733+79T>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 20/24 | chr10 | 68786297 | |||||||
| chr10:68786351 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2733+133G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 20/24 | chr10 | 68786351 | |||||||
| chr10:68786372 | T | C | 1 | a0001c0001t0001g0004 | 2 | HG00738.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2733+154T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 20/24 | chr10 | 68786372 | |||||||
| chr10:68786399 | G | A | 1 | a0001c0001t0001g0004 | 2 | HG00738.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2734-147G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 20/24 | chr10 | 68786399 | |||||||
| chr10:68786466 | C | T | 36 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(33): Show |
37 | HG00741.hp1 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.2734-80C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 20/24 | chr10 | 68786466 | |||||||
| chr10:68786475 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2734-71C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 20/24 | chr10 | 68786475 | |||||||
| chr10:68786491 | G | A | 1 | a0001c0001t0001g0296 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2734-55G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 20/24 | chr10 | 68786491 | |||||||
| chr10:68786756 | G | C | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2880+64G>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 21/24 | chr10 | 68786756 | |||||||
| chr10:68786855 | C | T | 7 | a0001c0002t0001g0115 a0001c0002t0001g0122 a0001c0002t0001g0127 others(4): Show |
7 | NA18947.hp2 NA18949.hp1 NA18977.hp2 others(4): Show |
intron_variant | MODIFIER | c.2880+163C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 21/24 | chr10 | 68786855 | |||||||
| chr10:68786958 | G | A | 1 | a0001c0001t0001g0304 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2880+266G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 21/24 | chr10 | 68786958 | |||||||
| chr10:68787019 | A | G | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2880+327A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 21/24 | chr10 | 68787019 | |||||||
| chr10:68787027 | A | G | 1 | a0001c0001t0001g0246 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2880+335A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 21/24 | chr10 | 68787027 | |||||||
| chr10:68787194 | T | C | 1 | a0001c0002t0001g0124 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2880+502T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 21/24 | chr10 | 68787194 | |||||||
| chr10:68787295 | C | T | 3 | a0001c0001t0001g0168 a0001c0001t0001g0199 a0001c0001t0001g0251 |
3 | NA18975.hp1 NA18982.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.2880+603C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 21/24 | chr10 | 68787295 | |||||||
| chr10:68787526 | A | G | 1 | a0001c0001t0018g0088 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2881-401A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 21/24 | chr10 | 68787526 | |||||||
| chr10:68787530 | A | C | 1 | a0001c0001t0001g0195 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2881-397A>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 21/24 | chr10 | 68787530 | |||||||
| chr10:68787703 | C | T | 1 | a0001c0002t0001g0095 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2881-224C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 21/24 | chr10 | 68787703 | |||||||
| chr10:68787712 | G | A | 1 | a0001c0003t0002g0352 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2881-215G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 21/24 | chr10 | 68787712 | |||||||
| chr10:68787727 | C | T | 1 | a0001c0002t0001g0130 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2881-200C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 21/24 | chr10 | 68787727 | |||||||
| chr10:68787765 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2881-162G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 21/24 | chr10 | 68787765 | |||||||
| chr10:68787813 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2881-114C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 21/24 | chr10 | 68787813 | |||||||
| chr10:68788131 | TTTATA | T | 6 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0023 others(3): Show |
6 | HG01123.hp2 HG01256.hp1 HG01257.hp1 others(3): Show |
splice_acceptor_variant&splice_region_variant&intron_variant | HIGH | c.3002-6_3002-2delTT others(3): Show |
CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr10 | 68788131 | ||||||
| chr10:68788367 | C | T | 2 | a0001c0003t0002g0061 a0001c0003t0002g0063 |
2 | HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.3187+39C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 23/24 | chr10 | 68788367 | |||||||
| chr10:68788672 | A | G | 7 | a0001c0003t0002g0066 a0001c0003t0004g0067 a0001c0003t0004g0068 others(4): Show |
7 | HG02559.hp1 HG02647.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.3187+344A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 23/24 | chr10 | 68788672 | |||||||
| chr10:68788673 | T | C | 3 | a0001c0001t0007g0350 a0001c0001t0007g0351 a0001c0001t0010g0353 |
3 | HG02280.hp1 HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.3187+345T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 23/24 | chr10 | 68788673 | |||||||
| chr10:68788871 | T | C | 1 | a0001c0003t0002g0052 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.3187+543T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 23/24 | chr10 | 68788871 | |||||||
| chr10:68788908 | G | A | 9 | a0001c0003t0002g0064 a0001c0003t0002g0065 a0001c0003t0002g0066 others(6): Show |
9 | HG01081.hp1 HG02559.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.3187+580G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 23/24 | chr10 | 68788908 | |||||||
| chr10:68789399 | C | T | 1 | a0001c0002t0001g0151 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.3188-311C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 23/24 | chr10 | 68789399 | |||||||
| chr10:68789459 | C | T | 1 | a0001c0001t0010g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3188-251C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 23/24 | chr10 | 68789459 | |||||||
| chr10:68789481 | A | T | 2 | a0001c0001t0007g0350 a0001c0001t0007g0351 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.3188-229A>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 23/24 | chr10 | 68789481 | |||||||
| chr10:68789516 | G | A | 66 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(63): Show |
66 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.3188-194G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 23/24 | chr10 | 68789516 | |||||||
| chr10:68789613 | A | G | 1 | a0001c0002t0001g0120 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.3188-97A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 23/24 | chr10 | 68789613 | |||||||
| chr10:68790004 | G | A | 1 | a0001c0001t0001g0207 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3393+89G>A | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 24/24 | chr10 | 68790004 | |||||||
| chr10:68790354 | T | TA | 10 | a0001c0001t0001g0289 a0001c0001t0001g0303 a0001c0001t0001g0313 others(7): Show |
10 | HG01934.hp2 HG02293.hp1 NA18942.hp1 others(7): Show |
intron_variant | MODIFIER | c.3393+455dupA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr10 | 68790354 | ||||||
| chr10:68790354 | TA | T | 7 | a0001c0001t0001g0195 a0001c0001t0001g0276 a0001c0001t0007g0350 others(4): Show |
7 | HG00099.hp2 HG02280.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.3393+455delA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr10 | 68790354 | ||||||
| chr10:68790418 | A | G | 36 | a0001c0003t0002g0047 a0001c0003t0002g0048 a0001c0003t0002g0051 others(33): Show |
36 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.3393+503A>G | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 24/24 | chr10 | 68790418 | |||||||
| chr10:68790553 | G | T | 1 | a0001c0001t0001g0085 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3393+638G>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 24/24 | chr10 | 68790553 | |||||||
| chr10:68790589 | C | T | 1 | a0001c0001t0001g0239 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.3394-618C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 24/24 | chr10 | 68790589 | |||||||
| chr10:68790804 | T | C | 167 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0014 others(164): Show |
168 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(165): Show |
intron_variant | MODIFIER | c.3394-403T>C | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 24/24 | chr10 | 68790804 | |||||||
| chr10:68790864 | C | CA | 8 | a0001c0001t0001g0015 a0001c0001t0001g0032 a0001c0001t0001g0037 others(5): Show |
8 | HG01361.hp1 HG02602.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.3394-327dupA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr10 | 68790864 | ||||||
| chr10:68790864 | CA | C | 23 | a0001c0001t0001g0191 a0001c0001t0001g0249 a0001c0001t0001g0276 others(20): Show |
23 | HG00558.hp1 HG00639.hp2 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.3394-327delA | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr10 | 68790864 | ||||||
| chr10:68790887 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.3394-320C>T | CCAR1 | ENSG00000060339.14 | transcript | ENST00000265872.11 | protein_coding | 24/24 | chr10 | 68790887 |