Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9648 |
| ensemblid | ENSG00000135968.22 |
| hgncid | 23218 |
| symbol | GCC2 |
| name | GRIP and coiled-coil domain containing 2 |
| refseq_nuc | NM_181453.4 |
| refseq_prot | NP_852118.2 |
| ensembl_nuc | ENST00000309863.11 |
| ensembl_prot | ENSP00000307939.5 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 108449206 |
| end | 108509415 |
| strand | + |
| ver | v1.2 |
| region | chr2:108449206-108509415 |
| region5000 | chr2:108444206-108514415 |
| regionname0 | GCC2_chr2_108449206_108509415 |
| regionname5000 | GCC2_chr2_108444206_108514415 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 1684 | 252 | 75 | 47 | 71 | 16 | 42 | 64 | GCC2_chr2_108444206_108514415 | GCC2 | MEDLV others(1679): Show |
chr2 | 108444206 | 108514415 |
| a0002 | 0/0 | 1684 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | MEDLV others(1679): Show |
chr2 | 108444206 | 108514415 |
| a0003 | 0/0 | 1684 | 7 | 0 | 0 | 7 | 0 | 0 | 7 | GCC2_chr2_108444206_108514415 | GCC2 | MEDLV others(1679): Show |
chr2 | 108444206 | 108514415 |
| a0004 | 0/0 | 1684 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | MEDLV others(1679): Show |
chr2 | 108444206 | 108514415 |
| a0005 | 0/0 | 1684 | 2 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | MEDLV others(1679): Show |
chr2 | 108444206 | 108514415 |
| a0006 | 0/0 | 1684 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | MEDLV others(1679): Show |
chr2 | 108444206 | 108514415 |
| a0007 | 0/0 | 1684 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | MEDLV others(1679): Show |
chr2 | 108444206 | 108514415 |
| a0008 | 0/0 | 1684 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | MEDLV others(1679): Show |
chr2 | 108444206 | 108514415 |
| a0009 | 0/0 | 1684 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | MEDLV others(1679): Show |
chr2 | 108444206 | 108514415 |
| a0010 | 0/1 | 1684 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | MEDLV others(1679): Show |
chr2 | 108444206 | 108514415 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 5052 | 151 | 57 | 27 | 26 | 10 | 30 | GCC2_chr2_108444206_108514415 | GCC2 | ATGGA others(5047): Show |
chr2 | 108444206 | 108514415 | ||
| a0001c0002 | 0/0 | 5052 | 83 | 12 | 13 | 41 | 6 | 11 | GCC2_chr2_108444206_108514415 | GCC2 | ATGGA others(5047): Show |
chr2 | 108444206 | 108514415 | ||
| a0001c0005 | 0/0 | 5052 | 5 | 0 | 5 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | ATGGA others(5047): Show |
chr2 | 108444206 | 108514415 | ||
| a0001c0006 | 0/0 | 5052 | 4 | 4 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | ATGGA others(5047): Show |
chr2 | 108444206 | 108514415 | ||
| a0001c0008 | 0/0 | 5052 | 3 | 0 | 0 | 3 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | ATGGA others(5047): Show |
chr2 | 108444206 | 108514415 | ||
| a0001c0009 | 0/0 | 5052 | 2 | 0 | 2 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | ATGGA others(5047): Show |
chr2 | 108444206 | 108514415 | ||
| a0001c0011 | 0/0 | 5052 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | ATGGA others(5047): Show |
chr2 | 108444206 | 108514415 | ||
| a0001c0012 | 0/0 | 5052 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | ATGGA others(5047): Show |
chr2 | 108444206 | 108514415 | ||
| a0001c0015 | 0/0 | 5052 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | ATGGA others(5047): Show |
chr2 | 108444206 | 108514415 | ||
| a0001c0019 | 0/0 | 5052 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | ATGGA others(5047): Show |
chr2 | 108444206 | 108514415 | ||
| a0002c0004 | 0/0 | 5052 | 7 | 7 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | ATGGA others(5047): Show |
chr2 | 108444206 | 108514415 | ||
| a0003c0003 | 0/0 | 5052 | 7 | 0 | 0 | 7 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | ATGGA others(5047): Show |
chr2 | 108444206 | 108514415 | ||
| a0004c0007 | 0/0 | 5052 | 3 | 3 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | ATGGA others(5047): Show |
chr2 | 108444206 | 108514415 | ||
| a0005c0010 | 0/0 | 5052 | 2 | 1 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | ATGGA others(5047): Show |
chr2 | 108444206 | 108514415 | ||
| a0006c0017 | 0/0 | 5052 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | ATGGA others(5047): Show |
chr2 | 108444206 | 108514415 | ||
| a0007c0016 | 0/0 | 5052 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | ATGGA others(5047): Show |
chr2 | 108444206 | 108514415 | ||
| a0008c0014 | 0/0 | 5052 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | ATGGA others(5047): Show |
chr2 | 108444206 | 108514415 | ||
| a0009c0018 | 0/0 | 5052 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | ATGGA others(5047): Show |
chr2 | 108444206 | 108514415 | ||
| a0010c0013 | 0/1 | 5052 | 1 | 0 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | ATGGA others(5047): Show |
chr2 | 108444206 | 108514415 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 6910 | 39 | 10 | 7 | 13 | 2 | 7 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6905): Show |
chr2 | 108444206 | 108514415 |
| a0001c0001t0003 | 0/0 | 6910 | 24 | 5 | 4 | 2 | 2 | 11 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6905): Show |
chr2 | 108444206 | 108514415 |
| a0001c0001t0004 | 0/0 | 6910 | 14 | 1 | 6 | 0 | 2 | 5 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6905): Show |
chr2 | 108444206 | 108514415 |
| a0001c0001t0005 | 0/0 | 6910 | 10 | 8 | 2 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6905): Show |
chr2 | 108444206 | 108514415 |
| a0001c0001t0006 | 0/0 | 6910 | 9 | 0 | 1 | 6 | 0 | 2 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6905): Show |
chr2 | 108444206 | 108514415 |
| a0001c0001t0007 | 0/0 | 6910 | 7 | 7 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6905): Show |
chr2 | 108444206 | 108514415 |
| a0001c0001t0009 | 0/0 | 6910 | 5 | 4 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6905): Show |
chr2 | 108444206 | 108514415 |
| a0001c0001t0010 | 0/0 | 6910 | 5 | 4 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6905): Show |
chr2 | 108444206 | 108514415 |
| a0001c0001t0011 | 0/0 | 6910 | 5 | 4 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6905): Show |
chr2 | 108444206 | 108514415 |
| a0001c0001t0015 | 0/0 | 6910 | 3 | 0 | 3 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6905): Show |
chr2 | 108444206 | 108514415 |
| a0001c0001t0016 | 0/0 | 6910 | 3 | 0 | 0 | 3 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6905): Show |
chr2 | 108444206 | 108514415 |
| a0001c0001t0017 | 0/0 | 6910 | 3 | 0 | 0 | 0 | 0 | 3 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6905): Show |
chr2 | 108444206 | 108514415 |
| a0001c0001t0019 | 0/0 | 6910 | 2 | 1 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6905): Show |
chr2 | 108444206 | 108514415 |
| a0001c0001t0024 | 0/0 | 6910 | 2 | 2 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6905): Show |
chr2 | 108444206 | 108514415 |
| a0001c0001t0025 | 0/0 | 6912 | 2 | 2 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6907): Show |
chr2 | 108444206 | 108514415 |
| a0001c0001t0026 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6905): Show |
chr2 | 108444206 | 108514415 |
| a0001c0001t0027 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6905): Show |
chr2 | 108444206 | 108514415 |
| a0001c0001t0028 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6905): Show |
chr2 | 108444206 | 108514415 |
| a0001c0001t0029 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6905): Show |
chr2 | 108444206 | 108514415 |
| a0001c0001t0033 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6905): Show |
chr2 | 108444206 | 108514415 |
| a0001c0001t0036 | 0/0 | 6912 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6907): Show |
chr2 | 108444206 | 108514415 |
| a0001c0001t0037 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6905): Show |
chr2 | 108444206 | 108514415 |
| a0001c0001t0038 | 0/0 | 6912 | 1 | 0 | 0 | 0 | 1 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6907): Show |
chr2 | 108444206 | 108514415 |
| a0001c0001t0039 | 0/0 | 6910 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6905): Show |
chr2 | 108444206 | 108514415 |
| a0001c0001t0040 | 0/0 | 6910 | 1 | 0 | 0 | 0 | 1 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6905): Show |
chr2 | 108444206 | 108514415 |
| a0001c0001t0041 | 1/0 | 6909 | 1 | 0 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6904): Show |
chr2 | 108444206 | 108514415 |
| a0001c0001t0042 | 0/0 | 6910 | 1 | 0 | 0 | 0 | 1 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6905): Show |
chr2 | 108444206 | 108514415 |
| a0001c0001t0043 | 0/0 | 6910 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6905): Show |
chr2 | 108444206 | 108514415 |
| a0001c0001t0044 | 0/0 | 6910 | 1 | 0 | 0 | 0 | 1 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6905): Show |
chr2 | 108444206 | 108514415 |
| a0001c0001t0045 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6905): Show |
chr2 | 108444206 | 108514415 |
| a0001c0001t0048 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6905): Show |
chr2 | 108444206 | 108514415 |
| a0001c0001t0049 | 0/0 | 6910 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6905): Show |
chr2 | 108444206 | 108514415 |
| a0001c0001t0053 | 0/0 | 6912 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6907): Show |
chr2 | 108444206 | 108514415 |
| a0001c0002t0001 | 0/0 | 6907 | 67 | 5 | 10 | 40 | 4 | 8 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6902): Show |
chr2 | 108444206 | 108514415 |
| a0001c0002t0008 | 0/0 | 6912 | 6 | 0 | 2 | 0 | 2 | 2 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6907): Show |
chr2 | 108444206 | 108514415 |
| a0001c0002t0013 | 0/0 | 6905 | 3 | 3 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6900): Show |
chr2 | 108444206 | 108514415 |
| a0001c0002t0021 | 0/0 | 6907 | 2 | 1 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6902): Show |
chr2 | 108444206 | 108514415 |
| a0001c0002t0023 | 0/0 | 6905 | 2 | 2 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6900): Show |
chr2 | 108444206 | 108514415 |
| a0001c0002t0034 | 0/0 | 6907 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6902): Show |
chr2 | 108444206 | 108514415 |
| a0001c0002t0035 | 0/0 | 6907 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6902): Show |
chr2 | 108444206 | 108514415 |
| a0001c0002t0052 | 0/0 | 6905 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6900): Show |
chr2 | 108444206 | 108514415 |
| a0001c0005t0001 | 0/0 | 6907 | 5 | 0 | 5 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6902): Show |
chr2 | 108444206 | 108514415 |
| a0001c0006t0018 | 0/0 | 6910 | 3 | 3 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6905): Show |
chr2 | 108444206 | 108514415 |
| a0001c0006t0032 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6905): Show |
chr2 | 108444206 | 108514415 |
| a0001c0008t0014 | 0/0 | 6910 | 3 | 0 | 0 | 3 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6905): Show |
chr2 | 108444206 | 108514415 |
| a0001c0009t0003 | 0/0 | 6910 | 2 | 0 | 2 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6905): Show |
chr2 | 108444206 | 108514415 |
| a0001c0011t0002 | 0/0 | 6910 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6905): Show |
chr2 | 108444206 | 108514415 |
| a0001c0012t0046 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6905): Show |
chr2 | 108444206 | 108514415 |
| a0001c0015t0001 | 0/0 | 6907 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6902): Show |
chr2 | 108444206 | 108514415 |
| a0001c0019t0010 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6905): Show |
chr2 | 108444206 | 108514415 |
| a0002c0004t0012 | 0/0 | 6910 | 4 | 4 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6905): Show |
chr2 | 108444206 | 108514415 |
| a0002c0004t0030 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6905): Show |
chr2 | 108444206 | 108514415 |
| a0002c0004t0031 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6905): Show |
chr2 | 108444206 | 108514415 |
| a0002c0004t0051 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6905): Show |
chr2 | 108444206 | 108514415 |
| a0003c0003t0003 | 0/0 | 6910 | 7 | 0 | 0 | 7 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6905): Show |
chr2 | 108444206 | 108514415 |
| a0004c0007t0022 | 0/0 | 6910 | 2 | 2 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6905): Show |
chr2 | 108444206 | 108514415 |
| a0004c0007t0047 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6905): Show |
chr2 | 108444206 | 108514415 |
| a0005c0010t0020 | 0/0 | 6907 | 2 | 1 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6902): Show |
chr2 | 108444206 | 108514415 |
| a0006c0017t0050 | 0/0 | 6910 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6905): Show |
chr2 | 108444206 | 108514415 |
| a0007c0016t0002 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6905): Show |
chr2 | 108444206 | 108514415 |
| a0008c0014t0009 | 0/0 | 6910 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6905): Show |
chr2 | 108444206 | 108514415 |
| a0009c0018t0001 | 0/0 | 6907 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6902): Show |
chr2 | 108444206 | 108514415 |
| a0010c0013t0008 | 0/1 | 6912 | 1 | 0 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | AGAGG others(6907): Show |
chr2 | 108444206 | 108514415 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0003g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0004g0001 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0004g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0004g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0004g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0004g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0004g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0004g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0004g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0004g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0004g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0004g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0004g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0005g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0005g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0005g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0005g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0005g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0005g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0005g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0005g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0005g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0006g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0006g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0006g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0006g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0006g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0006g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0006g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0006g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0006g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0007g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0007g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0007g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0007g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0007g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0007g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0009g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0009g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0009g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0009g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0009g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0010g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0010g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0010g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0010g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0010g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0011g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0011g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0011g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0011g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0011g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0015g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0015g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0015g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0016g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0016g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0016g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0017g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0017g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0017g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0019g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0019g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0024g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0024g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0025g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0025g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0026g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0027g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0028g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0029g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0033g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0036g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0037g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0038g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0039g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0040g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0041g0245 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0042g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0043g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0044g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0045g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0048g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0049g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0001t0053g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0008g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0008g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0008g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0008g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0008g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0008g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0013g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0013g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0013g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0021g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0021g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0023g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0023g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0034g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0035g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0002t0052g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0005t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0005t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0005t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0005t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0005t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0006t0018g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0006t0018g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0006t0018g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0006t0032g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0008t0014g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0008t0014g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0008t0014g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0009t0003g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0011t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0012t0046g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0015t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0001c0019t0010g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0002c0004t0012g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0002c0004t0012g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0002c0004t0012g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0002c0004t0012g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0002c0004t0030g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0002c0004t0031g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0002c0004t0051g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0003c0003t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0003c0003t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0003c0003t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0003c0003t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0003c0003t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0003c0003t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0003c0003t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0004c0007t0022g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0004c0007t0022g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0004c0007t0047g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0005c0010t0020g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0005c0010t0020g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0006c0017t0050g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0007c0016t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0008c0014t0009g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0009c0018t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| a0010c0013t0008g0091 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0069 | EUR | GBR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0211 | EUR | GBR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0038 | EUR | GBR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0001 | EUR | GBR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG00280 | hp1 | a0001 | c0001 | t0004 | g0001 | EUR | FIN | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0037 | EUR | FIN | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0101 | EUR | FIN | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG00323 | hp2 | a0001 | c0002 | t0008 | g0021 | EUR | FIN | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0142 | AMR | PUR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG00639 | hp2 | a0001 | c0002 | t0008 | g0019 | AMR | PUR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG00642 | hp1 | a0001 | c0001 | t0015 | g0240 | AMR | PUR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG00642 | hp2 | a0001 | c0001 | t0053 | g0172 | AMR | PUR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG00673 | hp1 | a0001 | c0015 | t0001 | g0070 | EAS | CHS | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0071 | EAS | CHS | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0199 | AMR | PUR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0197 | AMR | PUR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0244 | AMR | PUR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0205 | AMR | PUR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0068 | AMR | PUR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0022 | AMR | PUR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG01074 | hp1 | a0001 | c0001 | t0005 | g0004 | AMR | PUR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0145 | AMR | PUR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG01099 | hp1 | a0001 | c0001 | t0004 | g0247 | AMR | PUR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG01099 | hp2 | a0001 | c0001 | t0005 | g0094 | AMR | PUR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG01106 | hp1 | a0001 | c0001 | t0004 | g0248 | AMR | PUR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0060 | AMR | PUR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0017 | AMR | PUR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG01109 | hp2 | a0001 | c0001 | t0006 | g0222 | AMR | PUR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG01167 | hp1 | a0001 | c0005 | t0001 | g0029 | AMR | PUR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0151 | AMR | PUR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG01175 | hp1 | a0001 | c0001 | t0009 | g0218 | AMR | PUR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG01175 | hp2 | a0001 | c0001 | t0015 | g0243 | AMR | PUR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG01192 | hp1 | a0001 | c0002 | t0034 | g0074 | AMR | PUR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG01192 | hp2 | a0001 | c0001 | t0004 | g0236 | AMR | PUR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0206 | AMR | PUR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG01243 | hp2 | a0001 | c0001 | t0011 | g0140 | AMR | PUR | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG01256 | hp1 | a0001 | c0002 | t0008 | g0018 | AMR | CLM | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG01256 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | CLM | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG01257 | hp1 | a0001 | c0001 | t0015 | g0241 | AMR | CLM | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG01257 | hp2 | a0001 | c0009 | t0003 | g0005 | AMR | CLM | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG01258 | hp1 | a0001 | c0009 | t0003 | g0005 | AMR | CLM | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG01258 | hp2 | a0001 | c0001 | t0004 | g0237 | AMR | CLM | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG01261 | hp1 | a0006 | c0017 | t0050 | g0162 | AMR | CLM | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG01261 | hp2 | a0001 | c0001 | t0043 | g0242 | AMR | CLM | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0039 | AMR | CLM | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0176 | AMR | CLM | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0132 | AMR | CLM | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG01361 | hp2 | a0001 | c0005 | t0001 | g0053 | AMR | CLM | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG01515 | hp1 | a0001 | c0001 | t0042 | g0249 | EUR | IBS | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG01515 | hp2 | a0001 | c0001 | t0044 | g0233 | EUR | IBS | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG01516 | hp1 | a0001 | c0001 | t0040 | g0171 | EUR | IBS | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG01516 | hp2 | a0001 | c0001 | t0038 | g0246 | EUR | IBS | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG01884 | hp1 | a0001 | c0001 | t0025 | g0100 | AFR | ACB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG01884 | hp2 | a0001 | c0001 | t0007 | g0258 | AFR | ACB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG01891 | hp1 | a0001 | c0001 | t0007 | g0261 | AFR | ACB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0115 | AFR | ACB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0013 | AMR | PEL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG01928 | hp2 | a0001 | c0005 | t0001 | g0052 | AMR | PEL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG01981 | hp1 | a0001 | c0005 | t0001 | g0034 | AMR | PEL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0106 | AMR | PEL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0213 | AMR | PEL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0043 | AMR | PEL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0050 | EAS | KHV | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02040 | hp2 | a0005 | c0010 | t0020 | g0157 | EAS | KHV | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02055 | hp1 | a0001 | c0001 | t0011 | g0131 | AFR | ACB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02055 | hp2 | a0001 | c0001 | t0024 | g0256 | AFR | ACB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0105 | EAS | KHV | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0042 | EAS | KHV | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0174 | AFR | ACB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02145 | hp2 | a0001 | c0001 | t0005 | g0103 | AFR | ACB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02148 | hp1 | a0001 | c0005 | t0001 | g0051 | AMR | PEL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0062 | AMR | PEL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02257 | hp1 | a0001 | c0001 | t0029 | g0216 | AFR | ACB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02257 | hp2 | a0001 | c0001 | t0033 | g0260 | AFR | ACB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0136 | AFR | ACB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02258 | hp2 | a0002 | c0004 | t0012 | g0165 | AFR | ACB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02280 | hp1 | a0001 | c0001 | t0026 | g0008 | AFR | ACB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02280 | hp2 | a0001 | c0001 | t0010 | g0264 | AFR | ACB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02451 | hp1 | a0001 | c0001 | t0007 | g0009 | AFR | ACB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0102 | AFR | ACB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02572 | hp1 | a0001 | c0001 | t0011 | g0149 | AFR | GWD | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02572 | hp2 | a0001 | c0001 | t0045 | g0152 | AFR | GWD | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0119 | SAS | PJL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0203 | SAS | PJL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02622 | hp1 | a0001 | c0001 | t0048 | g0146 | AFR | GWD | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0139 | AFR | GWD | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0027 | AFR | GWD | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02630 | hp2 | a0001 | c0006 | t0032 | g0007 | AFR | GWD | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02647 | hp1 | a0004 | c0007 | t0022 | g0232 | AFR | GWD | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02647 | hp2 | a0001 | c0006 | t0018 | g0148 | AFR | GWD | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02698 | hp1 | a0001 | c0001 | t0004 | g0238 | SAS | PJL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02698 | hp2 | a0001 | c0001 | t0019 | g0163 | SAS | PJL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0214 | AFR | GWD | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0036 | AFR | GWD | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02723 | hp1 | a0001 | c0001 | t0007 | g0009 | AFR | GWD | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0227 | AFR | GWD | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02735 | hp1 | a0001 | c0001 | t0006 | g0195 | SAS | PJL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02735 | hp2 | a0001 | c0001 | t0010 | g0250 | SAS | PJL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0104 | SAS | PJL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02738 | hp2 | a0001 | c0001 | t0004 | g0234 | SAS | PJL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02818 | hp1 | a0001 | c0001 | t0009 | g0178 | AFR | GWD | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0141 | AFR | GWD | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02886 | hp1 | a0001 | c0001 | t0011 | g0150 | AFR | GWD | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0016 | AFR | GWD | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02895 | hp1 | a0001 | c0002 | t0023 | g0156 | AFR | GWD | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02895 | hp2 | a0001 | c0001 | t0010 | g0255 | AFR | GWD | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | GWD | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0226 | AFR | GWD | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02897 | hp1 | a0001 | c0002 | t0023 | g0154 | AFR | GWD | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0224 | AFR | GWD | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02922 | hp1 | a0002 | c0004 | t0012 | g0168 | AFR | ESN | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02922 | hp2 | a0001 | c0001 | t0007 | g0257 | AFR | ESN | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02965 | hp1 | a0007 | c0016 | t0002 | g0183 | AFR | ESN | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02965 | hp2 | a0001 | c0001 | t0009 | g0220 | AFR | ESN | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02976 | hp1 | a0001 | c0001 | t0025 | g0099 | AFR | ESN | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02976 | hp2 | a0001 | c0001 | t0005 | g0095 | AFR | ESN | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0202 | SAS | PJL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0118 | SAS | PJL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG03041 | hp1 | a0001 | c0002 | t0052 | g0155 | AFR | GWD | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG03041 | hp2 | a0001 | c0001 | t0036 | g0116 | AFR | GWD | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG03098 | hp1 | a0001 | c0001 | t0010 | g0266 | AFR | MSL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0181 | AFR | MSL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG03130 | hp1 | a0001 | c0001 | t0007 | g0262 | AFR | ESN | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG03130 | hp2 | a0001 | c0001 | t0024 | g0265 | AFR | ESN | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG03195 | hp1 | a0001 | c0006 | t0018 | g0007 | AFR | ESN | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG03195 | hp2 | a0002 | c0004 | t0012 | g0166 | AFR | ESN | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG03209 | hp1 | a0001 | c0001 | t0011 | g0130 | AFR | MSL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0182 | AFR | MSL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG03225 | hp1 | a0001 | c0001 | t0027 | g0215 | AFR | MSL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG03225 | hp2 | a0002 | c0004 | t0051 | g0167 | AFR | MSL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0117 | SAS | PJL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG03239 | hp2 | a0001 | c0001 | t0004 | g0235 | SAS | PJL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG03453 | hp1 | a0002 | c0004 | t0012 | g0169 | AFR | MSL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG03453 | hp2 | a0001 | c0019 | t0010 | g0153 | AFR | MSL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG03486 | hp1 | a0002 | c0004 | t0031 | g0170 | AFR | MSL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG03486 | hp2 | a0004 | c0007 | t0022 | g0231 | AFR | MSL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0126 | SAS | PJL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG03491 | hp2 | a0001 | c0001 | t0017 | g0096 | SAS | PJL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0055 | SAS | PJL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG03492 | hp2 | a0001 | c0001 | t0017 | g0097 | SAS | PJL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG03516 | hp1 | a0001 | c0001 | t0037 | g0135 | AFR | ESN | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0225 | AFR | ESN | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0144 | AFR | GWD | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0006 | AFR | MSL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG03579 | hp2 | a0001 | c0001 | t0009 | g0221 | AFR | MSL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0193 | SAS | PJL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0120 | SAS | PJL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0031 | SAS | PJL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0124 | SAS | PJL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0035 | SAS | STU | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG03688 | hp2 | a0001 | c0001 | t0004 | g0239 | SAS | STU | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG03704 | hp1 | a0001 | c0001 | t0006 | g0212 | SAS | PJL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0129 | SAS | PJL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG03710 | hp1 | a0001 | c0002 | t0008 | g0085 | SAS | PJL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0133 | SAS | PJL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0128 | SAS | BEB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0040 | SAS | BEB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG03927 | hp1 | a0001 | c0002 | t0021 | g0087 | SAS | BEB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0254 | SAS | BEB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0177 | SAS | BEB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0056 | SAS | BEB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0054 | SAS | STU | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0229 | SAS | STU | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG04184 | hp1 | a0001 | c0001 | t0017 | g0127 | SAS | BEB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0073 | SAS | BEB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0180 | SAS | STU | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0098 | SAS | STU | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG04228 | hp1 | a0001 | c0002 | t0008 | g0020 | SAS | STU | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG04228 | hp2 | a0001 | c0011 | t0002 | g0201 | SAS | STU | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA18522 | hp1 | a0008 | c0014 | t0009 | g0217 | AFR | YRI | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA18522 | hp2 | a0001 | c0001 | t0005 | g0006 | AFR | YRI | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0079 | EAS | CHB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0032 | EAS | CHB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA18939 | hp2 | a0001 | c0001 | t0006 | g0208 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA18940 | hp2 | a0001 | c0001 | t0049 | g0123 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA18942 | hp1 | a0001 | c0001 | t0006 | g0179 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA18947 | hp1 | a0003 | c0003 | t0003 | g0108 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA18947 | hp2 | a0001 | c0001 | t0006 | g0210 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA18954 | hp2 | a0001 | c0008 | t0014 | g0160 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA18960 | hp1 | a0003 | c0003 | t0003 | g0111 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0121 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA18963 | hp1 | a0001 | c0001 | t0006 | g0209 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA18969 | hp2 | a0001 | c0001 | t0006 | g0190 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA18970 | hp2 | a0001 | c0008 | t0014 | g0161 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA18989 | hp1 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA18989 | hp2 | a0001 | c0002 | t0035 | g0064 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA18994 | hp1 | a0001 | c0001 | t0016 | g0122 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA18997 | hp2 | a0009 | c0018 | t0001 | g0063 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA19030 | hp1 | a0001 | c0001 | t0028 | g0207 | AFR | LWK | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA19030 | hp2 | a0004 | c0007 | t0047 | g0252 | AFR | LWK | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA19043 | hp1 | a0001 | c0002 | t0013 | g0090 | AFR | LWK | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA19043 | hp2 | a0005 | c0010 | t0020 | g0158 | AFR | LWK | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA19056 | hp1 | a0001 | c0001 | t0016 | g0114 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA19062 | hp2 | a0003 | c0003 | t0003 | g0112 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA19066 | hp2 | a0003 | c0003 | t0003 | g0113 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA19067 | hp1 | a0003 | c0003 | t0003 | g0107 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA19067 | hp2 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA19074 | hp1 | a0003 | c0003 | t0003 | g0109 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA19080 | hp2 | a0003 | c0003 | t0003 | g0110 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA19081 | hp2 | a0001 | c0001 | t0016 | g0125 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA19082 | hp2 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA19083 | hp1 | a0001 | c0001 | t0006 | g0173 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA19088 | hp2 | a0001 | c0008 | t0014 | g0159 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA19089 | hp1 | a0001 | c0001 | t0039 | g0138 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA19089 | hp2 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0223 | AFR | YRI | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0137 | AFR | YRI | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA20129 | hp1 | a0001 | c0002 | t0021 | g0002 | AFR | ASW | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA20129 | hp2 | a0001 | c0002 | t0013 | g0089 | AFR | ASW | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0204 | EUR | TSI | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA20752 | hp2 | a0001 | c0002 | t0008 | g0080 | EUR | TSI | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0012 | EUR | TSI | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0004 | EUR | TSI | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0191 | SAS | GIH | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0014 | SAS | GIH | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0092 | AMR | CLM | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0058 | AMR | CLM | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0093 | AFR | ACB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02486 | hp2 | a0001 | c0006 | t0018 | g0147 | AFR | ACB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0251 | AFR | ACB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG02559 | hp2 | a0001 | c0002 | t0013 | g0088 | AFR | ACB | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG03471 | hp1 | a0002 | c0004 | t0030 | g0164 | AFR | MSL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0143 | AFR | MSL | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG06807 | hp1 | a0001 | c0012 | t0046 | g0175 | AFR | USA | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| HG06807 | hp2 | a0001 | c0001 | t0007 | g0259 | AFR | USA | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA20300 | hp1 | a0001 | c0001 | t0010 | g0263 | AFR | USA | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA20300 | hp2 | a0001 | c0001 | t0009 | g0219 | AFR | USA | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA21309 | hp1 | a0001 | c0001 | t0019 | g0200 | AFR | LWK | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0134 | AFR | LWK | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| homoSapiens | chm13v2 | a0010 | c0013 | t0008 | g0091 | REF | REF | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0041 | g0245 | REF | REF | GCC2_chr2_108444206_108514415 | GCC2 | chr2 | 108444206 | 108514415 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:108452435 | C | G | 1 | a0002 | 7 | HG02258.hp2 HG02922.hp1 HG03195.hp2 others(4): Show |
missense_variant | MODERATE | c.185C>G | p.Pro62Arg | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/23 | 254/6909 | 185/5055 | 62/1684 | chr2 | 108452435 | |||
| chr2:108470281 | A | G | 1 | a0009 | 1 | NA18997.hp2 | missense_variant | MODERATE | c.952A>G | p.Ile318Val | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 6/23 | 1021/6909 | 952/5055 | 318/1684 | chr2 | 108470281 | |||
| chr2:108470716 | A | C | 1 | a0006 | 1 | HG01261.hp1 | missense_variant | MODERATE | c.1387A>C | p.Lys463Gln | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 6/23 | 1456/6909 | 1387/5055 | 463/1684 | chr2 | 108470716 | |||
| chr2:108470867 | C | T | 1 | a0007 | 1 | HG02965.hp1 | missense_variant | MODERATE | c.1538C>T | p.Ala513Val | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 6/23 | 1607/6909 | 1538/5055 | 513/1684 | chr2 | 108470867 | |||
| chr2:108471107 | C | G | 1 | a0005 | 2 | HG02040.hp2 NA19043.hp2 |
missense_variant | MODERATE | c.1778C>G | p.Thr593Ser | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 6/23 | 1847/6909 | 1778/5055 | 593/1684 | chr2 | 108471107 | |||
| chr2:108471875 | A | G | 1 | a0008 | 1 | NA18522.hp1 | missense_variant | MODERATE | c.2546A>G | p.Glu849Gly | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 6/23 | 2615/6909 | 2546/5055 | 849/1684 | chr2 | 108471875 | |||
| chr2:108482398 | A | G | 1 | a0003 | 7 | NA18947.hp1 NA18960.hp1 NA19062.hp2 others(4): Show |
missense_variant | MODERATE | c.3292A>G | p.Met1098Val | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 11/23 | 3361/6909 | 3292/5055 | 1098/1684 | chr2 | 108482398 | |||
| chr2:108483075 | C | G | 1 | a0004 | 3 | HG02647.hp1 HG03486.hp2 NA19030.hp2 |
missense_variant | MODERATE | c.3359C>G | p.Thr1120Ser | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 12/23 | 3428/6909 | 3359/5055 | 1120/1684 | chr2 | 108483075 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:108470109 | A | G | 1 | a0001c0019 | 1 | HG03453.hp2 | synonymous_variant | LOW | c.780A>G | p.Glu260Glu | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 6/23 | 849/6909 | 780/5055 | 260/1684 | chr2 | 108470109 | |||
| chr2:108470358 | A | G | 2 | a0001c0008 a0006c0017 |
4 | HG01261.hp1 NA18954.hp2 NA18970.hp2 others(1): Show |
synonymous_variant | LOW | c.1029A>G | p.Glu343Glu | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 6/23 | 1098/6909 | 1029/5055 | 343/1684 | chr2 | 108470358 | |||
| chr2:108471240 | C | T | 1 | a0001c0006 | 4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
synonymous_variant | LOW | c.1911C>T | p.Tyr637Tyr | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 6/23 | 1980/6909 | 1911/5055 | 637/1684 | chr2 | 108471240 | |||
| chr2:108471471 | A | G | 1 | a0001c0015 | 1 | HG00673.hp1 | synonymous_variant | LOW | c.2142A>G | p.Gln714Gln | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 6/23 | 2211/6909 | 2142/5055 | 714/1684 | chr2 | 108471471 | |||
| chr2:108471819 | G | A | 1 | a0001c0005 | 5 | HG01167.hp1 HG01361.hp2 HG01928.hp2 others(2): Show |
synonymous_variant | LOW | c.2490G>A | p.Lys830Lys | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 6/23 | 2559/6909 | 2490/5055 | 830/1684 | chr2 | 108471819 | |||
| chr2:108489925 | A | G | 5 | a0001c0002 a0001c0005 a0001c0015 others(2): Show |
92 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(89): Show |
synonymous_variant | LOW | c.4140A>G | p.Gln1380Gln | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 18/23 | 4209/6909 | 4140/5055 | 1380/1684 | chr2 | 108489925 | |||
| chr2:108492627 | T | A | 1 | a0001c0011 | 1 | HG04228.hp2 | synonymous_variant | LOW | c.4284T>A | p.Thr1428Thr | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/23 | 4353/6909 | 4284/5055 | 1428/1684 | chr2 | 108492627 | |||
| chr2:108492780 | G | T | 1 | a0002c0004 | 7 | HG02258.hp2 HG02922.hp1 HG03195.hp2 others(4): Show |
synonymous_variant | LOW | c.4437G>T | p.Pro1479Pro | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/23 | 4506/6909 | 4437/5055 | 1479/1684 | chr2 | 108492780 | |||
| chr2:108495412 | G | A | 1 | a0001c0009 | 2 | HG01257.hp2 HG01258.hp1 |
synonymous_variant | LOW | c.4569G>A | p.Thr1523Thr | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 20/23 | 4638/6909 | 4569/5055 | 1523/1684 | chr2 | 108495412 | |||
| chr2:108497028 | C | T | 1 | a0001c0012 | 1 | HG06807.hp1 | synonymous_variant | LOW | c.4701C>T | p.Ser1567Ser | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/23 | 4770/6909 | 4701/5055 | 1567/1684 | chr2 | 108497028 | |||
| chr2:108499744 | G | A | 1 | a0005c0010 | 2 | HG02040.hp2 NA19043.hp2 |
synonymous_variant | LOW | c.4974G>A | p.Ala1658Ala | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/23 | 5043/6909 | 4974/5055 | 1658/1684 | chr2 | 108499744 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:108507786 | T | A | 11 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0009 others(8): Show |
62 | HG00099.hp2 HG00738.hp1 HG00738.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*156T>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 156 | chr2 | 108507786 | ||||||
| chr2:108507816 | G | A | 1 | a0001c0001t0026 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*186G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 186 | chr2 | 108507816 | ||||||
| chr2:108507823 | G | C | 13 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0009 others(10): Show |
64 | HG00099.hp2 HG00738.hp1 HG00738.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*193G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 193 | chr2 | 108507823 | ||||||
| chr2:108507852 | T | C | 7 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0033 others(4): Show |
22 | HG01109.hp2 HG01884.hp2 HG01891.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*222T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 222 | chr2 | 108507852 | ||||||
| chr2:108507900 | C | A | 10 | a0001c0002t0001 a0001c0002t0008 a0001c0002t0013 others(7): Show |
89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*270C>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 270 | chr2 | 108507900 | ||||||
| chr2:108507919 | G | A | 3 | a0001c0001t0011 a0001c0001t0036 a0001c0001t0037 |
7 | HG01243.hp2 HG02055.hp1 HG02572.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*289G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 289 | chr2 | 108507919 | ||||||
| chr2:108508056 | T | G | 1 | a0001c0001t0038 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*426T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 426 | chr2 | 108508056 | ||||||
| chr2:108508066 | A | C | 2 | a0001c0001t0038 a0002c0004t0031 |
2 | HG01516.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*436A>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 436 | chr2 | 108508066 | ||||||
| chr2:108508068 | G | C | 1 | a0001c0001t0039 | 1 | NA19089.hp1 | 3_prime_UTR_variant | MODIFIER | c.*438G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 438 | chr2 | 108508068 | ||||||
| chr2:108508069 | C | G | 1 | a0001c0001t0039 | 1 | NA19089.hp1 | 3_prime_UTR_variant | MODIFIER | c.*439C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 439 | chr2 | 108508069 | ||||||
| chr2:108508078 | T | C | 9 | a0001c0001t0036 a0001c0002t0001 a0001c0002t0008 others(6): Show |
85 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*448T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 448 | chr2 | 108508078 | ||||||
| chr2:108508080 | C | T | 8 | a0001c0002t0001 a0001c0002t0008 a0001c0002t0021 others(5): Show |
84 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*450C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 450 | chr2 | 108508080 | ||||||
| chr2:108508100 | A | ATT | 13 | a0001c0001t0025 a0001c0001t0036 a0001c0001t0038 others(10): Show |
91 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*470_*471insTT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 471 | chr2 | 108508100 | ||||||
| chr2:108508101 | C | G | 13 | a0001c0001t0025 a0001c0001t0036 a0001c0001t0038 others(10): Show |
91 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*471C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 471 | chr2 | 108508101 | ||||||
| chr2:108508103 | C | A | 13 | a0001c0001t0025 a0001c0001t0036 a0001c0001t0038 others(10): Show |
91 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*473C>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 473 | chr2 | 108508103 | ||||||
| chr2:108508157 | G | A | 2 | a0001c0001t0038 a0001c0001t0053 |
2 | HG00642.hp2 HG01516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*527G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 527 | chr2 | 108508157 | ||||||
| chr2:108508160 | A | G | 2 | a0001c0001t0038 a0001c0001t0053 |
2 | HG00642.hp2 HG01516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*530A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 530 | chr2 | 108508160 | ||||||
| chr2:108508176 | G | A | 1 | a0001c0001t0038 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*546G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 546 | chr2 | 108508176 | ||||||
| chr2:108508205 | G | T | 2 | a0001c0001t0038 a0001c0001t0053 |
2 | HG00642.hp2 HG01516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*575G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 575 | chr2 | 108508205 | ||||||
| chr2:108508207 | T | C | 1 | a0001c0001t0040 | 1 | HG01516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*577T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 577 | chr2 | 108508207 | ||||||
| chr2:108508267 | G | A | 1 | a0001c0001t0038 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*637G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 637 | chr2 | 108508267 | ||||||
| chr2:108508321 | A | G | 35 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(32): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
3_prime_UTR_variant | MODIFIER | c.*691A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 691 | chr2 | 108508321 | ||||||
| chr2:108508381 | A | T | 1 | a0001c0001t0044 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*751A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 751 | chr2 | 108508381 | ||||||
| chr2:108508392 | T | C | 2 | a0001c0001t0019 a0001c0001t0027 |
3 | HG02698.hp2 HG03225.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*762T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 762 | chr2 | 108508392 | ||||||
| chr2:108508447 | A | C | 2 | a0001c0002t0023 a0001c0002t0052 |
3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*817A>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 817 | chr2 | 108508447 | ||||||
| chr2:108508451 | G | A | 1 | a0001c0001t0024 | 2 | HG02055.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*821G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 821 | chr2 | 108508451 | ||||||
| chr2:108508463 | A | AC | 49 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(46): Show |
182 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(179): Show |
3_prime_UTR_variant | MODIFIER | c.*834dupC | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 835 | INFO_REALIGN_3_PRIME | chr2 | 108508463 | |||||
| chr2:108508464 | CACTT | C | 12 | a0001c0002t0001 a0001c0002t0008 a0001c0002t0013 others(9): Show |
92 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*835_*838delACTT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 835 | chr2 | 108508464 | ||||||
| chr2:108508469 | G | C | 12 | a0001c0002t0001 a0001c0002t0008 a0001c0002t0013 others(9): Show |
92 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*839G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 839 | chr2 | 108508469 | ||||||
| chr2:108508471 | G | C | 12 | a0001c0002t0001 a0001c0002t0008 a0001c0002t0013 others(9): Show |
92 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*841G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 841 | chr2 | 108508471 | ||||||
| chr2:108508519 | T | TGCATG | 1 | a0001c0002t0008 | 6 | HG00323.hp2 HG00639.hp2 HG01256.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*890_*894dupGCATG | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 895 | INFO_REALIGN_3_PRIME | chr2 | 108508519 | |||||
| chr2:108508526 | A | G | 4 | a0002c0004t0012 a0002c0004t0030 a0002c0004t0031 others(1): Show |
7 | HG02258.hp2 HG02922.hp1 HG03195.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*896A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 896 | chr2 | 108508526 | ||||||
| chr2:108508580 | A | C | 9 | a0001c0001t0017 a0001c0001t0033 a0001c0001t0038 others(6): Show |
14 | HG01261.hp1 HG01261.hp2 HG01516.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*950A>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 950 | chr2 | 108508580 | ||||||
| chr2:108508662 | G | C | 1 | a0001c0002t0034 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1032G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 1032 | chr2 | 108508662 | ||||||
| chr2:108508708 | A | G | 12 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0011 others(9): Show |
60 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*1078A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 1078 | chr2 | 108508708 | ||||||
| chr2:108508711 | G | T | 6 | a0001c0001t0015 a0001c0001t0027 a0001c0001t0044 others(3): Show |
10 | HG00642.hp1 HG01175.hp2 HG01257.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1081G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 1081 | chr2 | 108508711 | ||||||
| chr2:108508724 | C | T | 5 | a0001c0001t0015 a0001c0001t0027 a0001c0001t0029 others(2): Show |
8 | HG00642.hp1 HG01175.hp2 HG01257.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1094C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 1094 | chr2 | 108508724 | ||||||
| chr2:108508764 | T | G | 2 | a0001c0001t0048 a0004c0007t0022 |
3 | HG02622.hp1 HG02647.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1134T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 1134 | chr2 | 108508764 | ||||||
| chr2:108508765 | C | G | 5 | a0001c0001t0016 a0001c0001t0042 a0001c0001t0049 others(2): Show |
12 | HG00323.hp2 HG00639.hp2 HG01256.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1135C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 1135 | chr2 | 108508765 | ||||||
| chr2:108508799 | T | G | 2 | a0002c0004t0030 a0002c0004t0031 |
2 | HG03471.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1169T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 1169 | chr2 | 108508799 | ||||||
| chr2:108508813 | A | G | 1 | a0001c0012t0046 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1183A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 1183 | chr2 | 108508813 | ||||||
| chr2:108508857 | G | A | 1 | a0001c0002t0035 | 1 | NA18989.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1227G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 1227 | chr2 | 108508857 | ||||||
| chr2:108509026 | A | T | 1 | a0001c0001t0039 | 1 | NA19089.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1396A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 1396 | chr2 | 108509026 | ||||||
| chr2:108509050 | A | C | 1 | a0001c0002t0052 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1420A>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 1420 | chr2 | 108509050 | ||||||
| chr2:108509117 | T | C | 1 | a0001c0002t0052 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1487T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 1487 | chr2 | 108509117 | ||||||
| chr2:108509164 | A | G | 1 | a0001c0001t0028 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1534A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 1534 | chr2 | 108509164 | ||||||
| chr2:108509206 | T | C | 2 | a0001c0006t0018 a0001c0006t0032 |
4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1576T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 1576 | chr2 | 108509206 | ||||||
| chr2:108509230 | T | C | 1 | a0002c0004t0051 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1600T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 1600 | chr2 | 108509230 | ||||||
| chr2:108509322 | A | G | 1 | a0001c0001t0045 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1692A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 23/23 | 1692 | chr2 | 108509322 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:108449402 | T | C | 161 | a0001c0001t0002g0151 a0001c0001t0003g0004 a0001c0001t0003g0098 others(158): Show |
164 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.6+122T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 1/22 | chr2 | 108449402 | |||||||
| chr2:108449434 | C | T | 13 | a0001c0001t0007g0009 a0001c0001t0007g0257 a0001c0001t0007g0258 others(10): Show |
14 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.6+154C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 1/22 | chr2 | 108449434 | |||||||
| chr2:108449463 | T | C | 86 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(83): Show |
87 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.7-170T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 1/22 | chr2 | 108449463 | |||||||
| chr2:108449492 | CCGTCCGC others(7): Show |
C | 1 | a0001c0001t0004g0254 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.7-139_7-126delGTCC others(10): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr2 | 108449492 | ||||||
| chr2:108449517 | C | A | 1 | a0001c0001t0019g0163 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.7-116C>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 1/22 | chr2 | 108449517 | |||||||
| chr2:108449554 | C | T | 1 | a0001c0001t0004g0254 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.7-79C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 1/22 | chr2 | 108449554 | |||||||
| chr2:108449598 | T | A | 1 | a0001c0001t0004g0254 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.7-35T>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 1/22 | chr2 | 108449598 | |||||||
| chr2:108449722 | A | G | 1 | a0001c0001t0004g0254 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.63+33A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | chr2 | 108449722 | |||||||
| chr2:108449778 | AT | A | 68 | a0001c0001t0002g0151 a0001c0001t0003g0004 a0001c0001t0003g0098 others(65): Show |
70 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(67): Show |
intron_variant | MODIFIER | c.63+102delT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr2 | 108449778 | ||||||
| chr2:108449792 | A | T | 1 | a0001c0001t0004g0254 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.63+103A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | chr2 | 108449792 | |||||||
| chr2:108449798 | C | T | 2 | a0001c0001t0045g0152 a0001c0019t0010g0153 |
2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.63+109C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | chr2 | 108449798 | |||||||
| chr2:108449810 | G | T | 2 | a0001c0002t0001g0092 a0001c0002t0001g0093 |
2 | HG01123.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.63+121G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | chr2 | 108449810 | |||||||
| chr2:108449855 | C | T | 4 | a0001c0008t0014g0159 a0001c0008t0014g0160 a0001c0008t0014g0161 others(1): Show |
4 | HG01261.hp1 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+166C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | chr2 | 108449855 | |||||||
| chr2:108449874 | AAG | A | 16 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(13): Show |
17 | HG00323.hp1 HG01074.hp1 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.63+187_63+188delGA | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr2 | 108449874 | ||||||
| chr2:108449888 | G | A | 167 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(164): Show |
170 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.63+199G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | chr2 | 108449888 | |||||||
| chr2:108449968 | G | A | 83 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(80): Show |
84 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.63+279G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | chr2 | 108449968 | |||||||
| chr2:108450003 | C | A | 1 | a0002c0004t0030g0164 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.63+314C>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | chr2 | 108450003 | |||||||
| chr2:108450030 | T | C | 1 | a0001c0001t0040g0171 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.63+341T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | chr2 | 108450030 | |||||||
| chr2:108450076 | T | C | 2 | a0001c0001t0045g0152 a0001c0019t0010g0153 |
2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.63+387T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | chr2 | 108450076 | |||||||
| chr2:108450115 | T | G | 7 | a0003c0003t0003g0107 a0003c0003t0003g0108 a0003c0003t0003g0109 others(4): Show |
7 | NA18947.hp1 NA18960.hp1 NA19062.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+426T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | chr2 | 108450115 | |||||||
| chr2:108450132 | T | C | 1 | a0001c0001t0053g0172 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.63+443T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | chr2 | 108450132 | |||||||
| chr2:108450196 | A | G | 1 | a0001c0001t0002g0253 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.63+507A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | chr2 | 108450196 | |||||||
| chr2:108450237 | G | C | 1 | a0001c0002t0001g0012 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.63+548G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | chr2 | 108450237 | |||||||
| chr2:108450340 | T | C | 1 | a0001c0001t0006g0173 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.63+651T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | chr2 | 108450340 | |||||||
| chr2:108450343 | G | T | 160 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(157): Show |
163 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.63+654G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | chr2 | 108450343 | |||||||
| chr2:108450610 | G | A | 69 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(66): Show |
71 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.64-418G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | chr2 | 108450610 | |||||||
| chr2:108450647 | C | T | 83 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(80): Show |
84 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.64-381C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | chr2 | 108450647 | |||||||
| chr2:108450663 | C | T | 1 | a0004c0007t0047g0252 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.64-365C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | chr2 | 108450663 | |||||||
| chr2:108450774 | T | C | 3 | a0001c0002t0023g0154 a0001c0002t0023g0156 a0001c0002t0052g0155 |
3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.64-254T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | chr2 | 108450774 | |||||||
| chr2:108450805 | T | C | 246 | a0001c0001t0002g0008 a0001c0001t0002g0151 a0001c0001t0002g0174 others(243): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.64-223T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | chr2 | 108450805 | |||||||
| chr2:108450881 | C | T | 87 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(84): Show |
88 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.64-147C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | chr2 | 108450881 | |||||||
| chr2:108450882 | A | T | 1 | a0001c0002t0001g0011 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.64-146A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | chr2 | 108450882 | |||||||
| chr2:108450903 | G | A | 88 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(85): Show |
89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.64-125G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | chr2 | 108450903 | |||||||
| chr2:108450904 | T | A | 88 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(85): Show |
89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.64-124T>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 2/22 | chr2 | 108450904 | |||||||
| chr2:108451169 | G | A | 4 | a0001c0008t0014g0159 a0001c0008t0014g0160 a0001c0008t0014g0161 others(1): Show |
4 | HG01261.hp1 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.148+57G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 3/22 | chr2 | 108451169 | |||||||
| chr2:108451232 | T | G | 88 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(85): Show |
89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.148+120T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 3/22 | chr2 | 108451232 | |||||||
| chr2:108451320 | T | G | 1 | a0003c0003t0003g0107 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.148+208T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 3/22 | chr2 | 108451320 | |||||||
| chr2:108451329 | A | G | 2 | a0001c0001t0011g0149 a0001c0001t0011g0150 |
2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.148+217A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 3/22 | chr2 | 108451329 | |||||||
| chr2:108451396 | G | C | 1 | a0001c0001t0002g0174 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.148+284G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 3/22 | chr2 | 108451396 | |||||||
| chr2:108451454 | G | A | 4 | a0001c0008t0014g0159 a0001c0008t0014g0160 a0001c0008t0014g0161 others(1): Show |
4 | HG01261.hp1 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.148+342G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 3/22 | chr2 | 108451454 | |||||||
| chr2:108451519 | C | T | 160 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(157): Show |
163 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.148+407C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 3/22 | chr2 | 108451519 | |||||||
| chr2:108451606 | CT | C | 86 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(83): Show |
87 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.148+504delT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr2 | 108451606 | ||||||
| chr2:108451827 | T | TTCTCTC | 7 | a0002c0004t0012g0165 a0002c0004t0012g0166 a0002c0004t0012g0168 others(4): Show |
7 | HG02258.hp2 HG02922.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.149-562_149-557dup others(6): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr2 | 108451827 | ||||||
| chr2:108451841 | C | CT | 17 | a0001c0001t0002g0228 a0001c0001t0002g0229 a0001c0001t0002g0230 others(14): Show |
18 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.149-540dupT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr2 | 108451841 | ||||||
| chr2:108451841 | C | CTT | 7 | a0001c0008t0014g0159 a0001c0008t0014g0160 a0001c0008t0014g0161 others(4): Show |
7 | HG01261.hp1 HG02647.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.149-541_149-540dup others(2): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr2 | 108451841 | ||||||
| chr2:108451841 | CT | C | 89 | a0001c0001t0016g0114 a0001c0001t0044g0233 a0001c0002t0001g0002 others(86): Show |
90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.149-540delT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr2 | 108451841 | ||||||
| chr2:108451859 | T | C | 1 | a0001c0002t0008g0085 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.149-540T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 3/22 | chr2 | 108451859 | |||||||
| chr2:108451936 | C | T | 88 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(85): Show |
89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.149-463C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 3/22 | chr2 | 108451936 | |||||||
| chr2:108452032 | C | T | 69 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(66): Show |
71 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.149-367C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 3/22 | chr2 | 108452032 | |||||||
| chr2:108452052 | C | G | 6 | a0001c0001t0045g0152 a0001c0006t0018g0007 a0001c0006t0018g0147 others(3): Show |
6 | HG02486.hp2 HG02572.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.149-347C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 3/22 | chr2 | 108452052 | |||||||
| chr2:108452275 | A | C | 3 | a0001c0002t0023g0154 a0001c0002t0023g0156 a0001c0002t0052g0155 |
3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.149-124A>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 3/22 | chr2 | 108452275 | |||||||
| chr2:108452552 | T | C | 160 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(157): Show |
163 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.216+86T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108452552 | |||||||
| chr2:108452691 | C | CT | 17 | a0001c0001t0002g0174 a0001c0001t0006g0190 a0001c0001t0006g0222 others(14): Show |
18 | HG01109.hp2 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.216+246dupT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108452691 | ||||||
| chr2:108452691 | CT | C | 10 | a0001c0001t0002g0193 a0001c0001t0002g0197 a0001c0001t0002g0211 others(7): Show |
10 | HG00099.hp2 HG00738.hp2 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.216+246delT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108452691 | ||||||
| chr2:108452691 | CTT | C | 7 | a0001c0001t0003g0101 a0001c0001t0003g0144 a0001c0002t0001g0081 others(4): Show |
7 | HG00323.hp1 HG02559.hp2 HG03540.hp2 others(4): Show |
intron_variant | MODIFIER | c.216+245_216+246del others(2): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108452691 | ||||||
| chr2:108452691 | CTTT | C | 140 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0102 others(137): Show |
143 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.216+244_216+246del others(3): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108452691 | ||||||
| chr2:108452746 | T | G | 1 | a0001c0002t0052g0155 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.216+280T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108452746 | |||||||
| chr2:108452839 | G | A | 2 | a0001c0001t0002g0176 a0001c0001t0002g0177 |
2 | HG01346.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.216+373G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108452839 | |||||||
| chr2:108452898 | T | C | 1 | a0001c0001t0003g0115 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.216+432T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108452898 | |||||||
| chr2:108452934 | C | T | 1 | a0001c0001t0002g0227 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.216+468C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108452934 | |||||||
| chr2:108452976 | G | A | 63 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(60): Show |
65 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(62): Show |
intron_variant | MODIFIER | c.216+510G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108452976 | |||||||
| chr2:108452984 | G | A | 1 | a0001c0001t0009g0178 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.216+518G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108452984 | |||||||
| chr2:108453033 | C | T | 1 | a0001c0001t0010g0250 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.216+567C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108453033 | |||||||
| chr2:108453073 | T | C | 1 | a0001c0012t0046g0175 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.216+607T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108453073 | |||||||
| chr2:108453100 | A | G | 1 | a0002c0004t0031g0170 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.216+634A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108453100 | |||||||
| chr2:108453109 | T | C | 4 | a0001c0006t0018g0007 a0001c0006t0018g0147 a0001c0006t0018g0148 others(1): Show |
4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.216+643T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108453109 | |||||||
| chr2:108453482 | C | T | 1 | a0001c0002t0001g0084 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.216+1016C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108453482 | |||||||
| chr2:108453508 | A | G | 1 | a0001c0002t0001g0083 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.216+1042A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108453508 | |||||||
| chr2:108453645 | C | T | 2 | a0001c0001t0004g0248 a0001c0001t0042g0249 |
2 | HG01106.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.216+1179C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108453645 | |||||||
| chr2:108453785 | T | TA | 9 | a0001c0001t0002g0151 a0001c0001t0002g0180 a0001c0001t0002g0253 others(6): Show |
9 | HG01167.hp2 HG02486.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.216+1336dupA | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108453785 | ||||||
| chr2:108453785 | TA | T | 136 | a0001c0001t0002g0226 a0001c0001t0003g0115 a0001c0001t0003g0117 others(133): Show |
138 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.216+1336delA | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108453785 | ||||||
| chr2:108453785 | TAA | T | 18 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(15): Show |
19 | HG00323.hp1 HG01074.hp1 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.216+1335_216+1336d others(4): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108453785 | ||||||
| chr2:108454009 | G | T | 88 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(85): Show |
89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.216+1543G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108454009 | |||||||
| chr2:108454062 | C | T | 88 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(85): Show |
89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.216+1596C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108454062 | |||||||
| chr2:108454100 | C | T | 3 | a0001c0002t0023g0154 a0001c0002t0023g0156 a0001c0002t0052g0155 |
3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.216+1634C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108454100 | |||||||
| chr2:108454178 | A | G | 167 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(164): Show |
170 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.216+1712A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108454178 | |||||||
| chr2:108454242 | G | A | 14 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(11): Show |
15 | HG00323.hp1 HG01074.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.216+1776G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108454242 | |||||||
| chr2:108454437 | G | T | 1 | a0001c0002t0001g0011 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.216+1971G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108454437 | |||||||
| chr2:108454670 | C | G | 1 | a0001c0002t0001g0079 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.216+2204C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108454670 | |||||||
| chr2:108454714 | C | T | 13 | a0001c0001t0007g0009 a0001c0001t0007g0257 a0001c0001t0007g0258 others(10): Show |
14 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.216+2248C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108454714 | |||||||
| chr2:108454731 | T | C | 2 | a0001c0002t0001g0013 a0001c0002t0001g0014 |
2 | HG01928.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.216+2265T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108454731 | |||||||
| chr2:108454896 | AT | A | 44 | a0001c0001t0002g0176 a0001c0001t0002g0177 a0001c0001t0002g0180 others(41): Show |
44 | HG00099.hp2 HG00738.hp1 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.216+2441delT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108454896 | ||||||
| chr2:108454963 | G | A | 1 | a0001c0002t0001g0015 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.216+2497G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108454963 | |||||||
| chr2:108454977 | CTA | C | 160 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(157): Show |
163 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.216+2514_216+2515d others(4): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108454977 | ||||||
| chr2:108455017 | A | G | 88 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(85): Show |
89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.216+2551A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108455017 | |||||||
| chr2:108455168 | G | A | 1 | a0001c0001t0024g0256 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.216+2702G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108455168 | |||||||
| chr2:108455219 | C | A | 13 | a0001c0001t0007g0009 a0001c0001t0007g0257 a0001c0001t0007g0258 others(10): Show |
14 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.216+2753C>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108455219 | |||||||
| chr2:108455285 | C | G | 1 | a0001c0001t0010g0266 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.216+2819C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108455285 | |||||||
| chr2:108455366 | G | A | 59 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(56): Show |
61 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.216+2900G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108455366 | |||||||
| chr2:108455456 | C | A | 1 | a0001c0001t0036g0116 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.216+2990C>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108455456 | |||||||
| chr2:108455475 | ACCTTTAA others(3): Show |
A | 1 | a0001c0001t0002g0230 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.216+3010_216+3019d others(12): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108455475 | |||||||
| chr2:108455518 | C | T | 88 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(85): Show |
89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.216+3052C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108455518 | |||||||
| chr2:108455591 | CAG | C | 88 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(85): Show |
89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.216+3128_216+3129d others(4): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108455591 | ||||||
| chr2:108455616 | G | T | 6 | a0001c0001t0010g0255 a0001c0001t0010g0263 a0001c0001t0010g0264 others(3): Show |
6 | HG02055.hp2 HG02280.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.216+3150G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108455616 | |||||||
| chr2:108455662 | A | G | 1 | a0001c0002t0001g0078 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.216+3196A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108455662 | |||||||
| chr2:108455720 | G | A | 2 | a0001c0002t0023g0154 a0001c0002t0023g0156 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.216+3254G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108455720 | |||||||
| chr2:108455950 | T | C | 2 | a0001c0001t0045g0152 a0001c0019t0010g0153 |
2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.216+3484T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108455950 | |||||||
| chr2:108455958 | C | G | 1 | a0003c0003t0003g0113 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.216+3492C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108455958 | |||||||
| chr2:108456007 | C | T | 1 | a0001c0001t0010g0255 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.216+3541C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108456007 | |||||||
| chr2:108456025 | C | T | 3 | a0001c0002t0023g0154 a0001c0002t0023g0156 a0001c0002t0052g0155 |
3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.216+3559C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108456025 | |||||||
| chr2:108456129 | C | T | 1 | a0001c0002t0001g0077 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.216+3663C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108456129 | |||||||
| chr2:108456237 | G | A | 1 | a0001c0002t0001g0016 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.216+3771G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108456237 | |||||||
| chr2:108456274 | C | T | 1 | a0001c0008t0014g0159 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.216+3808C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108456274 | |||||||
| chr2:108456374 | A | T | 1 | a0001c0001t0048g0146 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.216+3908A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108456374 | |||||||
| chr2:108456673 | A | G | 1 | a0001c0001t0004g0247 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.216+4207A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108456673 | |||||||
| chr2:108456720 | G | A | 1 | a0001c0002t0052g0155 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.216+4254G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108456720 | |||||||
| chr2:108456766 | CAT | C | 88 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(85): Show |
89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.216+4302_216+4303d others(4): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108456766 | ||||||
| chr2:108456948 | T | TA | 40 | a0001c0001t0002g0181 a0001c0001t0003g0004 a0001c0001t0003g0098 others(37): Show |
42 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.216+4501dupA | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108456948 | ||||||
| chr2:108456948 | T | TAA | 21 | a0001c0001t0003g0115 a0001c0001t0003g0117 a0001c0001t0003g0118 others(18): Show |
21 | HG01891.hp2 HG02602.hp1 HG03017.hp2 others(18): Show |
intron_variant | MODIFIER | c.216+4500_216+4501d others(4): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108456948 | ||||||
| chr2:108456948 | TA | T | 91 | a0001c0001t0002g0213 a0001c0001t0006g0212 a0001c0001t0045g0152 others(88): Show |
92 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.216+4501delA | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108456948 | ||||||
| chr2:108456973 | G | A | 1 | a0001c0001t0004g0251 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.216+4507G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108456973 | |||||||
| chr2:108457061 | A | G | 10 | a0001c0001t0045g0152 a0001c0006t0018g0007 a0001c0006t0018g0147 others(7): Show |
10 | HG01261.hp1 HG02486.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.216+4595A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108457061 | |||||||
| chr2:108457119 | TATA | T | 69 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(66): Show |
71 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.216+4657_216+4659d others(5): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108457119 | ||||||
| chr2:108457125 | A | G | 2 | a0001c0002t0023g0154 a0001c0002t0023g0156 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.216+4659A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108457125 | |||||||
| chr2:108457248 | G | A | 3 | a0001c0001t0002g0214 a0001c0001t0027g0215 a0001c0001t0029g0216 |
3 | HG02257.hp1 HG02717.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.216+4782G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108457248 | |||||||
| chr2:108457390 | G | T | 1 | a0004c0007t0047g0252 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.216+4924G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108457390 | |||||||
| chr2:108457430 | C | T | 1 | a0001c0002t0052g0155 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.216+4964C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108457430 | |||||||
| chr2:108457545 | G | C | 69 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(66): Show |
71 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.216+5079G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108457545 | |||||||
| chr2:108457587 | T | C | 3 | a0001c0002t0023g0154 a0001c0002t0023g0156 a0001c0002t0052g0155 |
3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.216+5121T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108457587 | |||||||
| chr2:108457587 | T | G | 59 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(56): Show |
61 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.216+5121T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108457587 | |||||||
| chr2:108457745 | T | C | 4 | a0001c0006t0018g0007 a0001c0006t0018g0147 a0001c0006t0018g0148 others(1): Show |
4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.216+5279T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108457745 | |||||||
| chr2:108457908 | C | T | 88 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(85): Show |
89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.216+5442C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108457908 | |||||||
| chr2:108458057 | T | C | 6 | a0001c0002t0008g0018 a0001c0002t0008g0019 a0001c0002t0008g0020 others(3): Show |
6 | HG00323.hp2 HG00639.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.216+5591T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108458057 | |||||||
| chr2:108458069 | C | T | 1 | a0001c0002t0001g0076 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.216+5603C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108458069 | |||||||
| chr2:108458181 | C | T | 2 | a0001c0001t0045g0152 a0001c0019t0010g0153 |
2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.216+5715C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108458181 | |||||||
| chr2:108458182 | G | A | 4 | a0001c0006t0018g0007 a0001c0006t0018g0147 a0001c0006t0018g0148 others(1): Show |
4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.216+5716G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108458182 | |||||||
| chr2:108458238 | A | T | 1 | a0001c0001t0002g0211 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.216+5772A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108458238 | |||||||
| chr2:108458374 | C | CT | 11 | a0001c0001t0003g0117 a0001c0002t0001g0073 a0001c0002t0001g0075 others(8): Show |
11 | HG01192.hp1 HG02486.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.216+5928dupT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108458374 | ||||||
| chr2:108458374 | C | CTT | 53 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(50): Show |
54 | HG00323.hp1 HG01074.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.216+5927_216+5928d others(4): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108458374 | ||||||
| chr2:108458374 | C | CTTT | 10 | a0001c0001t0003g0105 a0001c0001t0003g0142 a0001c0001t0003g0144 others(7): Show |
11 | HG00639.hp1 HG01243.hp2 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.216+5926_216+5928d others(5): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108458374 | ||||||
| chr2:108458374 | CT | C | 89 | a0001c0001t0002g0008 a0001c0001t0002g0151 a0001c0001t0002g0180 others(86): Show |
91 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.216+5928delT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108458374 | ||||||
| chr2:108458379 | T | C | 3 | a0001c0001t0002g0182 a0001c0002t0052g0155 a0007c0016t0002g0183 |
3 | HG02965.hp1 HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.216+5913T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108458379 | |||||||
| chr2:108458430 | A | C | 69 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(66): Show |
71 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.216+5964A>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108458430 | |||||||
| chr2:108458446 | G | A | 1 | a0001c0002t0001g0022 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.216+5980G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108458446 | |||||||
| chr2:108458521 | T | C | 1 | a0001c0002t0001g0078 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.216+6055T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108458521 | |||||||
| chr2:108458680 | A | G | 1 | a0001c0001t0003g0129 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.216+6214A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108458680 | |||||||
| chr2:108458904 | C | T | 3 | a0001c0002t0023g0154 a0001c0002t0023g0156 a0001c0002t0052g0155 |
3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.216+6438C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108458904 | |||||||
| chr2:108459114 | A | G | 1 | a0001c0001t0002g0180 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.216+6648A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108459114 | |||||||
| chr2:108459245 | G | T | 2 | a0002c0004t0030g0164 a0002c0004t0031g0170 |
2 | HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.216+6779G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108459245 | |||||||
| chr2:108459252 | G | A | 1 | a0001c0002t0001g0023 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.216+6786G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108459252 | |||||||
| chr2:108459276 | G | A | 59 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(56): Show |
61 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.216+6810G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108459276 | |||||||
| chr2:108459352 | T | A | 59 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(56): Show |
61 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.216+6886T>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108459352 | |||||||
| chr2:108459481 | C | T | 69 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(66): Show |
71 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.216+7015C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108459481 | |||||||
| chr2:108459578 | G | A | 1 | a0001c0002t0013g0088 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.216+7112G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108459578 | |||||||
| chr2:108459649 | A | G | 4 | a0001c0006t0018g0007 a0001c0006t0018g0147 a0001c0006t0018g0148 others(1): Show |
4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.216+7183A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108459649 | |||||||
| chr2:108459669 | G | A | 11 | a0001c0001t0004g0001 a0001c0001t0004g0235 a0001c0001t0004g0236 others(8): Show |
13 | HG00140.hp2 HG00280.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.216+7203G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108459669 | |||||||
| chr2:108459745 | C | CT | 28 | a0001c0001t0002g0008 a0001c0001t0002g0174 a0001c0001t0002g0182 others(25): Show |
30 | HG00140.hp2 HG00280.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.216+7312dupT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | ||||||
| chr2:108459745 | C | CTT | 18 | a0001c0001t0002g0196 a0001c0001t0002g0197 a0001c0001t0002g0198 others(15): Show |
18 | HG00099.hp2 HG00738.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.216+7311_216+7312d others(4): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | ||||||
| chr2:108459745 | C | CTTT | 17 | a0001c0001t0002g0151 a0001c0001t0002g0176 a0001c0001t0002g0177 others(14): Show |
17 | HG01109.hp2 HG01167.hp2 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.216+7310_216+7312d others(5): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | ||||||
| chr2:108459745 | C | CTTTT | 9 | a0001c0001t0002g0205 a0001c0001t0002g0213 a0001c0001t0002g0224 others(6): Show |
9 | HG00741.hp2 HG01993.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.216+7309_216+7312d others(6): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | ||||||
| chr2:108459745 | C | CTTTTT | 7 | a0001c0001t0002g0206 a0001c0001t0028g0207 a0001c0002t0001g0030 others(4): Show |
7 | HG01167.hp1 HG01243.hp1 HG03669.hp1 others(4): Show |
intron_variant | MODIFIER | c.216+7308_216+7312d others(7): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | ||||||
| chr2:108459745 | C | CTTTTTT | 36 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(33): Show |
37 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.216+7307_216+7312d others(8): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | ||||||
| chr2:108459745 | C | CTTTTTTT | 33 | a0001c0002t0001g0013 a0001c0002t0001g0016 a0001c0002t0001g0050 others(30): Show |
33 | HG00323.hp2 HG01071.hp1 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.216+7306_216+7312d others(9): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | ||||||
| chr2:108459745 | C | CTTTTTTT others(1): Show |
9 | a0001c0002t0001g0014 a0001c0002t0001g0069 a0001c0002t0001g0071 others(6): Show |
9 | HG00099.hp1 HG00673.hp1 HG00673.hp2 others(6): Show |
intron_variant | MODIFIER | c.216+7305_216+7312d others(10): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | ||||||
| chr2:108459745 | C | CTTTTTTT others(3): Show |
1 | a0001c0002t0013g0090 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.216+7303_216+7312d others(12): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | ||||||
| chr2:108459745 | C | CTTTTTTT others(4): Show |
2 | a0001c0006t0018g0007 a0001c0006t0032g0007 |
2 | HG02630.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.216+7302_216+7312d others(13): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | ||||||
| chr2:108459745 | C | CTTTTTTT others(5): Show |
3 | a0001c0001t0003g0120 a0001c0001t0039g0138 a0001c0002t0001g0072 |
3 | HG03654.hp2 NA18998.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.216+7301_216+7312d others(14): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | ||||||
| chr2:108459745 | C | CTTTTTTT others(6): Show |
8 | a0001c0001t0003g0121 a0001c0001t0003g0124 a0001c0001t0005g0139 others(5): Show |
8 | HG02486.hp2 HG02622.hp2 HG03669.hp2 others(5): Show |
intron_variant | MODIFIER | c.216+7300_216+7312d others(15): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | ||||||
| chr2:108459745 | C | CTTTTTTT others(9): Show |
1 | a0001c0006t0018g0148 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.216+7297_216+7312d others(18): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | ||||||
| chr2:108459745 | C | CTTTTTTT others(10): Show |
2 | a0003c0003t0003g0107 a0003c0003t0003g0109 |
2 | NA19067.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.216+7296_216+7312d others(19): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | ||||||
| chr2:108459745 | C | CTTTTTTT others(11): Show |
3 | a0001c0001t0003g0126 a0003c0003t0003g0110 a0003c0003t0003g0112 |
3 | HG03491.hp1 NA19062.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.216+7295_216+7312d others(20): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | ||||||
| chr2:108459745 | C | CTTTTTTT others(12): Show |
1 | a0001c0001t0017g0127 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.216+7294_216+7312d others(21): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | ||||||
| chr2:108459745 | C | CTTTTTTT others(13): Show |
1 | a0001c0001t0003g0128 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.216+7293_216+7312d others(22): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | ||||||
| chr2:108459745 | C | CTTTTTTT others(16): Show |
2 | a0001c0001t0003g0117 a0003c0003t0003g0111 |
2 | HG03239.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.216+7290_216+7312d others(25): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | ||||||
| chr2:108459745 | CT | C | 7 | a0001c0001t0002g0184 a0001c0001t0002g0214 a0001c0001t0027g0215 others(4): Show |
7 | HG00642.hp2 HG01515.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.216+7312delT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | ||||||
| chr2:108459745 | CTTT | C | 11 | a0001c0001t0003g0132 a0001c0001t0003g0133 a0001c0001t0003g0134 others(8): Show |
12 | HG00639.hp1 HG01074.hp2 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.216+7310_216+7312d others(5): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | ||||||
| chr2:108459745 | CTTTT | C | 6 | a0001c0001t0011g0130 a0001c0001t0011g0131 a0001c0001t0011g0140 others(3): Show |
6 | HG01243.hp2 HG02055.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.216+7309_216+7312d others(6): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | ||||||
| chr2:108459745 | CTTTTTT | C | 6 | a0001c0001t0045g0152 a0001c0002t0001g0023 a0001c0002t0001g0024 others(3): Show |
6 | HG02572.hp2 NA18747.hp1 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.216+7307_216+7312d others(8): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | ||||||
| chr2:108459745 | CTTTTTTT others(6): Show |
C | 3 | a0001c0001t0003g0105 a0001c0012t0046g0175 a0002c0004t0031g0170 |
3 | HG02056.hp1 HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.216+7300_216+7312d others(15): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | ||||||
| chr2:108459745 | CTTTTTTT others(7): Show |
C | 14 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(11): Show |
15 | HG00323.hp1 HG01074.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.216+7299_216+7312d others(16): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | ||||||
| chr2:108459745 | CTTTTTTT others(9): Show |
C | 1 | a0005c0010t0020g0157 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.216+7297_216+7312d others(18): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | ||||||
| chr2:108459745 | CTTTTTTT others(10): Show |
C | 1 | a0005c0010t0020g0158 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.216+7296_216+7312d others(19): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | ||||||
| chr2:108459745 | CTTTTTTT others(12): Show |
C | 1 | a0001c0002t0052g0155 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.216+7294_216+7312d others(21): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | ||||||
| chr2:108459745 | CTTTTTTT others(13): Show |
C | 2 | a0001c0002t0023g0154 a0001c0002t0023g0156 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.216+7293_216+7312d others(22): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108459745 | ||||||
| chr2:108459854 | T | C | 69 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(66): Show |
71 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.216+7388T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108459854 | |||||||
| chr2:108459889 | C | T | 2 | a0005c0010t0020g0157 a0005c0010t0020g0158 |
2 | HG02040.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.216+7423C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108459889 | |||||||
| chr2:108459921 | T | C | 160 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(157): Show |
163 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.216+7455T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108459921 | |||||||
| chr2:108460001 | T | C | 160 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(157): Show |
163 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.216+7535T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108460001 | |||||||
| chr2:108460098 | A | G | 245 | a0001c0001t0002g0008 a0001c0001t0002g0151 a0001c0001t0002g0174 others(242): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.216+7632A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108460098 | |||||||
| chr2:108460387 | TC | T | 3 | a0001c0002t0023g0154 a0001c0002t0023g0156 a0001c0002t0052g0155 |
3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.216+7922delC | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108460387 | |||||||
| chr2:108460400 | C | T | 160 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(157): Show |
163 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.216+7934C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108460400 | |||||||
| chr2:108460523 | C | A | 1 | a0001c0001t0002g0182 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.216+8057C>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108460523 | |||||||
| chr2:108460524 | C | T | 86 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(83): Show |
87 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.216+8058C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108460524 | |||||||
| chr2:108460649 | C | G | 1 | a0001c0001t0038g0246 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.216+8183C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108460649 | |||||||
| chr2:108460822 | A | G | 2 | a0005c0010t0020g0157 a0005c0010t0020g0158 |
2 | HG02040.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.217-8158A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108460822 | |||||||
| chr2:108460860 | C | T | 3 | a0001c0002t0023g0154 a0001c0002t0023g0156 a0001c0002t0052g0155 |
3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.217-8120C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108460860 | |||||||
| chr2:108460904 | C | T | 1 | a0007c0016t0002g0183 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.217-8076C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108460904 | |||||||
| chr2:108460976 | A | T | 8 | a0001c0001t0002g0008 a0001c0001t0002g0174 a0001c0001t0002g0225 others(5): Show |
8 | HG01175.hp1 HG02145.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.217-8004A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108460976 | |||||||
| chr2:108460994 | C | A | 91 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(88): Show |
92 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.217-7986C>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108460994 | |||||||
| chr2:108461248 | G | T | 59 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(56): Show |
61 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.217-7732G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108461248 | |||||||
| chr2:108461291 | AT | A | 72 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(69): Show |
74 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(71): Show |
intron_variant | MODIFIER | c.217-7678delT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108461291 | ||||||
| chr2:108461302 | T | C | 7 | a0002c0004t0012g0165 a0002c0004t0012g0166 a0002c0004t0012g0168 others(4): Show |
7 | HG02258.hp2 HG02922.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.217-7678T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108461302 | |||||||
| chr2:108461348 | G | A | 9 | a0001c0001t0002g0008 a0001c0001t0002g0151 a0001c0001t0002g0174 others(6): Show |
9 | HG01167.hp2 HG01175.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.217-7632G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108461348 | |||||||
| chr2:108461460 | A | T | 3 | a0001c0002t0023g0154 a0001c0002t0023g0156 a0001c0002t0052g0155 |
3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.217-7520A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108461460 | |||||||
| chr2:108461616 | C | T | 1 | a0001c0002t0001g0083 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.217-7364C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108461616 | |||||||
| chr2:108461658 | A | G | 1 | a0001c0001t0003g0128 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.217-7322A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108461658 | |||||||
| chr2:108461693 | G | A | 1 | a0001c0002t0001g0050 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.217-7287G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108461693 | |||||||
| chr2:108461778 | G | A | 69 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(66): Show |
71 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.217-7202G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108461778 | |||||||
| chr2:108461830 | C | CTTT | 54 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(51): Show |
56 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(53): Show |
intron_variant | MODIFIER | c.217-7147_217-7145d others(5): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108461830 | ||||||
| chr2:108461830 | C | CTTTTT | 5 | a0001c0001t0045g0152 a0001c0006t0018g0147 a0001c0006t0018g0148 others(2): Show |
5 | HG02486.hp2 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.217-7149_217-7145d others(7): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108461830 | ||||||
| chr2:108461836 | C | CT | 11 | a0001c0001t0015g0240 a0001c0002t0013g0088 a0001c0002t0052g0155 others(8): Show |
11 | HG00642.hp1 HG02040.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.217-7129dupT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108461836 | ||||||
| chr2:108461836 | C | T | 63 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(60): Show |
65 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(62): Show |
intron_variant | MODIFIER | c.217-7144C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108461836 | |||||||
| chr2:108461864 | C | T | 3 | a0001c0001t0045g0152 a0001c0019t0010g0153 a0002c0004t0031g0170 |
3 | HG02572.hp2 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.217-7116C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108461864 | |||||||
| chr2:108461885 | C | T | 88 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(85): Show |
89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.217-7095C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108461885 | |||||||
| chr2:108461999 | A | AT | 89 | a0001c0001t0004g0254 a0001c0001t0028g0207 a0001c0002t0001g0002 others(86): Show |
90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.217-6969dupT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108461999 | ||||||
| chr2:108461999 | A | T | 4 | a0001c0006t0018g0007 a0001c0006t0018g0147 a0001c0006t0018g0148 others(1): Show |
4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.217-6981A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108461999 | |||||||
| chr2:108462004 | T | A | 1 | a0001c0001t0004g0234 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.217-6976T>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108462004 | |||||||
| chr2:108462073 | G | A | 5 | a0001c0005t0001g0029 a0001c0005t0001g0034 a0001c0005t0001g0051 others(2): Show |
5 | HG01167.hp1 HG01361.hp2 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.217-6907G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108462073 | |||||||
| chr2:108462083 | C | T | 2 | a0001c0002t0023g0154 a0001c0002t0023g0156 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.217-6897C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108462083 | |||||||
| chr2:108462084 | G | A | 1 | a0001c0001t0002g0211 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.217-6896G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108462084 | |||||||
| chr2:108462160 | C | T | 160 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(157): Show |
163 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.217-6820C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108462160 | |||||||
| chr2:108462241 | C | G | 1 | a0001c0001t0002g0204 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.217-6739C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108462241 | |||||||
| chr2:108462264 | G | A | 13 | a0001c0001t0007g0009 a0001c0001t0007g0257 a0001c0001t0007g0258 others(10): Show |
14 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.217-6716G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108462264 | |||||||
| chr2:108462294 | C | T | 1 | a0001c0001t0019g0163 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.217-6686C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108462294 | |||||||
| chr2:108462336 | A | T | 1 | a0001c0002t0001g0068 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.217-6644A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108462336 | |||||||
| chr2:108462411 | G | A | 1 | a0001c0001t0053g0172 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.217-6569G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108462411 | |||||||
| chr2:108462494 | A | AAAAT | 69 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(66): Show |
71 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.217-6468_217-6465d others(6): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108462494 | ||||||
| chr2:108462524 | C | G | 69 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(66): Show |
71 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.217-6456C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108462524 | |||||||
| chr2:108462540 | A | G | 59 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(56): Show |
61 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.217-6440A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108462540 | |||||||
| chr2:108462541 | TGTCACAA others(7): Show |
T | 85 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(82): Show |
86 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.217-6437_217-6424d others(16): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108462541 | ||||||
| chr2:108462542 | GTCACAAA others(2): Show |
G | 3 | a0001c0002t0001g0049 a0001c0002t0001g0067 a0001c0002t0008g0021 |
3 | HG00323.hp2 NA18950.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.217-6437_217-6429d others(11): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108462542 | |||||||
| chr2:108462555 | CGCTT | C | 3 | a0001c0002t0001g0049 a0001c0002t0001g0067 a0001c0002t0008g0021 |
3 | HG00323.hp2 NA18950.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.217-6424_217-6421d others(6): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108462555 | |||||||
| chr2:108462560 | C | CT | 9 | a0001c0001t0002g0184 a0001c0001t0002g0230 a0001c0001t0003g0121 others(6): Show |
9 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.217-6400dupT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108462560 | ||||||
| chr2:108462560 | C | CTT | 59 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(56): Show |
61 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.217-6401_217-6400d others(4): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108462560 | ||||||
| chr2:108462560 | C | CTTT | 5 | a0001c0001t0011g0131 a0001c0001t0011g0150 a0001c0001t0016g0125 others(2): Show |
5 | HG02055.hp1 HG02886.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.217-6402_217-6400d others(5): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108462560 | ||||||
| chr2:108462560 | C | T | 3 | a0001c0002t0001g0049 a0001c0002t0001g0067 a0001c0002t0008g0021 |
3 | HG00323.hp2 NA18950.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.217-6420C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108462560 | |||||||
| chr2:108462560 | CT | C | 6 | a0001c0001t0006g0190 a0001c0001t0010g0250 a0001c0002t0008g0018 others(3): Show |
6 | HG01167.hp1 HG01256.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.217-6400delT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108462560 | ||||||
| chr2:108462597 | C | T | 15 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(12): Show |
16 | HG00323.hp1 HG01074.hp1 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.217-6383C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108462597 | |||||||
| chr2:108462624 | G | A | 86 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(83): Show |
87 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.217-6356G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108462624 | |||||||
| chr2:108462649 | A | G | 1 | a0001c0001t0004g0235 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.217-6331A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108462649 | |||||||
| chr2:108462656 | G | C | 3 | a0001c0002t0013g0088 a0001c0002t0013g0089 a0001c0002t0013g0090 |
3 | HG02559.hp2 NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.217-6324G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108462656 | |||||||
| chr2:108462692 | A | G | 1 | a0001c0019t0010g0153 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.217-6288A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108462692 | |||||||
| chr2:108462789 | A | G | 1 | a0001c0002t0001g0082 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.217-6191A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108462789 | |||||||
| chr2:108462789 | A | T | 2 | a0001c0001t0045g0152 a0001c0019t0010g0153 |
2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.217-6191A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108462789 | |||||||
| chr2:108462838 | C | T | 1 | a0001c0002t0001g0093 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.217-6142C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108462838 | |||||||
| chr2:108462950 | T | G | 1 | a0001c0001t0009g0221 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.217-6030T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108462950 | |||||||
| chr2:108463438 | A | G | 264 | a0001c0001t0002g0008 a0001c0001t0002g0151 a0001c0001t0002g0174 others(261): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.217-5542A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108463438 | |||||||
| chr2:108463446 | G | A | 160 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(157): Show |
163 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.217-5534G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108463446 | |||||||
| chr2:108463481 | T | G | 1 | a0001c0001t0002g0206 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.217-5499T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108463481 | |||||||
| chr2:108463553 | G | T | 3 | a0002c0004t0012g0166 a0002c0004t0012g0169 a0002c0004t0051g0167 |
3 | HG03195.hp2 HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.217-5427G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108463553 | |||||||
| chr2:108463655 | A | C | 2 | a0005c0010t0020g0157 a0005c0010t0020g0158 |
2 | HG02040.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.217-5325A>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108463655 | |||||||
| chr2:108463745 | G | T | 1 | a0001c0002t0013g0088 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.217-5235G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108463745 | |||||||
| chr2:108463776 | C | T | 59 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(56): Show |
61 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.217-5204C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108463776 | |||||||
| chr2:108463959 | T | G | 1 | a0001c0012t0046g0175 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.217-5021T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108463959 | |||||||
| chr2:108463987 | A | G | 1 | a0001c0001t0048g0146 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.217-4993A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108463987 | |||||||
| chr2:108464010 | G | A | 1 | a0001c0002t0052g0155 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.217-4970G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108464010 | |||||||
| chr2:108464167 | A | G | 69 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(66): Show |
71 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.217-4813A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108464167 | |||||||
| chr2:108464282 | G | C | 1 | a0001c0002t0001g0035 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.217-4698G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108464282 | |||||||
| chr2:108464286 | C | T | 1 | a0001c0001t0004g0251 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.217-4694C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108464286 | |||||||
| chr2:108464367 | G | C | 2 | a0001c0002t0013g0089 a0001c0002t0013g0090 |
2 | NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.217-4613G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108464367 | |||||||
| chr2:108464458 | G | T | 69 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(66): Show |
71 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.217-4522G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108464458 | |||||||
| chr2:108464610 | G | T | 65 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(62): Show |
67 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(64): Show |
intron_variant | MODIFIER | c.217-4370G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108464610 | |||||||
| chr2:108464643 | G | T | 65 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(62): Show |
67 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(64): Show |
intron_variant | MODIFIER | c.217-4337G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108464643 | |||||||
| chr2:108464690 | T | C | 2 | a0001c0002t0023g0154 a0001c0002t0023g0156 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.217-4290T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108464690 | |||||||
| chr2:108464740 | A | C | 1 | a0001c0001t0002g0189 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.217-4240A>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108464740 | |||||||
| chr2:108464745 | A | T | 65 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(62): Show |
67 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(64): Show |
intron_variant | MODIFIER | c.217-4235A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108464745 | |||||||
| chr2:108464793 | G | A | 86 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(83): Show |
87 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.217-4187G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108464793 | |||||||
| chr2:108464899 | T | G | 3 | a0004c0007t0022g0231 a0004c0007t0022g0232 a0004c0007t0047g0252 |
3 | HG02647.hp1 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.217-4081T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108464899 | |||||||
| chr2:108464930 | C | T | 1 | a0001c0002t0052g0155 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.217-4050C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108464930 | |||||||
| chr2:108465012 | C | G | 40 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(37): Show |
41 | HG00323.hp1 HG01074.hp1 HG01099.hp2 others(38): Show |
intron_variant | MODIFIER | c.217-3968C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108465012 | |||||||
| chr2:108465154 | A | G | 1 | a0001c0002t0021g0087 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.217-3826A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108465154 | |||||||
| chr2:108465232 | T | G | 4 | a0001c0001t0003g0098 a0001c0001t0003g0105 a0001c0001t0017g0096 others(1): Show |
4 | HG02056.hp1 HG03491.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.217-3748T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108465232 | |||||||
| chr2:108465293 | C | T | 4 | a0001c0006t0018g0007 a0001c0006t0018g0147 a0001c0006t0018g0148 others(1): Show |
4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.217-3687C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108465293 | |||||||
| chr2:108465356 | CTT | C | 3 | a0001c0002t0023g0154 a0001c0002t0023g0156 a0001c0002t0052g0155 |
3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.217-3620_217-3619d others(4): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108465356 | ||||||
| chr2:108465461 | A | G | 4 | a0001c0008t0014g0159 a0001c0008t0014g0160 a0001c0008t0014g0161 others(1): Show |
4 | HG01261.hp1 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.217-3519A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108465461 | |||||||
| chr2:108465596 | A | T | 50 | a0001c0002t0001g0003 a0001c0002t0001g0010 a0001c0002t0001g0011 others(47): Show |
51 | HG00673.hp1 HG00673.hp2 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.217-3384A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108465596 | |||||||
| chr2:108465768 | C | T | 2 | a0005c0010t0020g0157 a0005c0010t0020g0158 |
2 | HG02040.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.217-3212C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108465768 | |||||||
| chr2:108465919 | A | C | 1 | a0001c0001t0009g0178 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.217-3061A>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108465919 | |||||||
| chr2:108465928 | C | T | 4 | a0001c0008t0014g0159 a0001c0008t0014g0160 a0001c0008t0014g0161 others(1): Show |
4 | HG01261.hp1 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.217-3052C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108465928 | |||||||
| chr2:108466064 | G | T | 1 | a0001c0001t0009g0221 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.217-2916G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108466064 | |||||||
| chr2:108466185 | C | G | 88 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(85): Show |
89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.217-2795C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108466185 | |||||||
| chr2:108466209 | G | A | 65 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(62): Show |
67 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(64): Show |
intron_variant | MODIFIER | c.217-2771G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108466209 | |||||||
| chr2:108466249 | G | A | 2 | a0001c0001t0045g0152 a0001c0019t0010g0153 |
2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.217-2731G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108466249 | |||||||
| chr2:108466263 | G | C | 63 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(60): Show |
65 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(62): Show |
intron_variant | MODIFIER | c.217-2717G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108466263 | |||||||
| chr2:108466343 | C | T | 11 | a0001c0001t0003g0132 a0001c0001t0003g0133 a0001c0001t0003g0134 others(8): Show |
12 | HG00639.hp1 HG01074.hp2 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.217-2637C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108466343 | |||||||
| chr2:108466464 | T | TTTTA | 53 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(50): Show |
55 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(52): Show |
intron_variant | MODIFIER | c.217-2496_217-2493d others(6): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108466464 | ||||||
| chr2:108466673 | T | C | 88 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(85): Show |
89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.217-2307T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108466673 | |||||||
| chr2:108466757 | C | G | 59 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(56): Show |
61 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.217-2223C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108466757 | |||||||
| chr2:108466760 | C | T | 1 | a0002c0004t0031g0170 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.217-2220C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108466760 | |||||||
| chr2:108466935 | T | A | 2 | a0001c0002t0013g0089 a0001c0002t0013g0090 |
2 | NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.217-2045T>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108466935 | |||||||
| chr2:108466943 | T | A | 1 | a0001c0002t0001g0054 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.217-2037T>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108466943 | |||||||
| chr2:108466943 | T | G | 1 | a0001c0002t0001g0058 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.217-2037T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108466943 | |||||||
| chr2:108467035 | G | T | 69 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(66): Show |
71 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.217-1945G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108467035 | |||||||
| chr2:108467361 | A | G | 2 | a0001c0001t0045g0152 a0001c0019t0010g0153 |
2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.217-1619A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108467361 | |||||||
| chr2:108467444 | A | C | 4 | a0001c0006t0018g0007 a0001c0006t0018g0147 a0001c0006t0018g0148 others(1): Show |
4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.217-1536A>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108467444 | |||||||
| chr2:108467651 | G | T | 69 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(66): Show |
71 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.217-1329G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108467651 | |||||||
| chr2:108467821 | A | G | 69 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(66): Show |
71 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.217-1159A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108467821 | |||||||
| chr2:108468067 | CT | C | 164 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(161): Show |
167 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.217-901delT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108468067 | ||||||
| chr2:108468145 | C | T | 69 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(66): Show |
71 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.217-835C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108468145 | |||||||
| chr2:108468369 | A | G | 59 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(56): Show |
61 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.217-611A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108468369 | |||||||
| chr2:108468375 | A | G | 69 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(66): Show |
71 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.217-605A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108468375 | |||||||
| chr2:108468486 | A | AT | 7 | a0001c0001t0011g0130 a0001c0001t0011g0131 a0001c0001t0011g0140 others(4): Show |
7 | HG01243.hp2 HG02055.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.217-485dupT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108468486 | ||||||
| chr2:108468651 | A | C | 3 | a0001c0001t0002g0199 a0001c0001t0002g0205 a0001c0001t0002g0213 |
3 | HG00738.hp1 HG00741.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.217-329A>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108468651 | |||||||
| chr2:108468756 | C | T | 63 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(60): Show |
65 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(62): Show |
intron_variant | MODIFIER | c.217-224C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108468756 | |||||||
| chr2:108468852 | A | AATGTGTT others(306): Show |
1 | a0001c0002t0001g0066 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.217-112_217-111ins others(313): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr2 | 108468852 | ||||||
| chr2:108468852 | A | G | 3 | a0001c0002t0001g0031 a0001c0002t0001g0057 a0001c0002t0001g0076 |
3 | HG03669.hp1 NA18955.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.217-128A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108468852 | |||||||
| chr2:108468917 | A | G | 83 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(80): Show |
84 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.217-63A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 4/22 | chr2 | 108468917 | |||||||
| chr2:108469106 | C | A | 1 | a0001c0002t0001g0036 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.321+22C>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 5/22 | chr2 | 108469106 | |||||||
| chr2:108469198 | CAAAG | C | 86 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(83): Show |
87 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.321+118_321+121del others(4): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr2 | 108469198 | ||||||
| chr2:108469532 | A | G | 1 | a0001c0002t0001g0026 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.322-119A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 5/22 | chr2 | 108469532 | |||||||
| chr2:108472137 | A | G | 2 | a0001c0001t0045g0152 a0001c0019t0010g0153 |
2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2787+21A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 6/22 | chr2 | 108472137 | |||||||
| chr2:108472179 | G | A | 1 | a0001c0001t0004g0254 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2787+63G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 6/22 | chr2 | 108472179 | |||||||
| chr2:108472222 | A | AT | 7 | a0002c0004t0012g0165 a0002c0004t0012g0166 a0002c0004t0012g0168 others(4): Show |
7 | HG02258.hp2 HG02922.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.2787+109dupT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr2 | 108472222 | ||||||
| chr2:108472256 | A | G | 7 | a0001c0001t0011g0130 a0001c0001t0011g0131 a0001c0001t0011g0140 others(4): Show |
7 | HG01243.hp2 HG02055.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.2787+140A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 6/22 | chr2 | 108472256 | |||||||
| chr2:108472350 | G | T | 65 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(62): Show |
67 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(64): Show |
intron_variant | MODIFIER | c.2787+234G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 6/22 | chr2 | 108472350 | |||||||
| chr2:108472412 | G | A | 167 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(164): Show |
170 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.2787+296G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 6/22 | chr2 | 108472412 | |||||||
| chr2:108472540 | A | G | 160 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(157): Show |
163 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.2788-287A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 6/22 | chr2 | 108472540 | |||||||
| chr2:108472542 | T | C | 1 | a0001c0001t0002g0224 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2788-285T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 6/22 | chr2 | 108472542 | |||||||
| chr2:108472548 | T | C | 1 | a0001c0001t0002g0224 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2788-279T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 6/22 | chr2 | 108472548 | |||||||
| chr2:108472575 | T | C | 1 | a0001c0001t0002g0224 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2788-252T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 6/22 | chr2 | 108472575 | |||||||
| chr2:108472607 | CT | C | 5 | a0001c0001t0045g0152 a0001c0002t0023g0154 a0001c0002t0023g0156 others(2): Show |
5 | HG02572.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.2788-207delT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr2 | 108472607 | ||||||
| chr2:108472612 | T | C | 1 | a0001c0001t0002g0224 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2788-215T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 6/22 | chr2 | 108472612 | |||||||
| chr2:108472620 | T | A | 1 | a0001c0001t0015g0243 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2788-207T>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 6/22 | chr2 | 108472620 | |||||||
| chr2:108472644 | T | C | 3 | a0001c0002t0023g0154 a0001c0002t0023g0156 a0001c0002t0052g0155 |
3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2788-183T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 6/22 | chr2 | 108472644 | |||||||
| chr2:108472803 | T | G | 1 | a0005c0010t0020g0158 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2788-24T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 6/22 | chr2 | 108472803 | |||||||
| chr2:108472948 | C | G | 160 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(157): Show |
163 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.2860+49C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108472948 | |||||||
| chr2:108472954 | G | A | 1 | a0004c0007t0047g0252 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2860+55G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108472954 | |||||||
| chr2:108473010 | C | T | 1 | a0001c0002t0001g0017 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2860+111C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108473010 | |||||||
| chr2:108473154 | A | G | 4 | a0001c0006t0018g0007 a0001c0006t0018g0147 a0001c0006t0018g0148 others(1): Show |
4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.2860+255A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108473154 | |||||||
| chr2:108473211 | A | G | 3 | a0001c0002t0023g0154 a0001c0002t0023g0156 a0001c0002t0052g0155 |
3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2860+312A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108473211 | |||||||
| chr2:108473239 | G | A | 69 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(66): Show |
71 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.2860+340G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108473239 | |||||||
| chr2:108473289 | A | G | 69 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(66): Show |
71 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.2860+390A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108473289 | |||||||
| chr2:108473312 | T | TA | 7 | a0001c0006t0018g0007 a0001c0006t0018g0147 a0001c0006t0032g0007 others(4): Show |
7 | HG01261.hp1 HG02486.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.2860+429dupA | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr2 | 108473312 | ||||||
| chr2:108473312 | TA | T | 131 | a0001c0001t0002g0008 a0001c0001t0002g0151 a0001c0001t0002g0174 others(128): Show |
134 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.2860+429delA | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr2 | 108473312 | ||||||
| chr2:108473439 | C | A | 2 | a0001c0002t0001g0041 a0001c0002t0001g0075 |
2 | NA19057.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.2860+540C>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108473439 | |||||||
| chr2:108473483 | C | A | 2 | a0001c0001t0045g0152 a0001c0019t0010g0153 |
2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2860+584C>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108473483 | |||||||
| chr2:108473496 | A | G | 59 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(56): Show |
61 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.2860+597A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108473496 | |||||||
| chr2:108473555 | C | T | 3 | a0001c0002t0023g0154 a0001c0002t0023g0156 a0001c0002t0052g0155 |
3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2860+656C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108473555 | |||||||
| chr2:108473655 | G | A | 160 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(157): Show |
163 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.2860+756G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108473655 | |||||||
| chr2:108473730 | G | T | 2 | a0001c0002t0008g0018 a0001c0002t0008g0020 |
2 | HG01256.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.2860+831G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108473730 | |||||||
| chr2:108473811 | G | C | 69 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(66): Show |
71 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.2860+912G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108473811 | |||||||
| chr2:108473882 | G | A | 4 | a0001c0006t0018g0007 a0001c0006t0018g0147 a0001c0006t0018g0148 others(1): Show |
4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.2860+983G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108473882 | |||||||
| chr2:108473891 | C | T | 5 | a0001c0001t0003g0124 a0001c0006t0018g0007 a0001c0006t0018g0147 others(2): Show |
5 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2860+992C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108473891 | |||||||
| chr2:108473904 | A | T | 44 | a0001c0001t0002g0176 a0001c0001t0002g0177 a0001c0001t0002g0180 others(41): Show |
44 | HG00099.hp2 HG00738.hp1 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.2860+1005A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108473904 | |||||||
| chr2:108473928 | C | T | 1 | a0001c0002t0001g0065 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2860+1029C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108473928 | |||||||
| chr2:108473954 | C | T | 1 | a0001c0002t0035g0064 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2860+1055C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108473954 | |||||||
| chr2:108473982 | T | C | 1 | a0001c0001t0003g0126 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2860+1083T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108473982 | |||||||
| chr2:108473996 | C | CA | 89 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(86): Show |
90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.2860+1109dupA | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr2 | 108473996 | ||||||
| chr2:108474027 | G | A | 1 | a0005c0010t0020g0158 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2860+1128G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108474027 | |||||||
| chr2:108474051 | G | A | 1 | a0001c0001t0003g0120 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2860+1152G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108474051 | |||||||
| chr2:108474083 | G | A | 63 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(60): Show |
65 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(62): Show |
intron_variant | MODIFIER | c.2860+1184G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108474083 | |||||||
| chr2:108474152 | C | T | 1 | a0001c0002t0001g0031 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2860+1253C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108474152 | |||||||
| chr2:108474190 | A | G | 1 | a0002c0004t0012g0165 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2860+1291A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108474190 | |||||||
| chr2:108474357 | G | C | 2 | a0001c0002t0013g0089 a0001c0002t0013g0090 |
2 | NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2861-1178G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108474357 | |||||||
| chr2:108474537 | C | T | 1 | a0001c0001t0039g0138 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2861-998C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108474537 | |||||||
| chr2:108474538 | A | G | 1 | a0001c0002t0001g0015 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2861-997A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108474538 | |||||||
| chr2:108474769 | G | A | 1 | a0001c0001t0003g0132 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2861-766G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108474769 | |||||||
| chr2:108475023 | C | G | 90 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(87): Show |
91 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.2861-512C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108475023 | |||||||
| chr2:108475099 | G | C | 88 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(85): Show |
89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.2861-436G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108475099 | |||||||
| chr2:108475313 | A | C | 4 | a0001c0008t0014g0159 a0001c0008t0014g0160 a0001c0008t0014g0161 others(1): Show |
4 | HG01261.hp1 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2861-222A>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108475313 | |||||||
| chr2:108475353 | A | G | 7 | a0002c0004t0012g0165 a0002c0004t0012g0166 a0002c0004t0012g0168 others(4): Show |
7 | HG02258.hp2 HG02922.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.2861-182A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108475353 | |||||||
| chr2:108475360 | G | A | 59 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(56): Show |
61 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.2861-175G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108475360 | |||||||
| chr2:108475377 | A | C | 14 | a0001c0001t0007g0009 a0001c0001t0007g0257 a0001c0001t0007g0258 others(11): Show |
15 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.2861-158A>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108475377 | |||||||
| chr2:108475458 | C | T | 1 | a0001c0002t0001g0047 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2861-77C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108475458 | |||||||
| chr2:108475504 | C | T | 1 | a0001c0001t0003g0134 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2861-31C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108475504 | |||||||
| chr2:108475505 | G | A | 1 | a0001c0001t0043g0242 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2861-30G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 7/22 | chr2 | 108475505 | |||||||
| chr2:108475657 | A | G | 3 | a0001c0002t0023g0154 a0001c0002t0023g0156 a0001c0002t0052g0155 |
3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2961+22A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 8/22 | chr2 | 108475657 | |||||||
| chr2:108475665 | G | A | 86 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(83): Show |
87 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.2961+30G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 8/22 | chr2 | 108475665 | |||||||
| chr2:108475689 | A | G | 1 | a0002c0004t0030g0164 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2961+54A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 8/22 | chr2 | 108475689 | |||||||
| chr2:108475902 | C | T | 1 | a0001c0002t0001g0035 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3060+52C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108475902 | |||||||
| chr2:108476023 | C | T | 69 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(66): Show |
71 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.3060+173C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108476023 | |||||||
| chr2:108476054 | C | CT | 34 | a0001c0001t0002g0177 a0001c0001t0002g0184 a0001c0001t0002g0185 others(31): Show |
34 | HG00741.hp1 HG01106.hp1 HG01175.hp2 others(31): Show |
intron_variant | MODIFIER | c.3060+230dupT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 108476054 | ||||||
| chr2:108476054 | C | CTTTTTTT others(4): Show |
2 | a0001c0008t0014g0159 a0001c0008t0014g0160 |
2 | NA18954.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.3060+220_3060+230d others(13): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 108476054 | ||||||
| chr2:108476054 | C | CTTTTTTT others(5): Show |
1 | a0001c0008t0014g0161 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.3060+219_3060+230d others(14): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 108476054 | ||||||
| chr2:108476054 | C | CTTTTTTT others(6): Show |
1 | a0006c0017t0050g0162 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3060+218_3060+230d others(15): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 108476054 | ||||||
| chr2:108476054 | CT | C | 81 | a0001c0001t0002g0224 a0001c0001t0006g0222 a0001c0001t0045g0152 others(78): Show |
82 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.3060+230delT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 108476054 | ||||||
| chr2:108476054 | CTTTTTTT others(3): Show |
C | 59 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(56): Show |
61 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.3060+221_3060+230d others(12): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 108476054 | ||||||
| chr2:108476055 | T | C | 8 | a0001c0002t0001g0056 a0001c0002t0001g0073 a0001c0002t0001g0075 others(5): Show |
8 | HG01361.hp2 HG01981.hp1 HG03942.hp2 others(5): Show |
intron_variant | MODIFIER | c.3060+205T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108476055 | |||||||
| chr2:108476056 | T | C | 77 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(74): Show |
78 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.3060+206T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108476056 | |||||||
| chr2:108476090 | T | G | 69 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(66): Show |
71 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.3060+240T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108476090 | |||||||
| chr2:108476125 | A | G | 1 | a0001c0001t0003g0129 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3060+275A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108476125 | |||||||
| chr2:108476206 | C | T | 63 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(60): Show |
65 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(62): Show |
intron_variant | MODIFIER | c.3060+356C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108476206 | |||||||
| chr2:108476341 | C | T | 4 | a0001c0006t0018g0007 a0001c0006t0018g0147 a0001c0006t0018g0148 others(1): Show |
4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.3060+491C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108476341 | |||||||
| chr2:108476406 | G | A | 86 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(83): Show |
87 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.3060+556G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108476406 | |||||||
| chr2:108477047 | T | C | 4 | a0001c0002t0001g0002 a0001c0002t0001g0016 a0001c0002t0001g0036 others(1): Show |
4 | HG02717.hp2 HG02886.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.3060+1197T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108477047 | |||||||
| chr2:108477063 | A | C | 1 | a0001c0001t0003g0144 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3060+1213A>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108477063 | |||||||
| chr2:108477214 | C | T | 1 | a0001c0002t0035g0064 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.3060+1364C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108477214 | |||||||
| chr2:108477360 | C | T | 4 | a0001c0006t0018g0007 a0001c0006t0018g0147 a0001c0006t0018g0148 others(1): Show |
4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.3060+1510C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108477360 | |||||||
| chr2:108477380 | A | G | 70 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(67): Show |
72 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(69): Show |
intron_variant | MODIFIER | c.3060+1530A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108477380 | |||||||
| chr2:108477392 | C | T | 3 | a0001c0002t0001g0066 a0001c0002t0001g0071 a0009c0018t0001g0063 |
3 | HG00673.hp2 NA18997.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.3060+1542C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108477392 | |||||||
| chr2:108477395 | G | A | 1 | a0001c0002t0001g0076 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.3060+1545G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108477395 | |||||||
| chr2:108477405 | T | C | 4 | a0001c0008t0014g0159 a0001c0008t0014g0160 a0001c0008t0014g0161 others(1): Show |
4 | HG01261.hp1 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.3060+1555T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108477405 | |||||||
| chr2:108477416 | T | C | 7 | a0001c0001t0011g0130 a0001c0001t0011g0131 a0001c0001t0011g0140 others(4): Show |
7 | HG01243.hp2 HG02055.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.3060+1566T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108477416 | |||||||
| chr2:108477507 | C | G | 2 | a0001c0001t0045g0152 a0001c0019t0010g0153 |
2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3060+1657C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108477507 | |||||||
| chr2:108477764 | G | A | 11 | a0001c0001t0003g0132 a0001c0001t0003g0133 a0001c0001t0003g0134 others(8): Show |
12 | HG00639.hp1 HG01074.hp2 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.3060+1914G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108477764 | |||||||
| chr2:108477825 | C | G | 1 | a0001c0001t0002g0206 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3060+1975C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108477825 | |||||||
| chr2:108477921 | C | G | 3 | a0001c0002t0023g0154 a0001c0002t0023g0156 a0001c0002t0052g0155 |
3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3060+2071C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108477921 | |||||||
| chr2:108478070 | G | GA | 69 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(66): Show |
71 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.3060+2221dupA | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 108478070 | ||||||
| chr2:108478127 | A | G | 4 | a0001c0006t0018g0007 a0001c0006t0018g0147 a0001c0006t0018g0148 others(1): Show |
4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.3060+2277A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108478127 | |||||||
| chr2:108478169 | C | A | 2 | a0001c0002t0008g0018 a0001c0002t0008g0020 |
2 | HG01256.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.3060+2319C>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108478169 | |||||||
| chr2:108478201 | G | A | 1 | a0001c0002t0001g0078 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.3060+2351G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108478201 | |||||||
| chr2:108478237 | T | TTGTATAA others(3): Show |
69 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(66): Show |
71 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.3060+2388_3060+238 others(14): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 108478237 | ||||||
| chr2:108478240 | G | GTATAATT others(6): Show |
69 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(66): Show |
71 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.3060+2391_3060+239 others(17): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 108478240 | ||||||
| chr2:108478303 | G | T | 13 | a0001c0001t0007g0009 a0001c0001t0007g0257 a0001c0001t0007g0258 others(10): Show |
14 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.3060+2453G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108478303 | |||||||
| chr2:108478430 | C | A | 1 | a0001c0001t0002g0204 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.3060+2580C>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108478430 | |||||||
| chr2:108478491 | T | C | 1 | a0003c0003t0003g0112 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.3060+2641T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108478491 | |||||||
| chr2:108479100 | G | C | 4 | a0001c0006t0018g0007 a0001c0006t0018g0147 a0001c0006t0018g0148 others(1): Show |
4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.3061-2597G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108479100 | |||||||
| chr2:108479138 | T | G | 2 | a0001c0001t0025g0099 a0001c0001t0025g0100 |
2 | HG01884.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.3061-2559T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108479138 | |||||||
| chr2:108479157 | C | T | 69 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(66): Show |
71 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.3061-2540C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108479157 | |||||||
| chr2:108479180 | A | G | 91 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(88): Show |
92 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.3061-2517A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108479180 | |||||||
| chr2:108479261 | G | A | 1 | a0001c0002t0001g0017 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3061-2436G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108479261 | |||||||
| chr2:108479430 | T | C | 160 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(157): Show |
163 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.3061-2267T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108479430 | |||||||
| chr2:108479556 | G | A | 1 | a0001c0002t0052g0155 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3061-2141G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108479556 | |||||||
| chr2:108479635 | T | C | 2 | a0004c0007t0022g0231 a0004c0007t0022g0232 |
2 | HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.3061-2062T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108479635 | |||||||
| chr2:108479663 | G | A | 1 | a0003c0003t0003g0111 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.3061-2034G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108479663 | |||||||
| chr2:108479816 | T | C | 2 | a0001c0002t0023g0154 a0001c0002t0023g0156 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3061-1881T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108479816 | |||||||
| chr2:108479930 | C | T | 14 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(11): Show |
15 | HG00323.hp1 HG01074.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.3061-1767C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108479930 | |||||||
| chr2:108479980 | C | CA | 46 | a0001c0001t0002g0151 a0001c0001t0002g0176 a0001c0001t0002g0177 others(43): Show |
46 | HG00642.hp1 HG00642.hp2 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.3061-1688dupA | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 108479980 | ||||||
| chr2:108479980 | C | CAA | 15 | a0001c0001t0002g0008 a0001c0001t0002g0174 a0001c0001t0002g0223 others(12): Show |
15 | HG01109.hp2 HG01175.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.3061-1689_3061-168 others(6): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 108479980 | ||||||
| chr2:108479980 | C | CAAA | 8 | a0001c0001t0002g0214 a0001c0001t0007g0009 a0001c0001t0007g0257 others(5): Show |
9 | HG01884.hp2 HG01891.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.3061-1690_3061-168 others(7): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 108479980 | ||||||
| chr2:108479980 | CAAAAAAA others(4): Show |
C | 7 | a0001c0001t0011g0131 a0001c0001t0011g0140 a0001c0001t0016g0122 others(4): Show |
7 | HG01243.hp2 HG02055.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.3061-1698_3061-168 others(15): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 108479980 | ||||||
| chr2:108479980 | CAAAAAAA others(5): Show |
C | 62 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(59): Show |
64 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(61): Show |
intron_variant | MODIFIER | c.3061-1699_3061-168 others(16): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 108479980 | ||||||
| chr2:108479980 | CAAAAAAA others(9): Show |
C | 4 | a0001c0002t0001g0042 a0001c0002t0001g0048 a0001c0002t0001g0049 others(1): Show |
4 | HG02056.hp2 HG03927.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.3061-1703_3061-168 others(20): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 108479980 | ||||||
| chr2:108479980 | CAAAAAAA others(10): Show |
C | 82 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(79): Show |
83 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.3061-1704_3061-168 others(21): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 108479980 | ||||||
| chr2:108480006 | A | AC | 3 | a0001c0002t0023g0154 a0001c0002t0023g0156 a0001c0002t0052g0155 |
3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3061-1691_3061-169 others(5): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108480006 | |||||||
| chr2:108480009 | A | C | 69 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(66): Show |
71 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.3061-1688A>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108480009 | |||||||
| chr2:108480211 | C | A | 1 | a0005c0010t0020g0158 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3061-1486C>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108480211 | |||||||
| chr2:108480214 | C | A | 3 | a0001c0002t0023g0154 a0001c0002t0023g0156 a0001c0002t0052g0155 |
3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3061-1483C>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108480214 | |||||||
| chr2:108480448 | C | A | 4 | a0001c0008t0014g0159 a0001c0008t0014g0160 a0001c0008t0014g0161 others(1): Show |
4 | HG01261.hp1 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.3061-1249C>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108480448 | |||||||
| chr2:108480487 | C | T | 7 | a0002c0004t0012g0165 a0002c0004t0012g0166 a0002c0004t0012g0168 others(4): Show |
7 | HG02258.hp2 HG02922.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.3061-1210C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108480487 | |||||||
| chr2:108480500 | G | A | 1 | a0001c0001t0040g0171 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.3061-1197G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108480500 | |||||||
| chr2:108480558 | A | G | 2 | a0001c0001t0003g0136 a0001c0001t0005g0137 |
2 | HG02258.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3061-1139A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108480558 | |||||||
| chr2:108480674 | C | T | 1 | a0001c0001t0009g0219 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3061-1023C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108480674 | |||||||
| chr2:108480678 | C | T | 2 | a0001c0002t0023g0154 a0001c0002t0023g0156 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3061-1019C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108480678 | |||||||
| chr2:108480758 | AG | A | 157 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(154): Show |
160 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.3061-935delG | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 108480758 | ||||||
| chr2:108480845 | C | T | 1 | a0001c0002t0008g0080 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.3061-852C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108480845 | |||||||
| chr2:108480870 | TAAC | T | 88 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(85): Show |
89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.3061-824_3061-822d others(5): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr2 | 108480870 | ||||||
| chr2:108480904 | G | A | 1 | a0001c0001t0003g0106 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3061-793G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108480904 | |||||||
| chr2:108480912 | A | T | 1 | a0001c0002t0001g0031 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3061-785A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108480912 | |||||||
| chr2:108481564 | G | A | 6 | a0001c0002t0008g0018 a0001c0002t0008g0019 a0001c0002t0008g0020 others(3): Show |
6 | HG00323.hp2 HG00639.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.3061-133G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 9/22 | chr2 | 108481564 | |||||||
| chr2:108481928 | C | A | 59 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(56): Show |
61 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.3180+112C>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 10/22 | chr2 | 108481928 | |||||||
| chr2:108482023 | GTTGT | G | 2 | a0005c0010t0020g0157 a0005c0010t0020g0158 |
2 | HG02040.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3180+219_3180+222d others(6): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr2 | 108482023 | ||||||
| chr2:108482461 | A | G | 3 | a0001c0002t0023g0154 a0001c0002t0023g0156 a0001c0002t0052g0155 |
3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3345+10A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 11/22 | chr2 | 108482461 | |||||||
| chr2:108482538 | T | C | 86 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(83): Show |
87 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.3345+87T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 11/22 | chr2 | 108482538 | |||||||
| chr2:108482542 | A | G | 60 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(57): Show |
62 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(59): Show |
intron_variant | MODIFIER | c.3345+91A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 11/22 | chr2 | 108482542 | |||||||
| chr2:108482700 | G | A | 1 | a0001c0002t0013g0088 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3345+249G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 11/22 | chr2 | 108482700 | |||||||
| chr2:108482780 | C | G | 59 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(56): Show |
61 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.3346-282C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 11/22 | chr2 | 108482780 | |||||||
| chr2:108482870 | C | T | 3 | a0004c0007t0022g0231 a0004c0007t0022g0232 a0004c0007t0047g0252 |
3 | HG02647.hp1 HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3346-192C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 11/22 | chr2 | 108482870 | |||||||
| chr2:108482929 | C | T | 52 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(49): Show |
54 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(51): Show |
intron_variant | MODIFIER | c.3346-133C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 11/22 | chr2 | 108482929 | |||||||
| chr2:108482999 | C | G | 1 | a0001c0001t0042g0249 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.3346-63C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 11/22 | chr2 | 108482999 | |||||||
| chr2:108483021 | A | G | 160 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(157): Show |
163 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.3346-41A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 11/22 | chr2 | 108483021 | |||||||
| chr2:108483250 | A | G | 7 | a0003c0003t0003g0107 a0003c0003t0003g0108 a0003c0003t0003g0109 others(4): Show |
7 | NA18947.hp1 NA18960.hp1 NA19062.hp2 others(4): Show |
intron_variant | MODIFIER | c.3450+84A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 12/22 | chr2 | 108483250 | |||||||
| chr2:108483322 | C | G | 2 | a0001c0001t0003g0120 a0001c0001t0003g0124 |
2 | HG03654.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.3450+156C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 12/22 | chr2 | 108483322 | |||||||
| chr2:108483369 | A | G | 1 | a0001c0001t0005g0095 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3450+203A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 12/22 | chr2 | 108483369 | |||||||
| chr2:108483409 | G | A | 101 | a0001c0001t0002g0008 a0001c0001t0002g0151 a0001c0001t0002g0174 others(98): Show |
104 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.3450+243G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 12/22 | chr2 | 108483409 | |||||||
| chr2:108483440 | G | C | 1 | a0001c0002t0001g0092 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.3450+274G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 12/22 | chr2 | 108483440 | |||||||
| chr2:108483484 | C | A | 2 | a0001c0001t0045g0152 a0001c0019t0010g0153 |
2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3450+318C>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 12/22 | chr2 | 108483484 | |||||||
| chr2:108483621 | A | G | 3 | a0001c0002t0023g0154 a0001c0002t0023g0156 a0001c0002t0052g0155 |
3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3450+455A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 12/22 | chr2 | 108483621 | |||||||
| chr2:108483882 | G | A | 1 | a0001c0002t0001g0037 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.3451-267G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 12/22 | chr2 | 108483882 | |||||||
| chr2:108484108 | G | C | 1 | a0001c0002t0052g0155 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3451-41G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 12/22 | chr2 | 108484108 | |||||||
| chr2:108484354 | A | G | 1 | a0001c0002t0001g0062 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.3613+43A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 13/22 | chr2 | 108484354 | |||||||
| chr2:108485169 | G | A | 3 | a0001c0002t0023g0154 a0001c0002t0023g0156 a0001c0002t0052g0155 |
3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3614-467G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 13/22 | chr2 | 108485169 | |||||||
| chr2:108485199 | A | T | 1 | a0001c0001t0003g0129 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3614-437A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 13/22 | chr2 | 108485199 | |||||||
| chr2:108485260 | A | G | 3 | a0001c0002t0023g0154 a0001c0002t0023g0156 a0001c0002t0052g0155 |
3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3614-376A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 13/22 | chr2 | 108485260 | |||||||
| chr2:108485322 | T | TA | 7 | a0002c0004t0012g0165 a0002c0004t0012g0166 a0002c0004t0012g0168 others(4): Show |
7 | HG02258.hp2 HG02922.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.3614-302dupA | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr2 | 108485322 | ||||||
| chr2:108485574 | T | C | 4 | a0001c0008t0014g0159 a0001c0008t0014g0160 a0001c0008t0014g0161 others(1): Show |
4 | HG01261.hp1 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.3614-62T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 13/22 | chr2 | 108485574 | |||||||
| chr2:108486035 | C | A | 86 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(83): Show |
87 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.3792+127C>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 15/22 | chr2 | 108486035 | |||||||
| chr2:108486078 | G | A | 184 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(181): Show |
188 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.3792+170G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 15/22 | chr2 | 108486078 | |||||||
| chr2:108486189 | A | G | 4 | a0001c0006t0018g0007 a0001c0006t0018g0147 a0001c0006t0018g0148 others(1): Show |
4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.3792+281A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 15/22 | chr2 | 108486189 | |||||||
| chr2:108486488 | T | C | 1 | a0001c0001t0011g0131 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3793-23T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 15/22 | chr2 | 108486488 | |||||||
| chr2:108486652 | C | T | 88 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(85): Show |
89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
splice_region_variant&intron_variant | LOW | c.3930+4C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 16/22 | chr2 | 108486652 | |||||||
| chr2:108486808 | A | C | 3 | a0001c0002t0023g0154 a0001c0002t0023g0156 a0001c0002t0052g0155 |
3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3930+160A>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 16/22 | chr2 | 108486808 | |||||||
| chr2:108486822 | C | G | 2 | a0001c0002t0001g0031 a0001c0002t0001g0076 |
2 | HG03669.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.3930+174C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 16/22 | chr2 | 108486822 | |||||||
| chr2:108486827 | G | A | 2 | a0005c0010t0020g0157 a0005c0010t0020g0158 |
2 | HG02040.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3930+179G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 16/22 | chr2 | 108486827 | |||||||
| chr2:108487053 | G | A | 88 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(85): Show |
89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.3930+405G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 16/22 | chr2 | 108487053 | |||||||
| chr2:108487166 | A | G | 2 | a0001c0001t0003g0136 a0001c0001t0005g0137 |
2 | HG02258.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3930+518A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 16/22 | chr2 | 108487166 | |||||||
| chr2:108487204 | A | G | 59 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(56): Show |
61 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.3931-495A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 16/22 | chr2 | 108487204 | |||||||
| chr2:108487324 | T | A | 14 | a0001c0001t0007g0009 a0001c0001t0007g0257 a0001c0001t0007g0258 others(11): Show |
15 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.3931-375T>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 16/22 | chr2 | 108487324 | |||||||
| chr2:108487381 | A | G | 2 | a0005c0010t0020g0157 a0005c0010t0020g0158 |
2 | HG02040.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3931-318A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 16/22 | chr2 | 108487381 | |||||||
| chr2:108487900 | A | AT | 11 | a0001c0001t0002g0199 a0001c0001t0002g0203 a0001c0001t0006g0222 others(8): Show |
11 | HG00738.hp1 HG01106.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.4052+103dupT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr2 | 108487900 | ||||||
| chr2:108487900 | AT | A | 56 | a0001c0001t0002g0214 a0001c0001t0003g0004 a0001c0001t0003g0098 others(53): Show |
58 | HG00639.hp1 HG01074.hp1 HG01074.hp2 others(55): Show |
intron_variant | MODIFIER | c.4052+103delT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr2 | 108487900 | ||||||
| chr2:108487900 | ATT | A | 8 | a0001c0001t0003g0101 a0001c0001t0011g0130 a0001c0001t0011g0131 others(5): Show |
8 | HG00323.hp1 HG01243.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.4052+102_4052+103d others(4): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr2 | 108487900 | ||||||
| chr2:108487901 | T | A | 1 | a0001c0002t0052g0155 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.4052+81T>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 17/22 | chr2 | 108487901 | |||||||
| chr2:108487956 | G | C | 2 | a0001c0002t0023g0154 a0001c0002t0023g0156 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4052+136G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 17/22 | chr2 | 108487956 | |||||||
| chr2:108487992 | G | A | 3 | a0001c0001t0002g0181 a0001c0001t0002g0227 a0001c0001t0019g0200 |
3 | HG02723.hp2 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.4052+172G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 17/22 | chr2 | 108487992 | |||||||
| chr2:108488008 | G | C | 160 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(157): Show |
163 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.4052+188G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 17/22 | chr2 | 108488008 | |||||||
| chr2:108488051 | G | A | 1 | a0001c0001t0002g0204 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.4052+231G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 17/22 | chr2 | 108488051 | |||||||
| chr2:108488187 | G | A | 86 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(83): Show |
87 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.4052+367G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 17/22 | chr2 | 108488187 | |||||||
| chr2:108488195 | C | T | 1 | a0001c0001t0004g0234 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.4052+375C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 17/22 | chr2 | 108488195 | |||||||
| chr2:108488203 | G | C | 1 | a0001c0002t0001g0054 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.4052+383G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 17/22 | chr2 | 108488203 | |||||||
| chr2:108488311 | C | A | 1 | a0001c0001t0002g0227 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.4052+491C>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 17/22 | chr2 | 108488311 | |||||||
| chr2:108488411 | T | A | 1 | a0001c0001t0004g0251 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.4052+591T>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 17/22 | chr2 | 108488411 | |||||||
| chr2:108488488 | A | C | 1 | a0001c0001t0003g0119 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.4052+668A>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 17/22 | chr2 | 108488488 | |||||||
| chr2:108488738 | A | G | 244 | a0001c0001t0002g0008 a0001c0001t0002g0151 a0001c0001t0002g0174 others(241): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.4052+918A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 17/22 | chr2 | 108488738 | |||||||
| chr2:108488921 | T | C | 1 | a0001c0002t0001g0030 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.4053-917T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 17/22 | chr2 | 108488921 | |||||||
| chr2:108489146 | A | C | 1 | a0001c0001t0010g0264 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4053-692A>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 17/22 | chr2 | 108489146 | |||||||
| chr2:108489155 | C | G | 4 | a0001c0006t0018g0007 a0001c0006t0018g0147 a0001c0006t0018g0148 others(1): Show |
4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.4053-683C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 17/22 | chr2 | 108489155 | |||||||
| chr2:108489205 | A | G | 32 | a0001c0001t0002g0176 a0001c0001t0002g0177 a0001c0001t0002g0180 others(29): Show |
32 | HG00099.hp2 HG00738.hp2 HG01346.hp2 others(29): Show |
intron_variant | MODIFIER | c.4053-633A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 17/22 | chr2 | 108489205 | |||||||
| chr2:108489376 | G | A | 1 | a0001c0001t0003g0115 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.4053-462G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 17/22 | chr2 | 108489376 | |||||||
| chr2:108489395 | G | A | 1 | a0001c0002t0001g0010 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.4053-443G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 17/22 | chr2 | 108489395 | |||||||
| chr2:108489471 | C | T | 8 | a0001c0002t0001g0033 a0002c0004t0012g0165 a0002c0004t0012g0166 others(5): Show |
8 | HG02258.hp2 HG02922.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.4053-367C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 17/22 | chr2 | 108489471 | |||||||
| chr2:108489514 | C | CA | 6 | a0001c0001t0002g0196 a0001c0001t0045g0152 a0001c0002t0023g0154 others(3): Show |
6 | HG02572.hp2 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.4053-311dupA | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr2 | 108489514 | ||||||
| chr2:108489678 | T | TG | 91 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(88): Show |
92 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.4053-160_4053-159i others(3): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 17/22 | chr2 | 108489678 | |||||||
| chr2:108490037 | C | T | 2 | a0005c0010t0020g0157 a0005c0010t0020g0158 |
2 | HG02040.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.4229+23C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 18/22 | chr2 | 108490037 | |||||||
| chr2:108490222 | A | T | 4 | a0001c0006t0018g0007 a0001c0006t0018g0147 a0001c0006t0018g0148 others(1): Show |
4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.4229+208A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 18/22 | chr2 | 108490222 | |||||||
| chr2:108490585 | T | TAA | 160 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(157): Show |
163 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.4229+571_4229+572i others(4): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 18/22 | chr2 | 108490585 | |||||||
| chr2:108490632 | T | C | 4 | a0001c0008t0014g0159 a0001c0008t0014g0160 a0001c0008t0014g0161 others(1): Show |
4 | HG01261.hp1 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.4229+618T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 18/22 | chr2 | 108490632 | |||||||
| chr2:108490635 | T | C | 1 | a0001c0001t0003g0144 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4229+621T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 18/22 | chr2 | 108490635 | |||||||
| chr2:108490709 | T | C | 1 | a0001c0001t0011g0130 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.4229+695T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 18/22 | chr2 | 108490709 | |||||||
| chr2:108490994 | T | C | 1 | a0002c0004t0012g0169 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4229+980T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 18/22 | chr2 | 108490994 | |||||||
| chr2:108491067 | T | C | 6 | a0001c0001t0010g0255 a0001c0001t0010g0263 a0001c0001t0010g0264 others(3): Show |
6 | HG02055.hp2 HG02280.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.4229+1053T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 18/22 | chr2 | 108491067 | |||||||
| chr2:108491093 | T | TTATC | 7 | a0002c0004t0012g0165 a0002c0004t0012g0166 a0002c0004t0012g0168 others(4): Show |
7 | HG02258.hp2 HG02922.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.4229+1083_4229+108 others(8): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr2 | 108491093 | ||||||
| chr2:108491198 | A | T | 1 | a0004c0007t0047g0252 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4229+1184A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 18/22 | chr2 | 108491198 | |||||||
| chr2:108491618 | A | T | 2 | a0001c0001t0045g0152 a0001c0019t0010g0153 |
2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4230-955A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 18/22 | chr2 | 108491618 | |||||||
| chr2:108491619 | A | G | 2 | a0001c0001t0045g0152 a0001c0019t0010g0153 |
2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4230-954A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 18/22 | chr2 | 108491619 | |||||||
| chr2:108491777 | A | AT | 6 | a0001c0001t0003g0142 a0001c0001t0003g0144 a0001c0001t0005g0006 others(3): Show |
7 | HG00639.hp1 HG02622.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.4230-793dupT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr2 | 108491777 | ||||||
| chr2:108491780 | T | A | 1 | a0001c0002t0023g0156 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.4230-793T>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 18/22 | chr2 | 108491780 | |||||||
| chr2:108491781 | A | T | 26 | a0001c0001t0003g0098 a0001c0001t0003g0101 a0001c0001t0003g0104 others(23): Show |
28 | HG00323.hp1 HG00639.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.4230-792A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 18/22 | chr2 | 108491781 | |||||||
| chr2:108491785 | A | T | 125 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(122): Show |
128 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.4230-788A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 18/22 | chr2 | 108491785 | |||||||
| chr2:108491789 | T | A | 1 | a0001c0001t0007g0262 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.4230-784T>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 18/22 | chr2 | 108491789 | |||||||
| chr2:108492004 | T | C | 184 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(181): Show |
188 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.4230-569T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 18/22 | chr2 | 108492004 | |||||||
| chr2:108492141 | G | T | 1 | a0001c0002t0013g0088 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4230-432G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 18/22 | chr2 | 108492141 | |||||||
| chr2:108492142 | T | G | 5 | a0002c0004t0012g0165 a0002c0004t0012g0166 a0002c0004t0012g0168 others(2): Show |
5 | HG02258.hp2 HG02922.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.4230-431T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 18/22 | chr2 | 108492142 | |||||||
| chr2:108492834 | G | A | 4 | a0001c0006t0018g0007 a0001c0006t0018g0147 a0001c0006t0018g0148 others(1): Show |
4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.4447+44G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108492834 | |||||||
| chr2:108492869 | TAAGA | T | 59 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(56): Show |
61 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.4447+86_4447+89del others(4): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 108492869 | ||||||
| chr2:108492887 | A | G | 1 | a0009c0018t0001g0063 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.4447+97A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108492887 | |||||||
| chr2:108492888 | G | T | 1 | a0001c0015t0001g0070 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.4447+98G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108492888 | |||||||
| chr2:108492963 | C | A | 1 | a0003c0003t0003g0110 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.4447+173C>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108492963 | |||||||
| chr2:108493016 | C | T | 1 | a0001c0002t0021g0087 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.4447+226C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108493016 | |||||||
| chr2:108493085 | G | A | 1 | a0001c0001t0003g0117 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4447+295G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108493085 | |||||||
| chr2:108493153 | G | A | 3 | a0001c0002t0023g0154 a0001c0002t0023g0156 a0001c0002t0052g0155 |
3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.4447+363G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108493153 | |||||||
| chr2:108493158 | C | T | 4 | a0001c0006t0018g0007 a0001c0006t0018g0147 a0001c0006t0018g0148 others(1): Show |
4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.4447+368C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108493158 | |||||||
| chr2:108493241 | C | T | 1 | a0001c0001t0002g0229 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.4447+451C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108493241 | |||||||
| chr2:108493264 | A | G | 1 | a0001c0001t0010g0250 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.4447+474A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108493264 | |||||||
| chr2:108493306 | T | C | 1 | a0002c0004t0031g0170 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.4447+516T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108493306 | |||||||
| chr2:108493436 | G | A | 1 | a0001c0001t0017g0127 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.4447+646G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108493436 | |||||||
| chr2:108493503 | A | T | 1 | a0001c0001t0029g0216 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.4447+713A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108493503 | |||||||
| chr2:108493570 | T | C | 91 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(88): Show |
92 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.4447+780T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108493570 | |||||||
| chr2:108493729 | G | A | 7 | a0002c0004t0012g0165 a0002c0004t0012g0166 a0002c0004t0012g0168 others(4): Show |
7 | HG02258.hp2 HG02922.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.4447+939G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108493729 | |||||||
| chr2:108493774 | A | T | 1 | a0002c0004t0030g0164 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4447+984A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108493774 | |||||||
| chr2:108493892 | CA | C | 7 | a0002c0004t0012g0165 a0002c0004t0012g0166 a0002c0004t0012g0168 others(4): Show |
7 | HG02258.hp2 HG02922.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.4447+1107delA | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr2 | 108493892 | ||||||
| chr2:108494123 | C | G | 4 | a0001c0006t0018g0007 a0001c0006t0018g0147 a0001c0006t0018g0148 others(1): Show |
4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.4448-1168C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494123 | |||||||
| chr2:108494147 | T | A | 1 | a0001c0001t0002g0181 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4448-1144T>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494147 | |||||||
| chr2:108494202 | A | G | 1 | a0001c0001t0005g0141 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.4448-1089A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494202 | |||||||
| chr2:108494333 | C | T | 1 | a0001c0001t0003g0145 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.4448-958C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494333 | |||||||
| chr2:108494337 | A | G | 3 | a0001c0001t0002g0214 a0001c0001t0027g0215 a0001c0001t0029g0216 |
3 | HG02257.hp1 HG02717.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.4448-954A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494337 | |||||||
| chr2:108494560 | A | C | 22 | a0001c0001t0003g0117 a0001c0001t0003g0118 a0001c0001t0003g0119 others(19): Show |
22 | HG02602.hp1 HG03017.hp2 HG03239.hp1 others(19): Show |
intron_variant | MODIFIER | c.4448-731A>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494560 | |||||||
| chr2:108494568 | A | G | 1 | a0001c0002t0001g0013 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.4448-723A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494568 | |||||||
| chr2:108494572 | G | A | 1 | a0001c0001t0003g0142 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.4448-719G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494572 | |||||||
| chr2:108494605 | A | G | 1 | a0001c0002t0001g0040 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.4448-686A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494605 | |||||||
| chr2:108494731 | A | G | 7 | a0003c0003t0003g0107 a0003c0003t0003g0108 a0003c0003t0003g0109 others(4): Show |
7 | NA18947.hp1 NA18960.hp1 NA19062.hp2 others(4): Show |
intron_variant | MODIFIER | c.4448-560A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494731 | |||||||
| chr2:108494766 | T | G | 7 | a0003c0003t0003g0107 a0003c0003t0003g0108 a0003c0003t0003g0109 others(4): Show |
7 | NA18947.hp1 NA18960.hp1 NA19062.hp2 others(4): Show |
intron_variant | MODIFIER | c.4448-525T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494766 | |||||||
| chr2:108494779 | G | C | 7 | a0003c0003t0003g0107 a0003c0003t0003g0108 a0003c0003t0003g0109 others(4): Show |
7 | NA18947.hp1 NA18960.hp1 NA19062.hp2 others(4): Show |
intron_variant | MODIFIER | c.4448-512G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494779 | |||||||
| chr2:108494783 | C | T | 88 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(85): Show |
89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.4448-508C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494783 | |||||||
| chr2:108494787 | T | G | 7 | a0003c0003t0003g0107 a0003c0003t0003g0108 a0003c0003t0003g0109 others(4): Show |
7 | NA18947.hp1 NA18960.hp1 NA19062.hp2 others(4): Show |
intron_variant | MODIFIER | c.4448-504T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494787 | |||||||
| chr2:108494801 | T | G | 7 | a0003c0003t0003g0107 a0003c0003t0003g0108 a0003c0003t0003g0109 others(4): Show |
7 | NA18947.hp1 NA18960.hp1 NA19062.hp2 others(4): Show |
intron_variant | MODIFIER | c.4448-490T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494801 | |||||||
| chr2:108494803 | C | G | 7 | a0003c0003t0003g0107 a0003c0003t0003g0108 a0003c0003t0003g0109 others(4): Show |
7 | NA18947.hp1 NA18960.hp1 NA19062.hp2 others(4): Show |
intron_variant | MODIFIER | c.4448-488C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494803 | |||||||
| chr2:108494807 | G | C | 2 | a0001c0002t0023g0154 a0001c0002t0023g0156 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4448-484G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494807 | |||||||
| chr2:108494813 | G | T | 7 | a0003c0003t0003g0107 a0003c0003t0003g0108 a0003c0003t0003g0109 others(4): Show |
7 | NA18947.hp1 NA18960.hp1 NA19062.hp2 others(4): Show |
intron_variant | MODIFIER | c.4448-478G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494813 | |||||||
| chr2:108494819 | T | TG | 7 | a0003c0003t0003g0107 a0003c0003t0003g0108 a0003c0003t0003g0109 others(4): Show |
7 | NA18947.hp1 NA18960.hp1 NA19062.hp2 others(4): Show |
intron_variant | MODIFIER | c.4448-472_4448-471i others(3): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494819 | |||||||
| chr2:108494821 | G | T | 7 | a0003c0003t0003g0107 a0003c0003t0003g0108 a0003c0003t0003g0109 others(4): Show |
7 | NA18947.hp1 NA18960.hp1 NA19062.hp2 others(4): Show |
intron_variant | MODIFIER | c.4448-470G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494821 | |||||||
| chr2:108494826 | G | T | 7 | a0003c0003t0003g0107 a0003c0003t0003g0108 a0003c0003t0003g0109 others(4): Show |
7 | NA18947.hp1 NA18960.hp1 NA19062.hp2 others(4): Show |
intron_variant | MODIFIER | c.4448-465G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494826 | |||||||
| chr2:108494839 | A | C | 7 | a0003c0003t0003g0107 a0003c0003t0003g0108 a0003c0003t0003g0109 others(4): Show |
7 | NA18947.hp1 NA18960.hp1 NA19062.hp2 others(4): Show |
intron_variant | MODIFIER | c.4448-452A>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494839 | |||||||
| chr2:108494845 | A | G | 9 | a0003c0003t0003g0107 a0003c0003t0003g0108 a0003c0003t0003g0109 others(6): Show |
9 | HG02647.hp1 HG03486.hp2 NA18947.hp1 others(6): Show |
intron_variant | MODIFIER | c.4448-446A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494845 | |||||||
| chr2:108494853 | G | A | 2 | a0004c0007t0022g0231 a0004c0007t0022g0232 |
2 | HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.4448-438G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494853 | |||||||
| chr2:108494868 | A | G | 2 | a0001c0002t0023g0154 a0001c0002t0023g0156 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4448-423A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494868 | |||||||
| chr2:108494890 | G | A | 2 | a0001c0001t0011g0149 a0001c0001t0011g0150 |
2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.4448-401G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494890 | |||||||
| chr2:108494908 | T | C | 2 | a0001c0001t0011g0149 a0001c0001t0011g0150 |
2 | HG02572.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.4448-383T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494908 | |||||||
| chr2:108494929 | A | G | 1 | a0001c0001t0045g0152 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4448-362A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494929 | |||||||
| chr2:108494966 | C | T | 10 | a0001c0001t0003g0106 a0001c0001t0003g0128 a0001c0006t0018g0007 others(7): Show |
10 | HG01261.hp1 HG01981.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.4448-325C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494966 | |||||||
| chr2:108494971 | C | G | 1 | a0001c0001t0004g0234 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.4448-320C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494971 | |||||||
| chr2:108494977 | G | A | 8 | a0001c0001t0004g0234 a0001c0001t0011g0130 a0001c0001t0011g0140 others(5): Show |
8 | HG01243.hp2 HG02572.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.4448-314G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108494977 | |||||||
| chr2:108495031 | T | C | 1 | a0005c0010t0020g0158 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4448-260T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108495031 | |||||||
| chr2:108495107 | A | G | 7 | a0001c0001t0002g0192 a0001c0001t0004g0254 a0001c0001t0045g0152 others(4): Show |
7 | HG02572.hp2 HG03453.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.4448-184A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108495107 | |||||||
| chr2:108495110 | T | C | 7 | a0001c0001t0002g0192 a0001c0001t0004g0254 a0001c0001t0045g0152 others(4): Show |
7 | HG02572.hp2 HG03453.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.4448-181T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108495110 | |||||||
| chr2:108495135 | C | T | 1 | a0001c0002t0001g0054 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.4448-156C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108495135 | |||||||
| chr2:108495183 | T | C | 3 | a0001c0001t0006g0173 a0001c0001t0006g0179 a0001c0001t0006g0190 |
3 | NA18942.hp1 NA18969.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.4448-108T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108495183 | |||||||
| chr2:108495204 | T | G | 89 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(86): Show |
90 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.4448-87T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108495204 | |||||||
| chr2:108495224 | T | C | 1 | a0001c0001t0015g0243 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.4448-67T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108495224 | |||||||
| chr2:108495238 | A | T | 4 | a0001c0006t0018g0007 a0001c0006t0018g0147 a0001c0006t0018g0148 others(1): Show |
4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.4448-53A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108495238 | |||||||
| chr2:108495264 | A | G | 4 | a0001c0006t0018g0007 a0001c0006t0018g0147 a0001c0006t0018g0148 others(1): Show |
4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.4448-27A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 19/22 | chr2 | 108495264 | |||||||
| chr2:108495710 | G | A | 2 | a0001c0002t0001g0058 a0001c0002t0001g0060 |
2 | HG01106.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.4642+225G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 20/22 | chr2 | 108495710 | |||||||
| chr2:108495741 | G | A | 1 | a0001c0001t0002g0253 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.4642+256G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 20/22 | chr2 | 108495741 | |||||||
| chr2:108495742 | T | C | 1 | a0001c0001t0002g0253 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.4642+257T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 20/22 | chr2 | 108495742 | |||||||
| chr2:108495802 | G | A | 1 | a0001c0002t0001g0092 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.4642+317G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 20/22 | chr2 | 108495802 | |||||||
| chr2:108495810 | CA | C | 3 | a0001c0002t0023g0154 a0001c0002t0023g0156 a0001c0002t0052g0155 |
3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.4642+326delA | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 20/22 | chr2 | 108495810 | |||||||
| chr2:108495828 | G | C | 2 | a0002c0004t0012g0165 a0002c0004t0012g0168 |
2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.4642+343G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 20/22 | chr2 | 108495828 | |||||||
| chr2:108496031 | A | G | 3 | a0001c0001t0002g0199 a0001c0001t0002g0205 a0001c0001t0002g0213 |
3 | HG00738.hp1 HG00741.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.4642+546A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 20/22 | chr2 | 108496031 | |||||||
| chr2:108496051 | T | C | 91 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(88): Show |
92 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.4642+566T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 20/22 | chr2 | 108496051 | |||||||
| chr2:108496147 | T | C | 1 | a0001c0001t0009g0221 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4642+662T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 20/22 | chr2 | 108496147 | |||||||
| chr2:108496167 | G | A | 91 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(88): Show |
92 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.4642+682G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 20/22 | chr2 | 108496167 | |||||||
| chr2:108496199 | G | C | 184 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(181): Show |
188 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.4642+714G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 20/22 | chr2 | 108496199 | |||||||
| chr2:108496233 | C | G | 2 | a0001c0002t0001g0054 a0001c0002t0001g0069 |
2 | HG00099.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.4643-737C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 20/22 | chr2 | 108496233 | |||||||
| chr2:108496244 | A | T | 1 | a0009c0018t0001g0063 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.4643-726A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 20/22 | chr2 | 108496244 | |||||||
| chr2:108496258 | G | C | 3 | a0001c0002t0023g0154 a0001c0002t0023g0156 a0001c0002t0052g0155 |
3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.4643-712G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 20/22 | chr2 | 108496258 | |||||||
| chr2:108496332 | C | T | 2 | a0005c0010t0020g0157 a0005c0010t0020g0158 |
2 | HG02040.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.4643-638C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 20/22 | chr2 | 108496332 | |||||||
| chr2:108496637 | C | A | 1 | a0001c0001t0003g0142 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.4643-333C>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 20/22 | chr2 | 108496637 | |||||||
| chr2:108496924 | T | G | 1 | a0005c0010t0020g0158 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4643-46T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 20/22 | chr2 | 108496924 | |||||||
| chr2:108496954 | GAAC | G | 4 | a0001c0008t0014g0159 a0001c0008t0014g0160 a0001c0008t0014g0161 others(1): Show |
4 | HG01261.hp1 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.4643-11_4643-9delA others(2): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr2 | 108496954 | ||||||
| chr2:108497234 | A | G | 1 | a0004c0007t0047g0252 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4782+125A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | chr2 | 108497234 | |||||||
| chr2:108497354 | G | T | 4 | a0001c0002t0008g0019 a0001c0002t0008g0021 a0001c0002t0008g0080 others(1): Show |
4 | HG00323.hp2 HG00639.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.4782+245G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | chr2 | 108497354 | |||||||
| chr2:108497622 | T | C | 1 | a0001c0001t0009g0221 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4782+513T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | chr2 | 108497622 | |||||||
| chr2:108498101 | T | C | 1 | a0001c0002t0001g0076 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.4782+992T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | chr2 | 108498101 | |||||||
| chr2:108498102 | G | C | 1 | a0001c0002t0001g0076 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.4782+993G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | chr2 | 108498102 | |||||||
| chr2:108498121 | G | A | 4 | a0001c0006t0018g0007 a0001c0006t0018g0147 a0001c0006t0018g0148 others(1): Show |
4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.4782+1012G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | chr2 | 108498121 | |||||||
| chr2:108498151 | A | AACCTAAA others(1): Show |
4 | a0001c0008t0014g0159 a0001c0008t0014g0160 a0001c0008t0014g0161 others(1): Show |
4 | HG01261.hp1 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.4782+1043_4782+105 others(12): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr2 | 108498151 | ||||||
| chr2:108498183 | C | CT | 28 | a0001c0001t0002g0151 a0001c0001t0002g0192 a0001c0001t0002g0194 others(25): Show |
28 | HG00673.hp1 HG00741.hp2 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.4782+1104dupT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr2 | 108498183 | ||||||
| chr2:108498183 | C | CTT | 8 | a0001c0001t0002g0008 a0001c0001t0002g0223 a0001c0001t0002g0224 others(5): Show |
8 | HG02280.hp1 HG02738.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.4782+1103_4782+110 others(6): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr2 | 108498183 | ||||||
| chr2:108498183 | C | CTTT | 9 | a0001c0001t0006g0222 a0001c0001t0009g0218 a0001c0001t0009g0219 others(6): Show |
9 | HG01109.hp2 HG01175.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.4782+1102_4782+110 others(7): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr2 | 108498183 | ||||||
| chr2:108498183 | CT | C | 95 | a0001c0001t0002g0196 a0001c0001t0003g0117 a0001c0001t0003g0118 others(92): Show |
97 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.4782+1104delT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr2 | 108498183 | ||||||
| chr2:108498183 | CTT | C | 9 | a0001c0001t0007g0009 a0001c0001t0007g0257 a0001c0001t0007g0258 others(6): Show |
10 | HG01071.hp1 HG01884.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.4782+1103_4782+110 others(6): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr2 | 108498183 | ||||||
| chr2:108498227 | G | A | 1 | a0001c0001t0003g0133 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.4782+1118G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | chr2 | 108498227 | |||||||
| chr2:108498235 | T | A | 167 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(164): Show |
170 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.4782+1126T>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | chr2 | 108498235 | |||||||
| chr2:108498260 | A | G | 2 | a0001c0002t0001g0012 a0001c0002t0001g0022 |
2 | HG01071.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.4782+1151A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | chr2 | 108498260 | |||||||
| chr2:108498276 | A | G | 1 | a0001c0001t0002g0192 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.4782+1167A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | chr2 | 108498276 | |||||||
| chr2:108498356 | C | T | 1 | a0001c0001t0002g0181 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4783-1197C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | chr2 | 108498356 | |||||||
| chr2:108498485 | C | T | 1 | a0001c0001t0006g0173 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.4783-1068C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | chr2 | 108498485 | |||||||
| chr2:108498545 | T | C | 1 | a0001c0002t0052g0155 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.4783-1008T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | chr2 | 108498545 | |||||||
| chr2:108498651 | C | T | 1 | a0001c0001t0011g0150 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.4783-902C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | chr2 | 108498651 | |||||||
| chr2:108498736 | A | G | 246 | a0001c0001t0002g0008 a0001c0001t0002g0151 a0001c0001t0002g0174 others(243): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.4783-817A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | chr2 | 108498736 | |||||||
| chr2:108498973 | C | T | 1 | a0001c0002t0001g0093 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4783-580C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | chr2 | 108498973 | |||||||
| chr2:108499082 | C | CTT | 160 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(157): Show |
163 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.4783-471_4783-470i others(4): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | chr2 | 108499082 | |||||||
| chr2:108499194 | C | G | 44 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(41): Show |
45 | HG00323.hp1 HG01074.hp1 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.4783-359C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | chr2 | 108499194 | |||||||
| chr2:108499210 | A | G | 1 | a0002c0004t0051g0167 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4783-343A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | chr2 | 108499210 | |||||||
| chr2:108499278 | C | T | 2 | a0004c0007t0022g0231 a0004c0007t0022g0232 |
2 | HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.4783-275C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | chr2 | 108499278 | |||||||
| chr2:108499336 | C | T | 4 | a0001c0008t0014g0159 a0001c0008t0014g0160 a0001c0008t0014g0161 others(1): Show |
4 | HG01261.hp1 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.4783-217C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | chr2 | 108499336 | |||||||
| chr2:108499337 | G | A | 1 | a0001c0002t0001g0056 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.4783-216G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | chr2 | 108499337 | |||||||
| chr2:108499363 | C | T | 1 | a0002c0004t0012g0165 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4783-190C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | chr2 | 108499363 | |||||||
| chr2:108499399 | G | A | 4 | a0001c0006t0018g0007 a0001c0006t0018g0147 a0001c0006t0018g0148 others(1): Show |
4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.4783-154G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | chr2 | 108499399 | |||||||
| chr2:108499549 | C | A | 1 | a0004c0007t0022g0232 | 1 | HG02647.hp1 | splice_region_variant&intron_variant | LOW | c.4783-4C>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 21/22 | chr2 | 108499549 | |||||||
| chr2:108499970 | G | A | 2 | a0001c0002t0023g0154 a0001c0002t0023g0156 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4984+216G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108499970 | |||||||
| chr2:108500157 | CAT | C | 154 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(151): Show |
157 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.4984+409_4984+410d others(4): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr2 | 108500157 | ||||||
| chr2:108500177 | G | A | 7 | a0003c0003t0003g0107 a0003c0003t0003g0108 a0003c0003t0003g0109 others(4): Show |
7 | NA18947.hp1 NA18960.hp1 NA19062.hp2 others(4): Show |
intron_variant | MODIFIER | c.4984+423G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108500177 | |||||||
| chr2:108500243 | G | A | 59 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(56): Show |
61 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.4984+489G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108500243 | |||||||
| chr2:108500329 | A | G | 1 | a0001c0001t0002g0198 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.4984+575A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108500329 | |||||||
| chr2:108500390 | A | G | 160 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(157): Show |
163 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.4984+636A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108500390 | |||||||
| chr2:108500412 | T | C | 91 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(88): Show |
92 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.4984+658T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108500412 | |||||||
| chr2:108500488 | G | A | 1 | a0001c0002t0001g0054 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.4984+734G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108500488 | |||||||
| chr2:108500540 | A | G | 2 | a0001c0001t0045g0152 a0001c0019t0010g0153 |
2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4984+786A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108500540 | |||||||
| chr2:108500658 | G | C | 91 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(88): Show |
92 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.4984+904G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108500658 | |||||||
| chr2:108500664 | T | C | 2 | a0001c0002t0023g0154 a0001c0002t0023g0156 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4984+910T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108500664 | |||||||
| chr2:108500705 | G | T | 90 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(87): Show |
91 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.4984+951G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108500705 | |||||||
| chr2:108500768 | T | G | 3 | a0001c0008t0014g0159 a0001c0008t0014g0160 a0001c0008t0014g0161 |
3 | NA18954.hp2 NA18970.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.4984+1014T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108500768 | |||||||
| chr2:108500798 | A | C | 7 | a0001c0001t0011g0130 a0001c0001t0011g0131 a0001c0001t0011g0140 others(4): Show |
7 | HG01243.hp2 HG02055.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.4984+1044A>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108500798 | |||||||
| chr2:108500906 | G | C | 2 | a0005c0010t0020g0157 a0005c0010t0020g0158 |
2 | HG02040.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.4984+1152G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108500906 | |||||||
| chr2:108500997 | C | T | 2 | a0001c0002t0001g0077 a0006c0017t0050g0162 |
2 | HG01261.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.4984+1243C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108500997 | |||||||
| chr2:108501019 | A | G | 5 | a0001c0002t0001g0028 a0001c0002t0023g0154 a0001c0002t0023g0156 others(2): Show |
5 | HG01261.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.4984+1265A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501019 | |||||||
| chr2:108501059 | G | A | 50 | a0001c0002t0001g0003 a0001c0002t0001g0010 a0001c0002t0001g0011 others(47): Show |
51 | HG00673.hp1 HG00673.hp2 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.4984+1305G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501059 | |||||||
| chr2:108501082 | G | T | 11 | a0001c0001t0002g0008 a0001c0001t0002g0151 a0001c0001t0002g0174 others(8): Show |
11 | HG01109.hp2 HG01167.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.4984+1328G>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501082 | |||||||
| chr2:108501087 | C | T | 1 | a0001c0002t0013g0088 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4984+1333C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501087 | |||||||
| chr2:108501089 | A | G | 1 | a0001c0002t0001g0075 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.4984+1335A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501089 | |||||||
| chr2:108501098 | C | T | 1 | a0001c0002t0001g0075 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.4984+1344C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501098 | |||||||
| chr2:108501105 | C | T | 1 | a0001c0002t0001g0062 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.4984+1351C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501105 | |||||||
| chr2:108501113 | A | G | 1 | a0001c0002t0001g0028 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.4984+1359A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501113 | |||||||
| chr2:108501121 | C | A | 12 | a0001c0001t0002g0008 a0001c0001t0002g0151 a0001c0001t0002g0174 others(9): Show |
12 | HG01109.hp2 HG01167.hp2 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.4984+1367C>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501121 | |||||||
| chr2:108501124 | C | T | 12 | a0001c0001t0002g0008 a0001c0001t0002g0151 a0001c0001t0002g0174 others(9): Show |
12 | HG01109.hp2 HG01167.hp2 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.4984+1370C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501124 | |||||||
| chr2:108501130 | G | A | 10 | a0001c0001t0002g0008 a0001c0001t0002g0151 a0001c0001t0002g0174 others(7): Show |
10 | HG01167.hp2 HG01175.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.4984+1376G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501130 | |||||||
| chr2:108501145 | G | A | 7 | a0002c0004t0012g0165 a0002c0004t0012g0166 a0002c0004t0012g0168 others(4): Show |
7 | HG02258.hp2 HG02922.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.4984+1391G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501145 | |||||||
| chr2:108501165 | T | G | 1 | a0002c0004t0012g0165 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4984+1411T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501165 | |||||||
| chr2:108501175 | C | T | 195 | a0001c0001t0002g0008 a0001c0001t0002g0151 a0001c0001t0002g0174 others(192): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.4984+1421C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501175 | |||||||
| chr2:108501189 | G | A | 200 | a0001c0001t0002g0008 a0001c0001t0002g0151 a0001c0001t0002g0174 others(197): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.4984+1435G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501189 | |||||||
| chr2:108501217 | C | T | 1 | a0001c0001t0017g0127 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.4984+1463C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501217 | |||||||
| chr2:108501231 | C | T | 1 | a0001c0001t0005g0103 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.4984+1477C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501231 | |||||||
| chr2:108501232 | G | A | 67 | a0001c0001t0002g0191 a0001c0001t0007g0009 a0001c0001t0007g0257 others(64): Show |
69 | HG00673.hp1 HG00673.hp2 HG01071.hp1 others(66): Show |
intron_variant | MODIFIER | c.4984+1478G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501232 | |||||||
| chr2:108501270 | C | A | 1 | a0001c0001t0002g0191 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.4984+1516C>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501270 | |||||||
| chr2:108501277 | G | A | 149 | a0001c0001t0002g0181 a0001c0001t0002g0186 a0001c0001t0002g0227 others(146): Show |
152 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.4984+1523G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501277 | |||||||
| chr2:108501281 | A | G | 4 | a0001c0001t0002g0203 a0001c0002t0001g0015 a0001c0002t0001g0040 others(1): Show |
4 | HG02602.hp2 HG03834.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.4984+1527A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501281 | |||||||
| chr2:108501481 | C | T | 5 | a0001c0001t0003g0133 a0001c0008t0014g0159 a0001c0008t0014g0160 others(2): Show |
5 | HG01261.hp1 HG03710.hp2 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.4984+1727C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501481 | |||||||
| chr2:108501519 | A | G | 178 | a0001c0001t0002g0008 a0001c0001t0002g0151 a0001c0001t0002g0174 others(175): Show |
181 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.4984+1765A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501519 | |||||||
| chr2:108501541 | T | A | 2 | a0001c0002t0023g0154 a0001c0002t0023g0156 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4984+1787T>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501541 | |||||||
| chr2:108501582 | T | C | 1 | a0001c0006t0018g0147 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.4984+1828T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501582 | |||||||
| chr2:108501594 | C | T | 4 | a0001c0001t0015g0240 a0001c0001t0015g0241 a0001c0001t0015g0243 others(1): Show |
4 | HG00642.hp1 HG01175.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.4984+1840C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501594 | |||||||
| chr2:108501676 | G | C | 167 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(164): Show |
170 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.4984+1922G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501676 | |||||||
| chr2:108501687 | A | G | 4 | a0001c0008t0014g0159 a0001c0008t0014g0160 a0001c0008t0014g0161 others(1): Show |
4 | HG01261.hp1 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.4984+1933A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501687 | |||||||
| chr2:108501771 | A | T | 59 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(56): Show |
61 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.4984+2017A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501771 | |||||||
| chr2:108501935 | A | G | 88 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(85): Show |
89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.4984+2181A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108501935 | |||||||
| chr2:108502204 | A | G | 1 | a0001c0002t0001g0031 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.4984+2450A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108502204 | |||||||
| chr2:108502264 | C | G | 63 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(60): Show |
65 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(62): Show |
intron_variant | MODIFIER | c.4984+2510C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108502264 | |||||||
| chr2:108502328 | G | A | 63 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(60): Show |
65 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(62): Show |
intron_variant | MODIFIER | c.4984+2574G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108502328 | |||||||
| chr2:108502395 | A | G | 52 | a0001c0002t0001g0003 a0001c0002t0001g0010 a0001c0002t0001g0011 others(49): Show |
53 | HG00673.hp1 HG00673.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.4984+2641A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108502395 | |||||||
| chr2:108502469 | C | G | 2 | a0001c0002t0001g0044 a0001c0002t0001g0048 |
2 | NA18954.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.4984+2715C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108502469 | |||||||
| chr2:108502618 | TACATTCT others(14): Show |
T | 2 | a0001c0001t0045g0152 a0001c0019t0010g0153 |
2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4984+2865_4984+288 others(25): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108502618 | |||||||
| chr2:108502655 | C | T | 157 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(154): Show |
160 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.4984+2901C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108502655 | |||||||
| chr2:108502656 | A | G | 157 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(154): Show |
160 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.4984+2902A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108502656 | |||||||
| chr2:108502721 | T | C | 1 | a0009c0018t0001g0063 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.4984+2967T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108502721 | |||||||
| chr2:108502749 | C | T | 2 | a0005c0010t0020g0157 a0005c0010t0020g0158 |
2 | HG02040.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.4984+2995C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108502749 | |||||||
| chr2:108502779 | C | T | 1 | a0001c0002t0052g0155 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.4984+3025C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108502779 | |||||||
| chr2:108502811 | T | A | 1 | a0001c0001t0002g0204 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.4984+3057T>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108502811 | |||||||
| chr2:108502848 | G | A | 5 | a0001c0001t0004g0236 a0001c0001t0004g0238 a0001c0001t0004g0244 others(2): Show |
5 | HG00741.hp1 HG01106.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.4984+3094G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108502848 | |||||||
| chr2:108502897 | C | T | 1 | a0001c0002t0001g0065 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.4984+3143C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108502897 | |||||||
| chr2:108502898 | G | A | 3 | a0001c0001t0002g0230 a0001c0001t0002g0253 a0001c0001t0011g0130 |
3 | HG03209.hp1 NA18997.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.4984+3144G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108502898 | |||||||
| chr2:108502911 | A | G | 4 | a0001c0006t0018g0007 a0001c0006t0018g0147 a0001c0006t0018g0148 others(1): Show |
4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.4984+3157A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108502911 | |||||||
| chr2:108502923 | CA | C | 152 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(149): Show |
155 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.4984+3185delA | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr2 | 108502923 | ||||||
| chr2:108502939 | AG | A | 30 | a0001c0001t0002g0176 a0001c0001t0002g0177 a0001c0001t0002g0180 others(27): Show |
30 | HG00099.hp2 HG00738.hp2 HG01346.hp2 others(27): Show |
intron_variant | MODIFIER | c.4984+3186delG | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108502939 | |||||||
| chr2:108502940 | G | A | 2 | a0001c0001t0006g0173 a0001c0001t0006g0210 |
2 | NA18947.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.4984+3186G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108502940 | |||||||
| chr2:108502956 | A | G | 4 | a0001c0008t0014g0159 a0001c0008t0014g0160 a0001c0008t0014g0161 others(1): Show |
4 | HG01261.hp1 NA18954.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.4984+3202A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108502956 | |||||||
| chr2:108503003 | A | C | 4 | a0001c0006t0018g0007 a0001c0006t0018g0147 a0001c0006t0018g0148 others(1): Show |
4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.4984+3249A>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108503003 | |||||||
| chr2:108503175 | A | AG | 87 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(84): Show |
88 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.4984+3421_4984+342 others(5): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108503175 | |||||||
| chr2:108503175 | A | G | 1 | a0001c0002t0001g0069 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.4984+3421A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108503175 | |||||||
| chr2:108503178 | G | A | 1 | a0001c0001t0029g0216 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.4984+3424G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108503178 | |||||||
| chr2:108503425 | C | G | 4 | a0001c0001t0015g0240 a0001c0001t0015g0241 a0001c0001t0015g0243 others(1): Show |
4 | HG00642.hp1 HG01175.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.4984+3671C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108503425 | |||||||
| chr2:108503627 | G | A | 1 | a0001c0001t0028g0207 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4984+3873G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108503627 | |||||||
| chr2:108503913 | A | G | 3 | a0001c0002t0023g0154 a0001c0002t0023g0156 a0001c0002t0052g0155 |
3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.4985-3647A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108503913 | |||||||
| chr2:108503962 | C | G | 160 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(157): Show |
163 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.4985-3598C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108503962 | |||||||
| chr2:108504020 | A | T | 3 | a0001c0001t0002g0214 a0001c0001t0027g0215 a0001c0001t0029g0216 |
3 | HG02257.hp1 HG02717.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.4985-3540A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108504020 | |||||||
| chr2:108504099 | A | G | 2 | a0001c0002t0023g0154 a0001c0002t0023g0156 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4985-3461A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108504099 | |||||||
| chr2:108504119 | C | T | 88 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(85): Show |
89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.4985-3441C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108504119 | |||||||
| chr2:108504123 | A | T | 4 | a0001c0002t0001g0031 a0001c0002t0001g0032 a0001c0002t0001g0061 others(1): Show |
4 | HG03669.hp1 HG03710.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.4985-3437A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108504123 | |||||||
| chr2:108504482 | T | C | 1 | a0001c0001t0003g0106 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.4985-3078T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108504482 | |||||||
| chr2:108504585 | C | T | 88 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(85): Show |
89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.4985-2975C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108504585 | |||||||
| chr2:108504590 | C | T | 1 | a0001c0001t0002g0151 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.4985-2970C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108504590 | |||||||
| chr2:108504759 | T | C | 2 | a0001c0001t0002g0192 a0001c0001t0002g0198 |
2 | NA18940.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.4985-2801T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108504759 | |||||||
| chr2:108504789 | T | G | 2 | a0005c0010t0020g0157 a0005c0010t0020g0158 |
2 | HG02040.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.4985-2771T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108504789 | |||||||
| chr2:108504951 | C | A | 91 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(88): Show |
92 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.4985-2609C>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108504951 | |||||||
| chr2:108504994 | T | A | 91 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(88): Show |
92 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.4985-2566T>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108504994 | |||||||
| chr2:108505027 | C | T | 1 | a0001c0012t0046g0175 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.4985-2533C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108505027 | |||||||
| chr2:108505132 | G | A | 1 | a0001c0001t0004g0234 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.4985-2428G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108505132 | |||||||
| chr2:108505138 | C | G | 2 | a0004c0007t0022g0231 a0004c0007t0022g0232 |
2 | HG02647.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.4985-2422C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108505138 | |||||||
| chr2:108505160 | A | C | 1 | a0005c0010t0020g0158 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4985-2400A>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108505160 | |||||||
| chr2:108505187 | T | G | 1 | a0001c0001t0038g0246 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.4985-2373T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108505187 | |||||||
| chr2:108505261 | C | T | 3 | a0001c0001t0002g0176 a0001c0001t0002g0177 a0001c0001t0002g0202 |
3 | HG01346.hp2 HG03017.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.4985-2299C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108505261 | |||||||
| chr2:108505338 | G | A | 1 | a0001c0001t0005g0139 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4985-2222G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108505338 | |||||||
| chr2:108505451 | G | C | 10 | a0001c0001t0002g0008 a0001c0001t0002g0151 a0001c0001t0002g0174 others(7): Show |
10 | HG01167.hp2 HG01175.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.4985-2109G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108505451 | |||||||
| chr2:108505629 | G | A | 5 | a0001c0001t0019g0163 a0001c0001t0045g0152 a0001c0002t0013g0089 others(2): Show |
5 | HG02572.hp2 HG02698.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.4985-1931G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108505629 | |||||||
| chr2:108505643 | A | G | 15 | a0001c0001t0002g0008 a0001c0001t0002g0151 a0001c0001t0002g0174 others(12): Show |
15 | HG01109.hp2 HG01167.hp2 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.4985-1917A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108505643 | |||||||
| chr2:108505702 | A | G | 2 | a0001c0001t0003g0120 a0001c0001t0003g0124 |
2 | HG03654.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.4985-1858A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108505702 | |||||||
| chr2:108505708 | C | T | 1 | a0001c0002t0001g0076 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.4985-1852C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108505708 | |||||||
| chr2:108505748 | T | A | 167 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(164): Show |
170 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.4985-1812T>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108505748 | |||||||
| chr2:108505770 | G | C | 7 | a0002c0004t0012g0165 a0002c0004t0012g0166 a0002c0004t0012g0168 others(4): Show |
7 | HG02258.hp2 HG02922.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.4985-1790G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108505770 | |||||||
| chr2:108505879 | G | C | 91 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(88): Show |
92 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.4985-1681G>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108505879 | |||||||
| chr2:108505953 | A | G | 1 | a0001c0001t0048g0146 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4985-1607A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108505953 | |||||||
| chr2:108505958 | A | T | 91 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(88): Show |
92 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.4985-1602A>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108505958 | |||||||
| chr2:108506107 | T | A | 1 | a0002c0004t0012g0165 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4985-1453T>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108506107 | |||||||
| chr2:108506330 | C | G | 1 | a0001c0002t0001g0068 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.4985-1230C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108506330 | |||||||
| chr2:108506406 | G | GA | 23 | a0001c0001t0003g0117 a0001c0001t0003g0118 a0001c0001t0003g0119 others(20): Show |
23 | HG02602.hp1 HG02622.hp2 HG03017.hp2 others(20): Show |
intron_variant | MODIFIER | c.4985-1148dupA | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr2 | 108506406 | ||||||
| chr2:108506453 | G | A | 1 | a0001c0012t0046g0175 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.4985-1107G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108506453 | |||||||
| chr2:108506578 | C | T | 1 | a0005c0010t0020g0158 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4985-982C>T | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108506578 | |||||||
| chr2:108506654 | T | C | 86 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(83): Show |
87 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.4985-906T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108506654 | |||||||
| chr2:108506664 | A | C | 2 | a0001c0001t0045g0152 a0001c0019t0010g0153 |
2 | HG02572.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4985-896A>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108506664 | |||||||
| chr2:108506737 | T | C | 91 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(88): Show |
92 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.4985-823T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108506737 | |||||||
| chr2:108506775 | A | G | 1 | a0001c0001t0002g0253 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.4985-785A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108506775 | |||||||
| chr2:108506814 | G | A | 2 | a0001c0002t0023g0154 a0001c0002t0023g0156 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4985-746G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108506814 | |||||||
| chr2:108506871 | A | ATAGAGGA others(323): Show |
1 | a0001c0002t0052g0155 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.4985-685_4985-684i others(332): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr2 | 108506871 | ||||||
| chr2:108506876 | A | G | 91 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(88): Show |
92 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.4985-684A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108506876 | |||||||
| chr2:108507030 | C | G | 2 | a0001c0002t0001g0041 a0001c0002t0001g0075 |
2 | NA19057.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.4985-530C>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108507030 | |||||||
| chr2:108507031 | T | A | 88 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(85): Show |
89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.4985-529T>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108507031 | |||||||
| chr2:108507089 | T | C | 4 | a0001c0001t0002g0180 a0001c0001t0002g0193 a0001c0001t0002g0197 others(1): Show |
4 | HG00099.hp2 HG00738.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.4985-471T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108507089 | |||||||
| chr2:108507219 | G | A | 1 | a0002c0004t0012g0165 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.4985-341G>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108507219 | |||||||
| chr2:108507228 | CA | C | 91 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(88): Show |
92 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.4985-324delA | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr2 | 108507228 | ||||||
| chr2:108507336 | T | C | 1 | a0005c0010t0020g0158 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4985-224T>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108507336 | |||||||
| chr2:108507404 | A | G | 1 | a0001c0001t0002g0188 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.4985-156A>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108507404 | |||||||
| chr2:108507405 | A | AC | 91 | a0001c0001t0002g0187 a0001c0001t0002g0213 a0001c0001t0003g0105 others(88): Show |
92 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.4985-144dupC | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr2 | 108507405 | ||||||
| chr2:108507405 | A | ACC | 28 | a0001c0001t0003g0119 a0001c0001t0005g0139 a0001c0002t0001g0013 others(25): Show |
28 | HG01109.hp1 HG01192.hp1 HG01928.hp1 others(25): Show |
intron_variant | MODIFIER | c.4985-145_4985-144d others(4): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr2 | 108507405 | ||||||
| chr2:108507405 | AC | A | 29 | a0001c0001t0002g0008 a0001c0001t0002g0151 a0001c0001t0002g0174 others(26): Show |
29 | HG01109.hp2 HG01167.hp2 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.4985-144delC | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr2 | 108507405 | ||||||
| chr2:108507417 | A | C | 3 | a0001c0002t0023g0154 a0001c0002t0023g0156 a0001c0011t0002g0201 |
3 | HG02895.hp1 HG02897.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.4985-143A>C | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108507417 | |||||||
| chr2:108507494 | T | A | 91 | a0001c0002t0001g0002 a0001c0002t0001g0003 a0001c0002t0001g0010 others(88): Show |
92 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.4985-66T>A | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108507494 | |||||||
| chr2:108507532 | C | CT | 86 | a0001c0001t0027g0215 a0001c0002t0001g0002 a0001c0002t0001g0003 others(83): Show |
87 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.4985-17dupT | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr2 | 108507532 | ||||||
| chr2:108507532 | C | CTT | 5 | a0001c0002t0008g0085 a0001c0008t0014g0159 a0001c0008t0014g0160 others(2): Show |
5 | HG01261.hp1 HG03710.hp1 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.4985-18_4985-17dup others(2): Show |
GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr2 | 108507532 | ||||||
| chr2:108507540 | T | G | 59 | a0001c0001t0003g0004 a0001c0001t0003g0098 a0001c0001t0003g0101 others(56): Show |
61 | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.4985-20T>G | GCC2 | ENSG00000135968.22 | transcript | ENST00000309863.11 | protein_coding | 22/22 | chr2 | 108507540 |