Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5516 |
| ensemblid | ENSG00000104695.13 |
| hgncid | 9300 |
| symbol | PPP2CB |
| name | protein phosphatase 2 catalytic subunit beta |
| refseq_nuc | NM_001009552.2 |
| refseq_prot | NP_001009552.1 |
| ensembl_nuc | ENST00000221138.9 |
| ensembl_prot | ENSP00000221138.4 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 30785616 |
| end | 30812818 |
| strand | - |
| ver | v1.2 |
| region | chr8:30785616-30812818 |
| region5000 | chr8:30780616-30817818 |
| regionname0 | PPP2CB_chr8_30785616_30812818 |
| regionname5000 | PPP2CB_chr8_30780616_30817818 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 309 | 303 | 90 | 54 | 111 | 10 | 36 | 91 | PPP2CB_chr8_30780616_30817818 | PPP2CB | MDDKA others(304): Show |
chr8 | 30780616 | 30817818 |
| a0002 | 0/0 | 309 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PPP2CB_chr8_30780616_30817818 | PPP2CB | MDDKA others(304): Show |
chr8 | 30780616 | 30817818 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 927 | 299 | 90 | 53 | 109 | 10 | 35 | PPP2CB_chr8_30780616_30817818 | PPP2CB | ATGGA others(922): Show |
chr8 | 30780616 | 30817818 | ||
| a0001c0002 | 0/0 | 927 | 2 | 0 | 0 | 2 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | ATGGA others(922): Show |
chr8 | 30780616 | 30817818 | ||
| a0001c0004 | 0/0 | 927 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | ATGGA others(922): Show |
chr8 | 30780616 | 30817818 | ||
| a0001c0005 | 0/0 | 927 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2CB_chr8_30780616_30817818 | PPP2CB | ATGGA others(922): Show |
chr8 | 30780616 | 30817818 | ||
| a0002c0003 | 0/0 | 927 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | ATGGA others(922): Show |
chr8 | 30780616 | 30817818 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1946 | 120 | 7 | 22 | 67 | 8 | 14 | PPP2CB_chr8_30780616_30817818 | PPP2CB | GAGAG others(1941): Show |
chr8 | 30780616 | 30817818 |
| a0001c0001t0002 | 0/0 | 1946 | 106 | 52 | 21 | 22 | 0 | 11 | PPP2CB_chr8_30780616_30817818 | PPP2CB | GAGAG others(1941): Show |
chr8 | 30780616 | 30817818 |
| a0001c0001t0003 | 0/0 | 1950 | 55 | 15 | 9 | 20 | 2 | 9 | PPP2CB_chr8_30780616_30817818 | PPP2CB | GAGAG others(1945): Show |
chr8 | 30780616 | 30817818 |
| a0001c0001t0004 | 0/0 | 1946 | 6 | 6 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | GAGAG others(1941): Show |
chr8 | 30780616 | 30817818 |
| a0001c0001t0005 | 0/0 | 1946 | 3 | 3 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | GAGAG others(1941): Show |
chr8 | 30780616 | 30817818 |
| a0001c0001t0006 | 0/0 | 1950 | 2 | 2 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | GAGAG others(1945): Show |
chr8 | 30780616 | 30817818 |
| a0001c0001t0007 | 0/0 | 1946 | 2 | 2 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | GAGAG others(1941): Show |
chr8 | 30780616 | 30817818 |
| a0001c0001t0008 | 0/0 | 1946 | 2 | 1 | 1 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | GAGAG others(1941): Show |
chr8 | 30780616 | 30817818 |
| a0001c0001t0009 | 0/0 | 1946 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | GAGAG others(1941): Show |
chr8 | 30780616 | 30817818 |
| a0001c0001t0010 | 0/0 | 1950 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | GAGAG others(1945): Show |
chr8 | 30780616 | 30817818 |
| a0001c0001t0011 | 0/0 | 1946 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2CB_chr8_30780616_30817818 | PPP2CB | GAGAG others(1941): Show |
chr8 | 30780616 | 30817818 |
| a0001c0002t0001 | 0/0 | 1946 | 2 | 0 | 0 | 2 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | GAGAG others(1941): Show |
chr8 | 30780616 | 30817818 |
| a0001c0004t0001 | 0/0 | 1946 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | GAGAG others(1941): Show |
chr8 | 30780616 | 30817818 |
| a0001c0005t0001 | 0/0 | 1946 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2CB_chr8_30780616_30817818 | PPP2CB | GAGAG others(1941): Show |
chr8 | 30780616 | 30817818 |
| a0002c0003t0001 | 0/0 | 1946 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | GAGAG others(1941): Show |
chr8 | 30780616 | 30817818 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/1 | 26 | 0 | 7 | 15 | 1 | 2 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0003 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0006 | 0/0 | 6 | 0 | 1 | 4 | 0 | 1 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 1 | 1 | 1 | 1 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0018 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0004 | 0/0 | 8 | 0 | 5 | 3 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0005 | 0/0 | 8 | 0 | 5 | 2 | 0 | 1 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0007 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0008 | 0/0 | 4 | 1 | 0 | 1 | 0 | 2 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0021 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0003g0002 | 0/0 | 14 | 0 | 3 | 9 | 0 | 2 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0003g0013 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0003g0014 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0003g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0003g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0003g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0003g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0003g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0003g0030 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0003g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0004g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0004g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0005g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0005g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0005g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0006g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0006g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0007g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0008g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0008g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0009g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0010g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0001t0011g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0004t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0001c0005t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| a0002c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0167 | EUR | GBR | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0030 | EUR | GBR | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0164 | EUR | GBR | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0165 | EUR | GBR | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0136 | EUR | FIN | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0161 | EUR | FIN | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0027 | AMR | PUR | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0109 | AMR | PUR | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0053 | AMR | PUR | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG01071 | hp2 | a0001 | c0004 | t0001 | g0123 | AMR | PUR | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0059 | AMR | PUR | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0069 | AMR | PUR | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0027 | AMR | PUR | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0013 | AMR | PUR | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0139 | AMR | CLM | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0181 | EUR | IBS | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | ACB | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0064 | AFR | ACB | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0055 | AMR | PEL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | PEL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0056 | AMR | PEL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | PEL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0044 | AMR | PEL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0113 | EAS | KHV | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | KHV | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | ACB | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | PEL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02148 | hp2 | a0001 | c0001 | t0008 | g0168 | AMR | PEL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | CDX | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0095 | AFR | ACB | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02257 | hp2 | a0001 | c0001 | t0007 | g0023 | AFR | ACB | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0085 | AFR | ACB | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0024 | AFR | ACB | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0050 | AFR | ACB | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | PEL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0052 | AMR | PEL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | ACB | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0088 | AFR | ACB | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0108 | AFR | GWD | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0061 | AFR | GWD | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | GWD | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0141 | AFR | GWD | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0065 | AFR | GWD | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0087 | AFR | GWD | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0105 | AFR | GWD | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0076 | SAS | PJL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | GWD | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0024 | AFR | GWD | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02723 | hp2 | a0001 | c0001 | t0005 | g0106 | AFR | GWD | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0030 | SAS | PJL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02735 | hp2 | a0001 | c0005 | t0001 | g0172 | SAS | PJL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02738 | hp1 | a0001 | c0001 | t0011 | g0149 | SAS | PJL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0060 | SAS | PJL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | GWD | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0058 | AFR | GWD | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0101 | AFR | GWD | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0142 | AFR | GWD | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0097 | AFR | GWD | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02896 | hp2 | a0001 | c0001 | t0006 | g0036 | AFR | GWD | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0063 | AFR | GWD | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0070 | AFR | ESN | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0099 | AFR | ESN | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0071 | AFR | ESN | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ESN | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | ESN | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0091 | AFR | ESN | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0074 | AFR | ESN | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0068 | AFR | GWD | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0133 | AFR | GWD | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0104 | AFR | MSL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | MSL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0062 | AFR | ESN | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0045 | AFR | ESN | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0072 | AFR | MSL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0025 | AFR | MSL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | MSL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | MSL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0031 | AFR | MSL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0025 | AFR | MSL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | MSL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0103 | AFR | MSL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0014 | SAS | PJL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0014 | SAS | PJL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0073 | AFR | ESN | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0079 | AFR | ESN | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0140 | AFR | GWD | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0132 | AFR | GWD | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0049 | AFR | MSL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0138 | AFR | MSL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0092 | SAS | STU | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0134 | SAS | PJL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0084 | SAS | PJL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0135 | SAS | PJL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | BEB | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | BEB | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0078 | SAS | BEB | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | BEB | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0114 | SAS | BEB | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | BEB | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | BEB | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0082 | SAS | BEB | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0089 | SAS | STU | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | STU | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | STU | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0137 | SAS | STU | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | STU | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18522 | hp1 | a0001 | c0001 | t0007 | g0023 | AFR | YRI | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0051 | AFR | YRI | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | CHB | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0098 | AFR | YRI | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0086 | AFR | YRI | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0175 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0189 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18968 | hp1 | a0002 | c0003 | t0001 | g0183 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18974 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA19001 | hp2 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0046 | AFR | LWK | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0115 | AFR | LWK | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA19043 | hp1 | a0001 | c0001 | t0009 | g0035 | AFR | LWK | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | LWK | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA19076 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0112 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0100 | AFR | YRI | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0047 | AFR | YRI | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0083 | AFR | ASW | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ASW | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0160 | EUR | TSI | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | GIH | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0090 | SAS | GIH | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0014 | AMR | CLM | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0111 | AFR | ACB | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02486 | hp1 | a0001 | c0001 | t0010 | g0107 | AFR | ACB | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0102 | AFR | ACB | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0031 | AFR | ACB | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | ACB | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG03471 | hp1 | a0001 | c0001 | t0008 | g0125 | AFR | MSL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | MSL | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | USA | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| HG06807 | hp2 | a0001 | c0001 | t0006 | g0037 | AFR | USA | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | USA | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0093 | AFR | USA | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0048 | AFR | LWK | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | LWK | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0001 | REF | REF | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0018 | REF | REF | PPP2CB_chr8_30780616_30817818 | PPP2CB | chr8 | 30780616 | 30817818 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:30799745 | A | T | 1 | a0002 | 1 | NA18968.hp1 | missense_variant | MODERATE | c.113T>A | p.Ile38Asn | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 2/7 | 510/1946 | 113/930 | 38/309 | chr8 | 30799745 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:30793971 | A | G | 1 | a0001c0004 | 1 | HG01071.hp2 | synonymous_variant | LOW | c.684T>C | p.Phe228Phe | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 5/7 | 1081/1946 | 684/930 | 228/309 | chr8 | 30793971 | |||
| chr8:30794243 | G | A | 1 | a0001c0002 | 2 | NA18944.hp2 NA18967.hp1 |
synonymous_variant | LOW | c.525C>T | p.Asp175Asp | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 4/7 | 922/1946 | 525/930 | 175/309 | chr8 | 30794243 | |||
| chr8:30799615 | T | C | 1 | a0001c0005 | 1 | HG02735.hp2 | synonymous_variant | LOW | c.243A>G | p.Leu81Leu | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 2/7 | 640/1946 | 243/930 | 81/309 | chr8 | 30799615 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:30785629 | T | C | 1 | a0001c0001t0008 | 2 | HG02148.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*606A>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 7/7 | 606 | chr8 | 30785629 | ||||||
| chr8:30785725 | T | C | 2 | a0001c0001t0005 a0001c0001t0007 |
5 | HG02257.hp2 HG02486.hp2 HG02723.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*510A>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 7/7 | 510 | chr8 | 30785725 | ||||||
| chr8:30785837 | G | A | 1 | a0001c0001t0011 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*398C>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 7/7 | 398 | chr8 | 30785837 | ||||||
| chr8:30785938 | A | T | 1 | a0001c0001t0010 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*297T>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 7/7 | 297 | chr8 | 30785938 | ||||||
| chr8:30786022 | C | CCTAT | 3 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0010 |
58 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*212_*213insATAG | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 7/7 | 212 | chr8 | 30786022 | ||||||
| chr8:30786039 | T | A | 1 | a0001c0001t0004 | 6 | HG02258.hp2 HG02647.hp2 HG02717.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*196A>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 7/7 | 196 | chr8 | 30786039 | ||||||
| chr8:30786115 | A | C | 1 | a0001c0001t0007 | 2 | HG02257.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*120T>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 7/7 | 120 | chr8 | 30786115 | ||||||
| chr8:30812550 | G | T | 1 | a0001c0001t0009 | 1 | NA19043.hp1 | 5_prime_UTR_variant | MODIFIER | c.-129C>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/7 | 129 | chr8 | 30812550 | ||||||
| chr8:30812647 | G | T | 3 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0009 |
109 | HG00733.hp2 HG00738.hp2 HG01081.hp1 others(106): Show |
5_prime_UTR_variant | MODIFIER | c.-226C>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/7 | 226 | chr8 | 30812647 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:30786497 | A | ATGGTGAA others(306): Show |
21 | a0001c0001t0002g0004 a0001c0001t0002g0010 a0001c0001t0002g0019 others(18): Show |
31 | HG00738.hp2 HG01081.hp1 HG01168.hp2 others(28): Show |
intron_variant | MODIFIER | c.858-191_858-190ins others(313): Show |
PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 6/6 | chr8 | 30786497 | |||||||
| chr8:30786497 | A | ATGGTGAA others(307): Show |
3 | a0001c0001t0002g0038 a0001c0001t0002g0041 a0001c0001t0002g0101 |
3 | HG02809.hp1 HG02818.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.858-191_858-190ins others(314): Show |
PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 6/6 | chr8 | 30786497 | |||||||
| chr8:30786497 | A | ATGGTGAA others(310): Show |
3 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0105 |
5 | HG02258.hp2 HG02647.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.858-191_858-190ins others(317): Show |
PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 6/6 | chr8 | 30786497 | |||||||
| chr8:30786497 | A | ATGGTGAA others(311): Show |
1 | a0001c0001t0004g0104 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.858-191_858-190ins others(318): Show |
PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 6/6 | chr8 | 30786497 | |||||||
| chr8:30786509 | TAAG | T | 5 | a0001c0001t0002g0007 a0001c0001t0002g0058 a0001c0001t0002g0065 others(2): Show |
9 | HG02280.hp1 HG02572.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.858-205_858-203del others(3): Show |
PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 6/6 | chr8 | 30786509 | |||||||
| chr8:30786536 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.858-229G>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 6/6 | chr8 | 30786536 | |||||||
| chr8:30786641 | TTAATAA | T | 190 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(187): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.858-340_858-335del others(6): Show |
PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 6/6 | chr8 | 30786641 | |||||||
| chr8:30786662 | C | CT | 14 | a0001c0001t0001g0124 a0001c0001t0001g0127 a0001c0001t0001g0130 others(11): Show |
15 | HG01109.hp1 HG01928.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.858-356dupA | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 6/6 | chr8 | 30786662 | |||||||
| chr8:30786662 | CT | C | 10 | a0001c0001t0001g0158 a0001c0001t0001g0161 a0001c0001t0003g0013 others(7): Show |
12 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.858-356delA | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 6/6 | chr8 | 30786662 | |||||||
| chr8:30786822 | C | T | 1 | a0001c0001t0002g0064 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.858-515G>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 6/6 | chr8 | 30786822 | |||||||
| chr8:30786835 | C | A | 5 | a0001c0001t0002g0007 a0001c0001t0002g0058 a0001c0001t0002g0068 others(2): Show |
9 | HG02280.hp1 HG02572.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.858-528G>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 6/6 | chr8 | 30786835 | |||||||
| chr8:30786838 | A | AT | 81 | a0001c0001t0001g0166 a0001c0001t0002g0004 a0001c0001t0002g0005 others(78): Show |
114 | HG00733.hp2 HG00738.hp2 HG01081.hp1 others(111): Show |
intron_variant | MODIFIER | c.858-532dupA | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 6/6 | chr8 | 30786838 | |||||||
| chr8:30786857 | G | A | 16 | a0001c0001t0003g0002 a0001c0001t0003g0014 a0001c0001t0003g0015 others(13): Show |
37 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(34): Show |
intron_variant | MODIFIER | c.858-550C>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 6/6 | chr8 | 30786857 | |||||||
| chr8:30786916 | C | T | 1 | a0001c0001t0004g0104 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.858-609G>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 6/6 | chr8 | 30786916 | |||||||
| chr8:30786923 | C | T | 1 | a0001c0001t0002g0101 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.858-616G>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 6/6 | chr8 | 30786923 | |||||||
| chr8:30787001 | G | A | 1 | a0001c0001t0001g0190 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.858-694C>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 6/6 | chr8 | 30787001 | |||||||
| chr8:30787233 | T | C | 1 | a0001c0001t0003g0194 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.858-926A>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 6/6 | chr8 | 30787233 | |||||||
| chr8:30787375 | T | G | 31 | a0001c0001t0002g0008 a0001c0001t0002g0012 a0001c0001t0002g0022 others(28): Show |
37 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(34): Show |
intron_variant | MODIFIER | c.858-1068A>C | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 6/6 | chr8 | 30787375 | |||||||
| chr8:30787408 | T | C | 3 | a0001c0001t0002g0045 a0001c0001t0002g0061 a0001c0001t0002g0064 |
3 | HG01891.hp2 HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.858-1101A>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 6/6 | chr8 | 30787408 | |||||||
| chr8:30787678 | A | C | 1 | a0001c0001t0001g0174 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.858-1371T>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 6/6 | chr8 | 30787678 | |||||||
| chr8:30787801 | T | G | 1 | a0001c0001t0002g0053 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.858-1494A>C | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 6/6 | chr8 | 30787801 | |||||||
| chr8:30787818 | C | T | 1 | a0001c0001t0003g0132 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.858-1511G>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 6/6 | chr8 | 30787818 | |||||||
| chr8:30788007 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.858-1700G>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 6/6 | chr8 | 30788007 | |||||||
| chr8:30788444 | T | C | 30 | a0001c0001t0003g0002 a0001c0001t0003g0013 a0001c0001t0003g0014 others(27): Show |
55 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.858-2137A>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 6/6 | chr8 | 30788444 | |||||||
| chr8:30788549 | C | A | 6 | a0001c0001t0003g0013 a0001c0001t0003g0031 a0001c0001t0003g0109 others(3): Show |
9 | HG00738.hp1 HG01243.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.858-2242G>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 6/6 | chr8 | 30788549 | |||||||
| chr8:30788934 | C | A | 1 | a0001c0001t0002g0097 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.857+2263G>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 6/6 | chr8 | 30788934 | |||||||
| chr8:30789023 | C | T | 3 | a0001c0001t0001g0121 a0001c0001t0001g0164 a0001c0001t0001g0177 |
3 | HG00140.hp1 HG03927.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.857+2174G>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 6/6 | chr8 | 30789023 | |||||||
| chr8:30789036 | T | A | 1 | a0001c0001t0003g0138 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.857+2161A>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 6/6 | chr8 | 30789036 | |||||||
| chr8:30789049 | C | CT | 25 | a0001c0001t0002g0004 a0001c0001t0002g0010 a0001c0001t0002g0019 others(22): Show |
35 | HG00738.hp2 HG01081.hp1 HG01168.hp2 others(32): Show |
intron_variant | MODIFIER | c.857+2147dupA | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 6/6 | chr8 | 30789049 | |||||||
| chr8:30789049 | CT | C | 22 | a0001c0001t0003g0002 a0001c0001t0003g0014 a0001c0001t0003g0015 others(19): Show |
44 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.857+2147delA | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 6/6 | chr8 | 30789049 | |||||||
| chr8:30789144 | C | T | 2 | a0001c0001t0004g0024 a0001c0001t0004g0105 |
3 | HG02258.hp2 HG02647.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.857+2053G>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 6/6 | chr8 | 30789144 | |||||||
| chr8:30789317 | A | C | 4 | a0001c0001t0002g0045 a0001c0001t0002g0061 a0001c0001t0002g0100 others(1): Show |
5 | HG02257.hp2 HG02615.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.857+1880T>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 6/6 | chr8 | 30789317 | |||||||
| chr8:30789330 | G | A | 3 | a0001c0001t0002g0060 a0001c0001t0002g0067 a0001c0001t0002g0082 |
3 | HG02451.hp1 HG02738.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.857+1867C>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 6/6 | chr8 | 30789330 | |||||||
| chr8:30789390 | T | A | 1 | a0001c0001t0002g0093 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.857+1807A>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 6/6 | chr8 | 30789390 | |||||||
| chr8:30789692 | G | A | 3 | a0001c0001t0003g0111 a0001c0001t0003g0132 a0001c0001t0003g0133 |
3 | HG02109.hp2 HG03041.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.857+1505C>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 6/6 | chr8 | 30789692 | |||||||
| chr8:30789700 | AATG | A | 8 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0104 others(5): Show |
11 | HG02257.hp2 HG02258.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.857+1494_857+1496d others(5): Show |
PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 6/6 | chr8 | 30789700 | |||||||
| chr8:30789727 | A | C | 19 | a0001c0001t0003g0002 a0001c0001t0003g0014 a0001c0001t0003g0015 others(16): Show |
39 | HG00280.hp1 HG00408.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.857+1470T>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 6/6 | chr8 | 30789727 | |||||||
| chr8:30789930 | C | G | 1 | a0001c0001t0009g0035 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.857+1267G>C | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 6/6 | chr8 | 30789930 | |||||||
| chr8:30789941 | T | C | 2 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
4 | HG01256.hp2 HG01258.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.857+1256A>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 6/6 | chr8 | 30789941 | |||||||
| chr8:30789993 | C | T | 1 | a0001c0001t0001g0163 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.857+1204G>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 6/6 | chr8 | 30789993 | |||||||
| chr8:30790148 | G | C | 7 | a0001c0001t0003g0013 a0001c0001t0003g0031 a0001c0001t0003g0108 others(4): Show |
10 | HG00738.hp1 HG01243.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.857+1049C>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 6/6 | chr8 | 30790148 | |||||||
| chr8:30790156 | AT | A | 31 | a0001c0001t0003g0002 a0001c0001t0003g0013 a0001c0001t0003g0014 others(28): Show |
56 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.857+1040delA | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 6/6 | chr8 | 30790156 | |||||||
| chr8:30790280 | C | T | 1 | a0001c0001t0002g0072 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.857+917G>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 6/6 | chr8 | 30790280 | |||||||
| chr8:30790322 | T | C | 1 | a0001c0001t0002g0022 | 2 | NA18989.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.857+875A>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 6/6 | chr8 | 30790322 | |||||||
| chr8:30790488 | T | C | 7 | a0001c0001t0002g0005 a0001c0001t0002g0011 a0001c0001t0002g0020 others(4): Show |
18 | HG00733.hp2 HG01099.hp2 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.857+709A>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 6/6 | chr8 | 30790488 | |||||||
| chr8:30790817 | T | C | 1 | a0001c0001t0002g0056 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.857+380A>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 6/6 | chr8 | 30790817 | |||||||
| chr8:30790867 | C | T | 8 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0104 others(5): Show |
11 | HG02257.hp2 HG02258.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.857+330G>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 6/6 | chr8 | 30790867 | |||||||
| chr8:30790911 | G | A | 1 | a0001c0001t0002g0042 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.857+286C>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 6/6 | chr8 | 30790911 | |||||||
| chr8:30791171 | T | C | 1 | a0001c0001t0010g0107 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.857+26A>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 6/6 | chr8 | 30791171 | |||||||
| chr8:30791429 | G | A | 1 | a0001c0001t0010g0107 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.739-114C>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 5/6 | chr8 | 30791429 | |||||||
| chr8:30791477 | T | C | 9 | a0001c0001t0002g0073 a0001c0001t0004g0024 a0001c0001t0004g0025 others(6): Show |
12 | HG02257.hp2 HG02258.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.739-162A>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 5/6 | chr8 | 30791477 | |||||||
| chr8:30791662 | A | G | 1 | a0001c0001t0002g0065 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.739-347T>C | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 5/6 | chr8 | 30791662 | |||||||
| chr8:30791703 | G | A | 3 | a0001c0001t0002g0091 a0001c0001t0002g0095 a0001c0001t0002g0099 |
3 | HG02257.hp1 HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.739-388C>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 5/6 | chr8 | 30791703 | |||||||
| chr8:30791738 | T | C | 7 | a0001c0001t0003g0013 a0001c0001t0003g0031 a0001c0001t0003g0108 others(4): Show |
10 | HG00738.hp1 HG01243.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.739-423A>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 5/6 | chr8 | 30791738 | |||||||
| chr8:30791854 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.739-539C>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 5/6 | chr8 | 30791854 | |||||||
| chr8:30791858 | A | G | 31 | a0001c0001t0003g0002 a0001c0001t0003g0013 a0001c0001t0003g0014 others(28): Show |
56 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.739-543T>C | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 5/6 | chr8 | 30791858 | |||||||
| chr8:30791862 | A | G | 31 | a0001c0001t0003g0002 a0001c0001t0003g0013 a0001c0001t0003g0014 others(28): Show |
56 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.739-547T>C | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 5/6 | chr8 | 30791862 | |||||||
| chr8:30791864 | GTA | G | 23 | a0001c0001t0002g0004 a0001c0001t0002g0010 a0001c0001t0002g0019 others(20): Show |
33 | HG00738.hp2 HG01081.hp1 HG01168.hp2 others(30): Show |
intron_variant | MODIFIER | c.739-551_739-550del others(2): Show |
PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 5/6 | chr8 | 30791864 | |||||||
| chr8:30791868 | ATATGTGT others(67): Show |
A | 1 | a0001c0001t0001g0118 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.739-627_739-554del others(74): Show |
PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 5/6 | chr8 | 30791868 | |||||||
| chr8:30791941 | T | G | 7 | a0001c0001t0002g0005 a0001c0001t0002g0011 a0001c0001t0002g0020 others(4): Show |
18 | HG00733.hp2 HG01099.hp2 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.739-626A>C | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 5/6 | chr8 | 30791941 | |||||||
| chr8:30791945 | T | C | 1 | a0001c0001t0002g0098 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.739-630A>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 5/6 | chr8 | 30791945 | |||||||
| chr8:30791966 | GTGTGTAT others(1): Show |
G | 78 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(75): Show |
109 | HG00733.hp2 HG00738.hp2 HG01081.hp1 others(106): Show |
intron_variant | MODIFIER | c.739-659_739-652del others(8): Show |
PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 5/6 | chr8 | 30791966 | |||||||
| chr8:30791987 | C | T | 1 | a0001c0001t0002g0048 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.739-672G>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 5/6 | chr8 | 30791987 | |||||||
| chr8:30792003 | TAC | T | 4 | a0001c0001t0002g0007 a0001c0001t0002g0058 a0001c0001t0002g0071 others(1): Show |
8 | HG02280.hp1 HG02572.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.739-690_739-689del others(2): Show |
PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 5/6 | chr8 | 30792003 | |||||||
| chr8:30792014 | ATG | A | 34 | a0001c0001t0002g0008 a0001c0001t0002g0012 a0001c0001t0002g0022 others(31): Show |
40 | HG01891.hp2 HG02257.hp1 HG02258.hp1 others(37): Show |
intron_variant | MODIFIER | c.739-701_739-700del others(2): Show |
PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 5/6 | chr8 | 30792014 | |||||||
| chr8:30792027 | T | A | 8 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0104 others(5): Show |
11 | HG02257.hp2 HG02258.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.739-712A>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 5/6 | chr8 | 30792027 | |||||||
| chr8:30792060 | ATG | A | 8 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0104 others(5): Show |
11 | HG02257.hp2 HG02258.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.739-747_739-746del others(2): Show |
PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 5/6 | chr8 | 30792060 | |||||||
| chr8:30792066 | G | GTA | 31 | a0001c0001t0003g0002 a0001c0001t0003g0013 a0001c0001t0003g0014 others(28): Show |
56 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.739-753_739-752dup others(2): Show |
PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 5/6 | chr8 | 30792066 | |||||||
| chr8:30792187 | T | C | 26 | a0001c0001t0002g0004 a0001c0001t0002g0010 a0001c0001t0002g0019 others(23): Show |
36 | HG00738.hp2 HG01081.hp1 HG01168.hp2 others(33): Show |
intron_variant | MODIFIER | c.739-872A>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 5/6 | chr8 | 30792187 | |||||||
| chr8:30792275 | G | A | 1 | a0001c0001t0002g0051 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.739-960C>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 5/6 | chr8 | 30792275 | |||||||
| chr8:30792501 | C | G | 4 | a0001c0001t0003g0013 a0001c0001t0003g0108 a0001c0001t0003g0109 others(1): Show |
6 | HG00738.hp1 HG01243.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.739-1186G>C | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 5/6 | chr8 | 30792501 | |||||||
| chr8:30792633 | T | A | 2 | a0001c0001t0003g0114 a0001c0001t0003g0135 |
2 | HG03710.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.738+1284A>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 5/6 | chr8 | 30792633 | |||||||
| chr8:30792908 | T | A | 1 | a0001c0001t0001g0170 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.738+1009A>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 5/6 | chr8 | 30792908 | |||||||
| chr8:30792918 | C | T | 2 | a0001c0001t0003g0139 a0001c0001t0003g0140 |
2 | HG01255.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.738+999G>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 5/6 | chr8 | 30792918 | |||||||
| chr8:30792938 | C | T | 1 | a0001c0001t0002g0048 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.738+979G>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 5/6 | chr8 | 30792938 | |||||||
| chr8:30793133 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.738+784G>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 5/6 | chr8 | 30793133 | |||||||
| chr8:30793234 | A | G | 2 | a0001c0001t0002g0080 a0001c0001t0002g0081 |
2 | NA18974.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.738+683T>C | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 5/6 | chr8 | 30793234 | |||||||
| chr8:30793330 | C | T | 78 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(75): Show |
109 | HG00733.hp2 HG00738.hp2 HG01081.hp1 others(106): Show |
intron_variant | MODIFIER | c.738+587G>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 5/6 | chr8 | 30793330 | |||||||
| chr8:30793536 | G | C | 1 | a0001c0001t0001g0169 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.738+381C>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 5/6 | chr8 | 30793536 | |||||||
| chr8:30793690 | A | T | 39 | a0001c0001t0003g0002 a0001c0001t0003g0013 a0001c0001t0003g0014 others(36): Show |
67 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.738+227T>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 5/6 | chr8 | 30793690 | |||||||
| chr8:30793698 | C | T | 27 | a0001c0001t0003g0002 a0001c0001t0003g0014 a0001c0001t0003g0015 others(24): Show |
50 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.738+219G>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 5/6 | chr8 | 30793698 | |||||||
| chr8:30793819 | T | C | 24 | a0001c0001t0003g0002 a0001c0001t0003g0014 a0001c0001t0003g0015 others(21): Show |
47 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.738+98A>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 5/6 | chr8 | 30793819 | |||||||
| chr8:30794343 | A | G | 3 | a0001c0001t0005g0102 a0001c0001t0005g0103 a0001c0001t0005g0106 |
3 | HG02486.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.487-62T>C | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 3/6 | chr8 | 30794343 | |||||||
| chr8:30794387 | T | A | 1 | a0001c0001t0005g0102 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.487-106A>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 3/6 | chr8 | 30794387 | |||||||
| chr8:30794424 | C | CTTCTCTG others(77): Show |
1 | a0001c0001t0001g0153 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.487-227_487-144dup others(84): Show |
PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 3/6 | chr8 | 30794424 | |||||||
| chr8:30794473 | C | CT | 24 | a0001c0001t0002g0004 a0001c0001t0002g0010 a0001c0001t0002g0019 others(21): Show |
34 | HG00738.hp2 HG01168.hp2 HG01258.hp1 others(31): Show |
intron_variant | MODIFIER | c.487-193dupA | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 3/6 | chr8 | 30794473 | |||||||
| chr8:30794473 | CT | C | 7 | a0001c0001t0002g0005 a0001c0001t0002g0011 a0001c0001t0002g0020 others(4): Show |
18 | HG00733.hp2 HG01099.hp2 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.487-193delA | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 3/6 | chr8 | 30794473 | |||||||
| chr8:30794552 | ATTTC | A | 31 | a0001c0001t0003g0002 a0001c0001t0003g0013 a0001c0001t0003g0014 others(28): Show |
56 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.487-275_487-272del others(4): Show |
PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 3/6 | chr8 | 30794552 | |||||||
| chr8:30794695 | T | C | 1 | a0001c0001t0002g0100 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.487-414A>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 3/6 | chr8 | 30794695 | |||||||
| chr8:30794847 | C | T | 4 | a0001c0001t0003g0013 a0001c0001t0003g0108 a0001c0001t0003g0109 others(1): Show |
6 | HG00738.hp1 HG01243.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.487-566G>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 3/6 | chr8 | 30794847 | |||||||
| chr8:30794859 | A | C | 1 | a0001c0001t0001g0162 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.487-578T>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 3/6 | chr8 | 30794859 | |||||||
| chr8:30795113 | ATTTTGAT others(5): Show |
A | 2 | a0001c0001t0003g0114 a0001c0001t0003g0135 |
2 | HG03710.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.487-844_487-833del others(12): Show |
PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 3/6 | chr8 | 30795113 | |||||||
| chr8:30795119 | A | AT | 33 | a0001c0001t0001g0001 a0001c0001t0001g0131 a0001c0001t0001g0162 others(30): Show |
53 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.487-839dupA | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 3/6 | chr8 | 30795119 | |||||||
| chr8:30795119 | A | ATT | 6 | a0001c0001t0001g0127 a0001c0001t0003g0002 a0001c0001t0003g0026 others(3): Show |
6 | HG00735.hp2 HG03704.hp1 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.487-840_487-839dup others(2): Show |
PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 3/6 | chr8 | 30795119 | |||||||
| chr8:30795119 | AT | A | 7 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0158 others(4): Show |
8 | HG00733.hp1 HG01361.hp1 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.487-839delA | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 3/6 | chr8 | 30795119 | |||||||
| chr8:30795152 | C | T | 1 | a0001c0001t0002g0054 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.487-871G>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 3/6 | chr8 | 30795152 | |||||||
| chr8:30795193 | G | A | 1 | a0001c0001t0001g0176 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.487-912C>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 3/6 | chr8 | 30795193 | |||||||
| chr8:30795234 | G | A | 1 | a0001c0001t0002g0088 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.487-953C>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 3/6 | chr8 | 30795234 | |||||||
| chr8:30795318 | T | C | 1 | a0001c0001t0002g0092 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.487-1037A>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 3/6 | chr8 | 30795318 | |||||||
| chr8:30795360 | C | T | 78 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(75): Show |
109 | HG00733.hp2 HG00738.hp2 HG01081.hp1 others(106): Show |
intron_variant | MODIFIER | c.487-1079G>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 3/6 | chr8 | 30795360 | |||||||
| chr8:30795410 | T | C | 114 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(111): Show |
173 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.487-1129A>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 3/6 | chr8 | 30795410 | |||||||
| chr8:30795610 | G | A | 1 | a0001c0001t0001g0170 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.487-1329C>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 3/6 | chr8 | 30795610 | |||||||
| chr8:30795737 | G | A | 1 | a0001c0001t0002g0083 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.487-1456C>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 3/6 | chr8 | 30795737 | |||||||
| chr8:30795979 | G | T | 34 | a0001c0001t0002g0008 a0001c0001t0002g0012 a0001c0001t0002g0022 others(31): Show |
40 | HG01891.hp2 HG02257.hp1 HG02258.hp1 others(37): Show |
intron_variant | MODIFIER | c.486+1602C>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 3/6 | chr8 | 30795979 | |||||||
| chr8:30795995 | T | C | 8 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0104 others(5): Show |
11 | HG02257.hp2 HG02258.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.486+1586A>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 3/6 | chr8 | 30795995 | |||||||
| chr8:30796393 | T | C | 1 | a0001c0001t0001g0119 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.486+1188A>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 3/6 | chr8 | 30796393 | |||||||
| chr8:30796446 | T | C | 3 | a0001c0001t0003g0013 a0001c0001t0003g0108 a0001c0001t0003g0109 |
5 | HG00738.hp1 HG01243.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.486+1135A>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 3/6 | chr8 | 30796446 | |||||||
| chr8:30796732 | T | C | 4 | a0001c0001t0003g0013 a0001c0001t0003g0108 a0001c0001t0003g0109 others(1): Show |
6 | HG00738.hp1 HG01243.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.486+849A>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 3/6 | chr8 | 30796732 | |||||||
| chr8:30796804 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.486+777C>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 3/6 | chr8 | 30796804 | |||||||
| chr8:30796837 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.486+744A>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 3/6 | chr8 | 30796837 | |||||||
| chr8:30796843 | T | A | 3 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 |
3 | HG01255.hp2 HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.486+738A>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 3/6 | chr8 | 30796843 | |||||||
| chr8:30796912 | C | T | 1 | a0001c0001t0002g0079 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.486+669G>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 3/6 | chr8 | 30796912 | |||||||
| chr8:30796913 | G | A | 1 | a0001c0001t0002g0067 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.486+668C>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 3/6 | chr8 | 30796913 | |||||||
| chr8:30797018 | A | AT | 40 | a0001c0001t0001g0017 a0001c0001t0001g0110 a0001c0001t0001g0151 others(37): Show |
48 | HG00735.hp1 HG01891.hp2 HG01928.hp2 others(45): Show |
intron_variant | MODIFIER | c.486+562dupA | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 3/6 | chr8 | 30797018 | |||||||
| chr8:30797167 | A | G | 1 | a0001c0001t0003g0136 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.486+414T>C | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 3/6 | chr8 | 30797167 | |||||||
| chr8:30797293 | G | A | 1 | a0001c0001t0002g0075 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.486+288C>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 3/6 | chr8 | 30797293 | |||||||
| chr8:30797323 | A | G | 1 | a0001c0001t0002g0085 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.486+258T>C | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 3/6 | chr8 | 30797323 | |||||||
| chr8:30797393 | T | G | 1 | a0001c0001t0001g0126 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.486+188A>C | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 3/6 | chr8 | 30797393 | |||||||
| chr8:30797409 | A | T | 8 | a0001c0001t0003g0013 a0001c0001t0003g0031 a0001c0001t0003g0108 others(5): Show |
11 | HG00738.hp1 HG01243.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.486+172T>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 3/6 | chr8 | 30797409 | |||||||
| chr8:30797483 | C | A | 1 | a0001c0001t0001g0034 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.486+98G>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 3/6 | chr8 | 30797483 | |||||||
| chr8:30797522 | A | G | 1 | a0001c0001t0002g0067 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.486+59T>C | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 3/6 | chr8 | 30797522 | |||||||
| chr8:30797847 | G | A | 76 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(73): Show |
107 | HG00733.hp2 HG00738.hp2 HG01081.hp1 others(104): Show |
intron_variant | MODIFIER | c.313-93C>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 2/6 | chr8 | 30797847 | |||||||
| chr8:30797997 | A | C | 1 | a0001c0001t0003g0139 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.313-243T>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 2/6 | chr8 | 30797997 | |||||||
| chr8:30798183 | T | G | 1 | a0001c0001t0002g0070 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.313-429A>C | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 2/6 | chr8 | 30798183 | |||||||
| chr8:30798223 | C | A | 2 | a0001c0001t0003g0015 a0001c0001t0003g0112 |
4 | NA18954.hp2 NA18973.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.313-469G>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 2/6 | chr8 | 30798223 | |||||||
| chr8:30798295 | A | G | 1 | a0001c0001t0002g0065 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.313-541T>C | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 2/6 | chr8 | 30798295 | |||||||
| chr8:30798725 | A | G | 1 | a0001c0001t0001g0152 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.312+821T>C | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 2/6 | chr8 | 30798725 | |||||||
| chr8:30798836 | T | C | 1 | a0001c0001t0002g0043 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.312+710A>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 2/6 | chr8 | 30798836 | |||||||
| chr8:30799117 | C | T | 1 | a0001c0001t0001g0033 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.312+429G>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 2/6 | chr8 | 30799117 | |||||||
| chr8:30799259 | G | C | 1 | a0001c0001t0002g0038 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.312+287C>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 2/6 | chr8 | 30799259 | |||||||
| chr8:30799371 | G | A | 2 | a0001c0001t0003g0028 a0001c0001t0003g0142 |
3 | HG02615.hp2 HG02886.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.312+175C>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 2/6 | chr8 | 30799371 | |||||||
| chr8:30799460 | A | C | 8 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0104 others(5): Show |
11 | HG02257.hp2 HG02258.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.312+86T>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 2/6 | chr8 | 30799460 | |||||||
| chr8:30799465 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.312+81T>C | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 2/6 | chr8 | 30799465 | |||||||
| chr8:30800036 | C | A | 1 | a0001c0001t0001g0190 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.103-281G>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30800036 | |||||||
| chr8:30800079 | T | C | 7 | a0001c0001t0002g0005 a0001c0001t0002g0011 a0001c0001t0002g0020 others(4): Show |
18 | HG00733.hp2 HG01099.hp2 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.103-324A>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30800079 | |||||||
| chr8:30800249 | C | T | 1 | a0001c0001t0001g0185 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.103-494G>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30800249 | |||||||
| chr8:30800449 | C | T | 1 | a0001c0001t0002g0068 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.103-694G>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30800449 | |||||||
| chr8:30800462 | A | G | 4 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0104 others(1): Show |
6 | HG02258.hp2 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.103-707T>C | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30800462 | |||||||
| chr8:30800694 | C | G | 1 | a0001c0001t0001g0121 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.103-939G>C | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30800694 | |||||||
| chr8:30800767 | T | C | 1 | a0001c0001t0002g0084 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.103-1012A>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30800767 | |||||||
| chr8:30800879 | G | A | 1 | a0001c0001t0002g0067 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.103-1124C>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30800879 | |||||||
| chr8:30800896 | G | A | 3 | a0001c0001t0003g0031 a0001c0001t0003g0115 a0001c0001t0003g0138 |
4 | HG02559.hp1 HG03453.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.103-1141C>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30800896 | |||||||
| chr8:30800933 | G | A | 3 | a0001c0001t0003g0031 a0001c0001t0003g0115 a0001c0001t0003g0138 |
4 | HG02559.hp1 HG03453.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.103-1178C>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30800933 | |||||||
| chr8:30800970 | G | T | 23 | a0001c0001t0002g0004 a0001c0001t0002g0010 a0001c0001t0002g0019 others(20): Show |
33 | HG00738.hp2 HG01081.hp1 HG01168.hp2 others(30): Show |
intron_variant | MODIFIER | c.103-1215C>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30800970 | |||||||
| chr8:30801337 | C | T | 1 | a0001c0001t0001g0173 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.103-1582G>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30801337 | |||||||
| chr8:30801466 | G | A | 35 | a0001c0001t0002g0008 a0001c0001t0002g0012 a0001c0001t0002g0022 others(32): Show |
42 | HG01891.hp2 HG02257.hp1 HG02257.hp2 others(39): Show |
intron_variant | MODIFIER | c.103-1711C>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30801466 | |||||||
| chr8:30801488 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.103-1733G>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30801488 | |||||||
| chr8:30801535 | GA | G | 86 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(83): Show |
120 | HG00733.hp2 HG00738.hp2 HG01081.hp1 others(117): Show |
intron_variant | MODIFIER | c.103-1781delT | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30801535 | |||||||
| chr8:30801535 | GAA | G | 4 | a0001c0001t0003g0013 a0001c0001t0003g0108 a0001c0001t0003g0109 others(1): Show |
6 | HG00738.hp1 HG01243.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.103-1782_103-1781d others(4): Show |
PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30801535 | |||||||
| chr8:30801609 | G | C | 1 | a0001c0001t0001g0173 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.103-1854C>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30801609 | |||||||
| chr8:30801726 | A | T | 1 | a0001c0001t0002g0074 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.103-1971T>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30801726 | |||||||
| chr8:30801784 | A | G | 1 | a0001c0001t0001g0185 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.103-2029T>C | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30801784 | |||||||
| chr8:30801833 | T | C | 76 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(73): Show |
107 | HG00733.hp2 HG00738.hp2 HG01081.hp1 others(104): Show |
intron_variant | MODIFIER | c.103-2078A>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30801833 | |||||||
| chr8:30802347 | A | G | 1 | a0001c0001t0004g0104 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.103-2592T>C | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30802347 | |||||||
| chr8:30802482 | T | C | 2 | a0001c0001t0003g0028 a0001c0001t0003g0142 |
3 | HG02615.hp2 HG02886.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.103-2727A>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30802482 | |||||||
| chr8:30802546 | A | C | 8 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0104 others(5): Show |
11 | HG02257.hp2 HG02258.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.103-2791T>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30802546 | |||||||
| chr8:30802690 | C | T | 1 | a0001c0001t0002g0086 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.103-2935G>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30802690 | |||||||
| chr8:30802853 | A | C | 1 | a0001c0001t0002g0065 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.103-3098T>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30802853 | |||||||
| chr8:30802879 | T | C | 1 | a0001c0001t0002g0085 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.103-3124A>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30802879 | |||||||
| chr8:30802886 | C | T | 8 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0104 others(5): Show |
11 | HG02257.hp2 HG02258.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.103-3131G>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30802886 | |||||||
| chr8:30803076 | C | A | 8 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0104 others(5): Show |
11 | HG02257.hp2 HG02258.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.103-3321G>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30803076 | |||||||
| chr8:30803229 | C | T | 2 | a0001c0001t0006g0036 a0001c0001t0006g0037 |
2 | HG02896.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.103-3474G>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30803229 | |||||||
| chr8:30803300 | T | C | 3 | a0001c0001t0002g0086 a0001c0001t0002g0087 a0001c0001t0002g0088 |
3 | HG02451.hp2 HG02647.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.103-3545A>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30803300 | |||||||
| chr8:30803355 | C | T | 1 | a0001c0001t0002g0067 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.103-3600G>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30803355 | |||||||
| chr8:30803375 | T | A | 2 | a0001c0001t0003g0028 a0001c0001t0003g0142 |
3 | HG02615.hp2 HG02886.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.103-3620A>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30803375 | |||||||
| chr8:30803482 | C | T | 3 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0181 |
3 | HG00280.hp2 HG01515.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.103-3727G>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30803482 | |||||||
| chr8:30803540 | C | CT | 3 | a0001c0001t0003g0031 a0001c0001t0003g0115 a0001c0001t0003g0138 |
4 | HG02559.hp1 HG03453.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.103-3786dupA | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30803540 | |||||||
| chr8:30803543 | T | A | 1 | a0001c0001t0002g0086 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.103-3788A>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30803543 | |||||||
| chr8:30803543 | T | TA | 8 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0104 others(5): Show |
11 | HG02257.hp2 HG02258.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.103-3789dupT | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30803543 | |||||||
| chr8:30803783 | T | TAATTTC | 117 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(114): Show |
176 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.103-4029_103-4028i others(8): Show |
PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30803783 | |||||||
| chr8:30803784 | G | A | 117 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(114): Show |
176 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.103-4029C>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30803784 | |||||||
| chr8:30803785 | G | A | 117 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(114): Show |
176 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.103-4030C>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30803785 | |||||||
| chr8:30803819 | A | AT | 7 | a0001c0001t0001g0159 a0001c0001t0002g0038 a0001c0001t0002g0039 others(4): Show |
7 | HG00738.hp2 HG01981.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.103-4065dupA | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30803819 | |||||||
| chr8:30803819 | AT | A | 10 | a0001c0001t0001g0180 a0001c0001t0002g0078 a0001c0001t0002g0089 others(7): Show |
13 | HG01256.hp1 HG02257.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.103-4065delA | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30803819 | |||||||
| chr8:30803839 | C | T | 3 | a0001c0001t0005g0102 a0001c0001t0005g0103 a0001c0001t0005g0106 |
3 | HG02486.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.103-4084G>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30803839 | |||||||
| chr8:30803856 | G | A | 3 | a0001c0001t0002g0012 a0001c0001t0002g0063 a0001c0001t0002g0093 |
5 | HG02723.hp1 HG02818.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.103-4101C>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30803856 | |||||||
| chr8:30803879 | C | T | 76 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(73): Show |
107 | HG00733.hp2 HG00738.hp2 HG01081.hp1 others(104): Show |
intron_variant | MODIFIER | c.103-4124G>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30803879 | |||||||
| chr8:30803907 | C | T | 2 | a0001c0001t0001g0158 a0001c0001t0001g0180 |
2 | HG00733.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.103-4152G>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30803907 | |||||||
| chr8:30803968 | G | A | 23 | a0001c0001t0002g0004 a0001c0001t0002g0010 a0001c0001t0002g0019 others(20): Show |
33 | HG00738.hp2 HG01081.hp1 HG01168.hp2 others(30): Show |
intron_variant | MODIFIER | c.103-4213C>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30803968 | |||||||
| chr8:30804073 | G | A | 3 | a0001c0001t0005g0102 a0001c0001t0005g0103 a0001c0001t0005g0106 |
3 | HG02486.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.103-4318C>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30804073 | |||||||
| chr8:30804080 | T | A | 1 | a0001c0001t0005g0106 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.103-4325A>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30804080 | |||||||
| chr8:30804186 | C | G | 10 | a0001c0001t0002g0005 a0001c0001t0002g0011 a0001c0001t0002g0020 others(7): Show |
21 | HG00733.hp2 HG01099.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.103-4431G>C | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30804186 | |||||||
| chr8:30804318 | C | T | 1 | a0001c0001t0002g0067 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.103-4563G>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30804318 | |||||||
| chr8:30804324 | C | G | 2 | a0001c0001t0001g0151 a0001c0001t0001g0157 |
2 | NA18967.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.103-4569G>C | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30804324 | |||||||
| chr8:30804507 | T | C | 1 | a0001c0001t0001g0156 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.103-4752A>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30804507 | |||||||
| chr8:30804553 | G | A | 10 | a0001c0001t0001g0003 a0001c0001t0001g0120 a0001c0001t0001g0127 others(7): Show |
19 | HG00423.hp2 HG02074.hp1 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.103-4798C>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30804553 | |||||||
| chr8:30804557 | T | C | 3 | a0001c0001t0003g0139 a0001c0001t0003g0140 a0001c0001t0003g0141 |
3 | HG01255.hp2 HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.103-4802A>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30804557 | |||||||
| chr8:30804605 | T | A | 1 | a0001c0001t0001g0155 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.103-4850A>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30804605 | |||||||
| chr8:30804628 | G | A | 1 | a0001c0001t0002g0065 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.103-4873C>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30804628 | |||||||
| chr8:30804672 | C | G | 1 | a0001c0001t0006g0036 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.103-4917G>C | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30804672 | |||||||
| chr8:30804764 | T | C | 1 | a0001c0001t0003g0109 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.103-5009A>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30804764 | |||||||
| chr8:30804917 | C | A | 3 | a0001c0001t0002g0011 a0001c0001t0002g0020 a0001c0001t0002g0072 |
6 | HG01891.hp1 HG02717.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.103-5162G>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30804917 | |||||||
| chr8:30805052 | A | T | 1 | a0001c0001t0003g0132 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.103-5297T>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30805052 | |||||||
| chr8:30805216 | T | A | 19 | a0001c0001t0003g0002 a0001c0001t0003g0014 a0001c0001t0003g0015 others(16): Show |
40 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.103-5461A>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30805216 | |||||||
| chr8:30805237 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.103-5482C>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30805237 | |||||||
| chr8:30805402 | C | T | 31 | a0001c0001t0003g0002 a0001c0001t0003g0013 a0001c0001t0003g0014 others(28): Show |
56 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.103-5647G>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30805402 | |||||||
| chr8:30805482 | C | G | 7 | a0001c0001t0002g0005 a0001c0001t0002g0011 a0001c0001t0002g0020 others(4): Show |
18 | HG00733.hp2 HG01099.hp2 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.103-5727G>C | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30805482 | |||||||
| chr8:30805521 | C | G | 2 | a0001c0001t0002g0011 a0001c0001t0002g0020 |
5 | HG01891.hp1 HG02717.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.103-5766G>C | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30805521 | |||||||
| chr8:30805545 | G | C | 23 | a0001c0001t0002g0004 a0001c0001t0002g0010 a0001c0001t0002g0019 others(20): Show |
33 | HG00738.hp2 HG01081.hp1 HG01168.hp2 others(30): Show |
intron_variant | MODIFIER | c.103-5790C>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30805545 | |||||||
| chr8:30805572 | A | C | 78 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(75): Show |
109 | HG00733.hp2 HG00738.hp2 HG01081.hp1 others(106): Show |
intron_variant | MODIFIER | c.103-5817T>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30805572 | |||||||
| chr8:30805626 | T | C | 2 | a0001c0001t0002g0077 a0001c0001t0002g0094 |
2 | NA19079.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.103-5871A>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30805626 | |||||||
| chr8:30805764 | T | C | 31 | a0001c0001t0003g0002 a0001c0001t0003g0013 a0001c0001t0003g0014 others(28): Show |
56 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.103-6009A>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30805764 | |||||||
| chr8:30805952 | A | G | 1 | a0001c0001t0001g0156 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.103-6197T>C | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30805952 | |||||||
| chr8:30806046 | A | AT | 19 | a0001c0001t0001g0016 a0001c0001t0001g0110 a0001c0001t0001g0118 others(16): Show |
22 | HG00423.hp1 HG00423.hp2 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.102+6273dupA | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30806046 | |||||||
| chr8:30806046 | AT | A | 9 | a0001c0001t0001g0116 a0001c0001t0001g0178 a0001c0001t0002g0064 others(6): Show |
13 | HG00099.hp2 HG00280.hp1 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.102+6273delA | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30806046 | |||||||
| chr8:30806214 | A | AT | 7 | a0001c0001t0001g0143 a0001c0001t0001g0150 a0001c0001t0002g0038 others(4): Show |
7 | HG02809.hp1 HG02896.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.102+6105dupA | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30806214 | |||||||
| chr8:30806244 | C | A | 4 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0104 others(1): Show |
6 | HG02258.hp2 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.102+6076G>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30806244 | |||||||
| chr8:30806354 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.102+5966C>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30806354 | |||||||
| chr8:30806487 | C | T | 1 | a0001c0001t0002g0047 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.102+5833G>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30806487 | |||||||
| chr8:30806909 | T | C | 2 | a0001c0001t0002g0046 a0001c0001t0002g0100 |
2 | NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.102+5411A>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30806909 | |||||||
| chr8:30807140 | C | G | 117 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(114): Show |
176 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.102+5180G>C | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30807140 | |||||||
| chr8:30807437 | T | A | 33 | a0001c0001t0003g0002 a0001c0001t0003g0013 a0001c0001t0003g0014 others(30): Show |
58 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.102+4883A>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30807437 | |||||||
| chr8:30807578 | G | C | 1 | a0001c0001t0004g0104 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.102+4742C>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30807578 | |||||||
| chr8:30807640 | G | C | 1 | a0001c0001t0003g0137 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.102+4680C>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30807640 | |||||||
| chr8:30807762 | T | C | 76 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(73): Show |
107 | HG00733.hp2 HG00738.hp2 HG01081.hp1 others(104): Show |
intron_variant | MODIFIER | c.102+4558A>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30807762 | |||||||
| chr8:30807789 | C | T | 1 | a0001c0001t0002g0046 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.102+4531G>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30807789 | |||||||
| chr8:30808080 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.102+4240C>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30808080 | |||||||
| chr8:30808124 | A | G | 117 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(114): Show |
176 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.102+4196T>C | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30808124 | |||||||
| chr8:30808142 | C | T | 34 | a0001c0001t0002g0008 a0001c0001t0002g0012 a0001c0001t0002g0022 others(31): Show |
40 | HG01891.hp2 HG02257.hp1 HG02258.hp1 others(37): Show |
intron_variant | MODIFIER | c.102+4178G>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30808142 | |||||||
| chr8:30808162 | G | A | 3 | a0001c0001t0005g0102 a0001c0001t0005g0103 a0001c0001t0005g0106 |
3 | HG02486.hp2 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.102+4158C>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30808162 | |||||||
| chr8:30808251 | G | A | 1 | a0001c0001t0002g0065 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.102+4069C>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30808251 | |||||||
| chr8:30808348 | C | T | 1 | a0001c0001t0004g0104 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.102+3972G>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30808348 | |||||||
| chr8:30808360 | A | C | 26 | a0001c0001t0003g0002 a0001c0001t0003g0014 a0001c0001t0003g0015 others(23): Show |
49 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.102+3960T>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30808360 | |||||||
| chr8:30808416 | G | C | 50 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0008 others(47): Show |
71 | HG00733.hp2 HG01099.hp2 HG01123.hp1 others(68): Show |
intron_variant | MODIFIER | c.102+3904C>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30808416 | |||||||
| chr8:30808452 | C | T | 117 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(114): Show |
176 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(173): Show |
intron_variant | MODIFIER | c.102+3868G>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30808452 | |||||||
| chr8:30808550 | A | G | 1 | a0001c0001t0002g0052 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.102+3770T>C | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30808550 | |||||||
| chr8:30808744 | G | A | 16 | a0001c0001t0002g0004 a0001c0001t0002g0010 a0001c0001t0002g0039 others(13): Show |
25 | HG00738.hp2 HG01081.hp1 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.102+3576C>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30808744 | |||||||
| chr8:30808890 | C | T | 1 | a0001c0001t0001g0117 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.102+3430G>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30808890 | |||||||
| chr8:30808922 | C | CT | 7 | a0001c0001t0001g0148 a0001c0001t0001g0192 a0001c0001t0005g0102 others(4): Show |
8 | HG02257.hp2 HG02486.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.102+3397dupA | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30808922 | |||||||
| chr8:30808922 | CT | C | 85 | a0001c0001t0001g0009 a0001c0001t0001g0129 a0001c0001t0001g0147 others(82): Show |
123 | HG00733.hp2 HG00738.hp2 HG01081.hp1 others(120): Show |
intron_variant | MODIFIER | c.102+3397delA | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30808922 | |||||||
| chr8:30808922 | CTTTTTTT others(5): Show |
C | 16 | a0001c0001t0003g0002 a0001c0001t0003g0014 a0001c0001t0003g0015 others(13): Show |
37 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(34): Show |
intron_variant | MODIFIER | c.102+3386_102+3397d others(14): Show |
PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30808922 | |||||||
| chr8:30808976 | G | A | 74 | a0001c0001t0002g0004 a0001c0001t0002g0005 a0001c0001t0002g0007 others(71): Show |
105 | HG00733.hp2 HG00738.hp2 HG01081.hp1 others(102): Show |
intron_variant | MODIFIER | c.102+3344C>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30808976 | |||||||
| chr8:30808983 | G | A | 1 | a0001c0001t0002g0095 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.102+3337C>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30808983 | |||||||
| chr8:30809052 | G | T | 1 | a0001c0001t0002g0067 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.102+3268C>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30809052 | |||||||
| chr8:30809065 | A | G | 1 | a0001c0001t0002g0065 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.102+3255T>C | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30809065 | |||||||
| chr8:30809076 | AT | A | 35 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0002g0008 others(32): Show |
41 | HG01081.hp1 HG01099.hp1 HG01891.hp2 others(38): Show |
intron_variant | MODIFIER | c.102+3243delA | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30809076 | |||||||
| chr8:30809234 | C | T | 3 | a0001c0001t0001g0116 a0001c0001t0001g0146 a0001c0001t0001g0147 |
3 | HG02523.hp2 NA18950.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.102+3086G>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30809234 | |||||||
| chr8:30809481 | C | T | 1 | a0001c0001t0002g0100 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.102+2839G>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30809481 | |||||||
| chr8:30809651 | A | G | 19 | a0001c0001t0003g0002 a0001c0001t0003g0014 a0001c0001t0003g0015 others(16): Show |
40 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(37): Show |
intron_variant | MODIFIER | c.102+2669T>C | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30809651 | |||||||
| chr8:30809709 | G | C | 4 | a0001c0001t0001g0110 a0001c0001t0001g0186 a0001c0001t0001g0187 others(1): Show |
4 | HG00735.hp1 HG01496.hp2 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.102+2611C>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30809709 | |||||||
| chr8:30809772 | A | T | 1 | a0001c0001t0001g0145 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.102+2548T>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30809772 | |||||||
| chr8:30809916 | G | C | 1 | a0001c0001t0003g0109 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.102+2404C>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30809916 | |||||||
| chr8:30809933 | T | TC | 11 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0190 others(8): Show |
14 | HG02145.hp2 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.102+2386dupG | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30809933 | |||||||
| chr8:30809933 | TC | T | 108 | a0001c0001t0001g0033 a0001c0001t0002g0004 a0001c0001t0002g0005 others(105): Show |
165 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.102+2386delG | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30809933 | |||||||
| chr8:30809937 | C | A | 2 | a0001c0001t0002g0097 a0001c0001t0002g0098 |
2 | HG02895.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.102+2383G>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30809937 | |||||||
| chr8:30810060 | T | C | 1 | a0001c0001t0002g0099 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.102+2260A>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30810060 | |||||||
| chr8:30810240 | C | T | 23 | a0001c0001t0002g0004 a0001c0001t0002g0010 a0001c0001t0002g0019 others(20): Show |
33 | HG00738.hp2 HG01081.hp1 HG01168.hp2 others(30): Show |
intron_variant | MODIFIER | c.102+2080G>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30810240 | |||||||
| chr8:30810416 | G | A | 2 | a0001c0001t0002g0044 a0001c0001t0002g0059 |
2 | HG01081.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.102+1904C>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30810416 | |||||||
| chr8:30810544 | T | C | 34 | a0001c0001t0002g0008 a0001c0001t0002g0012 a0001c0001t0002g0022 others(31): Show |
40 | HG01891.hp2 HG02257.hp1 HG02258.hp1 others(37): Show |
intron_variant | MODIFIER | c.102+1776A>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30810544 | |||||||
| chr8:30810644 | AT | A | 2 | a0001c0001t0003g0028 a0001c0001t0003g0142 |
3 | HG02615.hp2 HG02886.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.102+1675delA | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30810644 | |||||||
| chr8:30810653 | T | C | 1 | a0001c0001t0002g0046 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.102+1667A>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30810653 | |||||||
| chr8:30811087 | A | G | 3 | a0001c0001t0001g0032 a0001c0001t0001g0143 a0001c0001t0001g0144 |
4 | HG01952.hp1 NA18959.hp2 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.102+1233T>C | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30811087 | |||||||
| chr8:30811169 | C | T | 1 | a0001c0001t0002g0065 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.102+1151G>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30811169 | |||||||
| chr8:30811209 | T | C | 31 | a0001c0001t0003g0002 a0001c0001t0003g0013 a0001c0001t0003g0014 others(28): Show |
56 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.102+1111A>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30811209 | |||||||
| chr8:30811334 | T | TTC | 1 | a0001c0001t0003g0015 | 3 | NA18954.hp2 NA18973.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.102+985_102+986ins others(2): Show |
PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30811334 | |||||||
| chr8:30811505 | A | AT | 49 | a0001c0001t0001g0006 a0001c0001t0001g0116 a0001c0001t0001g0117 others(46): Show |
77 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.102+814dupA | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30811505 | |||||||
| chr8:30811505 | A | ATT | 13 | a0001c0001t0001g0110 a0001c0001t0002g0038 a0001c0001t0003g0026 others(10): Show |
16 | HG00735.hp2 HG01109.hp2 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.102+813_102+814dup others(2): Show |
PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30811505 | |||||||
| chr8:30811505 | AT | A | 40 | a0001c0001t0002g0005 a0001c0001t0002g0007 a0001c0001t0002g0008 others(37): Show |
58 | HG00733.hp2 HG01099.hp2 HG01123.hp1 others(55): Show |
intron_variant | MODIFIER | c.102+814delA | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30811505 | |||||||
| chr8:30811599 | G | T | 8 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0104 others(5): Show |
11 | HG02257.hp2 HG02258.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.102+721C>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30811599 | |||||||
| chr8:30811672 | A | AT | 4 | a0001c0001t0003g0013 a0001c0001t0003g0108 a0001c0001t0003g0109 others(1): Show |
6 | HG00738.hp1 HG01243.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.102+647dupA | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30811672 | |||||||
| chr8:30811936 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.102+384C>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30811936 | |||||||
| chr8:30811967 | T | C | 1 | a0001c0001t0001g0193 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.102+353A>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30811967 | |||||||
| chr8:30811972 | G | A | 1 | a0001c0001t0003g0194 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.102+348C>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30811972 | |||||||
| chr8:30812122 | G | A | 1 | a0001c0001t0002g0100 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.102+198C>T | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30812122 | |||||||
| chr8:30812216 | C | T | 8 | a0001c0001t0004g0024 a0001c0001t0004g0025 a0001c0001t0004g0104 others(5): Show |
11 | HG02257.hp2 HG02258.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.102+104G>A | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30812216 | |||||||
| chr8:30812256 | G | C | 1 | a0001c0001t0002g0101 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.102+64C>G | PPP2CB | ENSG00000104695.13 | transcript | ENST00000221138.9 | protein_coding | 1/6 | chr8 | 30812256 |