Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10492 |
| ensemblid | ENSG00000135316.20 |
| hgncid | 16918 |
| symbol | SYNCRIP |
| name | synaptotagmin binding cytoplasmic RNA interacting protein |
| refseq_nuc | NM_006372.5 |
| refseq_prot | NP_006363.4 |
| ensembl_nuc | ENST00000369622.8 |
| ensembl_prot | ENSP00000358635.3 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 85613976 |
| end | 85642886 |
| strand | - |
| ver | v1.2 |
| region | chr6:85613976-85642886 |
| region5000 | chr6:85608976-85647886 |
| regionname0 | SYNCRIP_chr6_85613976_85642886 |
| regionname5000 | SYNCRIP_chr6_85608976_85647886 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 623 | 361 | 84 | 48 | 179 | 14 | 34 | 141 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | MATEH others(618): Show |
chr6 | 85608976 | 85647886 |
| a0002 | 0/0 | 623 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | MATEH others(618): Show |
chr6 | 85608976 | 85647886 |
| a0003 | 0/0 | 623 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | MATEH others(618): Show |
chr6 | 85608976 | 85647886 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1869 | 359 | 84 | 48 | 177 | 14 | 34 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | ATGGC others(1864): Show |
chr6 | 85608976 | 85647886 | ||
| a0001c0003 | 0/0 | 1869 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | ATGGC others(1864): Show |
chr6 | 85608976 | 85647886 | ||
| a0001c0004 | 0/0 | 1869 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | ATGGC others(1864): Show |
chr6 | 85608976 | 85647886 | ||
| a0002c0002 | 0/0 | 1869 | 2 | 0 | 2 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | ATGGC others(1864): Show |
chr6 | 85608976 | 85647886 | ||
| a0003c0005 | 0/0 | 1869 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | ATGGC others(1864): Show |
chr6 | 85608976 | 85647886 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2754 | 356 | 84 | 48 | 175 | 14 | 33 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | ACTCG others(2749): Show |
chr6 | 85608976 | 85647886 |
| a0001c0001t0002 | 0/0 | 2754 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | ACTCG others(2749): Show |
chr6 | 85608976 | 85647886 |
| a0001c0001t0003 | 0/0 | 2754 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | ACTCG others(2749): Show |
chr6 | 85608976 | 85647886 |
| a0001c0001t0004 | 0/0 | 2754 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | ACTCG others(2749): Show |
chr6 | 85608976 | 85647886 |
| a0001c0003t0001 | 0/0 | 2754 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | ACTCG others(2749): Show |
chr6 | 85608976 | 85647886 |
| a0001c0004t0001 | 0/0 | 2754 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | ACTCG others(2749): Show |
chr6 | 85608976 | 85647886 |
| a0002c0002t0001 | 0/0 | 2754 | 2 | 0 | 2 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | ACTCG others(2749): Show |
chr6 | 85608976 | 85647886 |
| a0003c0005t0001 | 0/0 | 2754 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | ACTCG others(2749): Show |
chr6 | 85608976 | 85647886 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0002 | 0/0 | 6 | 5 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0003 | 0/0 | 5 | 1 | 0 | 4 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0008 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0014 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0017 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0198 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0274 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0001t0004g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0003t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0001c0004t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0002c0002t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| a0003c0005t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | GBR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0169 | EUR | GBR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0034 | EUR | FIN | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0146 | EUR | FIN | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | CHS | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | CHS | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | CHS | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | CHS | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0030 | AMR | CLM | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | CLM | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0030 | AMR | CLM | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | CLM | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | CLM | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0235 | EUR | IBS | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0273 | EUR | IBS | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0140 | EUR | IBS | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0272 | EUR | IBS | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | ACB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | KHV | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | KHV | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | KHV | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0292 | EAS | KHV | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CDX | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CDX | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CDX | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CDX | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | KHV | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | GWD | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | ESN | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | ESN | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | ESN | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0270 | SAS | PJL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | MSL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | ESN | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ESN | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | MSL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | MSL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | MSL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | MSL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | MSL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | MSL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | MSL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | MSL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | STU | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | STU | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | BEB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | BEB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0287 | SAS | BEB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | BEB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | BEB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | BEB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | STU | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | BEB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0267 | SAS | BEB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | STU | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | STU | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0290 | SAS | STU | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | STU | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | YRI | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | CHB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | CHB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | YRI | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | YRI | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18957 | hp1 | a0003 | c0005 | t0001 | g0238 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18971 | hp2 | a0001 | c0003 | t0001 | g0206 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18977 | hp1 | a0001 | c0004 | t0001 | g0185 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0291 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | LWK | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | LWK | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | LWK | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | LWK | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | YRI | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | YRI | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | TSI | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0234 | EUR | TSI | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0139 | EUR | TSI | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0156 | EUR | TSI | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0289 | SAS | GIH | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | GIH | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | MSL | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | USA | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | USA | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | USA | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | USA | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0274 | REF | REF | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0198 | REF | REF | SYNCRIP_chr6_85608976_85647886 | SYNCRIP | chr6 | 85608976 | 85647886 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:85614856 | G | A | 1 | a0002 | 2 | HG01257.hp1 HG01258.hp1 |
missense_variant | MODERATE | c.1772C>T | p.Ala591Val | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 11/11 | 1874/2754 | 1772/1872 | 591/623 | chr6 | 85614856 | |||
| chr6:85641393 | T | G | 1 | a0003 | 1 | NA18957.hp1 | missense_variant | MODERATE | c.47A>C | p.Asp16Ala | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 2/11 | 149/2754 | 47/1872 | 16/623 | chr6 | 85641393 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:85615152 | T | C | 1 | a0001c0003 | 1 | NA18971.hp2 | synonymous_variant | LOW | c.1476A>G | p.Gln492Gln | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 11/11 | 1578/2754 | 1476/1872 | 492/623 | chr6 | 85615152 | |||
| chr6:85637279 | G | A | 1 | a0001c0004 | 1 | NA18977.hp1 | synonymous_variant | LOW | c.453C>T | p.Ser151Ser | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 5/11 | 555/2754 | 453/1872 | 151/623 | chr6 | 85637279 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:85642807 | G | A | 1 | a0001c0001t0002 | 1 | HG04204.hp1 | 5_prime_UTR_variant | MODIFIER | c.-23C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 1/11 | 1368 | chr6 | 85642807 | ||||||
| chr6:85642817 | G | A | 1 | a0001c0001t0003 | 1 | NA18998.hp1 | 5_prime_UTR_variant | MODIFIER | c.-33C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 1/11 | 1378 | chr6 | 85642817 | ||||||
| chr6:85642860 | T | G | 1 | a0001c0001t0004 | 1 | HG02080.hp2 | 5_prime_UTR_variant | MODIFIER | c.-76A>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 1/11 | 1421 | chr6 | 85642860 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:85615548 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1281-201A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85615548 | |||||||
| chr6:85615633 | T | G | 1 | a0001c0001t0001g0159 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1281-286A>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85615633 | |||||||
| chr6:85615855 | T | C | 3 | a0001c0001t0001g0161 a0001c0001t0001g0170 a0001c0001t0001g0189 |
3 | NA18980.hp1 NA18995.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.1281-508A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85615855 | |||||||
| chr6:85615914 | C | T | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(171): Show |
215 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(212): Show |
intron_variant | MODIFIER | c.1281-567G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85615914 | |||||||
| chr6:85615947 | A | C | 2 | a0001c0001t0001g0049 a0001c0001t0001g0050 |
2 | HG02145.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1281-600T>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85615947 | |||||||
| chr6:85616084 | A | G | 1 | a0001c0001t0001g0282 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1281-737T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85616084 | |||||||
| chr6:85616190 | C | T | 1 | a0001c0001t0001g0029 | 2 | HG00735.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.1281-843G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85616190 | |||||||
| chr6:85616295 | G | A | 3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | HG01258.hp2 HG02055.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.1281-948C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85616295 | |||||||
| chr6:85616387 | G | A | 6 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0242 others(3): Show |
6 | HG02886.hp2 HG02965.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1281-1040C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85616387 | |||||||
| chr6:85616567 | ACCCACCT others(17): Show |
A | 2 | a0001c0001t0001g0162 a0001c0001t0001g0167 |
2 | HG01433.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1281-1244_1281-122 others(28): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85616567 | |||||||
| chr6:85616693 | C | T | 2 | a0001c0001t0001g0215 a0001c0001t0001g0216 |
2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1281-1346G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85616693 | |||||||
| chr6:85616750 | T | C | 2 | a0001c0001t0001g0184 a0001c0001t0001g0202 |
2 | HG01074.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.1281-1403A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85616750 | |||||||
| chr6:85616782 | C | A | 1 | a0001c0001t0001g0064 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1281-1435G>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85616782 | |||||||
| chr6:85616898 | G | A | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1281-1551C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85616898 | |||||||
| chr6:85616924 | T | C | 2 | a0001c0001t0001g0195 a0001c0001t0001g0197 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1281-1577A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85616924 | |||||||
| chr6:85616945 | C | G | 4 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(1): Show |
4 | HG02109.hp1 HG02630.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1281-1598G>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85616945 | |||||||
| chr6:85617013 | A | G | 4 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(1): Show |
4 | HG02109.hp1 HG02630.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1281-1666T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85617013 | |||||||
| chr6:85617152 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1280+1666C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85617152 | |||||||
| chr6:85617160 | G | C | 1 | a0001c0001t0001g0064 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1280+1658C>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85617160 | |||||||
| chr6:85617174 | G | C | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1280+1644C>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85617174 | |||||||
| chr6:85617197 | T | TA | 9 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0058 others(6): Show |
11 | HG01884.hp2 HG02109.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1280+1620dupT | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85617197 | |||||||
| chr6:85617197 | TA | T | 16 | a0001c0001t0001g0047 a0001c0001t0001g0051 a0001c0001t0001g0052 others(13): Show |
16 | HG01070.hp2 HG01517.hp2 HG01934.hp2 others(13): Show |
intron_variant | MODIFIER | c.1280+1620delT | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85617197 | |||||||
| chr6:85617229 | A | G | 1 | a0001c0001t0001g0102 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1280+1589T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85617229 | |||||||
| chr6:85617283 | A | G | 1 | a0001c0001t0001g0079 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1280+1535T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85617283 | |||||||
| chr6:85617327 | CCTCT | C | 3 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0231 |
3 | HG00423.hp1 HG02074.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.1280+1487_1280+149 others(8): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85617327 | |||||||
| chr6:85617453 | C | T | 4 | a0001c0001t0001g0006 a0001c0001t0001g0154 a0001c0001t0001g0192 others(1): Show |
7 | HG01175.hp1 HG01261.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.1280+1365G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85617453 | |||||||
| chr6:85617488 | G | C | 1 | a0001c0001t0001g0183 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1280+1330C>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85617488 | |||||||
| chr6:85617647 | G | A | 1 | a0001c0001t0001g0270 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1280+1171C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85617647 | |||||||
| chr6:85617751 | G | A | 9 | a0001c0001t0001g0058 a0001c0001t0001g0126 a0001c0001t0001g0237 others(6): Show |
9 | HG01884.hp2 HG02109.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.1280+1067C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85617751 | |||||||
| chr6:85617778 | G | A | 3 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0036 |
10 | NA18944.hp2 NA18952.hp2 NA18968.hp1 others(7): Show |
intron_variant | MODIFIER | c.1280+1040C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85617778 | |||||||
| chr6:85617975 | A | G | 1 | a0001c0001t0001g0184 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1280+843T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85617975 | |||||||
| chr6:85618019 | T | C | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1280+799A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85618019 | |||||||
| chr6:85618142 | C | G | 140 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(137): Show |
173 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.1280+676G>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85618142 | |||||||
| chr6:85618149 | A | AG | 4 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(1): Show |
4 | HG02647.hp1 HG03130.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1280+668dupC | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85618149 | |||||||
| chr6:85618230 | T | A | 6 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(3): Show |
6 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1280+588A>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85618230 | |||||||
| chr6:85618256 | A | G | 1 | a0001c0001t0001g0081 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1280+562T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85618256 | |||||||
| chr6:85618425 | C | CAGCT | 8 | a0001c0001t0001g0126 a0001c0001t0001g0237 a0001c0001t0001g0240 others(5): Show |
8 | HG01884.hp2 HG02886.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1280+389_1280+392d others(6): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85618425 | |||||||
| chr6:85618635 | T | C | 1 | a0001c0001t0001g0191 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1280+183A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85618635 | |||||||
| chr6:85618713 | A | T | 140 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(137): Show |
173 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.1280+105T>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 10/10 | chr6 | 85618713 | |||||||
| chr6:85619049 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1159-110G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 9/10 | chr6 | 85619049 | |||||||
| chr6:85619075 | T | C | 1 | a0001c0001t0001g0253 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1159-136A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 9/10 | chr6 | 85619075 | |||||||
| chr6:85619174 | CA | C | 3 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 |
3 | HG02145.hp1 HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1158+93delT | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 9/10 | chr6 | 85619174 | |||||||
| chr6:85619187 | A | G | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | NA18991.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1158+81T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 9/10 | chr6 | 85619187 | |||||||
| chr6:85619421 | G | T | 1 | a0001c0001t0001g0205 | 1 | NA18959.hp2 | splice_region_variant&intron_variant | LOW | c.1009-4C>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85619421 | |||||||
| chr6:85619535 | T | A | 1 | a0001c0001t0001g0279 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1009-118A>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85619535 | |||||||
| chr6:85619535 | T | TA | 81 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(78): Show |
90 | HG00408.hp2 HG00423.hp2 HG00735.hp2 others(87): Show |
intron_variant | MODIFIER | c.1009-119dupT | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85619535 | |||||||
| chr6:85619715 | C | T | 2 | a0001c0001t0001g0171 a0001c0001t0001g0177 |
2 | HG02698.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1009-298G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85619715 | |||||||
| chr6:85619797 | G | GTA | 51 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(48): Show |
75 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.1009-382_1009-381d others(4): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85619797 | |||||||
| chr6:85619824 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1009-407G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85619824 | |||||||
| chr6:85619842 | A | C | 1 | a0001c0001t0001g0250 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1009-425T>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85619842 | |||||||
| chr6:85619886 | C | G | 1 | a0001c0001t0001g0213 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1009-469G>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85619886 | |||||||
| chr6:85620111 | T | C | 4 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(1): Show |
4 | HG02109.hp1 HG02630.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1009-694A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85620111 | |||||||
| chr6:85620141 | G | A | 25 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0031 others(22): Show |
33 | HG00423.hp1 HG00544.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.1009-724C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85620141 | |||||||
| chr6:85620204 | C | T | 1 | a0001c0001t0001g0259 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1009-787G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85620204 | |||||||
| chr6:85620359 | T | G | 1 | a0001c0001t0001g0058 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1009-942A>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85620359 | |||||||
| chr6:85620397 | T | C | 51 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(48): Show |
75 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.1009-980A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85620397 | |||||||
| chr6:85620415 | G | A | 51 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(48): Show |
75 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.1009-998C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85620415 | |||||||
| chr6:85620880 | A | C | 1 | a0001c0001t0001g0058 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1009-1463T>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85620880 | |||||||
| chr6:85621322 | A | G | 4 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(1): Show |
4 | HG02818.hp1 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1008+1160T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85621322 | |||||||
| chr6:85621347 | C | G | 1 | a0001c0001t0001g0191 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1008+1135G>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85621347 | |||||||
| chr6:85621409 | C | T | 2 | a0001c0001t0001g0162 a0001c0001t0001g0167 |
2 | HG01433.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1008+1073G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85621409 | |||||||
| chr6:85621601 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1008+881C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85621601 | |||||||
| chr6:85621607 | T | TA | 7 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0141 others(4): Show |
9 | HG00280.hp1 HG00544.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1008+874dupT | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85621607 | |||||||
| chr6:85621607 | TA | T | 115 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(112): Show |
132 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.1008+874delT | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85621607 | |||||||
| chr6:85621607 | TAA | T | 14 | a0001c0001t0001g0063 a0001c0001t0001g0074 a0001c0001t0001g0075 others(11): Show |
14 | HG01168.hp1 HG01884.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.1008+873_1008+874d others(4): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85621607 | |||||||
| chr6:85621609 | A | T | 1 | a0001c0001t0001g0072 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1008+873T>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85621609 | |||||||
| chr6:85621640 | A | G | 2 | a0001c0001t0001g0022 a0001c0001t0001g0038 |
3 | HG02280.hp2 HG02922.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1008+842T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85621640 | |||||||
| chr6:85621731 | G | T | 1 | a0001c0001t0001g0083 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1008+751C>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85621731 | |||||||
| chr6:85621800 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1008+682C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85621800 | |||||||
| chr6:85621819 | T | A | 1 | a0001c0001t0001g0145 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1008+663A>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85621819 | |||||||
| chr6:85621913 | T | TGTAGGCG others(41): Show |
2 | a0001c0001t0001g0055 a0001c0001t0001g0056 |
2 | HG02559.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1008+521_1008+568d others(50): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85621913 | |||||||
| chr6:85621918 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1008+564C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85621918 | |||||||
| chr6:85622016 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1008+466G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85622016 | |||||||
| chr6:85622031 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1008+451G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85622031 | |||||||
| chr6:85622064 | T | C | 1 | a0001c0001t0001g0069 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1008+418A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85622064 | |||||||
| chr6:85622155 | C | T | 1 | a0001c0001t0001g0150 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1008+327G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85622155 | |||||||
| chr6:85622169 | C | T | 56 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(53): Show |
80 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.1008+313G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85622169 | |||||||
| chr6:85622181 | G | C | 1 | a0001c0001t0001g0064 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1008+301C>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85622181 | |||||||
| chr6:85622231 | C | T | 21 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0031 others(18): Show |
29 | HG00423.hp1 HG00544.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.1008+251G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85622231 | |||||||
| chr6:85622256 | T | C | 1 | a0001c0001t0001g0067 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1008+226A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85622256 | |||||||
| chr6:85622274 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1008+208G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85622274 | |||||||
| chr6:85622416 | C | T | 6 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(3): Show |
6 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1008+66G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 8/10 | chr6 | 85622416 | |||||||
| chr6:85622725 | A | C | 2 | a0001c0001t0001g0013 a0001c0001t0001g0157 |
4 | HG02451.hp2 HG03139.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-38T>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85622725 | |||||||
| chr6:85622875 | T | C | 3 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 |
3 | HG02145.hp1 HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.803-188A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85622875 | |||||||
| chr6:85623044 | A | G | 5 | a0001c0001t0001g0025 a0001c0001t0001g0045 a0001c0001t0001g0046 others(2): Show |
6 | HG02559.hp1 HG02647.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.803-357T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623044 | |||||||
| chr6:85623258 | G | A | 3 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0036 |
10 | NA18944.hp2 NA18952.hp2 NA18968.hp1 others(7): Show |
intron_variant | MODIFIER | c.803-571C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623258 | |||||||
| chr6:85623311 | C | T | 51 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(48): Show |
75 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.803-624G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623311 | |||||||
| chr6:85623374 | G | A | 6 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(3): Show |
6 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.802+603C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623374 | |||||||
| chr6:85623532 | C | G | 75 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(72): Show |
83 | HG00408.hp2 HG00423.hp2 HG00735.hp2 others(80): Show |
intron_variant | MODIFIER | c.802+445G>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623532 | |||||||
| chr6:85623561 | C | CCCAAAAA others(6): Show |
2 | a0001c0001t0001g0088 a0001c0001t0001g0101 |
2 | HG00408.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.802+415_802+416ins others(13): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623561 | |||||||
| chr6:85623562 | C | CAAAAAA | 15 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0031 others(12): Show |
23 | HG00423.hp1 HG01070.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.802+409_802+414dup others(6): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623562 | |||||||
| chr6:85623562 | C | CAAAAAAA others(7): Show |
2 | a0001c0001t0001g0213 a0001c0001t0001g0214 |
2 | HG02818.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.802+401_802+414dup others(14): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623562 | |||||||
| chr6:85623562 | C | CAAAAAAA others(11): Show |
1 | a0001c0001t0001g0215 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.802+397_802+414dup others(18): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623562 | |||||||
| chr6:85623562 | C | CAAAAAAA others(12): Show |
1 | a0001c0001t0001g0216 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.802+396_802+414dup others(19): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623562 | |||||||
| chr6:85623562 | C | CCAA | 4 | a0001c0001t0001g0062 a0001c0001t0001g0125 a0001c0001t0001g0130 others(1): Show |
4 | HG03098.hp2 HG03130.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.802+414_802+415ins others(3): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623562 | |||||||
| chr6:85623562 | C | CCAAA | 3 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0131 |
3 | HG02145.hp1 HG02647.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.802+414_802+415ins others(4): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623562 | |||||||
| chr6:85623562 | C | CCAAAAAA | 7 | a0001c0001t0001g0035 a0001c0001t0001g0050 a0001c0001t0001g0254 others(4): Show |
8 | HG01168.hp2 HG01169.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.802+414_802+415ins others(7): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623562 | |||||||
| chr6:85623562 | C | CCAAAAAA others(4): Show |
15 | a0001c0001t0001g0010 a0001c0001t0001g0037 a0001c0001t0001g0059 others(12): Show |
17 | HG01168.hp1 HG01358.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.802+414_802+415ins others(11): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623562 | |||||||
| chr6:85623562 | C | CCAAAAAA others(5): Show |
19 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0046 others(16): Show |
22 | HG00735.hp2 HG01109.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.802+414_802+415ins others(12): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623562 | |||||||
| chr6:85623562 | C | CCAAAAAA others(6): Show |
12 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0078 others(9): Show |
12 | HG02165.hp2 HG02523.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.802+414_802+415ins others(13): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623562 | |||||||
| chr6:85623562 | C | CCAAAAAA others(7): Show |
13 | a0001c0001t0001g0011 a0001c0001t0001g0026 a0001c0001t0001g0027 others(10): Show |
17 | HG00423.hp2 HG02135.hp2 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.802+414_802+415ins others(14): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623562 | |||||||
| chr6:85623562 | C | CCAAAAAA others(8): Show |
10 | a0001c0001t0001g0045 a0001c0001t0001g0066 a0001c0001t0001g0068 others(7): Show |
10 | HG01255.hp1 HG01975.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.802+414_802+415ins others(15): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623562 | |||||||
| chr6:85623562 | C | CCAAAAAA others(9): Show |
2 | a0001c0001t0001g0093 a0001c0001t0001g0100 |
2 | HG01928.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.802+414_802+415ins others(16): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623562 | |||||||
| chr6:85623562 | C | CCAAAAAA others(10): Show |
2 | a0001c0001t0001g0064 a0001c0001t0001g0077 |
2 | HG03471.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.802+414_802+415ins others(17): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623562 | |||||||
| chr6:85623562 | C | CCAAAAAA others(11): Show |
1 | a0001c0001t0001g0086 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.802+414_802+415ins others(18): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623562 | |||||||
| chr6:85623562 | C | CCAAAAAA others(13): Show |
1 | a0001c0001t0001g0279 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.802+414_802+415ins others(20): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623562 | |||||||
| chr6:85623562 | CA | C | 93 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(90): Show |
121 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.802+414delT | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623562 | |||||||
| chr6:85623562 | CAAA | C | 8 | a0001c0001t0001g0126 a0001c0001t0001g0237 a0001c0001t0001g0240 others(5): Show |
8 | HG01884.hp2 HG02886.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.802+412_802+414del others(3): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623562 | |||||||
| chr6:85623563 | A | C | 45 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(42): Show |
68 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.802+414T>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623563 | |||||||
| chr6:85623566 | A | C | 1 | a0001c0001t0001g0279 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.802+411T>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623566 | |||||||
| chr6:85623567 | A | C | 1 | a0001c0001t0001g0107 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.802+410T>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623567 | |||||||
| chr6:85623571 | A | AAAAAAAA others(14): Show |
2 | a0001c0001t0001g0051 a0001c0001t0001g0056 |
2 | HG02559.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.802+405_802+406ins others(21): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623571 | |||||||
| chr6:85623571 | A | AAAAAAAA others(13): Show |
3 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0055 |
3 | HG02630.hp1 HG02630.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.802+405_802+406ins others(20): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623571 | |||||||
| chr6:85623571 | A | AAAAAAAA others(13): Show |
1 | a0001c0001t0001g0053 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.802+405_802+406ins others(20): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623571 | |||||||
| chr6:85623571 | A | C | 1 | a0001c0001t0001g0078 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.802+406T>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623571 | |||||||
| chr6:85623573 | A | C | 4 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0087 others(1): Show |
6 | NA18956.hp2 NA18969.hp1 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.802+404T>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623573 | |||||||
| chr6:85623579 | A | AAAAAAAA others(14): Show |
4 | a0001c0001t0001g0247 a0001c0001t0001g0251 a0001c0001t0001g0266 others(1): Show |
4 | HG02071.hp2 NA19058.hp1 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.802+397_802+398ins others(21): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623579 | |||||||
| chr6:85623579 | A | AAAAAAAC others(14): Show |
1 | a0001c0001t0001g0259 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.802+397_802+398ins others(21): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623579 | |||||||
| chr6:85623579 | A | AAAAAAAC others(13): Show |
37 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(34): Show |
60 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.802+397_802+398ins others(20): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623579 | |||||||
| chr6:85623579 | A | AAAAAAAC others(13): Show |
1 | a0001c0001t0001g0252 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.802+397_802+398ins others(20): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623579 | |||||||
| chr6:85623579 | A | AAAAAAAC others(14): Show |
1 | a0001c0001t0001g0283 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.802+397_802+398ins others(21): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623579 | |||||||
| chr6:85623579 | A | C | 7 | a0001c0001t0001g0035 a0001c0001t0001g0254 a0001c0001t0001g0257 others(4): Show |
8 | HG01106.hp2 HG01168.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.802+398T>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623579 | |||||||
| chr6:85623583 | A | AAAAAAAA others(9): Show |
1 | a0001c0001t0001g0133 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.802+393_802+394ins others(16): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623583 | |||||||
| chr6:85623595 | G | A | 1 | a0001c0001t0001g0255 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.802+382C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623595 | |||||||
| chr6:85623888 | T | C | 1 | a0001c0001t0001g0242 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.802+89A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 7/10 | chr6 | 85623888 | |||||||
| chr6:85624115 | G | A | 2 | a0001c0001t0001g0082 a0001c0001t0001g0135 |
2 | HG02523.hp1 NA18979.hp2 |
splice_region_variant&intron_variant | LOW | c.667-3C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85624115 | |||||||
| chr6:85624138 | T | C | 1 | a0001c0001t0001g0083 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.667-26A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85624138 | |||||||
| chr6:85624186 | A | T | 1 | a0001c0001t0001g0214 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.667-74T>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85624186 | |||||||
| chr6:85624303 | T | G | 1 | a0001c0001t0001g0164 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.667-191A>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85624303 | |||||||
| chr6:85624342 | C | G | 4 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(1): Show |
4 | HG02818.hp1 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.667-230G>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85624342 | |||||||
| chr6:85624372 | G | A | 25 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0031 others(22): Show |
33 | HG00423.hp1 HG00544.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.667-260C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85624372 | |||||||
| chr6:85624669 | T | G | 1 | a0001c0001t0001g0153 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.667-557A>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85624669 | |||||||
| chr6:85624681 | A | G | 1 | a0001c0001t0001g0128 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.667-569T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85624681 | |||||||
| chr6:85624708 | A | G | 1 | a0001c0001t0001g0057 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.667-596T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85624708 | |||||||
| chr6:85624716 | T | C | 2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | HG02647.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.667-604A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85624716 | |||||||
| chr6:85624718 | G | C | 1 | a0001c0001t0001g0129 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.667-606C>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85624718 | |||||||
| chr6:85624956 | A | G | 9 | a0001c0001t0001g0058 a0001c0001t0001g0126 a0001c0001t0001g0237 others(6): Show |
9 | HG01884.hp2 HG02109.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.667-844T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85624956 | |||||||
| chr6:85625130 | C | T | 139 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(136): Show |
172 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.667-1018G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85625130 | |||||||
| chr6:85625212 | T | A | 1 | a0001c0001t0001g0250 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.667-1100A>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85625212 | |||||||
| chr6:85625243 | C | T | 25 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0031 others(22): Show |
33 | HG00423.hp1 HG00544.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.667-1131G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85625243 | |||||||
| chr6:85625246 | C | G | 75 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(72): Show |
83 | HG00408.hp2 HG00423.hp2 HG00735.hp2 others(80): Show |
intron_variant | MODIFIER | c.667-1134G>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85625246 | |||||||
| chr6:85625358 | T | C | 3 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0231 |
3 | HG00423.hp1 HG02074.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.667-1246A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85625358 | |||||||
| chr6:85625363 | A | T | 1 | a0001c0001t0001g0193 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.667-1251T>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85625363 | |||||||
| chr6:85625379 | G | A | 1 | a0001c0001t0001g0156 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.667-1267C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85625379 | |||||||
| chr6:85625380 | G | GT | 10 | a0001c0001t0001g0036 a0001c0001t0001g0058 a0001c0001t0001g0077 others(7): Show |
11 | HG02055.hp1 HG02109.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.667-1269dupA | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85625380 | |||||||
| chr6:85625432 | A | T | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(178): Show |
222 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(219): Show |
intron_variant | MODIFIER | c.667-1320T>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85625432 | |||||||
| chr6:85625466 | C | A | 2 | a0001c0001t0001g0116 a0001c0001t0001g0122 |
2 | HG01891.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.667-1354G>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85625466 | |||||||
| chr6:85625513 | G | A | 1 | a0001c0001t0001g0165 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.667-1401C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85625513 | |||||||
| chr6:85625576 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.667-1464G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85625576 | |||||||
| chr6:85625584 | C | T | 3 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 |
3 | HG02647.hp1 HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.667-1472G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85625584 | |||||||
| chr6:85625632 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.667-1520G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85625632 | |||||||
| chr6:85625747 | C | A | 4 | a0001c0001t0001g0065 a0001c0001t0001g0067 a0001c0001t0001g0068 others(1): Show |
4 | NA18944.hp1 NA19009.hp1 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.667-1635G>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85625747 | |||||||
| chr6:85626080 | T | C | 8 | a0001c0001t0001g0006 a0001c0001t0001g0154 a0001c0001t0001g0155 others(5): Show |
11 | HG00099.hp2 HG01069.hp1 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.667-1968A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85626080 | |||||||
| chr6:85626315 | A | C | 1 | a0001c0001t0001g0061 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.667-2203T>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85626315 | |||||||
| chr6:85626340 | T | C | 5 | a0001c0001t0001g0025 a0001c0001t0001g0045 a0001c0001t0001g0046 others(2): Show |
6 | HG02559.hp1 HG02647.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.667-2228A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85626340 | |||||||
| chr6:85626385 | GA | G | 3 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 |
3 | HG02145.hp1 HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.667-2274delT | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85626385 | |||||||
| chr6:85626491 | T | C | 3 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0001t0001g0283 |
3 | HG00609.hp2 NA18981.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.667-2379A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85626491 | |||||||
| chr6:85626582 | T | G | 51 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(48): Show |
75 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.667-2470A>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85626582 | |||||||
| chr6:85626619 | G | C | 141 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(138): Show |
174 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.667-2507C>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85626619 | |||||||
| chr6:85626686 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.667-2574T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85626686 | |||||||
| chr6:85626949 | C | T | 6 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(3): Show |
6 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.667-2837G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85626949 | |||||||
| chr6:85626972 | T | C | 75 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(72): Show |
83 | HG00408.hp2 HG00423.hp2 HG00735.hp2 others(80): Show |
intron_variant | MODIFIER | c.667-2860A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85626972 | |||||||
| chr6:85627037 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.667-2925C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85627037 | |||||||
| chr6:85627083 | C | T | 2 | a0001c0001t0001g0055 a0001c0001t0001g0056 |
2 | HG02559.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.667-2971G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85627083 | |||||||
| chr6:85627092 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.667-2980C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85627092 | |||||||
| chr6:85627270 | C | CA | 18 | a0001c0001t0001g0064 a0001c0001t0001g0085 a0001c0001t0001g0086 others(15): Show |
18 | HG01928.hp2 HG02135.hp1 HG02818.hp2 others(15): Show |
intron_variant | MODIFIER | c.667-3159dupT | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85627270 | |||||||
| chr6:85627271 | A | G | 1 | a0001c0001t0001g0110 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.667-3159T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85627271 | |||||||
| chr6:85627393 | A | G | 3 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 |
3 | HG02647.hp1 HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.667-3281T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85627393 | |||||||
| chr6:85627465 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.667-3353G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85627465 | |||||||
| chr6:85627607 | A | G | 2 | a0001c0001t0001g0184 a0001c0001t0001g0202 |
2 | HG01074.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.667-3495T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85627607 | |||||||
| chr6:85627619 | T | TAATTTAA others(3): Show |
1 | a0001c0001t0001g0193 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.667-3517_667-3508d others(12): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85627619 | |||||||
| chr6:85627705 | C | A | 1 | a0001c0001t0001g0159 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.667-3593G>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85627705 | |||||||
| chr6:85627729 | T | C | 1 | a0001c0001t0001g0064 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.667-3617A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85627729 | |||||||
| chr6:85628089 | T | A | 1 | a0001c0001t0001g0147 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.667-3977A>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85628089 | |||||||
| chr6:85628271 | G | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0071 |
2 | HG00735.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.667-4159C>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85628271 | |||||||
| chr6:85628276 | G | C | 1 | a0001c0001t0001g0200 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.667-4164C>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85628276 | |||||||
| chr6:85628330 | A | G | 2 | a0001c0001t0001g0247 a0001c0001t0001g0265 |
2 | NA18985.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.667-4218T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85628330 | |||||||
| chr6:85628340 | T | A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0041 a0001c0001t0001g0043 |
4 | HG02132.hp1 NA18940.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.667-4228A>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85628340 | |||||||
| chr6:85628561 | G | T | 4 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(1): Show |
4 | HG02109.hp1 HG02630.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.667-4449C>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85628561 | |||||||
| chr6:85628562 | A | T | 4 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(1): Show |
4 | HG02109.hp1 HG02630.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.667-4450T>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85628562 | |||||||
| chr6:85628679 | G | C | 1 | a0001c0001t0001g0239 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.667-4567C>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85628679 | |||||||
| chr6:85628868 | C | G | 1 | a0001c0001t0001g0048 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.667-4756G>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85628868 | |||||||
| chr6:85629009 | CT | C | 25 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0031 others(22): Show |
33 | HG00423.hp1 HG00544.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.667-4898delA | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85629009 | |||||||
| chr6:85629052 | A | T | 1 | a0001c0001t0001g0058 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.667-4940T>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85629052 | |||||||
| chr6:85629066 | A | C | 1 | a0001c0001t0001g0250 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.667-4954T>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85629066 | |||||||
| chr6:85629088 | T | C | 3 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 |
3 | HG02647.hp1 HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.667-4976A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85629088 | |||||||
| chr6:85629176 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.667-5064T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85629176 | |||||||
| chr6:85629378 | T | C | 1 | a0001c0001t0001g0179 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.667-5266A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85629378 | |||||||
| chr6:85629516 | C | CA | 63 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0023 others(60): Show |
72 | HG00423.hp1 HG00609.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.667-5405dupT | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85629516 | |||||||
| chr6:85629516 | C | CAA | 36 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0018 others(33): Show |
54 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.667-5406_667-5405d others(4): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85629516 | |||||||
| chr6:85629516 | C | CAAA | 23 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0246 others(20): Show |
32 | HG00609.hp2 HG02071.hp2 HG02083.hp2 others(29): Show |
intron_variant | MODIFIER | c.667-5407_667-5405d others(5): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85629516 | |||||||
| chr6:85629552 | G | A | 1 | a0001c0001t0001g0168 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.667-5440C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85629552 | |||||||
| chr6:85629587 | G | A | 21 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0031 others(18): Show |
29 | HG00423.hp1 HG00544.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.667-5475C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85629587 | |||||||
| chr6:85629683 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.667-5571C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85629683 | |||||||
| chr6:85629846 | T | C | 2 | a0001c0001t0001g0269 a0001c0001t0001g0289 |
2 | HG06807.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.667-5734A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85629846 | |||||||
| chr6:85629853 | G | A | 3 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 |
3 | HG02145.hp1 HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.667-5741C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85629853 | |||||||
| chr6:85629917 | G | C | 1 | a0001c0001t0001g0048 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.667-5805C>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85629917 | |||||||
| chr6:85629961 | T | C | 1 | a0001c0001t0001g0069 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.667-5849A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85629961 | |||||||
| chr6:85629979 | C | G | 1 | a0001c0001t0001g0107 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.667-5867G>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85629979 | |||||||
| chr6:85629981 | C | CA | 82 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(79): Show |
90 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.667-5870dupT | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85629981 | |||||||
| chr6:85630084 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.667-5972C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85630084 | |||||||
| chr6:85630205 | C | T | 1 | a0001c0001t0001g0234 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.667-6093G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85630205 | |||||||
| chr6:85630255 | G | A | 1 | a0001c0001t0001g0258 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.667-6143C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85630255 | |||||||
| chr6:85630310 | G | T | 8 | a0001c0001t0001g0126 a0001c0001t0001g0237 a0001c0001t0001g0240 others(5): Show |
8 | HG01884.hp2 HG02886.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.667-6198C>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85630310 | |||||||
| chr6:85630363 | A | G | 2 | a0001c0001t0001g0218 a0001c0001t0001g0219 |
2 | HG01109.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.667-6251T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85630363 | |||||||
| chr6:85630388 | C | T | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(277): Show |
352 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(349): Show |
intron_variant | MODIFIER | c.667-6276G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85630388 | |||||||
| chr6:85630519 | C | T | 24 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0060 others(21): Show |
26 | HG00735.hp2 HG01168.hp1 HG02165.hp1 others(23): Show |
intron_variant | MODIFIER | c.667-6407G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85630519 | |||||||
| chr6:85630678 | T | C | 1 | a0001c0001t0001g0129 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.666+6289A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85630678 | |||||||
| chr6:85630690 | A | AT | 3 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 |
3 | HG02647.hp1 HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.666+6276dupA | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85630690 | |||||||
| chr6:85630978 | C | T | 1 | a0001c0001t0001g0044 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.666+5989G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85630978 | |||||||
| chr6:85631025 | C | T | 3 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 |
3 | HG02145.hp1 HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.666+5942G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85631025 | |||||||
| chr6:85631119 | A | T | 3 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 |
3 | HG02145.hp1 HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.666+5848T>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85631119 | |||||||
| chr6:85631130 | G | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(178): Show |
222 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(219): Show |
intron_variant | MODIFIER | c.666+5837C>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85631130 | |||||||
| chr6:85631310 | G | A | 1 | a0001c0001t0001g0174 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.666+5657C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85631310 | |||||||
| chr6:85631339 | C | CA | 7 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0177 others(4): Show |
7 | HG00544.hp2 HG01496.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.666+5627dupT | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85631339 | |||||||
| chr6:85631339 | C | CAAA | 42 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(39): Show |
66 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.666+5625_666+5627d others(5): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85631339 | |||||||
| chr6:85631339 | C | CAAAA | 6 | a0001c0001t0001g0065 a0001c0001t0001g0259 a0001c0001t0001g0260 others(3): Show |
6 | HG00597.hp1 HG03017.hp1 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.666+5624_666+5627d others(6): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85631339 | |||||||
| chr6:85631339 | C | CAAAAAAA | 8 | a0001c0001t0001g0025 a0001c0001t0001g0045 a0001c0001t0001g0046 others(5): Show |
9 | HG01433.hp2 HG02145.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.666+5621_666+5627d others(9): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85631339 | |||||||
| chr6:85631339 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0001g0075 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.666+5617_666+5627d others(13): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85631339 | |||||||
| chr6:85631339 | C | CAAAAAAA others(5): Show |
28 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0027 others(25): Show |
33 | HG00423.hp2 HG01255.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.666+5616_666+5627d others(14): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85631339 | |||||||
| chr6:85631339 | C | CAAAAAAA others(6): Show |
27 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0001g0061 others(24): Show |
30 | HG00408.hp2 HG00735.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.666+5615_666+5627d others(15): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85631339 | |||||||
| chr6:85631339 | C | CAAAAAAA others(7): Show |
9 | a0001c0001t0001g0073 a0001c0001t0001g0110 a0001c0001t0001g0111 others(6): Show |
9 | HG01358.hp2 HG03017.hp2 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.666+5614_666+5627d others(16): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85631339 | |||||||
| chr6:85631339 | C | CAAAAAAA others(8): Show |
4 | a0001c0001t0001g0059 a0001c0001t0001g0092 a0001c0001t0001g0106 others(1): Show |
4 | HG01109.hp1 HG03942.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.666+5613_666+5627d others(17): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85631339 | |||||||
| chr6:85631339 | C | CAAAAAAA others(9): Show |
1 | a0001c0001t0001g0127 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.666+5612_666+5627d others(18): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85631339 | |||||||
| chr6:85631339 | C | CAAAAAAA others(10): Show |
2 | a0001c0001t0001g0114 a0001c0001t0001g0122 |
2 | HG01891.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.666+5627_666+5628i others(19): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85631339 | |||||||
| chr6:85631339 | C | CAAAAAAA others(11): Show |
2 | a0001c0001t0001g0060 a0001c0001t0001g0115 |
2 | HG02895.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.666+5627_666+5628i others(20): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85631339 | |||||||
| chr6:85631339 | C | CAAAAAAA others(12): Show |
1 | a0001c0001t0001g0116 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.666+5627_666+5628i others(21): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85631339 | |||||||
| chr6:85631339 | C | CAAAAAAA others(18): Show |
1 | a0001c0001t0001g0130 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.666+5627_666+5628i others(27): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85631339 | |||||||
| chr6:85631339 | C | CAAAAAAA others(38): Show |
1 | a0001c0001t0001g0132 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.666+5627_666+5628i others(47): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85631339 | |||||||
| chr6:85631339 | C | CAAAAAAA others(44): Show |
1 | a0001c0001t0001g0064 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.666+5627_666+5628i others(53): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85631339 | |||||||
| chr6:85631721 | C | T | 1 | a0001c0001t0001g0288 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.666+5246G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85631721 | |||||||
| chr6:85631754 | C | G | 1 | a0001c0001t0001g0217 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.666+5213G>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85631754 | |||||||
| chr6:85631849 | C | T | 4 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(1): Show |
4 | HG02647.hp1 HG03130.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.666+5118G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85631849 | |||||||
| chr6:85631891 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.666+5076G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85631891 | |||||||
| chr6:85631893 | T | C | 2 | a0001c0001t0001g0126 a0001c0001t0001g0237 |
2 | HG01884.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.666+5074A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85631893 | |||||||
| chr6:85632041 | G | C | 1 | a0001c0001t0001g0048 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.666+4926C>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85632041 | |||||||
| chr6:85632198 | A | G | 2 | a0001c0001t0001g0228 a0001c0001t0001g0229 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.666+4769T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85632198 | |||||||
| chr6:85632260 | T | A | 1 | a0001c0001t0001g0093 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.666+4707A>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85632260 | |||||||
| chr6:85632463 | T | C | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | HG02071.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.666+4504A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85632463 | |||||||
| chr6:85632641 | T | TA | 7 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(4): Show |
7 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.666+4325dupT | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85632641 | |||||||
| chr6:85632765 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.666+4202C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85632765 | |||||||
| chr6:85632936 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.666+4031C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85632936 | |||||||
| chr6:85632961 | G | A | 139 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(136): Show |
172 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.666+4006C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85632961 | |||||||
| chr6:85632981 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.666+3986C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85632981 | |||||||
| chr6:85633088 | TAAAAAAA others(4): Show |
T | 1 | a0001c0001t0001g0058 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.666+3868_666+3878d others(13): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85633088 | |||||||
| chr6:85633180 | C | T | 2 | a0001c0001t0001g0215 a0001c0001t0001g0216 |
2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.666+3787G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85633180 | |||||||
| chr6:85633188 | A | G | 2 | a0001c0001t0001g0215 a0001c0001t0001g0216 |
2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.666+3779T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85633188 | |||||||
| chr6:85633257 | AAAAC | A | 73 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(70): Show |
81 | HG00408.hp2 HG00423.hp2 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.666+3706_666+3709d others(6): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85633257 | |||||||
| chr6:85633261 | C | CAAAT | 6 | a0001c0001t0001g0019 a0001c0001t0001g0033 a0001c0001t0001g0162 others(3): Show |
6 | HG01175.hp2 HG01261.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.666+3702_666+3705d others(6): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85633261 | |||||||
| chr6:85633261 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.666+3706G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85633261 | |||||||
| chr6:85633261 | CAAAT | C | 48 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0025 others(45): Show |
57 | HG00423.hp1 HG00544.hp2 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.666+3702_666+3705d others(6): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85633261 | |||||||
| chr6:85633269 | T | C | 25 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0031 others(22): Show |
33 | HG00423.hp1 HG00544.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.666+3698A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85633269 | |||||||
| chr6:85633294 | T | C | 3 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 |
3 | HG02647.hp1 HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.666+3673A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85633294 | |||||||
| chr6:85633355 | G | C | 1 | a0001c0001t0001g0028 | 2 | NA18948.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.666+3612C>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85633355 | |||||||
| chr6:85633373 | C | G | 3 | a0001c0001t0001g0118 a0001c0001t0001g0123 a0001c0001t0001g0125 |
3 | HG02818.hp2 HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.666+3594G>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85633373 | |||||||
| chr6:85633528 | T | C | 3 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0036 |
10 | NA18944.hp2 NA18952.hp2 NA18968.hp1 others(7): Show |
intron_variant | MODIFIER | c.666+3439A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85633528 | |||||||
| chr6:85633575 | A | G | 4 | a0001c0001t0001g0212 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | NA18948.hp2 NA18961.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.666+3392T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85633575 | |||||||
| chr6:85633688 | T | C | 11 | a0001c0001t0001g0016 a0001c0001t0001g0029 a0001c0001t0001g0125 others(8): Show |
15 | HG00735.hp1 HG01106.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.666+3279A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85633688 | |||||||
| chr6:85633731 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.666+3236G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85633731 | |||||||
| chr6:85633763 | C | A | 2 | a0001c0001t0001g0215 a0001c0001t0001g0216 |
2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.666+3204G>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85633763 | |||||||
| chr6:85633793 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.666+3174G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85633793 | |||||||
| chr6:85633950 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.666+3017C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85633950 | |||||||
| chr6:85633996 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.666+2971C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85633996 | |||||||
| chr6:85634161 | T | A | 3 | a0001c0001t0001g0182 a0001c0001t0001g0201 a0001c0001t0001g0285 |
3 | HG00597.hp2 HG02027.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.666+2806A>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85634161 | |||||||
| chr6:85634237 | C | CTCGA | 4 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(1): Show |
4 | HG02647.hp1 HG03209.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.666+2726_666+2729d others(6): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85634237 | |||||||
| chr6:85634239 | C | T | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.666+2728G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85634239 | |||||||
| chr6:85634240 | G | A | 4 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(1): Show |
4 | HG02109.hp1 HG02630.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.666+2727C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85634240 | |||||||
| chr6:85634317 | C | CTATAAAT others(4): Show |
1 | a0001c0001t0001g0133 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.666+2639_666+2649d others(13): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85634317 | |||||||
| chr6:85634386 | G | A | 1 | a0001c0001t0001g0283 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.666+2581C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85634386 | |||||||
| chr6:85634512 | G | A | 5 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(2): Show |
5 | HG02109.hp1 HG02630.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.666+2455C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85634512 | |||||||
| chr6:85634522 | C | T | 4 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(1): Show |
4 | HG02818.hp1 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.666+2445G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85634522 | |||||||
| chr6:85634532 | A | G | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 |
3 | HG00280.hp2 HG01081.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.666+2435T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85634532 | |||||||
| chr6:85634542 | C | T | 1 | a0001c0001t0001g0074 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.666+2425G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85634542 | |||||||
| chr6:85634578 | G | A | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(178): Show |
222 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(219): Show |
intron_variant | MODIFIER | c.666+2389C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85634578 | |||||||
| chr6:85634581 | G | GT | 54 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(51): Show |
78 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.666+2385dupA | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85634581 | |||||||
| chr6:85634633 | G | A | 25 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0031 others(22): Show |
33 | HG00423.hp1 HG00544.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.666+2334C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85634633 | |||||||
| chr6:85634907 | T | C | 4 | a0001c0001t0001g0025 a0001c0001t0001g0045 a0001c0001t0001g0046 others(1): Show |
5 | HG02647.hp2 HG02895.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.666+2060A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85634907 | |||||||
| chr6:85634949 | T | G | 1 | a0001c0001t0001g0276 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.666+2018A>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85634949 | |||||||
| chr6:85634990 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.666+1977G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85634990 | |||||||
| chr6:85635168 | A | G | 2 | a0001c0001t0001g0275 a0001c0001t0001g0276 |
2 | HG01433.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.666+1799T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85635168 | |||||||
| chr6:85635321 | T | C | 51 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(48): Show |
75 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.666+1646A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85635321 | |||||||
| chr6:85635353 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.666+1614A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85635353 | |||||||
| chr6:85635553 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.666+1414A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85635553 | |||||||
| chr6:85635702 | G | A | 2 | a0001c0001t0001g0055 a0001c0001t0001g0056 |
2 | HG02559.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.666+1265C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85635702 | |||||||
| chr6:85635774 | C | CA | 107 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(104): Show |
134 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.666+1192dupT | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85635774 | |||||||
| chr6:85635774 | C | CAA | 39 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0025 others(36): Show |
43 | HG00597.hp1 HG00735.hp2 HG01106.hp2 others(40): Show |
intron_variant | MODIFIER | c.666+1191_666+1192d others(4): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85635774 | |||||||
| chr6:85635774 | C | CAAA | 8 | a0001c0001t0001g0064 a0001c0001t0001g0106 a0001c0001t0001g0108 others(5): Show |
8 | HG01884.hp2 HG03098.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.666+1190_666+1192d others(5): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85635774 | |||||||
| chr6:85635774 | CA | C | 8 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(5): Show |
11 | HG01257.hp1 HG01975.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.666+1192delT | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85635774 | |||||||
| chr6:85635774 | CAAA | C | 21 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0031 others(18): Show |
29 | HG00423.hp1 HG00544.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.666+1190_666+1192d others(5): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85635774 | |||||||
| chr6:85636071 | A | G | 3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | HG01258.hp2 HG02055.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.666+896T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85636071 | |||||||
| chr6:85636119 | A | G | 3 | a0001c0001t0001g0141 a0001c0001t0001g0186 a0001c0001t0001g0187 |
3 | HG03492.hp1 HG03688.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.666+848T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85636119 | |||||||
| chr6:85636177 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.666+790C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85636177 | |||||||
| chr6:85636216 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.666+751C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85636216 | |||||||
| chr6:85636220 | G | A | 75 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(72): Show |
83 | HG00408.hp2 HG00423.hp2 HG00735.hp2 others(80): Show |
intron_variant | MODIFIER | c.666+747C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85636220 | |||||||
| chr6:85636287 | A | C | 1 | a0001c0001t0001g0064 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.666+680T>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85636287 | |||||||
| chr6:85636326 | A | G | 75 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(72): Show |
83 | HG00408.hp2 HG00423.hp2 HG00735.hp2 others(80): Show |
intron_variant | MODIFIER | c.666+641T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85636326 | |||||||
| chr6:85636424 | G | A | 2 | a0001c0001t0001g0126 a0001c0001t0001g0237 |
2 | HG01884.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.666+543C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85636424 | |||||||
| chr6:85636784 | A | C | 1 | a0001c0001t0001g0249 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.666+183T>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85636784 | |||||||
| chr6:85636841 | A | G | 6 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(3): Show |
6 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.666+126T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85636841 | |||||||
| chr6:85636891 | T | C | 2 | a0001c0001t0001g0184 a0001c0001t0001g0202 |
2 | HG01074.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.666+76A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 6/10 | chr6 | 85636891 | |||||||
| chr6:85637471 | TAA | T | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(178): Show |
222 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(219): Show |
intron_variant | MODIFIER | c.376-117_376-116del others(2): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85637471 | |||||||
| chr6:85637527 | T | C | 40 | a0001c0001t0001g0011 a0001c0001t0001g0026 a0001c0001t0001g0027 others(37): Show |
44 | HG00408.hp2 HG00423.hp2 HG01255.hp1 others(41): Show |
intron_variant | MODIFIER | c.376-171A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85637527 | |||||||
| chr6:85637830 | G | C | 1 | a0001c0001t0001g0058 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.376-474C>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85637830 | |||||||
| chr6:85637887 | C | T | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(178): Show |
222 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(219): Show |
intron_variant | MODIFIER | c.376-531G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85637887 | |||||||
| chr6:85637972 | G | A | 1 | a0001c0001t0001g0235 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.376-616C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85637972 | |||||||
| chr6:85638286 | T | C | 1 | a0001c0001t0001g0058 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.376-930A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85638286 | |||||||
| chr6:85638341 | A | G | 1 | a0001c0001t0001g0248 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.376-985T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85638341 | |||||||
| chr6:85638380 | C | CA | 15 | a0001c0001t0001g0025 a0001c0001t0001g0044 a0001c0001t0001g0046 others(12): Show |
16 | HG01168.hp1 HG01975.hp1 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.376-1025dupT | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85638380 | |||||||
| chr6:85638380 | C | CAA | 31 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0026 others(28): Show |
36 | HG00423.hp2 HG00735.hp2 HG01358.hp2 others(33): Show |
intron_variant | MODIFIER | c.376-1026_376-1025d others(4): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85638380 | |||||||
| chr6:85638380 | C | CAAA | 17 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0094 others(14): Show |
17 | HG00408.hp2 HG01255.hp1 HG01928.hp2 others(14): Show |
intron_variant | MODIFIER | c.376-1027_376-1025d others(5): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85638380 | |||||||
| chr6:85638380 | C | CAAAA | 21 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0053 others(18): Show |
24 | HG01109.hp1 HG02109.hp1 HG02165.hp1 others(21): Show |
intron_variant | MODIFIER | c.376-1028_376-1025d others(6): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85638380 | |||||||
| chr6:85638380 | C | CAAAAA | 10 | a0001c0001t0001g0033 a0001c0001t0001g0061 a0001c0001t0001g0118 others(7): Show |
11 | HG01891.hp2 HG02132.hp2 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.376-1029_376-1025d others(7): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85638380 | |||||||
| chr6:85638380 | C | CAAAAAA | 13 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0123 others(10): Show |
15 | HG00280.hp1 HG00544.hp1 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.376-1030_376-1025d others(8): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85638380 | |||||||
| chr6:85638380 | C | CAAAAAAA | 7 | a0001c0001t0001g0243 a0001c0001t0001g0244 a0001c0001t0001g0245 others(4): Show |
7 | HG00741.hp1 HG01515.hp2 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.376-1031_376-1025d others(9): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85638380 | |||||||
| chr6:85638380 | C | CAAAAAAA others(1): Show |
8 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0036 others(5): Show |
15 | HG00099.hp1 HG01433.hp2 HG02698.hp2 others(12): Show |
intron_variant | MODIFIER | c.376-1032_376-1025d others(10): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85638380 | |||||||
| chr6:85638380 | C | CAAAAAAA others(2): Show |
8 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0278 others(5): Show |
12 | HG00597.hp1 HG00609.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.376-1033_376-1025d others(11): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85638380 | |||||||
| chr6:85638380 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0134 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.376-1034_376-1025d others(12): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85638380 | |||||||
| chr6:85638380 | CA | C | 97 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(94): Show |
126 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.376-1025delT | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85638380 | |||||||
| chr6:85638380 | CAAAAAA | C | 19 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0032 others(16): Show |
29 | HG02027.hp2 HG02083.hp2 HG02109.hp2 others(26): Show |
intron_variant | MODIFIER | c.376-1030_376-1025d others(8): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85638380 | |||||||
| chr6:85638380 | CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0001g0126 a0001c0001t0001g0237 |
2 | HG01884.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.376-1035_376-1025d others(13): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85638380 | |||||||
| chr6:85638463 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.376-1107T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85638463 | |||||||
| chr6:85638585 | T | C | 1 | a0001c0001t0001g0232 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.376-1229A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85638585 | |||||||
| chr6:85638620 | A | G | 1 | a0001c0001t0001g0139 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.376-1264T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85638620 | |||||||
| chr6:85638820 | G | A | 21 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0031 others(18): Show |
29 | HG00423.hp1 HG00544.hp2 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.375+1401C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85638820 | |||||||
| chr6:85638848 | C | T | 4 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0137 others(1): Show |
7 | HG01074.hp1 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.375+1373G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85638848 | |||||||
| chr6:85638992 | G | A | 1 | a0001c0001t0001g0284 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.375+1229C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85638992 | |||||||
| chr6:85639002 | G | A | 3 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 |
3 | HG02145.hp1 HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.375+1219C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85639002 | |||||||
| chr6:85639025 | T | C | 25 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0031 others(22): Show |
33 | HG00423.hp1 HG00544.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.375+1196A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85639025 | |||||||
| chr6:85639080 | C | T | 6 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(3): Show |
6 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.375+1141G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85639080 | |||||||
| chr6:85639150 | G | A | 2 | a0001c0001t0001g0126 a0001c0001t0001g0237 |
2 | HG01884.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.375+1071C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85639150 | |||||||
| chr6:85639385 | T | C | 51 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(48): Show |
75 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.375+836A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85639385 | |||||||
| chr6:85639415 | T | C | 1 | a0001c0001t0001g0203 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.375+806A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85639415 | |||||||
| chr6:85639453 | C | T | 3 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 |
3 | HG03492.hp2 HG03704.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.375+768G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85639453 | |||||||
| chr6:85639584 | C | T | 6 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0242 others(3): Show |
6 | HG02886.hp2 HG02965.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.375+637G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85639584 | |||||||
| chr6:85639636 | A | C | 1 | a0001c0001t0001g0058 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.375+585T>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85639636 | |||||||
| chr6:85639672 | G | A | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | NA18991.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.375+549C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85639672 | |||||||
| chr6:85639688 | T | G | 1 | a0001c0001t0001g0129 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.375+533A>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85639688 | |||||||
| chr6:85639714 | A | G | 4 | a0001c0001t0001g0025 a0001c0001t0001g0045 a0001c0001t0001g0046 others(1): Show |
5 | HG02647.hp2 HG02895.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.375+507T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85639714 | |||||||
| chr6:85639726 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.375+495G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85639726 | |||||||
| chr6:85639852 | T | C | 56 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(53): Show |
80 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.375+369A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85639852 | |||||||
| chr6:85639952 | A | T | 1 | a0001c0001t0001g0212 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.375+269T>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85639952 | |||||||
| chr6:85639969 | T | C | 1 | a0001c0001t0001g0135 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.375+252A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85639969 | |||||||
| chr6:85640027 | G | C | 9 | a0001c0001t0001g0007 a0001c0001t0001g0204 a0001c0001t0001g0205 others(6): Show |
12 | HG02074.hp2 HG02683.hp1 NA18946.hp1 others(9): Show |
intron_variant | MODIFIER | c.375+194C>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85640027 | |||||||
| chr6:85640097 | T | C | 2 | a0001c0001t0001g0055 a0001c0001t0001g0056 |
2 | HG02559.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.375+124A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85640097 | |||||||
| chr6:85640135 | A | G | 1 | a0001c0001t0001g0247 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.375+86T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 4/10 | chr6 | 85640135 | |||||||
| chr6:85640676 | C | T | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(172): Show |
216 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(213): Show |
intron_variant | MODIFIER | c.149-112G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 2/10 | chr6 | 85640676 | |||||||
| chr6:85640687 | G | GA | 33 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0031 others(30): Show |
41 | HG00423.hp1 HG00544.hp2 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.149-124dupT | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 2/10 | chr6 | 85640687 | |||||||
| chr6:85640698 | A | C | 1 | a0001c0001t0001g0057 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.149-134T>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 2/10 | chr6 | 85640698 | |||||||
| chr6:85640779 | T | G | 4 | a0001c0001t0001g0008 a0001c0001t0001g0234 a0001c0001t0001g0235 others(1): Show |
7 | HG01069.hp2 HG01071.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.149-215A>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 2/10 | chr6 | 85640779 | |||||||
| chr6:85640838 | TAC | T | 6 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(3): Show |
6 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.149-276_149-275del others(2): Show |
SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 2/10 | chr6 | 85640838 | |||||||
| chr6:85641007 | A | G | 3 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 |
3 | HG02145.hp1 HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.148+285T>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 2/10 | chr6 | 85641007 | |||||||
| chr6:85641046 | T | C | 1 | a0001c0001t0001g0237 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.148+246A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 2/10 | chr6 | 85641046 | |||||||
| chr6:85641496 | G | T | 4 | a0001c0001t0001g0025 a0001c0001t0001g0045 a0001c0001t0001g0046 others(1): Show |
5 | HG02647.hp2 HG02895.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-12-45C>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 1/10 | chr6 | 85641496 | |||||||
| chr6:85641865 | G | C | 1 | a0001c0001t0001g0239 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-12-414C>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 1/10 | chr6 | 85641865 | |||||||
| chr6:85642004 | G | C | 1 | a0001c0001t0003g0291 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-12-553C>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 1/10 | chr6 | 85642004 | |||||||
| chr6:85642083 | C | T | 1 | a0001c0001t0001g0246 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-12-632G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 1/10 | chr6 | 85642083 | |||||||
| chr6:85642223 | G | A | 6 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0242 others(3): Show |
6 | HG02886.hp2 HG02965.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-13+574C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 1/10 | chr6 | 85642223 | |||||||
| chr6:85642298 | G | A | 52 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(49): Show |
76 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.-13+499C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 1/10 | chr6 | 85642298 | |||||||
| chr6:85642339 | C | G | 9 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0039 others(6): Show |
11 | HG00609.hp1 HG02040.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.-13+458G>C | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 1/10 | chr6 | 85642339 | |||||||
| chr6:85642449 | G | A | 1 | a0001c0001t0001g0286 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-13+348C>T | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 1/10 | chr6 | 85642449 | |||||||
| chr6:85642458 | C | T | 1 | a0001c0001t0001g0009 | 3 | NA18951.hp1 NA18970.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.-13+339G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 1/10 | chr6 | 85642458 | |||||||
| chr6:85642468 | C | T | 3 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0038 |
5 | HG02280.hp2 HG02615.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-13+329G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 1/10 | chr6 | 85642468 | |||||||
| chr6:85642651 | T | C | 1 | a0001c0001t0001g0287 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-13+146A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 1/10 | chr6 | 85642651 | |||||||
| chr6:85642711 | C | T | 1 | a0001c0001t0001g0037 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-13+86G>A | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 1/10 | chr6 | 85642711 | |||||||
| chr6:85642718 | T | C | 1 | a0001c0001t0001g0288 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-13+79A>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 1/10 | chr6 | 85642718 | |||||||
| chr6:85642761 | G | C | 1 | a0001c0001t0001g0289 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-13+36C>G | SYNCRIP | ENSG00000135316.20 | transcript | ENST00000369622.8 | protein_coding | 1/10 | chr6 | 85642761 |