Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 391059 |
| ensemblid | ENSG00000156869.14 |
| hgncid | 27622 |
| symbol | FRRS1 |
| name | ferric chelate reductase 1 |
| refseq_nuc | NM_001361041.2 |
| refseq_prot | NP_001347970.1 |
| ensembl_nuc | ENST00000646001.2 |
| ensembl_prot | ENSP00000496583.2 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 99703970 |
| end | 99766635 |
| strand | - |
| ver | v1.2 |
| region | chr1:99703970-99766635 |
| region5000 | chr1:99698970-99771635 |
| regionname0 | FRRS1_chr1_99703970_99766635 |
| regionname5000 | FRRS1_chr1_99698970_99771635 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 592 | 256 | 52 | 54 | 106 | 4 | 38 | 78 | FRRS1_chr1_99698970_99771635 | FRRS1 | MAVSG others(587): Show |
chr1 | 99698970 | 99771635 |
| a0002 | 0/0 | 592 | 56 | 32 | 6 | 16 | 0 | 2 | 14 | FRRS1_chr1_99698970_99771635 | FRRS1 | MAVSG others(587): Show |
chr1 | 99698970 | 99771635 |
| a0003 | 0/0 | 592 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | MAVSG others(587): Show |
chr1 | 99698970 | 99771635 |
| a0004 | 0/0 | 592 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | MAVSG others(587): Show |
chr1 | 99698970 | 99771635 |
| a0005 | 0/0 | 592 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | MAVSG others(587): Show |
chr1 | 99698970 | 99771635 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1776 | 126 | 7 | 27 | 72 | 2 | 17 | FRRS1_chr1_99698970_99771635 | FRRS1 | ATGGC others(1771): Show |
chr1 | 99698970 | 99771635 | ||
| a0001c0002 | 0/1 | 1776 | 115 | 41 | 25 | 33 | 2 | 13 | FRRS1_chr1_99698970_99771635 | FRRS1 | ATGGC others(1771): Show |
chr1 | 99698970 | 99771635 | ||
| a0001c0004 | 0/0 | 1776 | 15 | 4 | 2 | 1 | 0 | 8 | FRRS1_chr1_99698970_99771635 | FRRS1 | ATGGC others(1771): Show |
chr1 | 99698970 | 99771635 | ||
| a0002c0003 | 0/0 | 1776 | 54 | 31 | 6 | 16 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | ATGGC others(1771): Show |
chr1 | 99698970 | 99771635 | ||
| a0002c0007 | 0/0 | 1776 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | ATGGC others(1771): Show |
chr1 | 99698970 | 99771635 | ||
| a0002c0008 | 0/0 | 1776 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | ATGGC others(1771): Show |
chr1 | 99698970 | 99771635 | ||
| a0003c0005 | 0/0 | 1776 | 2 | 2 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | ATGGC others(1771): Show |
chr1 | 99698970 | 99771635 | ||
| a0003c0006 | 0/0 | 1776 | 2 | 2 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | ATGGC others(1771): Show |
chr1 | 99698970 | 99771635 | ||
| a0004c0010 | 0/0 | 1776 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | ATGGC others(1771): Show |
chr1 | 99698970 | 99771635 | ||
| a0005c0009 | 0/0 | 1776 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | ATGGC others(1771): Show |
chr1 | 99698970 | 99771635 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 6971 | 54 | 3 | 11 | 28 | 1 | 10 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6966): Show |
chr1 | 99698970 | 99771635 |
| a0001c0001t0003 | 0/0 | 6971 | 30 | 1 | 0 | 28 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6966): Show |
chr1 | 99698970 | 99771635 |
| a0001c0001t0006 | 0/0 | 6971 | 14 | 1 | 10 | 0 | 1 | 2 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6966): Show |
chr1 | 99698970 | 99771635 |
| a0001c0001t0013 | 0/0 | 6973 | 5 | 1 | 0 | 4 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6968): Show |
chr1 | 99698970 | 99771635 |
| a0001c0001t0020 | 0/0 | 6968 | 3 | 0 | 2 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6963): Show |
chr1 | 99698970 | 99771635 |
| a0001c0001t0030 | 0/0 | 6971 | 2 | 0 | 0 | 2 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6966): Show |
chr1 | 99698970 | 99771635 |
| a0001c0001t0031 | 0/0 | 6973 | 2 | 0 | 1 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6968): Show |
chr1 | 99698970 | 99771635 |
| a0001c0001t0032 | 0/0 | 6972 | 2 | 0 | 1 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6967): Show |
chr1 | 99698970 | 99771635 |
| a0001c0001t0033 | 0/0 | 6972 | 2 | 0 | 0 | 2 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6967): Show |
chr1 | 99698970 | 99771635 |
| a0001c0001t0034 | 0/0 | 6973 | 2 | 0 | 0 | 2 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6968): Show |
chr1 | 99698970 | 99771635 |
| a0001c0001t0060 | 0/0 | 6970 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6965): Show |
chr1 | 99698970 | 99771635 |
| a0001c0001t0061 | 0/0 | 6970 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6965): Show |
chr1 | 99698970 | 99771635 |
| a0001c0001t0062 | 0/0 | 6972 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6967): Show |
chr1 | 99698970 | 99771635 |
| a0001c0001t0063 | 0/0 | 6971 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6966): Show |
chr1 | 99698970 | 99771635 |
| a0001c0001t0064 | 0/0 | 6973 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6968): Show |
chr1 | 99698970 | 99771635 |
| a0001c0001t0065 | 0/0 | 6976 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6971): Show |
chr1 | 99698970 | 99771635 |
| a0001c0001t0066 | 0/0 | 6973 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6968): Show |
chr1 | 99698970 | 99771635 |
| a0001c0001t0067 | 0/0 | 6971 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6966): Show |
chr1 | 99698970 | 99771635 |
| a0001c0001t0068 | 0/0 | 6971 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6966): Show |
chr1 | 99698970 | 99771635 |
| a0001c0001t0069 | 0/0 | 6971 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6966): Show |
chr1 | 99698970 | 99771635 |
| a0001c0002t0002 | 0/0 | 6971 | 25 | 8 | 5 | 11 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6966): Show |
chr1 | 99698970 | 99771635 |
| a0001c0002t0004 | 0/0 | 6971 | 27 | 9 | 3 | 9 | 1 | 5 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6966): Show |
chr1 | 99698970 | 99771635 |
| a0001c0002t0007 | 0/0 | 6971 | 9 | 2 | 7 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6966): Show |
chr1 | 99698970 | 99771635 |
| a0001c0002t0008 | 0/0 | 6970 | 5 | 5 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6965): Show |
chr1 | 99698970 | 99771635 |
| a0001c0002t0009 | 0/0 | 6971 | 9 | 0 | 2 | 4 | 0 | 3 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6966): Show |
chr1 | 99698970 | 99771635 |
| a0001c0002t0012 | 0/0 | 6971 | 5 | 0 | 2 | 3 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6966): Show |
chr1 | 99698970 | 99771635 |
| a0001c0002t0016 | 0/0 | 6971 | 4 | 0 | 3 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6966): Show |
chr1 | 99698970 | 99771635 |
| a0001c0002t0019 | 0/0 | 6973 | 3 | 3 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6968): Show |
chr1 | 99698970 | 99771635 |
| a0001c0002t0024 | 0/0 | 6973 | 2 | 0 | 1 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6968): Show |
chr1 | 99698970 | 99771635 |
| a0001c0002t0025 | 0/0 | 6970 | 2 | 1 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6965): Show |
chr1 | 99698970 | 99771635 |
| a0001c0002t0026 | 0/0 | 6972 | 2 | 2 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6967): Show |
chr1 | 99698970 | 99771635 |
| a0001c0002t0027 | 0/0 | 6976 | 2 | 2 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6971): Show |
chr1 | 99698970 | 99771635 |
| a0001c0002t0028 | 0/0 | 6972 | 2 | 0 | 1 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6967): Show |
chr1 | 99698970 | 99771635 |
| a0001c0002t0029 | 0/0 | 6971 | 2 | 2 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6966): Show |
chr1 | 99698970 | 99771635 |
| a0001c0002t0042 | 0/0 | 6968 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6963): Show |
chr1 | 99698970 | 99771635 |
| a0001c0002t0043 | 0/0 | 6971 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6966): Show |
chr1 | 99698970 | 99771635 |
| a0001c0002t0044 | 0/0 | 6970 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6965): Show |
chr1 | 99698970 | 99771635 |
| a0001c0002t0045 | 0/0 | 6971 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6966): Show |
chr1 | 99698970 | 99771635 |
| a0001c0002t0046 | 0/0 | 6973 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6968): Show |
chr1 | 99698970 | 99771635 |
| a0001c0002t0047 | 0/0 | 6972 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6967): Show |
chr1 | 99698970 | 99771635 |
| a0001c0002t0048 | 0/0 | 6971 | 1 | 0 | 0 | 0 | 1 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6966): Show |
chr1 | 99698970 | 99771635 |
| a0001c0002t0049 | 0/0 | 6973 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6968): Show |
chr1 | 99698970 | 99771635 |
| a0001c0002t0051 | 0/0 | 6972 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6967): Show |
chr1 | 99698970 | 99771635 |
| a0001c0002t0052 | 0/0 | 6984 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6979): Show |
chr1 | 99698970 | 99771635 |
| a0001c0002t0053 | 0/0 | 6952 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6947): Show |
chr1 | 99698970 | 99771635 |
| a0001c0002t0054 | 0/1 | 6962 | 1 | 0 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6957): Show |
chr1 | 99698970 | 99771635 |
| a0001c0002t0055 | 0/0 | 6971 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6966): Show |
chr1 | 99698970 | 99771635 |
| a0001c0002t0056 | 0/0 | 6971 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6966): Show |
chr1 | 99698970 | 99771635 |
| a0001c0002t0057 | 0/0 | 6971 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6966): Show |
chr1 | 99698970 | 99771635 |
| a0001c0002t0058 | 0/0 | 6971 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6966): Show |
chr1 | 99698970 | 99771635 |
| a0001c0004t0002 | 0/0 | 6971 | 6 | 0 | 2 | 0 | 0 | 4 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6966): Show |
chr1 | 99698970 | 99771635 |
| a0001c0004t0007 | 0/0 | 6971 | 4 | 0 | 0 | 1 | 0 | 3 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6966): Show |
chr1 | 99698970 | 99771635 |
| a0001c0004t0008 | 0/0 | 6970 | 4 | 4 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6965): Show |
chr1 | 99698970 | 99771635 |
| a0001c0004t0050 | 0/0 | 6971 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6966): Show |
chr1 | 99698970 | 99771635 |
| a0002c0003t0005 | 0/0 | 6972 | 19 | 6 | 5 | 8 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6967): Show |
chr1 | 99698970 | 99771635 |
| a0002c0003t0010 | 0/0 | 6972 | 4 | 4 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6967): Show |
chr1 | 99698970 | 99771635 |
| a0002c0003t0011 | 0/0 | 6967 | 5 | 0 | 0 | 5 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6962): Show |
chr1 | 99698970 | 99771635 |
| a0002c0003t0014 | 0/0 | 6963 | 4 | 1 | 1 | 1 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6958): Show |
chr1 | 99698970 | 99771635 |
| a0002c0003t0015 | 0/0 | 6973 | 4 | 3 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6968): Show |
chr1 | 99698970 | 99771635 |
| a0002c0003t0017 | 0/0 | 6969 | 3 | 3 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6964): Show |
chr1 | 99698970 | 99771635 |
| a0002c0003t0018 | 0/0 | 6973 | 3 | 3 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6968): Show |
chr1 | 99698970 | 99771635 |
| a0002c0003t0021 | 0/0 | 6964 | 2 | 2 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6959): Show |
chr1 | 99698970 | 99771635 |
| a0002c0003t0022 | 0/0 | 6967 | 2 | 2 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6962): Show |
chr1 | 99698970 | 99771635 |
| a0002c0003t0023 | 0/0 | 6970 | 2 | 2 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6965): Show |
chr1 | 99698970 | 99771635 |
| a0002c0003t0035 | 0/0 | 6969 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6964): Show |
chr1 | 99698970 | 99771635 |
| a0002c0003t0036 | 0/0 | 6970 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6965): Show |
chr1 | 99698970 | 99771635 |
| a0002c0003t0037 | 0/0 | 6970 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6965): Show |
chr1 | 99698970 | 99771635 |
| a0002c0003t0038 | 0/0 | 6973 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6968): Show |
chr1 | 99698970 | 99771635 |
| a0002c0003t0039 | 0/0 | 6973 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6968): Show |
chr1 | 99698970 | 99771635 |
| a0002c0003t0040 | 0/0 | 6973 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6968): Show |
chr1 | 99698970 | 99771635 |
| a0002c0007t0041 | 0/0 | 6973 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6968): Show |
chr1 | 99698970 | 99771635 |
| a0002c0008t0059 | 0/0 | 6972 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6967): Show |
chr1 | 99698970 | 99771635 |
| a0003c0005t0010 | 0/0 | 6972 | 2 | 2 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6967): Show |
chr1 | 99698970 | 99771635 |
| a0003c0006t0010 | 0/0 | 6972 | 2 | 2 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6967): Show |
chr1 | 99698970 | 99771635 |
| a0004c0010t0005 | 0/0 | 6972 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6967): Show |
chr1 | 99698970 | 99771635 |
| a0005c0009t0005 | 0/0 | 6972 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | AGTTG others(6967): Show |
chr1 | 99698970 | 99771635 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0001g0188 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0003g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0003g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0003g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0006g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0006g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0006g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0006g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0006g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0006g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0006g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0006g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0006g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0006g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0006g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0006g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0006g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0006g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0013g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0013g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0013g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0013g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0013g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0020g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0020g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0020g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0030g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0030g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0031g0017 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0032g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0032g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0033g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0033g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0034g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0034g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0060g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0061g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0062g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0063g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0064g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0065g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0066g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0067g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0068g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0001t0069g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0002g0003 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0004g0001 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0004g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0004g0009 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0004g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0004g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0004g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0004g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0004g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0004g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0004g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0004g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0007g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0007g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0007g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0007g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0007g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0007g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0007g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0008g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0008g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0008g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0008g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0009g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0009g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0009g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0009g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0009g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0009g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0009g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0009g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0012g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0012g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0012g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0012g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0012g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0016g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0016g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0016g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0016g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0019g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0019g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0019g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0024g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0024g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0025g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0025g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0026g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0026g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0027g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0028g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0028g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0029g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0042g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0043g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0044g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0045g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0046g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0047g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0048g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0049g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0051g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0052g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0053g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0054g0091 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0055g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0056g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0057g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0002t0058g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0004t0002g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0004t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0004t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0004t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0004t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0004t0007g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0004t0007g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0004t0007g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0004t0007g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0004t0008g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0004t0008g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0004t0008g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0004t0008g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0001c0004t0050g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0002c0003t0005g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0002c0003t0005g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0002c0003t0005g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0002c0003t0005g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0002c0003t0005g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0002c0003t0005g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0002c0003t0005g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0002c0003t0005g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0002c0003t0005g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0002c0003t0005g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0002c0003t0005g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0002c0003t0005g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0002c0003t0005g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0002c0003t0005g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0002c0003t0005g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0002c0003t0005g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0002c0003t0005g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0002c0003t0005g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0002c0003t0010g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0002c0003t0010g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0002c0003t0010g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0002c0003t0011g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0002c0003t0011g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0002c0003t0011g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0002c0003t0011g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0002c0003t0011g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0002c0003t0014g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0002c0003t0014g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0002c0003t0014g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0002c0003t0015g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0002c0003t0015g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0002c0003t0015g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0002c0003t0015g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0002c0003t0017g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0002c0003t0017g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0002c0003t0018g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0002c0003t0018g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0002c0003t0018g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0002c0003t0021g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0002c0003t0021g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0002c0003t0022g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0002c0003t0023g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0002c0003t0023g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0002c0003t0035g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0002c0003t0036g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0002c0003t0037g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0002c0003t0038g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0002c0003t0039g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0002c0003t0040g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0002c0007t0041g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0002c0008t0059g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0003c0005t0010g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0003c0005t0010g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0003c0006t0010g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0003c0006t0010g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0004c0010t0005g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| a0005c0009t0005g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG00423 | hp2 | a0001 | c0002 | t0004 | g0012 | EAS | CHS | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG00621 | hp1 | a0001 | c0002 | t0004 | g0062 | EAS | CHS | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG00621 | hp2 | a0001 | c0002 | t0009 | g0088 | EAS | CHS | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG00639 | hp2 | a0001 | c0002 | t0002 | g0075 | AMR | PUR | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG00642 | hp1 | a0001 | c0001 | t0006 | g0181 | AMR | PUR | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG00673 | hp1 | a0001 | c0002 | t0009 | g0071 | EAS | CHS | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG00673 | hp2 | a0002 | c0003 | t0011 | g0237 | EAS | CHS | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG00735 | hp1 | a0002 | c0003 | t0014 | g0027 | AMR | PUR | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG00735 | hp2 | a0002 | c0003 | t0005 | g0277 | AMR | PUR | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG00738 | hp1 | a0001 | c0002 | t0012 | g0072 | AMR | PUR | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG00741 | hp1 | a0001 | c0002 | t0004 | g0067 | AMR | PUR | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG00741 | hp2 | a0001 | c0001 | t0006 | g0136 | AMR | PUR | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG01069 | hp1 | a0002 | c0003 | t0005 | g0066 | AMR | PUR | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG01069 | hp2 | a0001 | c0001 | t0020 | g0153 | AMR | PUR | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG01074 | hp1 | a0002 | c0003 | t0005 | g0249 | AMR | PUR | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG01081 | hp1 | a0001 | c0004 | t0002 | g0008 | AMR | PUR | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG01081 | hp2 | a0001 | c0001 | t0066 | g0135 | AMR | PUR | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG01106 | hp1 | a0001 | c0002 | t0016 | g0219 | AMR | PUR | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG01106 | hp2 | a0001 | c0001 | t0006 | g0130 | AMR | PUR | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG01109 | hp1 | a0001 | c0001 | t0063 | g0133 | AMR | PUR | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG01109 | hp2 | a0002 | c0003 | t0005 | g0267 | AMR | PUR | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG01167 | hp2 | a0001 | c0002 | t0024 | g0116 | AMR | PUR | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG01192 | hp1 | a0001 | c0004 | t0002 | g0008 | AMR | PUR | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG01192 | hp2 | a0001 | c0002 | t0007 | g0235 | AMR | PUR | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG01255 | hp1 | a0001 | c0001 | t0006 | g0127 | AMR | CLM | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG01255 | hp2 | a0001 | c0002 | t0007 | g0239 | AMR | CLM | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG01256 | hp2 | a0001 | c0002 | t0028 | g0216 | AMR | CLM | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG01257 | hp1 | a0001 | c0002 | t0016 | g0222 | AMR | CLM | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG01257 | hp2 | a0001 | c0001 | t0006 | g0128 | AMR | CLM | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG01261 | hp1 | a0001 | c0002 | t0016 | g0220 | AMR | CLM | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG01261 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | CLM | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG01346 | hp1 | a0001 | c0002 | t0009 | g0011 | AMR | CLM | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG01346 | hp2 | a0001 | c0001 | t0031 | g0017 | AMR | CLM | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG01361 | hp1 | a0001 | c0002 | t0004 | g0068 | AMR | CLM | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG01433 | hp1 | a0001 | c0001 | t0006 | g0183 | AMR | CLM | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG01433 | hp2 | a0001 | c0001 | t0032 | g0156 | AMR | CLM | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG01496 | hp2 | a0001 | c0001 | t0006 | g0193 | AMR | CLM | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG01515 | hp1 | a0001 | c0001 | t0006 | g0118 | EUR | IBS | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG01515 | hp2 | a0001 | c0002 | t0048 | g0070 | EUR | IBS | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG01884 | hp1 | a0001 | c0004 | t0008 | g0044 | AFR | ACB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG01884 | hp2 | a0001 | c0002 | t0019 | g0256 | AFR | ACB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG01891 | hp1 | a0002 | c0003 | t0023 | g0268 | AFR | ACB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG01891 | hp2 | a0002 | c0003 | t0005 | g0230 | AFR | ACB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG01928 | hp1 | a0001 | c0002 | t0007 | g0007 | AMR | PEL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG01928 | hp2 | a0001 | c0002 | t0012 | g0052 | AMR | PEL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG01934 | hp2 | a0001 | c0002 | t0007 | g0241 | AMR | PEL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG01943 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PEL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG01943 | hp2 | a0001 | c0001 | t0006 | g0139 | AMR | PEL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG01978 | hp1 | a0002 | c0003 | t0005 | g0248 | AMR | PEL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG01978 | hp2 | a0001 | c0001 | t0020 | g0189 | AMR | PEL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG01981 | hp1 | a0001 | c0002 | t0007 | g0007 | AMR | PEL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG01993 | hp1 | a0001 | c0002 | t0051 | g0234 | AMR | PEL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG01993 | hp2 | a0001 | c0002 | t0002 | g0082 | AMR | PEL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02027 | hp1 | a0001 | c0002 | t0009 | g0069 | EAS | KHV | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0211 | EAS | KHV | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02055 | hp1 | a0001 | c0002 | t0026 | g0101 | AFR | ACB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02055 | hp2 | a0001 | c0002 | t0027 | g0010 | AFR | ACB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0200 | EAS | KHV | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02080 | hp1 | a0002 | c0003 | t0011 | g0233 | EAS | KHV | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02132 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | KHV | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02135 | hp1 | a0001 | c0001 | t0013 | g0147 | EAS | KHV | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02135 | hp2 | a0001 | c0002 | t0002 | g0085 | EAS | KHV | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02145 | hp1 | a0002 | c0003 | t0039 | g0109 | AFR | ACB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02145 | hp2 | a0001 | c0002 | t0002 | g0258 | AFR | ACB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02148 | hp1 | a0001 | c0002 | t0009 | g0011 | AMR | PEL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02148 | hp2 | a0001 | c0002 | t0007 | g0232 | AMR | PEL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0024 | EAS | CDX | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | CDX | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | CDX | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02165 | hp2 | a0001 | c0001 | t0034 | g0120 | EAS | CDX | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02257 | hp1 | a0001 | c0002 | t0029 | g0026 | AFR | ACB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02257 | hp2 | a0002 | c0003 | t0015 | g0092 | AFR | ACB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02258 | hp1 | a0002 | c0003 | t0015 | g0264 | AFR | ACB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02258 | hp2 | a0001 | c0002 | t0004 | g0058 | AFR | ACB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02280 | hp2 | a0002 | c0003 | t0015 | g0263 | AFR | ACB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02293 | hp1 | a0001 | c0001 | t0006 | g0138 | AMR | PEL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02293 | hp2 | a0001 | c0002 | t0007 | g0007 | AMR | PEL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02300 | hp1 | a0001 | c0002 | t0002 | g0221 | AMR | PEL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02451 | hp1 | a0001 | c0002 | t0026 | g0100 | AFR | ACB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02451 | hp2 | a0003 | c0005 | t0010 | g0047 | AFR | ACB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02572 | hp1 | a0002 | c0003 | t0005 | g0244 | AFR | GWD | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02572 | hp2 | a0001 | c0002 | t0002 | g0112 | AFR | GWD | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02622 | hp1 | a0002 | c0003 | t0010 | g0102 | AFR | GWD | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02622 | hp2 | a0001 | c0002 | t0004 | g0004 | AFR | GWD | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02630 | hp2 | a0001 | c0002 | t0004 | g0090 | AFR | GWD | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02647 | hp1 | a0001 | c0002 | t0002 | g0257 | AFR | GWD | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02647 | hp2 | a0001 | c0002 | t0004 | g0057 | AFR | GWD | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02683 | hp1 | a0001 | c0004 | t0007 | g0036 | SAS | PJL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02683 | hp2 | a0001 | c0002 | t0004 | g0049 | SAS | PJL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02698 | hp2 | a0001 | c0002 | t0004 | g0029 | SAS | PJL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02717 | hp1 | a0002 | c0003 | t0005 | g0231 | AFR | GWD | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02717 | hp2 | a0001 | c0002 | t0002 | g0111 | AFR | GWD | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02735 | hp1 | a0001 | c0002 | t0009 | g0074 | SAS | PJL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02738 | hp2 | a0001 | c0002 | t0002 | g0226 | SAS | PJL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02809 | hp1 | a0002 | c0003 | t0018 | g0097 | AFR | GWD | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02809 | hp2 | a0002 | c0003 | t0010 | g0015 | AFR | GWD | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02886 | hp1 | a0002 | c0003 | t0018 | g0096 | AFR | GWD | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02886 | hp2 | a0001 | c0001 | t0064 | g0161 | AFR | GWD | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02895 | hp1 | a0002 | c0003 | t0035 | g0275 | AFR | GWD | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02895 | hp2 | a0001 | c0002 | t0004 | g0004 | AFR | GWD | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02896 | hp1 | a0002 | c0003 | t0017 | g0014 | AFR | GWD | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02896 | hp2 | a0002 | c0003 | t0021 | g0265 | AFR | GWD | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02897 | hp1 | a0001 | c0002 | t0004 | g0050 | AFR | GWD | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02897 | hp2 | a0002 | c0003 | t0017 | g0014 | AFR | GWD | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02922 | hp1 | a0002 | c0003 | t0005 | g0025 | AFR | ESN | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02922 | hp2 | a0001 | c0004 | t0008 | g0045 | AFR | ESN | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02965 | hp1 | a0002 | c0003 | t0005 | g0025 | AFR | ESN | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02965 | hp2 | a0001 | c0002 | t0008 | g0108 | AFR | ESN | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02970 | hp1 | a0002 | c0003 | t0017 | g0103 | AFR | ESN | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02970 | hp2 | a0003 | c0006 | t0010 | g0114 | AFR | ESN | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02976 | hp1 | a0001 | c0002 | t0008 | g0107 | AFR | ESN | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02976 | hp2 | a0003 | c0005 | t0010 | g0046 | AFR | ESN | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG03017 | hp2 | a0001 | c0001 | t0065 | g0141 | SAS | PJL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG03041 | hp1 | a0001 | c0002 | t0053 | g0243 | AFR | GWD | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG03041 | hp2 | a0003 | c0006 | t0010 | g0113 | AFR | GWD | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG03098 | hp1 | a0002 | c0003 | t0038 | g0270 | AFR | MSL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG03098 | hp2 | a0001 | c0002 | t0019 | g0094 | AFR | MSL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ESN | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG03130 | hp2 | a0001 | c0002 | t0002 | g0260 | AFR | ESN | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG03195 | hp1 | a0001 | c0002 | t0056 | g0247 | AFR | ESN | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG03195 | hp2 | a0002 | c0003 | t0010 | g0110 | AFR | ESN | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG03209 | hp1 | a0001 | c0002 | t0002 | g0254 | AFR | MSL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG03209 | hp2 | a0001 | c0002 | t0008 | g0016 | AFR | MSL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG03225 | hp1 | a0001 | c0002 | t0043 | g0279 | AFR | MSL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG03225 | hp2 | a0001 | c0002 | t0004 | g0004 | AFR | MSL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG03239 | hp1 | a0001 | c0001 | t0069 | g0131 | SAS | PJL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG03239 | hp2 | a0001 | c0001 | t0006 | g0099 | SAS | PJL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG03453 | hp1 | a0001 | c0002 | t0046 | g0262 | AFR | MSL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG03453 | hp2 | a0002 | c0003 | t0037 | g0106 | AFR | MSL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG03486 | hp1 | a0001 | c0002 | t0008 | g0065 | AFR | MSL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG03486 | hp2 | a0001 | c0002 | t0007 | g0246 | AFR | MSL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG03490 | hp1 | a0001 | c0002 | t0004 | g0009 | SAS | PJL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG03491 | hp1 | a0001 | c0004 | t0002 | g0040 | SAS | PJL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG03491 | hp2 | a0001 | c0002 | t0009 | g0086 | SAS | PJL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG03516 | hp1 | a0002 | c0003 | t0018 | g0218 | AFR | ESN | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG03516 | hp2 | a0001 | c0004 | t0008 | g0043 | AFR | ESN | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG03540 | hp1 | a0002 | c0007 | t0041 | g0048 | AFR | GWD | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG03540 | hp2 | a0001 | c0002 | t0004 | g0064 | AFR | GWD | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG03579 | hp1 | a0002 | c0003 | t0010 | g0015 | AFR | MSL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG03579 | hp2 | a0002 | c0003 | t0021 | g0266 | AFR | MSL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG03669 | hp1 | a0001 | c0002 | t0055 | g0055 | SAS | PJL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG03669 | hp2 | a0002 | c0008 | t0059 | g0167 | SAS | PJL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | STU | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG03688 | hp2 | a0001 | c0001 | t0006 | g0140 | SAS | STU | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG03704 | hp1 | a0002 | c0003 | t0014 | g0240 | SAS | PJL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG03704 | hp2 | a0001 | c0001 | t0061 | g0151 | SAS | PJL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG03710 | hp1 | a0001 | c0004 | t0002 | g0038 | SAS | PJL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG03710 | hp2 | a0001 | c0002 | t0004 | g0001 | SAS | PJL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0126 | SAS | BEB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG03927 | hp2 | a0001 | c0002 | t0024 | g0115 | SAS | BEB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | STU | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG04115 | hp2 | a0001 | c0004 | t0002 | g0042 | SAS | STU | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG04184 | hp1 | a0001 | c0004 | t0050 | g0030 | SAS | BEB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG04184 | hp2 | a0001 | c0002 | t0016 | g0225 | SAS | BEB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG04199 | hp1 | a0001 | c0002 | t0004 | g0083 | SAS | STU | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG04199 | hp2 | a0001 | c0002 | t0049 | g0223 | SAS | STU | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG04204 | hp1 | a0001 | c0001 | t0031 | g0017 | SAS | STU | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG04204 | hp2 | a0001 | c0004 | t0007 | g0037 | SAS | STU | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG04228 | hp1 | a0001 | c0004 | t0002 | g0039 | SAS | STU | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | STU | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18522 | hp1 | a0002 | c0003 | t0023 | g0215 | AFR | YRI | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18522 | hp2 | a0001 | c0002 | t0002 | g0105 | AFR | YRI | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0198 | EAS | CHB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18612 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | CHB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0213 | EAS | CHB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0132 | EAS | CHB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18906 | hp1 | a0001 | c0002 | t0025 | g0261 | AFR | YRI | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18906 | hp2 | a0001 | c0002 | t0008 | g0016 | AFR | YRI | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18942 | hp1 | a0001 | c0002 | t0002 | g0056 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18944 | hp2 | a0001 | c0002 | t0004 | g0063 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18947 | hp1 | a0002 | c0003 | t0040 | g0272 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18947 | hp2 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18948 | hp1 | a0002 | c0003 | t0014 | g0217 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18948 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18951 | hp1 | a0001 | c0002 | t0025 | g0053 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18952 | hp1 | a0001 | c0002 | t0044 | g0079 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18953 | hp1 | a0001 | c0002 | t0002 | g0076 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18953 | hp2 | a0001 | c0001 | t0013 | g0160 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18959 | hp1 | a0001 | c0001 | t0032 | g0145 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18959 | hp2 | a0001 | c0002 | t0012 | g0051 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18962 | hp1 | a0002 | c0003 | t0011 | g0253 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18964 | hp1 | a0001 | c0001 | t0062 | g0199 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18964 | hp2 | a0001 | c0002 | t0002 | g0080 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18967 | hp2 | a0004 | c0010 | t0005 | g0250 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18968 | hp1 | a0001 | c0002 | t0012 | g0060 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18968 | hp2 | a0001 | c0001 | t0068 | g0164 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18970 | hp2 | a0002 | c0003 | t0005 | g0242 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18974 | hp1 | a0001 | c0002 | t0002 | g0054 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18974 | hp2 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18975 | hp1 | a0001 | c0001 | t0033 | g0214 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18978 | hp1 | a0002 | c0003 | t0015 | g0274 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18978 | hp2 | a0001 | c0002 | t0004 | g0073 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18980 | hp1 | a0002 | c0003 | t0005 | g0252 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18982 | hp2 | a0002 | c0003 | t0011 | g0228 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18983 | hp1 | a0001 | c0001 | t0020 | g0178 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18983 | hp2 | a0002 | c0003 | t0005 | g0271 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18984 | hp1 | a0002 | c0003 | t0005 | g0251 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18984 | hp2 | a0001 | c0001 | t0067 | g0171 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18987 | hp2 | a0001 | c0004 | t0007 | g0041 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18993 | hp1 | a0002 | c0003 | t0005 | g0227 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18993 | hp2 | a0001 | c0001 | t0030 | g0149 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18998 | hp1 | a0002 | c0003 | t0005 | g0229 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA19000 | hp1 | a0002 | c0003 | t0005 | g0276 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA19000 | hp2 | a0001 | c0002 | t0057 | g0089 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA19002 | hp2 | a0001 | c0002 | t0002 | g0032 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0123 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA19004 | hp2 | a0002 | c0003 | t0011 | g0238 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA19005 | hp1 | a0001 | c0001 | t0013 | g0150 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA19007 | hp2 | a0001 | c0002 | t0009 | g0095 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA19010 | hp1 | a0001 | c0001 | t0034 | g0121 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA19010 | hp2 | a0001 | c0001 | t0013 | g0186 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA19030 | hp1 | a0001 | c0002 | t0002 | g0224 | AFR | LWK | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA19030 | hp2 | a0001 | c0002 | t0027 | g0010 | AFR | LWK | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA19043 | hp1 | a0001 | c0002 | t0007 | g0117 | AFR | LWK | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA19043 | hp2 | a0002 | c0003 | t0022 | g0013 | AFR | LWK | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA19057 | hp1 | a0001 | c0001 | t0060 | g0098 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0155 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0212 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA19063 | hp2 | a0001 | c0002 | t0002 | g0081 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA19066 | hp1 | a0001 | c0002 | t0042 | g0078 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA19068 | hp1 | a0005 | c0009 | t0005 | g0236 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA19070 | hp1 | a0001 | c0002 | t0012 | g0061 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA19072 | hp1 | a0001 | c0002 | t0002 | g0033 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA19072 | hp2 | a0001 | c0001 | t0030 | g0148 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA19079 | hp2 | a0001 | c0002 | t0002 | g0077 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA19080 | hp2 | a0002 | c0003 | t0005 | g0273 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA19082 | hp1 | a0001 | c0002 | t0028 | g0093 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA19082 | hp2 | a0001 | c0001 | t0033 | g0204 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA19083 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA19083 | hp2 | a0001 | c0002 | t0004 | g0084 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA19089 | hp1 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA19089 | hp2 | a0001 | c0002 | t0058 | g0031 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA19091 | hp1 | a0001 | c0002 | t0004 | g0001 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA19240 | hp1 | a0002 | c0003 | t0036 | g0269 | AFR | YRI | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA19240 | hp2 | a0002 | c0003 | t0022 | g0013 | AFR | YRI | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0184 | EUR | TSI | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA20752 | hp2 | a0001 | c0002 | t0004 | g0009 | EUR | TSI | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA20905 | hp1 | a0001 | c0002 | t0009 | g0087 | SAS | GIH | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA20905 | hp2 | a0001 | c0004 | t0007 | g0035 | SAS | GIH | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG01123 | hp1 | a0001 | c0002 | t0004 | g0001 | AMR | CLM | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG01123 | hp2 | a0001 | c0001 | t0006 | g0134 | AMR | CLM | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02109 | hp1 | a0002 | c0003 | t0014 | g0027 | AFR | ACB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02109 | hp2 | a0001 | c0002 | t0019 | g0278 | AFR | ACB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02486 | hp1 | a0001 | c0002 | t0052 | g0259 | AFR | ACB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02486 | hp2 | a0001 | c0002 | t0047 | g0034 | AFR | ACB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02559 | hp1 | a0001 | c0001 | t0013 | g0191 | AFR | ACB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG02559 | hp2 | a0001 | c0002 | t0004 | g0059 | AFR | ACB | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG03471 | hp1 | a0001 | c0004 | t0008 | g0028 | AFR | MSL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| HG03471 | hp2 | a0001 | c0002 | t0029 | g0026 | AFR | MSL | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18955 | hp1 | a0001 | c0002 | t0004 | g0012 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0208 | EAS | JPT | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0207 | AFR | USA | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA20300 | hp2 | a0001 | c0002 | t0045 | g0255 | AFR | USA | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA21309 | hp1 | a0002 | c0003 | t0005 | g0245 | AFR | LWK | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| NA21309 | hp2 | a0001 | c0001 | t0006 | g0210 | AFR | LWK | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0054 | g0091 | REF | REF | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0188 | REF | REF | FRRS1_chr1_99698970_99771635 | FRRS1 | chr1 | 99698970 | 99771635 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:99709114 | C | T | 4 | a0002 a0003 a0004 others(1): Show |
62 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(59): Show |
missense_variant | MODERATE | c.1693G>A | p.Ala565Thr | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 1827/6971 | 1693/1779 | 565/592 | chr1 | 99709114 | |||
| chr1:99710875 | C | T | 1 | a0005 | 1 | NA19068.hp1 | missense_variant | MODERATE | c.1555G>A | p.Gly519Arg | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 15/17 | 1689/6971 | 1555/1779 | 519/592 | chr1 | 99710875 | |||
| chr1:99712143 | G | A | 1 | a0003 | 4 | HG02451.hp2 HG02970.hp2 HG02976.hp2 others(1): Show |
missense_variant | MODERATE | c.1442C>T | p.Thr481Ile | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 14/17 | 1576/6971 | 1442/1779 | 481/592 | chr1 | 99712143 | |||
| chr1:99740911 | T | G | 1 | a0004 | 1 | NA18967.hp2 | missense_variant | MODERATE | c.458A>C | p.Tyr153Ser | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/17 | 592/6971 | 458/1779 | 153/592 | chr1 | 99740911 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:99738092 | C | T | 8 | a0001c0002 a0001c0004 a0002c0003 others(5): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
synonymous_variant | LOW | c.753G>A | p.Gln251Gln | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/17 | 887/6971 | 753/1779 | 251/592 | chr1 | 99738092 | |||
| chr1:99738137 | G | A | 8 | a0001c0002 a0001c0004 a0002c0003 others(5): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
synonymous_variant | LOW | c.708C>T | p.Ser236Ser | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/17 | 842/6971 | 708/1779 | 236/592 | chr1 | 99738137 | |||
| chr1:99742262 | C | G | 3 | a0001c0004 a0002c0007 a0003c0005 |
18 | HG01081.hp1 HG01192.hp1 HG01884.hp1 others(15): Show |
synonymous_variant | LOW | c.345G>C | p.Val115Val | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 5/17 | 479/6971 | 345/1779 | 115/592 | chr1 | 99742262 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:99704004 | T | C | 1 | a0001c0002t0047 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5024A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 5024 | chr1 | 99704004 | ||||||
| chr1:99704546 | T | C | 11 | a0001c0002t0046 a0002c0003t0005 a0002c0003t0011 others(8): Show |
40 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*4482A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 4482 | chr1 | 99704546 | ||||||
| chr1:99704946 | T | C | 41 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0031 others(38): Show |
141 | HG00408.hp1 HG00642.hp1 HG00673.hp2 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*4082A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 4082 | chr1 | 99704946 | ||||||
| chr1:99705017 | C | T | 1 | a0002c0003t0036 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4011G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 4011 | chr1 | 99705017 | ||||||
| chr1:99705083 | G | A | 3 | a0001c0002t0019 a0001c0002t0027 a0001c0002t0052 |
6 | HG01884.hp2 HG02055.hp2 HG02109.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3945C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 3945 | chr1 | 99705083 | ||||||
| chr1:99705424 | C | T | 2 | a0001c0001t0063 a0001c0001t0066 |
2 | HG01081.hp2 HG01109.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3604G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 3604 | chr1 | 99705424 | ||||||
| chr1:99705695 | T | A | 1 | a0001c0002t0026 | 2 | HG02055.hp1 HG02451.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3333A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 3333 | chr1 | 99705695 | ||||||
| chr1:99705854 | A | G | 30 | a0001c0001t0031 a0001c0001t0065 a0001c0002t0019 others(27): Show |
75 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*3174T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 3174 | chr1 | 99705854 | ||||||
| chr1:99706170 | T | C | 2 | a0001c0002t0019 a0001c0002t0052 |
4 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2858A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 2858 | chr1 | 99706170 | ||||||
| chr1:99706212 | T | A | 2 | a0001c0002t0019 a0001c0002t0052 |
4 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2816A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 2816 | chr1 | 99706212 | ||||||
| chr1:99706223 | C | CA | 16 | a0001c0002t0019 a0001c0002t0052 a0002c0003t0005 others(13): Show |
51 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*2804_*2805insT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 2804 | chr1 | 99706223 | ||||||
| chr1:99706223 | C | CAA | 9 | a0001c0002t0046 a0002c0003t0015 a0002c0003t0018 others(6): Show |
16 | HG01891.hp1 HG02145.hp1 HG02257.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2804_*2805insTT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 2804 | chr1 | 99706223 | ||||||
| chr1:99706223 | C | CAAA | 3 | a0001c0001t0031 a0001c0002t0024 a0001c0002t0049 |
5 | HG01167.hp2 HG01346.hp2 HG03927.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2804_*2805insTTT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 2804 | chr1 | 99706223 | ||||||
| chr1:99706223 | C | CAAAA | 2 | a0001c0001t0065 a0001c0002t0027 |
3 | HG02055.hp2 HG03017.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2804_*2805insTTTT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 2804 | chr1 | 99706223 | ||||||
| chr1:99706224 | C | A | 30 | a0001c0001t0031 a0001c0001t0065 a0001c0002t0019 others(27): Show |
75 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*2804G>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 2804 | chr1 | 99706224 | ||||||
| chr1:99706269 | G | A | 1 | a0001c0002t0045 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2759C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 2759 | chr1 | 99706269 | ||||||
| chr1:99706408 | CA | C | 27 | a0001c0001t0031 a0001c0001t0061 a0001c0001t0065 others(24): Show |
69 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*2619delT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 2619 | chr1 | 99706408 | ||||||
| chr1:99706542 | G | A | 1 | a0001c0002t0047 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2486C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 2486 | chr1 | 99706542 | ||||||
| chr1:99706750 | C | T | 1 | a0001c0002t0046 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2278G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 2278 | chr1 | 99706750 | ||||||
| chr1:99706891 | C | CA | 30 | a0001c0001t0062 a0001c0001t0064 a0001c0002t0019 others(27): Show |
74 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*2136dupT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 2136 | chr1 | 99706891 | ||||||
| chr1:99706891 | CA | C | 4 | a0001c0001t0060 a0001c0002t0008 a0001c0002t0025 others(1): Show |
12 | HG01884.hp1 HG02922.hp2 HG02965.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2136delT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 2136 | chr1 | 99706891 | ||||||
| chr1:99706944 | A | G | 1 | a0001c0002t0024 | 2 | HG01167.hp2 HG03927.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2084T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 2084 | chr1 | 99706944 | ||||||
| chr1:99707196 | G | C | 1 | a0001c0001t0030 | 2 | NA18993.hp2 NA19072.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1832C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 1832 | chr1 | 99707196 | ||||||
| chr1:99707345 | G | A | 7 | a0001c0001t0069 a0001c0002t0004 a0001c0002t0009 others(4): Show |
45 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1683C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 1683 | chr1 | 99707345 | ||||||
| chr1:99707678 | T | C | 1 | a0001c0002t0048 | 1 | HG01515.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1350A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 1350 | chr1 | 99707678 | ||||||
| chr1:99707742 | C | T | 2 | a0001c0002t0043 a0001c0002t0053 |
2 | HG03041.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1286G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 1286 | chr1 | 99707742 | ||||||
| chr1:99707973 | G | A | 22 | a0002c0003t0005 a0002c0003t0010 a0002c0003t0011 others(19): Show |
62 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*1055C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 1055 | chr1 | 99707973 | ||||||
| chr1:99708174 | T | C | 6 | a0001c0001t0006 a0001c0001t0031 a0001c0001t0063 others(3): Show |
20 | HG00642.hp1 HG00741.hp2 HG01081.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*854A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 854 | chr1 | 99708174 | ||||||
| chr1:99708368 | G | A | 1 | a0001c0002t0049 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*660C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 660 | chr1 | 99708368 | ||||||
| chr1:99708375 | A | G | 22 | a0002c0003t0005 a0002c0003t0010 a0002c0003t0011 others(19): Show |
62 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*653T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 653 | chr1 | 99708375 | ||||||
| chr1:99708441 | A | T | 1 | a0001c0002t0024 | 2 | HG01167.hp2 HG03927.hp2 |
3_prime_UTR_variant | MODIFIER | c.*587T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 587 | chr1 | 99708441 | ||||||
| chr1:99708461 | G | T | 1 | a0002c0003t0038 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*567C>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 567 | chr1 | 99708461 | ||||||
| chr1:99708549 | G | A | 1 | a0001c0004t0050 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*479C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 479 | chr1 | 99708549 | ||||||
| chr1:99708597 | C | CA | 5 | a0001c0001t0032 a0001c0001t0033 a0001c0001t0064 others(2): Show |
8 | HG01256.hp2 HG01433.hp2 HG01993.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*430dupT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 430 | chr1 | 99708597 | ||||||
| chr1:99708597 | C | CAA | 4 | a0001c0001t0013 a0001c0001t0034 a0001c0001t0065 others(1): Show |
9 | HG01081.hp2 HG02135.hp1 HG02165.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*429_*430dupTT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 430 | chr1 | 99708597 | ||||||
| chr1:99708597 | C | CAAAAAAA others(4): Show |
1 | a0001c0002t0052 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*420_*430dupTTTTTT others(5): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 430 | chr1 | 99708597 | ||||||
| chr1:99708597 | CAAA | C | 7 | a0001c0001t0020 a0001c0002t0042 a0002c0003t0017 others(4): Show |
12 | HG01069.hp2 HG01891.hp1 HG01978.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*428_*430delTTT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 428 | chr1 | 99708597 | ||||||
| chr1:99708597 | CAAAAA | C | 2 | a0002c0003t0011 a0002c0003t0022 |
7 | HG00673.hp2 HG02080.hp1 NA18962.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*426_*430delTTTTT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 426 | chr1 | 99708597 | ||||||
| chr1:99708597 | CAAAAAAA others(2): Show |
C | 2 | a0002c0003t0014 a0002c0003t0021 |
6 | HG00735.hp1 HG02109.hp1 HG02896.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*422_*430delTTTTTT others(3): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 422 | chr1 | 99708597 | ||||||
| chr1:99708616 | AAAAAAAA others(12): Show |
A | 1 | a0001c0002t0053 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*411delATATAT others(13): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 393 | chr1 | 99708616 | ||||||
| chr1:99708618 | AAAAAAAA others(2): Show |
A | 3 | a0002c0003t0005 a0002c0003t0038 a0005c0009t0005 |
11 | HG01109.hp2 HG01891.hp2 HG02717.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*401_*409delATTTTT others(3): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 401 | chr1 | 99708618 | ||||||
| chr1:99708618 | AAAAAAAA others(4): Show |
A | 1 | a0002c0008t0059 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*399_*409delATATTT others(5): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 399 | chr1 | 99708618 | ||||||
| chr1:99708618 | AAAAAAAA others(12): Show |
A | 1 | a0001c0002t0043 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*391_*409delATATAT others(13): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 391 | chr1 | 99708618 | ||||||
| chr1:99708619 | A | T | 1 | a0002c0007t0041 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*409T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 409 | chr1 | 99708619 | ||||||
| chr1:99708620 | AAAAAAAT others(4): Show |
A | 1 | a0001c0002t0002 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*397_*407delATATAT others(5): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 397 | chr1 | 99708620 | ||||||
| chr1:99708620 | AAAAAAAT others(8): Show |
A | 1 | a0001c0002t0004 | 2 | HG00741.hp1 HG01361.hp1 |
3_prime_UTR_variant | MODIFIER | c.*393_*407delATATAT others(9): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 393 | chr1 | 99708620 | ||||||
| chr1:99708620 | AAAAAAAT others(10): Show |
A | 1 | a0001c0002t0026 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*391_*407delATATAT others(11): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 391 | chr1 | 99708620 | ||||||
| chr1:99708621 | A | T | 8 | a0002c0003t0005 a0002c0003t0010 a0002c0003t0011 others(5): Show |
8 | HG02145.hp1 HG02886.hp1 HG02895.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*407T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 407 | chr1 | 99708621 | ||||||
| chr1:99708621 | AAAAAATA others(3): Show |
A | 1 | a0001c0002t0004 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*397_*406delATATAT others(4): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 397 | chr1 | 99708621 | ||||||
| chr1:99708621 | AAAAAATA others(9): Show |
A | 1 | a0001c0002t0026 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*391_*406delATATAT others(10): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 391 | chr1 | 99708621 | ||||||
| chr1:99708623 | A | T | 11 | a0001c0001t0001 a0002c0003t0005 a0002c0003t0010 others(8): Show |
17 | HG00642.hp2 HG00673.hp2 HG01891.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*405T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 405 | chr1 | 99708623 | ||||||
| chr1:99708623 | AAAATATA others(3): Show |
A | 1 | a0001c0002t0002 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*395_*404delATATAT others(4): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 395 | chr1 | 99708623 | ||||||
| chr1:99708623 | AAAATATA others(19): Show |
A | 1 | a0001c0002t0002 | 1 | NA19072.hp1 | 3_prime_UTR_variant | MODIFIER | c.*379_*404delATATAT others(20): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 379 | chr1 | 99708623 | ||||||
| chr1:99708624 | AAATAT | A | 2 | a0001c0001t0001 a0001c0002t0002 |
8 | HG00639.hp2 HG01261.hp2 HG01993.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*399_*403delATATT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 399 | chr1 | 99708624 | ||||||
| chr1:99708624 | AAATATAT others(4): Show |
A | 1 | a0001c0002t0002 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*393_*403delATATAT others(5): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 393 | chr1 | 99708624 | ||||||
| chr1:99708625 | A | AAAAAAAA others(13): Show |
1 | a0001c0004t0002 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*402_*403insATATAT others(14): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 402 | chr1 | 99708625 | ||||||
| chr1:99708625 | A | AAAAAAAA others(5): Show |
1 | a0001c0002t0019 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*402_*403insATTTTT others(6): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 402 | chr1 | 99708625 | ||||||
| chr1:99708625 | A | AAAAAAAA others(9): Show |
1 | a0001c0001t0001 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*402_*403insATATAT others(10): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 402 | chr1 | 99708625 | ||||||
| chr1:99708625 | A | AAAAAAAA others(13): Show |
1 | a0001c0004t0002 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*402_*403insATATAT others(14): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 402 | chr1 | 99708625 | ||||||
| chr1:99708625 | A | AAAAAAAA others(8): Show |
1 | a0001c0004t0002 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*402_*403insATATAT others(9): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 402 | chr1 | 99708625 | ||||||
| chr1:99708625 | A | AAAAAAAA others(7): Show |
1 | a0001c0004t0002 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*402_*403insATATAT others(8): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 402 | chr1 | 99708625 | ||||||
| chr1:99708625 | A | AAAAAAAT others(4): Show |
1 | a0001c0002t0024 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*402_*403insATATAT others(5): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 402 | chr1 | 99708625 | ||||||
| chr1:99708625 | A | AAAAAAAT others(6): Show |
1 | a0001c0004t0002 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*402_*403insATATAT others(7): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 402 | chr1 | 99708625 | ||||||
| chr1:99708625 | A | AAAAATAT others(4): Show |
1 | a0001c0004t0002 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*402_*403insATATAT others(5): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 402 | chr1 | 99708625 | ||||||
| chr1:99708625 | A | AAAAATAT others(6): Show |
1 | a0001c0004t0007 | 1 | NA18987.hp2 | 3_prime_UTR_variant | MODIFIER | c.*402_*403insATATAT others(7): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 402 | chr1 | 99708625 | ||||||
| chr1:99708625 | A | AAAAATAT others(8): Show |
1 | a0001c0004t0007 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*402_*403insATATAT others(9): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 402 | chr1 | 99708625 | ||||||
| chr1:99708625 | A | AAAT | 5 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(2): Show |
6 | HG02080.hp2 HG02280.hp1 HG03130.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*402_*403insATT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 402 | chr1 | 99708625 | ||||||
| chr1:99708625 | A | AT | 3 | a0001c0001t0006 a0001c0001t0031 a0001c0001t0063 |
3 | HG00642.hp1 HG01109.hp1 HG01346.hp2 |
3_prime_UTR_variant | MODIFIER | c.*402_*403insA | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 402 | chr1 | 99708625 | ||||||
| chr1:99708625 | A | T | 20 | a0001c0001t0001 a0001c0001t0031 a0001c0002t0007 others(17): Show |
36 | HG00642.hp2 HG00673.hp2 HG01069.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*403T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 403 | chr1 | 99708625 | ||||||
| chr1:99708625 | AAT | A | 5 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(2): Show |
15 | HG00408.hp2 HG00423.hp1 HG00609.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*401_*402delAT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 401 | chr1 | 99708625 | ||||||
| chr1:99708625 | AATAT | A | 6 | a0001c0001t0003 a0001c0001t0062 a0001c0002t0002 others(3): Show |
7 | HG01934.hp2 HG02027.hp2 HG02486.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*399_*402delATAT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 399 | chr1 | 99708625 | ||||||
| chr1:99708625 | AATATATA others(1): Show |
A | 5 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0012 others(2): Show |
8 | HG00423.hp2 HG02647.hp2 HG02698.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*395_*402delATATAT others(2): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 395 | chr1 | 99708625 | ||||||
| chr1:99708625 | AATATATA others(3): Show |
A | 7 | a0001c0001t0001 a0001c0002t0002 a0001c0002t0004 others(4): Show |
19 | HG00621.hp1 HG00621.hp2 HG00673.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*393_*402delATATAT others(4): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 393 | chr1 | 99708625 | ||||||
| chr1:99708626 | AT | A | 5 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(2): Show |
12 | HG00639.hp1 HG01255.hp1 HG01361.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*401delA | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 401 | chr1 | 99708626 | ||||||
| chr1:99708626 | ATAT | A | 5 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(2): Show |
35 | HG00408.hp1 HG00741.hp2 HG01106.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*399_*401delATA | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 399 | chr1 | 99708626 | ||||||
| chr1:99708626 | ATATAT | A | 7 | a0001c0001t0001 a0001c0001t0003 a0001c0002t0002 others(4): Show |
10 | HG01943.hp1 HG01981.hp1 HG02055.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*397_*401delATATA | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 397 | chr1 | 99708626 | ||||||
| chr1:99708626 | ATATATAT others(2): Show |
A | 8 | a0001c0001t0068 a0001c0001t0069 a0001c0002t0004 others(5): Show |
16 | HG00738.hp1 HG01106.hp1 HG01257.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*393_*401delATATAT others(3): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 393 | chr1 | 99708626 | ||||||
| chr1:99708626 | ATATATAT others(4): Show |
A | 5 | a0001c0001t0001 a0001c0002t0004 a0001c0002t0007 others(2): Show |
9 | HG02257.hp1 HG02300.hp2 HG03471.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*391_*401delATATAT others(5): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 391 | chr1 | 99708626 | ||||||
| chr1:99708627 | T | A | 10 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0013 others(7): Show |
19 | HG00738.hp2 HG01256.hp1 HG01256.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*401A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 401 | chr1 | 99708627 | ||||||
| chr1:99708629 | T | A | 8 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(5): Show |
25 | HG00408.hp2 HG00639.hp1 HG01361.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*399A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 399 | chr1 | 99708629 | ||||||
| chr1:99708631 | T | A | 8 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0033 others(5): Show |
34 | HG00408.hp1 HG00408.hp2 HG01192.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*397A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 397 | chr1 | 99708631 | ||||||
| chr1:99708633 | T | A | 6 | a0001c0001t0001 a0001c0001t0003 a0001c0002t0002 others(3): Show |
10 | HG00408.hp1 HG01361.hp2 HG01981.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*395A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 395 | chr1 | 99708633 | ||||||
| chr1:99708635 | T | A | 5 | a0001c0001t0067 a0001c0002t0002 a0001c0002t0004 others(2): Show |
5 | HG02698.hp2 HG04184.hp2 NA18959.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*393A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 393 | chr1 | 99708635 | ||||||
| chr1:99708637 | T | A | 8 | a0001c0001t0067 a0001c0001t0068 a0001c0001t0069 others(5): Show |
23 | HG00621.hp2 HG00673.hp1 HG00738.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*391A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 391 | chr1 | 99708637 | ||||||
| chr1:99708639 | T | A | 5 | a0001c0002t0012 a0001c0002t0029 a0001c0002t0055 others(2): Show |
10 | HG00738.hp1 HG01928.hp2 HG02257.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*389A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 389 | chr1 | 99708639 | ||||||
| chr1:99708641 | T | A | 1 | a0001c0002t0057 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*387A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 387 | chr1 | 99708641 | ||||||
| chr1:99708654 | A | G | 21 | a0002c0003t0005 a0002c0003t0010 a0002c0003t0011 others(18): Show |
61 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*374T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 374 | chr1 | 99708654 | ||||||
| chr1:99708662 | A | C | 22 | a0002c0003t0005 a0002c0003t0010 a0002c0003t0011 others(19): Show |
62 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*366T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 366 | chr1 | 99708662 | ||||||
| chr1:99708899 | T | C | 1 | a0001c0002t0058 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*129A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 17/17 | 129 | chr1 | 99708899 | ||||||
| chr1:99748931 | C | T | 54 | a0001c0002t0002 a0001c0002t0004 a0001c0002t0007 others(51): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
5_prime_UTR_variant | MODIFIER | c.-35G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 2/17 | 163 | chr1 | 99748931 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:99709316 | T | A | 1 | a0001c0001t0006g0136 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1625-57A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 15/16 | chr1 | 99709316 | |||||||
| chr1:99709320 | T | A | 66 | a0001c0002t0019g0094 a0001c0002t0019g0256 a0001c0002t0019g0278 others(63): Show |
72 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(69): Show |
intron_variant | MODIFIER | c.1625-61A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 15/16 | chr1 | 99709320 | |||||||
| chr1:99709321 | A | T | 1 | a0001c0002t0004g0057 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1625-62T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 15/16 | chr1 | 99709321 | |||||||
| chr1:99709685 | C | T | 3 | a0002c0003t0010g0015 a0002c0003t0010g0102 a0002c0003t0022g0013 |
5 | HG02622.hp1 HG02809.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1625-426G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 15/16 | chr1 | 99709685 | |||||||
| chr1:99709686 | A | G | 57 | a0002c0003t0005g0025 a0002c0003t0005g0066 a0002c0003t0005g0227 others(54): Show |
62 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.1625-427T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 15/16 | chr1 | 99709686 | |||||||
| chr1:99709739 | G | A | 1 | a0002c0003t0015g0092 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1625-480C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 15/16 | chr1 | 99709739 | |||||||
| chr1:99709817 | A | C | 57 | a0002c0003t0005g0025 a0002c0003t0005g0066 a0002c0003t0005g0227 others(54): Show |
62 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.1625-558T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 15/16 | chr1 | 99709817 | |||||||
| chr1:99709992 | A | C | 1 | a0001c0002t0004g0064 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1625-733T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 15/16 | chr1 | 99709992 | |||||||
| chr1:99710065 | G | A | 57 | a0002c0003t0005g0025 a0002c0003t0005g0066 a0002c0003t0005g0227 others(54): Show |
62 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.1624+741C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 15/16 | chr1 | 99710065 | |||||||
| chr1:99710091 | G | C | 7 | a0001c0001t0001g0005 a0001c0001t0001g0194 a0001c0001t0013g0147 others(4): Show |
9 | HG02135.hp1 NA18954.hp2 NA18959.hp1 others(6): Show |
intron_variant | MODIFIER | c.1624+715C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 15/16 | chr1 | 99710091 | |||||||
| chr1:99710099 | C | G | 1 | a0001c0001t0003g0201 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1624+707G>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 15/16 | chr1 | 99710099 | |||||||
| chr1:99710142 | G | T | 31 | a0002c0003t0005g0025 a0002c0003t0005g0066 a0002c0003t0005g0227 others(28): Show |
33 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.1624+664C>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 15/16 | chr1 | 99710142 | |||||||
| chr1:99710202 | A | G | 57 | a0002c0003t0005g0025 a0002c0003t0005g0066 a0002c0003t0005g0227 others(54): Show |
62 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.1624+604T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 15/16 | chr1 | 99710202 | |||||||
| chr1:99710208 | G | A | 57 | a0002c0003t0005g0025 a0002c0003t0005g0066 a0002c0003t0005g0227 others(54): Show |
62 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.1624+598C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 15/16 | chr1 | 99710208 | |||||||
| chr1:99710210 | C | A | 57 | a0002c0003t0005g0025 a0002c0003t0005g0066 a0002c0003t0005g0227 others(54): Show |
62 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.1624+596G>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 15/16 | chr1 | 99710210 | |||||||
| chr1:99710353 | T | TCTGG | 62 | a0001c0002t0019g0094 a0001c0002t0019g0278 a0001c0002t0026g0100 others(59): Show |
67 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.1624+449_1624+452d others(6): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 15/16 | chr1 | 99710353 | |||||||
| chr1:99710507 | A | C | 1 | a0001c0002t0002g0226 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1624+299T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 15/16 | chr1 | 99710507 | |||||||
| chr1:99710528 | C | A | 57 | a0002c0003t0005g0025 a0002c0003t0005g0066 a0002c0003t0005g0227 others(54): Show |
62 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.1624+278G>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 15/16 | chr1 | 99710528 | |||||||
| chr1:99710689 | A | G | 2 | a0001c0001t0001g0021 a0001c0001t0001g0177 |
3 | HG00423.hp1 HG02015.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1624+117T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 15/16 | chr1 | 99710689 | |||||||
| chr1:99710735 | G | A | 1 | a0002c0003t0005g0245 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1624+71C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 15/16 | chr1 | 99710735 | |||||||
| chr1:99710760 | T | G | 2 | a0001c0002t0019g0256 a0001c0002t0047g0034 |
2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1624+46A>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 15/16 | chr1 | 99710760 | |||||||
| chr1:99711015 | T | C | 2 | a0001c0002t0024g0115 a0001c0002t0024g0116 |
2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1481-66A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 14/16 | chr1 | 99711015 | |||||||
| chr1:99711278 | C | T | 1 | a0001c0001t0031g0017 | 2 | HG01346.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1481-329G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 14/16 | chr1 | 99711278 | |||||||
| chr1:99711279 | G | T | 1 | a0001c0001t0006g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1481-330C>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 14/16 | chr1 | 99711279 | |||||||
| chr1:99711341 | A | G | 1 | a0002c0003t0014g0027 | 2 | HG00735.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1481-392T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 14/16 | chr1 | 99711341 | |||||||
| chr1:99711586 | C | G | 1 | a0001c0002t0042g0078 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1480+519G>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 14/16 | chr1 | 99711586 | |||||||
| chr1:99711717 | A | C | 2 | a0001c0002t0024g0115 a0001c0002t0024g0116 |
2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1480+388T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 14/16 | chr1 | 99711717 | |||||||
| chr1:99711970 | G | A | 31 | a0002c0003t0005g0025 a0002c0003t0005g0066 a0002c0003t0005g0227 others(28): Show |
33 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.1480+135C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 14/16 | chr1 | 99711970 | |||||||
| chr1:99712099 | T | C | 2 | a0001c0002t0019g0256 a0001c0002t0047g0034 |
2 | HG01884.hp2 HG02486.hp2 |
splice_region_variant&intron_variant | LOW | c.1480+6A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 14/16 | chr1 | 99712099 | |||||||
| chr1:99712397 | A | G | 1 | a0002c0003t0005g0248 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1421+21T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 13/16 | chr1 | 99712397 | |||||||
| chr1:99712399 | A | G | 1 | a0001c0001t0001g0176 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1421+19T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 13/16 | chr1 | 99712399 | |||||||
| chr1:99712413 | A | G | 1 | a0001c0002t0002g0077 | 1 | NA19079.hp2 | splice_region_variant&intron_variant | LOW | c.1421+5T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 13/16 | chr1 | 99712413 | |||||||
| chr1:99712728 | T | C | 1 | a0002c0003t0005g0066 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1324-213A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 12/16 | chr1 | 99712728 | |||||||
| chr1:99712885 | C | T | 1 | a0002c0003t0021g0265 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1324-370G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 12/16 | chr1 | 99712885 | |||||||
| chr1:99712998 | G | GGGACTAG others(558): Show |
49 | a0002c0003t0005g0025 a0002c0003t0005g0066 a0002c0003t0005g0227 others(46): Show |
51 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.1324-484_1324-483i others(567): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 12/16 | chr1 | 99712998 | |||||||
| chr1:99713152 | A | C | 49 | a0002c0003t0005g0025 a0002c0003t0005g0066 a0002c0003t0005g0227 others(46): Show |
51 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.1324-637T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 12/16 | chr1 | 99713152 | |||||||
| chr1:99713266 | T | C | 4 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0157 others(1): Show |
6 | HG00738.hp2 HG01256.hp1 HG01981.hp2 others(3): Show |
intron_variant | MODIFIER | c.1324-751A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 12/16 | chr1 | 99713266 | |||||||
| chr1:99713343 | G | T | 3 | a0001c0002t0019g0094 a0001c0002t0019g0278 a0001c0002t0052g0259 |
3 | HG02109.hp2 HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1324-828C>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 12/16 | chr1 | 99713343 | |||||||
| chr1:99713494 | G | A | 49 | a0002c0003t0005g0025 a0002c0003t0005g0066 a0002c0003t0005g0227 others(46): Show |
51 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.1324-979C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 12/16 | chr1 | 99713494 | |||||||
| chr1:99713565 | A | G | 2 | a0002c0003t0010g0110 a0002c0003t0039g0109 |
2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1324-1050T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 12/16 | chr1 | 99713565 | |||||||
| chr1:99713743 | T | C | 150 | a0001c0001t0001g0104 a0001c0001t0001g0129 a0001c0001t0001g0137 others(147): Show |
168 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(165): Show |
intron_variant | MODIFIER | c.1324-1228A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 12/16 | chr1 | 99713743 | |||||||
| chr1:99713934 | C | T | 1 | a0001c0001t0034g0120 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1324-1419G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 12/16 | chr1 | 99713934 | |||||||
| chr1:99714060 | A | G | 1 | a0002c0003t0005g0066 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1323+1526T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 12/16 | chr1 | 99714060 | |||||||
| chr1:99714112 | C | T | 2 | a0001c0002t0043g0279 a0001c0002t0053g0243 |
2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1323+1474G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 12/16 | chr1 | 99714112 | |||||||
| chr1:99714185 | CT | C | 6 | a0001c0001t0030g0149 a0001c0002t0002g0033 a0001c0002t0002g0081 others(3): Show |
6 | HG02145.hp1 HG03195.hp2 NA18993.hp1 others(3): Show |
intron_variant | MODIFIER | c.1323+1400delA | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 12/16 | chr1 | 99714185 | |||||||
| chr1:99714247 | G | A | 1 | a0001c0001t0067g0171 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1323+1339C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 12/16 | chr1 | 99714247 | |||||||
| chr1:99714329 | G | A | 2 | a0001c0004t0008g0043 a0001c0004t0008g0044 |
2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1323+1257C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 12/16 | chr1 | 99714329 | |||||||
| chr1:99714393 | A | G | 3 | a0001c0002t0019g0094 a0001c0002t0019g0278 a0001c0002t0052g0259 |
3 | HG02109.hp2 HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1323+1193T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 12/16 | chr1 | 99714393 | |||||||
| chr1:99714478 | G | A | 14 | a0002c0003t0015g0092 a0002c0003t0015g0263 a0002c0003t0015g0264 others(11): Show |
14 | HG01891.hp1 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1323+1108C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 12/16 | chr1 | 99714478 | |||||||
| chr1:99714536 | C | T | 52 | a0001c0002t0019g0094 a0001c0002t0019g0278 a0001c0002t0052g0259 others(49): Show |
54 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.1323+1050G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 12/16 | chr1 | 99714536 | |||||||
| chr1:99714970 | T | C | 2 | a0001c0002t0026g0100 a0001c0002t0026g0101 |
2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1323+616A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 12/16 | chr1 | 99714970 | |||||||
| chr1:99715108 | C | T | 1 | a0002c0003t0035g0275 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1323+478G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 12/16 | chr1 | 99715108 | |||||||
| chr1:99715127 | G | A | 4 | a0001c0002t0002g0105 a0001c0002t0002g0111 a0001c0002t0002g0112 others(1): Show |
4 | HG02572.hp2 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1323+459C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 12/16 | chr1 | 99715127 | |||||||
| chr1:99715198 | G | T | 1 | a0001c0001t0003g0125 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1323+388C>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 12/16 | chr1 | 99715198 | |||||||
| chr1:99715489 | C | T | 2 | a0001c0001t0006g0134 a0001c0001t0006g0181 |
2 | HG00642.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.1323+97G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 12/16 | chr1 | 99715489 | |||||||
| chr1:99715537 | T | C | 2 | a0001c0002t0009g0088 a0001c0002t0012g0051 |
2 | HG00621.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.1323+49A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 12/16 | chr1 | 99715537 | |||||||
| chr1:99715823 | A | C | 2 | a0001c0001t0001g0166 a0001c0001t0001g0184 |
2 | HG00642.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1237-151T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 11/16 | chr1 | 99715823 | |||||||
| chr1:99715824 | GA | G | 7 | a0001c0002t0019g0094 a0001c0002t0052g0259 a0002c0003t0018g0218 others(4): Show |
7 | HG01891.hp1 HG02486.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1237-153delT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 11/16 | chr1 | 99715824 | |||||||
| chr1:99715870 | T | C | 52 | a0001c0002t0019g0094 a0001c0002t0019g0278 a0001c0002t0052g0259 others(49): Show |
54 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.1237-198A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 11/16 | chr1 | 99715870 | |||||||
| chr1:99715916 | T | C | 150 | a0001c0001t0001g0104 a0001c0001t0001g0129 a0001c0001t0001g0137 others(147): Show |
168 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(165): Show |
intron_variant | MODIFIER | c.1237-244A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 11/16 | chr1 | 99715916 | |||||||
| chr1:99716218 | A | G | 4 | a0003c0005t0010g0046 a0003c0005t0010g0047 a0003c0006t0010g0113 others(1): Show |
4 | HG02451.hp2 HG02970.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1237-546T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 11/16 | chr1 | 99716218 | |||||||
| chr1:99716264 | A | C | 1 | a0001c0001t0006g0138 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1237-592T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 11/16 | chr1 | 99716264 | |||||||
| chr1:99716275 | G | A | 1 | a0001c0004t0008g0043 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1237-603C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 11/16 | chr1 | 99716275 | |||||||
| chr1:99716277 | T | G | 1 | a0001c0001t0001g0172 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1237-605A>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 11/16 | chr1 | 99716277 | |||||||
| chr1:99716320 | A | T | 1 | a0002c0003t0040g0272 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1237-648T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 11/16 | chr1 | 99716320 | |||||||
| chr1:99716341 | G | A | 145 | a0001c0001t0001g0129 a0001c0001t0001g0137 a0001c0001t0001g0172 others(142): Show |
162 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(159): Show |
intron_variant | MODIFIER | c.1237-669C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 11/16 | chr1 | 99716341 | |||||||
| chr1:99716414 | T | C | 2 | a0001c0002t0026g0100 a0001c0002t0026g0101 |
2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1237-742A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 11/16 | chr1 | 99716414 | |||||||
| chr1:99716474 | G | A | 2 | a0001c0002t0024g0115 a0001c0002t0024g0116 |
2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1237-802C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 11/16 | chr1 | 99716474 | |||||||
| chr1:99716503 | G | A | 49 | a0002c0003t0005g0025 a0002c0003t0005g0066 a0002c0003t0005g0227 others(46): Show |
51 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.1237-831C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 11/16 | chr1 | 99716503 | |||||||
| chr1:99716895 | T | G | 148 | a0001c0001t0001g0104 a0001c0001t0001g0129 a0001c0001t0001g0137 others(145): Show |
166 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(163): Show |
intron_variant | MODIFIER | c.1236+515A>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 11/16 | chr1 | 99716895 | |||||||
| chr1:99716923 | T | C | 1 | a0001c0004t0008g0043 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1236+487A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 11/16 | chr1 | 99716923 | |||||||
| chr1:99716927 | G | A | 2 | a0001c0002t0026g0100 a0001c0002t0026g0101 |
2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1236+483C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 11/16 | chr1 | 99716927 | |||||||
| chr1:99717023 | T | C | 1 | a0001c0002t0019g0278 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1236+387A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 11/16 | chr1 | 99717023 | |||||||
| chr1:99717144 | C | G | 1 | a0001c0001t0064g0161 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1236+266G>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 11/16 | chr1 | 99717144 | |||||||
| chr1:99717279 | G | A | 1 | a0001c0002t0009g0087 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1236+131C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 11/16 | chr1 | 99717279 | |||||||
| chr1:99717328 | C | T | 110 | a0001c0001t0001g0129 a0001c0001t0001g0137 a0001c0001t0001g0172 others(107): Show |
129 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(126): Show |
intron_variant | MODIFIER | c.1236+82G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 11/16 | chr1 | 99717328 | |||||||
| chr1:99717794 | T | C | 1 | a0001c0002t0024g0115 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1121-269A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 10/16 | chr1 | 99717794 | |||||||
| chr1:99717801 | C | A | 12 | a0001c0001t0001g0137 a0001c0001t0001g0172 a0001c0001t0067g0171 others(9): Show |
12 | HG01074.hp2 HG01106.hp1 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1121-276G>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 10/16 | chr1 | 99717801 | |||||||
| chr1:99718047 | C | T | 2 | a0001c0004t0008g0043 a0001c0004t0008g0044 |
2 | HG01884.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1121-522G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 10/16 | chr1 | 99718047 | |||||||
| chr1:99718096 | G | A | 1 | a0001c0002t0043g0279 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1121-571C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 10/16 | chr1 | 99718096 | |||||||
| chr1:99718188 | T | A | 1 | a0002c0003t0011g0238 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1121-663A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 10/16 | chr1 | 99718188 | |||||||
| chr1:99718338 | G | C | 20 | a0001c0001t0001g0129 a0001c0002t0007g0117 a0001c0002t0007g0246 others(17): Show |
22 | HG01081.hp1 HG01192.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.1121-813C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 10/16 | chr1 | 99718338 | |||||||
| chr1:99718428 | A | T | 1 | a0001c0004t0007g0041 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1121-903T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 10/16 | chr1 | 99718428 | |||||||
| chr1:99718456 | G | A | 1 | a0001c0002t0027g0010 | 2 | HG02055.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1121-931C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 10/16 | chr1 | 99718456 | |||||||
| chr1:99718474 | G | A | 1 | a0001c0002t0027g0010 | 2 | HG02055.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1121-949C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 10/16 | chr1 | 99718474 | |||||||
| chr1:99718612 | A | G | 1 | a0001c0001t0001g0197 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1120+922T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 10/16 | chr1 | 99718612 | |||||||
| chr1:99718788 | T | C | 2 | a0001c0002t0004g0004 a0001c0002t0004g0050 |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1120+746A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 10/16 | chr1 | 99718788 | |||||||
| chr1:99718902 | T | G | 49 | a0002c0003t0005g0025 a0002c0003t0005g0066 a0002c0003t0005g0227 others(46): Show |
51 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.1120+632A>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 10/16 | chr1 | 99718902 | |||||||
| chr1:99718987 | A | G | 1 | a0001c0001t0001g0163 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1120+547T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 10/16 | chr1 | 99718987 | |||||||
| chr1:99719044 | T | C | 3 | a0001c0002t0008g0016 a0001c0002t0008g0107 a0001c0002t0008g0108 |
4 | HG02965.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1120+490A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 10/16 | chr1 | 99719044 | |||||||
| chr1:99719070 | CA | C | 55 | a0001c0002t0019g0094 a0001c0002t0019g0256 a0001c0002t0019g0278 others(52): Show |
58 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.1120+463delT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 10/16 | chr1 | 99719070 | |||||||
| chr1:99719070 | CAA | C | 109 | a0001c0001t0001g0129 a0001c0001t0001g0137 a0001c0001t0001g0172 others(106): Show |
127 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(124): Show |
intron_variant | MODIFIER | c.1120+462_1120+463d others(4): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 10/16 | chr1 | 99719070 | |||||||
| chr1:99719122 | G | T | 2 | a0001c0002t0024g0115 a0001c0002t0024g0116 |
2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1120+412C>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 10/16 | chr1 | 99719122 | |||||||
| chr1:99719349 | C | A | 2 | a0001c0002t0024g0115 a0001c0002t0024g0116 |
2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1120+185G>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 10/16 | chr1 | 99719349 | |||||||
| chr1:99719407 | C | CA | 104 | a0001c0001t0001g0137 a0001c0001t0001g0172 a0001c0001t0001g0196 others(101): Show |
123 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(120): Show |
intron_variant | MODIFIER | c.1120+126dupT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 10/16 | chr1 | 99719407 | |||||||
| chr1:99719407 | C | CAA | 54 | a0001c0002t0002g0081 a0001c0002t0002g0224 a0001c0002t0004g0058 others(51): Show |
56 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.1120+125_1120+126d others(4): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 10/16 | chr1 | 99719407 | |||||||
| chr1:99719407 | CA | C | 9 | a0001c0001t0001g0154 a0001c0001t0001g0179 a0001c0001t0003g0122 others(6): Show |
9 | HG01256.hp2 NA18998.hp2 NA19003.hp1 others(6): Show |
intron_variant | MODIFIER | c.1120+126delT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 10/16 | chr1 | 99719407 | |||||||
| chr1:99719726 | G | T | 109 | a0001c0001t0001g0129 a0001c0001t0001g0137 a0001c0001t0001g0172 others(106): Show |
127 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(124): Show |
intron_variant | MODIFIER | c.1007-79C>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99719726 | |||||||
| chr1:99719853 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1007-206A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99719853 | |||||||
| chr1:99719864 | G | C | 1 | a0001c0002t0027g0010 | 2 | HG02055.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1007-217C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99719864 | |||||||
| chr1:99719893 | G | C | 2 | a0001c0002t0026g0100 a0001c0002t0026g0101 |
2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1007-246C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99719893 | |||||||
| chr1:99719902 | T | C | 2 | a0001c0001t0001g0166 a0001c0001t0001g0184 |
2 | HG00642.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1007-255A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99719902 | |||||||
| chr1:99720199 | A | T | 1 | a0002c0003t0015g0092 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1007-552T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99720199 | |||||||
| chr1:99720350 | T | C | 2 | a0001c0002t0043g0279 a0001c0002t0053g0243 |
2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1007-703A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99720350 | |||||||
| chr1:99720370 | G | A | 54 | a0001c0002t0019g0094 a0001c0002t0019g0278 a0001c0002t0026g0100 others(51): Show |
56 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.1007-723C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99720370 | |||||||
| chr1:99720420 | G | A | 7 | a0002c0003t0010g0015 a0002c0003t0010g0102 a0002c0003t0010g0110 others(4): Show |
10 | HG02145.hp1 HG02622.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1007-773C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99720420 | |||||||
| chr1:99720834 | A | AAC | 9 | a0001c0001t0001g0018 a0001c0001t0001g0157 a0001c0001t0001g0166 others(6): Show |
10 | HG00642.hp2 HG01256.hp1 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.1007-1189_1007-118 others(6): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99720834 | |||||||
| chr1:99720834 | AAC | A | 42 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0173 others(39): Show |
47 | HG00423.hp1 HG00642.hp1 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.1007-1189_1007-118 others(6): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99720834 | |||||||
| chr1:99720834 | AACAC | A | 22 | a0001c0001t0001g0137 a0001c0001t0001g0146 a0001c0001t0001g0170 others(19): Show |
22 | HG01074.hp2 HG01106.hp1 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.1007-1191_1007-118 others(8): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99720834 | |||||||
| chr1:99720834 | AACACAC | A | 64 | a0001c0001t0001g0129 a0001c0001t0001g0172 a0001c0001t0001g0209 others(61): Show |
71 | HG00609.hp1 HG00621.hp1 HG00673.hp2 others(68): Show |
intron_variant | MODIFIER | c.1007-1193_1007-118 others(10): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99720834 | |||||||
| chr1:99720834 | AACACACA others(1): Show |
A | 11 | a0001c0001t0032g0145 a0001c0001t0032g0156 a0001c0002t0004g0084 others(8): Show |
11 | HG01109.hp2 HG01433.hp2 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.1007-1195_1007-118 others(12): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99720834 | |||||||
| chr1:99720834 | AACACACA others(3): Show |
A | 65 | a0001c0001t0001g0206 a0001c0001t0069g0131 a0001c0002t0002g0003 others(62): Show |
79 | HG00423.hp2 HG00621.hp2 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.1007-1197_1007-118 others(14): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99720834 | |||||||
| chr1:99720834 | AACACACA others(5): Show |
A | 11 | a0001c0002t0004g0058 a0001c0002t0004g0059 a0001c0002t0019g0278 others(8): Show |
11 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1007-1199_1007-118 others(16): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99720834 | |||||||
| chr1:99720834 | AACACACA others(7): Show |
A | 1 | a0001c0002t0002g0221 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1007-1201_1007-118 others(18): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99720834 | |||||||
| chr1:99720984 | A | G | 20 | a0001c0001t0001g0129 a0001c0002t0007g0117 a0001c0002t0007g0246 others(17): Show |
22 | HG01081.hp1 HG01192.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.1007-1337T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99720984 | |||||||
| chr1:99720987 | C | T | 1 | a0001c0001t0003g0132 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1007-1340G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99720987 | |||||||
| chr1:99721129 | C | G | 107 | a0001c0001t0001g0129 a0001c0001t0001g0137 a0001c0001t0001g0172 others(104): Show |
125 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(122): Show |
intron_variant | MODIFIER | c.1007-1482G>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99721129 | |||||||
| chr1:99721242 | G | A | 2 | a0001c0002t0024g0115 a0001c0002t0024g0116 |
2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1007-1595C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99721242 | |||||||
| chr1:99721349 | T | G | 1 | a0001c0002t0004g0068 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1007-1702A>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99721349 | |||||||
| chr1:99721364 | G | A | 6 | a0001c0001t0001g0129 a0001c0004t0002g0008 a0001c0004t0002g0038 others(3): Show |
7 | HG01081.hp1 HG01192.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1007-1717C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99721364 | |||||||
| chr1:99721475 | T | C | 31 | a0002c0003t0005g0025 a0002c0003t0005g0066 a0002c0003t0005g0227 others(28): Show |
33 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.1007-1828A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99721475 | |||||||
| chr1:99721796 | G | A | 110 | a0001c0001t0001g0129 a0001c0001t0001g0137 a0001c0001t0001g0172 others(107): Show |
128 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(125): Show |
intron_variant | MODIFIER | c.1007-2149C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99721796 | |||||||
| chr1:99721872 | T | C | 266 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0019 others(263): Show |
305 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(302): Show |
intron_variant | MODIFIER | c.1007-2225A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99721872 | |||||||
| chr1:99721908 | T | C | 1 | a0002c0003t0014g0240 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1007-2261A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99721908 | |||||||
| chr1:99722329 | T | A | 1 | a0001c0002t0009g0087 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1007-2682A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99722329 | |||||||
| chr1:99722388 | T | G | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | HG00738.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.1007-2741A>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99722388 | |||||||
| chr1:99722435 | G | A | 3 | a0001c0001t0003g0203 a0001c0001t0003g0205 a0001c0001t0033g0204 |
3 | NA18944.hp1 NA19079.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.1007-2788C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99722435 | |||||||
| chr1:99722452 | A | G | 1 | a0001c0002t0019g0278 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1007-2805T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99722452 | |||||||
| chr1:99722458 | A | T | 4 | a0002c0003t0015g0263 a0002c0003t0015g0264 a0002c0003t0021g0265 others(1): Show |
4 | HG02258.hp1 HG02280.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1007-2811T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99722458 | |||||||
| chr1:99722475 | A | G | 1 | a0002c0003t0037g0106 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1007-2828T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99722475 | |||||||
| chr1:99722567 | C | A | 54 | a0001c0002t0019g0094 a0001c0002t0019g0278 a0001c0002t0026g0100 others(51): Show |
56 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.1007-2920G>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99722567 | |||||||
| chr1:99722611 | A | G | 1 | a0001c0001t0001g0206 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1007-2964T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99722611 | |||||||
| chr1:99722760 | C | T | 77 | a0001c0001t0001g0137 a0001c0001t0001g0172 a0001c0001t0001g0206 others(74): Show |
90 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(87): Show |
intron_variant | MODIFIER | c.1007-3113G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99722760 | |||||||
| chr1:99722905 | A | T | 5 | a0002c0003t0005g0271 a0002c0003t0005g0273 a0002c0003t0005g0276 others(2): Show |
5 | NA18947.hp1 NA18978.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.1007-3258T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99722905 | |||||||
| chr1:99723015 | G | A | 7 | a0001c0001t0006g0099 a0001c0001t0006g0138 a0001c0001t0006g0139 others(4): Show |
8 | HG01346.hp2 HG01943.hp2 HG01993.hp1 others(5): Show |
intron_variant | MODIFIER | c.1007-3368C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99723015 | |||||||
| chr1:99723116 | A | C | 5 | a0001c0001t0003g0122 a0001c0001t0003g0123 a0001c0001t0003g0124 others(2): Show |
5 | NA19003.hp1 NA19010.hp1 NA19062.hp1 others(2): Show |
intron_variant | MODIFIER | c.1007-3469T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99723116 | |||||||
| chr1:99723378 | A | C | 1 | a0002c0003t0005g0267 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1007-3731T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99723378 | |||||||
| chr1:99723574 | A | G | 2 | a0001c0001t0001g0165 a0001c0001t0013g0186 |
2 | NA18971.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.1007-3927T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99723574 | |||||||
| chr1:99723658 | G | A | 1 | a0001c0002t0009g0095 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1007-4011C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99723658 | |||||||
| chr1:99723664 | C | T | 2 | a0001c0002t0019g0094 a0001c0002t0052g0259 |
2 | HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1007-4017G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99723664 | |||||||
| chr1:99723785 | G | A | 1 | a0001c0002t0019g0278 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1007-4138C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99723785 | |||||||
| chr1:99724244 | A | C | 1 | a0001c0001t0001g0185 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1006+4249T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99724244 | |||||||
| chr1:99724431 | C | G | 49 | a0002c0003t0005g0025 a0002c0003t0005g0066 a0002c0003t0005g0227 others(46): Show |
51 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.1006+4062G>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99724431 | |||||||
| chr1:99724454 | A | G | 3 | a0001c0001t0001g0173 a0001c0002t0019g0256 a0001c0002t0047g0034 |
3 | HG01496.hp1 HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1006+4039T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99724454 | |||||||
| chr1:99724541 | G | A | 107 | a0001c0001t0001g0129 a0001c0001t0001g0137 a0001c0001t0001g0172 others(104): Show |
125 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(122): Show |
intron_variant | MODIFIER | c.1006+3952C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99724541 | |||||||
| chr1:99724677 | T | C | 1 | a0001c0004t0002g0039 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1006+3816A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99724677 | |||||||
| chr1:99724735 | A | G | 2 | a0002c0003t0015g0263 a0002c0003t0015g0264 |
2 | HG02258.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1006+3758T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99724735 | |||||||
| chr1:99725128 | G | A | 1 | a0002c0003t0005g0245 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1006+3365C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99725128 | |||||||
| chr1:99725274 | G | A | 79 | a0001c0001t0001g0137 a0001c0001t0001g0172 a0001c0001t0001g0206 others(76): Show |
92 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(89): Show |
intron_variant | MODIFIER | c.1006+3219C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99725274 | |||||||
| chr1:99725287 | C | A | 54 | a0001c0002t0019g0094 a0001c0002t0019g0278 a0001c0002t0026g0100 others(51): Show |
56 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.1006+3206G>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99725287 | |||||||
| chr1:99725532 | G | A | 2 | a0002c0003t0021g0265 a0002c0003t0021g0266 |
2 | HG02896.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1006+2961C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99725532 | |||||||
| chr1:99725673 | G | A | 1 | a0001c0002t0024g0116 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1006+2820C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99725673 | |||||||
| chr1:99725737 | G | A | 2 | a0001c0002t0019g0256 a0001c0002t0047g0034 |
2 | HG01884.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1006+2756C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99725737 | |||||||
| chr1:99726335 | C | T | 65 | a0001c0001t0001g0206 a0001c0001t0069g0131 a0001c0002t0002g0003 others(62): Show |
78 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.1006+2158G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99726335 | |||||||
| chr1:99726714 | C | T | 2 | a0001c0002t0026g0100 a0001c0002t0026g0101 |
2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1006+1779G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99726714 | |||||||
| chr1:99727064 | T | G | 2 | a0001c0001t0003g0213 a0001c0001t0062g0199 |
2 | NA18747.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.1006+1429A>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99727064 | |||||||
| chr1:99727438 | C | T | 9 | a0001c0002t0019g0094 a0001c0002t0019g0278 a0001c0002t0026g0100 others(6): Show |
9 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1006+1055G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99727438 | |||||||
| chr1:99727472 | C | T | 1 | a0002c0003t0038g0270 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1006+1021G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99727472 | |||||||
| chr1:99727948 | T | A | 1 | a0002c0003t0037g0106 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1006+545A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99727948 | |||||||
| chr1:99728012 | C | T | 1 | a0002c0003t0015g0092 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1006+481G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99728012 | |||||||
| chr1:99728044 | C | T | 4 | a0001c0001t0001g0119 a0001c0001t0001g0152 a0001c0001t0020g0153 others(1): Show |
4 | HG01069.hp2 HG01167.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.1006+449G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99728044 | |||||||
| chr1:99728266 | AT | A | 14 | a0002c0003t0015g0092 a0002c0003t0015g0263 a0002c0003t0015g0264 others(11): Show |
14 | HG01891.hp1 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1006+226delA | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99728266 | |||||||
| chr1:99728282 | G | A | 4 | a0002c0003t0015g0263 a0002c0003t0015g0264 a0002c0003t0021g0265 others(1): Show |
4 | HG02258.hp1 HG02280.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1006+211C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99728282 | |||||||
| chr1:99728404 | C | A | 1 | a0001c0001t0069g0131 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1006+89G>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99728404 | |||||||
| chr1:99728415 | G | C | 2 | a0001c0002t0026g0100 a0001c0002t0026g0101 |
2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1006+78C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 9/16 | chr1 | 99728415 | |||||||
| chr1:99728644 | C | CAA | 3 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0195 |
3 | HG00639.hp1 HG01934.hp1 HG04115.hp1 |
splice_region_variant&intron_variant | LOW | c.859-6_859-5dupTT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 8/16 | chr1 | 99728644 | |||||||
| chr1:99728749 | C | G | 172 | a0001c0001t0001g0137 a0001c0001t0001g0172 a0001c0001t0001g0206 others(169): Show |
195 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(192): Show |
intron_variant | MODIFIER | c.859-109G>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 8/16 | chr1 | 99728749 | |||||||
| chr1:99729056 | G | T | 1 | a0001c0002t0002g0257 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.859-416C>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 8/16 | chr1 | 99729056 | |||||||
| chr1:99729075 | T | G | 2 | a0001c0001t0001g0172 a0001c0001t0067g0171 |
2 | NA18984.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.859-435A>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 8/16 | chr1 | 99729075 | |||||||
| chr1:99729082 | A | G | 1 | a0001c0001t0003g0200 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.859-442T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 8/16 | chr1 | 99729082 | |||||||
| chr1:99729174 | CAAA | C | 3 | a0001c0002t0019g0094 a0001c0002t0019g0278 a0001c0002t0052g0259 |
3 | HG02109.hp2 HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.858+473_858+475del others(3): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 8/16 | chr1 | 99729174 | |||||||
| chr1:99729290 | C | T | 3 | a0001c0001t0001g0180 a0001c0001t0001g0196 a0001c0001t0064g0161 |
3 | HG02280.hp1 HG02886.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.858+360G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 8/16 | chr1 | 99729290 | |||||||
| chr1:99729322 | C | CCT | 172 | a0001c0001t0001g0137 a0001c0001t0001g0172 a0001c0001t0001g0206 others(169): Show |
195 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(192): Show |
intron_variant | MODIFIER | c.858+326_858+327dup others(2): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 8/16 | chr1 | 99729322 | |||||||
| chr1:99729338 | G | A | 63 | a0001c0001t0001g0206 a0001c0001t0069g0131 a0001c0002t0002g0003 others(60): Show |
77 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.858+312C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 8/16 | chr1 | 99729338 | |||||||
| chr1:99729340 | CTGTA | C | 63 | a0001c0001t0001g0206 a0001c0001t0069g0131 a0001c0002t0002g0003 others(60): Show |
77 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.858+306_858+309del others(4): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 8/16 | chr1 | 99729340 | |||||||
| chr1:99729347 | C | CT | 63 | a0001c0001t0001g0206 a0001c0001t0069g0131 a0001c0002t0002g0003 others(60): Show |
77 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.858+302dupA | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 8/16 | chr1 | 99729347 | |||||||
| chr1:99729406 | G | A | 172 | a0001c0001t0001g0137 a0001c0001t0001g0172 a0001c0001t0001g0206 others(169): Show |
195 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(192): Show |
intron_variant | MODIFIER | c.858+244C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 8/16 | chr1 | 99729406 | |||||||
| chr1:99729458 | C | T | 172 | a0001c0001t0001g0137 a0001c0001t0001g0172 a0001c0001t0001g0206 others(169): Show |
195 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(192): Show |
intron_variant | MODIFIER | c.858+192G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 8/16 | chr1 | 99729458 | |||||||
| chr1:99729461 | C | G | 172 | a0001c0001t0001g0137 a0001c0001t0001g0172 a0001c0001t0001g0206 others(169): Show |
195 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(192): Show |
intron_variant | MODIFIER | c.858+189G>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 8/16 | chr1 | 99729461 | |||||||
| chr1:99729921 | A | G | 172 | a0001c0001t0001g0137 a0001c0001t0001g0172 a0001c0001t0001g0206 others(169): Show |
195 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(192): Show |
intron_variant | MODIFIER | c.760-173T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99729921 | |||||||
| chr1:99730029 | G | A | 1 | a0001c0002t0019g0278 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.760-281C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99730029 | |||||||
| chr1:99730260 | C | T | 171 | a0001c0001t0001g0137 a0001c0001t0001g0172 a0001c0001t0067g0171 others(168): Show |
194 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(191): Show |
intron_variant | MODIFIER | c.760-512G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99730260 | |||||||
| chr1:99730561 | A | T | 2 | a0001c0002t0024g0115 a0001c0002t0024g0116 |
2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.760-813T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99730561 | |||||||
| chr1:99730563 | A | T | 168 | a0001c0001t0001g0137 a0001c0001t0069g0131 a0001c0002t0002g0003 others(165): Show |
191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.760-815T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99730563 | |||||||
| chr1:99730585 | G | A | 1 | a0001c0001t0003g0126 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.760-837C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99730585 | |||||||
| chr1:99730593 | C | T | 2 | a0002c0003t0018g0096 a0002c0003t0018g0097 |
2 | HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.760-845G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99730593 | |||||||
| chr1:99730595 | A | C | 1 | a0002c0003t0037g0106 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.760-847T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99730595 | |||||||
| chr1:99730613 | G | A | 2 | a0001c0001t0001g0144 a0001c0002t0016g0225 |
2 | HG02155.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.760-865C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99730613 | |||||||
| chr1:99730634 | A | G | 12 | a0001c0002t0002g0003 a0001c0002t0002g0075 a0001c0002t0002g0076 others(9): Show |
15 | HG00621.hp2 HG00639.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.760-886T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99730634 | |||||||
| chr1:99730643 | A | G | 1 | a0002c0003t0005g0267 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.760-895T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99730643 | |||||||
| chr1:99730652 | G | A | 160 | a0001c0001t0001g0137 a0001c0002t0002g0003 a0001c0002t0002g0032 others(157): Show |
183 | HG00423.hp2 HG00621.hp2 HG00639.hp2 others(180): Show |
intron_variant | MODIFIER | c.760-904C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99730652 | |||||||
| chr1:99730664 | C | G | 2 | a0001c0001t0003g0132 a0001c0002t0007g0235 |
2 | HG01192.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.760-916G>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99730664 | |||||||
| chr1:99730683 | T | A | 1 | a0001c0002t0002g0254 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.760-935A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99730683 | |||||||
| chr1:99730683 | T | C | 5 | a0001c0002t0004g0004 a0001c0002t0004g0050 a0001c0002t0004g0073 others(2): Show |
7 | HG02027.hp1 HG02257.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.760-935A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99730683 | |||||||
| chr1:99730695 | G | A | 1 | a0001c0002t0007g0239 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.760-947C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99730695 | |||||||
| chr1:99730728 | A | G | 1 | a0001c0004t0007g0036 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.760-980T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99730728 | |||||||
| chr1:99730760 | A | G | 1 | a0002c0003t0005g0277 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.760-1012T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99730760 | |||||||
| chr1:99730824 | G | A | 61 | a0001c0001t0001g0137 a0001c0001t0001g0192 a0001c0002t0002g0221 others(58): Show |
64 | HG00673.hp2 HG01074.hp1 HG01074.hp2 others(61): Show |
intron_variant | MODIFIER | c.760-1076C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99730824 | |||||||
| chr1:99730866 | C | CA | 152 | a0001c0001t0001g0137 a0001c0001t0001g0162 a0001c0001t0001g0185 others(149): Show |
173 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(170): Show |
intron_variant | MODIFIER | c.760-1119dupT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99730866 | |||||||
| chr1:99730866 | C | CAA | 17 | a0001c0002t0002g0081 a0001c0002t0002g0226 a0001c0002t0002g0254 others(14): Show |
18 | HG01081.hp1 HG01192.hp1 HG02080.hp1 others(15): Show |
intron_variant | MODIFIER | c.760-1120_760-1119d others(4): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99730866 | |||||||
| chr1:99730866 | CA | C | 8 | a0001c0001t0001g0005 a0001c0001t0001g0194 a0001c0001t0013g0147 others(5): Show |
10 | HG02135.hp1 NA18954.hp2 NA18959.hp1 others(7): Show |
intron_variant | MODIFIER | c.760-1119delT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99730866 | |||||||
| chr1:99731054 | C | T | 108 | a0001c0001t0001g0137 a0001c0002t0002g0105 a0001c0002t0002g0111 others(105): Show |
118 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(115): Show |
intron_variant | MODIFIER | c.760-1306G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99731054 | |||||||
| chr1:99731105 | A | G | 75 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(72): Show |
86 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.760-1357T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99731105 | |||||||
| chr1:99731241 | A | G | 1 | a0001c0001t0006g0099 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.760-1493T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99731241 | |||||||
| chr1:99731295 | A | G | 1 | a0001c0002t0012g0061 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.760-1547T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99731295 | |||||||
| chr1:99731434 | T | G | 1 | a0002c0003t0010g0102 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.760-1686A>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99731434 | |||||||
| chr1:99731503 | T | C | 58 | a0001c0002t0002g0221 a0001c0002t0002g0224 a0001c0002t0002g0226 others(55): Show |
61 | HG00673.hp2 HG01074.hp1 HG01106.hp1 others(58): Show |
intron_variant | MODIFIER | c.760-1755A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99731503 | |||||||
| chr1:99731922 | A | G | 1 | a0001c0002t0002g0075 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.760-2174T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99731922 | |||||||
| chr1:99731935 | A | C | 1 | a0001c0002t0016g0220 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.760-2187T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99731935 | |||||||
| chr1:99732010 | T | C | 2 | a0002c0003t0023g0268 a0002c0003t0035g0275 |
2 | HG01891.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.760-2262A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99732010 | |||||||
| chr1:99732048 | T | C | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.760-2300A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99732048 | |||||||
| chr1:99732067 | G | C | 3 | a0001c0002t0019g0278 a0001c0002t0026g0100 a0001c0002t0026g0101 |
3 | HG02055.hp1 HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.760-2319C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99732067 | |||||||
| chr1:99732207 | C | T | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.760-2459G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99732207 | |||||||
| chr1:99732268 | C | A | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.760-2520G>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99732268 | |||||||
| chr1:99732503 | T | C | 96 | a0001c0002t0002g0105 a0001c0002t0002g0111 a0001c0002t0002g0112 others(93): Show |
105 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(102): Show |
intron_variant | MODIFIER | c.760-2755A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99732503 | |||||||
| chr1:99732542 | C | T | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.760-2794G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99732542 | |||||||
| chr1:99732600 | A | G | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.760-2852T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99732600 | |||||||
| chr1:99732707 | T | C | 9 | a0001c0002t0007g0117 a0001c0002t0008g0016 a0001c0002t0008g0107 others(6): Show |
10 | HG02145.hp1 HG02965.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.760-2959A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99732707 | |||||||
| chr1:99732741 | T | G | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.760-2993A>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99732741 | |||||||
| chr1:99732831 | T | C | 8 | a0001c0002t0007g0117 a0001c0002t0008g0016 a0001c0002t0008g0107 others(5): Show |
9 | HG02145.hp1 HG02965.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.760-3083A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99732831 | |||||||
| chr1:99732843 | A | G | 96 | a0001c0002t0002g0105 a0001c0002t0002g0111 a0001c0002t0002g0112 others(93): Show |
105 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(102): Show |
intron_variant | MODIFIER | c.760-3095T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99732843 | |||||||
| chr1:99732844 | AT | A | 93 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0019 others(90): Show |
109 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.760-3097delA | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99732844 | |||||||
| chr1:99732844 | ATTT | A | 57 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(54): Show |
70 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.760-3099_760-3097d others(5): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99732844 | |||||||
| chr1:99732844 | ATTTT | A | 109 | a0001c0002t0002g0105 a0001c0002t0002g0111 a0001c0002t0002g0112 others(106): Show |
119 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(116): Show |
intron_variant | MODIFIER | c.760-3100_760-3097d others(6): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99732844 | |||||||
| chr1:99732871 | T | A | 1 | a0001c0002t0007g0117 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.760-3123A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99732871 | |||||||
| chr1:99732954 | C | T | 1 | a0002c0003t0037g0106 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.760-3206G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99732954 | |||||||
| chr1:99733000 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.760-3252G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99733000 | |||||||
| chr1:99733045 | G | A | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.760-3297C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99733045 | |||||||
| chr1:99733151 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.760-3403C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99733151 | |||||||
| chr1:99733243 | C | T | 66 | a0001c0002t0002g0221 a0001c0002t0002g0224 a0001c0002t0002g0226 others(63): Show |
70 | HG00673.hp2 HG00735.hp2 HG01074.hp1 others(67): Show |
intron_variant | MODIFIER | c.760-3495G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99733243 | |||||||
| chr1:99733249 | A | C | 1 | a0002c0003t0005g0271 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.760-3501T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99733249 | |||||||
| chr1:99733333 | C | T | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.760-3585G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99733333 | |||||||
| chr1:99733546 | C | T | 2 | a0001c0002t0012g0060 a0001c0002t0057g0089 |
2 | NA18968.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.760-3798G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99733546 | |||||||
| chr1:99733579 | G | A | 1 | a0002c0003t0005g0231 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.760-3831C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99733579 | |||||||
| chr1:99733583 | G | A | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.760-3835C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99733583 | |||||||
| chr1:99733644 | C | A | 1 | a0002c0003t0014g0240 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.760-3896G>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99733644 | |||||||
| chr1:99733646 | A | G | 1 | a0002c0003t0005g0229 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.760-3898T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99733646 | |||||||
| chr1:99733675 | A | G | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.760-3927T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99733675 | |||||||
| chr1:99733694 | A | G | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.760-3946T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99733694 | |||||||
| chr1:99733888 | C | T | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.760-4140G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99733888 | |||||||
| chr1:99734011 | C | T | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.759+4075G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99734011 | |||||||
| chr1:99734012 | A | G | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.759+4074T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99734012 | |||||||
| chr1:99734279 | G | A | 1 | a0001c0002t0007g0117 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.759+3807C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99734279 | |||||||
| chr1:99734504 | GT | G | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.759+3581delA | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99734504 | |||||||
| chr1:99734506 | G | C | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.759+3580C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99734506 | |||||||
| chr1:99734539 | G | A | 1 | a0001c0002t0004g0049 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.759+3547C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99734539 | |||||||
| chr1:99734628 | C | T | 59 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(56): Show |
72 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.759+3458G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99734628 | |||||||
| chr1:99734723 | A | G | 12 | a0001c0002t0002g0105 a0001c0002t0002g0111 a0001c0002t0002g0112 others(9): Show |
13 | HG02145.hp1 HG02572.hp2 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.759+3363T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99734723 | |||||||
| chr1:99734730 | G | C | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.759+3356C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99734730 | |||||||
| chr1:99734823 | G | C | 12 | a0001c0002t0002g0105 a0001c0002t0002g0111 a0001c0002t0002g0112 others(9): Show |
13 | HG02145.hp1 HG02572.hp2 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.759+3263C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99734823 | |||||||
| chr1:99734885 | T | A | 2 | a0001c0004t0002g0039 a0001c0004t0002g0040 |
2 | HG03491.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.759+3201A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99734885 | |||||||
| chr1:99734992 | G | A | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.759+3094C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99734992 | |||||||
| chr1:99735053 | A | C | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.759+3033T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99735053 | |||||||
| chr1:99735124 | G | A | 5 | a0002c0003t0018g0218 a0002c0003t0023g0215 a0002c0003t0023g0268 others(2): Show |
5 | HG01891.hp1 HG02895.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.759+2962C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99735124 | |||||||
| chr1:99735169 | A | G | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.759+2917T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99735169 | |||||||
| chr1:99735176 | G | T | 1 | a0001c0002t0016g0219 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.759+2910C>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99735176 | |||||||
| chr1:99735397 | T | C | 1 | a0001c0002t0028g0093 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.759+2689A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99735397 | |||||||
| chr1:99735456 | G | A | 2 | a0001c0001t0001g0163 a0001c0001t0001g0190 |
2 | HG02015.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.759+2630C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99735456 | |||||||
| chr1:99735565 | G | C | 1 | a0001c0002t0012g0051 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.759+2521C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99735565 | |||||||
| chr1:99735581 | C | T | 5 | a0002c0003t0018g0218 a0002c0003t0023g0215 a0002c0003t0023g0268 others(2): Show |
5 | HG01891.hp1 HG02895.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.759+2505G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99735581 | |||||||
| chr1:99735688 | G | T | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.759+2398C>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99735688 | |||||||
| chr1:99735736 | T | C | 4 | a0002c0003t0015g0263 a0002c0003t0015g0264 a0002c0003t0021g0265 others(1): Show |
4 | HG02258.hp1 HG02280.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.759+2350A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99735736 | |||||||
| chr1:99735764 | C | T | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.759+2322G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99735764 | |||||||
| chr1:99735814 | C | T | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.759+2272G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99735814 | |||||||
| chr1:99735868 | C | T | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.759+2218G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99735868 | |||||||
| chr1:99735894 | G | A | 7 | a0001c0002t0047g0034 a0002c0003t0010g0015 a0002c0003t0010g0102 others(4): Show |
11 | HG00735.hp1 HG02109.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.759+2192C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99735894 | |||||||
| chr1:99736052 | T | C | 2 | a0001c0002t0024g0115 a0001c0002t0024g0116 |
2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.759+2034A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736052 | |||||||
| chr1:99736104 | A | G | 1 | a0001c0002t0002g0111 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.759+1982T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736104 | |||||||
| chr1:99736346 | A | T | 25 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(22): Show |
28 | HG00408.hp2 HG00423.hp1 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.759+1740T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736346 | |||||||
| chr1:99736422 | G | A | 1 | a0001c0002t0019g0278 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.759+1664C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736422 | |||||||
| chr1:99736527 | C | A | 1 | a0001c0001t0001g0195 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.759+1559G>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736527 | |||||||
| chr1:99736553 | A | G | 266 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0019 others(263): Show |
305 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(302): Show |
intron_variant | MODIFIER | c.759+1533T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736553 | |||||||
| chr1:99736560 | A | G | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.759+1526T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736560 | |||||||
| chr1:99736561 | T | C | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.759+1525A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736561 | |||||||
| chr1:99736577 | C | A | 1 | a0002c0003t0014g0027 | 2 | HG00735.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.759+1509G>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736577 | |||||||
| chr1:99736629 | A | G | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.759+1457T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736629 | |||||||
| chr1:99736631 | A | G | 21 | a0001c0002t0002g0056 a0001c0002t0002g0082 a0001c0002t0002g0085 others(18): Show |
21 | HG00673.hp1 HG00735.hp2 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.759+1455T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736631 | |||||||
| chr1:99736632 | G | A | 21 | a0001c0002t0002g0056 a0001c0002t0002g0082 a0001c0002t0002g0085 others(18): Show |
21 | HG00673.hp1 HG00735.hp2 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.759+1454C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736632 | |||||||
| chr1:99736632 | GT | G | 146 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(143): Show |
169 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(166): Show |
intron_variant | MODIFIER | c.759+1453delA | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736632 | |||||||
| chr1:99736633 | T | G | 21 | a0001c0002t0002g0056 a0001c0002t0002g0082 a0001c0002t0002g0085 others(18): Show |
21 | HG00673.hp1 HG00735.hp2 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.759+1453A>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736633 | |||||||
| chr1:99736667 | T | C | 57 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(54): Show |
70 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.759+1419A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736667 | |||||||
| chr1:99736676 | C | G | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.759+1410G>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736676 | |||||||
| chr1:99736719 | T | C | 93 | a0001c0002t0002g0221 a0001c0002t0002g0224 a0001c0002t0002g0226 others(90): Show |
102 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(99): Show |
intron_variant | MODIFIER | c.759+1367A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736719 | |||||||
| chr1:99736719 | T | G | 4 | a0001c0001t0001g0023 a0001c0001t0001g0163 a0001c0001t0001g0182 others(1): Show |
5 | HG02015.hp2 HG02132.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.759+1367A>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736719 | |||||||
| chr1:99736759 | TAA | T | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.759+1325_759+1326d others(4): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736759 | |||||||
| chr1:99736772 | T | TAATAA | 166 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(163): Show |
189 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(186): Show |
intron_variant | MODIFIER | c.759+1309_759+1313d others(7): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736772 | |||||||
| chr1:99736790 | T | A | 1 | a0002c0003t0023g0268 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.759+1296A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736790 | |||||||
| chr1:99736792 | A | T | 1 | a0002c0003t0023g0268 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.759+1294T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736792 | |||||||
| chr1:99736795 | T | A | 1 | a0002c0003t0023g0268 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.759+1291A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736795 | |||||||
| chr1:99736796 | A | T | 1 | a0002c0003t0023g0268 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.759+1290T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736796 | |||||||
| chr1:99736810 | A | AT | 166 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(163): Show |
189 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(186): Show |
intron_variant | MODIFIER | c.759+1275dupA | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736810 | |||||||
| chr1:99736812 | A | C | 59 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(56): Show |
72 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.759+1274T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736812 | |||||||
| chr1:99736813 | A | T | 1 | a0002c0003t0023g0268 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.759+1273T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736813 | |||||||
| chr1:99736820 | G | C | 17 | a0001c0004t0002g0008 a0001c0004t0002g0038 a0001c0004t0002g0039 others(14): Show |
18 | HG01081.hp1 HG01192.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.759+1266C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736820 | |||||||
| chr1:99736833 | T | TA | 108 | a0001c0002t0002g0105 a0001c0002t0002g0111 a0001c0002t0002g0112 others(105): Show |
118 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(115): Show |
intron_variant | MODIFIER | c.759+1252dupT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736833 | |||||||
| chr1:99736872 | C | A | 1 | a0001c0001t0006g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.759+1214G>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736872 | |||||||
| chr1:99736906 | A | T | 2 | a0001c0002t0024g0115 a0001c0002t0024g0116 |
2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.759+1180T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99736906 | |||||||
| chr1:99737032 | C | T | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.759+1054G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99737032 | |||||||
| chr1:99737034 | T | C | 1 | a0001c0004t0002g0040 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.759+1052A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99737034 | |||||||
| chr1:99737045 | A | C | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.759+1041T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99737045 | |||||||
| chr1:99737046 | C | CCCTT | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.759+1039_759+1040i others(6): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99737046 | |||||||
| chr1:99737068 | T | C | 1 | a0001c0002t0002g0105 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.759+1018A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99737068 | |||||||
| chr1:99737124 | T | C | 1 | a0001c0001t0068g0164 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.759+962A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99737124 | |||||||
| chr1:99737167 | G | A | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.759+919C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99737167 | |||||||
| chr1:99737273 | T | TA | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.759+812dupT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99737273 | |||||||
| chr1:99737287 | C | G | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.759+799G>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99737287 | |||||||
| chr1:99737344 | T | C | 2 | a0001c0002t0024g0115 a0001c0002t0024g0116 |
2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.759+742A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99737344 | |||||||
| chr1:99737549 | C | T | 12 | a0001c0002t0002g0105 a0001c0002t0002g0111 a0001c0002t0002g0112 others(9): Show |
13 | HG02145.hp1 HG02572.hp2 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.759+537G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99737549 | |||||||
| chr1:99737726 | T | C | 1 | a0002c0003t0005g0242 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.759+360A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99737726 | |||||||
| chr1:99737782 | G | A | 5 | a0002c0003t0010g0015 a0002c0003t0010g0102 a0002c0003t0017g0014 others(2): Show |
8 | HG02622.hp1 HG02809.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.759+304C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99737782 | |||||||
| chr1:99737868 | G | T | 2 | a0001c0002t0004g0004 a0001c0002t0004g0050 |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.759+218C>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99737868 | |||||||
| chr1:99737876 | G | A | 2 | a0002c0003t0018g0096 a0002c0003t0018g0097 |
2 | HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.759+210C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99737876 | |||||||
| chr1:99737888 | G | C | 2 | a0001c0002t0026g0100 a0001c0002t0026g0101 |
2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.759+198C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99737888 | |||||||
| chr1:99737899 | C | T | 2 | a0001c0002t0004g0058 a0001c0002t0004g0059 |
2 | HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.759+187G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99737899 | |||||||
| chr1:99737937 | T | G | 1 | a0002c0003t0015g0264 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.759+149A>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99737937 | |||||||
| chr1:99737945 | C | T | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.759+141G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99737945 | |||||||
| chr1:99737971 | G | A | 1 | a0001c0002t0007g0117 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.759+115C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99737971 | |||||||
| chr1:99738015 | A | G | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.759+71T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99738015 | |||||||
| chr1:99738041 | G | A | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.759+45C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 7/16 | chr1 | 99738041 | |||||||
| chr1:99738346 | C | T | 27 | a0001c0002t0024g0115 a0001c0002t0024g0116 a0001c0002t0043g0279 others(24): Show |
32 | HG00735.hp1 HG01081.hp1 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.577-78G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99738346 | |||||||
| chr1:99738443 | G | A | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.577-175C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99738443 | |||||||
| chr1:99738533 | G | A | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.577-265C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99738533 | |||||||
| chr1:99738577 | A | T | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.577-309T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99738577 | |||||||
| chr1:99738746 | T | C | 69 | a0001c0002t0002g0221 a0001c0002t0002g0224 a0001c0002t0002g0226 others(66): Show |
73 | HG00673.hp2 HG00735.hp2 HG01074.hp1 others(70): Show |
intron_variant | MODIFIER | c.577-478A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99738746 | |||||||
| chr1:99738812 | C | T | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.577-544G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99738812 | |||||||
| chr1:99738877 | C | T | 1 | a0001c0001t0003g0201 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.577-609G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99738877 | |||||||
| chr1:99738892 | C | A | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.577-624G>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99738892 | |||||||
| chr1:99738896 | C | T | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.577-628G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99738896 | |||||||
| chr1:99738925 | T | C | 1 | a0001c0001t0003g0024 | 2 | HG02155.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.577-657A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99738925 | |||||||
| chr1:99739090 | G | T | 2 | a0001c0001t0001g0162 a0001c0001t0001g0185 |
2 | HG00408.hp2 HG00609.hp2 |
intron_variant | MODIFIER | c.577-822C>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99739090 | |||||||
| chr1:99739221 | G | A | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.577-953C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99739221 | |||||||
| chr1:99739261 | C | A | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.577-993G>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99739261 | |||||||
| chr1:99739294 | A | C | 2 | a0001c0001t0001g0165 a0001c0001t0013g0186 |
2 | NA18971.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.577-1026T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99739294 | |||||||
| chr1:99739491 | G | T | 1 | a0001c0001t0006g0127 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.577-1223C>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99739491 | |||||||
| chr1:99739533 | G | A | 9 | a0001c0002t0002g0221 a0001c0002t0002g0224 a0001c0002t0002g0226 others(6): Show |
9 | HG01106.hp1 HG01256.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.576+1260C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99739533 | |||||||
| chr1:99739546 | G | T | 2 | a0002c0003t0017g0014 a0002c0003t0017g0103 |
3 | HG02896.hp1 HG02897.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.576+1247C>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99739546 | |||||||
| chr1:99739740 | A | G | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.576+1053T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99739740 | |||||||
| chr1:99739852 | T | C | 1 | a0001c0001t0001g0194 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.576+941A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99739852 | |||||||
| chr1:99739880 | G | GT | 107 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0019 others(104): Show |
123 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.576+912dupA | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99739880 | |||||||
| chr1:99739896 | A | C | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.576+897T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99739896 | |||||||
| chr1:99739993 | G | A | 25 | a0001c0001t0001g0206 a0001c0001t0003g0002 a0001c0001t0003g0006 others(22): Show |
32 | HG00408.hp1 HG02027.hp2 HG02056.hp2 others(29): Show |
intron_variant | MODIFIER | c.576+800C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99739993 | |||||||
| chr1:99740032 | A | G | 17 | a0001c0002t0007g0007 a0001c0002t0007g0232 a0001c0002t0007g0235 others(14): Show |
19 | HG00673.hp2 HG01192.hp2 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.576+761T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99740032 | |||||||
| chr1:99740194 | A | C | 1 | a0001c0002t0002g0111 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.576+599T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99740194 | |||||||
| chr1:99740218 | GA | G | 60 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(57): Show |
74 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.576+574delT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99740218 | |||||||
| chr1:99740596 | T | G | 1 | a0001c0001t0001g0159 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.576+197A>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99740596 | |||||||
| chr1:99740729 | C | T | 1 | a0001c0002t0047g0034 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.576+64G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99740729 | |||||||
| chr1:99740736 | G | A | 1 | a0001c0001t0003g0201 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.576+57C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 6/16 | chr1 | 99740736 | |||||||
| chr1:99741065 | A | G | 8 | a0001c0002t0019g0278 a0001c0002t0026g0100 a0001c0002t0026g0101 others(5): Show |
11 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.429-125T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 5/16 | chr1 | 99741065 | |||||||
| chr1:99741108 | C | T | 1 | a0001c0001t0069g0131 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.429-168G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 5/16 | chr1 | 99741108 | |||||||
| chr1:99741109 | G | C | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.429-169C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 5/16 | chr1 | 99741109 | |||||||
| chr1:99741245 | T | C | 74 | a0001c0002t0002g0221 a0001c0002t0002g0224 a0001c0002t0002g0226 others(71): Show |
81 | HG00673.hp2 HG00735.hp2 HG01074.hp1 others(78): Show |
intron_variant | MODIFIER | c.429-305A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 5/16 | chr1 | 99741245 | |||||||
| chr1:99741267 | T | C | 7 | a0001c0001t0001g0129 a0001c0001t0006g0099 a0001c0001t0006g0138 others(4): Show |
8 | HG01346.hp2 HG01943.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.429-327A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 5/16 | chr1 | 99741267 | |||||||
| chr1:99741324 | C | G | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.429-384G>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 5/16 | chr1 | 99741324 | |||||||
| chr1:99741340 | C | A | 66 | a0001c0002t0002g0221 a0001c0002t0002g0224 a0001c0002t0002g0226 others(63): Show |
70 | HG00673.hp2 HG00735.hp2 HG01074.hp1 others(67): Show |
intron_variant | MODIFIER | c.429-400G>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 5/16 | chr1 | 99741340 | |||||||
| chr1:99741424 | T | C | 1 | a0001c0002t0043g0279 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.429-484A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 5/16 | chr1 | 99741424 | |||||||
| chr1:99741602 | A | C | 2 | a0001c0002t0047g0034 a0002c0003t0014g0027 |
3 | HG00735.hp1 HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.428+577T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 5/16 | chr1 | 99741602 | |||||||
| chr1:99741641 | C | T | 1 | a0001c0002t0002g0054 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.428+538G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 5/16 | chr1 | 99741641 | |||||||
| chr1:99741651 | T | C | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.428+528A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 5/16 | chr1 | 99741651 | |||||||
| chr1:99741745 | A | G | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.428+434T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 5/16 | chr1 | 99741745 | |||||||
| chr1:99741771 | C | T | 1 | a0001c0002t0019g0278 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.428+408G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 5/16 | chr1 | 99741771 | |||||||
| chr1:99741939 | A | G | 1 | a0001c0001t0006g0130 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.428+240T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 5/16 | chr1 | 99741939 | |||||||
| chr1:99742553 | A | G | 2 | a0002c0003t0010g0110 a0002c0003t0039g0109 |
2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.334-280T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99742553 | |||||||
| chr1:99742598 | T | C | 1 | a0001c0001t0006g0183 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.334-325A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99742598 | |||||||
| chr1:99742719 | C | T | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.334-446G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99742719 | |||||||
| chr1:99742755 | T | A | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.334-482A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99742755 | |||||||
| chr1:99742759 | C | T | 8 | a0001c0002t0019g0278 a0001c0002t0026g0100 a0001c0002t0026g0101 others(5): Show |
11 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.334-486G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99742759 | |||||||
| chr1:99742783 | A | G | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.334-510T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99742783 | |||||||
| chr1:99742808 | T | C | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.334-535A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99742808 | |||||||
| chr1:99742872 | T | C | 76 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(73): Show |
87 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.334-599A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99742872 | |||||||
| chr1:99743174 | A | G | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.334-901T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99743174 | |||||||
| chr1:99743195 | G | A | 1 | a0001c0001t0001g0184 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.334-922C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99743195 | |||||||
| chr1:99743384 | T | A | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.334-1111A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99743384 | |||||||
| chr1:99743388 | T | C | 2 | a0002c0003t0005g0251 a0002c0003t0005g0252 |
2 | NA18980.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.334-1115A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99743388 | |||||||
| chr1:99743400 | G | A | 1 | a0001c0004t0007g0041 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.334-1127C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99743400 | |||||||
| chr1:99743645 | A | C | 1 | a0001c0002t0007g0232 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.334-1372T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99743645 | |||||||
| chr1:99743708 | T | C | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.334-1435A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99743708 | |||||||
| chr1:99743747 | G | A | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.334-1474C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99743747 | |||||||
| chr1:99743825 | G | A | 2 | a0002c0003t0018g0096 a0002c0003t0018g0097 |
2 | HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.334-1552C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99743825 | |||||||
| chr1:99743924 | G | A | 2 | a0001c0001t0001g0162 a0001c0001t0001g0185 |
2 | HG00408.hp2 HG00609.hp2 |
intron_variant | MODIFIER | c.334-1651C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99743924 | |||||||
| chr1:99744059 | G | C | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.334-1786C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99744059 | |||||||
| chr1:99744064 | T | TAAAA | 72 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(69): Show |
86 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.334-1795_334-1792d others(6): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99744064 | |||||||
| chr1:99744064 | T | TAAAAA | 17 | a0001c0002t0002g0105 a0001c0002t0002g0111 a0001c0002t0002g0112 others(14): Show |
18 | HG01167.hp2 HG02145.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.334-1796_334-1792d others(7): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99744064 | |||||||
| chr1:99744075 | A | AAAAAG | 5 | a0001c0002t0019g0278 a0001c0002t0026g0100 a0001c0002t0026g0101 others(2): Show |
6 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.334-1803_334-1802i others(7): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99744075 | |||||||
| chr1:99744075 | A | AAAAG | 65 | a0001c0002t0002g0221 a0001c0002t0002g0224 a0001c0002t0002g0226 others(62): Show |
69 | HG00673.hp2 HG00735.hp2 HG01074.hp1 others(66): Show |
intron_variant | MODIFIER | c.334-1806_334-1803d others(6): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99744075 | |||||||
| chr1:99744153 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.334-1880C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99744153 | |||||||
| chr1:99744164 | T | C | 5 | a0002c0003t0005g0271 a0002c0003t0005g0273 a0002c0003t0005g0276 others(2): Show |
5 | NA18947.hp1 NA18978.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.334-1891A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99744164 | |||||||
| chr1:99744213 | G | A | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.334-1940C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99744213 | |||||||
| chr1:99744403 | A | G | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.334-2130T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99744403 | |||||||
| chr1:99744424 | T | C | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.334-2151A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99744424 | |||||||
| chr1:99744452 | A | C | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.334-2179T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99744452 | |||||||
| chr1:99744510 | G | C | 22 | a0001c0002t0024g0115 a0001c0002t0024g0116 a0001c0002t0043g0279 others(19): Show |
24 | HG00735.hp1 HG01081.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.334-2237C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99744510 | |||||||
| chr1:99744553 | A | G | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.334-2280T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99744553 | |||||||
| chr1:99744578 | G | A | 22 | a0001c0002t0024g0115 a0001c0002t0024g0116 a0001c0002t0043g0279 others(19): Show |
24 | HG00735.hp1 HG01081.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.334-2305C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99744578 | |||||||
| chr1:99744599 | T | C | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.334-2326A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99744599 | |||||||
| chr1:99744707 | AC | A | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.334-2435delG | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99744707 | |||||||
| chr1:99744709 | C | G | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.334-2436G>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99744709 | |||||||
| chr1:99744723 | C | T | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.334-2450G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99744723 | |||||||
| chr1:99744865 | G | A | 1 | a0002c0003t0011g0253 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.333+2429C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99744865 | |||||||
| chr1:99744969 | CA | C | 95 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0019 others(92): Show |
110 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.333+2324delT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99744969 | |||||||
| chr1:99744969 | CAA | C | 7 | a0001c0001t0001g0129 a0001c0001t0001g0163 a0001c0001t0003g0198 others(4): Show |
7 | HG01255.hp1 HG01257.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.333+2323_333+2324d others(4): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99744969 | |||||||
| chr1:99744969 | CAAAAAAA others(3): Show |
C | 1 | a0001c0004t0002g0042 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.333+2315_333+2324d others(12): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99744969 | |||||||
| chr1:99744969 | CAAAAAAA others(4): Show |
C | 10 | a0001c0002t0058g0031 a0001c0004t0002g0008 a0001c0004t0002g0038 others(7): Show |
11 | HG01081.hp1 HG01192.hp1 HG02683.hp1 others(8): Show |
intron_variant | MODIFIER | c.333+2314_333+2324d others(13): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99744969 | |||||||
| chr1:99744969 | CAAAAAAA others(5): Show |
C | 156 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(153): Show |
178 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(175): Show |
intron_variant | MODIFIER | c.333+2313_333+2324d others(14): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99744969 | |||||||
| chr1:99744969 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0003g0024 | 2 | HG02155.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.333+2312_333+2324d others(15): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99744969 | |||||||
| chr1:99745259 | A | G | 57 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(54): Show |
70 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.333+2035T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99745259 | |||||||
| chr1:99745279 | G | C | 1 | a0002c0003t0037g0106 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.333+2015C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99745279 | |||||||
| chr1:99745323 | T | G | 1 | a0001c0001t0013g0160 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.333+1971A>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99745323 | |||||||
| chr1:99745366 | C | T | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.333+1928G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99745366 | |||||||
| chr1:99745407 | G | A | 2 | a0002c0003t0018g0096 a0002c0003t0018g0097 |
2 | HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.333+1887C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99745407 | |||||||
| chr1:99745416 | G | T | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.333+1878C>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99745416 | |||||||
| chr1:99745428 | A | T | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.333+1866T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99745428 | |||||||
| chr1:99745449 | C | T | 2 | a0001c0002t0024g0115 a0001c0002t0024g0116 |
2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.333+1845G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99745449 | |||||||
| chr1:99745482 | G | C | 57 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(54): Show |
70 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.333+1812C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99745482 | |||||||
| chr1:99745548 | G | T | 16 | a0001c0004t0002g0008 a0001c0004t0002g0038 a0001c0004t0002g0039 others(13): Show |
17 | HG01081.hp1 HG01192.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.333+1746C>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99745548 | |||||||
| chr1:99745561 | A | T | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.333+1733T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99745561 | |||||||
| chr1:99745607 | C | T | 1 | a0002c0003t0005g0231 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.333+1687G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99745607 | |||||||
| chr1:99745683 | C | CTAAATAA others(5): Show |
165 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(162): Show |
188 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(185): Show |
intron_variant | MODIFIER | c.333+1610_333+1611i others(14): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99745683 | |||||||
| chr1:99745683 | C | CTAAATAA others(9): Show |
1 | a0001c0004t0008g0044 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.333+1610_333+1611i others(18): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99745683 | |||||||
| chr1:99745755 | T | C | 2 | a0001c0002t0024g0115 a0001c0002t0024g0116 |
2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.333+1539A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99745755 | |||||||
| chr1:99745763 | C | T | 1 | a0001c0004t0002g0008 | 2 | HG01081.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.333+1531G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99745763 | |||||||
| chr1:99745888 | C | A | 4 | a0002c0003t0015g0263 a0002c0003t0015g0264 a0002c0003t0021g0265 others(1): Show |
4 | HG02258.hp1 HG02280.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.333+1406G>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99745888 | |||||||
| chr1:99745888 | C | G | 163 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(160): Show |
186 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(183): Show |
intron_variant | MODIFIER | c.333+1406G>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99745888 | |||||||
| chr1:99746003 | G | GTAC | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.333+1290_333+1291i others(5): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99746003 | |||||||
| chr1:99746004 | C | A | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.333+1290G>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99746004 | |||||||
| chr1:99746044 | A | G | 3 | a0001c0002t0004g0057 a0001c0002t0004g0090 a0001c0002t0027g0010 |
4 | HG02055.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.333+1250T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99746044 | |||||||
| chr1:99746171 | A | G | 1 | a0001c0001t0001g0162 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.333+1123T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99746171 | |||||||
| chr1:99746285 | T | C | 15 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(12): Show |
18 | HG00639.hp2 HG01261.hp2 HG01943.hp1 others(15): Show |
intron_variant | MODIFIER | c.333+1009A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99746285 | |||||||
| chr1:99746319 | T | C | 2 | a0001c0002t0002g0260 a0001c0002t0052g0259 |
2 | HG02486.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.333+975A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99746319 | |||||||
| chr1:99746482 | A | G | 1 | a0001c0001t0003g0207 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.333+812T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99746482 | |||||||
| chr1:99746556 | G | C | 1 | a0001c0001t0003g0143 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.333+738C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99746556 | |||||||
| chr1:99746884 | C | T | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.333+410G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99746884 | |||||||
| chr1:99746989 | A | G | 1 | a0001c0002t0002g0056 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.333+305T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99746989 | |||||||
| chr1:99746997 | C | T | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.333+297G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99746997 | |||||||
| chr1:99747016 | T | C | 1 | a0001c0001t0003g0207 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.333+278A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99747016 | |||||||
| chr1:99747069 | C | T | 1 | a0001c0001t0064g0161 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.333+225G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99747069 | |||||||
| chr1:99747106 | AAC | A | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.333+186_333+187del others(2): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99747106 | |||||||
| chr1:99747237 | G | T | 12 | a0001c0002t0002g0105 a0001c0002t0002g0111 a0001c0002t0002g0112 others(9): Show |
13 | HG02145.hp1 HG02572.hp2 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.333+57C>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 4/16 | chr1 | 99747237 | |||||||
| chr1:99747492 | G | C | 1 | a0001c0004t0008g0045 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.197-62C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 3/16 | chr1 | 99747492 | |||||||
| chr1:99747557 | T | A | 2 | a0001c0002t0024g0115 a0001c0002t0024g0116 |
2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.197-127A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 3/16 | chr1 | 99747557 | |||||||
| chr1:99747559 | T | C | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.197-129A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 3/16 | chr1 | 99747559 | |||||||
| chr1:99747595 | T | C | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.197-165A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 3/16 | chr1 | 99747595 | |||||||
| chr1:99747743 | C | T | 1 | a0001c0002t0055g0055 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.197-313G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 3/16 | chr1 | 99747743 | |||||||
| chr1:99747752 | T | C | 1 | a0001c0001t0001g0190 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.197-322A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 3/16 | chr1 | 99747752 | |||||||
| chr1:99747910 | G | T | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.197-480C>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 3/16 | chr1 | 99747910 | |||||||
| chr1:99748167 | T | TAA | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.196+405_196+406ins others(2): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 3/16 | chr1 | 99748167 | |||||||
| chr1:99748351 | AG | A | 67 | a0001c0002t0002g0221 a0001c0002t0002g0224 a0001c0002t0002g0226 others(64): Show |
72 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(69): Show |
intron_variant | MODIFIER | c.196+221delC | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 3/16 | chr1 | 99748351 | |||||||
| chr1:99748382 | C | T | 1 | a0001c0002t0002g0054 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.196+191G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 3/16 | chr1 | 99748382 | |||||||
| chr1:99748408 | T | C | 1 | a0002c0003t0017g0103 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.196+165A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 3/16 | chr1 | 99748408 | |||||||
| chr1:99748835 | T | A | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.-1+62A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 2/16 | chr1 | 99748835 | |||||||
| chr1:99748863 | T | C | 1 | a0001c0001t0013g0191 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-1+34A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 2/16 | chr1 | 99748863 | |||||||
| chr1:99749022 | G | A | 56 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(53): Show |
69 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.-105-21C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99749022 | |||||||
| chr1:99749078 | C | T | 56 | a0001c0002t0002g0221 a0001c0002t0002g0224 a0001c0002t0002g0226 others(53): Show |
60 | HG00673.hp2 HG00735.hp2 HG01074.hp1 others(57): Show |
intron_variant | MODIFIER | c.-105-77G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99749078 | |||||||
| chr1:99749122 | G | A | 1 | a0001c0002t0016g0225 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-105-121C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99749122 | |||||||
| chr1:99749138 | T | G | 2 | a0001c0002t0024g0115 a0001c0002t0024g0116 |
2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-105-137A>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99749138 | |||||||
| chr1:99749169 | G | A | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.-105-168C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99749169 | |||||||
| chr1:99749221 | G | C | 57 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(54): Show |
70 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.-105-220C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99749221 | |||||||
| chr1:99749280 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-105-279G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99749280 | |||||||
| chr1:99749434 | G | A | 1 | a0001c0002t0004g0029 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-105-433C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99749434 | |||||||
| chr1:99749442 | T | C | 59 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(56): Show |
72 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.-105-441A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99749442 | |||||||
| chr1:99749453 | G | A | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.-105-452C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99749453 | |||||||
| chr1:99749718 | G | A | 1 | a0001c0002t0012g0051 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-105-717C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99749718 | |||||||
| chr1:99749779 | A | C | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.-105-778T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99749779 | |||||||
| chr1:99749914 | T | A | 1 | a0001c0002t0009g0086 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-105-913A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99749914 | |||||||
| chr1:99750051 | G | C | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.-105-1050C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99750051 | |||||||
| chr1:99750064 | C | T | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.-105-1063G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99750064 | |||||||
| chr1:99750113 | T | C | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.-105-1112A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99750113 | |||||||
| chr1:99750163 | G | T | 1 | a0002c0003t0005g0230 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-105-1162C>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99750163 | |||||||
| chr1:99750293 | G | C | 2 | a0002c0003t0021g0265 a0002c0003t0021g0266 |
2 | HG02896.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-105-1292C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99750293 | |||||||
| chr1:99750325 | A | C | 1 | a0001c0002t0019g0278 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-105-1324T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99750325 | |||||||
| chr1:99750392 | T | C | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.-105-1391A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99750392 | |||||||
| chr1:99750425 | T | C | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.-105-1424A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99750425 | |||||||
| chr1:99750490 | T | A | 1 | a0001c0002t0004g0083 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-105-1489A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99750490 | |||||||
| chr1:99750677 | G | GA | 159 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(156): Show |
179 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(176): Show |
intron_variant | MODIFIER | c.-105-1677dupT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99750677 | |||||||
| chr1:99750677 | G | GAA | 8 | a0001c0002t0019g0278 a0001c0002t0026g0100 a0001c0002t0026g0101 others(5): Show |
11 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-105-1678_-105-167 others(6): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99750677 | |||||||
| chr1:99750752 | G | A | 2 | a0001c0002t0024g0115 a0001c0002t0024g0116 |
2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-105-1751C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99750752 | |||||||
| chr1:99750773 | G | T | 1 | a0001c0001t0064g0161 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-105-1772C>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99750773 | |||||||
| chr1:99750949 | A | C | 2 | a0002c0003t0018g0096 a0002c0003t0018g0097 |
2 | HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-105-1948T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99750949 | |||||||
| chr1:99751039 | C | G | 10 | a0001c0004t0002g0008 a0001c0004t0002g0038 a0001c0004t0002g0039 others(7): Show |
11 | HG01081.hp1 HG01192.hp1 HG02683.hp1 others(8): Show |
intron_variant | MODIFIER | c.-105-2038G>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99751039 | |||||||
| chr1:99751130 | C | A | 1 | a0001c0001t0001g0192 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-105-2129G>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99751130 | |||||||
| chr1:99751201 | T | TA | 7 | a0001c0001t0001g0206 a0001c0001t0003g0202 a0001c0001t0003g0203 others(4): Show |
7 | NA18944.hp1 NA18952.hp2 NA18975.hp1 others(4): Show |
intron_variant | MODIFIER | c.-105-2201dupT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99751201 | |||||||
| chr1:99751557 | T | C | 1 | a0001c0001t0013g0191 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-105-2556A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99751557 | |||||||
| chr1:99751712 | G | A | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.-105-2711C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99751712 | |||||||
| chr1:99751847 | A | G | 1 | a0001c0001t0032g0145 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-105-2846T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99751847 | |||||||
| chr1:99751920 | T | G | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.-105-2919A>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99751920 | |||||||
| chr1:99752027 | C | T | 1 | a0001c0002t0043g0279 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-105-3026G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99752027 | |||||||
| chr1:99752116 | T | G | 1 | a0001c0002t0019g0278 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-105-3115A>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99752116 | |||||||
| chr1:99752127 | C | A | 2 | a0001c0002t0024g0115 a0001c0002t0024g0116 |
2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-105-3126G>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99752127 | |||||||
| chr1:99752332 | G | A | 20 | a0001c0002t0024g0115 a0001c0002t0024g0116 a0001c0002t0043g0279 others(17): Show |
21 | HG01081.hp1 HG01167.hp2 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.-105-3331C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99752332 | |||||||
| chr1:99752632 | C | T | 22 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0019 others(19): Show |
27 | HG00738.hp2 HG01069.hp2 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.-105-3631G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99752632 | |||||||
| chr1:99752691 | A | G | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.-105-3690T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99752691 | |||||||
| chr1:99752694 | T | C | 3 | a0001c0002t0002g0085 a0001c0002t0004g0012 a0001c0002t0004g0084 |
4 | HG00423.hp2 HG02135.hp2 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.-105-3693A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99752694 | |||||||
| chr1:99752709 | A | T | 41 | a0001c0002t0002g0105 a0001c0002t0002g0111 a0001c0002t0002g0112 others(38): Show |
46 | HG01081.hp1 HG01167.hp2 HG01192.hp1 others(43): Show |
intron_variant | MODIFIER | c.-105-3708T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99752709 | |||||||
| chr1:99752863 | A | G | 1 | a0002c0003t0015g0092 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-105-3862T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99752863 | |||||||
| chr1:99752872 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-105-3871A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99752872 | |||||||
| chr1:99752904 | A | G | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.-105-3903T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99752904 | |||||||
| chr1:99752967 | C | A | 1 | a0001c0002t0009g0086 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-105-3966G>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99752967 | |||||||
| chr1:99753231 | A | AG | 164 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(161): Show |
187 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(184): Show |
intron_variant | MODIFIER | c.-105-4231_-105-423 others(5): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99753231 | |||||||
| chr1:99753232 | A | G | 1 | a0001c0002t0058g0031 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-105-4231T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99753232 | |||||||
| chr1:99753255 | T | C | 1 | a0001c0001t0006g0193 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-105-4254A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99753255 | |||||||
| chr1:99753403 | T | A | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.-105-4402A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99753403 | |||||||
| chr1:99753420 | G | A | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.-105-4419C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99753420 | |||||||
| chr1:99753454 | C | T | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.-105-4453G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99753454 | |||||||
| chr1:99753471 | A | G | 1 | a0001c0002t0025g0053 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-105-4470T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99753471 | |||||||
| chr1:99753490 | G | A | 2 | a0001c0002t0026g0100 a0001c0002t0026g0101 |
2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.-105-4489C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99753490 | |||||||
| chr1:99753539 | G | A | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.-105-4538C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99753539 | |||||||
| chr1:99753603 | T | TA | 18 | a0001c0002t0002g0221 a0001c0002t0002g0224 a0001c0002t0002g0226 others(15): Show |
18 | HG01106.hp1 HG01256.hp2 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.-105-4603dupT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99753603 | |||||||
| chr1:99753609 | A | G | 21 | a0001c0002t0024g0115 a0001c0002t0024g0116 a0001c0002t0043g0279 others(18): Show |
22 | HG01081.hp1 HG01167.hp2 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.-105-4608T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99753609 | |||||||
| chr1:99753639 | G | C | 1 | a0001c0002t0047g0034 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-105-4638C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99753639 | |||||||
| chr1:99753816 | G | A | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.-105-4815C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99753816 | |||||||
| chr1:99753874 | T | C | 1 | a0002c0003t0018g0097 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-105-4873A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99753874 | |||||||
| chr1:99753879 | T | C | 155 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(152): Show |
177 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(174): Show |
intron_variant | MODIFIER | c.-105-4878A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99753879 | |||||||
| chr1:99754120 | G | A | 1 | a0001c0002t0047g0034 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-105-5119C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99754120 | |||||||
| chr1:99754374 | G | A | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.-105-5373C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99754374 | |||||||
| chr1:99754495 | G | C | 4 | a0001c0002t0002g0254 a0001c0002t0025g0261 a0001c0002t0045g0255 others(1): Show |
4 | HG03209.hp1 HG03453.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-105-5494C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99754495 | |||||||
| chr1:99754507 | A | AAG | 11 | a0001c0001t0001g0137 a0001c0001t0006g0118 a0001c0001t0006g0128 others(8): Show |
11 | HG00741.hp2 HG01074.hp2 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.-105-5508_-105-550 others(6): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99754507 | |||||||
| chr1:99754507 | A | G | 6 | a0001c0002t0019g0278 a0002c0003t0010g0015 a0002c0003t0010g0102 others(3): Show |
9 | HG02109.hp2 HG02622.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.-105-5506T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99754507 | |||||||
| chr1:99754507 | AAG | A | 159 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(156): Show |
179 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(176): Show |
intron_variant | MODIFIER | c.-105-5508_-105-550 others(6): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99754507 | |||||||
| chr1:99754509 | G | A | 8 | a0001c0002t0019g0278 a0001c0002t0026g0100 a0001c0002t0026g0101 others(5): Show |
11 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-105-5508C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99754509 | |||||||
| chr1:99754641 | G | A | 2 | a0001c0002t0024g0115 a0001c0002t0024g0116 |
2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-105-5640C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99754641 | |||||||
| chr1:99754840 | C | T | 1 | a0001c0002t0019g0256 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-105-5839G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99754840 | |||||||
| chr1:99754869 | T | G | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.-105-5868A>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99754869 | |||||||
| chr1:99754904 | G | A | 168 | a0001c0001t0001g0194 a0001c0002t0002g0003 a0001c0002t0002g0032 others(165): Show |
191 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(188): Show |
intron_variant | MODIFIER | c.-105-5903C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99754904 | |||||||
| chr1:99754966 | G | C | 1 | a0001c0002t0009g0087 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-105-5965C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99754966 | |||||||
| chr1:99755044 | T | C | 1 | a0002c0003t0005g0267 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-105-6043A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99755044 | |||||||
| chr1:99755077 | T | A | 166 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(163): Show |
189 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(186): Show |
intron_variant | MODIFIER | c.-105-6076A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99755077 | |||||||
| chr1:99755080 | T | A | 2 | a0001c0002t0024g0115 a0001c0002t0024g0116 |
2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-105-6079A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99755080 | |||||||
| chr1:99755191 | C | A | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.-105-6190G>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99755191 | |||||||
| chr1:99755191 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-105-6190G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99755191 | |||||||
| chr1:99755263 | T | TA | 161 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(158): Show |
184 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(181): Show |
intron_variant | MODIFIER | c.-105-6263dupT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99755263 | |||||||
| chr1:99755264 | A | T | 1 | a0001c0001t0001g0209 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-105-6263T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99755264 | |||||||
| chr1:99755282 | C | T | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.-105-6281G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99755282 | |||||||
| chr1:99755335 | A | G | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.-105-6334T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99755335 | |||||||
| chr1:99755407 | C | T | 1 | a0001c0002t0045g0255 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-105-6406G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99755407 | |||||||
| chr1:99755408 | G | A | 1 | a0001c0002t0009g0088 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-105-6407C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99755408 | |||||||
| chr1:99755457 | G | A | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.-105-6456C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99755457 | |||||||
| chr1:99755622 | G | A | 1 | a0001c0002t0043g0279 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-105-6621C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99755622 | |||||||
| chr1:99755754 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-105-6753C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99755754 | |||||||
| chr1:99755808 | A | G | 1 | a0001c0002t0002g0254 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-105-6807T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99755808 | |||||||
| chr1:99755844 | C | T | 1 | a0002c0003t0005g0227 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-105-6843G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99755844 | |||||||
| chr1:99755845 | C | T | 1 | a0002c0003t0005g0227 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-105-6844G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99755845 | |||||||
| chr1:99755930 | T | A | 1 | a0001c0001t0001g0196 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-105-6929A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99755930 | |||||||
| chr1:99756047 | A | C | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.-105-7046T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99756047 | |||||||
| chr1:99756064 | G | A | 17 | a0001c0004t0002g0008 a0001c0004t0002g0038 a0001c0004t0002g0039 others(14): Show |
18 | HG01081.hp1 HG01192.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.-105-7063C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99756064 | |||||||
| chr1:99756332 | C | T | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.-105-7331G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99756332 | |||||||
| chr1:99756372 | C | T | 8 | a0001c0002t0019g0278 a0001c0002t0026g0100 a0001c0002t0026g0101 others(5): Show |
11 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-105-7371G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99756372 | |||||||
| chr1:99756450 | CA | C | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.-105-7450delT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99756450 | |||||||
| chr1:99756543 | T | A | 67 | a0001c0002t0002g0221 a0001c0002t0002g0224 a0001c0002t0002g0226 others(64): Show |
72 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(69): Show |
intron_variant | MODIFIER | c.-105-7542A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99756543 | |||||||
| chr1:99756547 | A | C | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.-105-7546T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99756547 | |||||||
| chr1:99756663 | A | T | 38 | a0001c0002t0007g0007 a0001c0002t0007g0232 a0001c0002t0007g0235 others(35): Show |
42 | HG00673.hp2 HG00735.hp2 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.-105-7662T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99756663 | |||||||
| chr1:99756684 | G | A | 7 | a0001c0002t0026g0100 a0001c0002t0026g0101 a0002c0003t0010g0015 others(4): Show |
10 | HG02055.hp1 HG02451.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.-105-7683C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99756684 | |||||||
| chr1:99756691 | T | C | 1 | a0001c0002t0047g0034 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-105-7690A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99756691 | |||||||
| chr1:99756731 | A | G | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.-105-7730T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99756731 | |||||||
| chr1:99756748 | T | A | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.-105-7747A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99756748 | |||||||
| chr1:99756847 | T | C | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.-105-7846A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99756847 | |||||||
| chr1:99756923 | A | T | 1 | a0001c0001t0001g0209 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-105-7922T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99756923 | |||||||
| chr1:99757080 | CT | C | 35 | a0001c0001t0001g0197 a0001c0001t0003g0125 a0001c0001t0003g0208 others(32): Show |
40 | HG00735.hp1 HG01167.hp2 HG01891.hp1 others(37): Show |
intron_variant | MODIFIER | c.-105-8080delA | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99757080 | |||||||
| chr1:99757097 | A | T | 8 | a0001c0002t0019g0278 a0001c0002t0026g0100 a0001c0002t0026g0101 others(5): Show |
11 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-105-8096T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99757097 | |||||||
| chr1:99757272 | T | C | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.-105-8271A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99757272 | |||||||
| chr1:99757297 | T | A | 11 | a0002c0003t0014g0027 a0002c0003t0015g0263 a0002c0003t0015g0264 others(8): Show |
12 | HG00735.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.-105-8296A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99757297 | |||||||
| chr1:99757501 | C | T | 1 | a0001c0004t0007g0035 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-105-8500G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99757501 | |||||||
| chr1:99757527 | A | G | 1 | a0001c0002t0047g0034 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-105-8526T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99757527 | |||||||
| chr1:99757598 | G | A | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.-105-8597C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99757598 | |||||||
| chr1:99757937 | G | C | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.-106+8670C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99757937 | |||||||
| chr1:99757948 | AG | A | 14 | a0001c0002t0002g0105 a0001c0002t0002g0111 a0001c0002t0002g0112 others(11): Show |
15 | HG01109.hp2 HG02145.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.-106+8658delC | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99757948 | |||||||
| chr1:99757949 | GGA | G | 153 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(150): Show |
175 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(172): Show |
intron_variant | MODIFIER | c.-106+8656_-106+865 others(6): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99757949 | |||||||
| chr1:99757950 | GA | G | 47 | a0001c0001t0001g0129 a0001c0001t0001g0137 a0001c0001t0001g0142 others(44): Show |
55 | HG00408.hp1 HG00741.hp2 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.-106+8656delT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99757950 | |||||||
| chr1:99758063 | G | C | 21 | a0001c0002t0024g0115 a0001c0002t0024g0116 a0001c0002t0043g0279 others(18): Show |
22 | HG01081.hp1 HG01167.hp2 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.-106+8544C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99758063 | |||||||
| chr1:99758446 | G | A | 5 | a0002c0003t0018g0218 a0002c0003t0023g0215 a0002c0003t0023g0268 others(2): Show |
5 | HG01891.hp1 HG02895.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.-106+8161C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99758446 | |||||||
| chr1:99758542 | G | A | 1 | a0001c0002t0004g0090 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-106+8065C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99758542 | |||||||
| chr1:99758570 | C | T | 2 | a0001c0002t0024g0115 a0001c0002t0024g0116 |
2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-106+8037G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99758570 | |||||||
| chr1:99758579 | C | T | 90 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(87): Show |
105 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(102): Show |
intron_variant | MODIFIER | c.-106+8028G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99758579 | |||||||
| chr1:99758609 | CAT | C | 165 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(162): Show |
188 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(185): Show |
intron_variant | MODIFIER | c.-106+7996_-106+799 others(6): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99758609 | |||||||
| chr1:99758663 | T | C | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.-106+7944A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99758663 | |||||||
| chr1:99758716 | TGGGCAAA others(16): Show |
T | 2 | a0002c0003t0018g0096 a0002c0003t0018g0097 |
2 | HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-106+7868_-106+789 others(27): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99758716 | |||||||
| chr1:99758740 | T | C | 2 | a0002c0003t0018g0096 a0002c0003t0018g0097 |
2 | HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-106+7867A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99758740 | |||||||
| chr1:99758827 | C | G | 166 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(163): Show |
189 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(186): Show |
intron_variant | MODIFIER | c.-106+7780G>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99758827 | |||||||
| chr1:99758843 | C | T | 165 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(162): Show |
188 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(185): Show |
intron_variant | MODIFIER | c.-106+7764G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99758843 | |||||||
| chr1:99758848 | G | A | 2 | a0002c0003t0018g0096 a0002c0003t0018g0097 |
2 | HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-106+7759C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99758848 | |||||||
| chr1:99758850 | G | A | 1 | a0002c0003t0015g0092 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-106+7757C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99758850 | |||||||
| chr1:99758894 | G | C | 26 | a0001c0001t0001g0206 a0001c0001t0001g0209 a0001c0001t0003g0002 others(23): Show |
33 | HG00408.hp1 HG00609.hp1 HG02027.hp2 others(30): Show |
intron_variant | MODIFIER | c.-106+7713C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99758894 | |||||||
| chr1:99758927 | C | T | 9 | a0001c0002t0002g0221 a0001c0002t0002g0224 a0001c0002t0002g0226 others(6): Show |
9 | HG01106.hp1 HG01256.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-106+7680G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99758927 | |||||||
| chr1:99759006 | C | G | 2 | a0002c0003t0018g0096 a0002c0003t0018g0097 |
2 | HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-106+7601G>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99759006 | |||||||
| chr1:99759050 | C | G | 80 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(77): Show |
94 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(91): Show |
intron_variant | MODIFIER | c.-106+7557G>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99759050 | |||||||
| chr1:99759055 | C | T | 2 | a0001c0002t0024g0115 a0001c0002t0024g0116 |
2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-106+7552G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99759055 | |||||||
| chr1:99759056 | G | C | 2 | a0002c0003t0018g0096 a0002c0003t0018g0097 |
2 | HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-106+7551C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99759056 | |||||||
| chr1:99759080 | A | G | 2 | a0002c0003t0018g0096 a0002c0003t0018g0097 |
2 | HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-106+7527T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99759080 | |||||||
| chr1:99759095 | C | T | 1 | a0002c0003t0022g0013 | 2 | NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-106+7512G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99759095 | |||||||
| chr1:99759391 | T | C | 1 | a0002c0003t0038g0270 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-106+7216A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99759391 | |||||||
| chr1:99759583 | A | G | 8 | a0001c0002t0019g0278 a0001c0002t0026g0100 a0001c0002t0026g0101 others(5): Show |
11 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-106+7024T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99759583 | |||||||
| chr1:99759628 | A | G | 1 | a0002c0003t0014g0217 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-106+6979T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99759628 | |||||||
| chr1:99759687 | T | C | 2 | a0003c0005t0010g0046 a0003c0005t0010g0047 |
2 | HG02451.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-106+6920A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99759687 | |||||||
| chr1:99759761 | C | T | 153 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(150): Show |
175 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(172): Show |
intron_variant | MODIFIER | c.-106+6846G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99759761 | |||||||
| chr1:99760041 | C | T | 5 | a0002c0003t0010g0015 a0002c0003t0010g0102 a0002c0003t0017g0014 others(2): Show |
8 | HG02622.hp1 HG02809.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-106+6566G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99760041 | |||||||
| chr1:99760149 | T | C | 2 | a0001c0002t0024g0115 a0001c0002t0024g0116 |
2 | HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-106+6458A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99760149 | |||||||
| chr1:99760258 | T | C | 7 | a0001c0002t0026g0100 a0001c0002t0026g0101 a0002c0003t0010g0015 others(4): Show |
10 | HG02055.hp1 HG02451.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.-106+6349A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99760258 | |||||||
| chr1:99760319 | G | A | 1 | a0001c0002t0007g0117 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-106+6288C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99760319 | |||||||
| chr1:99760532 | A | T | 1 | a0001c0002t0004g0009 | 2 | HG03490.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-106+6075T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99760532 | |||||||
| chr1:99760698 | G | A | 5 | a0002c0003t0005g0271 a0002c0003t0005g0273 a0002c0003t0005g0276 others(2): Show |
5 | NA18947.hp1 NA18978.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.-106+5909C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99760698 | |||||||
| chr1:99760709 | G | A | 2 | a0002c0003t0018g0096 a0002c0003t0018g0097 |
2 | HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-106+5898C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99760709 | |||||||
| chr1:99761178 | G | A | 5 | a0002c0003t0010g0015 a0002c0003t0010g0102 a0002c0003t0017g0014 others(2): Show |
8 | HG02622.hp1 HG02809.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-106+5429C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99761178 | |||||||
| chr1:99761191 | A | G | 2 | a0001c0002t0026g0100 a0001c0002t0026g0101 |
2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.-106+5416T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99761191 | |||||||
| chr1:99761215 | G | A | 1 | a0001c0001t0006g0210 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-106+5392C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99761215 | |||||||
| chr1:99761367 | A | G | 1 | a0001c0002t0019g0094 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-106+5240T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99761367 | |||||||
| chr1:99761538 | C | A | 1 | a0001c0001t0006g0099 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-106+5069G>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99761538 | |||||||
| chr1:99761788 | TA | T | 78 | a0001c0001t0003g0126 a0001c0002t0002g0003 a0001c0002t0002g0032 others(75): Show |
92 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(89): Show |
intron_variant | MODIFIER | c.-106+4818delT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99761788 | |||||||
| chr1:99761877 | A | G | 1 | a0001c0002t0002g0105 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-106+4730T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99761877 | |||||||
| chr1:99761896 | T | C | 2 | a0002c0003t0018g0096 a0002c0003t0018g0097 |
2 | HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-106+4711A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99761896 | |||||||
| chr1:99762401 | C | T | 1 | a0001c0002t0004g0049 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-106+4206G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99762401 | |||||||
| chr1:99762476 | T | C | 1 | a0001c0002t0028g0093 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-106+4131A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99762476 | |||||||
| chr1:99762479 | C | CTT | 56 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(53): Show |
69 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.-106+4126_-106+412 others(6): Show |
FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99762479 | |||||||
| chr1:99762513 | A | G | 1 | a0001c0002t0028g0216 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-106+4094T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99762513 | |||||||
| chr1:99762711 | A | C | 5 | a0001c0001t0003g0122 a0001c0001t0003g0123 a0001c0001t0003g0124 others(2): Show |
5 | NA19003.hp1 NA19010.hp1 NA19062.hp1 others(2): Show |
intron_variant | MODIFIER | c.-106+3896T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99762711 | |||||||
| chr1:99762890 | T | C | 1 | a0001c0002t0009g0095 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-106+3717A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99762890 | |||||||
| chr1:99762951 | T | C | 4 | a0001c0001t0003g0211 a0001c0001t0003g0212 a0001c0001t0003g0213 others(1): Show |
4 | HG02027.hp2 NA18747.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.-106+3656A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99762951 | |||||||
| chr1:99763250 | C | T | 1 | a0002c0003t0023g0215 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-106+3357G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99763250 | |||||||
| chr1:99763357 | A | G | 2 | a0001c0002t0026g0100 a0001c0002t0026g0101 |
2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.-106+3250T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99763357 | |||||||
| chr1:99763736 | T | C | 2 | a0002c0003t0018g0096 a0002c0003t0018g0097 |
2 | HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-106+2871A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99763736 | |||||||
| chr1:99763817 | G | A | 57 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(54): Show |
70 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.-106+2790C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99763817 | |||||||
| chr1:99763859 | A | G | 1 | a0001c0001t0034g0120 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-106+2748T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99763859 | |||||||
| chr1:99763868 | C | CA | 74 | a0001c0002t0002g0003 a0001c0002t0002g0054 a0001c0002t0002g0056 others(71): Show |
88 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.-106+2738dupT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99763868 | |||||||
| chr1:99763868 | CA | C | 89 | a0001c0001t0001g0119 a0001c0001t0006g0118 a0001c0002t0002g0105 others(86): Show |
98 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(95): Show |
intron_variant | MODIFIER | c.-106+2738delT | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99763868 | |||||||
| chr1:99764066 | T | A | 1 | a0002c0003t0005g0277 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-106+2541A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99764066 | |||||||
| chr1:99764321 | G | C | 1 | a0001c0002t0019g0094 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-106+2286C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99764321 | |||||||
| chr1:99764482 | A | T | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.-106+2125T>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99764482 | |||||||
| chr1:99764555 | C | T | 167 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(164): Show |
190 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(187): Show |
intron_variant | MODIFIER | c.-106+2052G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99764555 | |||||||
| chr1:99764582 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-106+2025G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99764582 | |||||||
| chr1:99764641 | C | T | 75 | a0001c0002t0002g0221 a0001c0002t0002g0224 a0001c0002t0002g0226 others(72): Show |
83 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(80): Show |
intron_variant | MODIFIER | c.-106+1966G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99764641 | |||||||
| chr1:99765123 | A | G | 1 | a0001c0002t0004g0029 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-106+1484T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99765123 | |||||||
| chr1:99765140 | A | C | 1 | a0001c0004t0008g0028 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-106+1467T>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99765140 | |||||||
| chr1:99765285 | C | T | 1 | a0001c0001t0006g0099 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-106+1322G>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99765285 | |||||||
| chr1:99765311 | T | C | 67 | a0001c0002t0002g0221 a0001c0002t0002g0224 a0001c0002t0002g0226 others(64): Show |
72 | HG00673.hp2 HG00735.hp1 HG00735.hp2 others(69): Show |
intron_variant | MODIFIER | c.-106+1296A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99765311 | |||||||
| chr1:99765511 | G | C | 2 | a0002c0003t0018g0096 a0002c0003t0018g0097 |
2 | HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-106+1096C>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99765511 | |||||||
| chr1:99765662 | G | A | 1 | a0001c0002t0043g0279 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-106+945C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99765662 | |||||||
| chr1:99765844 | G | T | 1 | a0001c0001t0060g0098 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-106+763C>A | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99765844 | |||||||
| chr1:99766138 | G | A | 1 | a0001c0002t0009g0095 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-106+469C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99766138 | |||||||
| chr1:99766143 | G | A | 1 | a0001c0002t0019g0278 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-106+464C>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99766143 | |||||||
| chr1:99766437 | T | A | 2 | a0002c0003t0018g0096 a0002c0003t0018g0097 |
2 | HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-106+170A>T | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99766437 | |||||||
| chr1:99766518 | A | G | 78 | a0001c0002t0002g0003 a0001c0002t0002g0032 a0001c0002t0002g0033 others(75): Show |
92 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(89): Show |
intron_variant | MODIFIER | c.-106+89T>C | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99766518 | |||||||
| chr1:99766564 | T | C | 1 | a0001c0002t0043g0279 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-106+43A>G | FRRS1 | ENSG00000156869.14 | transcript | ENST00000646001.2 | protein_coding | 1/16 | chr1 | 99766564 |