Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 6009 |
| ensemblid | ENSG00000106615.10 |
| hgncid | 10011 |
| symbol | RHEB |
| name | Ras homolog, mTORC1 binding |
| refseq_nuc | NM_005614.4 |
| refseq_prot | NP_005605.1 |
| ensembl_nuc | ENST00000262187.10 |
| ensembl_prot | ENSP00000262187.5 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 151466012 |
| end | 151519895 |
| strand | - |
| ver | v1.2 |
| region | chr7:151466012-151519895 |
| region5000 | chr7:151461012-151524895 |
| regionname0 | RHEB_chr7_151466012_151519895 |
| regionname5000 | RHEB_chr7_151461012_151524895 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 552 | 360 | 84 | 70 | 156 | 14 | 34 | RHEB_chr7_151461012_151524895 | RHEB | ATGCC others(547): Show |
chr7 | 151461012 | 151524895 | ||
| a0001c0002 | 0/0 | 552 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | ATGCC others(547): Show |
chr7 | 151461012 | 151524895 | ||
| a0001c0003 | 0/0 | 552 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | ATGCC others(547): Show |
chr7 | 151461012 | 151524895 | ||
| a0001c0004 | 0/0 | 552 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | ATGCC others(547): Show |
chr7 | 151461012 | 151524895 | ||
| a0001c0005 | 0/0 | 552 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | ATGCC others(547): Show |
chr7 | 151461012 | 151524895 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2046 | 299 | 59 | 60 | 135 | 12 | 31 | RHEB_chr7_151461012_151524895 | RHEB | GGGAG others(2041): Show |
chr7 | 151461012 | 151524895 |
| a0001c0001t0002 | 0/0 | 2055 | 40 | 14 | 10 | 15 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | GGGAG others(2050): Show |
chr7 | 151461012 | 151524895 |
| a0001c0001t0003 | 0/0 | 2042 | 7 | 7 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | GGGAG others(2037): Show |
chr7 | 151461012 | 151524895 |
| a0001c0001t0004 | 0/0 | 2046 | 3 | 0 | 0 | 3 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | GGGAG others(2041): Show |
chr7 | 151461012 | 151524895 |
| a0001c0001t0005 | 0/0 | 2046 | 2 | 2 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | GGGAG others(2041): Show |
chr7 | 151461012 | 151524895 |
| a0001c0001t0006 | 0/0 | 2046 | 2 | 0 | 0 | 2 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | GGGAG others(2041): Show |
chr7 | 151461012 | 151524895 |
| a0001c0001t0007 | 0/0 | 2046 | 1 | 0 | 0 | 0 | 1 | 0 | RHEB_chr7_151461012_151524895 | RHEB | GGGAG others(2041): Show |
chr7 | 151461012 | 151524895 |
| a0001c0001t0008 | 0/0 | 2046 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | GGGAG others(2041): Show |
chr7 | 151461012 | 151524895 |
| a0001c0001t0009 | 0/0 | 2046 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | GGGAG others(2041): Show |
chr7 | 151461012 | 151524895 |
| a0001c0001t0010 | 0/0 | 2046 | 1 | 0 | 0 | 0 | 1 | 0 | RHEB_chr7_151461012_151524895 | RHEB | GGGAG others(2041): Show |
chr7 | 151461012 | 151524895 |
| a0001c0001t0011 | 0/0 | 2046 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | GGGAG others(2041): Show |
chr7 | 151461012 | 151524895 |
| a0001c0001t0012 | 0/0 | 2046 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | GGGAG others(2041): Show |
chr7 | 151461012 | 151524895 |
| a0001c0001t0013 | 0/0 | 2046 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | GGGAG others(2041): Show |
chr7 | 151461012 | 151524895 |
| a0001c0002t0001 | 0/0 | 2046 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | GGGAG others(2041): Show |
chr7 | 151461012 | 151524895 |
| a0001c0003t0001 | 0/0 | 2046 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | GGGAG others(2041): Show |
chr7 | 151461012 | 151524895 |
| a0001c0004t0001 | 0/0 | 2046 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | GGGAG others(2041): Show |
chr7 | 151461012 | 151524895 |
| a0001c0005t0001 | 0/0 | 2046 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | GGGAG others(2041): Show |
chr7 | 151461012 | 151524895 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 10 | 0 | 3 | 7 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0002 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0003 | 0/0 | 6 | 0 | 5 | 0 | 1 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0004 | 0/0 | 5 | 0 | 2 | 0 | 0 | 3 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0013 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0020 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0183 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0002g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0003g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0003g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0003g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0003g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0004g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0005g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0005g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0006g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0007g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0008g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0009g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0010g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0011g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0012g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0001t0013g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0003t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0004t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| a0001c0005t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0196 | EUR | GBR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG00099 | hp2 | a0001 | c0001 | t0007 | g0038 | EUR | GBR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0099 | EUR | GBR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0215 | EUR | FIN | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0118 | EUR | FIN | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0171 | EUR | FIN | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG00323 | hp2 | a0001 | c0001 | t0010 | g0141 | EUR | FIN | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG00408 | hp2 | a0001 | c0001 | t0012 | g0230 | EAS | CHS | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | CHS | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | CHS | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | CHS | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | CHS | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0091 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0202 | AMR | CLM | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0241 | AMR | CLM | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | CLM | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0098 | AMR | CLM | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0021 | EUR | IBS | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | IBS | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0029 | EUR | IBS | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0120 | EUR | IBS | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0279 | AFR | ACB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | ACB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PEL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0068 | AMR | PEL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0065 | AMR | PEL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | KHV | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | KHV | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | KHV | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | ACB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | KHV | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | KHV | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | KHV | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | KHV | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | KHV | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | ACB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0287 | AFR | ACB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0070 | AMR | PEL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0064 | AMR | PEL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0284 | AFR | GWD | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02602 | hp2 | a0001 | c0001 | t0011 | g0188 | SAS | PJL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02615 | hp2 | a0001 | c0001 | t0013 | g0298 | AFR | GWD | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0053 | AFR | GWD | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0148 | AFR | GWD | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02717 | hp1 | a0001 | c0003 | t0001 | g0151 | AFR | GWD | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0271 | SAS | PJL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0055 | AFR | GWD | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0281 | AFR | GWD | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | GWD | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0060 | AFR | GWD | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0093 | AFR | GWD | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0280 | AFR | ESN | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | ESN | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0286 | AFR | ESN | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | ESN | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | ESN | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ESN | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0057 | AFR | GWD | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | MSL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | ESN | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ESN | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG03139 | hp1 | a0001 | c0001 | t0008 | g0039 | AFR | ESN | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | ESN | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0077 | AFR | ESN | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0045 | AFR | MSL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | MSL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | MSL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0282 | AFR | MSL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | MSL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | MSL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0090 | SAS | PJL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0289 | AFR | ESN | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | STU | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | STU | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | BEB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | BEB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | BEB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | BEB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | BEB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | BEB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | STU | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | BEB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | BEB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG04228 | hp1 | a0001 | c0001 | t0009 | g0061 | SAS | STU | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | STU | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | YRI | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | YRI | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | CHB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | CHB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | YRI | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18980 | hp1 | a0001 | c0001 | t0006 | g0032 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18981 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA19005 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA19007 | hp2 | a0001 | c0004 | t0001 | g0154 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA19043 | hp1 | a0001 | c0005 | t0001 | g0297 | AFR | LWK | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | LWK | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA19078 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | YRI | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0283 | AFR | YRI | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | ASW | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0054 | AFR | ASW | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0293 | EUR | TSI | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | TSI | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0290 | AFR | ACB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0056 | AFR | ACB | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0288 | AFR | MSL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | MSL | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA18955 | hp2 | a0001 | c0001 | t0006 | g0032 | EAS | JPT | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | USA | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | USA | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | LWK | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | LWK | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0183 | REF | REF | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0020 | REF | REF | RHEB_chr7_151461012_151524895 | RHEB | chr7 | 151461012 | 151524895 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:151467134 | T | C | 1 | a0001c0003 | 1 | HG02717.hp1 | synonymous_variant | LOW | c.540A>G | p.Ser180Ser | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 8/8 | 924/2046 | 540/555 | 180/184 | chr7 | 151467134 | |||
| chr7:151471432 | A | G | 1 | a0001c0002 | 1 | NA18942.hp1 | synonymous_variant | LOW | c.342T>C | p.Ile114Ile | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 6/8 | 726/2046 | 342/555 | 114/184 | chr7 | 151471432 | |||
| chr7:151490992 | T | C | 1 | a0001c0004 | 1 | NA19007.hp2 | synonymous_variant | LOW | c.75A>G | p.Gln25Gln | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/8 | 459/2046 | 75/555 | 25/184 | chr7 | 151490992 | |||
| chr7:151519479 | G | A | 1 | a0001c0005 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.33C>T | p.Ile11Ile | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/8 | 417/2046 | 33/555 | 11/184 | chr7 | 151519479 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:151466162 | CCAAA | C | 1 | a0001c0001t0003 | 7 | HG01884.hp2 HG02572.hp1 HG02818.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*953_*956delTTTG | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 8/8 | 953 | chr7 | 151466162 | ||||||
| chr7:151466192 | C | A | 1 | a0001c0001t0006 | 2 | NA18955.hp2 NA18980.hp1 |
3_prime_UTR_variant | MODIFIER | c.*927G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 8/8 | 927 | chr7 | 151466192 | ||||||
| chr7:151466308 | C | T | 1 | a0001c0001t0005 | 2 | HG02630.hp2 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*811G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 8/8 | 811 | chr7 | 151466308 | ||||||
| chr7:151466337 | C | G | 1 | a0001c0001t0010 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*782G>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 8/8 | 782 | chr7 | 151466337 | ||||||
| chr7:151466562 | C | CTGCGCAG others(2): Show |
1 | a0001c0001t0002 | 40 | HG00423.hp2 HG00735.hp1 HG01109.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*556_*557insTCCTGC others(3): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 8/8 | 556 | chr7 | 151466562 | ||||||
| chr7:151466715 | T | G | 1 | a0001c0001t0011 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*404A>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 8/8 | 404 | chr7 | 151466715 | ||||||
| chr7:151466721 | C | T | 1 | a0001c0001t0009 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*398G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 8/8 | 398 | chr7 | 151466721 | ||||||
| chr7:151466861 | C | T | 1 | a0001c0001t0013 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*258G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 8/8 | 258 | chr7 | 151466861 | ||||||
| chr7:151466905 | T | C | 1 | a0001c0001t0012 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*214A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 8/8 | 214 | chr7 | 151466905 | ||||||
| chr7:151467028 | A | C | 1 | a0001c0001t0003 | 7 | HG01884.hp2 HG02572.hp1 HG02818.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*91T>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 8/8 | 91 | chr7 | 151467028 | ||||||
| chr7:151519512 | C | A | 1 | a0001c0001t0013 | 1 | HG02615.hp2 | 5_prime_UTR_variant | MODIFIER | c.-1G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/8 | 1 | chr7 | 151519512 | ||||||
| chr7:151519707 | C | G | 1 | a0001c0001t0004 | 3 | NA18981.hp1 NA19005.hp2 NA19078.hp1 |
5_prime_UTR_variant | MODIFIER | c.-196G>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/8 | 196 | chr7 | 151519707 | ||||||
| chr7:151519850 | C | T | 1 | a0001c0001t0008 | 1 | HG03139.hp1 | 5_prime_UTR_variant | MODIFIER | c.-339G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/8 | 339 | chr7 | 151519850 | ||||||
| chr7:151519858 | A | G | 1 | a0001c0001t0007 | 1 | HG00099.hp2 | 5_prime_UTR_variant | MODIFIER | c.-347T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/8 | 347 | chr7 | 151519858 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:151467262 | G | A | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(102): Show |
130 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.463-51C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 7/7 | chr7 | 151467262 | |||||||
| chr7:151467275 | G | A | 1 | a0001c0001t0001g0174 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.463-64C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 7/7 | chr7 | 151467275 | |||||||
| chr7:151467386 | C | T | 10 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0050 others(7): Show |
10 | HG00735.hp1 HG01109.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.463-175G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 7/7 | chr7 | 151467386 | |||||||
| chr7:151467758 | T | C | 62 | a0001c0001t0001g0014 a0001c0001t0001g0044 a0001c0001t0001g0047 others(59): Show |
67 | HG00423.hp2 HG00735.hp1 HG01109.hp2 others(64): Show |
intron_variant | MODIFIER | c.463-547A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 7/7 | chr7 | 151467758 | |||||||
| chr7:151467759 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0184 |
2 | HG02523.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.463-548G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 7/7 | chr7 | 151467759 | |||||||
| chr7:151468010 | C | T | 2 | a0001c0001t0005g0045 a0001c0001t0005g0148 |
2 | HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.463-799G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 7/7 | chr7 | 151468010 | |||||||
| chr7:151468285 | C | T | 109 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(106): Show |
135 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.463-1074G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 7/7 | chr7 | 151468285 | |||||||
| chr7:151468391 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.463-1180C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 7/7 | chr7 | 151468391 | |||||||
| chr7:151468406 | G | A | 6 | a0001c0001t0001g0013 a0001c0001t0001g0253 a0001c0001t0001g0255 others(3): Show |
8 | HG01243.hp1 HG01943.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.463-1195C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 7/7 | chr7 | 151468406 | |||||||
| chr7:151468407 | C | T | 15 | a0001c0001t0001g0011 a0001c0001t0001g0085 a0001c0001t0001g0180 others(12): Show |
17 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(14): Show |
intron_variant | MODIFIER | c.463-1196G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 7/7 | chr7 | 151468407 | |||||||
| chr7:151468507 | C | T | 1 | a0001c0001t0001g0080 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.463-1296G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 7/7 | chr7 | 151468507 | |||||||
| chr7:151468594 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.463-1383C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 7/7 | chr7 | 151468594 | |||||||
| chr7:151469041 | T | A | 1 | a0001c0001t0002g0070 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.462+1530A>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 7/7 | chr7 | 151469041 | |||||||
| chr7:151469166 | A | C | 80 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(77): Show |
95 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.462+1405T>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 7/7 | chr7 | 151469166 | |||||||
| chr7:151469171 | GTTT | G | 5 | a0001c0001t0001g0013 a0001c0001t0001g0253 a0001c0001t0001g0255 others(2): Show |
7 | HG01243.hp1 HG01943.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.462+1397_462+1399d others(5): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 7/7 | chr7 | 151469171 | |||||||
| chr7:151469377 | A | G | 3 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0182 |
5 | HG01069.hp2 HG01071.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.462+1194T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 7/7 | chr7 | 151469377 | |||||||
| chr7:151469457 | G | A | 10 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0214 others(7): Show |
16 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.462+1114C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 7/7 | chr7 | 151469457 | |||||||
| chr7:151469517 | TC | T | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(103): Show |
131 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.462+1053delG | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 7/7 | chr7 | 151469517 | |||||||
| chr7:151469566 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.462+1005A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 7/7 | chr7 | 151469566 | |||||||
| chr7:151469755 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.462+816C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 7/7 | chr7 | 151469755 | |||||||
| chr7:151469845 | G | T | 1 | a0001c0001t0013g0298 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.462+726C>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 7/7 | chr7 | 151469845 | |||||||
| chr7:151469889 | G | C | 2 | a0001c0001t0002g0016 a0001c0001t0002g0078 |
3 | HG02040.hp1 HG02132.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.462+682C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 7/7 | chr7 | 151469889 | |||||||
| chr7:151470345 | T | G | 1 | a0001c0001t0001g0193 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.462+226A>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 7/7 | chr7 | 151470345 | |||||||
| chr7:151470360 | C | T | 1 | a0001c0001t0002g0060 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.462+211G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 7/7 | chr7 | 151470360 | |||||||
| chr7:151470741 | G | A | 7 | a0001c0001t0001g0014 a0001c0001t0001g0261 a0001c0001t0001g0262 others(4): Show |
9 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.381-89C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 6/7 | chr7 | 151470741 | |||||||
| chr7:151470754 | C | G | 1 | a0001c0001t0001g0293 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.381-102G>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 6/7 | chr7 | 151470754 | |||||||
| chr7:151470843 | A | G | 1 | a0001c0001t0002g0078 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.381-191T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 6/7 | chr7 | 151470843 | |||||||
| chr7:151470917 | T | A | 3 | a0001c0001t0002g0090 a0001c0001t0002g0091 a0001c0001t0002g0098 |
3 | HG01167.hp2 HG01358.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.381-265A>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 6/7 | chr7 | 151470917 | |||||||
| chr7:151470965 | A | G | 1 | a0001c0001t0005g0148 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.381-313T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 6/7 | chr7 | 151470965 | |||||||
| chr7:151471065 | G | A | 4 | a0001c0001t0002g0053 a0001c0001t0002g0054 a0001c0001t0002g0055 others(1): Show |
4 | HG02486.hp2 HG02622.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.380+329C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 6/7 | chr7 | 151471065 | |||||||
| chr7:151471200 | T | C | 1 | a0001c0001t0001g0252 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.380+194A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 6/7 | chr7 | 151471200 | |||||||
| chr7:151471307 | A | G | 1 | a0001c0001t0001g0268 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.380+87T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 6/7 | chr7 | 151471307 | |||||||
| chr7:151471329 | CAAT | C | 108 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(105): Show |
133 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.380+62_380+64delAT others(1): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 6/7 | chr7 | 151471329 | |||||||
| chr7:151471448 | G | A | 149 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(146): Show |
179 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(176): Show |
splice_region_variant&intron_variant | LOW | c.333-7C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 5/7 | chr7 | 151471448 | |||||||
| chr7:151471618 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.276-13T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151471618 | |||||||
| chr7:151471656 | T | A | 1 | a0001c0001t0001g0092 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.276-51A>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151471656 | |||||||
| chr7:151471744 | C | T | 149 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(146): Show |
179 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.276-139G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151471744 | |||||||
| chr7:151471804 | G | A | 1 | a0001c0001t0001g0203 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.276-199C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151471804 | |||||||
| chr7:151471940 | C | T | 1 | a0001c0001t0001g0175 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.276-335G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151471940 | |||||||
| chr7:151472000 | A | G | 4 | a0001c0001t0001g0036 a0001c0001t0001g0059 a0001c0001t0001g0252 others(1): Show |
5 | HG01952.hp2 HG02630.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.276-395T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151472000 | |||||||
| chr7:151472097 | A | G | 3 | a0001c0001t0001g0034 a0001c0001t0001g0237 a0001c0001t0001g0245 |
4 | HG02109.hp2 HG02280.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.276-492T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151472097 | |||||||
| chr7:151472183 | C | T | 1 | a0001c0003t0001g0151 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.276-578G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151472183 | |||||||
| chr7:151472189 | C | A | 1 | a0001c0001t0001g0242 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.276-584G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151472189 | |||||||
| chr7:151472522 | C | T | 7 | a0001c0001t0001g0014 a0001c0001t0001g0261 a0001c0001t0001g0262 others(4): Show |
9 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.276-917G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151472522 | |||||||
| chr7:151472534 | C | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0081 |
3 | NA18945.hp2 NA18956.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.276-929G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151472534 | |||||||
| chr7:151472658 | C | T | 1 | a0001c0001t0001g0268 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.276-1053G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151472658 | |||||||
| chr7:151472704 | G | A | 14 | a0001c0001t0001g0014 a0001c0001t0001g0261 a0001c0001t0001g0262 others(11): Show |
16 | HG01884.hp2 HG02145.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.276-1099C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151472704 | |||||||
| chr7:151472730 | C | T | 1 | a0001c0003t0001g0151 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.276-1125G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151472730 | |||||||
| chr7:151472774 | T | C | 2 | a0001c0001t0001g0126 a0001c0001t0002g0125 |
2 | HG00558.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.276-1169A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151472774 | |||||||
| chr7:151472933 | C | T | 108 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(105): Show |
133 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.276-1328G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151472933 | |||||||
| chr7:151473165 | G | A | 5 | a0001c0001t0001g0013 a0001c0001t0001g0253 a0001c0001t0001g0255 others(2): Show |
7 | HG01243.hp1 HG01943.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.276-1560C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151473165 | |||||||
| chr7:151473184 | G | A | 14 | a0001c0001t0001g0014 a0001c0001t0001g0261 a0001c0001t0001g0262 others(11): Show |
16 | HG01884.hp2 HG02145.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.276-1579C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151473184 | |||||||
| chr7:151473199 | G | A | 2 | a0001c0001t0001g0277 a0001c0001t0001g0278 |
2 | HG01891.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.276-1594C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151473199 | |||||||
| chr7:151473385 | C | T | 1 | a0001c0001t0003g0284 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.276-1780G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151473385 | |||||||
| chr7:151473581 | C | T | 7 | a0001c0001t0001g0014 a0001c0001t0001g0261 a0001c0001t0001g0262 others(4): Show |
9 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.276-1976G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151473581 | |||||||
| chr7:151473757 | T | TA | 39 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(36): Show |
42 | HG00423.hp2 HG00735.hp1 HG01109.hp2 others(39): Show |
intron_variant | MODIFIER | c.276-2153dupT | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151473757 | |||||||
| chr7:151473829 | T | C | 13 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0268 others(10): Show |
13 | HG01884.hp2 HG02257.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.276-2224A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151473829 | |||||||
| chr7:151473865 | T | G | 1 | a0001c0001t0001g0195 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.276-2260A>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151473865 | |||||||
| chr7:151473994 | A | T | 28 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0037 others(25): Show |
31 | HG00423.hp2 HG01167.hp2 HG01358.hp2 others(28): Show |
intron_variant | MODIFIER | c.276-2389T>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151473994 | |||||||
| chr7:151474186 | GT | G | 157 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(154): Show |
188 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.276-2582delA | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151474186 | |||||||
| chr7:151474250 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.276-2645G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151474250 | |||||||
| chr7:151474266 | C | T | 20 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0018 others(17): Show |
24 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.276-2661G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151474266 | |||||||
| chr7:151474269 | C | T | 2 | a0001c0001t0005g0045 a0001c0001t0005g0148 |
2 | HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.276-2664G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151474269 | |||||||
| chr7:151474330 | G | A | 46 | a0001c0001t0001g0013 a0001c0001t0001g0044 a0001c0001t0001g0047 others(43): Show |
51 | HG00423.hp2 HG00735.hp1 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.276-2725C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151474330 | |||||||
| chr7:151474528 | A | G | 8 | a0001c0001t0001g0013 a0001c0001t0001g0034 a0001c0001t0001g0237 others(5): Show |
11 | HG01243.hp1 HG01943.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.275+2805T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151474528 | |||||||
| chr7:151474574 | A | G | 5 | a0001c0001t0001g0013 a0001c0001t0001g0224 a0001c0001t0001g0255 others(2): Show |
7 | HG01243.hp1 HG01943.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.275+2759T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151474574 | |||||||
| chr7:151474576 | G | T | 144 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(141): Show |
176 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.275+2757C>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151474576 | |||||||
| chr7:151474672 | T | C | 5 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(2): Show |
5 | HG02280.hp1 HG02886.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.275+2661A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151474672 | |||||||
| chr7:151474995 | G | A | 158 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(155): Show |
189 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.275+2338C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151474995 | |||||||
| chr7:151475124 | T | C | 21 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0018 others(18): Show |
25 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(22): Show |
intron_variant | MODIFIER | c.275+2209A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151475124 | |||||||
| chr7:151475196 | A | G | 108 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(105): Show |
133 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.275+2137T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151475196 | |||||||
| chr7:151475389 | T | C | 3 | a0001c0001t0001g0024 a0001c0001t0001g0122 a0001c0001t0001g0139 |
4 | HG00735.hp2 HG00738.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.275+1944A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151475389 | |||||||
| chr7:151475391 | G | A | 20 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0253 others(17): Show |
24 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.275+1942C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151475391 | |||||||
| chr7:151475414 | C | A | 6 | a0001c0001t0001g0014 a0001c0001t0001g0261 a0001c0001t0001g0262 others(3): Show |
8 | HG02145.hp2 HG02717.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.275+1919G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151475414 | |||||||
| chr7:151475533 | G | A | 1 | a0001c0001t0001g0012 | 3 | NA18981.hp2 NA19057.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.275+1800C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151475533 | |||||||
| chr7:151475625 | A | G | 2 | a0001c0001t0001g0229 a0001c0001t0012g0230 |
2 | HG00408.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.275+1708T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151475625 | |||||||
| chr7:151475705 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.275+1628G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151475705 | |||||||
| chr7:151475792 | T | C | 27 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0024 others(24): Show |
35 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(32): Show |
intron_variant | MODIFIER | c.275+1541A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151475792 | |||||||
| chr7:151475837 | A | G | 1 | a0001c0001t0001g0236 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.275+1496T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151475837 | |||||||
| chr7:151475859 | A | T | 1 | a0001c0001t0001g0212 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.275+1474T>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151475859 | |||||||
| chr7:151476082 | A | G | 1 | a0001c0001t0001g0239 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.275+1251T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151476082 | |||||||
| chr7:151476129 | G | A | 1 | a0001c0001t0001g0026 | 2 | NA18986.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.275+1204C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151476129 | |||||||
| chr7:151476152 | T | C | 2 | a0001c0001t0001g0036 a0001c0001t0001g0277 |
3 | HG02630.hp1 HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.275+1181A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151476152 | |||||||
| chr7:151476161 | C | T | 3 | a0001c0001t0002g0015 a0001c0001t0002g0066 a0001c0001t0002g0152 |
4 | HG02027.hp1 HG02074.hp2 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.275+1172G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151476161 | |||||||
| chr7:151476642 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.275+691T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151476642 | |||||||
| chr7:151476740 | C | T | 3 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0143 |
3 | HG01256.hp2 HG01261.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.275+593G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151476740 | |||||||
| chr7:151476789 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.275+544T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151476789 | |||||||
| chr7:151476904 | T | C | 40 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(37): Show |
43 | HG00423.hp2 HG00735.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.275+429A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151476904 | |||||||
| chr7:151476963 | T | C | 108 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(105): Show |
133 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.275+370A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151476963 | |||||||
| chr7:151477084 | T | A | 1 | a0001c0001t0001g0296 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.275+249A>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151477084 | |||||||
| chr7:151477130 | C | G | 2 | a0001c0001t0001g0214 a0001c0001t0001g0219 |
2 | HG01192.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.275+203G>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151477130 | |||||||
| chr7:151477200 | C | A | 115 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(112): Show |
140 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.275+133G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151477200 | |||||||
| chr7:151477222 | G | A | 2 | a0001c0001t0005g0045 a0001c0001t0005g0148 |
2 | HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.275+111C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151477222 | |||||||
| chr7:151477246 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.275+87G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151477246 | |||||||
| chr7:151477286 | T | G | 1 | a0001c0001t0002g0093 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.275+47A>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 4/7 | chr7 | 151477286 | |||||||
| chr7:151477452 | T | C | 7 | a0001c0001t0001g0014 a0001c0001t0001g0261 a0001c0001t0001g0262 others(4): Show |
9 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.193-37A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151477452 | |||||||
| chr7:151477516 | C | T | 7 | a0001c0001t0001g0014 a0001c0001t0001g0261 a0001c0001t0001g0262 others(4): Show |
9 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.193-101G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151477516 | |||||||
| chr7:151477553 | A | G | 1 | a0001c0003t0001g0151 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.193-138T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151477553 | |||||||
| chr7:151477591 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.193-176C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151477591 | |||||||
| chr7:151477947 | G | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0122 |
3 | HG00735.hp2 HG00738.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.193-532C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151477947 | |||||||
| chr7:151478009 | T | C | 1 | a0001c0001t0001g0203 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.193-594A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151478009 | |||||||
| chr7:151478132 | C | A | 2 | a0001c0001t0001g0224 a0001c0001t0001g0225 |
2 | HG02976.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.193-717G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151478132 | |||||||
| chr7:151478258 | T | G | 3 | a0001c0001t0001g0108 a0001c0001t0001g0112 a0001c0001t0001g0113 |
3 | HG02109.hp1 HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.193-843A>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151478258 | |||||||
| chr7:151478342 | T | C | 1 | a0001c0001t0001g0133 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.193-927A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151478342 | |||||||
| chr7:151478363 | T | C | 19 | a0001c0001t0001g0014 a0001c0001t0001g0261 a0001c0001t0001g0262 others(16): Show |
21 | HG01884.hp2 HG02145.hp2 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.193-948A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151478363 | |||||||
| chr7:151478372 | G | A | 108 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(105): Show |
133 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.193-957C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151478372 | |||||||
| chr7:151478387 | G | GA | 20 | a0001c0001t0001g0014 a0001c0001t0001g0199 a0001c0001t0001g0261 others(17): Show |
22 | HG01884.hp2 HG02145.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.193-973dupT | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151478387 | |||||||
| chr7:151478431 | C | A | 2 | a0001c0001t0001g0224 a0001c0001t0001g0225 |
2 | HG02976.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.193-1016G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151478431 | |||||||
| chr7:151478550 | A | G | 2 | a0001c0001t0001g0185 a0001c0001t0001g0200 |
2 | HG00423.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.193-1135T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151478550 | |||||||
| chr7:151478649 | T | C | 1 | a0001c0001t0002g0015 | 2 | NA18954.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.193-1234A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151478649 | |||||||
| chr7:151478871 | G | A | 1 | a0001c0001t0001g0058 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.193-1456C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151478871 | |||||||
| chr7:151478878 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.193-1463C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151478878 | |||||||
| chr7:151478937 | AT | A | 15 | a0001c0001t0001g0014 a0001c0001t0001g0212 a0001c0001t0001g0261 others(12): Show |
17 | HG01884.hp2 HG02145.hp2 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.193-1523delA | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151478937 | |||||||
| chr7:151479006 | C | T | 1 | a0001c0001t0001g0029 | 2 | HG01515.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.193-1591G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151479006 | |||||||
| chr7:151479406 | G | C | 2 | a0001c0001t0002g0046 a0001c0001t0002g0049 |
2 | HG00735.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.193-1991C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151479406 | |||||||
| chr7:151479407 | G | T | 1 | a0001c0001t0001g0080 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.193-1992C>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151479407 | |||||||
| chr7:151479409 | A | G | 1 | a0001c0001t0001g0255 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.193-1994T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151479409 | |||||||
| chr7:151479412 | A | G | 1 | a0001c0001t0001g0255 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.193-1997T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151479412 | |||||||
| chr7:151479465 | A | G | 1 | a0001c0001t0001g0260 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.193-2050T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151479465 | |||||||
| chr7:151479500 | G | A | 3 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0050 |
3 | HG02280.hp1 HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.193-2085C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151479500 | |||||||
| chr7:151479512 | C | A | 6 | a0001c0001t0003g0057 a0001c0001t0003g0279 a0001c0001t0003g0281 others(3): Show |
6 | HG01884.hp2 HG02572.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.193-2097G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151479512 | |||||||
| chr7:151479539 | T | C | 2 | a0001c0001t0001g0088 a0001c0001t0001g0204 |
2 | HG03927.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.193-2124A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151479539 | |||||||
| chr7:151479543 | C | T | 3 | a0001c0001t0001g0123 a0001c0001t0001g0155 a0001c0001t0001g0156 |
3 | HG00544.hp2 HG04115.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.193-2128G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151479543 | |||||||
| chr7:151479544 | G | A | 1 | a0001c0001t0001g0247 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.193-2129C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151479544 | |||||||
| chr7:151479551 | C | T | 1 | a0001c0001t0001g0238 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.193-2136G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151479551 | |||||||
| chr7:151479552 | G | A | 3 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0050 |
3 | HG02280.hp1 HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.193-2137C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151479552 | |||||||
| chr7:151479624 | A | T | 4 | a0001c0001t0002g0064 a0001c0001t0002g0068 a0001c0001t0002g0069 others(1): Show |
4 | HG01943.hp2 HG02293.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.193-2209T>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151479624 | |||||||
| chr7:151479640 | G | A | 8 | a0001c0001t0001g0014 a0001c0001t0001g0109 a0001c0001t0001g0254 others(5): Show |
10 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.193-2225C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151479640 | |||||||
| chr7:151479642 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.193-2227G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151479642 | |||||||
| chr7:151479645 | A | T | 4 | a0001c0001t0001g0109 a0001c0001t0001g0267 a0001c0001t0001g0268 others(1): Show |
4 | HG02257.hp2 HG02572.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-2230T>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151479645 | |||||||
| chr7:151479649 | C | A | 1 | a0001c0001t0001g0109 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.193-2234G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151479649 | |||||||
| chr7:151479662 | G | A | 2 | a0001c0001t0005g0045 a0001c0001t0005g0148 |
2 | HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.193-2247C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151479662 | |||||||
| chr7:151479664 | T | C | 26 | a0001c0001t0001g0248 a0001c0001t0002g0015 a0001c0001t0002g0016 others(23): Show |
28 | HG00423.hp2 HG00544.hp1 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.193-2249A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151479664 | |||||||
| chr7:151479678 | G | C | 1 | a0001c0001t0001g0221 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.193-2263C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151479678 | |||||||
| chr7:151479682 | C | CA | 146 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(143): Show |
174 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.193-2268dupT | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151479682 | |||||||
| chr7:151479682 | C | CAA | 13 | a0001c0001t0001g0014 a0001c0001t0001g0180 a0001c0001t0001g0181 others(10): Show |
15 | HG01109.hp1 HG01433.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.193-2269_193-2268d others(4): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151479682 | |||||||
| chr7:151479682 | CAAAAAAA others(1): Show |
C | 7 | a0001c0001t0003g0057 a0001c0001t0003g0279 a0001c0001t0003g0280 others(4): Show |
7 | HG01884.hp2 HG02572.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.193-2275_193-2268d others(10): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151479682 | |||||||
| chr7:151479863 | G | A | 1 | a0001c0003t0001g0151 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.193-2448C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151479863 | |||||||
| chr7:151480031 | C | T | 178 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(175): Show |
211 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.193-2616G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151480031 | |||||||
| chr7:151480048 | T | C | 198 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(195): Show |
235 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.193-2633A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151480048 | |||||||
| chr7:151480061 | G | A | 1 | a0001c0001t0001g0278 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.193-2646C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151480061 | |||||||
| chr7:151480099 | T | C | 1 | a0001c0001t0001g0239 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.193-2684A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151480099 | |||||||
| chr7:151480309 | C | T | 11 | a0001c0001t0001g0014 a0001c0001t0001g0254 a0001c0001t0001g0261 others(8): Show |
13 | HG02145.hp2 HG02257.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.193-2894G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151480309 | |||||||
| chr7:151480412 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.193-2997G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151480412 | |||||||
| chr7:151480529 | G | C | 7 | a0001c0001t0001g0014 a0001c0001t0001g0261 a0001c0001t0001g0262 others(4): Show |
9 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.193-3114C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151480529 | |||||||
| chr7:151480678 | TATTA | T | 5 | a0001c0001t0001g0013 a0001c0001t0001g0253 a0001c0001t0001g0255 others(2): Show |
7 | HG01243.hp1 HG01943.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.193-3267_193-3264d others(6): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151480678 | |||||||
| chr7:151480685 | TA | T | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(103): Show |
129 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.193-3271delT | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151480685 | |||||||
| chr7:151480686 | A | T | 2 | a0001c0001t0001g0243 a0001c0001t0006g0032 |
2 | HG01934.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.193-3271T>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151480686 | |||||||
| chr7:151480689 | A | T | 122 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(119): Show |
147 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.193-3274T>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151480689 | |||||||
| chr7:151480766 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.193-3351G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151480766 | |||||||
| chr7:151481066 | C | G | 30 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0027 others(27): Show |
43 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.193-3651G>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151481066 | |||||||
| chr7:151481092 | T | G | 169 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(166): Show |
200 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.192+3645A>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151481092 | |||||||
| chr7:151481130 | CT | C | 15 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0103 others(12): Show |
19 | HG01243.hp1 HG01943.hp1 HG01975.hp1 others(16): Show |
intron_variant | MODIFIER | c.192+3606delA | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151481130 | |||||||
| chr7:151481337 | T | A | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(104): Show |
132 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.192+3400A>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151481337 | |||||||
| chr7:151481382 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.192+3355C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151481382 | |||||||
| chr7:151481455 | C | G | 1 | a0001c0001t0001g0277 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.192+3282G>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151481455 | |||||||
| chr7:151481596 | C | T | 8 | a0001c0001t0001g0059 a0001c0001t0003g0057 a0001c0001t0003g0279 others(5): Show |
8 | HG01884.hp2 HG01952.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.192+3141G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151481596 | |||||||
| chr7:151481644 | A | G | 1 | a0001c0001t0001g0296 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.192+3093T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151481644 | |||||||
| chr7:151481766 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.192+2971G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151481766 | |||||||
| chr7:151481790 | C | T | 1 | a0001c0001t0001g0082 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.192+2947G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151481790 | |||||||
| chr7:151481814 | C | T | 2 | a0001c0001t0002g0046 a0001c0001t0002g0049 |
2 | HG00735.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.192+2923G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151481814 | |||||||
| chr7:151482321 | T | C | 1 | a0001c0001t0001g0059 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.192+2416A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151482321 | |||||||
| chr7:151482361 | C | T | 37 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(34): Show |
40 | HG00423.hp2 HG00673.hp1 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.192+2376G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151482361 | |||||||
| chr7:151482496 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.192+2241A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151482496 | |||||||
| chr7:151482528 | C | A | 1 | a0001c0001t0001g0207 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.192+2209G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151482528 | |||||||
| chr7:151482572 | A | G | 1 | a0001c0001t0002g0065 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.192+2165T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151482572 | |||||||
| chr7:151482852 | C | T | 39 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(36): Show |
42 | HG00423.hp2 HG00673.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.192+1885G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151482852 | |||||||
| chr7:151482994 | G | A | 7 | a0001c0001t0001g0014 a0001c0001t0001g0261 a0001c0001t0001g0262 others(4): Show |
9 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.192+1743C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151482994 | |||||||
| chr7:151483065 | C | T | 20 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0018 others(17): Show |
24 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.192+1672G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151483065 | |||||||
| chr7:151483070 | G | GC | 3 | a0001c0001t0001g0095 a0001c0001t0002g0016 a0001c0001t0002g0078 |
4 | HG00673.hp1 HG02040.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.192+1666dupG | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151483070 | |||||||
| chr7:151483277 | G | A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0122 a0001c0001t0001g0139 |
4 | HG00735.hp2 HG00738.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.192+1460C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151483277 | |||||||
| chr7:151483355 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.192+1382G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151483355 | |||||||
| chr7:151483517 | A | G | 196 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(193): Show |
233 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.192+1220T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151483517 | |||||||
| chr7:151483537 | G | T | 2 | a0001c0001t0001g0277 a0001c0001t0001g0278 |
2 | HG01891.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.192+1200C>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151483537 | |||||||
| chr7:151483549 | C | T | 1 | a0001c0001t0001g0172 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.192+1188G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151483549 | |||||||
| chr7:151483890 | T | A | 1 | a0001c0001t0001g0206 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.192+847A>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151483890 | |||||||
| chr7:151483965 | A | T | 2 | a0001c0001t0001g0127 a0001c0001t0001g0142 |
2 | HG02135.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.192+772T>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151483965 | |||||||
| chr7:151484046 | T | G | 1 | a0001c0001t0001g0277 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.192+691A>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151484046 | |||||||
| chr7:151484306 | T | C | 40 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(37): Show |
43 | HG00423.hp2 HG00673.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.192+431A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151484306 | |||||||
| chr7:151484536 | A | G | 1 | a0001c0001t0003g0284 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.192+201T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151484536 | |||||||
| chr7:151484559 | C | T | 1 | a0001c0001t0001g0027 | 2 | NA18962.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.192+178G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151484559 | |||||||
| chr7:151484573 | A | G | 2 | a0001c0001t0001g0267 a0001c0001t0001g0268 |
2 | HG02257.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.192+164T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151484573 | |||||||
| chr7:151484584 | G | A | 2 | a0001c0001t0001g0062 a0001c0001t0001g0128 |
2 | NA18952.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.192+153C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151484584 | |||||||
| chr7:151484584 | G | T | 7 | a0001c0001t0001g0014 a0001c0001t0001g0261 a0001c0001t0001g0262 others(4): Show |
9 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.192+153C>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 3/7 | chr7 | 151484584 | |||||||
| chr7:151484995 | G | A | 1 | a0001c0003t0001g0151 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.125-191C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151484995 | |||||||
| chr7:151485375 | A | C | 1 | a0001c0001t0002g0049 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.125-571T>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151485375 | |||||||
| chr7:151485571 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.125-767G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151485571 | |||||||
| chr7:151485759 | G | A | 47 | a0001c0001t0001g0014 a0001c0001t0001g0044 a0001c0001t0001g0047 others(44): Show |
52 | HG00423.hp2 HG00673.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.125-955C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151485759 | |||||||
| chr7:151485868 | A | G | 1 | a0001c0001t0002g0125 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.125-1064T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151485868 | |||||||
| chr7:151485931 | T | C | 1 | a0001c0001t0001g0254 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.125-1127A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151485931 | |||||||
| chr7:151486122 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.125-1318C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151486122 | |||||||
| chr7:151486679 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.125-1875G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151486679 | |||||||
| chr7:151486694 | G | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0122 |
3 | HG00735.hp2 HG00738.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.125-1890C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151486694 | |||||||
| chr7:151487129 | C | G | 1 | a0001c0001t0001g0121 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.125-2325G>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151487129 | |||||||
| chr7:151487439 | A | G | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(103): Show |
131 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.125-2635T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151487439 | |||||||
| chr7:151487464 | C | A | 1 | a0001c0001t0001g0113 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.125-2660G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151487464 | |||||||
| chr7:151487515 | G | T | 20 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0018 others(17): Show |
24 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.125-2711C>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151487515 | |||||||
| chr7:151487525 | GA | G | 29 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0035 others(26): Show |
34 | HG00558.hp1 HG00738.hp1 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.125-2722delT | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151487525 | |||||||
| chr7:151487531 | A | T | 9 | a0001c0001t0001g0036 a0001c0001t0001g0059 a0001c0001t0003g0057 others(6): Show |
10 | HG01884.hp2 HG01952.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.125-2727T>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151487531 | |||||||
| chr7:151487534 | A | T | 19 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0033 others(16): Show |
27 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.125-2730T>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151487534 | |||||||
| chr7:151487640 | G | C | 2 | a0001c0001t0001g0180 a0001c0001t0001g0181 |
2 | HG01433.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.125-2836C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151487640 | |||||||
| chr7:151487693 | C | A | 9 | a0001c0001t0001g0036 a0001c0001t0001g0059 a0001c0001t0003g0057 others(6): Show |
10 | HG01884.hp2 HG01952.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.125-2889G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151487693 | |||||||
| chr7:151487834 | A | G | 3 | a0001c0001t0001g0031 a0001c0001t0001g0196 a0001c0001t0001g0234 |
4 | HG00099.hp1 HG01346.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.125-3030T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151487834 | |||||||
| chr7:151487842 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.125-3038T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151487842 | |||||||
| chr7:151487877 | T | C | 1 | a0001c0001t0002g0286 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.124+3066A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151487877 | |||||||
| chr7:151487888 | A | T | 6 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(3): Show |
6 | HG02280.hp1 HG02886.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.124+3055T>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151487888 | |||||||
| chr7:151487899 | C | T | 175 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(172): Show |
208 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.124+3044G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151487899 | |||||||
| chr7:151488009 | T | C | 35 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(32): Show |
38 | HG00423.hp2 HG00673.hp1 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.124+2934A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151488009 | |||||||
| chr7:151488118 | A | G | 1 | a0001c0001t0001g0252 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.124+2825T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151488118 | |||||||
| chr7:151488169 | G | A | 44 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(41): Show |
47 | HG00423.hp2 HG00673.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.124+2774C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151488169 | |||||||
| chr7:151488281 | C | G | 1 | a0001c0001t0001g0195 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.124+2662G>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151488281 | |||||||
| chr7:151488357 | CTGAG | C | 3 | a0001c0001t0001g0252 a0001c0001t0001g0277 a0001c0001t0001g0278 |
3 | HG01891.hp1 HG02630.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.124+2582_124+2585d others(6): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151488357 | |||||||
| chr7:151488443 | T | C | 1 | a0001c0001t0001g0178 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.124+2500A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151488443 | |||||||
| chr7:151488529 | C | T | 1 | a0001c0001t0001g0194 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.124+2414G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151488529 | |||||||
| chr7:151488570 | G | A | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(234): Show |
296 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.124+2373C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151488570 | |||||||
| chr7:151488624 | A | C | 1 | a0001c0001t0001g0052 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.124+2319T>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151488624 | |||||||
| chr7:151488698 | A | C | 1 | a0001c0001t0002g0073 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.124+2245T>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151488698 | |||||||
| chr7:151488966 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.124+1977G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151488966 | |||||||
| chr7:151488982 | C | T | 5 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(2): Show |
5 | HG02280.hp1 HG02886.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.124+1961G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151488982 | |||||||
| chr7:151489011 | G | C | 1 | a0001c0001t0001g0164 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.124+1932C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151489011 | |||||||
| chr7:151489013 | T | C | 1 | a0001c0001t0001g0179 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.124+1930A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151489013 | |||||||
| chr7:151489085 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.124+1858G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151489085 | |||||||
| chr7:151489530 | G | C | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(102): Show |
130 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.124+1413C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151489530 | |||||||
| chr7:151489552 | T | C | 1 | a0001c0001t0001g0036 | 2 | HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.124+1391A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151489552 | |||||||
| chr7:151489560 | G | T | 1 | a0001c0001t0002g0055 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.124+1383C>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151489560 | |||||||
| chr7:151489611 | T | G | 7 | a0001c0001t0001g0014 a0001c0001t0001g0261 a0001c0001t0001g0262 others(4): Show |
9 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.124+1332A>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151489611 | |||||||
| chr7:151489632 | G | A | 1 | a0001c0001t0005g0045 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.124+1311C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151489632 | |||||||
| chr7:151489677 | T | G | 113 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(110): Show |
138 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.124+1266A>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151489677 | |||||||
| chr7:151489880 | G | A | 7 | a0001c0001t0003g0057 a0001c0001t0003g0279 a0001c0001t0003g0280 others(4): Show |
7 | HG01884.hp2 HG02572.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.124+1063C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151489880 | |||||||
| chr7:151489941 | C | A | 22 | a0001c0001t0001g0014 a0001c0001t0001g0044 a0001c0001t0001g0047 others(19): Show |
24 | HG00735.hp1 HG01109.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.124+1002G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151489941 | |||||||
| chr7:151490120 | A | C | 7 | a0001c0001t0001g0014 a0001c0001t0001g0261 a0001c0001t0001g0262 others(4): Show |
9 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.124+823T>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151490120 | |||||||
| chr7:151490172 | G | A | 15 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(12): Show |
15 | HG00735.hp1 HG01109.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.124+771C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151490172 | |||||||
| chr7:151490301 | A | T | 22 | a0001c0001t0001g0014 a0001c0001t0001g0044 a0001c0001t0001g0047 others(19): Show |
24 | HG00735.hp1 HG01109.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.124+642T>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151490301 | |||||||
| chr7:151490637 | G | C | 2 | a0001c0001t0001g0277 a0001c0001t0001g0278 |
2 | HG01891.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.124+306C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151490637 | |||||||
| chr7:151490705 | A | C | 1 | a0001c0001t0005g0045 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.124+238T>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151490705 | |||||||
| chr7:151490749 | A | G | 1 | a0001c0001t0001g0036 | 2 | HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.124+194T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 2/7 | chr7 | 151490749 | |||||||
| chr7:151491077 | C | A | 1 | a0001c0001t0001g0013 | 3 | HG01243.hp1 HG02647.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.53-63G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151491077 | |||||||
| chr7:151491211 | T | C | 1 | a0001c0001t0001g0028 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.53-197A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151491211 | |||||||
| chr7:151491345 | T | A | 1 | a0001c0001t0001g0092 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.53-331A>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151491345 | |||||||
| chr7:151491453 | C | T | 1 | a0001c0001t0001g0036 | 2 | HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.53-439G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151491453 | |||||||
| chr7:151491484 | C | G | 4 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0268 others(1): Show |
4 | HG02257.hp2 HG02572.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-470G>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151491484 | |||||||
| chr7:151491512 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.53-498C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151491512 | |||||||
| chr7:151491664 | G | C | 1 | a0001c0001t0001g0187 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.53-650C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151491664 | |||||||
| chr7:151491736 | CA | C | 138 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(135): Show |
166 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.53-723delT | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151491736 | |||||||
| chr7:151491960 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.53-946G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151491960 | |||||||
| chr7:151492077 | C | A | 3 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0182 |
5 | HG01069.hp2 HG01071.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.53-1063G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151492077 | |||||||
| chr7:151492126 | A | G | 11 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(8): Show |
11 | HG00735.hp1 HG01109.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.53-1112T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151492126 | |||||||
| chr7:151492378 | G | A | 9 | a0001c0001t0001g0013 a0001c0001t0001g0252 a0001c0001t0001g0253 others(6): Show |
11 | HG01243.hp1 HG01891.hp1 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.53-1364C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151492378 | |||||||
| chr7:151492445 | C | G | 1 | a0001c0001t0001g0243 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.53-1431G>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151492445 | |||||||
| chr7:151492509 | C | G | 2 | a0001c0001t0001g0030 a0001c0001t0011g0188 |
3 | HG02602.hp2 HG03834.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.53-1495G>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151492509 | |||||||
| chr7:151492567 | AG | A | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(103): Show |
131 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.53-1554delC | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151492567 | |||||||
| chr7:151492618 | T | TA | 19 | a0001c0001t0001g0011 a0001c0001t0001g0044 a0001c0001t0001g0047 others(16): Show |
21 | HG00735.hp1 HG01109.hp2 HG02071.hp1 others(18): Show |
intron_variant | MODIFIER | c.53-1605dupT | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151492618 | |||||||
| chr7:151492640 | G | C | 120 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(117): Show |
147 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.53-1626C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151492640 | |||||||
| chr7:151492689 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.53-1675G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151492689 | |||||||
| chr7:151492696 | C | A | 1 | a0001c0001t0001g0221 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.53-1682G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151492696 | |||||||
| chr7:151492696 | C | T | 15 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0027 others(12): Show |
26 | HG00323.hp1 HG00438.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.53-1682G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151492696 | |||||||
| chr7:151492703 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.53-1689G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151492703 | |||||||
| chr7:151492838 | A | AT | 17 | a0001c0001t0001g0014 a0001c0001t0001g0074 a0001c0001t0001g0084 others(14): Show |
19 | HG00280.hp2 HG00621.hp1 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.53-1825dupA | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151492838 | |||||||
| chr7:151492838 | A | ATT | 8 | a0001c0001t0001g0036 a0001c0001t0003g0057 a0001c0001t0003g0279 others(5): Show |
9 | HG01884.hp2 HG02572.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.53-1826_53-1825dup others(2): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151492838 | |||||||
| chr7:151492838 | A | ATTT | 97 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(94): Show |
121 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.53-1827_53-1825dup others(3): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151492838 | |||||||
| chr7:151492838 | A | ATTTT | 9 | a0001c0001t0001g0178 a0001c0001t0001g0191 a0001c0001t0001g0212 others(6): Show |
10 | HG00544.hp1 HG00741.hp1 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.53-1828_53-1825dup others(4): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151492838 | |||||||
| chr7:151492838 | AT | A | 13 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(10): Show |
13 | HG00735.hp1 HG01109.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.53-1825delA | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151492838 | |||||||
| chr7:151492986 | C | T | 7 | a0001c0001t0001g0014 a0001c0001t0001g0261 a0001c0001t0001g0262 others(4): Show |
9 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.53-1972G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151492986 | |||||||
| chr7:151492988 | C | T | 1 | a0001c0001t0001g0261 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.53-1974G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151492988 | |||||||
| chr7:151493025 | T | C | 1 | a0001c0001t0001g0036 | 2 | HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.53-2011A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151493025 | |||||||
| chr7:151493082 | C | T | 1 | a0001c0001t0001g0029 | 2 | HG01515.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.53-2068G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151493082 | |||||||
| chr7:151493088 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.53-2074C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151493088 | |||||||
| chr7:151493132 | C | T | 5 | a0001c0001t0001g0013 a0001c0001t0001g0253 a0001c0001t0001g0255 others(2): Show |
7 | HG01243.hp1 HG01943.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.53-2118G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151493132 | |||||||
| chr7:151493144 | A | C | 1 | a0001c0001t0001g0251 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.53-2130T>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151493144 | |||||||
| chr7:151493659 | A | C | 1 | a0001c0001t0001g0276 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.53-2645T>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151493659 | |||||||
| chr7:151493735 | C | T | 7 | a0001c0001t0003g0057 a0001c0001t0003g0279 a0001c0001t0003g0280 others(4): Show |
7 | HG01884.hp2 HG02572.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.53-2721G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151493735 | |||||||
| chr7:151493846 | A | C | 1 | a0001c0001t0001g0252 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.53-2832T>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151493846 | |||||||
| chr7:151493848 | A | G | 9 | a0001c0001t0001g0014 a0001c0001t0001g0254 a0001c0001t0001g0261 others(6): Show |
11 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.53-2834T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151493848 | |||||||
| chr7:151493904 | C | A | 1 | a0001c0001t0001g0059 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.53-2890G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151493904 | |||||||
| chr7:151494025 | T | C | 8 | a0001c0001t0001g0014 a0001c0001t0001g0254 a0001c0001t0001g0261 others(5): Show |
10 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.53-3011A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151494025 | |||||||
| chr7:151494122 | A | G | 1 | a0001c0001t0001g0190 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.53-3108T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151494122 | |||||||
| chr7:151494518 | T | C | 6 | a0001c0001t0002g0046 a0001c0001t0002g0049 a0001c0001t0002g0053 others(3): Show |
6 | HG00735.hp1 HG01109.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.53-3504A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151494518 | |||||||
| chr7:151494625 | G | A | 8 | a0001c0001t0001g0014 a0001c0001t0001g0261 a0001c0001t0001g0262 others(5): Show |
10 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.53-3611C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151494625 | |||||||
| chr7:151494654 | G | C | 1 | a0001c0001t0001g0084 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.53-3640C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151494654 | |||||||
| chr7:151494736 | C | A | 2 | a0001c0001t0001g0277 a0001c0001t0001g0278 |
2 | HG01891.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.53-3722G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151494736 | |||||||
| chr7:151494736 | C | T | 6 | a0001c0001t0001g0013 a0001c0001t0001g0253 a0001c0001t0001g0254 others(3): Show |
8 | HG01243.hp1 HG01943.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.53-3722G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151494736 | |||||||
| chr7:151494799 | C | A | 23 | a0001c0001t0001g0014 a0001c0001t0001g0044 a0001c0001t0001g0047 others(20): Show |
25 | HG00735.hp1 HG01109.hp2 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.53-3785G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151494799 | |||||||
| chr7:151494961 | C | T | 1 | a0001c0001t0001g0033 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.53-3947G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151494961 | |||||||
| chr7:151495007 | G | A | 6 | a0001c0001t0002g0037 a0001c0001t0002g0286 a0001c0001t0002g0287 others(3): Show |
7 | HG02055.hp1 HG02258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.53-3993C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151495007 | |||||||
| chr7:151495015 | G | C | 15 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(12): Show |
15 | HG00735.hp1 HG01109.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.53-4001C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151495015 | |||||||
| chr7:151495234 | C | G | 1 | a0001c0001t0001g0099 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.53-4220G>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151495234 | |||||||
| chr7:151495301 | T | A | 2 | a0001c0001t0001g0180 a0001c0001t0001g0181 |
2 | HG01433.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.53-4287A>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151495301 | |||||||
| chr7:151495576 | C | T | 132 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(129): Show |
162 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.53-4562G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151495576 | |||||||
| chr7:151495591 | T | C | 1 | a0001c0001t0010g0141 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.53-4577A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151495591 | |||||||
| chr7:151495674 | G | A | 15 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(12): Show |
15 | HG00735.hp1 HG01109.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.53-4660C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151495674 | |||||||
| chr7:151495722 | C | T | 2 | a0001c0001t0001g0224 a0001c0001t0001g0225 |
2 | HG02976.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.53-4708G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151495722 | |||||||
| chr7:151496029 | C | G | 2 | a0001c0001t0001g0010 a0001c0001t0001g0189 |
4 | HG02027.hp2 NA18944.hp1 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-5015G>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151496029 | |||||||
| chr7:151496080 | C | T | 2 | a0001c0001t0001g0030 a0001c0001t0011g0188 |
3 | HG02602.hp2 HG03834.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.53-5066G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151496080 | |||||||
| chr7:151496116 | C | T | 1 | a0001c0001t0001g0260 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.53-5102G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151496116 | |||||||
| chr7:151496126 | C | T | 2 | a0001c0001t0001g0266 a0001c0001t0001g0267 |
2 | HG02572.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.53-5112G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151496126 | |||||||
| chr7:151496282 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.53-5268G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151496282 | |||||||
| chr7:151496562 | G | A | 1 | a0001c0001t0001g0036 | 2 | HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.53-5548C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151496562 | |||||||
| chr7:151496588 | A | G | 7 | a0001c0001t0003g0057 a0001c0001t0003g0279 a0001c0001t0003g0280 others(4): Show |
7 | HG01884.hp2 HG02572.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.53-5574T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151496588 | |||||||
| chr7:151496658 | G | A | 7 | a0001c0001t0003g0057 a0001c0001t0003g0279 a0001c0001t0003g0280 others(4): Show |
7 | HG01884.hp2 HG02572.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.53-5644C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151496658 | |||||||
| chr7:151496945 | A | AT | 16 | a0001c0001t0001g0088 a0001c0001t0001g0102 a0001c0001t0001g0109 others(13): Show |
16 | HG00280.hp1 HG00544.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.53-5932dupA | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151496945 | |||||||
| chr7:151496945 | AT | A | 37 | a0001c0001t0001g0014 a0001c0001t0001g0044 a0001c0001t0001g0047 others(34): Show |
39 | HG00438.hp2 HG00735.hp1 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.53-5932delA | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151496945 | |||||||
| chr7:151497011 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.53-5997C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151497011 | |||||||
| chr7:151497020 | T | C | 148 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(145): Show |
178 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.53-6006A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151497020 | |||||||
| chr7:151497214 | T | C | 2 | a0001c0001t0001g0042 a0001c0001t0001g0184 |
2 | HG02523.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.53-6200A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151497214 | |||||||
| chr7:151497318 | T | C | 2 | a0001c0001t0001g0277 a0001c0001t0001g0278 |
2 | HG01891.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.53-6304A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151497318 | |||||||
| chr7:151497362 | C | T | 7 | a0001c0001t0001g0014 a0001c0001t0001g0261 a0001c0001t0001g0262 others(4): Show |
9 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.53-6348G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151497362 | |||||||
| chr7:151497387 | C | G | 20 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0018 others(17): Show |
24 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.53-6373G>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151497387 | |||||||
| chr7:151497724 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.53-6710G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151497724 | |||||||
| chr7:151497842 | C | A | 1 | a0001c0003t0001g0151 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.53-6828G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151497842 | |||||||
| chr7:151497943 | C | A | 1 | a0001c0001t0005g0045 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.53-6929G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151497943 | |||||||
| chr7:151497968 | C | G | 1 | a0001c0001t0001g0285 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.53-6954G>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151497968 | |||||||
| chr7:151498137 | A | C | 1 | a0001c0001t0001g0036 | 2 | HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.53-7123T>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151498137 | |||||||
| chr7:151498227 | A | G | 8 | a0001c0001t0001g0014 a0001c0001t0001g0261 a0001c0001t0001g0262 others(5): Show |
10 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.53-7213T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151498227 | |||||||
| chr7:151498242 | G | C | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(103): Show |
131 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.53-7228C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151498242 | |||||||
| chr7:151498448 | C | A | 1 | a0001c0001t0001g0036 | 2 | HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.53-7434G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151498448 | |||||||
| chr7:151498456 | A | C | 1 | a0001c0001t0001g0036 | 2 | HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.53-7442T>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151498456 | |||||||
| chr7:151498615 | C | T | 23 | a0001c0001t0001g0014 a0001c0001t0001g0044 a0001c0001t0001g0047 others(20): Show |
25 | HG00735.hp1 HG01109.hp2 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.53-7601G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151498615 | |||||||
| chr7:151498804 | T | TAAG | 24 | a0001c0001t0001g0014 a0001c0001t0001g0044 a0001c0001t0001g0047 others(21): Show |
26 | HG00735.hp1 HG01109.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.53-7793_53-7791dup others(3): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151498804 | |||||||
| chr7:151498901 | TC | T | 23 | a0001c0001t0001g0014 a0001c0001t0001g0044 a0001c0001t0001g0047 others(20): Show |
25 | HG00735.hp1 HG01109.hp2 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.53-7888delG | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151498901 | |||||||
| chr7:151499142 | G | A | 2 | a0001c0001t0001g0208 a0001c0001t0001g0272 |
2 | NA18949.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.53-8128C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151499142 | |||||||
| chr7:151499249 | TG | T | 4 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0268 others(1): Show |
4 | HG02257.hp2 HG02572.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-8236delC | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151499249 | |||||||
| chr7:151499329 | GC | G | 2 | a0001c0001t0002g0037 a0001c0001t0002g0289 |
3 | HG02055.hp1 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.53-8316delG | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151499329 | |||||||
| chr7:151499373 | G | C | 2 | a0001c0001t0001g0277 a0001c0001t0001g0278 |
2 | HG01891.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.53-8359C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151499373 | |||||||
| chr7:151499707 | T | C | 24 | a0001c0001t0001g0014 a0001c0001t0001g0044 a0001c0001t0001g0047 others(21): Show |
26 | HG00735.hp1 HG01109.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.53-8693A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151499707 | |||||||
| chr7:151499742 | C | G | 6 | a0001c0001t0001g0009 a0001c0001t0001g0187 a0001c0001t0001g0226 others(3): Show |
8 | NA18965.hp1 NA18974.hp2 NA18983.hp2 others(5): Show |
intron_variant | MODIFIER | c.53-8728G>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151499742 | |||||||
| chr7:151499861 | T | C | 7 | a0001c0001t0003g0057 a0001c0001t0003g0279 a0001c0001t0003g0280 others(4): Show |
7 | HG01884.hp2 HG02572.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.53-8847A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151499861 | |||||||
| chr7:151499884 | C | G | 1 | a0001c0001t0002g0063 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.53-8870G>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151499884 | |||||||
| chr7:151500017 | G | T | 8 | a0001c0001t0001g0014 a0001c0001t0001g0261 a0001c0001t0001g0262 others(5): Show |
10 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.53-9003C>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151500017 | |||||||
| chr7:151500039 | C | T | 1 | a0001c0001t0001g0036 | 2 | HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.53-9025G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151500039 | |||||||
| chr7:151500116 | A | T | 5 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(2): Show |
5 | HG02280.hp1 HG02886.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.53-9102T>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151500116 | |||||||
| chr7:151500154 | A | T | 1 | a0001c0001t0001g0079 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.53-9140T>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151500154 | |||||||
| chr7:151500194 | A | T | 1 | a0001c0001t0003g0280 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.53-9180T>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151500194 | |||||||
| chr7:151500367 | A | T | 1 | a0001c0001t0001g0109 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.53-9353T>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151500367 | |||||||
| chr7:151500400 | G | A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0122 a0001c0001t0001g0139 |
4 | HG00735.hp2 HG00738.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-9386C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151500400 | |||||||
| chr7:151500420 | C | CA | 3 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 |
3 | HG01943.hp1 NA20129.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.53-9407dupT | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151500420 | |||||||
| chr7:151500455 | A | C | 1 | a0001c0001t0004g0005 | 3 | NA18981.hp1 NA19005.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.53-9441T>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151500455 | |||||||
| chr7:151500585 | G | C | 9 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(6): Show |
9 | HG02257.hp2 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.53-9571C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151500585 | |||||||
| chr7:151500600 | C | A | 20 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0018 others(17): Show |
24 | HG00408.hp1 HG00438.hp2 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.53-9586G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151500600 | |||||||
| chr7:151500606 | A | G | 8 | a0001c0001t0001g0014 a0001c0001t0001g0254 a0001c0001t0001g0261 others(5): Show |
10 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.53-9592T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151500606 | |||||||
| chr7:151500649 | G | C | 9 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0221 others(6): Show |
11 | HG00673.hp2 HG02083.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.53-9635C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151500649 | |||||||
| chr7:151500690 | T | A | 2 | a0001c0001t0002g0046 a0001c0001t0002g0049 |
2 | HG00735.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.53-9676A>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151500690 | |||||||
| chr7:151500727 | T | G | 1 | a0001c0001t0001g0271 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.53-9713A>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151500727 | |||||||
| chr7:151500801 | T | C | 1 | a0001c0001t0001g0023 | 2 | HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.53-9787A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151500801 | |||||||
| chr7:151500974 | AC | A | 4 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0268 others(1): Show |
4 | HG02257.hp2 HG02572.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-9961delG | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151500974 | |||||||
| chr7:151501002 | A | G | 1 | a0001c0001t0005g0045 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.53-9988T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151501002 | |||||||
| chr7:151501037 | A | C | 4 | a0001c0001t0002g0053 a0001c0001t0002g0054 a0001c0001t0002g0055 others(1): Show |
4 | HG02486.hp2 HG02622.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-10023T>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151501037 | |||||||
| chr7:151501562 | T | G | 8 | a0001c0001t0001g0014 a0001c0001t0001g0254 a0001c0001t0001g0261 others(5): Show |
10 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.53-10548A>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151501562 | |||||||
| chr7:151501621 | T | C | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | HG02723.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.53-10607A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151501621 | |||||||
| chr7:151501725 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.53-10711C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151501725 | |||||||
| chr7:151501742 | C | T | 1 | a0001c0001t0009g0061 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.53-10728G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151501742 | |||||||
| chr7:151501774 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.53-10760A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151501774 | |||||||
| chr7:151501833 | C | T | 3 | a0001c0001t0001g0214 a0001c0001t0001g0218 a0001c0001t0001g0219 |
3 | HG01099.hp1 HG01192.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.53-10819G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151501833 | |||||||
| chr7:151501834 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.53-10820C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151501834 | |||||||
| chr7:151501964 | G | A | 1 | a0001c0001t0001g0036 | 2 | HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.53-10950C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151501964 | |||||||
| chr7:151502006 | C | T | 4 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0268 others(1): Show |
4 | HG02257.hp2 HG02572.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-10992G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151502006 | |||||||
| chr7:151502094 | G | C | 1 | a0001c0001t0001g0116 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.53-11080C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151502094 | |||||||
| chr7:151502162 | G | A | 1 | a0001c0001t0009g0061 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.53-11148C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151502162 | |||||||
| chr7:151502187 | G | T | 1 | a0001c0001t0001g0118 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.53-11173C>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151502187 | |||||||
| chr7:151502228 | C | CA | 11 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0050 others(8): Show |
11 | HG00438.hp2 HG01192.hp2 HG01952.hp1 others(8): Show |
intron_variant | MODIFIER | c.53-11215dupT | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151502228 | |||||||
| chr7:151502228 | CA | C | 115 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(112): Show |
140 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.53-11215delT | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151502228 | |||||||
| chr7:151502294 | G | C | 1 | a0001c0001t0002g0286 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.53-11280C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151502294 | |||||||
| chr7:151502411 | A | G | 2 | a0001c0001t0001g0127 a0001c0001t0001g0142 |
2 | HG02135.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.53-11397T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151502411 | |||||||
| chr7:151502421 | CA | C | 4 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0268 others(1): Show |
4 | HG02257.hp2 HG02572.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-11408delT | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151502421 | |||||||
| chr7:151502430 | AAACTTTA others(48): Show |
A | 1 | a0001c0001t0001g0138 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.53-11471_53-11417d others(57): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151502430 | |||||||
| chr7:151502524 | T | C | 1 | a0001c0001t0001g0267 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.53-11510A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151502524 | |||||||
| chr7:151502570 | A | G | 2 | a0001c0001t0001g0255 a0001c0001t0001g0257 |
2 | HG01943.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.53-11556T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151502570 | |||||||
| chr7:151502712 | C | G | 1 | a0001c0001t0001g0133 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.53-11698G>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151502712 | |||||||
| chr7:151502727 | G | A | 15 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(12): Show |
15 | HG00735.hp1 HG01109.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.53-11713C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151502727 | |||||||
| chr7:151502812 | A | G | 1 | a0001c0001t0001g0040 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.53-11798T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151502812 | |||||||
| chr7:151502931 | G | C | 1 | a0001c0001t0001g0085 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.53-11917C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151502931 | |||||||
| chr7:151503051 | C | T | 8 | a0001c0001t0001g0014 a0001c0001t0001g0261 a0001c0001t0001g0262 others(5): Show |
10 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.53-12037G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151503051 | |||||||
| chr7:151503053 | A | G | 1 | a0001c0001t0001g0062 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.53-12039T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151503053 | |||||||
| chr7:151503251 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.53-12237C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151503251 | |||||||
| chr7:151503481 | C | T | 1 | a0001c0001t0001g0029 | 2 | HG01515.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.53-12467G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151503481 | |||||||
| chr7:151503656 | G | A | 5 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(2): Show |
5 | HG02280.hp1 HG02886.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.53-12642C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151503656 | |||||||
| chr7:151503721 | T | C | 5 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(2): Show |
5 | HG02280.hp1 HG02886.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.53-12707A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151503721 | |||||||
| chr7:151503763 | G | GA | 16 | a0001c0001t0001g0014 a0001c0001t0001g0086 a0001c0001t0001g0103 others(13): Show |
18 | HG01943.hp1 HG01975.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.53-12750dupT | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151503763 | |||||||
| chr7:151503763 | GA | G | 32 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0027 others(29): Show |
45 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.53-12750delT | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151503763 | |||||||
| chr7:151503776 | A | AAT | 7 | a0001c0001t0001g0012 a0001c0001t0001g0044 a0001c0001t0001g0047 others(4): Show |
9 | HG01099.hp1 HG02280.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.53-12763_53-12762i others(4): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151503776 | |||||||
| chr7:151503776 | A | AT | 114 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(111): Show |
137 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.53-12763dupA | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151503776 | |||||||
| chr7:151503776 | A | T | 9 | a0001c0001t0001g0036 a0001c0001t0001g0161 a0001c0001t0002g0046 others(6): Show |
10 | HG00735.hp1 HG01109.hp2 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.53-12762T>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151503776 | |||||||
| chr7:151503802 | G | A | 3 | a0001c0001t0001g0212 a0001c0001t0001g0231 a0001c0001t0006g0032 |
4 | NA18955.hp2 NA18974.hp1 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-12788C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151503802 | |||||||
| chr7:151503822 | G | C | 1 | a0001c0001t0001g0213 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.53-12808C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151503822 | |||||||
| chr7:151503852 | T | G | 11 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(8): Show |
11 | HG00735.hp1 HG01109.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.53-12838A>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151503852 | |||||||
| chr7:151503913 | T | C | 23 | a0001c0001t0001g0014 a0001c0001t0001g0044 a0001c0001t0001g0047 others(20): Show |
25 | HG00735.hp1 HG01109.hp2 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.53-12899A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151503913 | |||||||
| chr7:151503945 | A | G | 2 | a0001c0001t0001g0266 a0001c0001t0001g0267 |
2 | HG02572.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.53-12931T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151503945 | |||||||
| chr7:151504018 | TAGG | T | 7 | a0001c0001t0001g0014 a0001c0001t0001g0261 a0001c0001t0001g0262 others(4): Show |
9 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.53-13007_53-13005d others(5): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151504018 | |||||||
| chr7:151504071 | G | T | 2 | a0001c0001t0001g0274 a0001c0001t0001g0275 |
2 | NA18968.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.53-13057C>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151504071 | |||||||
| chr7:151504213 | T | C | 238 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(235): Show |
290 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.53-13199A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151504213 | |||||||
| chr7:151504234 | C | A | 1 | a0001c0001t0001g0252 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.53-13220G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151504234 | |||||||
| chr7:151504473 | G | A | 1 | a0001c0001t0001g0252 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.53-13459C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151504473 | |||||||
| chr7:151504562 | C | A | 8 | a0001c0001t0001g0014 a0001c0001t0001g0261 a0001c0001t0001g0262 others(5): Show |
10 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.53-13548G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151504562 | |||||||
| chr7:151504637 | A | C | 2 | a0001c0001t0001g0277 a0001c0001t0001g0278 |
2 | HG01891.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.53-13623T>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151504637 | |||||||
| chr7:151504671 | C | T | 1 | a0001c0001t0001g0239 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.53-13657G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151504671 | |||||||
| chr7:151504672 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.53-13658C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151504672 | |||||||
| chr7:151504723 | C | T | 2 | a0001c0001t0001g0277 a0001c0001t0001g0278 |
2 | HG01891.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.53-13709G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151504723 | |||||||
| chr7:151504867 | C | CA | 7 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(4): Show |
7 | HG02280.hp1 HG02602.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.53-13854dupT | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151504867 | |||||||
| chr7:151505043 | G | GA | 12 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0096 others(9): Show |
18 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.53-14030dupT | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151505043 | |||||||
| chr7:151505043 | G | GAA | 11 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0219 others(8): Show |
13 | HG00673.hp2 HG01192.hp1 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.53-14031_53-14030d others(4): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151505043 | |||||||
| chr7:151505054 | C | A | 146 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(143): Show |
176 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.53-14040G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151505054 | |||||||
| chr7:151505102 | C | A | 1 | a0001c0001t0001g0104 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.53-14088G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151505102 | |||||||
| chr7:151505102 | C | CA | 27 | a0001c0001t0001g0013 a0001c0001t0001g0044 a0001c0001t0001g0047 others(24): Show |
29 | HG00735.hp1 HG01109.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.53-14089dupT | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151505102 | |||||||
| chr7:151505169 | C | CA | 8 | a0001c0001t0001g0006 a0001c0001t0001g0087 a0001c0001t0001g0088 others(5): Show |
10 | HG00597.hp2 HG02293.hp1 HG03927.hp2 others(7): Show |
intron_variant | MODIFIER | c.53-14156dupT | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151505169 | |||||||
| chr7:151505169 | CA | C | 144 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(141): Show |
174 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.53-14156delT | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151505169 | |||||||
| chr7:151505210 | T | G | 4 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0268 others(1): Show |
4 | HG02257.hp2 HG02572.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-14196A>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151505210 | |||||||
| chr7:151505250 | A | T | 1 | a0001c0001t0001g0101 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.52+14210T>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151505250 | |||||||
| chr7:151505550 | G | C | 1 | a0001c0001t0001g0223 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.52+13910C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151505550 | |||||||
| chr7:151505907 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.52+13553G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151505907 | |||||||
| chr7:151505935 | AAACT | A | 7 | a0001c0001t0001g0014 a0001c0001t0001g0261 a0001c0001t0001g0262 others(4): Show |
9 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.52+13521_52+13524d others(6): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151505935 | |||||||
| chr7:151505952 | T | C | 2 | a0001c0001t0001g0062 a0001c0001t0001g0128 |
2 | NA18952.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.52+13508A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151505952 | |||||||
| chr7:151505965 | A | G | 4 | a0001c0001t0002g0053 a0001c0001t0002g0054 a0001c0001t0002g0055 others(1): Show |
4 | HG02486.hp2 HG02622.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.52+13495T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151505965 | |||||||
| chr7:151505972 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.52+13488G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151505972 | |||||||
| chr7:151506013 | T | C | 1 | a0001c0001t0001g0027 | 2 | NA18962.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.52+13447A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151506013 | |||||||
| chr7:151506153 | G | GA | 5 | a0001c0001t0001g0008 a0001c0001t0001g0094 a0001c0001t0001g0126 others(2): Show |
7 | HG00558.hp2 NA18954.hp1 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.52+13306dupT | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151506153 | |||||||
| chr7:151506188 | C | CT | 10 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0108 others(7): Show |
13 | HG01106.hp1 HG01243.hp1 HG02300.hp1 others(10): Show |
intron_variant | MODIFIER | c.52+13271dupA | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151506188 | |||||||
| chr7:151506238 | G | C | 4 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0050 others(1): Show |
4 | HG02280.hp1 HG02886.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.52+13222C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151506238 | |||||||
| chr7:151506328 | G | A | 2 | a0001c0001t0001g0277 a0001c0001t0001g0278 |
2 | HG01891.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.52+13132C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151506328 | |||||||
| chr7:151506455 | G | A | 23 | a0001c0001t0001g0014 a0001c0001t0001g0044 a0001c0001t0001g0047 others(20): Show |
25 | HG00735.hp1 HG01109.hp2 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.52+13005C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151506455 | |||||||
| chr7:151506510 | T | C | 2 | a0001c0001t0001g0224 a0001c0001t0001g0225 |
2 | HG02976.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.52+12950A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151506510 | |||||||
| chr7:151506570 | T | C | 1 | a0001c0001t0001g0243 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.52+12890A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151506570 | |||||||
| chr7:151506936 | G | C | 15 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(12): Show |
15 | HG00735.hp1 HG01109.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.52+12524C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151506936 | |||||||
| chr7:151507156 | C | G | 8 | a0001c0001t0001g0014 a0001c0001t0001g0261 a0001c0001t0001g0262 others(5): Show |
10 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.52+12304G>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151507156 | |||||||
| chr7:151507258 | A | G | 2 | a0001c0001t0001g0157 a0001c0001t0001g0160 |
2 | HG00597.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.52+12202T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151507258 | |||||||
| chr7:151507275 | C | T | 2 | a0001c0001t0001g0277 a0001c0001t0001g0278 |
2 | HG01891.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.52+12185G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151507275 | |||||||
| chr7:151507400 | C | T | 129 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(126): Show |
155 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.52+12060G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151507400 | |||||||
| chr7:151507407 | A | AT | 129 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(126): Show |
155 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.52+12052dupA | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151507407 | |||||||
| chr7:151507407 | A | ATAT | 17 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0252 others(14): Show |
21 | HG01243.hp1 HG01891.hp1 HG01943.hp1 others(18): Show |
intron_variant | MODIFIER | c.52+12052_52+12053i others(5): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151507407 | |||||||
| chr7:151507453 | T | C | 1 | a0001c0001t0010g0141 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.52+12007A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151507453 | |||||||
| chr7:151507471 | CAT | C | 4 | a0001c0001t0001g0018 a0001c0001t0001g0074 a0001c0001t0001g0076 others(1): Show |
5 | HG00408.hp1 NA18941.hp2 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.52+11987_52+11988d others(4): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151507471 | |||||||
| chr7:151507473 | T | G | 7 | a0001c0001t0003g0057 a0001c0001t0003g0279 a0001c0001t0003g0280 others(4): Show |
7 | HG01884.hp2 HG02572.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.52+11987A>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151507473 | |||||||
| chr7:151507477 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.52+11983G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151507477 | |||||||
| chr7:151507598 | T | G | 1 | a0001c0003t0001g0151 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.52+11862A>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151507598 | |||||||
| chr7:151507618 | G | A | 1 | a0001c0001t0002g0073 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.52+11842C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151507618 | |||||||
| chr7:151507679 | A | C | 1 | a0001c0001t0001g0186 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.52+11781T>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151507679 | |||||||
| chr7:151507760 | T | C | 1 | a0001c0001t0001g0257 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.52+11700A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151507760 | |||||||
| chr7:151507930 | T | C | 1 | a0001c0001t0013g0298 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.52+11530A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151507930 | |||||||
| chr7:151508110 | T | A | 3 | a0001c0001t0002g0090 a0001c0001t0002g0091 a0001c0001t0002g0098 |
3 | HG01167.hp2 HG01358.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.52+11350A>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151508110 | |||||||
| chr7:151508125 | T | C | 146 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(143): Show |
176 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.52+11335A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151508125 | |||||||
| chr7:151508243 | T | C | 1 | a0001c0001t0001g0226 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.52+11217A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151508243 | |||||||
| chr7:151508420 | T | C | 3 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0001g0244 |
3 | HG00673.hp2 HG02083.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.52+11040A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151508420 | |||||||
| chr7:151508588 | A | C | 1 | a0001c0001t0001g0059 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.52+10872T>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151508588 | |||||||
| chr7:151508634 | G | GT | 119 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(116): Show |
146 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.52+10825dupA | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151508634 | |||||||
| chr7:151508634 | G | GTT | 8 | a0001c0001t0001g0036 a0001c0001t0003g0057 a0001c0001t0003g0279 others(5): Show |
9 | HG01884.hp2 HG02572.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.52+10824_52+10825d others(4): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151508634 | |||||||
| chr7:151508698 | C | G | 1 | a0001c0001t0001g0277 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.52+10762G>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151508698 | |||||||
| chr7:151508802 | T | C | 1 | a0001c0001t0001g0036 | 2 | HG02895.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.52+10658A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151508802 | |||||||
| chr7:151508810 | G | C | 1 | a0001c0001t0001g0275 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.52+10650C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151508810 | |||||||
| chr7:151509089 | G | A | 2 | a0001c0001t0001g0277 a0001c0001t0001g0278 |
2 | HG01891.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.52+10371C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151509089 | |||||||
| chr7:151509125 | C | G | 9 | a0001c0001t0001g0013 a0001c0001t0001g0252 a0001c0001t0001g0253 others(6): Show |
11 | HG01243.hp1 HG01891.hp1 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.52+10335G>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151509125 | |||||||
| chr7:151509140 | A | G | 146 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(143): Show |
176 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.52+10320T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151509140 | |||||||
| chr7:151509142 | G | A | 6 | a0001c0001t0002g0037 a0001c0001t0002g0286 a0001c0001t0002g0287 others(3): Show |
7 | HG02055.hp1 HG02258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.52+10318C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151509142 | |||||||
| chr7:151509161 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.52+10299G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151509161 | |||||||
| chr7:151509236 | G | A | 1 | a0001c0001t0001g0030 | 2 | HG03834.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.52+10224C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151509236 | |||||||
| chr7:151509270 | C | A | 7 | a0001c0001t0003g0057 a0001c0001t0003g0279 a0001c0001t0003g0280 others(4): Show |
7 | HG01884.hp2 HG02572.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.52+10190G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151509270 | |||||||
| chr7:151509553 | C | T | 144 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(141): Show |
174 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.52+9907G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151509553 | |||||||
| chr7:151509578 | C | T | 1 | a0001c0001t0001g0030 | 2 | HG03834.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.52+9882G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151509578 | |||||||
| chr7:151509604 | C | G | 9 | a0001c0001t0001g0013 a0001c0001t0001g0252 a0001c0001t0001g0253 others(6): Show |
11 | HG01243.hp1 HG01891.hp1 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.52+9856G>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151509604 | |||||||
| chr7:151509685 | T | G | 1 | a0001c0001t0001g0094 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.52+9775A>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151509685 | |||||||
| chr7:151509753 | T | C | 1 | a0001c0001t0003g0283 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.52+9707A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151509753 | |||||||
| chr7:151509807 | T | C | 5 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(2): Show |
5 | HG02280.hp1 HG02886.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.52+9653A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151509807 | |||||||
| chr7:151509839 | G | A | 7 | a0001c0001t0003g0057 a0001c0001t0003g0279 a0001c0001t0003g0280 others(4): Show |
7 | HG01884.hp2 HG02572.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.52+9621C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151509839 | |||||||
| chr7:151509858 | G | A | 15 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(12): Show |
15 | HG00735.hp1 HG01109.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.52+9602C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151509858 | |||||||
| chr7:151510049 | GAA | G | 15 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(12): Show |
15 | HG00735.hp1 HG01109.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.52+9409_52+9410del others(2): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151510049 | |||||||
| chr7:151510098 | C | T | 2 | a0001c0001t0001g0277 a0001c0001t0001g0278 |
2 | HG01891.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.52+9362G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151510098 | |||||||
| chr7:151510101 | T | C | 2 | a0001c0001t0001g0180 a0001c0001t0001g0181 |
2 | HG01433.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.52+9359A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151510101 | |||||||
| chr7:151510391 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.52+9069A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151510391 | |||||||
| chr7:151510530 | A | C | 1 | a0001c0001t0002g0075 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.52+8930T>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151510530 | |||||||
| chr7:151510847 | G | A | 1 | a0001c0001t0001g0252 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.52+8613C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151510847 | |||||||
| chr7:151510887 | G | A | 11 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(8): Show |
11 | HG00735.hp1 HG01109.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.52+8573C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151510887 | |||||||
| chr7:151510985 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.52+8475C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151510985 | |||||||
| chr7:151511091 | T | TA | 8 | a0001c0001t0001g0014 a0001c0001t0001g0261 a0001c0001t0001g0262 others(5): Show |
10 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.52+8368dupT | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151511091 | |||||||
| chr7:151511244 | G | A | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(103): Show |
131 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.52+8216C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151511244 | |||||||
| chr7:151511347 | T | C | 30 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0027 others(27): Show |
43 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.52+8113A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151511347 | |||||||
| chr7:151511379 | G | T | 1 | a0001c0001t0005g0045 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.52+8081C>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151511379 | |||||||
| chr7:151511449 | C | A | 146 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(143): Show |
176 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.52+8011G>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151511449 | |||||||
| chr7:151511572 | CT | C | 8 | a0001c0001t0001g0013 a0001c0001t0001g0231 a0001c0001t0001g0252 others(5): Show |
10 | HG01243.hp1 HG01943.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.52+7887delA | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151511572 | |||||||
| chr7:151511664 | C | CT | 13 | a0001c0001t0001g0014 a0001c0001t0001g0029 a0001c0001t0001g0106 others(10): Show |
16 | HG00735.hp1 HG01515.hp2 HG01516.hp1 others(13): Show |
intron_variant | MODIFIER | c.52+7795dupA | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151511664 | |||||||
| chr7:151511664 | C | CTT | 11 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(8): Show |
11 | HG01109.hp2 HG02280.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.52+7794_52+7795dup others(2): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151511664 | |||||||
| chr7:151511710 | C | T | 3 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0184 |
3 | HG02040.hp2 HG02523.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.52+7750G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151511710 | |||||||
| chr7:151511735 | C | G | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | HG00544.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.52+7725G>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151511735 | |||||||
| chr7:151511740 | G | A | 27 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0024 others(24): Show |
35 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(32): Show |
intron_variant | MODIFIER | c.52+7720C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151511740 | |||||||
| chr7:151511902 | T | C | 288 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(285): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.52+7558A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151511902 | |||||||
| chr7:151511926 | T | C | 1 | a0001c0001t0001g0232 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.52+7534A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151511926 | |||||||
| chr7:151511981 | A | C | 1 | a0001c0004t0001g0154 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.52+7479T>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151511981 | |||||||
| chr7:151512038 | G | C | 1 | a0001c0001t0001g0264 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.52+7422C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151512038 | |||||||
| chr7:151512108 | G | A | 2 | a0001c0001t0002g0060 a0001c0001t0002g0093 |
2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.52+7352C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151512108 | |||||||
| chr7:151512305 | G | A | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(103): Show |
131 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.52+7155C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151512305 | |||||||
| chr7:151512306 | T | C | 4 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0268 others(1): Show |
4 | HG02257.hp2 HG02572.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.52+7154A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151512306 | |||||||
| chr7:151512688 | C | T | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(103): Show |
131 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.52+6772G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151512688 | |||||||
| chr7:151512698 | A | T | 1 | a0001c0001t0001g0252 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.52+6762T>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151512698 | |||||||
| chr7:151512771 | A | G | 1 | a0001c0001t0001g0019 | 2 | HG01106.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.52+6689T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151512771 | |||||||
| chr7:151512891 | G | A | 4 | a0001c0001t0002g0053 a0001c0001t0002g0054 a0001c0001t0002g0055 others(1): Show |
4 | HG02486.hp2 HG02622.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.52+6569C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151512891 | |||||||
| chr7:151512894 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.52+6566G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151512894 | |||||||
| chr7:151513053 | G | A | 23 | a0001c0001t0001g0014 a0001c0001t0001g0044 a0001c0001t0001g0047 others(20): Show |
25 | HG00735.hp1 HG01109.hp2 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.52+6407C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151513053 | |||||||
| chr7:151513091 | A | G | 7 | a0001c0001t0003g0057 a0001c0001t0003g0279 a0001c0001t0003g0280 others(4): Show |
7 | HG01884.hp2 HG02572.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.52+6369T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151513091 | |||||||
| chr7:151513124 | C | T | 146 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(143): Show |
176 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.52+6336G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151513124 | |||||||
| chr7:151513272 | T | C | 11 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(8): Show |
11 | HG00735.hp1 HG01109.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.52+6188A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151513272 | |||||||
| chr7:151513525 | G | A | 114 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(111): Show |
140 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.52+5935C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151513525 | |||||||
| chr7:151513674 | T | C | 1 | a0001c0001t0001g0233 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.52+5786A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151513674 | |||||||
| chr7:151513739 | T | A | 7 | a0001c0001t0001g0014 a0001c0001t0001g0261 a0001c0001t0001g0262 others(4): Show |
9 | HG02145.hp2 HG02717.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.52+5721A>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151513739 | |||||||
| chr7:151513754 | G | A | 1 | a0001c0001t0001g0251 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.52+5706C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151513754 | |||||||
| chr7:151513819 | T | A | 1 | a0001c0001t0001g0265 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.52+5641A>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151513819 | |||||||
| chr7:151513841 | T | A | 4 | a0001c0001t0001g0062 a0001c0001t0001g0127 a0001c0001t0001g0128 others(1): Show |
4 | HG02135.hp2 NA18945.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.52+5619A>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151513841 | |||||||
| chr7:151513875 | T | G | 3 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0143 |
3 | HG01256.hp2 HG01261.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.52+5585A>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151513875 | |||||||
| chr7:151513975 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.52+5485C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151513975 | |||||||
| chr7:151514019 | G | C | 4 | a0001c0001t0002g0053 a0001c0001t0002g0054 a0001c0001t0002g0055 others(1): Show |
4 | HG02486.hp2 HG02622.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.52+5441C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151514019 | |||||||
| chr7:151514184 | A | G | 15 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(12): Show |
15 | HG00735.hp1 HG01109.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.52+5276T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151514184 | |||||||
| chr7:151514415 | G | A | 3 | a0001c0001t0001g0255 a0001c0001t0001g0256 a0001c0001t0001g0257 |
3 | HG01943.hp1 NA20129.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.52+5045C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151514415 | |||||||
| chr7:151514520 | T | G | 146 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(143): Show |
176 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.52+4940A>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151514520 | |||||||
| chr7:151514522 | G | A | 5 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(2): Show |
5 | HG02280.hp1 HG02886.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.52+4938C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151514522 | |||||||
| chr7:151514699 | C | T | 114 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(111): Show |
140 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.52+4761G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151514699 | |||||||
| chr7:151515068 | C | CAA | 113 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(110): Show |
139 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.52+4390_52+4391dup others(2): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151515068 | |||||||
| chr7:151515068 | C | CAAAA | 9 | a0001c0001t0001g0013 a0001c0001t0001g0252 a0001c0001t0001g0253 others(6): Show |
11 | HG01243.hp1 HG01943.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.52+4388_52+4391dup others(4): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151515068 | |||||||
| chr7:151515068 | C | CAAAAA | 15 | a0001c0001t0001g0014 a0001c0001t0001g0044 a0001c0001t0001g0261 others(12): Show |
17 | HG00735.hp1 HG01109.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.52+4387_52+4391dup others(5): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151515068 | |||||||
| chr7:151515068 | C | CAAAAAA | 7 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0050 others(4): Show |
7 | HG02280.hp1 HG02486.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.52+4386_52+4391dup others(6): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151515068 | |||||||
| chr7:151515068 | CA | C | 49 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0018 others(46): Show |
56 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.52+4391delT | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151515068 | |||||||
| chr7:151515138 | A | G | 146 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(143): Show |
176 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.52+4322T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151515138 | |||||||
| chr7:151515175 | A | G | 3 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0182 |
5 | HG01069.hp2 HG01071.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.52+4285T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151515175 | |||||||
| chr7:151515220 | A | G | 4 | a0001c0001t0002g0053 a0001c0001t0002g0054 a0001c0001t0002g0055 others(1): Show |
4 | HG02486.hp2 HG02622.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.52+4240T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151515220 | |||||||
| chr7:151515686 | T | C | 1 | a0001c0001t0001g0235 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.52+3774A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151515686 | |||||||
| chr7:151515853 | A | C | 1 | a0001c0001t0003g0279 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.52+3607T>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151515853 | |||||||
| chr7:151515943 | T | C | 15 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(12): Show |
15 | HG00735.hp1 HG01109.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.52+3517A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151515943 | |||||||
| chr7:151515980 | T | G | 1 | a0001c0001t0001g0131 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.52+3480A>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151515980 | |||||||
| chr7:151516043 | T | TTTAAC | 124 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(121): Show |
152 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.52+3416_52+3417ins others(5): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151516043 | |||||||
| chr7:151516126 | T | C | 146 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(143): Show |
176 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.52+3334A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151516126 | |||||||
| chr7:151516157 | G | A | 1 | a0001c0001t0001g0236 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.52+3303C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151516157 | |||||||
| chr7:151516390 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.52+3070G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151516390 | |||||||
| chr7:151516391 | G | A | 1 | a0001c0001t0005g0045 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.52+3069C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151516391 | |||||||
| chr7:151516407 | G | A | 4 | a0001c0001t0001g0034 a0001c0001t0001g0237 a0001c0001t0001g0245 others(1): Show |
5 | HG02109.hp2 HG02280.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.52+3053C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151516407 | |||||||
| chr7:151516617 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.52+2843A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151516617 | |||||||
| chr7:151516622 | C | CA | 38 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0001t0001g0026 others(35): Show |
52 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.52+2837dupT | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151516622 | |||||||
| chr7:151516622 | C | CAA | 8 | a0001c0001t0001g0144 a0001c0001t0001g0160 a0001c0001t0001g0161 others(5): Show |
8 | HG00597.hp1 HG02135.hp1 HG03834.hp2 others(5): Show |
intron_variant | MODIFIER | c.52+2836_52+2837dup others(2): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151516622 | |||||||
| chr7:151516622 | CA | C | 74 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0017 others(71): Show |
82 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.52+2837delT | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151516622 | |||||||
| chr7:151516622 | CAA | C | 114 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(111): Show |
142 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.52+2836_52+2837del others(2): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151516622 | |||||||
| chr7:151516881 | G | T | 146 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(143): Show |
176 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.52+2579C>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151516881 | |||||||
| chr7:151517352 | G | C | 1 | a0001c0001t0005g0045 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.52+2108C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151517352 | |||||||
| chr7:151517361 | T | C | 1 | a0001c0001t0001g0059 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.52+2099A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151517361 | |||||||
| chr7:151517368 | CG | C | 98 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(95): Show |
123 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.52+2091delC | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151517368 | |||||||
| chr7:151517369 | GGA | G | 4 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0180 others(1): Show |
4 | HG01433.hp1 HG01496.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.52+2089_52+2090del others(2): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151517369 | |||||||
| chr7:151517370 | G | A | 22 | a0001c0001t0001g0013 a0001c0001t0001g0036 a0001c0001t0001g0247 others(19): Show |
25 | HG00544.hp1 HG01243.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.52+2090C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151517370 | |||||||
| chr7:151517370 | G | GA | 16 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0048 others(13): Show |
16 | HG01109.hp2 HG01891.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.52+2089dupT | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151517370 | |||||||
| chr7:151517370 | G | GAA | 6 | a0001c0001t0001g0050 a0001c0001t0002g0049 a0001c0001t0002g0053 others(3): Show |
6 | HG00735.hp1 HG02486.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.52+2088_52+2089dup others(2): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151517370 | |||||||
| chr7:151517370 | GA | G | 17 | a0001c0001t0001g0074 a0001c0001t0001g0153 a0001c0001t0001g0167 others(14): Show |
18 | HG01943.hp2 HG01975.hp2 HG02015.hp2 others(15): Show |
intron_variant | MODIFIER | c.52+2089delT | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151517370 | |||||||
| chr7:151517371 | A | G | 1 | a0001c0001t0001g0062 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.52+2089T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151517371 | |||||||
| chr7:151517496 | T | A | 4 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0260 others(1): Show |
4 | NA18963.hp2 NA18988.hp2 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.52+1964A>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151517496 | |||||||
| chr7:151517620 | C | G | 123 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(120): Show |
151 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.52+1840G>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151517620 | |||||||
| chr7:151517690 | C | CA | 17 | a0001c0001t0001g0035 a0001c0001t0001g0047 a0001c0001t0001g0048 others(14): Show |
18 | HG00438.hp1 HG00735.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.52+1769dupT | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151517690 | |||||||
| chr7:151517690 | CA | C | 9 | a0001c0001t0001g0166 a0001c0001t0002g0060 a0001c0001t0003g0057 others(6): Show |
9 | HG01884.hp2 HG02572.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.52+1769delT | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151517690 | |||||||
| chr7:151517710 | T | G | 1 | a0001c0001t0001g0278 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.52+1750A>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151517710 | |||||||
| chr7:151517711 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.52+1749C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151517711 | |||||||
| chr7:151517777 | T | C | 2 | a0001c0001t0001g0274 a0001c0001t0001g0275 |
2 | NA18968.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.52+1683A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151517777 | |||||||
| chr7:151517783 | T | G | 15 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0027 others(12): Show |
26 | HG00323.hp1 HG00438.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.52+1677A>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151517783 | |||||||
| chr7:151517837 | T | C | 1 | a0001c0001t0001g0276 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.52+1623A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151517837 | |||||||
| chr7:151518009 | A | AAGCCCAG others(15): Show |
1 | a0001c0001t0001g0052 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.52+1450_52+1451ins others(22): Show |
RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151518009 | |||||||
| chr7:151518012 | G | C | 1 | a0001c0001t0001g0052 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.52+1448C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151518012 | |||||||
| chr7:151518047 | T | G | 2 | a0001c0001t0001g0277 a0001c0001t0001g0278 |
2 | HG01891.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.52+1413A>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151518047 | |||||||
| chr7:151518095 | C | T | 7 | a0001c0001t0003g0057 a0001c0001t0003g0279 a0001c0001t0003g0280 others(4): Show |
7 | HG01884.hp2 HG02572.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.52+1365G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151518095 | |||||||
| chr7:151518230 | G | C | 1 | a0001c0001t0002g0152 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.52+1230C>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151518230 | |||||||
| chr7:151518235 | G | A | 4 | a0001c0001t0002g0053 a0001c0001t0002g0054 a0001c0001t0002g0055 others(1): Show |
4 | HG02486.hp2 HG02622.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.52+1225C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151518235 | |||||||
| chr7:151518368 | T | C | 15 | a0001c0001t0001g0036 a0001c0001t0001g0285 a0001c0001t0002g0037 others(12): Show |
17 | HG01884.hp2 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.52+1092A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151518368 | |||||||
| chr7:151518399 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.52+1061G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151518399 | |||||||
| chr7:151518498 | T | C | 2 | a0001c0001t0001g0291 a0001c0001t0001g0292 |
2 | NA18992.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.52+962A>G | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151518498 | |||||||
| chr7:151518525 | A | T | 1 | a0001c0001t0001g0058 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.52+935T>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151518525 | |||||||
| chr7:151518696 | G | A | 1 | a0001c0001t0001g0293 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.52+764C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151518696 | |||||||
| chr7:151518864 | A | G | 183 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(180): Show |
227 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.52+596T>C | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151518864 | |||||||
| chr7:151518929 | C | T | 29 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0027 others(26): Show |
42 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.52+531G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151518929 | |||||||
| chr7:151519267 | G | A | 167 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(164): Show |
211 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.52+193C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151519267 | |||||||
| chr7:151519279 | G | A | 1 | a0001c0001t0001g0296 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.52+181C>T | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151519279 | |||||||
| chr7:151519401 | C | T | 1 | a0001c0001t0001g0040 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.52+59G>A | RHEB | ENSG00000106615.10 | transcript | ENST00000262187.10 | protein_coding | 1/7 | chr7 | 151519401 |