Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 50862 |
| ensemblid | ENSG00000110315.7 |
| hgncid | 21159 |
| symbol | RNF141 |
| name | ring finger protein 141 |
| refseq_nuc | NM_016422.4 |
| refseq_prot | NP_057506.2 |
| ensembl_nuc | ENST00000265981.7 |
| ensembl_prot | ENSP00000265981.2 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 10511673 |
| end | 10541187 |
| strand | - |
| ver | v1.2 |
| region | chr11:10511673-10541187 |
| region5000 | chr11:10506673-10546187 |
| regionname0 | RNF141_chr11_10511673_10541187 |
| regionname5000 | RNF141_chr11_10506673_10546187 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 230 | 370 | 97 | 68 | 145 | 16 | 42 | 117 | RNF141_chr11_10506673_10546187 | RNF141 | MGQQI others(225): Show |
chr11 | 10506673 | 10546187 |
| a0002 | 0/0 | 230 | 3 | 0 | 0 | 3 | 0 | 0 | 1 | RNF141_chr11_10506673_10546187 | RNF141 | MGQQI others(225): Show |
chr11 | 10506673 | 10546187 |
| a0003 | 0/0 | 230 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | MGQQI others(225): Show |
chr11 | 10506673 | 10546187 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 690 | 257 | 95 | 46 | 79 | 11 | 25 | RNF141_chr11_10506673_10546187 | RNF141 | ATGGG others(685): Show |
chr11 | 10506673 | 10546187 | ||
| a0001c0002 | 0/1 | 690 | 112 | 1 | 22 | 66 | 5 | 17 | RNF141_chr11_10506673_10546187 | RNF141 | ATGGG others(685): Show |
chr11 | 10506673 | 10546187 | ||
| a0001c0004 | 0/0 | 690 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | ATGGG others(685): Show |
chr11 | 10506673 | 10546187 | ||
| a0002c0003 | 0/0 | 690 | 3 | 0 | 0 | 3 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | ATGGG others(685): Show |
chr11 | 10506673 | 10546187 | ||
| a0003c0005 | 0/0 | 690 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | ATGGG others(685): Show |
chr11 | 10506673 | 10546187 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4049 | 13 | 11 | 1 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | AGGTC others(4044): Show |
chr11 | 10506673 | 10546187 |
| a0001c0001t0002 | 0/0 | 4048 | 74 | 10 | 15 | 37 | 6 | 6 | RNF141_chr11_10506673_10546187 | RNF141 | AGGTC others(4043): Show |
chr11 | 10506673 | 10546187 |
| a0001c0001t0003 | 0/0 | 4048 | 63 | 7 | 7 | 36 | 2 | 11 | RNF141_chr11_10506673_10546187 | RNF141 | AGGTC others(4043): Show |
chr11 | 10506673 | 10546187 |
| a0001c0001t0004 | 0/0 | 4048 | 25 | 18 | 5 | 0 | 0 | 2 | RNF141_chr11_10506673_10546187 | RNF141 | AGGTC others(4043): Show |
chr11 | 10506673 | 10546187 |
| a0001c0001t0005 | 0/0 | 4049 | 19 | 1 | 10 | 2 | 3 | 3 | RNF141_chr11_10506673_10546187 | RNF141 | AGGTC others(4044): Show |
chr11 | 10506673 | 10546187 |
| a0001c0001t0006 | 0/0 | 4046 | 17 | 13 | 2 | 0 | 0 | 2 | RNF141_chr11_10506673_10546187 | RNF141 | AGGTC others(4041): Show |
chr11 | 10506673 | 10546187 |
| a0001c0001t0007 | 0/0 | 4051 | 10 | 10 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | AGGTC others(4046): Show |
chr11 | 10506673 | 10546187 |
| a0001c0001t0008 | 1/0 | 4049 | 6 | 4 | 1 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | AGGTC others(4044): Show |
chr11 | 10506673 | 10546187 |
| a0001c0001t0009 | 0/0 | 4049 | 5 | 5 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | AGGTC others(4044): Show |
chr11 | 10506673 | 10546187 |
| a0001c0001t0010 | 0/0 | 4048 | 6 | 5 | 1 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | AGGTC others(4043): Show |
chr11 | 10506673 | 10546187 |
| a0001c0001t0011 | 0/0 | 4049 | 3 | 3 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | AGGTC others(4044): Show |
chr11 | 10506673 | 10546187 |
| a0001c0001t0012 | 0/0 | 4048 | 3 | 2 | 1 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | AGGTC others(4043): Show |
chr11 | 10506673 | 10546187 |
| a0001c0001t0013 | 0/0 | 4050 | 3 | 3 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | AGGTC others(4045): Show |
chr11 | 10506673 | 10546187 |
| a0001c0001t0014 | 0/0 | 4049 | 2 | 2 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | AGGTC others(4044): Show |
chr11 | 10506673 | 10546187 |
| a0001c0001t0015 | 0/0 | 4048 | 2 | 0 | 0 | 2 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | AGGTC others(4043): Show |
chr11 | 10506673 | 10546187 |
| a0001c0001t0016 | 0/0 | 4048 | 2 | 0 | 2 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | AGGTC others(4043): Show |
chr11 | 10506673 | 10546187 |
| a0001c0001t0017 | 0/0 | 4049 | 1 | 0 | 0 | 0 | 0 | 1 | RNF141_chr11_10506673_10546187 | RNF141 | AGGTC others(4044): Show |
chr11 | 10506673 | 10546187 |
| a0001c0001t0023 | 0/0 | 4048 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | AGGTC others(4043): Show |
chr11 | 10506673 | 10546187 |
| a0001c0001t0024 | 0/0 | 4049 | 1 | 0 | 1 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | AGGTC others(4044): Show |
chr11 | 10506673 | 10546187 |
| a0001c0001t0025 | 0/0 | 4048 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | AGGTC others(4043): Show |
chr11 | 10506673 | 10546187 |
| a0001c0002t0001 | 0/0 | 4049 | 103 | 0 | 21 | 61 | 5 | 16 | RNF141_chr11_10506673_10546187 | RNF141 | AGGTC others(4044): Show |
chr11 | 10506673 | 10546187 |
| a0001c0002t0003 | 0/0 | 4048 | 2 | 0 | 0 | 2 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | AGGTC others(4043): Show |
chr11 | 10506673 | 10546187 |
| a0001c0002t0005 | 0/0 | 4049 | 1 | 0 | 0 | 0 | 0 | 1 | RNF141_chr11_10506673_10546187 | RNF141 | AGGTC others(4044): Show |
chr11 | 10506673 | 10546187 |
| a0001c0002t0009 | 0/0 | 4049 | 1 | 0 | 1 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | AGGTC others(4044): Show |
chr11 | 10506673 | 10546187 |
| a0001c0002t0018 | 0/0 | 4051 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | AGGTC others(4046): Show |
chr11 | 10506673 | 10546187 |
| a0001c0002t0019 | 0/1 | 4049 | 1 | 0 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | AGGTC others(4044): Show |
chr11 | 10506673 | 10546187 |
| a0001c0002t0020 | 0/0 | 4049 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | AGGTC others(4044): Show |
chr11 | 10506673 | 10546187 |
| a0001c0002t0021 | 0/0 | 4049 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | AGGTC others(4044): Show |
chr11 | 10506673 | 10546187 |
| a0001c0002t0022 | 0/0 | 4049 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | AGGTC others(4044): Show |
chr11 | 10506673 | 10546187 |
| a0001c0004t0008 | 0/0 | 4049 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | AGGTC others(4044): Show |
chr11 | 10506673 | 10546187 |
| a0002c0003t0001 | 0/0 | 4049 | 3 | 0 | 0 | 3 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | AGGTC others(4044): Show |
chr11 | 10506673 | 10546187 |
| a0003c0005t0001 | 0/0 | 4049 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | AGGTC others(4044): Show |
chr11 | 10506673 | 10546187 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0004 | 0/0 | 5 | 2 | 0 | 3 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0041 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0045 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0003g0002 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0003g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0003g0011 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0003g0012 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0003g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0003g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0003g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0003g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0003g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0003g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0004g0009 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0004g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0004g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0004g0044 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0004g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0004g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0004g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0004g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0004g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0004g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0004g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0004g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0004g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0004g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0005g0005 | 0/0 | 5 | 1 | 4 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0005g0021 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0005g0048 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0005g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0005g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0005g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0005g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0005g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0005g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0005g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0005g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0005g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0006g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0006g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0006g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0006g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0006g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0006g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0006g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0006g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0006g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0006g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0006g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0006g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0006g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0006g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0006g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0007g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0007g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0007g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0007g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0007g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0007g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0007g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0007g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0007g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0008g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0008g0095 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0008g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0008g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0008g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0009g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0009g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0009g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0010g0001 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0011g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0011g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0011g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0012g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0012g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0012g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0013g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0013g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0013g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0014g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0014g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0015g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0015g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0016g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0017g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0023g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0024g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0001t0025g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0006 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0007 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0014 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0015 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0016 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0017 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0018 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0005g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0009g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0018g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0019g0126 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0020g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0021g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0002t0022g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0001c0004t0008g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0002c0003t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0002c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| a0003c0005t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0011 | EUR | GBR | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG00099 | hp2 | a0001 | c0001 | t0005 | g0021 | EUR | GBR | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0155 | EUR | GBR | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0238 | EUR | GBR | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0075 | EUR | FIN | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0233 | EUR | FIN | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0147 | EUR | FIN | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0116 | EUR | FIN | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG00438 | hp1 | a0001 | c0002 | t0003 | g0150 | EAS | CHS | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | CHS | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | CHS | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | CHS | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0154 | EAS | CHS | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0009 | AMR | PUR | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG00639 | hp2 | a0001 | c0001 | t0012 | g0209 | AMR | PUR | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG00642 | hp1 | a0001 | c0001 | t0005 | g0279 | AMR | PUR | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0074 | AMR | PUR | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0235 | AMR | PUR | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0033 | AMR | PUR | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | PUR | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0033 | AMR | PUR | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG00741 | hp2 | a0001 | c0001 | t0008 | g0025 | AMR | PUR | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01069 | hp1 | a0001 | c0001 | t0006 | g0063 | AMR | PUR | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0040 | AMR | PUR | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0035 | AMR | PUR | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0040 | AMR | PUR | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0212 | AMR | PUR | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0016 | AMR | PUR | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01081 | hp2 | a0001 | c0001 | t0006 | g0061 | AMR | PUR | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0237 | AMR | PUR | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01099 | hp2 | a0001 | c0001 | t0005 | g0281 | AMR | PUR | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01106 | hp1 | a0001 | c0001 | t0004 | g0225 | AMR | PUR | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0251 | AMR | PUR | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0177 | AMR | PUR | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01167 | hp2 | a0001 | c0001 | t0016 | g0049 | AMR | PUR | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0253 | AMR | PUR | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0201 | AMR | PUR | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0035 | AMR | PUR | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01169 | hp2 | a0001 | c0001 | t0016 | g0049 | AMR | PUR | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01175 | hp1 | a0001 | c0002 | t0009 | g0117 | AMR | PUR | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01175 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | PUR | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0015 | AMR | PUR | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0104 | AMR | PUR | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01243 | hp1 | a0001 | c0001 | t0024 | g0088 | AMR | PUR | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0130 | AMR | CLM | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0044 | AMR | CLM | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0046 | AMR | CLM | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01258 | hp1 | a0001 | c0001 | t0004 | g0216 | AMR | CLM | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0046 | AMR | CLM | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01261 | hp1 | a0001 | c0001 | t0005 | g0005 | AMR | CLM | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01261 | hp2 | a0001 | c0001 | t0004 | g0248 | AMR | CLM | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01346 | hp1 | a0001 | c0001 | t0005 | g0005 | AMR | CLM | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0141 | AMR | CLM | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0017 | AMR | CLM | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | CLM | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0031 | AMR | CLM | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01515 | hp1 | a0001 | c0001 | t0005 | g0021 | EUR | IBS | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0245 | EUR | IBS | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0172 | EUR | IBS | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0045 | EUR | IBS | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01517 | hp1 | a0001 | c0001 | t0005 | g0021 | EUR | IBS | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0045 | EUR | IBS | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01884 | hp1 | a0001 | c0001 | t0007 | g0269 | AFR | ACB | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01884 | hp2 | a0001 | c0001 | t0006 | g0050 | AFR | ACB | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0156 | AMR | PEL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01928 | hp2 | a0001 | c0001 | t0005 | g0275 | AMR | PEL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01934 | hp1 | a0001 | c0001 | t0005 | g0276 | AMR | PEL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0142 | AMR | PEL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01943 | hp1 | a0001 | c0001 | t0010 | g0001 | AMR | PEL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0135 | AMR | PEL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01975 | hp1 | a0001 | c0001 | t0005 | g0048 | AMR | PEL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0207 | AMR | PEL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0015 | AMR | PEL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0017 | AMR | PEL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0185 | AMR | PEL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | PEL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0042 | AMR | PEL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0140 | AMR | PEL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | KHV | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0093 | AFR | ACB | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02055 | hp2 | a0001 | c0001 | t0013 | g0190 | AFR | ACB | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | KHV | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02056 | hp2 | a0001 | c0002 | t0020 | g0194 | EAS | KHV | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02071 | hp1 | a0001 | c0002 | t0021 | g0159 | EAS | KHV | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0106 | EAS | KHV | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0076 | EAS | KHV | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0160 | EAS | KHV | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | KHV | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0182 | EAS | KHV | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | KHV | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02129 | hp2 | a0002 | c0003 | t0001 | g0022 | EAS | KHV | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02132 | hp1 | a0002 | c0003 | t0001 | g0022 | EAS | KHV | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | KHV | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | KHV | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0149 | EAS | KHV | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02145 | hp1 | a0001 | c0001 | t0007 | g0268 | AFR | ACB | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0098 | AFR | ACB | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0143 | EAS | CDX | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | CDX | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | CDX | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0168 | EAS | CDX | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02257 | hp1 | a0001 | c0001 | t0011 | g0180 | AFR | ACB | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | ACB | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0195 | AFR | ACB | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02258 | hp2 | a0001 | c0001 | t0010 | g0001 | AFR | ACB | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0208 | AMR | PEL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02273 | hp2 | a0001 | c0001 | t0005 | g0277 | AMR | PEL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02280 | hp1 | a0001 | c0001 | t0006 | g0060 | AFR | ACB | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02280 | hp2 | a0001 | c0001 | t0009 | g0151 | AFR | ACB | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0192 | AMR | PEL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02293 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | PEL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0224 | AMR | PEL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0115 | AMR | PEL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02451 | hp1 | a0001 | c0001 | t0008 | g0181 | AFR | ACB | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | KHV | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | KHV | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02572 | hp1 | a0001 | c0001 | t0006 | g0010 | AFR | GWD | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02572 | hp2 | a0001 | c0001 | t0012 | g0239 | AFR | GWD | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02602 | hp1 | a0001 | c0001 | t0005 | g0285 | SAS | PJL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0280 | SAS | PJL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02615 | hp1 | a0001 | c0001 | t0009 | g0193 | AFR | GWD | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02622 | hp1 | a0001 | c0001 | t0010 | g0001 | AFR | GWD | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02622 | hp2 | a0001 | c0001 | t0011 | g0113 | AFR | GWD | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0215 | AFR | GWD | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02630 | hp2 | a0001 | c0001 | t0007 | g0096 | AFR | GWD | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02647 | hp1 | a0003 | c0005 | t0001 | g0065 | AFR | GWD | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0016 | SAS | PJL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0153 | SAS | PJL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02723 | hp1 | a0001 | c0001 | t0008 | g0187 | AFR | GWD | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02723 | hp2 | a0001 | c0001 | t0007 | g0271 | AFR | GWD | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0082 | SAS | PJL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0007 | SAS | PJL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02738 | hp1 | a0001 | c0001 | t0005 | g0097 | SAS | PJL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0243 | SAS | PJL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02809 | hp1 | a0001 | c0001 | t0006 | g0051 | AFR | GWD | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02809 | hp2 | a0001 | c0001 | t0012 | g0262 | AFR | GWD | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0211 | AFR | GWD | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02818 | hp2 | a0001 | c0001 | t0009 | g0019 | AFR | GWD | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0218 | AFR | GWD | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0234 | AFR | GWD | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0043 | AFR | GWD | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02895 | hp2 | a0001 | c0001 | t0007 | g0047 | AFR | GWD | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02896 | hp1 | a0001 | c0001 | t0009 | g0019 | AFR | GWD | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0037 | AFR | GWD | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02897 | hp1 | a0001 | c0001 | t0007 | g0047 | AFR | GWD | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0037 | AFR | GWD | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02922 | hp1 | a0001 | c0001 | t0007 | g0272 | AFR | ESN | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0219 | AFR | ESN | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0249 | AFR | ESN | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02965 | hp2 | a0001 | c0001 | t0010 | g0001 | AFR | ESN | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02970 | hp1 | a0001 | c0001 | t0010 | g0001 | AFR | ESN | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02970 | hp2 | a0001 | c0001 | t0014 | g0184 | AFR | ESN | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0072 | AFR | ESN | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02976 | hp2 | a0001 | c0001 | t0013 | g0189 | AFR | ESN | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0024 | SAS | PJL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0014 | SAS | PJL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG03041 | hp1 | a0001 | c0001 | t0013 | g0191 | AFR | GWD | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0099 | AFR | GWD | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0264 | AFR | MSL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0214 | AFR | MSL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG03130 | hp1 | a0001 | c0001 | t0006 | g0010 | AFR | ESN | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0179 | AFR | ESN | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG03139 | hp1 | a0001 | c0001 | t0007 | g0273 | AFR | ESN | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG03139 | hp2 | a0001 | c0001 | t0006 | g0056 | AFR | ESN | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG03195 | hp1 | a0001 | c0001 | t0006 | g0055 | AFR | ESN | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0071 | AFR | ESN | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0054 | AFR | MSL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG03225 | hp1 | a0001 | c0001 | t0007 | g0164 | AFR | MSL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG03225 | hp2 | a0001 | c0001 | t0008 | g0025 | AFR | MSL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | MSL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG03453 | hp2 | a0001 | c0001 | t0014 | g0064 | AFR | MSL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0057 | AFR | MSL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0009 | AFR | MSL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0023 | SAS | PJL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0039 | SAS | PJL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0030 | SAS | PJL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0024 | SAS | PJL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0023 | SAS | PJL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0030 | SAS | PJL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ESN | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG03516 | hp2 | a0001 | c0001 | t0006 | g0010 | AFR | ESN | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG03540 | hp1 | a0001 | c0001 | t0007 | g0270 | AFR | GWD | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0263 | AFR | GWD | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0069 | AFR | MSL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0009 | AFR | MSL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0204 | SAS | PJL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0007 | SAS | PJL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG03669 | hp1 | a0001 | c0001 | t0006 | g0062 | SAS | PJL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0078 | SAS | PJL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG03688 | hp1 | a0001 | c0001 | t0006 | g0059 | SAS | STU | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG03688 | hp2 | a0001 | c0002 | t0005 | g0129 | SAS | STU | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG03704 | hp1 | a0001 | c0001 | t0004 | g0044 | SAS | PJL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0031 | SAS | PJL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0186 | SAS | PJL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0274 | SAS | PJL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0161 | SAS | BEB | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0012 | SAS | BEB | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0041 | SAS | BEB | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0079 | SAS | BEB | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0014 | SAS | BEB | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG03927 | hp2 | a0001 | c0001 | t0005 | g0278 | SAS | BEB | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0123 | SAS | BEB | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0183 | SAS | BEB | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0205 | SAS | STU | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0077 | SAS | STU | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0086 | SAS | STU | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0200 | SAS | STU | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG04228 | hp1 | a0001 | c0001 | t0017 | g0282 | SAS | STU | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0229 | SAS | STU | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18522 | hp1 | a0001 | c0001 | t0011 | g0133 | AFR | YRI | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | YRI | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18612 | hp1 | a0001 | c0001 | t0005 | g0283 | EAS | CHB | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0067 | EAS | CHB | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18906 | hp1 | a0001 | c0001 | t0006 | g0052 | AFR | YRI | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | YRI | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18952 | hp1 | a0001 | c0002 | t0001 | g0284 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18962 | hp1 | a0001 | c0001 | t0015 | g0087 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0199 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0169 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0157 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18967 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0286 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18977 | hp1 | a0001 | c0001 | t0025 | g0121 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0136 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18982 | hp2 | a0001 | c0001 | t0015 | g0089 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0111 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0266 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0144 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18985 | hp1 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18988 | hp1 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18988 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18989 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0267 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0131 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18997 | hp1 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18999 | hp2 | a0001 | c0002 | t0018 | g0138 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19006 | hp1 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19011 | hp1 | a0001 | c0002 | t0003 | g0122 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0197 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19030 | hp1 | a0001 | c0001 | t0006 | g0053 | AFR | LWK | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0258 | AFR | LWK | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19043 | hp1 | a0001 | c0001 | t0010 | g0001 | AFR | LWK | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | LWK | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19055 | hp2 | a0001 | c0002 | t0001 | g0170 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19058 | hp1 | a0001 | c0001 | t0005 | g0048 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19058 | hp2 | a0001 | c0002 | t0001 | g0167 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0242 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0146 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19067 | hp1 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19067 | hp2 | a0002 | c0003 | t0001 | g0066 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19075 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19075 | hp2 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19076 | hp1 | a0001 | c0002 | t0001 | g0139 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19076 | hp2 | a0001 | c0001 | t0003 | g0256 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19078 | hp1 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0198 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0127 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19087 | hp1 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0112 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0226 | AFR | YRI | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0265 | AFR | YRI | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | ASW | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA20129 | hp2 | a0001 | c0004 | t0008 | g0094 | AFR | ASW | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0213 | EUR | TSI | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0018 | EUR | TSI | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0236 | SAS | GIH | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0070 | SAS | GIH | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0247 | AFR | ACB | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0058 | AFR | ACB | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02486 | hp1 | a0001 | c0001 | t0009 | g0019 | AFR | ACB | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0068 | AFR | ACB | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0081 | AFR | ACB | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG02559 | hp2 | a0001 | c0002 | t0022 | g0165 | AFR | ACB | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG03471 | hp1 | a0001 | c0001 | t0023 | g0217 | AFR | MSL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0043 | AFR | MSL | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0255 | AFR | USA | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | USA | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0241 | AFR | USA | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | USA | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA21309 | hp1 | a0001 | c0001 | t0008 | g0101 | AFR | LWK | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0083 | AFR | LWK | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0019 | g0126 | REF | REF | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0008 | g0095 | REF | REF | RNF141_chr11_10506673_10546187 | RNF141 | chr11 | 10506673 | 10546187 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:10530666 | C | T | 1 | a0002 | 3 | HG02129.hp2 HG02132.hp1 NA19067.hp2 |
missense_variant | MODERATE | c.229G>A | p.Val77Ile | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/6 | 342/4049 | 229/693 | 77/230 | chr11 | 10530666 | |||
| chr11:10534085 | G | A | 1 | a0003 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.74C>T | p.Thr25Met | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/6 | 187/4049 | 74/693 | 25/230 | chr11 | 10534085 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:10519087 | A | G | 1 | a0001c0004 | 1 | NA20129.hp2 | synonymous_variant | LOW | c.489T>C | p.Ala163Ala | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 5/6 | 602/4049 | 489/693 | 163/230 | chr11 | 10519087 | |||
| chr11:10534042 | A | G | 2 | a0001c0002 a0002c0003 |
114 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(111): Show |
synonymous_variant | LOW | c.117T>C | p.Leu39Leu | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/6 | 230/4049 | 117/693 | 39/230 | chr11 | 10534042 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:10511814 | G | T | 1 | a0001c0002t0020 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3102C>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 6/6 | 3102 | chr11 | 10511814 | ||||||
| chr11:10512154 | A | G | 1 | a0001c0001t0007 | 10 | HG01884.hp1 HG02145.hp1 HG02630.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2762T>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 6/6 | 2762 | chr11 | 10512154 | ||||||
| chr11:10512229 | AGT | A | 1 | a0001c0001t0006 | 17 | HG01069.hp1 HG01081.hp2 HG01884.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2685_*2686delAC | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 6/6 | 2685 | chr11 | 10512229 | ||||||
| chr11:10512262 | C | A | 1 | a0001c0002t0021 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2654G>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 6/6 | 2654 | chr11 | 10512262 | ||||||
| chr11:10512405 | T | C | 5 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0015 others(2): Show |
84 | HG00140.hp2 HG00280.hp2 HG00558.hp2 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*2511A>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 6/6 | 2511 | chr11 | 10512405 | ||||||
| chr11:10512881 | T | C | 1 | a0001c0001t0014 | 2 | HG02970.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2035A>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 6/6 | 2035 | chr11 | 10512881 | ||||||
| chr11:10512964 | T | C | 1 | a0001c0002t0022 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1952A>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 6/6 | 1952 | chr11 | 10512964 | ||||||
| chr11:10513008 | A | C | 2 | a0001c0001t0004 a0001c0001t0023 |
26 | HG00639.hp1 HG01106.hp1 HG01256.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1908T>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 6/6 | 1908 | chr11 | 10513008 | ||||||
| chr11:10513319 | C | T | 15 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0009 others(12): Show |
156 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(153): Show |
3_prime_UTR_variant | MODIFIER | c.*1597G>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 6/6 | 1597 | chr11 | 10513319 | ||||||
| chr11:10513462 | C | T | 1 | a0001c0001t0025 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1454G>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 6/6 | 1454 | chr11 | 10513462 | ||||||
| chr11:10513474 | T | C | 1 | a0001c0001t0012 | 3 | HG00639.hp2 HG02572.hp2 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1442A>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 6/6 | 1442 | chr11 | 10513474 | ||||||
| chr11:10513687 | GT | G | 11 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(8): Show |
196 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
3_prime_UTR_variant | MODIFIER | c.*1228delA | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 6/6 | 1228 | chr11 | 10513687 | ||||||
| chr11:10513746 | C | T | 1 | a0001c0001t0023 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1170G>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 6/6 | 1170 | chr11 | 10513746 | ||||||
| chr11:10513802 | G | A | 9 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0010 others(6): Show |
104 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*1114C>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 6/6 | 1114 | chr11 | 10513802 | ||||||
| chr11:10514139 | A | C | 1 | a0001c0001t0010 | 6 | HG01943.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*777T>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 6/6 | 777 | chr11 | 10514139 | ||||||
| chr11:10514243 | G | GA | 1 | a0001c0001t0013 | 3 | HG02055.hp2 HG02976.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*672dupT | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 6/6 | 672 | chr11 | 10514243 | ||||||
| chr11:10514244 | A | C | 3 | a0001c0001t0005 a0001c0001t0017 a0001c0002t0005 |
21 | HG00099.hp2 HG00642.hp1 HG01099.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*672T>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 6/6 | 672 | chr11 | 10514244 | ||||||
| chr11:10514413 | C | CAT | 2 | a0001c0001t0007 a0001c0002t0018 |
11 | HG01884.hp1 HG02145.hp1 HG02630.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*501_*502dupAT | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 6/6 | 502 | chr11 | 10514413 | ||||||
| chr11:10514569 | A | G | 23 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(20): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
3_prime_UTR_variant | MODIFIER | c.*347T>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 6/6 | 347 | chr11 | 10514569 | ||||||
| chr11:10514743 | G | A | 1 | a0001c0002t0022 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*173C>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 6/6 | 173 | chr11 | 10514743 | ||||||
| chr11:10514751 | T | C | 8 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0010 others(5): Show |
101 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*165A>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 6/6 | 165 | chr11 | 10514751 | ||||||
| chr11:10514842 | C | T | 1 | a0001c0001t0017 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*74G>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 6/6 | 74 | chr11 | 10514842 | ||||||
| chr11:10541133 | G | A | 1 | a0001c0001t0016 | 2 | HG01167.hp2 HG01169.hp2 |
5_prime_UTR_variant | MODIFIER | c.-59C>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/6 | 6975 | chr11 | 10541133 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:10515177 | T | C | 122 | a0001c0001t0001g0073 a0001c0001t0001g0124 a0001c0001t0001g0125 others(119): Show |
156 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.543-111A>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 5/5 | chr11 | 10515177 | |||||||
| chr11:10515317 | C | T | 1 | a0001c0002t0001g0146 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.543-251G>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 5/5 | chr11 | 10515317 | |||||||
| chr11:10515374 | C | T | 2 | a0001c0002t0001g0155 a0001c0002t0001g0172 |
2 | HG00140.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.543-308G>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 5/5 | chr11 | 10515374 | |||||||
| chr11:10515388 | G | A | 2 | a0001c0001t0009g0019 a0001c0001t0009g0193 |
4 | HG02486.hp1 HG02615.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.543-322C>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 5/5 | chr11 | 10515388 | |||||||
| chr11:10515749 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.543-683G>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 5/5 | chr11 | 10515749 | |||||||
| chr11:10515991 | A | G | 1 | a0001c0001t0003g0077 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.543-925T>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 5/5 | chr11 | 10515991 | |||||||
| chr11:10516034 | G | T | 68 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0011 others(65): Show |
99 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.543-968C>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 5/5 | chr11 | 10516034 | |||||||
| chr11:10516133 | G | C | 1 | a0001c0002t0001g0128 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.543-1067C>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 5/5 | chr11 | 10516133 | |||||||
| chr11:10516174 | G | A | 185 | a0001c0001t0001g0073 a0001c0001t0001g0124 a0001c0001t0001g0125 others(182): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.543-1108C>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 5/5 | chr11 | 10516174 | |||||||
| chr11:10516368 | T | A | 1 | a0001c0001t0002g0206 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.543-1302A>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 5/5 | chr11 | 10516368 | |||||||
| chr11:10516414 | T | C | 1 | a0001c0001t0002g0244 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.543-1348A>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 5/5 | chr11 | 10516414 | |||||||
| chr11:10516427 | G | A | 1 | a0003c0005t0001g0065 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.543-1361C>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 5/5 | chr11 | 10516427 | |||||||
| chr11:10516577 | G | A | 1 | a0001c0002t0001g0153 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.543-1511C>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 5/5 | chr11 | 10516577 | |||||||
| chr11:10516623 | G | A | 70 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0011 others(67): Show |
101 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.543-1557C>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 5/5 | chr11 | 10516623 | |||||||
| chr11:10516641 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.543-1575C>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 5/5 | chr11 | 10516641 | |||||||
| chr11:10516781 | C | A | 53 | a0001c0001t0002g0004 a0001c0001t0002g0020 a0001c0001t0002g0038 others(50): Show |
67 | HG00140.hp2 HG00280.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.543-1715G>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 5/5 | chr11 | 10516781 | |||||||
| chr11:10516861 | A | G | 1 | a0001c0001t0003g0069 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.543-1795T>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 5/5 | chr11 | 10516861 | |||||||
| chr11:10517269 | C | T | 43 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0011 others(40): Show |
67 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.542+1765G>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 5/5 | chr11 | 10517269 | |||||||
| chr11:10517312 | A | G | 120 | a0001c0001t0001g0073 a0001c0001t0001g0124 a0001c0001t0001g0125 others(117): Show |
154 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.542+1722T>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 5/5 | chr11 | 10517312 | |||||||
| chr11:10517332 | G | C | 6 | a0001c0001t0001g0287 a0001c0001t0011g0113 a0001c0001t0011g0133 others(3): Show |
6 | HG02257.hp1 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.542+1702C>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 5/5 | chr11 | 10517332 | |||||||
| chr11:10517530 | C | T | 1 | a0001c0001t0006g0052 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.542+1504G>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 5/5 | chr11 | 10517530 | |||||||
| chr11:10517559 | G | C | 69 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0011 others(66): Show |
100 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.542+1475C>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 5/5 | chr11 | 10517559 | |||||||
| chr11:10517612 | CAG | C | 2 | a0001c0001t0003g0024 a0001c0001t0008g0025 |
4 | HG00741.hp2 HG03017.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.542+1420_542+1421d others(4): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 5/5 | chr11 | 10517612 | |||||||
| chr11:10517727 | A | G | 110 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0152 others(107): Show |
144 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.542+1307T>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 5/5 | chr11 | 10517727 | |||||||
| chr11:10517756 | GA | G | 5 | a0001c0001t0006g0059 a0001c0001t0006g0060 a0001c0001t0006g0061 others(2): Show |
5 | HG01069.hp1 HG01081.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.542+1277delT | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 5/5 | chr11 | 10517756 | |||||||
| chr11:10517771 | A | G | 1 | a0001c0001t0002g0206 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.542+1263T>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 5/5 | chr11 | 10517771 | |||||||
| chr11:10517854 | G | A | 2 | a0001c0001t0003g0011 a0001c0001t0003g0033 |
5 | HG00099.hp1 HG00738.hp1 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.542+1180C>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 5/5 | chr11 | 10517854 | |||||||
| chr11:10517968 | G | A | 2 | a0001c0002t0001g0155 a0001c0002t0001g0172 |
2 | HG00140.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.542+1066C>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 5/5 | chr11 | 10517968 | |||||||
| chr11:10518045 | G | C | 1 | a0001c0001t0002g0228 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.542+989C>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 5/5 | chr11 | 10518045 | |||||||
| chr11:10518091 | C | T | 1 | a0001c0004t0008g0094 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.542+943G>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 5/5 | chr11 | 10518091 | |||||||
| chr11:10518306 | T | C | 1 | a0001c0001t0008g0181 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.542+728A>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 5/5 | chr11 | 10518306 | |||||||
| chr11:10518339 | T | C | 283 | a0001c0001t0001g0073 a0001c0001t0001g0124 a0001c0001t0001g0125 others(280): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.542+695A>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 5/5 | chr11 | 10518339 | |||||||
| chr11:10518378 | G | A | 6 | a0001c0001t0003g0011 a0001c0001t0003g0033 a0001c0001t0003g0075 others(3): Show |
9 | HG00099.hp1 HG00280.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.542+656C>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 5/5 | chr11 | 10518378 | |||||||
| chr11:10518383 | C | T | 120 | a0001c0001t0001g0073 a0001c0001t0001g0124 a0001c0001t0001g0125 others(117): Show |
154 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.542+651G>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 5/5 | chr11 | 10518383 | |||||||
| chr11:10518466 | CTGAA | C | 80 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0020 others(77): Show |
100 | HG00140.hp2 HG00280.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.542+564_542+567del others(4): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 5/5 | chr11 | 10518466 | |||||||
| chr11:10518516 | A | C | 2 | a0001c0001t0003g0071 a0001c0001t0003g0179 |
2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.542+518T>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 5/5 | chr11 | 10518516 | |||||||
| chr11:10518541 | G | A | 1 | a0001c0001t0013g0189 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.542+493C>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 5/5 | chr11 | 10518541 | |||||||
| chr11:10518592 | T | C | 120 | a0001c0001t0001g0073 a0001c0001t0001g0124 a0001c0001t0001g0125 others(117): Show |
154 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.542+442A>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 5/5 | chr11 | 10518592 | |||||||
| chr11:10518620 | C | T | 9 | a0001c0001t0007g0047 a0001c0001t0007g0096 a0001c0001t0007g0164 others(6): Show |
10 | HG01884.hp1 HG02145.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.542+414G>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 5/5 | chr11 | 10518620 | |||||||
| chr11:10518784 | A | C | 120 | a0001c0001t0001g0073 a0001c0001t0001g0124 a0001c0001t0001g0125 others(117): Show |
154 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.542+250T>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 5/5 | chr11 | 10518784 | |||||||
| chr11:10518796 | A | G | 120 | a0001c0001t0001g0073 a0001c0001t0001g0124 a0001c0001t0001g0125 others(117): Show |
154 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.542+238T>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 5/5 | chr11 | 10518796 | |||||||
| chr11:10518823 | C | T | 1 | a0001c0001t0003g0069 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.542+211G>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 5/5 | chr11 | 10518823 | |||||||
| chr11:10518825 | A | G | 1 | a0001c0001t0002g0243 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.542+209T>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 5/5 | chr11 | 10518825 | |||||||
| chr11:10518864 | TAA | T | 120 | a0001c0001t0001g0073 a0001c0001t0001g0124 a0001c0001t0001g0125 others(117): Show |
154 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.542+168_542+169del others(2): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 5/5 | chr11 | 10518864 | |||||||
| chr11:10518870 | C | T | 16 | a0001c0001t0006g0010 a0001c0001t0006g0050 a0001c0001t0006g0051 others(13): Show |
18 | HG01069.hp1 HG01081.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.542+164G>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 5/5 | chr11 | 10518870 | |||||||
| chr11:10519383 | TAAAG | T | 4 | a0001c0002t0001g0115 a0001c0002t0001g0135 a0001c0002t0001g0140 others(1): Show |
4 | HG01934.hp2 HG01943.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.435-246_435-243del others(4): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10519383 | |||||||
| chr11:10519664 | A | AGGCTACT others(29): Show |
14 | a0001c0001t0005g0005 a0001c0001t0005g0021 a0001c0001t0005g0048 others(11): Show |
21 | HG00099.hp2 HG00642.hp1 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.435-524_435-523ins others(36): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10519664 | |||||||
| chr11:10519667 | G | T | 14 | a0001c0001t0005g0005 a0001c0001t0005g0021 a0001c0001t0005g0048 others(11): Show |
21 | HG00099.hp2 HG00642.hp1 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.435-526C>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10519667 | |||||||
| chr11:10519849 | G | A | 1 | a0001c0004t0008g0094 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.435-708C>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10519849 | |||||||
| chr11:10520066 | C | T | 70 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0011 others(67): Show |
101 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.435-925G>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10520066 | |||||||
| chr11:10520079 | T | C | 14 | a0001c0001t0005g0005 a0001c0001t0005g0021 a0001c0001t0005g0048 others(11): Show |
21 | HG00099.hp2 HG00642.hp1 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.435-938A>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10520079 | |||||||
| chr11:10520091 | G | T | 1 | a0001c0001t0006g0061 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.435-950C>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10520091 | |||||||
| chr11:10520154 | T | A | 122 | a0001c0001t0001g0073 a0001c0001t0001g0124 a0001c0001t0001g0125 others(119): Show |
156 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.435-1013A>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10520154 | |||||||
| chr11:10520257 | CTT | C | 76 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0020 others(73): Show |
96 | HG00140.hp2 HG00280.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.435-1118_435-1117d others(4): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10520257 | |||||||
| chr11:10520392 | C | T | 1 | a0001c0001t0008g0181 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.435-1251G>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10520392 | |||||||
| chr11:10520428 | C | T | 283 | a0001c0001t0001g0073 a0001c0001t0001g0124 a0001c0001t0001g0125 others(280): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.435-1287G>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10520428 | |||||||
| chr11:10520457 | T | C | 1 | a0001c0001t0002g0245 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.435-1316A>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10520457 | |||||||
| chr11:10520797 | A | C | 3 | a0001c0001t0013g0189 a0001c0001t0013g0190 a0001c0001t0013g0191 |
3 | HG02055.hp2 HG02976.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.435-1656T>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10520797 | |||||||
| chr11:10520945 | T | G | 3 | a0001c0001t0001g0073 a0001c0001t0001g0132 a0001c0001t0001g0148 |
3 | NA18522.hp2 NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.435-1804A>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10520945 | |||||||
| chr11:10520976 | T | C | 15 | a0001c0001t0006g0010 a0001c0001t0006g0050 a0001c0001t0006g0051 others(12): Show |
17 | HG01069.hp1 HG01081.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.435-1835A>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10520976 | |||||||
| chr11:10521024 | T | C | 2 | a0001c0001t0003g0083 a0001c0002t0001g0158 |
2 | NA19078.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.435-1883A>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10521024 | |||||||
| chr11:10521098 | G | C | 1 | a0001c0001t0013g0191 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.435-1957C>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10521098 | |||||||
| chr11:10521260 | C | G | 8 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0152 others(5): Show |
10 | HG01243.hp2 HG01891.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.435-2119G>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10521260 | |||||||
| chr11:10521548 | C | T | 1 | a0001c0001t0002g0264 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.435-2407G>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10521548 | |||||||
| chr11:10521568 | T | G | 2 | a0001c0001t0008g0181 a0001c0001t0008g0187 |
2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.435-2427A>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10521568 | |||||||
| chr11:10521734 | T | C | 1 | a0001c0002t0001g0192 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.435-2593A>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10521734 | |||||||
| chr11:10521749 | C | T | 68 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0011 others(65): Show |
99 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.435-2608G>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10521749 | |||||||
| chr11:10521828 | G | C | 2 | a0001c0001t0009g0019 a0001c0001t0009g0193 |
4 | HG02486.hp1 HG02615.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.435-2687C>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10521828 | |||||||
| chr11:10521971 | T | C | 15 | a0001c0001t0006g0010 a0001c0001t0006g0050 a0001c0001t0006g0051 others(12): Show |
17 | HG01069.hp1 HG01081.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.435-2830A>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10521971 | |||||||
| chr11:10522135 | T | A | 2 | a0001c0001t0012g0209 a0001c0001t0012g0262 |
2 | HG00639.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.435-2994A>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10522135 | |||||||
| chr11:10522157 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.435-3016C>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10522157 | |||||||
| chr11:10522193 | T | C | 9 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0080 others(6): Show |
19 | HG00621.hp2 HG01255.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.434+2999A>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10522193 | |||||||
| chr11:10522325 | G | A | 1 | a0001c0001t0003g0071 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.434+2867C>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10522325 | |||||||
| chr11:10522355 | G | T | 1 | a0001c0001t0011g0180 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.434+2837C>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10522355 | |||||||
| chr11:10522377 | C | A | 68 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0011 others(65): Show |
99 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.434+2815G>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10522377 | |||||||
| chr11:10522478 | A | T | 2 | a0001c0002t0001g0127 a0001c0002t0001g0145 |
2 | NA18993.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.434+2714T>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10522478 | |||||||
| chr11:10522536 | T | C | 1 | a0001c0002t0001g0182 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.434+2656A>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10522536 | |||||||
| chr11:10522694 | T | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0166 |
2 | HG01243.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.434+2498A>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10522694 | |||||||
| chr11:10522944 | A | G | 15 | a0001c0001t0006g0010 a0001c0001t0006g0050 a0001c0001t0006g0051 others(12): Show |
17 | HG01069.hp1 HG01081.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.434+2248T>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10522944 | |||||||
| chr11:10523027 | T | C | 2 | a0001c0001t0008g0181 a0001c0001t0008g0187 |
2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.434+2165A>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10523027 | |||||||
| chr11:10523128 | A | C | 1 | a0001c0002t0001g0158 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.434+2064T>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10523128 | |||||||
| chr11:10523192 | C | G | 1 | a0001c0001t0011g0133 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.434+2000G>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10523192 | |||||||
| chr11:10523275 | T | C | 4 | a0001c0001t0013g0189 a0001c0001t0013g0190 a0001c0001t0013g0191 others(1): Show |
4 | HG02055.hp2 HG02647.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.434+1917A>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10523275 | |||||||
| chr11:10523305 | C | T | 283 | a0001c0001t0001g0073 a0001c0001t0001g0124 a0001c0001t0001g0125 others(280): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.434+1887G>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10523305 | |||||||
| chr11:10523399 | T | C | 1 | a0001c0004t0008g0094 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.434+1793A>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10523399 | |||||||
| chr11:10523406 | A | G | 1 | a0001c0002t0001g0178 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.434+1786T>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10523406 | |||||||
| chr11:10523434 | G | T | 1 | a0001c0002t0001g0030 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.434+1758C>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10523434 | |||||||
| chr11:10523635 | C | G | 15 | a0001c0001t0006g0010 a0001c0001t0006g0050 a0001c0001t0006g0051 others(12): Show |
17 | HG01069.hp1 HG01081.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.434+1557G>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10523635 | |||||||
| chr11:10523637 | A | G | 5 | a0001c0001t0011g0113 a0001c0001t0011g0133 a0001c0001t0011g0180 others(2): Show |
5 | HG02257.hp1 HG02622.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.434+1555T>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10523637 | |||||||
| chr11:10523745 | GA | G | 205 | a0001c0001t0001g0073 a0001c0001t0001g0124 a0001c0001t0001g0125 others(202): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.434+1446delT | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10523745 | |||||||
| chr11:10523831 | C | A | 3 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0233 |
5 | HG00280.hp2 HG01256.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.434+1361G>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10523831 | |||||||
| chr11:10523857 | G | A | 184 | a0001c0001t0001g0073 a0001c0001t0001g0124 a0001c0001t0001g0125 others(181): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.434+1335C>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10523857 | |||||||
| chr11:10524108 | G | C | 2 | a0001c0001t0001g0132 a0001c0001t0001g0148 |
2 | NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.434+1084C>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10524108 | |||||||
| chr11:10524126 | A | G | 3 | a0001c0001t0001g0073 a0001c0001t0001g0132 a0001c0001t0001g0148 |
3 | NA18522.hp2 NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.434+1066T>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10524126 | |||||||
| chr11:10524166 | G | A | 63 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0020 others(60): Show |
83 | HG00140.hp2 HG00280.hp2 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.434+1026C>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10524166 | |||||||
| chr11:10524180 | C | T | 18 | a0001c0001t0006g0010 a0001c0001t0006g0050 a0001c0001t0006g0051 others(15): Show |
20 | HG00639.hp2 HG01069.hp1 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.434+1012G>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10524180 | |||||||
| chr11:10524217 | C | G | 96 | a0001c0001t0001g0073 a0001c0001t0001g0124 a0001c0001t0001g0125 others(93): Show |
121 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.434+975G>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10524217 | |||||||
| chr11:10524240 | C | T | 2 | a0001c0001t0001g0125 a0001c0001t0001g0166 |
2 | HG01243.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.434+952G>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10524240 | |||||||
| chr11:10524272 | G | A | 67 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0011 others(64): Show |
98 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.434+920C>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10524272 | |||||||
| chr11:10524333 | T | C | 187 | a0001c0001t0001g0073 a0001c0001t0001g0124 a0001c0001t0001g0125 others(184): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.434+859A>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10524333 | |||||||
| chr11:10524376 | G | A | 1 | a0001c0002t0001g0173 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.434+816C>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10524376 | |||||||
| chr11:10524404 | T | TA | 10 | a0001c0001t0002g0232 a0001c0001t0002g0246 a0001c0001t0002g0250 others(7): Show |
10 | HG00558.hp2 HG01168.hp1 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.434+787dupT | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10524404 | |||||||
| chr11:10524574 | G | A | 1 | a0001c0001t0002g0236 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.434+618C>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10524574 | |||||||
| chr11:10524604 | C | G | 2 | a0001c0001t0001g0132 a0001c0001t0001g0148 |
2 | NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.434+588G>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10524604 | |||||||
| chr11:10525081 | G | GA | 274 | a0001c0001t0001g0073 a0001c0001t0001g0124 a0001c0001t0001g0125 others(271): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.434+110dupT | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10525081 | |||||||
| chr11:10525090 | A | AG | 6 | a0001c0001t0002g0042 a0001c0001t0002g0093 a0001c0001t0002g0208 others(3): Show |
7 | HG01074.hp1 HG01981.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.434+101_434+102ins others(1): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10525090 | |||||||
| chr11:10525130 | A | G | 1 | a0001c0001t0008g0101 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.434+62T>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10525130 | |||||||
| chr11:10525176 | C | T | 2 | a0001c0001t0002g0040 a0001c0001t0002g0041 |
4 | HG00738.hp2 HG01069.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.434+16G>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 4/5 | chr11 | 10525176 | |||||||
| chr11:10525391 | A | G | 1 | a0001c0002t0001g0284 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.253-18T>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10525391 | |||||||
| chr11:10525503 | A | T | 2 | a0001c0001t0003g0071 a0001c0001t0003g0179 |
2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.253-130T>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10525503 | |||||||
| chr11:10525627 | G | C | 186 | a0001c0001t0001g0073 a0001c0001t0001g0124 a0001c0001t0001g0125 others(183): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.253-254C>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10525627 | |||||||
| chr11:10525867 | A | G | 1 | a0001c0001t0002g0230 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.253-494T>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10525867 | |||||||
| chr11:10526129 | T | C | 44 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0011 others(41): Show |
68 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.253-756A>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10526129 | |||||||
| chr11:10526141 | T | A | 1 | a0001c0001t0003g0079 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.253-768A>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10526141 | |||||||
| chr11:10526186 | G | A | 1 | a0001c0002t0001g0141 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.253-813C>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10526186 | |||||||
| chr11:10526212 | T | C | 1 | a0001c0004t0008g0094 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.253-839A>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10526212 | |||||||
| chr11:10526311 | A | G | 1 | a0001c0001t0002g0250 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.253-938T>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10526311 | |||||||
| chr11:10526384 | A | T | 1 | a0001c0004t0008g0094 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.253-1011T>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10526384 | |||||||
| chr11:10526498 | A | T | 1 | a0001c0001t0003g0024 | 2 | HG03017.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.253-1125T>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10526498 | |||||||
| chr11:10526501 | C | T | 44 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0011 others(41): Show |
68 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.253-1128G>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10526501 | |||||||
| chr11:10526599 | C | T | 3 | a0001c0002t0001g0137 a0001c0002t0001g0154 a0001c0002t0001g0168 |
3 | HG00621.hp1 HG02165.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.253-1226G>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10526599 | |||||||
| chr11:10526619 | T | G | 2 | a0001c0001t0014g0064 a0001c0001t0014g0184 |
2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.253-1246A>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10526619 | |||||||
| chr11:10526620 | A | T | 2 | a0001c0001t0014g0064 a0001c0001t0014g0184 |
2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.253-1247T>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10526620 | |||||||
| chr11:10526640 | G | A | 1 | a0003c0005t0001g0065 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.253-1267C>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10526640 | |||||||
| chr11:10526655 | C | T | 8 | a0001c0001t0003g0028 a0001c0001t0003g0034 a0001c0001t0003g0103 others(5): Show |
10 | HG02135.hp2 NA18947.hp1 NA18965.hp2 others(7): Show |
intron_variant | MODIFIER | c.253-1282G>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10526655 | |||||||
| chr11:10526985 | T | C | 3 | a0001c0001t0004g0037 a0001c0001t0004g0211 a0001c0001t0004g0241 |
4 | HG02818.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.253-1612A>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10526985 | |||||||
| chr11:10527168 | A | G | 1 | a0001c0004t0008g0094 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.253-1795T>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10527168 | |||||||
| chr11:10527344 | A | G | 1 | a0001c0001t0004g0219 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.253-1971T>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10527344 | |||||||
| chr11:10527645 | CG | C | 184 | a0001c0001t0001g0073 a0001c0001t0001g0124 a0001c0001t0001g0125 others(181): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.253-2273delC | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10527645 | |||||||
| chr11:10527652 | G | T | 20 | a0001c0001t0004g0009 a0001c0001t0004g0037 a0001c0001t0004g0043 others(17): Show |
26 | HG00639.hp1 HG01106.hp1 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.253-2279C>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10527652 | |||||||
| chr11:10527785 | G | C | 3 | a0001c0001t0006g0059 a0001c0001t0006g0060 a0001c0001t0006g0062 |
3 | HG02280.hp1 HG03669.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.253-2412C>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10527785 | |||||||
| chr11:10527828 | G | A | 2 | a0001c0001t0001g0132 a0001c0001t0001g0148 |
2 | NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.253-2455C>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10527828 | |||||||
| chr11:10527854 | C | T | 13 | a0001c0001t0005g0005 a0001c0001t0005g0021 a0001c0001t0005g0048 others(10): Show |
20 | HG00099.hp2 HG00642.hp1 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.253-2481G>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10527854 | |||||||
| chr11:10527921 | C | G | 184 | a0001c0001t0001g0073 a0001c0001t0001g0124 a0001c0001t0001g0125 others(181): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.253-2548G>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10527921 | |||||||
| chr11:10527926 | G | A | 184 | a0001c0001t0001g0073 a0001c0001t0001g0124 a0001c0001t0001g0125 others(181): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.253-2553C>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10527926 | |||||||
| chr11:10527937 | A | G | 1 | a0001c0002t0001g0104 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.253-2564T>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10527937 | |||||||
| chr11:10527950 | A | G | 1 | a0001c0001t0003g0149 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.253-2577T>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10527950 | |||||||
| chr11:10527960 | G | T | 9 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0080 others(6): Show |
19 | HG00621.hp2 HG01255.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.253-2587C>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10527960 | |||||||
| chr11:10528079 | T | C | 1 | a0001c0001t0004g0249 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.252+2564A>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10528079 | |||||||
| chr11:10528113 | G | A | 13 | a0001c0001t0005g0005 a0001c0001t0005g0021 a0001c0001t0005g0048 others(10): Show |
20 | HG00099.hp2 HG00642.hp1 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.252+2530C>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10528113 | |||||||
| chr11:10528117 | A | G | 1 | a0001c0004t0008g0094 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.252+2526T>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10528117 | |||||||
| chr11:10528319 | G | T | 1 | a0001c0001t0002g0224 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.252+2324C>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10528319 | |||||||
| chr11:10528401 | C | G | 1 | a0001c0001t0002g0230 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.252+2242G>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10528401 | |||||||
| chr11:10528556 | G | A | 3 | a0001c0001t0012g0209 a0001c0001t0012g0239 a0001c0001t0012g0262 |
3 | HG00639.hp2 HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.252+2087C>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10528556 | |||||||
| chr11:10528704 | T | C | 69 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0011 others(66): Show |
100 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.252+1939A>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10528704 | |||||||
| chr11:10528772 | T | C | 1 | a0001c0002t0001g0116 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.252+1871A>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10528772 | |||||||
| chr11:10528863 | A | C | 20 | a0001c0001t0004g0009 a0001c0001t0004g0037 a0001c0001t0004g0043 others(17): Show |
26 | HG00639.hp1 HG01106.hp1 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.252+1780T>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10528863 | |||||||
| chr11:10528874 | G | A | 1 | a0001c0001t0013g0191 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.252+1769C>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10528874 | |||||||
| chr11:10528900 | T | A | 116 | a0001c0001t0001g0073 a0001c0001t0001g0124 a0001c0001t0001g0125 others(113): Show |
148 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.252+1743A>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10528900 | |||||||
| chr11:10528903 | G | A | 2 | a0001c0001t0001g0073 a0001c0001t0012g0239 |
2 | HG02572.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.252+1740C>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10528903 | |||||||
| chr11:10529051 | TG | T | 116 | a0001c0001t0001g0073 a0001c0001t0001g0124 a0001c0001t0001g0125 others(113): Show |
148 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.252+1591delC | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10529051 | |||||||
| chr11:10529077 | C | G | 9 | a0001c0001t0007g0047 a0001c0001t0007g0096 a0001c0001t0007g0164 others(6): Show |
10 | HG01884.hp1 HG02145.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.252+1566G>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10529077 | |||||||
| chr11:10529139 | C | G | 2 | a0001c0001t0002g0253 a0001c0001t0002g0255 |
2 | HG01168.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.252+1504G>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10529139 | |||||||
| chr11:10529214 | T | C | 2 | a0001c0002t0001g0200 a0003c0005t0001g0065 |
2 | HG02647.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.252+1429A>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10529214 | |||||||
| chr11:10529254 | G | A | 1 | a0001c0002t0001g0142 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.252+1389C>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10529254 | |||||||
| chr11:10529417 | T | C | 3 | a0001c0002t0001g0123 a0001c0002t0001g0177 a0001c0002t0022g0165 |
3 | HG01167.hp1 HG02559.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.252+1226A>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10529417 | |||||||
| chr11:10529523 | T | C | 6 | a0001c0001t0002g0020 a0001c0001t0002g0202 a0001c0001t0002g0223 others(3): Show |
8 | NA18940.hp2 NA18952.hp2 NA18967.hp1 others(5): Show |
intron_variant | MODIFIER | c.252+1120A>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10529523 | |||||||
| chr11:10529559 | T | C | 187 | a0001c0001t0001g0073 a0001c0001t0001g0124 a0001c0001t0001g0125 others(184): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.252+1084A>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10529559 | |||||||
| chr11:10529829 | T | A | 1 | a0003c0005t0001g0065 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.252+814A>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10529829 | |||||||
| chr11:10529956 | T | C | 2 | a0001c0001t0003g0071 a0001c0001t0003g0179 |
2 | HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.252+687A>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10529956 | |||||||
| chr11:10529967 | C | T | 1 | a0001c0002t0018g0138 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.252+676G>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10529967 | |||||||
| chr11:10530050 | G | A | 1 | a0001c0002t0001g0106 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.252+593C>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10530050 | |||||||
| chr11:10530151 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.252+492A>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10530151 | |||||||
| chr11:10530475 | G | C | 186 | a0001c0001t0001g0073 a0001c0001t0001g0124 a0001c0001t0001g0125 others(183): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.252+168C>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10530475 | |||||||
| chr11:10530501 | G | A | 5 | a0001c0002t0001g0118 a0001c0002t0001g0119 a0001c0002t0001g0157 others(2): Show |
5 | HG02071.hp1 NA18944.hp1 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.252+142C>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10530501 | |||||||
| chr11:10530631 | C | T | 2 | a0001c0001t0001g0124 a0001c0001t0001g0152 |
2 | HG01891.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.252+12G>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 3/5 | chr11 | 10530631 | |||||||
| chr11:10530904 | T | C | 2 | a0001c0001t0002g0235 a0001c0001t0002g0237 |
2 | HG00733.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.144-153A>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10530904 | |||||||
| chr11:10531119 | G | C | 1 | a0001c0001t0012g0239 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.144-368C>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10531119 | |||||||
| chr11:10531125 | C | T | 15 | a0001c0001t0006g0010 a0001c0001t0006g0050 a0001c0001t0006g0051 others(12): Show |
17 | HG01069.hp1 HG01081.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.144-374G>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10531125 | |||||||
| chr11:10531155 | T | C | 69 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0011 others(66): Show |
100 | HG00099.hp1 HG00280.hp1 HG00621.hp2 others(97): Show |
intron_variant | MODIFIER | c.144-404A>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10531155 | |||||||
| chr11:10531176 | T | A | 15 | a0001c0001t0006g0010 a0001c0001t0006g0050 a0001c0001t0006g0051 others(12): Show |
17 | HG01069.hp1 HG01081.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.144-425A>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10531176 | |||||||
| chr11:10531186 | C | G | 69 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0011 others(66): Show |
100 | HG00099.hp1 HG00280.hp1 HG00621.hp2 others(97): Show |
intron_variant | MODIFIER | c.144-435G>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10531186 | |||||||
| chr11:10531204 | G | A | 188 | a0001c0001t0001g0073 a0001c0001t0001g0124 a0001c0001t0001g0125 others(185): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.144-453C>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10531204 | |||||||
| chr11:10531231 | C | T | 15 | a0001c0001t0006g0010 a0001c0001t0006g0050 a0001c0001t0006g0051 others(12): Show |
17 | HG01069.hp1 HG01081.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.144-480G>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10531231 | |||||||
| chr11:10531243 | C | T | 188 | a0001c0001t0001g0073 a0001c0001t0001g0124 a0001c0001t0001g0125 others(185): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.144-492G>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10531243 | |||||||
| chr11:10531319 | G | A | 3 | a0001c0001t0012g0209 a0001c0001t0012g0239 a0001c0001t0012g0262 |
3 | HG00639.hp2 HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.144-568C>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10531319 | |||||||
| chr11:10531374 | C | CA | 6 | a0001c0001t0002g0220 a0001c0001t0002g0263 a0001c0001t0002g0264 others(3): Show |
6 | HG02451.hp1 HG02723.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.144-624dupT | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10531374 | |||||||
| chr11:10531374 | C | CAA | 87 | a0001c0001t0001g0240 a0001c0001t0002g0004 a0001c0001t0002g0008 others(84): Show |
110 | HG00140.hp2 HG00558.hp2 HG00733.hp2 others(107): Show |
intron_variant | MODIFIER | c.144-625_144-624dup others(2): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10531374 | |||||||
| chr11:10531374 | C | CAAA | 181 | a0001c0001t0001g0073 a0001c0001t0001g0124 a0001c0001t0001g0125 others(178): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.144-626_144-624dup others(3): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10531374 | |||||||
| chr11:10531374 | C | CAAAA | 9 | a0001c0001t0003g0003 a0001c0001t0003g0068 a0001c0001t0003g0080 others(6): Show |
14 | HG02080.hp2 HG02155.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.144-627_144-624dup others(4): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10531374 | |||||||
| chr11:10531408 | T | C | 2 | a0001c0002t0001g0110 a0001c0002t0001g0144 |
2 | NA18962.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.144-657A>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10531408 | |||||||
| chr11:10531777 | C | T | 25 | a0001c0001t0003g0023 a0001c0001t0003g0069 a0001c0001t0003g0071 others(22): Show |
32 | HG00639.hp1 HG01106.hp1 HG01256.hp1 others(29): Show |
intron_variant | MODIFIER | c.144-1026G>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10531777 | |||||||
| chr11:10531808 | C | T | 132 | a0001c0001t0001g0073 a0001c0001t0001g0124 a0001c0001t0001g0125 others(129): Show |
165 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.144-1057G>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10531808 | |||||||
| chr11:10531821 | A | C | 1 | a0001c0001t0002g0245 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.144-1070T>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10531821 | |||||||
| chr11:10531821 | A | T | 14 | a0001c0001t0007g0047 a0001c0001t0007g0096 a0001c0001t0007g0164 others(11): Show |
15 | HG01884.hp1 HG02055.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.144-1070T>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10531821 | |||||||
| chr11:10531863 | C | T | 2 | a0001c0001t0007g0272 a0001c0001t0007g0273 |
2 | HG02922.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.144-1112G>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10531863 | |||||||
| chr11:10531947 | G | C | 6 | a0001c0001t0004g0037 a0001c0001t0004g0211 a0001c0001t0004g0218 others(3): Show |
7 | HG02818.hp1 HG02886.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.144-1196C>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10531947 | |||||||
| chr11:10532125 | C | T | 201 | a0001c0001t0001g0073 a0001c0001t0001g0124 a0001c0001t0001g0125 others(198): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.144-1374G>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10532125 | |||||||
| chr11:10532128 | C | T | 284 | a0001c0001t0001g0073 a0001c0001t0001g0124 a0001c0001t0001g0125 others(281): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.144-1377G>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10532128 | |||||||
| chr11:10532496 | T | TAC | 41 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0166 others(38): Show |
53 | HG00438.hp1 HG00639.hp1 HG01081.hp1 others(50): Show |
intron_variant | MODIFIER | c.143+1518_143+1519d others(4): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10532496 | |||||||
| chr11:10532496 | T | TACAC | 10 | a0001c0001t0001g0196 a0001c0002t0001g0119 a0001c0002t0001g0123 others(7): Show |
10 | HG00323.hp1 HG01167.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.143+1516_143+1519d others(6): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10532496 | |||||||
| chr11:10532496 | T | TACACAC | 3 | a0001c0002t0001g0107 a0001c0002t0001g0130 a0001c0002t0001g0153 |
3 | HG01255.hp1 HG02698.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.143+1514_143+1519d others(8): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10532496 | |||||||
| chr11:10532496 | TAC | T | 58 | a0001c0001t0001g0073 a0001c0001t0002g0234 a0001c0001t0003g0002 others(55): Show |
88 | HG00099.hp1 HG00280.hp1 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.143+1518_143+1519d others(4): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10532496 | |||||||
| chr11:10532496 | TACAC | T | 13 | a0001c0001t0001g0176 a0001c0001t0001g0210 a0001c0001t0002g0040 others(10): Show |
16 | HG00738.hp2 HG00741.hp2 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.143+1516_143+1519d others(6): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10532496 | |||||||
| chr11:10532496 | TACACAC | T | 26 | a0001c0001t0001g0287 a0001c0001t0002g0245 a0001c0001t0003g0083 others(23): Show |
34 | HG00099.hp2 HG00642.hp1 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.143+1514_143+1519d others(8): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10532496 | |||||||
| chr11:10532496 | TACACACA others(1): Show |
T | 51 | a0001c0001t0001g0240 a0001c0001t0002g0004 a0001c0001t0002g0008 others(48): Show |
68 | HG00140.hp2 HG00280.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.143+1512_143+1519d others(10): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10532496 | |||||||
| chr11:10532496 | TACACACA others(5): Show |
T | 1 | a0001c0001t0005g0097 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.143+1508_143+1519d others(14): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10532496 | |||||||
| chr11:10532496 | TACACACA others(11): Show |
T | 2 | a0001c0001t0001g0132 a0001c0001t0001g0148 |
2 | NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.143+1502_143+1519d others(20): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10532496 | |||||||
| chr11:10532529 | ACACACAC others(4): Show |
A | 7 | a0001c0001t0002g0042 a0001c0001t0002g0093 a0001c0001t0002g0208 others(4): Show |
8 | HG01074.hp1 HG01099.hp1 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.143+1476_143+1486d others(13): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10532529 | |||||||
| chr11:10532537 | A | ACACC | 10 | a0001c0002t0001g0006 a0001c0002t0001g0027 a0001c0002t0001g0032 others(7): Show |
10 | HG01346.hp2 HG01981.hp1 NA18969.hp1 others(7): Show |
intron_variant | MODIFIER | c.143+1478_143+1479i others(6): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10532537 | |||||||
| chr11:10532537 | A | ACC | 12 | a0001c0002t0001g0006 a0001c0002t0001g0015 a0001c0002t0001g0017 others(9): Show |
13 | HG00323.hp2 HG00558.hp1 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.143+1477_143+1478d others(4): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10532537 | |||||||
| chr11:10532537 | A | C | 48 | a0001c0001t0001g0176 a0001c0001t0001g0240 a0001c0001t0002g0004 others(45): Show |
60 | HG00140.hp2 HG00558.hp2 HG01106.hp2 others(57): Show |
intron_variant | MODIFIER | c.143+1479T>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10532537 | |||||||
| chr11:10532538 | C | CA | 3 | a0001c0002t0001g0015 a0001c0002t0001g0017 a0001c0002t0001g0142 |
3 | HG01192.hp1 HG01934.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.143+1477_143+1478i others(3): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10532538 | |||||||
| chr11:10532538 | C | CACA | 3 | a0001c0002t0001g0006 a0001c0002t0001g0127 a0001c0002t0001g0140 |
3 | HG00642.hp2 HG01993.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.143+1477_143+1478i others(5): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10532538 | |||||||
| chr11:10532539 | C | A | 8 | a0001c0002t0001g0013 a0001c0002t0001g0135 a0001c0002t0001g0136 others(5): Show |
10 | HG00140.hp1 HG00438.hp2 HG00621.hp1 others(7): Show |
intron_variant | MODIFIER | c.143+1477G>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10532539 | |||||||
| chr11:10532540 | C | A | 4 | a0001c0002t0001g0015 a0001c0002t0001g0017 a0001c0002t0001g0140 others(1): Show |
4 | HG01192.hp1 HG01934.hp2 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.143+1476G>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10532540 | |||||||
| chr11:10532541 | C | A | 1 | a0001c0002t0001g0137 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.143+1475G>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10532541 | |||||||
| chr11:10532541 | CA | C | 7 | a0001c0002t0001g0013 a0001c0002t0001g0135 a0001c0002t0001g0136 others(4): Show |
9 | HG00140.hp1 HG00438.hp2 HG00621.hp1 others(6): Show |
intron_variant | MODIFIER | c.143+1474delT | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10532541 | |||||||
| chr11:10532542 | A | C | 15 | a0001c0001t0002g0042 a0001c0001t0002g0093 a0001c0001t0002g0208 others(12): Show |
16 | HG00733.hp2 HG01074.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.143+1474T>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10532542 | |||||||
| chr11:10532983 | T | C | 9 | a0001c0001t0007g0047 a0001c0001t0007g0096 a0001c0001t0007g0164 others(6): Show |
10 | HG01884.hp1 HG02145.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.143+1033A>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10532983 | |||||||
| chr11:10533083 | C | T | 201 | a0001c0001t0001g0073 a0001c0001t0001g0124 a0001c0001t0001g0125 others(198): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.143+933G>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10533083 | |||||||
| chr11:10533337 | C | T | 71 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0011 others(68): Show |
102 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.143+679G>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10533337 | |||||||
| chr11:10533366 | A | G | 1 | a0001c0002t0001g0167 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.143+650T>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10533366 | |||||||
| chr11:10533380 | A | G | 15 | a0001c0001t0006g0010 a0001c0001t0006g0050 a0001c0001t0006g0051 others(12): Show |
17 | HG01069.hp1 HG01081.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.143+636T>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10533380 | |||||||
| chr11:10533399 | T | C | 9 | a0001c0001t0007g0047 a0001c0001t0007g0096 a0001c0001t0007g0164 others(6): Show |
10 | HG01884.hp1 HG02145.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.143+617A>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10533399 | |||||||
| chr11:10533430 | GTTAA | G | 17 | a0001c0001t0005g0005 a0001c0001t0005g0021 a0001c0001t0005g0048 others(14): Show |
24 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.143+582_143+585del others(4): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10533430 | |||||||
| chr11:10533540 | A | AAGT | 4 | a0001c0001t0003g0068 a0001c0001t0003g0072 a0001c0001t0003g0195 others(1): Show |
9 | HG01943.hp1 HG02258.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.143+475_143+476ins others(3): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10533540 | |||||||
| chr11:10533541 | G | A | 4 | a0001c0001t0003g0068 a0001c0001t0003g0072 a0001c0001t0003g0195 others(1): Show |
9 | HG01943.hp1 HG02258.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.143+475C>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10533541 | |||||||
| chr11:10533541 | G | GTA | 121 | a0001c0001t0001g0240 a0001c0001t0002g0004 a0001c0001t0002g0008 others(118): Show |
162 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.143+473_143+474dup others(2): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10533541 | |||||||
| chr11:10533541 | G | GTATA | 3 | a0001c0001t0012g0209 a0001c0001t0012g0239 a0001c0001t0012g0262 |
3 | HG00639.hp2 HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.143+471_143+474dup others(4): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10533541 | |||||||
| chr11:10533586 | A | C | 1 | a0001c0001t0013g0189 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.143+430T>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10533586 | |||||||
| chr11:10533722 | A | G | 2 | a0001c0002t0001g0153 a0001c0002t0001g0274 |
2 | HG02698.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.143+294T>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10533722 | |||||||
| chr11:10533835 | A | C | 1 | a0001c0001t0001g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.143+181T>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10533835 | |||||||
| chr11:10533962 | T | C | 1 | a0003c0005t0001g0065 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.143+54A>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 2/5 | chr11 | 10533962 | |||||||
| chr11:10534251 | G | A | 9 | a0001c0001t0007g0047 a0001c0001t0007g0096 a0001c0001t0007g0164 others(6): Show |
10 | HG01884.hp1 HG02145.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-47-46C>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10534251 | |||||||
| chr11:10534433 | A | G | 15 | a0001c0001t0006g0010 a0001c0001t0006g0050 a0001c0001t0006g0051 others(12): Show |
17 | HG01069.hp1 HG01081.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-47-228T>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10534433 | |||||||
| chr11:10534477 | T | TAC | 5 | a0001c0001t0002g0238 a0001c0001t0002g0253 a0001c0001t0002g0255 others(2): Show |
5 | HG00140.hp2 HG01168.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47-274_-47-273dup others(2): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10534477 | |||||||
| chr11:10534477 | TAC | T | 172 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0132 others(169): Show |
233 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.-47-274_-47-273del others(2): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10534477 | |||||||
| chr11:10534477 | TACAC | T | 3 | a0001c0001t0005g0278 a0001c0002t0001g0102 a0001c0002t0001g0167 |
3 | HG03927.hp2 NA19058.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.-47-276_-47-273del others(4): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10534477 | |||||||
| chr11:10534506 | A | G | 1 | a0001c0001t0003g0084 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-47-301T>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10534506 | |||||||
| chr11:10534595 | CA | C | 2 | a0001c0001t0002g0038 a0001c0001t0002g0206 |
3 | NA19054.hp1 NA19078.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.-47-391delT | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10534595 | |||||||
| chr11:10534714 | G | C | 118 | a0001c0001t0001g0073 a0001c0001t0001g0124 a0001c0001t0001g0125 others(115): Show |
150 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.-47-509C>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10534714 | |||||||
| chr11:10534864 | C | T | 1 | a0001c0001t0006g0061 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-47-659G>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10534864 | |||||||
| chr11:10534894 | A | T | 187 | a0001c0001t0001g0073 a0001c0001t0001g0124 a0001c0001t0001g0125 others(184): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.-47-689T>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10534894 | |||||||
| chr11:10535094 | A | C | 1 | a0001c0001t0002g0045 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-47-889T>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10535094 | |||||||
| chr11:10535291 | T | A | 1 | a0001c0001t0003g0070 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-47-1086A>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10535291 | |||||||
| chr11:10535356 | T | TA | 44 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0011 others(41): Show |
68 | HG00099.hp1 HG00280.hp1 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.-47-1152_-47-1151i others(3): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10535356 | |||||||
| chr11:10535357 | T | A | 44 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0011 others(41): Show |
68 | HG00099.hp1 HG00280.hp1 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.-47-1152A>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10535357 | |||||||
| chr11:10535357 | T | TA | 159 | a0001c0001t0001g0073 a0001c0001t0001g0124 a0001c0001t0001g0125 others(156): Show |
199 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.-47-1153dupT | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10535357 | |||||||
| chr11:10535372 | AAAC | A | 3 | a0001c0001t0012g0209 a0001c0001t0012g0239 a0001c0001t0012g0262 |
3 | HG00639.hp2 HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-47-1170_-47-1168d others(5): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10535372 | |||||||
| chr11:10535383 | T | C | 95 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0152 others(92): Show |
120 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.-47-1178A>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10535383 | |||||||
| chr11:10535425 | G | A | 1 | a0001c0002t0001g0183 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-47-1220C>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10535425 | |||||||
| chr11:10535463 | CA | C | 43 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0152 others(40): Show |
48 | HG00639.hp2 HG01069.hp1 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.-47-1259delT | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10535463 | |||||||
| chr11:10535463 | CAA | C | 145 | a0001c0001t0001g0240 a0001c0001t0002g0004 a0001c0001t0002g0008 others(142): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.-47-1260_-47-1259d others(4): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10535463 | |||||||
| chr11:10535599 | T | C | 1 | a0001c0001t0002g0202 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-47-1394A>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10535599 | |||||||
| chr11:10535693 | A | G | 1 | a0001c0001t0006g0059 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-47-1488T>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10535693 | |||||||
| chr11:10535710 | A | G | 3 | a0001c0002t0001g0123 a0001c0002t0001g0177 a0001c0002t0022g0165 |
3 | HG01167.hp1 HG02559.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-47-1505T>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10535710 | |||||||
| chr11:10535720 | C | T | 284 | a0001c0001t0001g0073 a0001c0001t0001g0124 a0001c0001t0001g0125 others(281): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.-47-1515G>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10535720 | |||||||
| chr11:10535812 | A | G | 15 | a0001c0001t0006g0010 a0001c0001t0006g0050 a0001c0001t0006g0051 others(12): Show |
17 | HG01069.hp1 HG01081.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-47-1607T>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10535812 | |||||||
| chr11:10535937 | T | A | 3 | a0001c0001t0005g0278 a0001c0001t0005g0279 a0001c0001t0005g0281 |
3 | HG00642.hp1 HG01099.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-47-1732A>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10535937 | |||||||
| chr11:10535961 | C | A | 204 | a0001c0001t0001g0073 a0001c0001t0001g0124 a0001c0001t0001g0125 others(201): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.-47-1756G>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10535961 | |||||||
| chr11:10536076 | T | A | 1 | a0001c0001t0007g0047 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-47-1871A>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10536076 | |||||||
| chr11:10536283 | C | T | 1 | a0001c0001t0002g0229 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-47-2078G>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10536283 | |||||||
| chr11:10536299 | C | G | 110 | a0001c0001t0001g0073 a0001c0001t0001g0124 a0001c0001t0001g0125 others(107): Show |
137 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.-47-2094G>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10536299 | |||||||
| chr11:10536301 | C | T | 1 | a0001c0001t0007g0164 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-47-2096G>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10536301 | |||||||
| chr11:10536324 | A | T | 25 | a0001c0001t0003g0023 a0001c0001t0003g0069 a0001c0001t0003g0071 others(22): Show |
32 | HG00639.hp1 HG01106.hp1 HG01256.hp1 others(29): Show |
intron_variant | MODIFIER | c.-47-2119T>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10536324 | |||||||
| chr11:10536336 | G | T | 204 | a0001c0001t0001g0073 a0001c0001t0001g0124 a0001c0001t0001g0125 others(201): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.-47-2131C>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10536336 | |||||||
| chr11:10536403 | T | C | 123 | a0001c0001t0001g0073 a0001c0001t0001g0124 a0001c0001t0001g0125 others(120): Show |
157 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.-47-2198A>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10536403 | |||||||
| chr11:10536439 | G | A | 2 | a0001c0001t0008g0181 a0001c0001t0008g0187 |
2 | HG02451.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-47-2234C>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10536439 | |||||||
| chr11:10536880 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-47-2675A>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10536880 | |||||||
| chr11:10536978 | T | C | 64 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0011 others(61): Show |
94 | HG00099.hp1 HG00280.hp1 HG00621.hp2 others(91): Show |
intron_variant | MODIFIER | c.-47-2773A>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10536978 | |||||||
| chr11:10537008 | T | A | 3 | a0001c0001t0002g0263 a0001c0001t0002g0264 a0001c0001t0002g0265 |
3 | HG03098.hp1 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-47-2803A>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10537008 | |||||||
| chr11:10537052 | C | G | 102 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0152 others(99): Show |
130 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.-47-2847G>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10537052 | |||||||
| chr11:10537230 | A | G | 64 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0011 others(61): Show |
94 | HG00099.hp1 HG00280.hp1 HG00621.hp2 others(91): Show |
intron_variant | MODIFIER | c.-47-3025T>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10537230 | |||||||
| chr11:10537279 | G | T | 1 | a0001c0001t0002g0246 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-47-3074C>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10537279 | |||||||
| chr11:10537280 | G | A | 1 | a0001c0001t0002g0246 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-47-3075C>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10537280 | |||||||
| chr11:10537281 | G | T | 1 | a0001c0001t0002g0246 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-47-3076C>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10537281 | |||||||
| chr11:10537283 | G | A | 1 | a0001c0001t0002g0246 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-47-3078C>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10537283 | |||||||
| chr11:10537284 | G | C | 1 | a0001c0001t0002g0246 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-47-3079C>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10537284 | |||||||
| chr11:10537291 | G | T | 1 | a0001c0001t0002g0246 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-47-3086C>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10537291 | |||||||
| chr11:10537293 | G | C | 1 | a0001c0001t0002g0246 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-47-3088C>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10537293 | |||||||
| chr11:10537295 | A | T | 1 | a0001c0001t0002g0246 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-47-3090T>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10537295 | |||||||
| chr11:10537296 | G | C | 1 | a0001c0001t0002g0246 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-47-3091C>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10537296 | |||||||
| chr11:10537297 | G | T | 1 | a0001c0001t0002g0246 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-47-3092C>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10537297 | |||||||
| chr11:10537298 | T | A | 1 | a0001c0001t0002g0246 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-47-3093A>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10537298 | |||||||
| chr11:10537299 | G | T | 1 | a0001c0001t0002g0246 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-47-3094C>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10537299 | |||||||
| chr11:10537300 | A | T | 1 | a0001c0001t0002g0246 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-47-3095T>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10537300 | |||||||
| chr11:10537315 | T | C | 1 | a0001c0001t0002g0246 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-47-3110A>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10537315 | |||||||
| chr11:10537320 | T | C | 1 | a0001c0001t0002g0246 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-47-3115A>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10537320 | |||||||
| chr11:10537322 | C | T | 1 | a0001c0001t0002g0246 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-47-3117G>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10537322 | |||||||
| chr11:10537332 | A | G | 1 | a0001c0001t0002g0246 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-47-3127T>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10537332 | |||||||
| chr11:10537335 | T | G | 1 | a0001c0001t0002g0246 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-47-3130A>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10537335 | |||||||
| chr11:10537338 | A | G | 1 | a0001c0001t0002g0246 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-47-3133T>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10537338 | |||||||
| chr11:10537346 | C | G | 1 | a0001c0001t0002g0246 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-47-3141G>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10537346 | |||||||
| chr11:10537349 | A | G | 1 | a0001c0001t0002g0246 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-47-3144T>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10537349 | |||||||
| chr11:10537353 | T | G | 1 | a0001c0001t0002g0246 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-47-3148A>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10537353 | |||||||
| chr11:10537356 | T | A | 1 | a0001c0001t0002g0246 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-47-3151A>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10537356 | |||||||
| chr11:10537357 | G | T | 1 | a0001c0001t0002g0246 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-47-3152C>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10537357 | |||||||
| chr11:10537359 | A | T | 1 | a0001c0001t0002g0246 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-47-3154T>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10537359 | |||||||
| chr11:10537363 | A | C | 1 | a0001c0001t0002g0246 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-47-3158T>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10537363 | |||||||
| chr11:10537368 | A | C | 1 | a0001c0001t0002g0246 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-47-3163T>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10537368 | |||||||
| chr11:10537373 | A | G | 1 | a0001c0001t0002g0246 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-47-3168T>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10537373 | |||||||
| chr11:10537377 | T | G | 1 | a0001c0001t0002g0246 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-47-3172A>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10537377 | |||||||
| chr11:10537379 | A | T | 1 | a0001c0001t0002g0246 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-47-3174T>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10537379 | |||||||
| chr11:10537380 | T | G | 1 | a0001c0001t0002g0246 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-47-3175A>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10537380 | |||||||
| chr11:10537381 | T | G | 1 | a0001c0001t0002g0246 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-47-3176A>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10537381 | |||||||
| chr11:10537384 | G | C | 1 | a0001c0001t0002g0246 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-47-3179C>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10537384 | |||||||
| chr11:10537387 | T | G | 1 | a0001c0001t0002g0246 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-47-3182A>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10537387 | |||||||
| chr11:10537390 | A | T | 1 | a0001c0001t0002g0246 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-47-3185T>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10537390 | |||||||
| chr11:10537391 | G | A | 1 | a0001c0001t0002g0246 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-47-3186C>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10537391 | |||||||
| chr11:10537396 | C | T | 1 | a0001c0001t0002g0246 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-47-3191G>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10537396 | |||||||
| chr11:10537399 | G | A | 1 | a0001c0001t0002g0246 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-47-3194C>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10537399 | |||||||
| chr11:10537400 | G | C | 1 | a0001c0001t0002g0246 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-47-3195C>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10537400 | |||||||
| chr11:10537407 | A | T | 1 | a0001c0001t0002g0246 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-47-3202T>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10537407 | |||||||
| chr11:10537412 | G | T | 1 | a0001c0001t0002g0246 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-47-3207C>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10537412 | |||||||
| chr11:10537425 | A | T | 1 | a0001c0001t0002g0246 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-47-3220T>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10537425 | |||||||
| chr11:10537426 | T | A | 1 | a0001c0001t0002g0246 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-47-3221A>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10537426 | |||||||
| chr11:10537623 | A | G | 4 | a0001c0001t0006g0010 a0001c0001t0006g0051 a0001c0001t0006g0053 others(1): Show |
6 | HG02572.hp1 HG02809.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47-3418T>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10537623 | |||||||
| chr11:10537801 | T | A | 43 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0011 others(40): Show |
67 | HG00099.hp1 HG00280.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.-48+3321A>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10537801 | |||||||
| chr11:10537886 | G | A | 2 | a0001c0001t0001g0174 a0001c0001t0001g0196 |
2 | HG01891.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.-48+3236C>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10537886 | |||||||
| chr11:10538236 | A | G | 66 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0011 others(63): Show |
96 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.-48+2886T>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10538236 | |||||||
| chr11:10538271 | G | C | 1 | a0001c0001t0012g0262 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-48+2851C>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10538271 | |||||||
| chr11:10538348 | T | C | 76 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0020 others(73): Show |
96 | HG00140.hp2 HG00280.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.-48+2774A>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10538348 | |||||||
| chr11:10538362 | C | T | 3 | a0001c0001t0013g0189 a0001c0001t0013g0190 a0001c0001t0013g0191 |
3 | HG02055.hp2 HG02976.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-48+2760G>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10538362 | |||||||
| chr11:10538561 | A | G | 107 | a0001c0001t0001g0073 a0001c0001t0001g0124 a0001c0001t0001g0125 others(104): Show |
135 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.-48+2561T>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10538561 | |||||||
| chr11:10538802 | C | T | 87 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0020 others(84): Show |
108 | HG00140.hp2 HG00280.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.-48+2320G>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10538802 | |||||||
| chr11:10538856 | A | C | 2 | a0001c0001t0002g0020 a0001c0001t0002g0228 |
4 | NA18940.hp2 NA18967.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+2266T>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10538856 | |||||||
| chr11:10538943 | G | A | 74 | a0001c0001t0002g0004 a0001c0001t0002g0008 a0001c0001t0002g0020 others(71): Show |
94 | HG00140.hp2 HG00280.hp2 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.-48+2179C>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10538943 | |||||||
| chr11:10539072 | C | T | 9 | a0001c0001t0007g0047 a0001c0001t0007g0096 a0001c0001t0007g0164 others(6): Show |
10 | HG01884.hp1 HG02145.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-48+2050G>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539072 | |||||||
| chr11:10539186 | T | C | 1 | a0001c0001t0006g0058 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-48+1936A>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539186 | |||||||
| chr11:10539209 | C | T | 1 | a0001c0001t0002g0204 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-48+1913G>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539209 | |||||||
| chr11:10539230 | C | G | 1 | a0001c0001t0002g0081 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-48+1892G>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539230 | |||||||
| chr11:10539485 | C | T | 13 | a0001c0001t0005g0005 a0001c0001t0005g0021 a0001c0001t0005g0048 others(10): Show |
20 | HG00099.hp2 HG00642.hp1 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.-48+1637G>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539485 | |||||||
| chr11:10539687 | C | CACATATA others(11): Show |
1 | a0001c0001t0003g0082 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-48+1434_-48+1435i others(20): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539687 | |||||||
| chr11:10539687 | C | CATATATA others(7): Show |
5 | a0001c0001t0006g0059 a0001c0001t0006g0060 a0001c0001t0006g0061 others(2): Show |
5 | HG01069.hp1 HG01081.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48+1434_-48+1435i others(16): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539687 | |||||||
| chr11:10539687 | C | CATATATA others(29): Show |
2 | a0001c0001t0006g0057 a0001c0001t0006g0058 |
2 | HG02109.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-48+1434_-48+1435i others(38): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539687 | |||||||
| chr11:10539687 | C | CATATATA others(31): Show |
2 | a0001c0001t0006g0010 a0001c0001t0006g0056 |
4 | HG02572.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48+1434_-48+1435i others(40): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539687 | |||||||
| chr11:10539687 | C | CATATATA others(33): Show |
3 | a0001c0001t0006g0053 a0001c0001t0006g0054 a0001c0001t0006g0055 |
3 | HG03195.hp1 HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-48+1434_-48+1435i others(42): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539687 | |||||||
| chr11:10539687 | C | CATATATA others(35): Show |
1 | a0001c0001t0006g0052 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-48+1434_-48+1435i others(44): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539687 | |||||||
| chr11:10539687 | C | CATATATA others(39): Show |
1 | a0001c0001t0006g0051 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-48+1434_-48+1435i others(48): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539687 | |||||||
| chr11:10539687 | C | CATATATA others(43): Show |
1 | a0001c0001t0006g0050 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-48+1434_-48+1435i others(52): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539687 | |||||||
| chr11:10539691 | C | CATATATA others(15): Show |
2 | a0001c0001t0002g0264 a0001c0001t0002g0265 |
2 | HG03098.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-48+1430_-48+1431i others(24): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539691 | |||||||
| chr11:10539691 | C | CATATATA others(19): Show |
2 | a0001c0001t0002g0263 a0001c0004t0008g0094 |
2 | HG03540.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-48+1430_-48+1431i others(28): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539691 | |||||||
| chr11:10539691 | C | CATATATA others(23): Show |
6 | a0001c0001t0002g0046 a0001c0001t0002g0258 a0001c0001t0002g0259 others(3): Show |
7 | HG00558.hp2 HG01256.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-48+1430_-48+1431i others(32): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539691 | |||||||
| chr11:10539691 | C | CATATATA others(25): Show |
3 | a0001c0001t0002g0020 a0001c0001t0002g0257 a0001c0001t0003g0256 |
5 | NA18940.hp2 NA18952.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.-48+1430_-48+1431i others(34): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539691 | |||||||
| chr11:10539691 | C | CATATATA others(27): Show |
11 | a0001c0001t0002g0045 a0001c0001t0002g0250 a0001c0001t0002g0251 others(8): Show |
12 | HG01106.hp2 HG01168.hp1 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.-48+1430_-48+1431i others(36): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539691 | |||||||
| chr11:10539691 | C | CATATATA others(29): Show |
11 | a0001c0001t0001g0240 a0001c0001t0002g0004 a0001c0001t0002g0243 others(8): Show |
20 | HG00639.hp1 HG01167.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.-48+1430_-48+1431i others(38): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539691 | |||||||
| chr11:10539691 | C | CATATATA others(31): Show |
17 | a0001c0001t0002g0093 a0001c0001t0002g0227 a0001c0001t0002g0228 others(14): Show |
18 | HG00140.hp2 HG00280.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.-48+1430_-48+1431i others(40): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539691 | |||||||
| chr11:10539691 | C | CATATATA others(33): Show |
13 | a0001c0001t0002g0041 a0001c0001t0002g0042 a0001c0001t0002g0220 others(10): Show |
15 | HG00738.hp2 HG01258.hp1 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.-48+1430_-48+1431i others(42): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539691 | |||||||
| chr11:10539691 | C | CATATATA others(35): Show |
8 | a0001c0001t0001g0210 a0001c0001t0002g0008 a0001c0001t0002g0039 others(5): Show |
13 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.-48+1430_-48+1431i others(44): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539691 | |||||||
| chr11:10539691 | C | CATATATA others(37): Show |
8 | a0001c0001t0002g0038 a0001c0001t0002g0204 a0001c0001t0002g0206 others(5): Show |
10 | HG00639.hp2 HG01975.hp2 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.-48+1430_-48+1431i others(46): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539691 | |||||||
| chr11:10539691 | C | CATATATA others(39): Show |
2 | a0001c0001t0002g0036 a0001c0001t0002g0203 |
3 | NA18953.hp1 NA18969.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.-48+1430_-48+1431i others(48): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539691 | |||||||
| chr11:10539691 | C | CATATATA others(41): Show |
1 | a0001c0001t0002g0202 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-48+1430_-48+1431i others(50): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539691 | |||||||
| chr11:10539691 | C | T | 186 | a0001c0001t0001g0073 a0001c0001t0001g0124 a0001c0001t0001g0125 others(183): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.-48+1431G>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539691 | |||||||
| chr11:10539699 | T | TA | 3 | a0001c0002t0001g0197 a0001c0002t0001g0198 a0001c0002t0001g0199 |
3 | NA18963.hp2 NA19012.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.-48+1422_-48+1423i others(3): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539699 | |||||||
| chr11:10539699 | T | TATATATA others(36): Show |
1 | a0001c0001t0007g0273 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-48+1422_-48+1423i others(45): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539699 | |||||||
| chr11:10539699 | T | TATATATA others(30): Show |
1 | a0001c0001t0007g0272 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-48+1422_-48+1423i others(39): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539699 | |||||||
| chr11:10539699 | T | TATATATA others(4): Show |
1 | a0001c0001t0003g0092 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-48+1422_-48+1423i others(13): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539699 | |||||||
| chr11:10539699 | T | TATATATA others(32): Show |
1 | a0001c0001t0007g0271 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-48+1422_-48+1423i others(41): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539699 | |||||||
| chr11:10539699 | T | TATATATA others(6): Show |
17 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0012 others(14): Show |
31 | HG00621.hp2 HG01243.hp1 HG01255.hp2 others(28): Show |
intron_variant | MODIFIER | c.-48+1422_-48+1423i others(15): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539699 | |||||||
| chr11:10539699 | T | TATATATA others(32): Show |
2 | a0001c0001t0007g0047 a0001c0001t0007g0269 |
3 | HG01884.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-48+1422_-48+1423i others(41): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539699 | |||||||
| chr11:10539699 | T | TATATATA others(34): Show |
1 | a0001c0001t0007g0270 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-48+1422_-48+1423i others(43): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539699 | |||||||
| chr11:10539699 | T | TATATATA others(8): Show |
4 | a0001c0001t0003g0024 a0001c0001t0003g0080 a0001c0001t0010g0001 others(1): Show |
10 | HG01943.hp1 HG02258.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.-48+1422_-48+1423i others(17): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539699 | |||||||
| chr11:10539699 | T | TATATATA others(32): Show |
1 | a0001c0001t0007g0268 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-48+1422_-48+1423i others(41): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539699 | |||||||
| chr11:10539699 | T | TATATATA others(10): Show |
5 | a0001c0001t0003g0034 a0001c0001t0003g0076 a0001c0001t0003g0077 others(2): Show |
6 | HG02080.hp1 HG03669.hp2 HG03834.hp2 others(3): Show |
intron_variant | MODIFIER | c.-48+1422_-48+1423i others(19): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539699 | |||||||
| chr11:10539699 | T | TATATATA others(32): Show |
1 | a0001c0001t0007g0096 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-48+1422_-48+1423i others(41): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539699 | |||||||
| chr11:10539699 | T | TATATATA others(12): Show |
7 | a0001c0001t0001g0073 a0001c0001t0002g0081 a0001c0001t0003g0011 others(4): Show |
10 | HG00099.hp1 HG00280.hp1 HG00733.hp1 others(7): Show |
intron_variant | MODIFIER | c.-48+1422_-48+1423i others(21): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539699 | |||||||
| chr11:10539699 | T | TATATATA others(14): Show |
5 | a0001c0001t0013g0189 a0001c0001t0013g0190 a0001c0001t0013g0191 others(2): Show |
5 | HG01981.hp1 HG02055.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-48+1422_-48+1423i others(23): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539699 | |||||||
| chr11:10539699 | T | TATATATA others(16): Show |
2 | a0001c0001t0003g0072 a0001c0001t0005g0285 |
2 | HG02602.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-48+1422_-48+1423i others(25): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539699 | |||||||
| chr11:10539699 | T | TATATATA others(18): Show |
4 | a0001c0001t0003g0071 a0001c0001t0008g0187 a0001c0001t0014g0184 others(1): Show |
4 | HG02723.hp1 HG02970.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48+1422_-48+1423i others(27): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539699 | |||||||
| chr11:10539699 | T | TATATATA others(38): Show |
1 | a0001c0001t0001g0196 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-48+1422_-48+1423i others(47): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539699 | |||||||
| chr11:10539699 | T | TATATATA others(20): Show |
6 | a0001c0001t0003g0069 a0001c0001t0003g0070 a0001c0001t0008g0181 others(3): Show |
6 | HG02083.hp2 HG02451.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.-48+1422_-48+1423i others(29): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539699 | |||||||
| chr11:10539699 | T | TATATATA others(24): Show |
8 | a0001c0001t0001g0287 a0001c0001t0003g0023 a0001c0001t0003g0179 others(5): Show |
12 | HG00099.hp2 HG01167.hp1 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.-48+1422_-48+1423i others(33): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539699 | |||||||
| chr11:10539699 | T | TATATATA others(26): Show |
13 | a0001c0001t0001g0166 a0001c0001t0001g0174 a0001c0001t0003g0175 others(10): Show |
15 | HG01516.hp1 HG02027.hp1 HG02083.hp1 others(12): Show |
intron_variant | MODIFIER | c.-48+1422_-48+1423i others(35): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539699 | |||||||
| chr11:10539699 | T | TATATATA others(28): Show |
20 | a0001c0001t0001g0152 a0001c0001t0003g0068 a0001c0001t0003g0162 others(17): Show |
24 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.-48+1422_-48+1423i others(37): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539699 | |||||||
| chr11:10539699 | T | TATATATA others(30): Show |
25 | a0001c0001t0001g0148 a0001c0001t0001g0176 a0001c0001t0003g0029 others(22): Show |
36 | HG00323.hp1 HG01071.hp1 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.-48+1422_-48+1423i others(39): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539699 | |||||||
| chr11:10539699 | T | TATATATA others(32): Show |
18 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0132 others(15): Show |
30 | HG00438.hp2 HG00642.hp2 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.-48+1422_-48+1423i others(41): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539699 | |||||||
| chr11:10539699 | T | TATATATA others(34): Show |
11 | a0001c0001t0005g0281 a0001c0001t0025g0121 a0001c0002t0001g0027 others(8): Show |
12 | HG00323.hp2 HG01099.hp2 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.-48+1422_-48+1423i others(43): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539699 | |||||||
| chr11:10539699 | T | TATATATA others(36): Show |
14 | a0001c0001t0003g0111 a0001c0001t0003g0112 a0001c0001t0005g0097 others(11): Show |
15 | HG00642.hp1 HG02273.hp2 HG02602.hp2 others(12): Show |
intron_variant | MODIFIER | c.-48+1422_-48+1423i others(45): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539699 | |||||||
| chr11:10539699 | T | TATATATA others(38): Show |
4 | a0001c0001t0005g0275 a0001c0001t0005g0276 a0001c0002t0001g0106 others(1): Show |
4 | HG01928.hp2 HG01934.hp1 HG02071.hp2 others(1): Show |
intron_variant | MODIFIER | c.-48+1422_-48+1423i others(47): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539699 | |||||||
| chr11:10539699 | T | TATATATA others(40): Show |
3 | a0001c0002t0001g0104 a0001c0002t0001g0105 a0001c0002t0001g0266 |
3 | HG01192.hp2 NA18984.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.-48+1422_-48+1423i others(49): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539699 | |||||||
| chr11:10539699 | T | TATATATA others(42): Show |
1 | a0001c0001t0003g0103 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-48+1422_-48+1423i others(51): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539699 | |||||||
| chr11:10539699 | T | TATATATA others(46): Show |
1 | a0003c0005t0001g0065 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-48+1422_-48+1423i others(55): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539699 | |||||||
| chr11:10539699 | T | TATATATA others(35): Show |
1 | a0001c0002t0001g0102 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-48+1422_-48+1423i others(44): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539699 | |||||||
| chr11:10539700 | T | A | 1 | a0001c0001t0003g0082 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-48+1422A>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539700 | |||||||
| chr11:10539700 | T | G | 8 | a0001c0001t0007g0047 a0001c0001t0007g0096 a0001c0001t0007g0268 others(5): Show |
9 | HG01884.hp1 HG02145.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-48+1422A>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539700 | |||||||
| chr11:10539701 | A | AC | 3 | a0001c0002t0001g0035 a0001c0002t0001g0200 a0001c0002t0001g0201 |
4 | HG01071.hp1 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-48+1420_-48+1421i others(3): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539701 | |||||||
| chr11:10539701 | A | AT | 168 | a0001c0001t0001g0073 a0001c0001t0001g0124 a0001c0001t0001g0125 others(165): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.-48+1420_-48+1421i others(3): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539701 | |||||||
| chr11:10539701 | A | ATATATAT others(44): Show |
1 | a0001c0002t0001g0199 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-48+1420_-48+1421i others(53): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539701 | |||||||
| chr11:10539701 | A | ATATATAT others(34): Show |
1 | a0001c0002t0001g0197 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-48+1420_-48+1421i others(43): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539701 | |||||||
| chr11:10539701 | A | ATATATAT others(32): Show |
1 | a0001c0002t0001g0198 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-48+1420_-48+1421i others(41): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539701 | |||||||
| chr11:10539701 | A | T | 1 | a0001c0001t0003g0082 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-48+1421T>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10539701 | |||||||
| chr11:10540273 | T | C | 1 | a0001c0002t0001g0274 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-48+849A>G | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10540273 | |||||||
| chr11:10540410 | C | A | 15 | a0001c0001t0005g0005 a0001c0001t0005g0021 a0001c0001t0005g0048 others(12): Show |
22 | HG00099.hp2 HG00642.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.-48+712G>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10540410 | |||||||
| chr11:10540457 | G | A | 2 | a0001c0001t0004g0098 a0001c0001t0004g0099 |
2 | HG02145.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-48+665C>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10540457 | |||||||
| chr11:10540458 | C | G | 2 | a0001c0001t0004g0098 a0001c0001t0004g0099 |
2 | HG02145.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-48+664G>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10540458 | |||||||
| chr11:10540593 | T | G | 228 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0132 others(225): Show |
290 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.-48+529A>C | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10540593 | |||||||
| chr11:10540623 | T | A | 1 | a0001c0001t0003g0286 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-48+499A>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10540623 | |||||||
| chr11:10540696 | G | T | 1 | a0001c0001t0014g0064 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-48+426C>A | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10540696 | |||||||
| chr11:10540714 | C | CGCTCTG | 15 | a0001c0001t0006g0010 a0001c0001t0006g0050 a0001c0001t0006g0051 others(12): Show |
17 | HG01069.hp1 HG01081.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-48+402_-48+407dup others(6): Show |
RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10540714 | |||||||
| chr11:10540888 | C | A | 1 | a0001c0001t0001g0287 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-48+234G>T | RNF141 | ENSG00000110315.7 | transcript | ENST00000265981.7 | protein_coding | 1/5 | chr11 | 10540888 |