Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 285533 |
| ensemblid | ENSG00000145428.15 |
| hgncid | 27735 |
| symbol | RNF175 |
| name | ring finger protein 175 |
| refseq_nuc | NM_173662.4 |
| refseq_prot | NP_775933.2 |
| ensembl_nuc | ENST00000347063.9 |
| ensembl_prot | ENSP00000340979.4 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 153710160 |
| end | 153760024 |
| strand | - |
| ver | v1.2 |
| region | chr4:153710160-153760024 |
| region5000 | chr4:153705160-153765024 |
| regionname0 | RNF175_chr4_153710160_153760024 |
| regionname5000 | RNF175_chr4_153705160_153765024 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 328 | 227 | 66 | 30 | 102 | 8 | 21 | 82 | RNF175_chr4_153705160_153765024 | RNF175 | MAAGT others(323): Show |
chr4 | 153705160 | 153765024 |
| a0002 | 0/0 | 328 | 67 | 0 | 12 | 49 | 4 | 2 | 37 | RNF175_chr4_153705160_153765024 | RNF175 | MAAGT others(323): Show |
chr4 | 153705160 | 153765024 |
| a0003 | 0/0 | 328 | 58 | 3 | 4 | 44 | 0 | 7 | 36 | RNF175_chr4_153705160_153765024 | RNF175 | MAAGT others(323): Show |
chr4 | 153705160 | 153765024 |
| a0004 | 0/0 | 328 | 17 | 0 | 9 | 0 | 2 | 6 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | MAAGT others(323): Show |
chr4 | 153705160 | 153765024 |
| a0005 | 1/0 | 328 | 12 | 9 | 1 | 0 | 0 | 1 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | MAAGT others(323): Show |
chr4 | 153705160 | 153765024 |
| a0006 | 0/1 | 328 | 3 | 0 | 1 | 0 | 0 | 1 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | MAAGT others(323): Show |
chr4 | 153705160 | 153765024 |
| a0007 | 0/0 | 328 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | MAAGT others(323): Show |
chr4 | 153705160 | 153765024 |
| a0008 | 0/0 | 328 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | MAAGT others(323): Show |
chr4 | 153705160 | 153765024 |
| a0009 | 0/0 | 328 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | MAAGT others(323): Show |
chr4 | 153705160 | 153765024 |
| a0010 | 0/0 | 328 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | MAAGT others(323): Show |
chr4 | 153705160 | 153765024 |
| a0011 | 0/0 | 328 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | MAAGT others(323): Show |
chr4 | 153705160 | 153765024 |
| a0012 | 0/0 | 328 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | MAAGT others(323): Show |
chr4 | 153705160 | 153765024 |
| a0013 | 0/0 | 328 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | MAAGT others(323): Show |
chr4 | 153705160 | 153765024 |
| a0014 | 0/0 | 328 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | MAAGT others(323): Show |
chr4 | 153705160 | 153765024 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 984 | 227 | 66 | 30 | 102 | 8 | 21 | RNF175_chr4_153705160_153765024 | RNF175 | ATGGC others(979): Show |
chr4 | 153705160 | 153765024 | ||
| a0002c0002 | 0/0 | 984 | 67 | 0 | 12 | 49 | 4 | 2 | RNF175_chr4_153705160_153765024 | RNF175 | ATGGC others(979): Show |
chr4 | 153705160 | 153765024 | ||
| a0003c0003 | 0/0 | 984 | 58 | 3 | 4 | 44 | 0 | 7 | RNF175_chr4_153705160_153765024 | RNF175 | ATGGC others(979): Show |
chr4 | 153705160 | 153765024 | ||
| a0004c0004 | 0/0 | 984 | 17 | 0 | 9 | 0 | 2 | 6 | RNF175_chr4_153705160_153765024 | RNF175 | ATGGC others(979): Show |
chr4 | 153705160 | 153765024 | ||
| a0005c0005 | 1/0 | 984 | 12 | 9 | 1 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | ATGGC others(979): Show |
chr4 | 153705160 | 153765024 | ||
| a0006c0006 | 0/1 | 984 | 3 | 0 | 1 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | ATGGC others(979): Show |
chr4 | 153705160 | 153765024 | ||
| a0007c0007 | 0/0 | 984 | 2 | 2 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | ATGGC others(979): Show |
chr4 | 153705160 | 153765024 | ||
| a0008c0008 | 0/0 | 984 | 2 | 0 | 0 | 0 | 0 | 2 | RNF175_chr4_153705160_153765024 | RNF175 | ATGGC others(979): Show |
chr4 | 153705160 | 153765024 | ||
| a0009c0010 | 0/0 | 984 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | ATGGC others(979): Show |
chr4 | 153705160 | 153765024 | ||
| a0010c0012 | 0/0 | 984 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | ATGGC others(979): Show |
chr4 | 153705160 | 153765024 | ||
| a0011c0011 | 0/0 | 984 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | ATGGC others(979): Show |
chr4 | 153705160 | 153765024 | ||
| a0012c0014 | 0/0 | 984 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | ATGGC others(979): Show |
chr4 | 153705160 | 153765024 | ||
| a0013c0009 | 0/0 | 984 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | ATGGC others(979): Show |
chr4 | 153705160 | 153765024 | ||
| a0014c0013 | 0/0 | 984 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | ATGGC others(979): Show |
chr4 | 153705160 | 153765024 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1358 | 226 | 66 | 30 | 102 | 8 | 20 | RNF175_chr4_153705160_153765024 | RNF175 | ATCTC others(1353): Show |
chr4 | 153705160 | 153765024 |
| a0001c0001t0003 | 0/0 | 1358 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | ATCTC others(1353): Show |
chr4 | 153705160 | 153765024 |
| a0002c0002t0001 | 0/0 | 1358 | 66 | 0 | 12 | 48 | 4 | 2 | RNF175_chr4_153705160_153765024 | RNF175 | ATCTC others(1353): Show |
chr4 | 153705160 | 153765024 |
| a0002c0002t0002 | 0/0 | 1358 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | ATCTC others(1353): Show |
chr4 | 153705160 | 153765024 |
| a0003c0003t0001 | 0/0 | 1358 | 58 | 3 | 4 | 44 | 0 | 7 | RNF175_chr4_153705160_153765024 | RNF175 | ATCTC others(1353): Show |
chr4 | 153705160 | 153765024 |
| a0004c0004t0001 | 0/0 | 1358 | 17 | 0 | 9 | 0 | 2 | 6 | RNF175_chr4_153705160_153765024 | RNF175 | ATCTC others(1353): Show |
chr4 | 153705160 | 153765024 |
| a0005c0005t0001 | 1/0 | 1358 | 12 | 9 | 1 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | ATCTC others(1353): Show |
chr4 | 153705160 | 153765024 |
| a0006c0006t0001 | 0/1 | 1358 | 3 | 0 | 1 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | ATCTC others(1353): Show |
chr4 | 153705160 | 153765024 |
| a0007c0007t0001 | 0/0 | 1358 | 2 | 2 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | ATCTC others(1353): Show |
chr4 | 153705160 | 153765024 |
| a0008c0008t0001 | 0/0 | 1358 | 2 | 0 | 0 | 0 | 0 | 2 | RNF175_chr4_153705160_153765024 | RNF175 | ATCTC others(1353): Show |
chr4 | 153705160 | 153765024 |
| a0009c0010t0001 | 0/0 | 1358 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | ATCTC others(1353): Show |
chr4 | 153705160 | 153765024 |
| a0010c0012t0001 | 0/0 | 1358 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | ATCTC others(1353): Show |
chr4 | 153705160 | 153765024 |
| a0011c0011t0001 | 0/0 | 1358 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | ATCTC others(1353): Show |
chr4 | 153705160 | 153765024 |
| a0012c0014t0001 | 0/0 | 1358 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | ATCTC others(1353): Show |
chr4 | 153705160 | 153765024 |
| a0013c0009t0001 | 0/0 | 1358 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | ATCTC others(1353): Show |
chr4 | 153705160 | 153765024 |
| a0014c0013t0001 | 0/0 | 1358 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | ATCTC others(1353): Show |
chr4 | 153705160 | 153765024 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 14 | 0 | 0 | 14 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0005 | 0/0 | 6 | 1 | 1 | 0 | 4 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0010 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0003 | 0/0 | 8 | 0 | 3 | 3 | 0 | 2 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0019 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0002 | 0/0 | 9 | 0 | 0 | 7 | 0 | 2 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0003c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0004c0004t0001g0014 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0004c0004t0001g0046 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0004c0004t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0004c0004t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0004c0004t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0004c0004t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0004c0004t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0004c0004t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0004c0004t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0004c0004t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0004c0004t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0004c0004t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0004c0004t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0005c0005t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0005c0005t0001g0132 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0005c0005t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0005c0005t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0005c0005t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0005c0005t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0005c0005t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0005c0005t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0005c0005t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0005c0005t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0006c0006t0001g0045 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0006c0006t0001g0275 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0007c0007t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0007c0007t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0008c0008t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0008c0008t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0009c0010t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0010c0012t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0011c0011t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0012c0014t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0013c0009t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| a0014c0013t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0004 | c0004 | t0001 | g0266 | EUR | GBR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG00280 | hp2 | a0002 | c0002 | t0001 | g0143 | EUR | FIN | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG00323 | hp1 | a0004 | c0004 | t0001 | g0265 | EUR | FIN | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG00323 | hp2 | a0002 | c0002 | t0001 | g0105 | EUR | FIN | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG00423 | hp1 | a0003 | c0003 | t0001 | g0061 | EAS | CHS | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0126 | EAS | CHS | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0108 | EAS | CHS | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG00558 | hp1 | a0003 | c0003 | t0001 | g0064 | EAS | CHS | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | CHS | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0083 | EAS | CHS | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG00609 | hp1 | a0003 | c0003 | t0001 | g0063 | EAS | CHS | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0016 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG00733 | hp1 | a0003 | c0003 | t0001 | g0025 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0085 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01070 | hp1 | a0003 | c0003 | t0001 | g0052 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0016 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0016 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01081 | hp1 | a0009 | c0010 | t0001 | g0051 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0090 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0088 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01167 | hp1 | a0003 | c0003 | t0001 | g0027 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01169 | hp1 | a0003 | c0003 | t0001 | g0027 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0019 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01243 | hp1 | a0004 | c0004 | t0001 | g0273 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01243 | hp2 | a0005 | c0005 | t0001 | g0260 | AMR | PUR | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0114 | AMR | CLM | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | CLM | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01257 | hp2 | a0004 | c0004 | t0001 | g0272 | AMR | CLM | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | CLM | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | CLM | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01346 | hp2 | a0006 | c0006 | t0001 | g0045 | AMR | CLM | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01358 | hp1 | a0004 | c0004 | t0001 | g0214 | AMR | CLM | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | CLM | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0093 | AMR | CLM | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | CLM | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0208 | EUR | IBS | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0098 | EUR | IBS | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | ACB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01891 | hp2 | a0007 | c0007 | t0001 | g0264 | AFR | ACB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01928 | hp1 | a0004 | c0004 | t0001 | g0271 | AMR | PEL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | PEL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | PEL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01952 | hp2 | a0004 | c0004 | t0001 | g0014 | AMR | PEL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PEL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01981 | hp1 | a0004 | c0004 | t0001 | g0014 | AMR | PEL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PEL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0127 | EAS | KHV | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02040 | hp2 | a0003 | c0003 | t0001 | g0004 | EAS | KHV | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02055 | hp1 | a0010 | c0012 | t0001 | g0236 | AFR | ACB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | KHV | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0150 | EAS | KHV | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | KHV | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02132 | hp2 | a0003 | c0003 | t0001 | g0002 | EAS | KHV | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0129 | EAS | KHV | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02135 | hp2 | a0003 | c0003 | t0001 | g0015 | EAS | KHV | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | ACB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02148 | hp1 | a0004 | c0004 | t0001 | g0014 | AMR | PEL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02155 | hp1 | a0003 | c0003 | t0001 | g0055 | EAS | CDX | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | CDX | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | CDX | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | CDX | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | ACB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | ACB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02273 | hp2 | a0004 | c0004 | t0001 | g0270 | AMR | PEL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | PEL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02300 | hp2 | a0004 | c0004 | t0001 | g0046 | AMR | PEL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02523 | hp2 | a0003 | c0003 | t0001 | g0074 | EAS | KHV | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02572 | hp2 | a0005 | c0005 | t0001 | g0178 | AFR | GWD | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02630 | hp2 | a0003 | c0003 | t0001 | g0068 | AFR | GWD | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | GWD | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02683 | hp1 | a0004 | c0004 | t0001 | g0014 | SAS | PJL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02698 | hp2 | a0004 | c0004 | t0001 | g0274 | SAS | PJL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | GWD | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02735 | hp1 | a0004 | c0004 | t0001 | g0046 | SAS | PJL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02738 | hp2 | a0003 | c0003 | t0001 | g0002 | SAS | PJL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02922 | hp1 | a0005 | c0005 | t0001 | g0180 | AFR | ESN | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ESN | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02970 | hp1 | a0005 | c0005 | t0001 | g0020 | AFR | ESN | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | ESN | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03017 | hp1 | a0006 | c0006 | t0001 | g0045 | SAS | PJL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0003 | SAS | PJL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | MSL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03098 | hp2 | a0005 | c0005 | t0001 | g0020 | AFR | MSL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03130 | hp2 | a0005 | c0005 | t0001 | g0193 | AFR | ESN | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ESN | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | ESN | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03209 | hp1 | a0012 | c0014 | t0001 | g0263 | AFR | MSL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | MSL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03225 | hp1 | a0003 | c0003 | t0001 | g0067 | AFR | MSL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03225 | hp2 | a0013 | c0009 | t0001 | g0049 | AFR | MSL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | MSL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03453 | hp2 | a0007 | c0007 | t0001 | g0189 | AFR | MSL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03486 | hp2 | a0005 | c0005 | t0001 | g0020 | AFR | MSL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03490 | hp2 | a0003 | c0003 | t0001 | g0026 | SAS | PJL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03491 | hp2 | a0008 | c0008 | t0001 | g0106 | SAS | PJL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03492 | hp1 | a0003 | c0003 | t0001 | g0026 | SAS | PJL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03492 | hp2 | a0008 | c0008 | t0001 | g0107 | SAS | PJL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | MSL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03579 | hp2 | a0005 | c0005 | t0001 | g0186 | AFR | MSL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0003 | SAS | PJL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03654 | hp2 | a0004 | c0004 | t0001 | g0206 | SAS | PJL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0281 | SAS | STU | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | STU | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03831 | hp1 | a0003 | c0003 | t0001 | g0071 | SAS | BEB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | BEB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | BEB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | BEB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG04115 | hp1 | a0003 | c0003 | t0001 | g0002 | SAS | STU | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | STU | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | BEB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG04184 | hp2 | a0004 | c0004 | t0001 | g0269 | SAS | BEB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | STU | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG04204 | hp2 | a0003 | c0003 | t0001 | g0025 | SAS | STU | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG04228 | hp1 | a0005 | c0005 | t0001 | g0185 | SAS | STU | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG04228 | hp2 | a0003 | c0003 | t0001 | g0058 | SAS | STU | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | YRI | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | YRI | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | CHB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | CHB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0149 | EAS | CHB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | CHB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18940 | hp1 | a0002 | c0002 | t0002 | g0047 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18940 | hp2 | a0003 | c0003 | t0001 | g0050 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18941 | hp2 | a0003 | c0003 | t0001 | g0062 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18942 | hp2 | a0003 | c0003 | t0001 | g0015 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18944 | hp1 | a0002 | c0002 | t0001 | g0102 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18945 | hp1 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0079 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18949 | hp1 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18950 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0117 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18952 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18953 | hp1 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18960 | hp1 | a0003 | c0003 | t0001 | g0072 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18960 | hp2 | a0002 | c0002 | t0001 | g0125 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18964 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18965 | hp1 | a0003 | c0003 | t0001 | g0073 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0101 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18972 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18972 | hp2 | a0003 | c0003 | t0001 | g0056 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18973 | hp1 | a0003 | c0003 | t0001 | g0078 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18977 | hp2 | a0003 | c0003 | t0001 | g0069 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0118 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18982 | hp2 | a0003 | c0003 | t0001 | g0066 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18983 | hp2 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18989 | hp1 | a0003 | c0003 | t0001 | g0077 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18989 | hp2 | a0002 | c0002 | t0001 | g0158 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18990 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18992 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18993 | hp1 | a0002 | c0002 | t0001 | g0142 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18997 | hp2 | a0002 | c0002 | t0001 | g0091 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18998 | hp1 | a0003 | c0003 | t0001 | g0053 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18999 | hp1 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0148 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19001 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19002 | hp2 | a0003 | c0003 | t0001 | g0075 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19005 | hp2 | a0003 | c0003 | t0001 | g0057 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19007 | hp1 | a0003 | c0003 | t0001 | g0076 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19012 | hp1 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19030 | hp1 | a0005 | c0005 | t0001 | g0190 | AFR | LWK | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | LWK | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19054 | hp1 | a0003 | c0003 | t0001 | g0054 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19057 | hp2 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19058 | hp1 | a0002 | c0002 | t0001 | g0092 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19062 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19062 | hp2 | a0003 | c0003 | t0001 | g0060 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19063 | hp1 | a0003 | c0003 | t0001 | g0015 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19065 | hp2 | a0014 | c0013 | t0001 | g0165 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19068 | hp2 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19072 | hp1 | a0003 | c0003 | t0001 | g0070 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19076 | hp2 | a0002 | c0002 | t0001 | g0121 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19078 | hp2 | a0002 | c0002 | t0001 | g0103 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19080 | hp1 | a0003 | c0003 | t0001 | g0059 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19080 | hp2 | a0002 | c0002 | t0001 | g0104 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19081 | hp2 | a0003 | c0003 | t0001 | g0028 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19082 | hp2 | a0003 | c0003 | t0001 | g0029 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19083 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19085 | hp2 | a0003 | c0003 | t0001 | g0029 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19087 | hp1 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19088 | hp2 | a0003 | c0003 | t0001 | g0065 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0119 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19090 | hp2 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | YRI | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | YRI | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | ASW | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA20129 | hp2 | a0005 | c0005 | t0001 | g0188 | AFR | ASW | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0040 | EUR | TSI | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0216 | EUR | TSI | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0089 | EUR | TSI | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0141 | EUR | TSI | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | GIH | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA20905 | hp2 | a0004 | c0004 | t0001 | g0267 | SAS | GIH | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | ACB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02109 | hp2 | a0003 | c0003 | t0001 | g0048 | AFR | ACB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG02559 | hp2 | a0011 | c0011 | t0001 | g0211 | AFR | ACB | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | MSL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | MSL | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | USA | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | USA | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18955 | hp1 | a0003 | c0003 | t0001 | g0028 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | USA | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | USA | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | LWK | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | LWK | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| homoSapiens | chm13v2 | a0006 | c0006 | t0001 | g0275 | REF | REF | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| homoSapiens | grch38p0 | a0005 | c0005 | t0001 | g0132 | REF | REF | RNF175_chr4_153705160_153765024 | RNF175 | chr4 | 153705160 | 153765024 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:153710391 | A | T | 12 | a0001 a0002 a0003 others(9): Show |
379 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(376): Show |
missense_variant | MODERATE | c.965T>A | p.Ile322Asn | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 9/9 | 1127/1358 | 965/987 | 322/328 | chr4 | 153710391 | |||
| chr4:153710398 | C | T | 1 | a0012 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.958G>A | p.Gly320Ser | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 9/9 | 1120/1358 | 958/987 | 320/328 | chr4 | 153710398 | |||
| chr4:153710411 | T | C | 2 | a0002 a0008 |
69 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(66): Show |
missense_variant | MODERATE | c.945A>G | p.Ile315Met | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 9/9 | 1107/1358 | 945/987 | 315/328 | chr4 | 153710411 | |||
| chr4:153710435 | C | G | 1 | a0004 | 17 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(14): Show |
missense_variant | MODERATE | c.921G>C | p.Leu307Phe | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 9/9 | 1083/1358 | 921/987 | 307/328 | chr4 | 153710435 | |||
| chr4:153715537 | A | C | 1 | a0009 | 1 | HG01081.hp1 | missense_variant | MODERATE | c.756T>G | p.Cys252Trp | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/9 | 918/1358 | 756/987 | 252/328 | chr4 | 153715537 | |||
| chr4:153715580 | A | G | 1 | a0013 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.713T>C | p.Leu238Pro | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/9 | 875/1358 | 713/987 | 238/328 | chr4 | 153715580 | |||
| chr4:153715646 | C | T | 1 | a0007 | 2 | HG01891.hp2 HG03453.hp2 |
missense_variant | MODERATE | c.647G>A | p.Arg216Gln | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/9 | 809/1358 | 647/987 | 216/328 | chr4 | 153715646 | |||
| chr4:153723385 | T | C | 2 | a0004 a0006 |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
missense_variant | MODERATE | c.475A>G | p.Met159Val | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/9 | 637/1358 | 475/987 | 159/328 | chr4 | 153723385 | |||
| chr4:153723390 | G | A | 1 | a0008 | 2 | HG03491.hp2 HG03492.hp2 |
missense_variant | MODERATE | c.470C>T | p.Ala157Val | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/9 | 632/1358 | 470/987 | 157/328 | chr4 | 153723390 | |||
| chr4:153728207 | C | T | 1 | a0014 | 1 | NA19065.hp2 | missense_variant&splice_region_variant | MODERATE | c.401G>A | p.Arg134Gln | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/9 | 563/1358 | 401/987 | 134/328 | chr4 | 153728207 | |||
| chr4:153748707 | C | T | 1 | a0010 | 1 | HG02055.hp1 | missense_variant | MODERATE | c.184G>A | p.Val62Ile | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/9 | 346/1358 | 184/987 | 62/328 | chr4 | 153748707 | |||
| chr4:153748734 | C | G | 1 | a0011 | 1 | HG02559.hp2 | missense_variant | MODERATE | c.157G>C | p.Val53Leu | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/9 | 319/1358 | 157/987 | 53/328 | chr4 | 153748734 | |||
| chr4:153759802 | C | T | 3 | a0003 a0009 a0013 |
60 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(57): Show |
missense_variant | MODERATE | c.61G>A | p.Glu21Lys | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/9 | 223/1358 | 61/987 | 21/328 | chr4 | 153759802 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:153759879 | C | T | 1 | a0002c0002t0002 | 1 | NA18940.hp1 | 5_prime_UTR_variant | MODIFIER | c.-17G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/9 | 17 | chr4 | 153759879 | ||||||
| chr4:153760016 | G | A | 1 | a0001c0001t0003 | 1 | HG03688.hp1 | 5_prime_UTR_variant | MODIFIER | c.-154C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/9 | 154 | chr4 | 153760016 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:153710851 | G | A | 8 | a0001c0001t0001g0037 a0001c0001t0001g0039 a0001c0001t0001g0041 others(5): Show |
11 | HG00408.hp1 HG00609.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.867-362C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 8/8 | chr4 | 153710851 | |||||||
| chr4:153710910 | A | G | 69 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0021 others(66): Show |
95 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.867-421T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 8/8 | chr4 | 153710910 | |||||||
| chr4:153711397 | G | A | 1 | a0001c0001t0001g0235 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.867-908C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 8/8 | chr4 | 153711397 | |||||||
| chr4:153711454 | A | G | 55 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(52): Show |
81 | HG00408.hp2 HG00438.hp2 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.867-965T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 8/8 | chr4 | 153711454 | |||||||
| chr4:153711686 | G | A | 25 | a0001c0001t0001g0005 a0001c0001t0001g0036 a0001c0001t0001g0043 others(22): Show |
32 | HG00099.hp2 HG00280.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.866+789C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 8/8 | chr4 | 153711686 | |||||||
| chr4:153711735 | A | G | 1 | a0001c0001t0001g0209 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.866+740T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 8/8 | chr4 | 153711735 | |||||||
| chr4:153711795 | A | G | 1 | a0001c0001t0001g0031 | 2 | HG00408.hp2 HG02027.hp2 |
intron_variant | MODIFIER | c.866+680T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 8/8 | chr4 | 153711795 | |||||||
| chr4:153711807 | C | A | 1 | a0002c0002t0001g0118 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.866+668G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 8/8 | chr4 | 153711807 | |||||||
| chr4:153711843 | C | T | 268 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(265): Show |
379 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(376): Show |
intron_variant | MODIFIER | c.866+632G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 8/8 | chr4 | 153711843 | |||||||
| chr4:153711846 | C | G | 1 | a0001c0001t0001g0036 | 2 | HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.866+629G>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 8/8 | chr4 | 153711846 | |||||||
| chr4:153712131 | C | G | 1 | a0001c0001t0001g0176 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.866+344G>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 8/8 | chr4 | 153712131 | |||||||
| chr4:153712428 | GA | G | 73 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0021 others(70): Show |
100 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.866+46delT | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 8/8 | chr4 | 153712428 | |||||||
| chr4:153712582 | G | C | 69 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(66): Show |
99 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(96): Show |
splice_region_variant&intron_variant | LOW | c.765-6C>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153712582 | |||||||
| chr4:153712695 | C | T | 1 | a0003c0003t0001g0059 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.765-119G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153712695 | |||||||
| chr4:153712853 | C | CT | 26 | a0001c0001t0001g0005 a0001c0001t0001g0036 a0001c0001t0001g0043 others(23): Show |
33 | HG00099.hp2 HG00280.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.765-278dupA | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153712853 | |||||||
| chr4:153713123 | A | C | 46 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0030 others(43): Show |
66 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.765-547T>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153713123 | |||||||
| chr4:153713266 | T | A | 2 | a0001c0001t0001g0200 a0001c0001t0001g0202 |
2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.765-690A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153713266 | |||||||
| chr4:153713351 | T | A | 1 | a0002c0002t0001g0096 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.765-775A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153713351 | |||||||
| chr4:153713583 | A | G | 2 | a0001c0001t0001g0200 a0001c0001t0001g0202 |
2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.765-1007T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153713583 | |||||||
| chr4:153713765 | A | G | 2 | a0001c0001t0001g0200 a0001c0001t0001g0202 |
2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.765-1189T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153713765 | |||||||
| chr4:153713836 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.765-1260G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153713836 | |||||||
| chr4:153713852 | G | A | 5 | a0001c0001t0001g0042 a0001c0001t0001g0176 a0001c0001t0001g0177 others(2): Show |
6 | HG02109.hp2 HG02280.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.765-1276C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153713852 | |||||||
| chr4:153713877 | T | C | 268 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(265): Show |
379 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(376): Show |
intron_variant | MODIFIER | c.765-1301A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153713877 | |||||||
| chr4:153713963 | T | G | 193 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(190): Show |
271 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.765-1387A>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153713963 | |||||||
| chr4:153713971 | G | A | 2 | a0001c0001t0001g0200 a0001c0001t0001g0202 |
2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.765-1395C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153713971 | |||||||
| chr4:153714156 | A | G | 1 | a0003c0003t0001g0064 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.764+1373T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153714156 | |||||||
| chr4:153714192 | G | A | 2 | a0002c0002t0001g0089 a0002c0002t0001g0090 |
2 | HG01099.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.764+1337C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153714192 | |||||||
| chr4:153714284 | C | G | 69 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(66): Show |
100 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.764+1245G>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153714284 | |||||||
| chr4:153714445 | C | T | 1 | a0007c0007t0001g0189 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.764+1084G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153714445 | |||||||
| chr4:153714474 | A | G | 7 | a0001c0001t0001g0035 a0001c0001t0001g0044 a0001c0001t0001g0179 others(4): Show |
9 | HG01884.hp2 HG01891.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.764+1055T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153714474 | |||||||
| chr4:153714620 | C | T | 1 | a0002c0002t0001g0143 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.764+909G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153714620 | |||||||
| chr4:153714698 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.764+831C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153714698 | |||||||
| chr4:153714864 | T | C | 1 | a0001c0001t0001g0213 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.764+665A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153714864 | |||||||
| chr4:153714877 | G | T | 1 | a0001c0001t0001g0152 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.764+652C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153714877 | |||||||
| chr4:153714887 | C | T | 68 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(65): Show |
99 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.764+642G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153714887 | |||||||
| chr4:153715004 | A | G | 1 | a0001c0001t0001g0191 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.764+525T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153715004 | |||||||
| chr4:153715011 | C | A | 1 | a0001c0001t0001g0040 | 2 | HG01975.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.764+518G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153715011 | |||||||
| chr4:153715098 | T | A | 1 | a0001c0001t0001g0226 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.764+431A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153715098 | |||||||
| chr4:153715167 | A | G | 1 | a0003c0003t0001g0074 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.764+362T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153715167 | |||||||
| chr4:153715374 | A | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0199 a0003c0003t0001g0048 |
4 | HG02109.hp2 HG02280.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.764+155T>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 7/8 | chr4 | 153715374 | |||||||
| chr4:153715924 | T | C | 1 | a0005c0005t0001g0190 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.631-262A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153715924 | |||||||
| chr4:153715927 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.631-265C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153715927 | |||||||
| chr4:153715978 | C | T | 2 | a0001c0001t0001g0200 a0001c0001t0001g0202 |
2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.631-316G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153715978 | |||||||
| chr4:153716048 | A | G | 2 | a0001c0001t0001g0200 a0001c0001t0001g0202 |
2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.631-386T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153716048 | |||||||
| chr4:153716054 | ACT | A | 67 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0021 others(64): Show |
93 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.631-394_631-393del others(2): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153716054 | |||||||
| chr4:153716063 | C | CA | 56 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0030 others(53): Show |
78 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.631-402dupT | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153716063 | |||||||
| chr4:153716063 | CA | C | 76 | a0001c0001t0001g0005 a0001c0001t0001g0036 a0001c0001t0001g0042 others(73): Show |
110 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.631-402delT | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153716063 | |||||||
| chr4:153716063 | CAA | C | 49 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(46): Show |
75 | HG00408.hp2 HG00438.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.631-403_631-402del others(2): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153716063 | |||||||
| chr4:153716063 | CAAAAAAA others(6): Show |
C | 14 | a0004c0004t0001g0014 a0004c0004t0001g0046 a0004c0004t0001g0206 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.631-414_631-402del others(13): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153716063 | |||||||
| chr4:153716107 | A | G | 2 | a0001c0001t0001g0200 a0001c0001t0001g0202 |
2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.631-445T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153716107 | |||||||
| chr4:153716109 | A | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0199 a0003c0003t0001g0048 |
4 | HG02109.hp2 HG02280.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.631-447T>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153716109 | |||||||
| chr4:153716128 | C | T | 1 | a0002c0002t0001g0121 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.631-466G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153716128 | |||||||
| chr4:153716236 | C | T | 1 | a0001c0001t0001g0191 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.631-574G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153716236 | |||||||
| chr4:153716399 | G | A | 5 | a0001c0001t0001g0042 a0001c0001t0001g0176 a0001c0001t0001g0177 others(2): Show |
6 | HG02109.hp2 HG02280.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.631-737C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153716399 | |||||||
| chr4:153716555 | C | G | 1 | a0001c0001t0001g0123 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.631-893G>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153716555 | |||||||
| chr4:153716612 | C | A | 54 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(51): Show |
80 | HG00408.hp2 HG00438.hp2 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.631-950G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153716612 | |||||||
| chr4:153716643 | C | A | 6 | a0003c0003t0001g0015 a0003c0003t0001g0029 a0003c0003t0001g0059 others(3): Show |
9 | HG02135.hp2 NA18942.hp2 NA18973.hp1 others(6): Show |
intron_variant | MODIFIER | c.631-981G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153716643 | |||||||
| chr4:153716694 | A | G | 1 | a0003c0003t0001g0063 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.631-1032T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153716694 | |||||||
| chr4:153716730 | G | A | 7 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(4): Show |
7 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.631-1068C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153716730 | |||||||
| chr4:153716742 | G | A | 5 | a0001c0001t0001g0042 a0001c0001t0001g0176 a0001c0001t0001g0177 others(2): Show |
6 | HG02109.hp2 HG02280.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.631-1080C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153716742 | |||||||
| chr4:153716850 | G | A | 7 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(4): Show |
7 | HG00642.hp2 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.631-1188C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153716850 | |||||||
| chr4:153716855 | T | C | 1 | a0003c0003t0001g0066 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.631-1193A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153716855 | |||||||
| chr4:153716933 | C | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0199 a0003c0003t0001g0048 |
4 | HG02109.hp2 HG02280.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.631-1271G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153716933 | |||||||
| chr4:153716962 | A | G | 2 | a0001c0001t0001g0200 a0001c0001t0001g0202 |
2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.631-1300T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153716962 | |||||||
| chr4:153716969 | G | T | 14 | a0004c0004t0001g0014 a0004c0004t0001g0046 a0004c0004t0001g0206 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.631-1307C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153716969 | |||||||
| chr4:153716974 | T | A | 70 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(67): Show |
101 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.631-1312A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153716974 | |||||||
| chr4:153717013 | C | T | 2 | a0001c0001t0001g0200 a0001c0001t0001g0202 |
2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.631-1351G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153717013 | |||||||
| chr4:153717049 | G | C | 1 | a0001c0001t0001g0213 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.631-1387C>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153717049 | |||||||
| chr4:153717465 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.631-1803C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153717465 | |||||||
| chr4:153717483 | A | T | 2 | a0001c0001t0001g0195 a0001c0001t0001g0196 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.631-1821T>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153717483 | |||||||
| chr4:153717507 | T | G | 1 | a0002c0002t0001g0102 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.631-1845A>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153717507 | |||||||
| chr4:153717534 | A | AAC | 128 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0018 others(125): Show |
187 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.631-1874_631-1873d others(4): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153717534 | |||||||
| chr4:153717534 | A | AACAC | 54 | a0001c0001t0001g0017 a0001c0001t0001g0030 a0001c0001t0001g0042 others(51): Show |
73 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.631-1876_631-1873d others(6): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153717534 | |||||||
| chr4:153717534 | A | AACACAC | 25 | a0001c0001t0001g0005 a0001c0001t0001g0036 a0001c0001t0001g0043 others(22): Show |
32 | HG00099.hp2 HG00280.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.631-1878_631-1873d others(8): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153717534 | |||||||
| chr4:153717534 | A | C | 5 | a0001c0001t0001g0032 a0001c0001t0001g0155 a0001c0001t0001g0167 others(2): Show |
6 | HG03704.hp1 HG03710.hp2 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.631-1872T>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153717534 | |||||||
| chr4:153717534 | AAC | A | 3 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0133 |
3 | HG02055.hp2 HG02647.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.631-1874_631-1873d others(4): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153717534 | |||||||
| chr4:153717590 | T | A | 2 | a0001c0001t0001g0200 a0001c0001t0001g0202 |
2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.631-1928A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153717590 | |||||||
| chr4:153717775 | T | C | 3 | a0001c0001t0001g0042 a0001c0001t0001g0199 a0003c0003t0001g0048 |
4 | HG02109.hp2 HG02280.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.631-2113A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153717775 | |||||||
| chr4:153717903 | G | T | 2 | a0001c0001t0001g0200 a0001c0001t0001g0202 |
2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.631-2241C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153717903 | |||||||
| chr4:153717944 | A | G | 2 | a0001c0001t0001g0200 a0001c0001t0001g0202 |
2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.630+2240T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153717944 | |||||||
| chr4:153717953 | G | A | 14 | a0004c0004t0001g0014 a0004c0004t0001g0046 a0004c0004t0001g0206 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.630+2231C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153717953 | |||||||
| chr4:153717953 | G | T | 11 | a0005c0005t0001g0020 a0005c0005t0001g0178 a0005c0005t0001g0180 others(8): Show |
13 | HG01243.hp2 HG01891.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.630+2231C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153717953 | |||||||
| chr4:153718054 | T | C | 1 | a0001c0001t0001g0177 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.630+2130A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718054 | |||||||
| chr4:153718208 | AGTTTTTT others(22): Show |
A | 2 | a0001c0001t0001g0200 a0001c0001t0001g0202 |
2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.630+1947_630+1975d others(31): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718208 | |||||||
| chr4:153718214 | TTTTG | T | 67 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0018 others(64): Show |
89 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.630+1966_630+1969d others(6): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718214 | |||||||
| chr4:153718214 | TTTTGTTT others(1): Show |
T | 5 | a0005c0005t0001g0020 a0005c0005t0001g0185 a0005c0005t0001g0193 others(2): Show |
5 | HG01891.hp2 HG03098.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.630+1962_630+1969d others(10): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718214 | |||||||
| chr4:153718218 | G | T | 56 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(53): Show |
82 | HG00408.hp2 HG00438.hp2 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.630+1966C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718218 | |||||||
| chr4:153718222 | G | GT | 43 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(40): Show |
64 | HG00408.hp2 HG00438.hp2 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.630+1961dupA | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718222 | |||||||
| chr4:153718222 | G | GTTTTGT | 14 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0035 others(11): Show |
17 | HG01884.hp2 HG01891.hp1 HG02027.hp1 others(14): Show |
intron_variant | MODIFIER | c.630+1961_630+1962i others(8): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718222 | |||||||
| chr4:153718222 | G | GTTTTTTT others(2): Show |
10 | a0001c0001t0001g0005 a0001c0001t0001g0036 a0001c0001t0001g0043 others(7): Show |
13 | HG00099.hp2 HG01515.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.630+1961_630+1962i others(11): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718222 | |||||||
| chr4:153718222 | G | GTTTTTTT others(3): Show |
5 | a0001c0001t0001g0005 a0001c0001t0001g0043 a0001c0001t0001g0216 others(2): Show |
7 | HG00280.hp1 HG00738.hp2 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.630+1961_630+1962i others(12): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718222 | |||||||
| chr4:153718222 | G | GTTTTTTT others(4): Show |
4 | a0001c0001t0001g0138 a0001c0001t0001g0140 a0001c0001t0001g0219 others(1): Show |
4 | HG01192.hp2 HG01261.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.630+1961_630+1962i others(13): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718222 | |||||||
| chr4:153718222 | G | GTTTTTTT others(5): Show |
1 | a0001c0001t0001g0139 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.630+1961_630+1962i others(14): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718222 | |||||||
| chr4:153718222 | G | GTTTTTTT others(6): Show |
1 | a0011c0011t0001g0211 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.630+1961_630+1962i others(15): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718222 | |||||||
| chr4:153718223 | TTTG | T | 63 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0021 others(60): Show |
82 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(79): Show |
intron_variant | MODIFIER | c.630+1958_630+1960d others(5): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718223 | |||||||
| chr4:153718223 | TTTGTTTG | T | 7 | a0005c0005t0001g0020 a0005c0005t0001g0178 a0005c0005t0001g0180 others(4): Show |
8 | HG01243.hp2 HG02572.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.630+1954_630+1960d others(9): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718223 | |||||||
| chr4:153718223 | TTTGTTTG others(4): Show |
T | 11 | a0004c0004t0001g0014 a0004c0004t0001g0046 a0004c0004t0001g0206 others(8): Show |
16 | HG00323.hp1 HG01243.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.630+1950_630+1960d others(13): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718223 | |||||||
| chr4:153718224 | TTG | T | 15 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0038 others(12): Show |
18 | HG00423.hp1 HG00738.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.630+1958_630+1959d others(4): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718224 | |||||||
| chr4:153718224 | TTGTTTG | T | 5 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0101 others(2): Show |
5 | HG00423.hp2 HG03017.hp2 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.630+1954_630+1959d others(8): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718224 | |||||||
| chr4:153718224 | TTGTTTGT others(3): Show |
T | 2 | a0004c0004t0001g0266 a0004c0004t0001g0274 |
2 | HG00099.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.630+1950_630+1959d others(12): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718224 | |||||||
| chr4:153718225 | TGTTTG | T | 30 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(27): Show |
43 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.630+1954_630+1958d others(7): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718225 | |||||||
| chr4:153718226 | G | T | 28 | a0001c0001t0001g0005 a0001c0001t0001g0036 a0001c0001t0001g0043 others(25): Show |
35 | HG00099.hp2 HG00280.hp1 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.630+1958C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718226 | |||||||
| chr4:153718227 | T | TTTTG | 28 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(25): Show |
41 | HG00408.hp2 HG00438.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.630+1956_630+1957i others(6): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718227 | |||||||
| chr4:153718227 | TTTGTTTG others(4): Show |
T | 1 | a0004c0004t0001g0269 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.630+1946_630+1956d others(13): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718227 | |||||||
| chr4:153718228 | T | TTTG | 15 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0023 others(12): Show |
21 | HG01081.hp2 HG01884.hp1 HG02083.hp1 others(18): Show |
intron_variant | MODIFIER | c.630+1955_630+1956i others(5): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718228 | |||||||
| chr4:153718230 | G | T | 219 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(216): Show |
306 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(303): Show |
intron_variant | MODIFIER | c.630+1954C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718230 | |||||||
| chr4:153718234 | G | T | 260 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(257): Show |
368 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(365): Show |
intron_variant | MODIFIER | c.630+1950C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718234 | |||||||
| chr4:153718238 | G | T | 273 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(270): Show |
386 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(383): Show |
intron_variant | MODIFIER | c.630+1946C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718238 | |||||||
| chr4:153718253 | G | T | 119 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0017 others(116): Show |
166 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.630+1931C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718253 | |||||||
| chr4:153718294 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.630+1890G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718294 | |||||||
| chr4:153718365 | C | T | 1 | a0001c0001t0001g0216 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.630+1819G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718365 | |||||||
| chr4:153718515 | T | G | 67 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0021 others(64): Show |
93 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.630+1669A>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718515 | |||||||
| chr4:153718522 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.630+1662C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718522 | |||||||
| chr4:153718795 | C | T | 1 | a0001c0001t0001g0191 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.630+1389G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718795 | |||||||
| chr4:153718878 | C | A | 4 | a0001c0001t0001g0134 a0001c0001t0001g0195 a0001c0001t0001g0196 others(1): Show |
4 | HG02723.hp2 HG02886.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.630+1306G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153718878 | |||||||
| chr4:153719011 | C | T | 1 | a0001c0001t0001g0191 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.630+1173G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153719011 | |||||||
| chr4:153719114 | G | A | 85 | a0001c0001t0001g0005 a0001c0001t0001g0036 a0001c0001t0001g0043 others(82): Show |
120 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.630+1070C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153719114 | |||||||
| chr4:153719177 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.630+1007G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153719177 | |||||||
| chr4:153719209 | A | G | 276 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(273): Show |
389 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(386): Show |
intron_variant | MODIFIER | c.630+975T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153719209 | |||||||
| chr4:153719337 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.630+847A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153719337 | |||||||
| chr4:153719379 | G | A | 68 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0021 others(65): Show |
94 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.630+805C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153719379 | |||||||
| chr4:153719405 | A | C | 73 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0021 others(70): Show |
99 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.630+779T>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153719405 | |||||||
| chr4:153719627 | C | A | 2 | a0003c0003t0001g0054 a0003c0003t0001g0061 |
2 | HG00423.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.630+557G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153719627 | |||||||
| chr4:153719700 | A | T | 95 | a0001c0001t0001g0005 a0001c0001t0001g0036 a0001c0001t0001g0043 others(92): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.630+484T>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153719700 | |||||||
| chr4:153719739 | T | C | 31 | a0001c0001t0001g0005 a0001c0001t0001g0036 a0001c0001t0001g0043 others(28): Show |
40 | HG00099.hp2 HG00280.hp1 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.630+445A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153719739 | |||||||
| chr4:153719758 | C | A | 1 | a0005c0005t0001g0186 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.630+426G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153719758 | |||||||
| chr4:153719781 | G | A | 95 | a0001c0001t0001g0005 a0001c0001t0001g0036 a0001c0001t0001g0043 others(92): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.630+403C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153719781 | |||||||
| chr4:153719790 | A | G | 95 | a0001c0001t0001g0005 a0001c0001t0001g0036 a0001c0001t0001g0043 others(92): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.630+394T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153719790 | |||||||
| chr4:153719791 | C | A | 95 | a0001c0001t0001g0005 a0001c0001t0001g0036 a0001c0001t0001g0043 others(92): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.630+393G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153719791 | |||||||
| chr4:153719920 | G | A | 95 | a0001c0001t0001g0005 a0001c0001t0001g0036 a0001c0001t0001g0043 others(92): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.630+264C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153719920 | |||||||
| chr4:153719922 | A | C | 3 | a0001c0001t0001g0033 a0001c0001t0001g0198 a0001c0001t0001g0259 |
4 | HG02451.hp1 HG02486.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.630+262T>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153719922 | |||||||
| chr4:153719971 | A | T | 14 | a0004c0004t0001g0014 a0004c0004t0001g0046 a0004c0004t0001g0206 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.630+213T>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153719971 | |||||||
| chr4:153719998 | G | T | 80 | a0001c0001t0001g0005 a0001c0001t0001g0036 a0001c0001t0001g0043 others(77): Show |
115 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.630+186C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 6/8 | chr4 | 153719998 | |||||||
| chr4:153720337 | T | C | 95 | a0001c0001t0001g0005 a0001c0001t0001g0036 a0001c0001t0001g0043 others(92): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.510-33A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153720337 | |||||||
| chr4:153720389 | A | C | 1 | a0001c0001t0001g0112 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.510-85T>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153720389 | |||||||
| chr4:153720413 | T | C | 3 | a0001c0001t0001g0179 a0001c0001t0001g0210 a0001c0001t0001g0212 |
3 | HG02818.hp2 HG03453.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.510-109A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153720413 | |||||||
| chr4:153720426 | ATG | A | 69 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0021 others(66): Show |
95 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.510-124_510-123del others(2): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153720426 | |||||||
| chr4:153720486 | T | C | 56 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0030 others(53): Show |
77 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.510-182A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153720486 | |||||||
| chr4:153720521 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.510-217A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153720521 | |||||||
| chr4:153720538 | T | A | 67 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0021 others(64): Show |
93 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.510-234A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153720538 | |||||||
| chr4:153720576 | G | A | 1 | a0002c0002t0001g0093 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.510-272C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153720576 | |||||||
| chr4:153720917 | C | T | 1 | a0003c0003t0001g0026 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.510-613G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153720917 | |||||||
| chr4:153721085 | T | A | 2 | a0007c0007t0001g0189 a0007c0007t0001g0264 |
2 | HG01891.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.510-781A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153721085 | |||||||
| chr4:153721120 | A | G | 65 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0021 others(62): Show |
91 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.510-816T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153721120 | |||||||
| chr4:153721149 | C | T | 49 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0030 others(46): Show |
70 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.510-845G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153721149 | |||||||
| chr4:153721157 | GT | G | 121 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0017 others(118): Show |
168 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(165): Show |
intron_variant | MODIFIER | c.510-854delA | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153721157 | |||||||
| chr4:153721546 | T | C | 219 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(216): Show |
306 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.510-1242A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153721546 | |||||||
| chr4:153721583 | G | C | 1 | a0001c0001t0001g0159 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.510-1279C>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153721583 | |||||||
| chr4:153721682 | G | A | 70 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0021 others(67): Show |
96 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(93): Show |
intron_variant | MODIFIER | c.510-1378C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153721682 | |||||||
| chr4:153721769 | G | A | 1 | a0001c0001t0001g0141 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.510-1465C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153721769 | |||||||
| chr4:153722035 | T | A | 2 | a0001c0001t0001g0042 a0003c0003t0001g0048 |
3 | HG02109.hp2 HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.509+1316A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153722035 | |||||||
| chr4:153722070 | G | T | 178 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(175): Show |
247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.509+1281C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153722070 | |||||||
| chr4:153722084 | T | C | 6 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(3): Show |
6 | HG00642.hp2 HG02109.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.509+1267A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153722084 | |||||||
| chr4:153722093 | T | C | 14 | a0004c0004t0001g0014 a0004c0004t0001g0046 a0004c0004t0001g0206 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.509+1258A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153722093 | |||||||
| chr4:153722225 | C | T | 2 | a0001c0001t0001g0200 a0001c0001t0001g0202 |
2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.509+1126G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153722225 | |||||||
| chr4:153722234 | G | A | 2 | a0001c0001t0001g0195 a0001c0001t0001g0196 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.509+1117C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153722234 | |||||||
| chr4:153722351 | G | A | 173 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(170): Show |
240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.509+1000C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153722351 | |||||||
| chr4:153722564 | C | CAA | 43 | a0002c0002t0001g0003 a0002c0002t0001g0006 a0002c0002t0001g0007 others(40): Show |
69 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.509+785_509+786dup others(2): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153722564 | |||||||
| chr4:153722646 | G | C | 1 | a0001c0001t0001g0176 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.509+705C>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153722646 | |||||||
| chr4:153722648 | A | G | 1 | a0001c0001t0001g0254 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.509+703T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153722648 | |||||||
| chr4:153722693 | G | A | 1 | a0001c0001t0001g0258 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.509+658C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153722693 | |||||||
| chr4:153722703 | C | T | 1 | a0012c0014t0001g0263 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.509+648G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153722703 | |||||||
| chr4:153722755 | C | G | 1 | a0001c0001t0001g0243 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.509+596G>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153722755 | |||||||
| chr4:153722767 | C | CA | 14 | a0001c0001t0001g0155 a0001c0001t0001g0159 a0001c0001t0001g0167 others(11): Show |
14 | HG00323.hp2 HG00438.hp2 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.509+583dupT | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153722767 | |||||||
| chr4:153722767 | CA | C | 50 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0031 others(47): Show |
64 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.509+583delT | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153722767 | |||||||
| chr4:153722767 | CAA | C | 5 | a0001c0001t0001g0042 a0001c0001t0001g0176 a0001c0001t0001g0199 others(2): Show |
6 | HG02109.hp2 HG02280.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.509+582_509+583del others(2): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153722767 | |||||||
| chr4:153722767 | CAAA | C | 66 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0021 others(63): Show |
91 | HG00423.hp1 HG00733.hp2 HG00738.hp1 others(88): Show |
intron_variant | MODIFIER | c.509+581_509+583del others(3): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153722767 | |||||||
| chr4:153722809 | A | G | 1 | a0001c0001t0001g0222 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.509+542T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153722809 | |||||||
| chr4:153722848 | A | G | 1 | a0001c0001t0001g0191 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.509+503T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153722848 | |||||||
| chr4:153723098 | C | T | 89 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0036 others(86): Show |
126 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.509+253G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153723098 | |||||||
| chr4:153723302 | T | C | 276 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(273): Show |
389 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(386): Show |
intron_variant | MODIFIER | c.509+49A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 5/8 | chr4 | 153723302 | |||||||
| chr4:153723551 | C | T | 1 | a0001c0001t0001g0204 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.402-93G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153723551 | |||||||
| chr4:153723561 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.402-103A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153723561 | |||||||
| chr4:153723655 | A | C | 74 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0021 others(71): Show |
102 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.402-197T>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153723655 | |||||||
| chr4:153723777 | G | A | 145 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(142): Show |
216 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(213): Show |
intron_variant | MODIFIER | c.402-319C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153723777 | |||||||
| chr4:153724029 | G | C | 43 | a0001c0001t0001g0209 a0002c0002t0001g0003 a0002c0002t0001g0006 others(40): Show |
69 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.402-571C>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153724029 | |||||||
| chr4:153724071 | G | A | 18 | a0001c0001t0001g0042 a0001c0001t0001g0176 a0001c0001t0001g0199 others(15): Show |
24 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.402-613C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153724071 | |||||||
| chr4:153724159 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.402-701C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153724159 | |||||||
| chr4:153724246 | G | C | 1 | a0001c0001t0001g0249 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.402-788C>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153724246 | |||||||
| chr4:153724280 | A | T | 1 | a0001c0001t0001g0111 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.402-822T>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153724280 | |||||||
| chr4:153724319 | G | A | 74 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0021 others(71): Show |
103 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(100): Show |
intron_variant | MODIFIER | c.402-861C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153724319 | |||||||
| chr4:153724322 | C | T | 2 | a0001c0001t0001g0200 a0001c0001t0001g0202 |
2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.402-864G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153724322 | |||||||
| chr4:153724441 | A | G | 14 | a0004c0004t0001g0014 a0004c0004t0001g0046 a0004c0004t0001g0206 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.402-983T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153724441 | |||||||
| chr4:153724545 | G | A | 271 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(268): Show |
383 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.402-1087C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153724545 | |||||||
| chr4:153724564 | C | T | 271 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(268): Show |
383 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.402-1106G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153724564 | |||||||
| chr4:153724595 | T | C | 271 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(268): Show |
383 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.402-1137A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153724595 | |||||||
| chr4:153724600 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.402-1142G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153724600 | |||||||
| chr4:153724658 | T | C | 228 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(225): Show |
314 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.402-1200A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153724658 | |||||||
| chr4:153724741 | G | T | 1 | a0001c0001t0001g0221 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.402-1283C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153724741 | |||||||
| chr4:153724774 | T | A | 52 | a0001c0001t0001g0042 a0001c0001t0001g0138 a0001c0001t0001g0139 others(49): Show |
79 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.402-1316A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153724774 | |||||||
| chr4:153724797 | T | C | 1 | a0001c0001t0001g0213 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.402-1339A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153724797 | |||||||
| chr4:153724909 | C | T | 1 | a0002c0002t0001g0104 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.402-1451G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153724909 | |||||||
| chr4:153724935 | ACGTGGGG others(101): Show |
A | 1 | a0002c0002t0001g0142 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.402-1585_402-1478d others(2): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153724935 | |||||||
| chr4:153724962 | A | ACGTGGGG others(47): Show |
4 | a0001c0001t0001g0116 a0003c0003t0001g0002 a0003c0003t0001g0055 others(1): Show |
5 | HG00609.hp1 HG02155.hp1 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.402-1558_402-1505d others(56): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153724962 | |||||||
| chr4:153724962 | ACGTGGGG others(74): Show |
A | 42 | a0002c0002t0001g0003 a0002c0002t0001g0006 a0002c0002t0001g0007 others(39): Show |
68 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.402-1585_402-1505d others(83): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153724962 | |||||||
| chr4:153724985 | AGCTGTGT others(47): Show |
A | 9 | a0001c0001t0001g0042 a0001c0001t0001g0138 a0001c0001t0001g0139 others(6): Show |
10 | HG01167.hp2 HG01192.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.402-1581_402-1528d others(56): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153724985 | |||||||
| chr4:153724990 | TGTGGGGG others(47): Show |
T | 54 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(51): Show |
78 | HG00408.hp2 HG00438.hp2 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.402-1586_402-1533d others(56): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153724990 | |||||||
| chr4:153725000 | C | CGGGCAGG others(47): Show |
1 | a0003c0003t0001g0002 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.402-1543_402-1542i others(56): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153725000 | |||||||
| chr4:153725024 | G | A | 1 | a0004c0004t0001g0274 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.402-1566C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153725024 | |||||||
| chr4:153725027 | C | T | 1 | a0001c0001t0001g0182 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.402-1569G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153725027 | |||||||
| chr4:153725082 | G | A | 7 | a0001c0001t0001g0042 a0001c0001t0001g0138 a0001c0001t0001g0139 others(4): Show |
8 | HG01167.hp2 HG01192.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.402-1624C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153725082 | |||||||
| chr4:153725108 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.402-1650A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153725108 | |||||||
| chr4:153725217 | C | T | 9 | a0001c0001t0001g0042 a0001c0001t0001g0138 a0001c0001t0001g0139 others(6): Show |
10 | HG01167.hp2 HG01192.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.402-1759G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153725217 | |||||||
| chr4:153725218 | A | G | 221 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(218): Show |
314 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.402-1760T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153725218 | |||||||
| chr4:153725267 | T | G | 44 | a0001c0001t0001g0209 a0002c0002t0001g0003 a0002c0002t0001g0006 others(41): Show |
70 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.402-1809A>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153725267 | |||||||
| chr4:153725270 | G | A | 9 | a0001c0001t0001g0009 a0001c0001t0001g0035 a0001c0001t0001g0044 others(6): Show |
15 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.402-1812C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153725270 | |||||||
| chr4:153725307 | T | G | 53 | a0001c0001t0001g0042 a0001c0001t0001g0138 a0001c0001t0001g0139 others(50): Show |
80 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.402-1849A>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153725307 | |||||||
| chr4:153725523 | T | C | 54 | a0001c0001t0001g0042 a0001c0001t0001g0138 a0001c0001t0001g0139 others(51): Show |
81 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.402-2065A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153725523 | |||||||
| chr4:153725600 | G | T | 224 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(221): Show |
317 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.402-2142C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153725600 | |||||||
| chr4:153725662 | C | A | 2 | a0003c0003t0001g0067 a0003c0003t0001g0068 |
2 | HG02630.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.402-2204G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153725662 | |||||||
| chr4:153725784 | T | C | 2 | a0001c0001t0001g0200 a0001c0001t0001g0202 |
2 | HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.402-2326A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153725784 | |||||||
| chr4:153725842 | A | G | 54 | a0001c0001t0001g0042 a0001c0001t0001g0138 a0001c0001t0001g0139 others(51): Show |
81 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.401+2365T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153725842 | |||||||
| chr4:153726073 | A | ATGTG | 5 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(2): Show |
5 | HG01167.hp2 HG02280.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.401+2130_401+2133d others(6): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153726073 | |||||||
| chr4:153726073 | A | ATGTGTG | 3 | a0001c0001t0001g0138 a0001c0001t0001g0176 a0001c0001t0001g0209 |
3 | HG01192.hp2 HG02280.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.401+2128_401+2133d others(8): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153726073 | |||||||
| chr4:153726073 | A | ATGTGTGT others(1): Show |
2 | a0001c0001t0001g0042 a0003c0003t0001g0048 |
3 | HG02109.hp2 HG02976.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.401+2126_401+2133d others(10): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153726073 | |||||||
| chr4:153726073 | ATG | A | 116 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(113): Show |
167 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.401+2132_401+2133d others(4): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153726073 | |||||||
| chr4:153726167 | G | A | 1 | a0003c0003t0001g0071 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.401+2040C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153726167 | |||||||
| chr4:153726229 | C | T | 9 | a0001c0001t0001g0042 a0001c0001t0001g0138 a0001c0001t0001g0139 others(6): Show |
10 | HG01167.hp2 HG01192.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.401+1978G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153726229 | |||||||
| chr4:153726320 | G | A | 1 | a0012c0014t0001g0263 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.401+1887C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153726320 | |||||||
| chr4:153726356 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.401+1851G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153726356 | |||||||
| chr4:153726395 | G | C | 1 | a0002c0002t0001g0148 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.401+1812C>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153726395 | |||||||
| chr4:153726470 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.401+1737A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153726470 | |||||||
| chr4:153726476 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.401+1731A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153726476 | |||||||
| chr4:153726479 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.401+1728A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153726479 | |||||||
| chr4:153726484 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.401+1723C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153726484 | |||||||
| chr4:153727000 | C | T | 45 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0030 others(42): Show |
65 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.401+1207G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153727000 | |||||||
| chr4:153727066 | C | T | 1 | a0001c0001t0001g0247 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.401+1141G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153727066 | |||||||
| chr4:153727072 | C | T | 22 | a0001c0001t0001g0001 a0001c0001t0001g0031 a0001c0001t0001g0081 others(19): Show |
36 | HG00408.hp2 HG00438.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.401+1135G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153727072 | |||||||
| chr4:153727129 | T | C | 4 | a0001c0001t0001g0035 a0001c0001t0001g0044 a0001c0001t0001g0181 others(1): Show |
6 | HG01884.hp2 HG01891.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.401+1078A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153727129 | |||||||
| chr4:153727153 | A | C | 1 | a0002c0002t0001g0148 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.401+1054T>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153727153 | |||||||
| chr4:153727652 | C | T | 45 | a0001c0001t0001g0097 a0001c0001t0001g0100 a0001c0001t0001g0123 others(42): Show |
71 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.401+555G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153727652 | |||||||
| chr4:153727653 | A | G | 134 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0012 others(131): Show |
198 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.401+554T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153727653 | |||||||
| chr4:153728020 | T | C | 2 | a0001c0001t0001g0177 a0001c0001t0001g0226 |
2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.401+187A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153728020 | |||||||
| chr4:153728116 | C | A | 1 | a0001c0001t0001g0162 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.401+91G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 4/8 | chr4 | 153728116 | |||||||
| chr4:153728657 | T | G | 1 | a0001c0001t0001g0230 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.247-296A>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153728657 | |||||||
| chr4:153728693 | G | C | 1 | a0001c0001t0001g0278 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.247-332C>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153728693 | |||||||
| chr4:153728954 | T | C | 100 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(97): Show |
134 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.247-593A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153728954 | |||||||
| chr4:153729106 | C | T | 2 | a0001c0001t0001g0230 a0004c0004t0001g0214 |
2 | HG01358.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.247-745G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153729106 | |||||||
| chr4:153729207 | C | G | 5 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(2): Show |
5 | HG00642.hp2 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.247-846G>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153729207 | |||||||
| chr4:153729277 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.247-916G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153729277 | |||||||
| chr4:153729307 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.247-946G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153729307 | |||||||
| chr4:153729308 | G | A | 136 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(133): Show |
210 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.247-947C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153729308 | |||||||
| chr4:153729342 | C | T | 142 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(139): Show |
216 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(213): Show |
intron_variant | MODIFIER | c.247-981G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153729342 | |||||||
| chr4:153729386 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.247-1025C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153729386 | |||||||
| chr4:153729544 | G | T | 1 | a0001c0001t0001g0177 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.247-1183C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153729544 | |||||||
| chr4:153729667 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.247-1306C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153729667 | |||||||
| chr4:153729735 | A | G | 59 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0030 others(56): Show |
90 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.247-1374T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153729735 | |||||||
| chr4:153729758 | G | T | 1 | a0001c0001t0001g0157 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.247-1397C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153729758 | |||||||
| chr4:153729796 | C | T | 136 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(133): Show |
210 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.247-1435G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153729796 | |||||||
| chr4:153729899 | C | CTCTT | 264 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(261): Show |
377 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(374): Show |
intron_variant | MODIFIER | c.247-1539_247-1538i others(6): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153729899 | |||||||
| chr4:153730048 | A | G | 2 | a0003c0003t0001g0056 a0003c0003t0001g0060 |
2 | NA18972.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.247-1687T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153730048 | |||||||
| chr4:153730202 | T | C | 153 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(150): Show |
230 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(227): Show |
intron_variant | MODIFIER | c.247-1841A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153730202 | |||||||
| chr4:153730297 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.247-1936C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153730297 | |||||||
| chr4:153730403 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.247-2042G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153730403 | |||||||
| chr4:153730444 | G | A | 1 | a0002c0002t0001g0114 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.247-2083C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153730444 | |||||||
| chr4:153730491 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.247-2130G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153730491 | |||||||
| chr4:153730610 | C | A | 1 | a0001c0001t0001g0177 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.247-2249G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153730610 | |||||||
| chr4:153730833 | C | T | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.247-2472G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153730833 | |||||||
| chr4:153730876 | A | G | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.247-2515T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153730876 | |||||||
| chr4:153730902 | A | AAG | 1 | a0002c0002t0001g0016 | 3 | HG00642.hp1 HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.247-2543_247-2542d others(4): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153730902 | |||||||
| chr4:153731082 | T | C | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.247-2721A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153731082 | |||||||
| chr4:153731142 | G | A | 266 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(263): Show |
379 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(376): Show |
intron_variant | MODIFIER | c.247-2781C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153731142 | |||||||
| chr4:153731177 | A | C | 1 | a0001c0001t0001g0177 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.247-2816T>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153731177 | |||||||
| chr4:153731295 | A | G | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.247-2934T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153731295 | |||||||
| chr4:153731409 | C | T | 5 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(2): Show |
5 | HG00642.hp2 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.247-3048G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153731409 | |||||||
| chr4:153731496 | T | G | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.247-3135A>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153731496 | |||||||
| chr4:153731529 | C | T | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.247-3168G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153731529 | |||||||
| chr4:153731665 | A | AAGAG | 13 | a0001c0001t0001g0268 a0004c0004t0001g0014 a0004c0004t0001g0046 others(10): Show |
18 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.247-3308_247-3305d others(6): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153731665 | |||||||
| chr4:153731676 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.247-3315C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153731676 | |||||||
| chr4:153731685 | G | A | 13 | a0001c0001t0001g0268 a0004c0004t0001g0014 a0004c0004t0001g0046 others(10): Show |
18 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.247-3324C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153731685 | |||||||
| chr4:153731685 | G | GAGGA | 58 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0030 others(55): Show |
89 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.247-3328_247-3325d others(6): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153731685 | |||||||
| chr4:153731685 | G | GAGGGAGG others(1): Show |
4 | a0002c0002t0001g0096 a0002c0002t0001g0101 a0002c0002t0001g0102 others(1): Show |
4 | NA18944.hp1 NA18969.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.247-3325_247-3324i others(10): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153731685 | |||||||
| chr4:153731929 | G | A | 1 | a0001c0001t0001g0163 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.247-3568C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153731929 | |||||||
| chr4:153732104 | C | T | 1 | a0001c0001t0003g0281 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.247-3743G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153732104 | |||||||
| chr4:153732164 | G | A | 10 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(7): Show |
10 | HG01167.hp2 HG01192.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.247-3803C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153732164 | |||||||
| chr4:153732231 | CA | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(137): Show |
214 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(211): Show |
intron_variant | MODIFIER | c.247-3871delT | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153732231 | |||||||
| chr4:153732238 | A | C | 100 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(97): Show |
134 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.247-3877T>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153732238 | |||||||
| chr4:153732250 | C | A | 1 | a0001c0001t0001g0115 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.247-3889G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153732250 | |||||||
| chr4:153732477 | C | T | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.247-4116G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153732477 | |||||||
| chr4:153732493 | C | G | 1 | a0001c0001t0001g0154 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.247-4132G>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153732493 | |||||||
| chr4:153732712 | C | T | 15 | a0001c0001t0001g0177 a0001c0001t0001g0200 a0001c0001t0001g0268 others(12): Show |
20 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.247-4351G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153732712 | |||||||
| chr4:153732713 | G | A | 4 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(1): Show |
4 | HG00642.hp2 HG02451.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.247-4352C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153732713 | |||||||
| chr4:153732915 | C | T | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.247-4554G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153732915 | |||||||
| chr4:153732924 | A | C | 47 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(44): Show |
72 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.247-4563T>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153732924 | |||||||
| chr4:153732945 | C | T | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.247-4584G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153732945 | |||||||
| chr4:153732989 | C | T | 1 | a0002c0002t0001g0127 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.247-4628G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153732989 | |||||||
| chr4:153732993 | C | T | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.247-4632G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153732993 | |||||||
| chr4:153732998 | G | A | 1 | a0001c0001t0001g0164 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.247-4637C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153732998 | |||||||
| chr4:153733171 | T | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(82): Show |
131 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.247-4810A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153733171 | |||||||
| chr4:153733332 | G | C | 3 | a0001c0001t0001g0215 a0001c0001t0001g0219 a0001c0001t0001g0220 |
3 | HG02818.hp1 HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.247-4971C>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153733332 | |||||||
| chr4:153733491 | A | C | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.247-5130T>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153733491 | |||||||
| chr4:153733513 | G | A | 75 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(72): Show |
118 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.247-5152C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153733513 | |||||||
| chr4:153733612 | G | A | 273 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(270): Show |
386 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(383): Show |
intron_variant | MODIFIER | c.247-5251C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153733612 | |||||||
| chr4:153733813 | CA | C | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.247-5453delT | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153733813 | |||||||
| chr4:153733854 | T | C | 9 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0181 others(6): Show |
11 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.247-5493A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153733854 | |||||||
| chr4:153733889 | CCACTGAT others(7): Show |
C | 1 | a0002c0002t0001g0126 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.247-5542_247-5529d others(16): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153733889 | |||||||
| chr4:153734019 | T | C | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.247-5658A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153734019 | |||||||
| chr4:153734188 | T | G | 1 | a0001c0001t0001g0177 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.247-5827A>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153734188 | |||||||
| chr4:153734220 | G | A | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.247-5859C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153734220 | |||||||
| chr4:153734336 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.247-5975G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153734336 | |||||||
| chr4:153734415 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.247-6054G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153734415 | |||||||
| chr4:153734495 | GAATT | G | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.247-6138_247-6135d others(6): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153734495 | |||||||
| chr4:153734571 | C | T | 1 | a0001c0001t0001g0241 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.247-6210G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153734571 | |||||||
| chr4:153734665 | C | CT | 8 | a0001c0001t0001g0139 a0001c0001t0001g0196 a0003c0003t0001g0015 others(5): Show |
11 | HG01167.hp2 HG02135.hp2 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.247-6305dupA | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153734665 | |||||||
| chr4:153734665 | C | CTT | 10 | a0001c0001t0001g0033 a0001c0001t0001g0137 a0001c0001t0001g0138 others(7): Show |
12 | HG01192.hp2 HG01884.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.247-6306_247-6305d others(4): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153734665 | |||||||
| chr4:153734665 | CT | C | 37 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0038 others(34): Show |
43 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(40): Show |
intron_variant | MODIFIER | c.247-6305delA | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153734665 | |||||||
| chr4:153734665 | CTT | C | 97 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(94): Show |
146 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.247-6306_247-6305d others(4): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153734665 | |||||||
| chr4:153734665 | CTTT | C | 21 | a0001c0001t0001g0177 a0001c0001t0001g0181 a0001c0001t0001g0217 others(18): Show |
26 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.247-6307_247-6305d others(5): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153734665 | |||||||
| chr4:153734665 | CTTTTTTT others(1): Show |
C | 5 | a0001c0001t0001g0100 a0001c0001t0001g0123 a0002c0002t0001g0007 others(2): Show |
9 | NA18947.hp2 NA18952.hp2 NA18961.hp1 others(6): Show |
intron_variant | MODIFIER | c.247-6312_247-6305d others(10): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153734665 | |||||||
| chr4:153734665 | CTTTTTTT others(2): Show |
C | 54 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0030 others(51): Show |
81 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.247-6313_247-6305d others(11): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153734665 | |||||||
| chr4:153734665 | CTTTTTTT others(3): Show |
C | 2 | a0002c0002t0001g0083 a0002c0002t0001g0090 |
2 | HG00597.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.247-6314_247-6305d others(12): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153734665 | |||||||
| chr4:153734665 | CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0001g0216 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.247-6319_247-6305d others(17): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153734665 | |||||||
| chr4:153734670 | T | C | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.247-6309A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153734670 | |||||||
| chr4:153734672 | T | C | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.247-6311A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153734672 | |||||||
| chr4:153734674 | T | C | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.247-6313A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153734674 | |||||||
| chr4:153734728 | C | T | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG01167.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.247-6367G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153734728 | |||||||
| chr4:153734777 | G | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(83): Show |
136 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.247-6416C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153734777 | |||||||
| chr4:153734800 | C | T | 2 | a0001c0001t0001g0204 a0001c0001t0001g0240 |
2 | HG03491.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.247-6439G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153734800 | |||||||
| chr4:153734801 | G | A | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.247-6440C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153734801 | |||||||
| chr4:153734825 | G | A | 1 | a0004c0004t0001g0266 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.247-6464C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153734825 | |||||||
| chr4:153734860 | T | G | 1 | a0014c0013t0001g0165 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.247-6499A>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153734860 | |||||||
| chr4:153734874 | C | A | 87 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(84): Show |
117 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.247-6513G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153734874 | |||||||
| chr4:153734914 | G | A | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.247-6553C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153734914 | |||||||
| chr4:153735006 | A | G | 1 | a0002c0002t0001g0121 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.247-6645T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153735006 | |||||||
| chr4:153735049 | C | T | 85 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(82): Show |
115 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.247-6688G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153735049 | |||||||
| chr4:153735108 | T | G | 168 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(165): Show |
250 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.247-6747A>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153735108 | |||||||
| chr4:153735227 | A | ATTT | 13 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(10): Show |
18 | HG00099.hp1 HG00323.hp1 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.247-6869_247-6867d others(5): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153735227 | |||||||
| chr4:153735244 | A | G | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.247-6883T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153735244 | |||||||
| chr4:153735258 | T | C | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.247-6897A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153735258 | |||||||
| chr4:153735347 | G | T | 45 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0021 others(42): Show |
66 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.247-6986C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153735347 | |||||||
| chr4:153735384 | T | C | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.247-7023A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153735384 | |||||||
| chr4:153735523 | C | T | 1 | a0012c0014t0001g0263 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.247-7162G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153735523 | |||||||
| chr4:153735640 | C | T | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.247-7279G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153735640 | |||||||
| chr4:153735693 | C | T | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.247-7332G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153735693 | |||||||
| chr4:153735747 | T | TA | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.247-7387_247-7386i others(3): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153735747 | |||||||
| chr4:153735851 | C | T | 1 | a0003c0003t0001g0056 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.247-7490G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153735851 | |||||||
| chr4:153735886 | T | C | 138 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(135): Show |
212 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.247-7525A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153735886 | |||||||
| chr4:153735955 | A | T | 2 | a0003c0003t0001g0028 a0003c0003t0001g0053 |
3 | NA18955.hp1 NA18998.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.247-7594T>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153735955 | |||||||
| chr4:153735999 | C | T | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.247-7638G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153735999 | |||||||
| chr4:153736208 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.247-7847G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153736208 | |||||||
| chr4:153736251 | T | C | 1 | a0001c0001t0001g0177 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.247-7890A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153736251 | |||||||
| chr4:153736427 | C | T | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.247-8066G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153736427 | |||||||
| chr4:153736455 | T | C | 1 | a0001c0001t0001g0177 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.247-8094A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153736455 | |||||||
| chr4:153736630 | A | T | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.247-8269T>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153736630 | |||||||
| chr4:153736710 | C | T | 4 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(1): Show |
4 | HG00642.hp2 HG02451.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.247-8349G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153736710 | |||||||
| chr4:153736722 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.247-8361G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153736722 | |||||||
| chr4:153736728 | C | T | 6 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(3): Show |
7 | HG00642.hp2 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.247-8367G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153736728 | |||||||
| chr4:153736737 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.247-8376C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153736737 | |||||||
| chr4:153736930 | G | A | 1 | a0004c0004t0001g0206 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.247-8569C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153736930 | |||||||
| chr4:153737050 | G | T | 1 | a0001c0001t0001g0137 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.247-8689C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153737050 | |||||||
| chr4:153737083 | A | T | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.247-8722T>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153737083 | |||||||
| chr4:153737112 | G | A | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.247-8751C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153737112 | |||||||
| chr4:153737160 | A | G | 13 | a0001c0001t0001g0268 a0004c0004t0001g0014 a0004c0004t0001g0046 others(10): Show |
18 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.247-8799T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153737160 | |||||||
| chr4:153737187 | T | C | 99 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(96): Show |
133 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.247-8826A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153737187 | |||||||
| chr4:153737239 | A | G | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.247-8878T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153737239 | |||||||
| chr4:153737336 | T | C | 4 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(1): Show |
4 | HG00642.hp2 HG02451.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.247-8975A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153737336 | |||||||
| chr4:153737460 | C | T | 2 | a0003c0003t0001g0048 a0013c0009t0001g0049 |
2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.247-9099G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153737460 | |||||||
| chr4:153737550 | T | C | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.247-9189A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153737550 | |||||||
| chr4:153737772 | CTGT | C | 61 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0030 others(58): Show |
92 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.247-9414_247-9412d others(5): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153737772 | |||||||
| chr4:153737876 | C | T | 152 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(149): Show |
231 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.247-9515G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153737876 | |||||||
| chr4:153738086 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.247-9725C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153738086 | |||||||
| chr4:153738122 | T | C | 1 | a0002c0002t0001g0117 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.247-9761A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153738122 | |||||||
| chr4:153738287 | C | T | 1 | a0001c0001t0001g0241 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.247-9926G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153738287 | |||||||
| chr4:153738344 | T | C | 1 | a0003c0003t0001g0075 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.247-9983A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153738344 | |||||||
| chr4:153738350 | A | AT | 78 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0030 others(75): Show |
114 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.247-9990dupA | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153738350 | |||||||
| chr4:153738376 | A | G | 160 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(157): Show |
242 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.247-10015T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153738376 | |||||||
| chr4:153738408 | G | C | 1 | a0001c0001t0001g0279 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.247-10047C>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153738408 | |||||||
| chr4:153738751 | T | C | 1 | a0002c0002t0001g0118 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.246+9894A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153738751 | |||||||
| chr4:153738820 | G | T | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.246+9825C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153738820 | |||||||
| chr4:153738828 | C | A | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.246+9817G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153738828 | |||||||
| chr4:153738980 | T | C | 5 | a0001c0001t0001g0128 a0002c0002t0001g0008 a0002c0002t0001g0119 others(2): Show |
9 | HG00423.hp2 HG02165.hp1 NA18946.hp2 others(6): Show |
intron_variant | MODIFIER | c.246+9665A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153738980 | |||||||
| chr4:153738997 | C | T | 2 | a0001c0001t0001g0130 a0001c0001t0001g0131 |
2 | HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.246+9648G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153738997 | |||||||
| chr4:153739077 | A | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(151): Show |
231 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(228): Show |
intron_variant | MODIFIER | c.246+9568T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153739077 | |||||||
| chr4:153739227 | C | T | 2 | a0003c0003t0001g0048 a0013c0009t0001g0049 |
2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.246+9418G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153739227 | |||||||
| chr4:153739313 | C | T | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.246+9332G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153739313 | |||||||
| chr4:153739487 | T | G | 2 | a0003c0003t0001g0048 a0013c0009t0001g0049 |
2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.246+9158A>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153739487 | |||||||
| chr4:153739660 | A | G | 1 | a0001c0001t0001g0177 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.246+8985T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153739660 | |||||||
| chr4:153739722 | C | T | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.246+8923G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153739722 | |||||||
| chr4:153739792 | C | T | 4 | a0001c0001t0001g0021 a0001c0001t0001g0194 a0001c0001t0001g0240 others(1): Show |
6 | HG00733.hp2 HG01109.hp2 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.246+8853G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153739792 | |||||||
| chr4:153739796 | G | A | 4 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0228 others(1): Show |
4 | HG02976.hp2 HG03471.hp1 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.246+8849C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153739796 | |||||||
| chr4:153739813 | C | A | 2 | a0001c0001t0001g0224 a0001c0001t0001g0225 |
2 | HG01255.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.246+8832G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153739813 | |||||||
| chr4:153740059 | AT | A | 13 | a0001c0001t0001g0268 a0004c0004t0001g0014 a0004c0004t0001g0046 others(10): Show |
18 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.246+8585delA | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153740059 | |||||||
| chr4:153740122 | A | G | 13 | a0001c0001t0001g0268 a0004c0004t0001g0014 a0004c0004t0001g0046 others(10): Show |
18 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.246+8523T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153740122 | |||||||
| chr4:153740166 | A | AT | 61 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0030 others(58): Show |
92 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.246+8478dupA | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153740166 | |||||||
| chr4:153740166 | AT | A | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.246+8478delA | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153740166 | |||||||
| chr4:153740534 | T | C | 146 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(143): Show |
220 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(217): Show |
intron_variant | MODIFIER | c.246+8111A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153740534 | |||||||
| chr4:153740603 | C | A | 61 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0030 others(58): Show |
92 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.246+8042G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153740603 | |||||||
| chr4:153740623 | T | C | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.246+8022A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153740623 | |||||||
| chr4:153740815 | A | G | 1 | a0007c0007t0001g0264 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.246+7830T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153740815 | |||||||
| chr4:153740923 | C | G | 273 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(270): Show |
386 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(383): Show |
intron_variant | MODIFIER | c.246+7722G>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153740923 | |||||||
| chr4:153741045 | C | T | 1 | a0001c0001t0001g0238 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.246+7600G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153741045 | |||||||
| chr4:153741075 | C | T | 19 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(16): Show |
24 | HG00099.hp1 HG00323.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.246+7570G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153741075 | |||||||
| chr4:153741171 | GT | G | 38 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(35): Show |
60 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.246+7473delA | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153741171 | |||||||
| chr4:153741246 | G | T | 2 | a0001c0001t0001g0250 a0010c0012t0001g0236 |
2 | HG01081.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.246+7399C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153741246 | |||||||
| chr4:153741279 | T | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(149): Show |
231 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.246+7366A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153741279 | |||||||
| chr4:153741310 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.246+7335G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153741310 | |||||||
| chr4:153741312 | G | A | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.246+7333C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153741312 | |||||||
| chr4:153741319 | C | T | 13 | a0001c0001t0001g0268 a0004c0004t0001g0014 a0004c0004t0001g0046 others(10): Show |
18 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.246+7326G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153741319 | |||||||
| chr4:153741451 | C | T | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.246+7194G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153741451 | |||||||
| chr4:153741463 | T | C | 1 | a0003c0003t0001g0072 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.246+7182A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153741463 | |||||||
| chr4:153741517 | T | C | 1 | a0001c0001t0001g0207 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.246+7128A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153741517 | |||||||
| chr4:153741557 | C | G | 1 | a0001c0001t0001g0192 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.246+7088G>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153741557 | |||||||
| chr4:153741741 | T | C | 2 | a0001c0001t0001g0120 a0001c0001t0001g0122 |
2 | NA19000.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.246+6904A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153741741 | |||||||
| chr4:153742131 | A | G | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.246+6514T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153742131 | |||||||
| chr4:153742142 | C | A | 1 | a0001c0001t0001g0203 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.246+6503G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153742142 | |||||||
| chr4:153742272 | C | CA | 89 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0021 others(86): Show |
119 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.246+6372dupT | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153742272 | |||||||
| chr4:153742272 | C | CAA | 103 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0081 others(100): Show |
152 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.246+6371_246+6372d others(4): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153742272 | |||||||
| chr4:153742272 | C | CAAA | 50 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(47): Show |
78 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.246+6370_246+6372d others(5): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153742272 | |||||||
| chr4:153742325 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.246+6320C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153742325 | |||||||
| chr4:153742739 | C | A | 152 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(149): Show |
231 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.246+5906G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153742739 | |||||||
| chr4:153742803 | A | G | 36 | a0001c0001t0001g0094 a0001c0001t0001g0124 a0003c0003t0001g0002 others(33): Show |
57 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.246+5842T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153742803 | |||||||
| chr4:153742913 | A | T | 2 | a0001c0001t0001g0130 a0001c0001t0001g0131 |
2 | HG02055.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.246+5732T>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153742913 | |||||||
| chr4:153742974 | A | G | 273 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(270): Show |
386 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(383): Show |
intron_variant | MODIFIER | c.246+5671T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153742974 | |||||||
| chr4:153743109 | C | T | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.246+5536G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153743109 | |||||||
| chr4:153743143 | G | A | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.246+5502C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153743143 | |||||||
| chr4:153743240 | A | T | 1 | a0001c0001t0001g0152 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.246+5405T>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153743240 | |||||||
| chr4:153743310 | A | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0249 |
5 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.246+5335T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153743310 | |||||||
| chr4:153743352 | C | T | 2 | a0003c0003t0001g0048 a0013c0009t0001g0049 |
2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.246+5293G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153743352 | |||||||
| chr4:153743371 | A | G | 91 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(88): Show |
137 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.246+5274T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153743371 | |||||||
| chr4:153743417 | G | A | 168 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(165): Show |
250 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.246+5228C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153743417 | |||||||
| chr4:153743545 | T | C | 1 | a0001c0001t0001g0168 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.246+5100A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153743545 | |||||||
| chr4:153743545 | T | G | 153 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(150): Show |
230 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(227): Show |
intron_variant | MODIFIER | c.246+5100A>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153743545 | |||||||
| chr4:153743556 | T | G | 1 | a0001c0001t0001g0123 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.246+5089A>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153743556 | |||||||
| chr4:153743636 | G | A | 167 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(164): Show |
249 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.246+5009C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153743636 | |||||||
| chr4:153743640 | G | C | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.246+5005C>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153743640 | |||||||
| chr4:153743642 | T | C | 13 | a0001c0001t0001g0268 a0004c0004t0001g0014 a0004c0004t0001g0046 others(10): Show |
18 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.246+5003A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153743642 | |||||||
| chr4:153743773 | G | T | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.246+4872C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153743773 | |||||||
| chr4:153743869 | T | C | 168 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(165): Show |
250 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.246+4776A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153743869 | |||||||
| chr4:153744051 | C | A | 1 | a0003c0003t0001g0025 | 2 | HG00733.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.246+4594G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153744051 | |||||||
| chr4:153744061 | C | G | 169 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(166): Show |
251 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.246+4584G>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153744061 | |||||||
| chr4:153744076 | G | C | 1 | a0001c0001t0001g0032 | 2 | HG03704.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.246+4569C>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153744076 | |||||||
| chr4:153744127 | A | G | 61 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0030 others(58): Show |
92 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.246+4518T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153744127 | |||||||
| chr4:153744147 | C | T | 2 | a0001c0001t0001g0192 a0001c0001t0001g0199 |
2 | HG02280.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.246+4498G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153744147 | |||||||
| chr4:153744278 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.246+4367G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153744278 | |||||||
| chr4:153744283 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.246+4362C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153744283 | |||||||
| chr4:153744295 | G | A | 34 | a0001c0001t0001g0005 a0001c0001t0001g0036 a0001c0001t0001g0043 others(31): Show |
42 | HG00099.hp2 HG00280.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.246+4350C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153744295 | |||||||
| chr4:153744426 | G | GA | 5 | a0001c0001t0001g0012 a0001c0001t0001g0166 a0001c0001t0001g0167 others(2): Show |
8 | NA18945.hp2 NA18955.hp2 NA18973.hp2 others(5): Show |
intron_variant | MODIFIER | c.246+4218dupT | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153744426 | |||||||
| chr4:153744426 | GA | G | 14 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(11): Show |
15 | HG01167.hp2 HG01192.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.246+4218delT | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153744426 | |||||||
| chr4:153744548 | A | G | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.246+4097T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153744548 | |||||||
| chr4:153744581 | C | A | 59 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0030 others(56): Show |
90 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.246+4064G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153744581 | |||||||
| chr4:153744747 | C | G | 1 | a0001c0001t0001g0237 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.246+3898G>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153744747 | |||||||
| chr4:153744826 | A | C | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.246+3819T>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153744826 | |||||||
| chr4:153744852 | C | T | 1 | a0002c0002t0001g0150 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.246+3793G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153744852 | |||||||
| chr4:153744908 | C | T | 1 | a0003c0003t0001g0052 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.246+3737G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153744908 | |||||||
| chr4:153745046 | A | G | 1 | a0001c0001t0001g0184 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.246+3599T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153745046 | |||||||
| chr4:153745094 | A | G | 15 | a0001c0001t0001g0033 a0001c0001t0001g0137 a0001c0001t0001g0138 others(12): Show |
16 | HG01167.hp2 HG01192.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.246+3551T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153745094 | |||||||
| chr4:153745169 | T | C | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.246+3476A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153745169 | |||||||
| chr4:153745695 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.246+2950A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153745695 | |||||||
| chr4:153745747 | A | T | 4 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(1): Show |
4 | HG00642.hp2 HG02451.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.246+2898T>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153745747 | |||||||
| chr4:153745965 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.246+2680G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153745965 | |||||||
| chr4:153746230 | G | A | 151 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(148): Show |
230 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.246+2415C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153746230 | |||||||
| chr4:153746294 | A | G | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.246+2351T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153746294 | |||||||
| chr4:153746295 | C | A | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.246+2350G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153746295 | |||||||
| chr4:153746432 | T | TCCATAGC others(30): Show |
1 | a0001c0001t0001g0169 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.246+2212_246+2213i others(39): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153746432 | |||||||
| chr4:153746432 | TCCGTAGC others(30): Show |
T | 1 | a0002c0002t0001g0149 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.246+2176_246+2212d others(39): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153746432 | |||||||
| chr4:153746435 | G | A | 150 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(147): Show |
229 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.246+2210C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153746435 | |||||||
| chr4:153746556 | TAGGCTGG others(30): Show |
T | 1 | a0002c0002t0001g0149 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.246+2052_246+2088d others(39): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153746556 | |||||||
| chr4:153746617 | C | A | 1 | a0004c0004t0001g0272 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.246+2028G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153746617 | |||||||
| chr4:153746689 | C | T | 3 | a0001c0001t0001g0177 a0003c0003t0001g0048 a0013c0009t0001g0049 |
3 | HG02109.hp2 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.246+1956G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153746689 | |||||||
| chr4:153746878 | C | T | 2 | a0001c0001t0001g0250 a0010c0012t0001g0236 |
2 | HG01081.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.246+1767G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153746878 | |||||||
| chr4:153746883 | A | G | 1 | a0001c0001t0001g0177 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.246+1762T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153746883 | |||||||
| chr4:153746891 | C | T | 2 | a0003c0003t0001g0048 a0011c0011t0001g0211 |
2 | HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.246+1754G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153746891 | |||||||
| chr4:153746900 | C | A | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.246+1745G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153746900 | |||||||
| chr4:153746951 | C | T | 2 | a0001c0001t0001g0250 a0010c0012t0001g0236 |
2 | HG01081.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.246+1694G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153746951 | |||||||
| chr4:153747076 | C | A | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.246+1569G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153747076 | |||||||
| chr4:153747095 | G | A | 1 | a0003c0003t0001g0072 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.246+1550C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153747095 | |||||||
| chr4:153747126 | C | A | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.246+1519G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153747126 | |||||||
| chr4:153747183 | A | G | 13 | a0001c0001t0001g0268 a0004c0004t0001g0014 a0004c0004t0001g0046 others(10): Show |
18 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.246+1462T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153747183 | |||||||
| chr4:153747221 | G | A | 1 | a0004c0004t0001g0273 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.246+1424C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153747221 | |||||||
| chr4:153747258 | G | C | 1 | a0003c0003t0001g0073 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.246+1387C>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153747258 | |||||||
| chr4:153747277 | T | C | 100 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(97): Show |
134 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.246+1368A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153747277 | |||||||
| chr4:153747455 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.246+1190C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153747455 | |||||||
| chr4:153747522 | T | C | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.246+1123A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153747522 | |||||||
| chr4:153747614 | C | T | 10 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(7): Show |
10 | HG01167.hp2 HG01192.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.246+1031G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153747614 | |||||||
| chr4:153747812 | G | A | 1 | a0001c0001t0001g0170 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.246+833C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153747812 | |||||||
| chr4:153748020 | C | T | 1 | a0003c0003t0001g0075 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.246+625G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153748020 | |||||||
| chr4:153748193 | A | G | 1 | a0001c0001t0001g0177 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.246+452T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153748193 | |||||||
| chr4:153748319 | C | T | 137 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(134): Show |
211 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(208): Show |
intron_variant | MODIFIER | c.246+326G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153748319 | |||||||
| chr4:153748446 | C | G | 1 | a0007c0007t0001g0264 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.246+199G>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153748446 | |||||||
| chr4:153748446 | C | T | 2 | a0003c0003t0001g0027 a0009c0010t0001g0051 |
3 | HG01081.hp1 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.246+199G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153748446 | |||||||
| chr4:153748581 | G | A | 13 | a0001c0001t0001g0268 a0004c0004t0001g0014 a0004c0004t0001g0046 others(10): Show |
18 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.246+64C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 3/8 | chr4 | 153748581 | |||||||
| chr4:153748793 | C | T | 10 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(7): Show |
10 | HG01167.hp2 HG01192.hp2 HG01884.hp1 others(7): Show |
splice_region_variant&intron_variant | LOW | c.105-7G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153748793 | |||||||
| chr4:153748841 | C | CAAAA | 13 | a0001c0001t0001g0268 a0004c0004t0001g0014 a0004c0004t0001g0046 others(10): Show |
18 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.105-59_105-56dupTT others(2): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153748841 | |||||||
| chr4:153748849 | A | C | 2 | a0001c0001t0001g0234 a0001c0001t0001g0235 |
2 | HG02004.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.105-63T>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153748849 | |||||||
| chr4:153749002 | T | C | 1 | a0007c0007t0001g0264 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.105-216A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153749002 | |||||||
| chr4:153749104 | G | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(149): Show |
231 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.105-318C>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153749104 | |||||||
| chr4:153749292 | T | C | 61 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0030 others(58): Show |
92 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.105-506A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153749292 | |||||||
| chr4:153749381 | T | C | 1 | a0001c0001t0001g0177 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.105-595A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153749381 | |||||||
| chr4:153749424 | A | T | 2 | a0003c0003t0001g0048 a0013c0009t0001g0049 |
2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.105-638T>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153749424 | |||||||
| chr4:153749506 | G | A | 1 | a0007c0007t0001g0264 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.105-720C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153749506 | |||||||
| chr4:153749607 | G | A | 3 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 |
3 | NA19000.hp1 NA19083.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.105-821C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153749607 | |||||||
| chr4:153749646 | T | C | 61 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0030 others(58): Show |
92 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.105-860A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153749646 | |||||||
| chr4:153749661 | A | G | 83 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(80): Show |
126 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.105-875T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153749661 | |||||||
| chr4:153749929 | T | C | 1 | a0001c0001t0001g0032 | 2 | HG03704.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.105-1143A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153749929 | |||||||
| chr4:153750244 | A | G | 13 | a0001c0001t0001g0268 a0004c0004t0001g0014 a0004c0004t0001g0046 others(10): Show |
18 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.104+1194T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153750244 | |||||||
| chr4:153750274 | G | A | 1 | a0001c0001t0001g0174 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.104+1164C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153750274 | |||||||
| chr4:153750303 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.104+1135T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153750303 | |||||||
| chr4:153750316 | T | A | 60 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0030 others(57): Show |
91 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.104+1122A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153750316 | |||||||
| chr4:153750323 | C | G | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.104+1115G>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153750323 | |||||||
| chr4:153750324 | T | C | 14 | a0001c0001t0001g0177 a0001c0001t0001g0268 a0004c0004t0001g0014 others(11): Show |
19 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.104+1114A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153750324 | |||||||
| chr4:153750657 | T | TAAACAAA others(1): Show |
106 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(103): Show |
141 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.104+773_104+780dup others(8): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153750657 | |||||||
| chr4:153750667 | A | G | 37 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0031 others(34): Show |
55 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.104+771T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153750667 | |||||||
| chr4:153750668 | G | A | 15 | a0001c0001t0001g0033 a0001c0001t0001g0137 a0001c0001t0001g0138 others(12): Show |
16 | HG01167.hp2 HG01192.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.104+770C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153750668 | |||||||
| chr4:153750669 | C | CAAACAAG others(2): Show |
15 | a0001c0001t0001g0033 a0001c0001t0001g0137 a0001c0001t0001g0138 others(12): Show |
16 | HG01167.hp2 HG01192.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.104+768_104+769ins others(9): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153750669 | |||||||
| chr4:153750836 | A | G | 1 | a0001c0001t0001g0177 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.104+602T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153750836 | |||||||
| chr4:153750876 | CTTTATGA others(19): Show |
C | 2 | a0001c0001t0001g0228 a0001c0001t0001g0229 |
2 | NA18954.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.104+536_104+561del others(26): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153750876 | |||||||
| chr4:153750878 | T | TTATGAGA others(19): Show |
13 | a0001c0001t0001g0268 a0004c0004t0001g0014 a0004c0004t0001g0046 others(10): Show |
18 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.104+534_104+559dup others(26): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153750878 | |||||||
| chr4:153750892 | T | TATTAATC others(19): Show |
1 | a0001c0001t0001g0177 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.104+545_104+546ins others(26): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153750892 | |||||||
| chr4:153750981 | G | T | 5 | a0002c0002t0001g0006 a0002c0002t0001g0011 a0002c0002t0001g0079 others(2): Show |
12 | HG00558.hp2 HG01433.hp2 NA18942.hp1 others(9): Show |
intron_variant | MODIFIER | c.104+457C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 2/8 | chr4 | 153750981 | |||||||
| chr4:153751553 | A | G | 1 | a0002c0002t0001g0149 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.67-78T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153751553 | |||||||
| chr4:153751695 | T | C | 1 | a0001c0001t0001g0124 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.67-220A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153751695 | |||||||
| chr4:153751893 | G | C | 1 | a0001c0001t0001g0249 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.67-418C>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153751893 | |||||||
| chr4:153751975 | T | C | 13 | a0001c0001t0001g0268 a0004c0004t0001g0014 a0004c0004t0001g0046 others(10): Show |
18 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.67-500A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153751975 | |||||||
| chr4:153752173 | G | T | 1 | a0002c0002t0001g0091 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.67-698C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153752173 | |||||||
| chr4:153752517 | T | C | 100 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(97): Show |
134 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.67-1042A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153752517 | |||||||
| chr4:153752598 | T | C | 1 | a0001c0001t0001g0250 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.67-1123A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153752598 | |||||||
| chr4:153752694 | T | C | 13 | a0001c0001t0001g0268 a0004c0004t0001g0014 a0004c0004t0001g0046 others(10): Show |
18 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.67-1219A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153752694 | |||||||
| chr4:153752770 | G | A | 3 | a0002c0002t0001g0008 a0002c0002t0001g0125 a0002c0002t0001g0126 |
7 | HG00423.hp2 HG02165.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.67-1295C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153752770 | |||||||
| chr4:153752853 | G | A | 1 | a0004c0004t0001g0274 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.67-1378C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153752853 | |||||||
| chr4:153752880 | A | G | 4 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 others(1): Show |
4 | NA18948.hp1 NA18971.hp1 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-1405T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153752880 | |||||||
| chr4:153752928 | G | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(70): Show |
116 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.67-1453C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153752928 | |||||||
| chr4:153752943 | G | T | 81 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(78): Show |
124 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.67-1468C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153752943 | |||||||
| chr4:153752968 | C | T | 1 | a0002c0002t0001g0148 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.67-1493G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153752968 | |||||||
| chr4:153752994 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.67-1519G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153752994 | |||||||
| chr4:153753040 | T | A | 53 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0021 others(50): Show |
75 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(72): Show |
intron_variant | MODIFIER | c.67-1565A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153753040 | |||||||
| chr4:153753048 | C | T | 110 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(107): Show |
144 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.67-1573G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153753048 | |||||||
| chr4:153753058 | G | A | 1 | a0003c0003t0001g0073 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.67-1583C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153753058 | |||||||
| chr4:153753071 | G | T | 4 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(1): Show |
4 | HG00642.hp2 HG02451.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.67-1596C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153753071 | |||||||
| chr4:153753072 | A | T | 4 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(1): Show |
4 | HG00642.hp2 HG02451.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.67-1597T>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153753072 | |||||||
| chr4:153753126 | C | T | 163 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(160): Show |
242 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.67-1651G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153753126 | |||||||
| chr4:153753227 | G | A | 1 | a0002c0002t0001g0127 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.67-1752C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153753227 | |||||||
| chr4:153753335 | GGCT | G | 10 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(7): Show |
10 | HG01167.hp2 HG01192.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.67-1863_67-1861del others(3): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153753335 | |||||||
| chr4:153753339 | A | C | 1 | a0001c0001t0001g0208 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.67-1864T>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153753339 | |||||||
| chr4:153753449 | C | T | 100 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(97): Show |
134 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.67-1974G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153753449 | |||||||
| chr4:153753542 | TTC | T | 82 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0030 others(79): Show |
118 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.67-2069_67-2068del others(2): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153753542 | |||||||
| chr4:153753542 | TTCTC | T | 3 | a0002c0002t0001g0088 a0002c0002t0001g0089 a0002c0002t0001g0090 |
3 | HG01099.hp2 HG01109.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.67-2071_67-2068del others(4): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153753542 | |||||||
| chr4:153753558 | CTCT | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(83): Show |
129 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.67-2086_67-2084del others(3): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153753558 | |||||||
| chr4:153753575 | G | A | 1 | a0001c0001t0001g0251 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.67-2100C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153753575 | |||||||
| chr4:153753596 | C | T | 160 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(157): Show |
234 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(231): Show |
intron_variant | MODIFIER | c.67-2121G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153753596 | |||||||
| chr4:153753690 | T | A | 81 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(78): Show |
124 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.67-2215A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153753690 | |||||||
| chr4:153753719 | A | G | 275 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(272): Show |
388 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(385): Show |
intron_variant | MODIFIER | c.67-2244T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153753719 | |||||||
| chr4:153753838 | C | T | 1 | a0003c0003t0001g0026 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.67-2363G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153753838 | |||||||
| chr4:153753896 | C | T | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-2421G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153753896 | |||||||
| chr4:153753903 | G | A | 2 | a0003c0003t0001g0048 a0013c0009t0001g0049 |
2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.67-2428C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153753903 | |||||||
| chr4:153753941 | C | T | 1 | a0004c0004t0001g0266 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.67-2466G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153753941 | |||||||
| chr4:153753947 | T | G | 273 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(270): Show |
386 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(383): Show |
intron_variant | MODIFIER | c.67-2472A>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153753947 | |||||||
| chr4:153753953 | G | A | 273 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(270): Show |
386 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(383): Show |
intron_variant | MODIFIER | c.67-2478C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153753953 | |||||||
| chr4:153753966 | A | C | 273 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(270): Show |
386 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(383): Show |
intron_variant | MODIFIER | c.67-2491T>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153753966 | |||||||
| chr4:153753986 | T | C | 1 | a0001c0001t0001g0175 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.67-2511A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153753986 | |||||||
| chr4:153754031 | G | A | 198 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(195): Show |
275 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.67-2556C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754031 | |||||||
| chr4:153754072 | C | T | 7 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0146 others(4): Show |
7 | HG00642.hp2 HG02109.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.67-2597G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754072 | |||||||
| chr4:153754095 | G | A | 198 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(195): Show |
275 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.67-2620C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754095 | |||||||
| chr4:153754131 | CT | C | 199 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(196): Show |
276 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.67-2657delA | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754131 | |||||||
| chr4:153754169 | C | CA | 70 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0030 others(67): Show |
102 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.67-2695dupT | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754169 | |||||||
| chr4:153754181 | A | AG | 195 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(192): Show |
272 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.67-2707_67-2706ins others(1): Show |
RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754181 | |||||||
| chr4:153754181 | A | G | 1 | a0001c0001t0001g0177 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.67-2706T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754181 | |||||||
| chr4:153754261 | G | T | 3 | a0001c0001t0001g0177 a0003c0003t0001g0048 a0013c0009t0001g0049 |
3 | HG02109.hp2 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.67-2786C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754261 | |||||||
| chr4:153754490 | T | A | 1 | a0001c0001t0001g0177 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.67-3015A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754490 | |||||||
| chr4:153754508 | A | C | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3033T>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754508 | |||||||
| chr4:153754511 | C | T | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3036G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754511 | |||||||
| chr4:153754514 | G | C | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3039C>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754514 | |||||||
| chr4:153754515 | G | A | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3040C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754515 | |||||||
| chr4:153754516 | T | A | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3041A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754516 | |||||||
| chr4:153754517 | T | C | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3042A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754517 | |||||||
| chr4:153754518 | T | A | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3043A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754518 | |||||||
| chr4:153754520 | G | A | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3045C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754520 | |||||||
| chr4:153754521 | G | A | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3046C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754521 | |||||||
| chr4:153754524 | C | A | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3049G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754524 | |||||||
| chr4:153754527 | T | G | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3052A>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754527 | |||||||
| chr4:153754530 | T | G | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3055A>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754530 | |||||||
| chr4:153754531 | G | A | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3056C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754531 | |||||||
| chr4:153754532 | A | G | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3057T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754532 | |||||||
| chr4:153754534 | T | A | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3059A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754534 | |||||||
| chr4:153754535 | T | G | 2 | a0001c0001t0001g0177 a0005c0005t0001g0185 |
2 | HG04228.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.67-3060A>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754535 | |||||||
| chr4:153754539 | T | A | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3064A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754539 | |||||||
| chr4:153754540 | T | A | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3065A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754540 | |||||||
| chr4:153754542 | T | A | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3067A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754542 | |||||||
| chr4:153754553 | A | G | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3078T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754553 | |||||||
| chr4:153754558 | A | C | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3083T>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754558 | |||||||
| chr4:153754560 | G | C | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3085C>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754560 | |||||||
| chr4:153754562 | T | C | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3087A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754562 | |||||||
| chr4:153754564 | G | C | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3089C>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754564 | |||||||
| chr4:153754566 | G | A | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3091C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754566 | |||||||
| chr4:153754567 | T | C | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3092A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754567 | |||||||
| chr4:153754568 | C | A | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3093G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754568 | |||||||
| chr4:153754569 | C | A | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3094G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754569 | |||||||
| chr4:153754570 | T | C | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3095A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754570 | |||||||
| chr4:153754574 | C | A | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3099G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754574 | |||||||
| chr4:153754576 | C | G | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3101G>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754576 | |||||||
| chr4:153754577 | C | G | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3102G>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754577 | |||||||
| chr4:153754580 | T | G | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3105A>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754580 | |||||||
| chr4:153754582 | C | G | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3107G>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754582 | |||||||
| chr4:153754583 | C | G | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3108G>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754583 | |||||||
| chr4:153754584 | T | A | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3109A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754584 | |||||||
| chr4:153754586 | T | G | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3111A>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754586 | |||||||
| chr4:153754587 | G | A | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3112C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754587 | |||||||
| chr4:153754590 | T | A | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3115A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754590 | |||||||
| chr4:153754592 | T | A | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3117A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754592 | |||||||
| chr4:153754598 | T | C | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3123A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754598 | |||||||
| chr4:153754600 | T | A | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3125A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754600 | |||||||
| chr4:153754603 | G | A | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3128C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754603 | |||||||
| chr4:153754604 | G | A | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3129C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754604 | |||||||
| chr4:153754608 | T | C | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3133A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754608 | |||||||
| chr4:153754610 | G | A | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3135C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754610 | |||||||
| chr4:153754610 | G | C | 1 | a0001c0001t0001g0254 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.67-3135C>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754610 | |||||||
| chr4:153754611 | G | C | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3136C>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754611 | |||||||
| chr4:153754613 | T | G | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3138A>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754613 | |||||||
| chr4:153754619 | C | G | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3144G>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754619 | |||||||
| chr4:153754622 | A | G | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3147T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754622 | |||||||
| chr4:153754623 | T | A | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3148A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754623 | |||||||
| chr4:153754625 | T | G | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3150A>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754625 | |||||||
| chr4:153754628 | T | A | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3153A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754628 | |||||||
| chr4:153754629 | T | A | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3154A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754629 | |||||||
| chr4:153754635 | C | T | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3160G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754635 | |||||||
| chr4:153754639 | A | T | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3164T>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754639 | |||||||
| chr4:153754640 | G | C | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3165C>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754640 | |||||||
| chr4:153754643 | T | C | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3168A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754643 | |||||||
| chr4:153754646 | G | C | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3171C>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754646 | |||||||
| chr4:153754648 | C | A | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3173G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754648 | |||||||
| chr4:153754651 | T | A | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3176A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754651 | |||||||
| chr4:153754662 | G | A | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3187C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754662 | |||||||
| chr4:153754664 | C | G | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3189G>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754664 | |||||||
| chr4:153754668 | T | A | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3193A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754668 | |||||||
| chr4:153754669 | C | A | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3194G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754669 | |||||||
| chr4:153754670 | C | A | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3195G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754670 | |||||||
| chr4:153754671 | T | G | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3196A>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754671 | |||||||
| chr4:153754673 | A | G | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3198T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754673 | |||||||
| chr4:153754675 | T | G | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3200A>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754675 | |||||||
| chr4:153754676 | C | A | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3201G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754676 | |||||||
| chr4:153754677 | C | G | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3202G>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754677 | |||||||
| chr4:153754679 | A | T | 1 | a0005c0005t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.67-3204T>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754679 | |||||||
| chr4:153754708 | C | T | 110 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(107): Show |
144 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.67-3233G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754708 | |||||||
| chr4:153754765 | G | A | 1 | a0001c0001t0001g0255 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.67-3290C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754765 | |||||||
| chr4:153754788 | A | G | 273 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(270): Show |
386 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(383): Show |
intron_variant | MODIFIER | c.67-3313T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754788 | |||||||
| chr4:153754938 | AT | A | 9 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0181 others(6): Show |
11 | HG01243.hp2 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.67-3464delA | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754938 | |||||||
| chr4:153754957 | G | A | 198 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(195): Show |
275 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.67-3482C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153754957 | |||||||
| chr4:153755055 | G | A | 1 | a0001c0001t0001g0262 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.67-3580C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153755055 | |||||||
| chr4:153755289 | A | G | 273 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(270): Show |
386 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(383): Show |
intron_variant | MODIFIER | c.67-3814T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153755289 | |||||||
| chr4:153755403 | A | G | 6 | a0001c0001t0001g0034 a0001c0001t0001g0204 a0001c0001t0001g0205 others(3): Show |
7 | HG01496.hp2 HG02698.hp1 HG03654.hp2 others(4): Show |
intron_variant | MODIFIER | c.67-3928T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153755403 | |||||||
| chr4:153755563 | C | G | 6 | a0001c0001t0001g0034 a0001c0001t0001g0204 a0001c0001t0001g0205 others(3): Show |
7 | HG01496.hp2 HG02698.hp1 HG03654.hp2 others(4): Show |
intron_variant | MODIFIER | c.67-4088G>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153755563 | |||||||
| chr4:153755574 | T | TA | 116 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(113): Show |
150 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.67-4100dupT | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153755574 | |||||||
| chr4:153755668 | G | C | 273 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(270): Show |
386 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(383): Show |
intron_variant | MODIFIER | c.66+4129C>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153755668 | |||||||
| chr4:153755669 | C | A | 1 | a0002c0002t0001g0129 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.66+4128G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153755669 | |||||||
| chr4:153755669 | C | CA | 72 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0030 others(69): Show |
108 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.66+4127dupT | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153755669 | |||||||
| chr4:153755670 | A | C | 198 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(195): Show |
275 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.66+4127T>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153755670 | |||||||
| chr4:153755802 | C | T | 3 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 |
3 | HG03041.hp1 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.66+3995G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153755802 | |||||||
| chr4:153755803 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.66+3994C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153755803 | |||||||
| chr4:153755822 | T | C | 12 | a0001c0001t0001g0033 a0001c0001t0001g0137 a0001c0001t0001g0138 others(9): Show |
13 | HG01167.hp2 HG01192.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.66+3975A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153755822 | |||||||
| chr4:153756271 | A | C | 118 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(115): Show |
152 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.66+3526T>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153756271 | |||||||
| chr4:153756297 | C | T | 2 | a0002c0002t0001g0142 a0002c0002t0001g0143 |
2 | HG00280.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.66+3500G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153756297 | |||||||
| chr4:153756391 | A | G | 23 | a0001c0001t0001g0033 a0001c0001t0001g0137 a0001c0001t0001g0138 others(20): Show |
24 | HG01167.hp2 HG01192.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.66+3406T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153756391 | |||||||
| chr4:153756413 | T | C | 198 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(195): Show |
275 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.66+3384A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153756413 | |||||||
| chr4:153756458 | T | C | 75 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0030 others(72): Show |
111 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.66+3339A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153756458 | |||||||
| chr4:153756482 | G | C | 119 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(116): Show |
153 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.66+3315C>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153756482 | |||||||
| chr4:153756516 | C | T | 8 | a0001c0001t0001g0184 a0001c0001t0001g0187 a0005c0005t0001g0185 others(5): Show |
8 | HG02615.hp1 HG03130.hp2 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.66+3281G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153756516 | |||||||
| chr4:153756704 | G | T | 118 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(115): Show |
152 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.66+3093C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153756704 | |||||||
| chr4:153756989 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.66+2808G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153756989 | |||||||
| chr4:153757051 | A | G | 7 | a0001c0001t0001g0033 a0001c0001t0001g0182 a0001c0001t0001g0183 others(4): Show |
8 | HG02451.hp1 HG02486.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.66+2746T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153757051 | |||||||
| chr4:153757084 | A | G | 1 | a0001c0001t0001g0177 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.66+2713T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153757084 | |||||||
| chr4:153757115 | C | A | 1 | a0001c0001t0001g0177 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.66+2682G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153757115 | |||||||
| chr4:153757160 | G | T | 1 | a0001c0001t0001g0082 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.66+2637C>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153757160 | |||||||
| chr4:153757211 | A | C | 198 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(195): Show |
275 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.66+2586T>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153757211 | |||||||
| chr4:153757471 | A | G | 273 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(270): Show |
386 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(383): Show |
intron_variant | MODIFIER | c.66+2326T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153757471 | |||||||
| chr4:153757583 | C | T | 1 | a0002c0002t0001g0079 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.66+2214G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153757583 | |||||||
| chr4:153757747 | C | G | 1 | a0001c0001t0001g0194 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.66+2050G>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153757747 | |||||||
| chr4:153758179 | A | G | 62 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0030 others(59): Show |
93 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.66+1618T>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153758179 | |||||||
| chr4:153758320 | G | C | 1 | a0005c0005t0001g0193 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.66+1477C>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153758320 | |||||||
| chr4:153758550 | G | A | 12 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(9): Show |
12 | HG02615.hp1 HG03130.hp2 HG03195.hp1 others(9): Show |
intron_variant | MODIFIER | c.66+1247C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153758550 | |||||||
| chr4:153758615 | G | A | 13 | a0001c0001t0001g0268 a0004c0004t0001g0014 a0004c0004t0001g0046 others(10): Show |
18 | HG00099.hp1 HG00323.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.66+1182C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153758615 | |||||||
| chr4:153758674 | C | A | 4 | a0003c0003t0001g0015 a0003c0003t0001g0029 a0003c0003t0001g0077 others(1): Show |
7 | HG02135.hp2 NA18942.hp2 NA18973.hp1 others(4): Show |
intron_variant | MODIFIER | c.66+1123G>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153758674 | |||||||
| chr4:153758713 | T | C | 201 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(198): Show |
283 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.66+1084A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153758713 | |||||||
| chr4:153758797 | C | T | 1 | a0003c0003t0001g0025 | 2 | HG00733.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.66+1000G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153758797 | |||||||
| chr4:153758829 | T | A | 162 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(159): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.66+968A>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153758829 | |||||||
| chr4:153758855 | T | C | 162 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(159): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.66+942A>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153758855 | |||||||
| chr4:153758894 | G | C | 50 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0012 others(47): Show |
72 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.66+903C>G | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153758894 | |||||||
| chr4:153759056 | C | T | 5 | a0001c0001t0001g0179 a0001c0001t0001g0181 a0005c0005t0001g0020 others(2): Show |
7 | HG02572.hp2 HG02922.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.66+741G>A | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153759056 | |||||||
| chr4:153759117 | T | G | 162 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0013 others(159): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.66+680A>C | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153759117 | |||||||
| chr4:153759344 | G | A | 6 | a0001c0001t0001g0024 a0001c0001t0001g0276 a0001c0001t0001g0277 others(3): Show |
8 | HG01346.hp1 HG01358.hp2 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.66+453C>T | RNF175 | ENSG00000145428.15 | transcript | ENST00000347063.9 | protein_coding | 1/8 | chr4 | 153759344 |