Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55819 |
| ensemblid | ENSG00000113269.14 |
| hgncid | 18280 |
| symbol | RNF130 |
| name | ring finger protein 130 |
| refseq_nuc | NM_018434.6 |
| refseq_prot | NP_060904.2 |
| ensembl_nuc | ENST00000521389.6 |
| ensembl_prot | ENSP00000430237.1 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 179955067 |
| end | 180071759 |
| strand | - |
| ver | v1.2 |
| region | chr5:179955067-180071759 |
| region5000 | chr5:179950067-180076759 |
| regionname0 | RNF130_chr5_179955067_180071759 |
| regionname5000 | RNF130_chr5_179950067_180076759 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 419 | 336 | 95 | 71 | 127 | 14 | 27 | 97 | RNF130_chr5_179950067_180076759 | RNF130 | MSCAG others(414): Show |
chr5 | 179950067 | 180076759 |
| a0002 | 0/0 | 419 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | MSCAG others(414): Show |
chr5 | 179950067 | 180076759 |
| a0003 | 0/0 | 419 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | MSCAG others(414): Show |
chr5 | 179950067 | 180076759 |
| a0004 | 0/0 | 419 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | MSCAG others(414): Show |
chr5 | 179950067 | 180076759 |
| a0005 | 0/0 | 419 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | MSCAG others(414): Show |
chr5 | 179950067 | 180076759 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1257 | 138 | 68 | 18 | 41 | 4 | 6 | RNF130_chr5_179950067_180076759 | RNF130 | ATGAG others(1252): Show |
chr5 | 179950067 | 180076759 | ||
| a0001c0002 | 0/1 | 1257 | 123 | 11 | 27 | 63 | 7 | 14 | RNF130_chr5_179950067_180076759 | RNF130 | ATGAG others(1252): Show |
chr5 | 179950067 | 180076759 | ||
| a0001c0003 | 0/0 | 1257 | 53 | 12 | 21 | 12 | 3 | 5 | RNF130_chr5_179950067_180076759 | RNF130 | ATGAG others(1252): Show |
chr5 | 179950067 | 180076759 | ||
| a0001c0004 | 0/0 | 1257 | 12 | 0 | 1 | 10 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | ATGAG others(1252): Show |
chr5 | 179950067 | 180076759 | ||
| a0001c0005 | 0/0 | 1257 | 4 | 4 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | ATGAG others(1252): Show |
chr5 | 179950067 | 180076759 | ||
| a0001c0006 | 0/0 | 1257 | 3 | 0 | 3 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | ATGAG others(1252): Show |
chr5 | 179950067 | 180076759 | ||
| a0001c0007 | 0/0 | 1257 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | ATGAG others(1252): Show |
chr5 | 179950067 | 180076759 | ||
| a0001c0011 | 0/0 | 1257 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | ATGAG others(1252): Show |
chr5 | 179950067 | 180076759 | ||
| a0001c0012 | 0/0 | 1257 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | ATGAG others(1252): Show |
chr5 | 179950067 | 180076759 | ||
| a0002c0010 | 0/0 | 1257 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | ATGAG others(1252): Show |
chr5 | 179950067 | 180076759 | ||
| a0003c0013 | 0/0 | 1257 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | ATGAG others(1252): Show |
chr5 | 179950067 | 180076759 | ||
| a0004c0009 | 0/0 | 1257 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | ATGAG others(1252): Show |
chr5 | 179950067 | 180076759 | ||
| a0005c0008 | 0/0 | 1257 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | ATGAG others(1252): Show |
chr5 | 179950067 | 180076759 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1904 | 137 | 67 | 18 | 41 | 4 | 6 | RNF130_chr5_179950067_180076759 | RNF130 | CTCTA others(1899): Show |
chr5 | 179950067 | 180076759 |
| a0001c0001t0002 | 0/0 | 1902 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | CTCTA others(1897): Show |
chr5 | 179950067 | 180076759 |
| a0001c0002t0001 | 0/1 | 1904 | 121 | 10 | 27 | 62 | 7 | 14 | RNF130_chr5_179950067_180076759 | RNF130 | CTCTA others(1899): Show |
chr5 | 179950067 | 180076759 |
| a0001c0002t0002 | 0/0 | 1902 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | CTCTA others(1897): Show |
chr5 | 179950067 | 180076759 |
| a0001c0002t0004 | 0/0 | 1904 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | CTCTA others(1899): Show |
chr5 | 179950067 | 180076759 |
| a0001c0003t0001 | 0/0 | 1904 | 49 | 8 | 21 | 12 | 3 | 5 | RNF130_chr5_179950067_180076759 | RNF130 | CTCTA others(1899): Show |
chr5 | 179950067 | 180076759 |
| a0001c0003t0002 | 0/0 | 1902 | 4 | 4 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | CTCTA others(1897): Show |
chr5 | 179950067 | 180076759 |
| a0001c0004t0001 | 0/0 | 1904 | 10 | 0 | 1 | 8 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | CTCTA others(1899): Show |
chr5 | 179950067 | 180076759 |
| a0001c0004t0004 | 0/0 | 1904 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | CTCTA others(1899): Show |
chr5 | 179950067 | 180076759 |
| a0001c0004t0005 | 0/0 | 1904 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | CTCTA others(1899): Show |
chr5 | 179950067 | 180076759 |
| a0001c0005t0001 | 0/0 | 1904 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | CTCTA others(1899): Show |
chr5 | 179950067 | 180076759 |
| a0001c0005t0003 | 0/0 | 1904 | 3 | 3 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | CTCTA others(1899): Show |
chr5 | 179950067 | 180076759 |
| a0001c0006t0001 | 0/0 | 1904 | 3 | 0 | 3 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | CTCTA others(1899): Show |
chr5 | 179950067 | 180076759 |
| a0001c0007t0001 | 0/0 | 1904 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | CTCTA others(1899): Show |
chr5 | 179950067 | 180076759 |
| a0001c0011t0001 | 0/0 | 1904 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | CTCTA others(1899): Show |
chr5 | 179950067 | 180076759 |
| a0001c0012t0001 | 0/0 | 1904 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | CTCTA others(1899): Show |
chr5 | 179950067 | 180076759 |
| a0002c0010t0001 | 0/0 | 1904 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | CTCTA others(1899): Show |
chr5 | 179950067 | 180076759 |
| a0003c0013t0001 | 0/0 | 1904 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | CTCTA others(1899): Show |
chr5 | 179950067 | 180076759 |
| a0004c0009t0001 | 0/0 | 1904 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | CTCTA others(1899): Show |
chr5 | 179950067 | 180076759 |
| a0005c0008t0001 | 0/0 | 1904 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | CTCTA others(1899): Show |
chr5 | 179950067 | 180076759 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0281 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0018 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0002t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0001 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0003t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0004t0001g0002 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0004t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0004t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0004t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0004t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0004t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0004t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0004t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0004t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0004t0004g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0004t0005g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0005t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0005t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0005t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0005t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0006t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0006t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0006t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0007t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0011t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0001c0012t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0002c0010t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0003c0013t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0004c0009t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| a0005c0008t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0050 | EUR | GBR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0121 | EUR | GBR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0303 | EUR | GBR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0021 | EUR | GBR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0257 | EUR | FIN | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00280 | hp2 | a0001 | c0003 | t0001 | g0168 | EUR | FIN | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0261 | EUR | FIN | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0063 | EUR | FIN | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | CHS | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00408 | hp2 | a0001 | c0003 | t0001 | g0154 | EAS | CHS | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0091 | EAS | CHS | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | CHS | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | CHS | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | CHS | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0066 | EAS | CHS | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00558 | hp2 | a0001 | c0003 | t0001 | g0181 | EAS | CHS | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0059 | EAS | CHS | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | CHS | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00642 | hp1 | a0001 | c0003 | t0001 | g0166 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0122 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | CHS | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0100 | EAS | CHS | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00733 | hp2 | a0001 | c0003 | t0001 | g0164 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0048 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0116 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0051 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0328 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01069 | hp1 | a0001 | c0003 | t0001 | g0187 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0054 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01071 | hp1 | a0001 | c0003 | t0001 | g0001 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01074 | hp1 | a0001 | c0003 | t0001 | g0165 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0074 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01081 | hp1 | a0001 | c0003 | t0001 | g0172 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0099 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0067 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01168 | hp1 | a0001 | c0003 | t0001 | g0001 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0053 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01169 | hp1 | a0001 | c0003 | t0001 | g0171 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0320 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01175 | hp1 | a0001 | c0003 | t0001 | g0153 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0068 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0123 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01243 | hp1 | a0001 | c0003 | t0001 | g0190 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01243 | hp2 | a0002 | c0010 | t0001 | g0031 | AMR | PUR | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0119 | AMR | CLM | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0070 | AMR | CLM | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01256 | hp1 | a0001 | c0003 | t0001 | g0183 | AMR | CLM | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0044 | AMR | CLM | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01257 | hp1 | a0001 | c0003 | t0001 | g0185 | AMR | CLM | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01257 | hp2 | a0001 | c0002 | t0001 | g0082 | AMR | CLM | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01258 | hp1 | a0001 | c0002 | t0001 | g0062 | AMR | CLM | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01258 | hp2 | a0001 | c0003 | t0001 | g0004 | AMR | CLM | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01261 | hp1 | a0001 | c0003 | t0001 | g0194 | AMR | CLM | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01261 | hp2 | a0001 | c0003 | t0001 | g0146 | AMR | CLM | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | CLM | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0315 | AMR | CLM | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0118 | AMR | CLM | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01361 | hp2 | a0001 | c0006 | t0001 | g0197 | AMR | CLM | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01433 | hp1 | a0001 | c0003 | t0001 | g0004 | AMR | CLM | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01433 | hp2 | a0001 | c0012 | t0001 | g0288 | AMR | CLM | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0055 | AMR | CLM | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01496 | hp2 | a0001 | c0003 | t0001 | g0147 | AMR | CLM | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0020 | EUR | IBS | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01516 | hp2 | a0001 | c0003 | t0001 | g0149 | EUR | IBS | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0015 | EUR | IBS | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01517 | hp2 | a0001 | c0003 | t0001 | g0150 | EUR | IBS | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | ACB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01884 | hp2 | a0001 | c0003 | t0002 | g0156 | AFR | ACB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0017 | AFR | ACB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01928 | hp1 | a0001 | c0003 | t0001 | g0175 | AMR | PEL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | PEL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01934 | hp1 | a0001 | c0006 | t0001 | g0198 | AMR | PEL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0117 | AMR | PEL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01943 | hp1 | a0001 | c0003 | t0001 | g0173 | AMR | PEL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0045 | AMR | PEL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0262 | AMR | PEL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01952 | hp2 | a0001 | c0003 | t0001 | g0148 | AMR | PEL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0080 | AMR | PEL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01975 | hp2 | a0001 | c0006 | t0001 | g0196 | AMR | PEL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0092 | AMR | PEL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0081 | AMR | PEL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PEL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0069 | AMR | PEL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0075 | AMR | PEL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0120 | AMR | PEL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02004 | hp2 | a0001 | c0003 | t0001 | g0174 | AMR | PEL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0112 | EAS | KHV | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0040 | EAS | KHV | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02055 | hp1 | a0003 | c0013 | t0001 | g0209 | AFR | ACB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | ACB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02056 | hp1 | a0001 | c0003 | t0001 | g0184 | EAS | KHV | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | KHV | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | KHV | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02074 | hp2 | a0001 | c0002 | t0004 | g0085 | EAS | KHV | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0111 | EAS | KHV | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0124 | EAS | KHV | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | KHV | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | KHV | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0009 | EAS | KHV | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | ACB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0115 | AFR | ACB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | CDX | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | CDX | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | CDX | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | CDX | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0056 | AFR | ACB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | ACB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0331 | AFR | ACB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0126 | AFR | ACB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02280 | hp2 | a0001 | c0003 | t0001 | g0157 | AFR | ACB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0087 | AMR | PEL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02293 | hp2 | a0001 | c0004 | t0001 | g0139 | AMR | PEL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02451 | hp1 | a0001 | c0003 | t0002 | g0159 | AFR | ACB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02572 | hp1 | a0001 | c0005 | t0003 | g0191 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02602 | hp1 | a0001 | c0003 | t0001 | g0162 | SAS | PJL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02602 | hp2 | a0004 | c0009 | t0001 | g0014 | SAS | PJL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0047 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02622 | hp2 | a0001 | c0003 | t0001 | g0189 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02630 | hp2 | a0001 | c0005 | t0003 | g0163 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0110 | SAS | PJL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0093 | SAS | PJL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0061 | SAS | PJL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0324 | SAS | PJL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02717 | hp2 | a0001 | c0002 | t0002 | g0132 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0133 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0010 | SAS | PJL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | PJL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0327 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ESN | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | ESN | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | ESN | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | ESN | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | ESN | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | ESN | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | ESN | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | ESN | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0078 | SAS | PJL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03017 | hp2 | a0001 | c0003 | t0001 | g0001 | SAS | PJL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03041 | hp1 | a0001 | c0003 | t0001 | g0160 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03098 | hp1 | a0001 | c0003 | t0001 | g0188 | AFR | MSL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | MSL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | ESN | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03139 | hp2 | a0001 | c0003 | t0001 | g0158 | AFR | ESN | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0326 | AFR | ESN | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | ESN | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | MSL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | MSL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | MSL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03453 | hp1 | a0001 | c0003 | t0001 | g0193 | AFR | MSL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | MSL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | MSL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0330 | AFR | MSL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0057 | SAS | PJL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0308 | SAS | PJL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0071 | SAS | PJL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0307 | SAS | PJL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | ESN | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | ESN | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0325 | AFR | MSL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | MSL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0284 | SAS | PJL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0322 | SAS | PJL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03704 | hp1 | a0001 | c0003 | t0001 | g0170 | SAS | PJL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0083 | SAS | PJL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0052 | SAS | PJL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0058 | SAS | PJL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0095 | SAS | BEB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03834 | hp2 | a0001 | c0004 | t0001 | g0002 | SAS | BEB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG04184 | hp1 | a0001 | c0003 | t0001 | g0152 | SAS | BEB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0032 | SAS | BEB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0114 | SAS | STU | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0016 | SAS | STU | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG04228 | hp1 | a0001 | c0003 | t0001 | g0182 | SAS | STU | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG04228 | hp2 | a0001 | c0007 | t0001 | g0008 | SAS | STU | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | YRI | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | YRI | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18612 | hp1 | a0001 | c0003 | t0001 | g0179 | EAS | CHB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0065 | EAS | CHB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0243 | AFR | YRI | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18939 | hp1 | a0001 | c0003 | t0001 | g0180 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0130 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18942 | hp2 | a0001 | c0003 | t0001 | g0003 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18943 | hp1 | a0001 | c0003 | t0001 | g0186 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18948 | hp1 | a0001 | c0003 | t0001 | g0176 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18951 | hp1 | a0001 | c0004 | t0001 | g0143 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0131 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18962 | hp1 | a0001 | c0004 | t0001 | g0140 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18971 | hp1 | a0001 | c0003 | t0001 | g0178 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18971 | hp2 | a0005 | c0008 | t0001 | g0128 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18974 | hp2 | a0001 | c0004 | t0001 | g0136 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18977 | hp2 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18987 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19004 | hp1 | a0001 | c0004 | t0001 | g0135 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19006 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19006 | hp2 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19030 | hp1 | a0001 | c0005 | t0001 | g0195 | AFR | LWK | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0134 | AFR | LWK | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | LWK | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19043 | hp2 | a0001 | c0003 | t0002 | g0155 | AFR | LWK | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19055 | hp1 | a0001 | c0004 | t0001 | g0138 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19055 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19056 | hp1 | a0001 | c0003 | t0001 | g0177 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0104 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19057 | hp2 | a0001 | c0011 | t0001 | g0145 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19065 | hp1 | a0001 | c0003 | t0001 | g0151 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0113 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19068 | hp1 | a0001 | c0004 | t0001 | g0141 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19070 | hp2 | a0001 | c0003 | t0001 | g0003 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19080 | hp2 | a0001 | c0004 | t0001 | g0002 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19081 | hp2 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19083 | hp2 | a0001 | c0004 | t0004 | g0144 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19086 | hp2 | a0001 | c0004 | t0001 | g0137 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19091 | hp2 | a0001 | c0004 | t0005 | g0142 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19240 | hp1 | a0001 | c0005 | t0003 | g0192 | AFR | YRI | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | YRI | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA20129 | hp1 | a0001 | c0003 | t0001 | g0161 | AFR | ASW | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0019 | AFR | ASW | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0260 | EUR | TSI | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0049 | EUR | TSI | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | CLM | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | CLM | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | ACB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0295 | AFR | ACB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0127 | AFR | ACB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | ACB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG02559 | hp2 | a0001 | c0003 | t0001 | g0167 | AFR | ACB | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | MSL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0030 | AFR | MSL | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0329 | AFR | USA | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | USA | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0297 | AFR | USA | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | USA | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA21309 | hp1 | a0001 | c0003 | t0002 | g0169 | AFR | LWK | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | LWK | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0018 | REF | REF | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0281 | REF | REF | RNF130_chr5_179950067_180076759 | RNF130 | chr5 | 179950067 | 180076759 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:179966923 | C | T | 1 | a0002 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.1033G>A | p.Asp345Asn | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 7/9 | 1090/1904 | 1033/1260 | 345/419 | chr5 | 179966923 | |||
| chr5:179966926 | C | T | 1 | a0003 | 1 | HG02055.hp1 | missense_variant | MODERATE | c.1030G>A | p.Gly344Ser | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 7/9 | 1087/1904 | 1030/1260 | 344/419 | chr5 | 179966926 | |||
| chr5:180013203 | C | T | 1 | a0004 | 1 | HG02602.hp2 | missense_variant | MODERATE | c.551G>A | p.Arg184Gln | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/9 | 608/1904 | 551/1260 | 184/419 | chr5 | 180013203 | |||
| chr5:180040533 | C | T | 1 | a0005 | 1 | NA18971.hp2 | missense_variant | MODERATE | c.362G>A | p.Arg121Gln | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/9 | 419/1904 | 362/1260 | 121/419 | chr5 | 180040533 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:179966867 | T | C | 1 | a0001c0005 | 4 | HG02572.hp1 HG02630.hp2 NA19030.hp1 others(1): Show |
synonymous_variant | LOW | c.1089A>G | p.Ser363Ser | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 7/9 | 1146/1904 | 1089/1260 | 363/419 | chr5 | 179966867 | |||
| chr5:180040553 | C | T | 1 | a0001c0012 | 1 | HG01433.hp2 | synonymous_variant | LOW | c.342G>A | p.Thr114Thr | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/9 | 399/1904 | 342/1260 | 114/419 | chr5 | 180040553 | |||
| chr5:180071529 | G | A | 1 | a0001c0006 | 3 | HG01361.hp2 HG01934.hp1 HG01975.hp2 |
synonymous_variant | LOW | c.174C>T | p.Arg58Arg | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/9 | 231/1904 | 174/1260 | 58/419 | chr5 | 180071529 | |||
| chr5:180071592 | C | T | 1 | a0001c0007 | 1 | HG04228.hp2 | synonymous_variant | LOW | c.111G>A | p.Ala37Ala | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/9 | 168/1904 | 111/1260 | 37/419 | chr5 | 180071592 | |||
| chr5:180071595 | C | T | 8 | a0001c0002 a0001c0003 a0001c0005 others(5): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(183): Show |
synonymous_variant | LOW | c.108G>A | p.Thr36Thr | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/9 | 165/1904 | 108/1260 | 36/419 | chr5 | 180071595 | |||
| chr5:180071652 | C | T | 1 | a0001c0011 | 1 | NA19057.hp2 | synonymous_variant | LOW | c.51G>A | p.Leu17Leu | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/9 | 108/1904 | 51/1260 | 17/419 | chr5 | 180071652 | |||
| chr5:180071658 | G | T | 6 | a0001c0002 a0001c0004 a0001c0007 others(3): Show |
138 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(135): Show |
synonymous_variant | LOW | c.45C>A | p.Leu15Leu | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/9 | 102/1904 | 45/1260 | 15/419 | chr5 | 180071658 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:179955136 | G | A | 1 | a0001c0004t0005 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*518C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 9/9 | 518 | chr5 | 179955136 | ||||||
| chr5:179955152 | A | C | 2 | a0001c0002t0004 a0001c0004t0004 |
2 | HG02074.hp2 NA19083.hp2 |
3_prime_UTR_variant | MODIFIER | c.*502T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 9/9 | 502 | chr5 | 179955152 | ||||||
| chr5:179955215 | TCA | T | 3 | a0001c0001t0002 a0001c0002t0002 a0001c0003t0002 |
6 | HG01884.hp2 HG02451.hp1 HG02717.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*437_*438delTG | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 9/9 | 437 | chr5 | 179955215 | ||||||
| chr5:179955594 | C | T | 1 | a0001c0005t0003 | 3 | HG02572.hp1 HG02630.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*60G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 9/9 | 60 | chr5 | 179955594 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:179955920 | G | A | 2 | a0001c0001t0001g0005 a0001c0001t0001g0255 |
3 | HG03209.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1245-251C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179955920 | |||||||
| chr5:179956531 | C | T | 3 | a0001c0001t0001g0276 a0001c0001t0001g0279 a0001c0002t0001g0123 |
3 | HG01192.hp2 HG01928.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.1245-862G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179956531 | |||||||
| chr5:179956575 | C | T | 4 | a0001c0003t0001g0174 a0001c0005t0003g0163 a0001c0005t0003g0191 others(1): Show |
4 | HG02004.hp2 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1245-906G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179956575 | |||||||
| chr5:179956634 | C | T | 1 | a0001c0002t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1245-965G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179956634 | |||||||
| chr5:179956757 | C | T | 3 | a0001c0002t0001g0101 a0001c0002t0001g0102 a0001c0002t0001g0103 |
3 | NA18979.hp1 NA19079.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1245-1088G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179956757 | |||||||
| chr5:179956815 | T | C | 189 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(186): Show |
197 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.1245-1146A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179956815 | |||||||
| chr5:179957222 | G | A | 1 | a0001c0003t0001g0179 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1245-1553C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179957222 | |||||||
| chr5:179957356 | G | A | 1 | a0001c0001t0001g0292 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1245-1687C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179957356 | |||||||
| chr5:179957626 | G | T | 1 | a0001c0001t0001g0286 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1245-1957C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179957626 | |||||||
| chr5:179957696 | T | C | 2 | a0001c0001t0001g0270 a0001c0002t0001g0091 |
2 | HG00438.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1245-2027A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179957696 | |||||||
| chr5:179957881 | CT | C | 209 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(206): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.1245-2213delA | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179957881 | |||||||
| chr5:179957904 | G | A | 4 | a0001c0001t0001g0315 a0001c0003t0001g0001 a0001c0003t0001g0171 others(1): Show |
6 | HG01069.hp1 HG01071.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.1245-2235C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179957904 | |||||||
| chr5:179957945 | T | C | 7 | a0001c0001t0001g0223 a0001c0001t0001g0225 a0001c0001t0001g0226 others(4): Show |
7 | HG02572.hp2 HG02818.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1245-2276A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179957945 | |||||||
| chr5:179957965 | C | T | 2 | a0001c0001t0001g0292 a0001c0001t0001g0295 |
2 | HG02486.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1245-2296G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179957965 | |||||||
| chr5:179957982 | A | G | 7 | a0001c0001t0001g0223 a0001c0001t0001g0225 a0001c0001t0001g0226 others(4): Show |
7 | HG02572.hp2 HG02818.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1245-2313T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179957982 | |||||||
| chr5:179957999 | T | G | 3 | a0001c0005t0003g0163 a0001c0005t0003g0191 a0001c0005t0003g0192 |
3 | HG02572.hp1 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1245-2330A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179957999 | |||||||
| chr5:179958022 | C | T | 1 | a0001c0003t0001g0153 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1245-2353G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179958022 | |||||||
| chr5:179958090 | G | A | 1 | a0001c0003t0001g0184 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1245-2421C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179958090 | |||||||
| chr5:179958131 | T | C | 208 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(205): Show |
216 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.1245-2462A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179958131 | |||||||
| chr5:179958152 | T | C | 2 | a0001c0001t0001g0264 a0001c0002t0001g0023 |
2 | HG02155.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.1245-2483A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179958152 | |||||||
| chr5:179958493 | G | A | 5 | a0001c0002t0001g0045 a0001c0002t0001g0048 a0001c0003t0001g0146 others(2): Show |
5 | HG00735.hp1 HG01261.hp2 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.1245-2824C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179958493 | |||||||
| chr5:179958672 | A | C | 140 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(137): Show |
148 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.1245-3003T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179958672 | |||||||
| chr5:179958919 | G | A | 1 | a0001c0002t0001g0064 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1245-3250C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179958919 | |||||||
| chr5:179959443 | C | T | 211 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(208): Show |
219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.1245-3774G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179959443 | |||||||
| chr5:179960005 | C | G | 1 | a0001c0002t0001g0123 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1244+3466G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179960005 | |||||||
| chr5:179960027 | A | G | 1 | a0001c0002t0001g0134 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1244+3444T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179960027 | |||||||
| chr5:179960190 | C | T | 2 | a0001c0003t0001g0149 a0001c0003t0001g0150 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1244+3281G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179960190 | |||||||
| chr5:179960366 | G | A | 10 | a0001c0001t0001g0204 a0001c0001t0001g0211 a0001c0001t0001g0212 others(7): Show |
10 | HG02717.hp1 HG02723.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1244+3105C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179960366 | |||||||
| chr5:179960369 | C | T | 29 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(26): Show |
31 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.1244+3102G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179960369 | |||||||
| chr5:179960479 | G | C | 2 | a0001c0002t0001g0030 a0001c0002t0001g0133 |
2 | HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1244+2992C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179960479 | |||||||
| chr5:179960632 | G | A | 1 | a0001c0003t0001g0157 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1244+2839C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179960632 | |||||||
| chr5:179960845 | GA | G | 197 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(194): Show |
205 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.1244+2625delT | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179960845 | |||||||
| chr5:179960882 | T | C | 8 | a0001c0001t0001g0237 a0001c0001t0001g0244 a0001c0001t0001g0245 others(5): Show |
8 | HG02055.hp2 HG02280.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1244+2589A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179960882 | |||||||
| chr5:179960894 | G | A | 1 | a0001c0005t0001g0195 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1244+2577C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179960894 | |||||||
| chr5:179960916 | T | C | 2 | a0001c0001t0001g0247 a0001c0001t0001g0249 |
2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1244+2555A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179960916 | |||||||
| chr5:179961061 | G | A | 2 | a0001c0001t0001g0247 a0001c0001t0001g0249 |
2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1244+2410C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179961061 | |||||||
| chr5:179961111 | T | TA | 22 | a0001c0001t0001g0203 a0001c0001t0001g0213 a0001c0001t0001g0216 others(19): Show |
22 | HG01243.hp2 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.1244+2359dupT | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179961111 | |||||||
| chr5:179961156 | G | A | 2 | a0001c0001t0001g0247 a0001c0001t0001g0249 |
2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1244+2315C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179961156 | |||||||
| chr5:179961212 | G | A | 2 | a0001c0001t0001g0286 a0001c0001t0001g0287 |
2 | HG01358.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1244+2259C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179961212 | |||||||
| chr5:179961249 | A | C | 1 | a0001c0002t0001g0056 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1244+2222T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179961249 | |||||||
| chr5:179961363 | C | T | 9 | a0001c0001t0001g0275 a0001c0002t0001g0079 a0001c0002t0001g0084 others(6): Show |
9 | NA18942.hp1 NA18943.hp2 NA18950.hp2 others(6): Show |
intron_variant | MODIFIER | c.1244+2108G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179961363 | |||||||
| chr5:179961586 | C | T | 22 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(19): Show |
24 | HG00408.hp2 HG00609.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.1244+1885G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179961586 | |||||||
| chr5:179961664 | T | C | 1 | a0001c0002t0001g0064 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1244+1807A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179961664 | |||||||
| chr5:179961714 | A | C | 1 | a0001c0002t0001g0090 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1244+1757T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179961714 | |||||||
| chr5:179961857 | G | T | 1 | a0001c0002t0001g0030 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1244+1614C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179961857 | |||||||
| chr5:179961859 | C | T | 1 | a0001c0001t0001g0292 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1244+1612G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179961859 | |||||||
| chr5:179961875 | G | A | 2 | a0001c0001t0001g0246 a0001c0003t0001g0158 |
2 | HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1244+1596C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179961875 | |||||||
| chr5:179961947 | T | C | 7 | a0001c0001t0001g0237 a0001c0001t0001g0244 a0001c0001t0001g0245 others(4): Show |
7 | HG02055.hp2 HG02896.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1244+1524A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179961947 | |||||||
| chr5:179961964 | A | C | 1 | a0001c0002t0001g0063 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1244+1507T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179961964 | |||||||
| chr5:179962124 | T | C | 1 | a0001c0003t0002g0155 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1244+1347A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179962124 | |||||||
| chr5:179962294 | C | T | 1 | a0001c0002t0001g0024 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1244+1177G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179962294 | |||||||
| chr5:179962391 | A | T | 7 | a0001c0001t0001g0237 a0001c0001t0001g0244 a0001c0001t0001g0245 others(4): Show |
7 | HG02055.hp2 HG02896.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1244+1080T>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179962391 | |||||||
| chr5:179962475 | T | C | 1 | a0001c0002t0001g0097 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1244+996A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179962475 | |||||||
| chr5:179962539 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1244+932G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179962539 | |||||||
| chr5:179962649 | A | G | 1 | a0001c0001t0001g0284 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1244+822T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179962649 | |||||||
| chr5:179962717 | C | T | 1 | a0001c0002t0001g0114 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1244+754G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179962717 | |||||||
| chr5:179962801 | C | T | 1 | a0001c0002t0001g0119 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1244+670G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179962801 | |||||||
| chr5:179962836 | G | A | 3 | a0001c0005t0003g0163 a0001c0005t0003g0191 a0001c0005t0003g0192 |
3 | HG02572.hp1 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1244+635C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179962836 | |||||||
| chr5:179962879 | C | G | 8 | a0001c0001t0001g0237 a0001c0001t0001g0244 a0001c0001t0001g0245 others(5): Show |
8 | HG02055.hp2 HG02280.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1244+592G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179962879 | |||||||
| chr5:179963003 | A | C | 142 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(139): Show |
150 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.1244+468T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179963003 | |||||||
| chr5:179963116 | G | A | 2 | a0001c0001t0001g0212 a0001c0001t0001g0218 |
2 | HG03098.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1244+355C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 8/8 | chr5 | 179963116 | |||||||
| chr5:179963682 | G | C | 1 | a0001c0001t0001g0278 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1151-118C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 7/8 | chr5 | 179963682 | |||||||
| chr5:179963995 | G | A | 1 | a0001c0005t0001g0195 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1151-431C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 7/8 | chr5 | 179963995 | |||||||
| chr5:179964061 | T | C | 1 | a0001c0003t0001g0153 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1151-497A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 7/8 | chr5 | 179964061 | |||||||
| chr5:179964192 | G | A | 1 | a0001c0003t0001g0161 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1151-628C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 7/8 | chr5 | 179964192 | |||||||
| chr5:179964584 | C | T | 4 | a0001c0005t0001g0195 a0001c0005t0003g0163 a0001c0005t0003g0191 others(1): Show |
4 | HG02572.hp1 HG02630.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1151-1020G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 7/8 | chr5 | 179964584 | |||||||
| chr5:179964811 | A | G | 29 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(26): Show |
31 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.1151-1247T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 7/8 | chr5 | 179964811 | |||||||
| chr5:179965075 | G | C | 3 | a0001c0005t0003g0163 a0001c0005t0003g0191 a0001c0005t0003g0192 |
3 | HG02572.hp1 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1151-1511C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 7/8 | chr5 | 179965075 | |||||||
| chr5:179965081 | C | T | 1 | a0001c0001t0001g0296 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1151-1517G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 7/8 | chr5 | 179965081 | |||||||
| chr5:179965120 | G | A | 1 | a0001c0001t0001g0325 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1151-1556C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 7/8 | chr5 | 179965120 | |||||||
| chr5:179965303 | G | A | 6 | a0001c0001t0002g0243 a0001c0002t0002g0132 a0001c0003t0002g0155 others(3): Show |
6 | HG01884.hp2 HG02451.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1150+1503C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 7/8 | chr5 | 179965303 | |||||||
| chr5:179965313 | C | T | 212 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(209): Show |
220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.1150+1493G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 7/8 | chr5 | 179965313 | |||||||
| chr5:179965325 | C | T | 3 | a0001c0005t0003g0163 a0001c0005t0003g0191 a0001c0005t0003g0192 |
3 | HG02572.hp1 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1150+1481G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 7/8 | chr5 | 179965325 | |||||||
| chr5:179965358 | A | G | 1 | a0001c0005t0001g0195 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1150+1448T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 7/8 | chr5 | 179965358 | |||||||
| chr5:179965379 | C | T | 3 | a0001c0001t0001g0238 a0001c0003t0001g0160 a0001c0003t0001g0161 |
3 | HG03041.hp1 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1150+1427G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 7/8 | chr5 | 179965379 | |||||||
| chr5:179965728 | A | G | 4 | a0001c0005t0001g0195 a0001c0005t0003g0163 a0001c0005t0003g0191 others(1): Show |
4 | HG02572.hp1 HG02630.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1150+1078T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 7/8 | chr5 | 179965728 | |||||||
| chr5:179965961 | G | A | 1 | a0001c0002t0001g0095 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1150+845C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 7/8 | chr5 | 179965961 | |||||||
| chr5:179966440 | G | A | 3 | a0001c0005t0003g0163 a0001c0005t0003g0191 a0001c0005t0003g0192 |
3 | HG02572.hp1 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1150+366C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 7/8 | chr5 | 179966440 | |||||||
| chr5:179966461 | A | G | 1 | a0001c0001t0001g0296 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1150+345T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 7/8 | chr5 | 179966461 | |||||||
| chr5:179966739 | C | T | 1 | a0001c0002t0001g0110 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1150+67G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 7/8 | chr5 | 179966739 | |||||||
| chr5:179966790 | G | A | 1 | a0001c0001t0001g0324 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1150+16C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 7/8 | chr5 | 179966790 | |||||||
| chr5:179967027 | G | A | 12 | a0001c0001t0001g0199 a0001c0001t0001g0260 a0001c0001t0001g0264 others(9): Show |
12 | HG00735.hp2 HG01071.hp2 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.946-17C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179967027 | |||||||
| chr5:179967096 | C | T | 1 | a0001c0005t0001g0195 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.946-86G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179967096 | |||||||
| chr5:179967249 | T | C | 12 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(9): Show |
12 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.946-239A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179967249 | |||||||
| chr5:179967343 | T | C | 1 | a0001c0012t0001g0288 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.946-333A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179967343 | |||||||
| chr5:179967438 | ATCTGGTA others(18): Show |
A | 2 | a0001c0002t0001g0029 a0001c0002t0001g0106 |
2 | NA18983.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.946-453_946-429del others(25): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179967438 | |||||||
| chr5:179967490 | A | T | 1 | a0001c0001t0001g0279 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.946-480T>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179967490 | |||||||
| chr5:179967583 | T | C | 1 | a0001c0001t0001g0267 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.946-573A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179967583 | |||||||
| chr5:179967666 | C | T | 1 | a0001c0001t0001g0292 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.946-656G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179967666 | |||||||
| chr5:179967695 | G | C | 1 | a0001c0001t0001g0241 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.946-685C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179967695 | |||||||
| chr5:179967810 | G | T | 13 | a0001c0001t0001g0203 a0001c0001t0001g0213 a0001c0001t0001g0216 others(10): Show |
13 | HG01243.hp2 HG01891.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.946-800C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179967810 | |||||||
| chr5:179967948 | A | G | 1 | a0001c0003t0001g0183 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.946-938T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179967948 | |||||||
| chr5:179967952 | T | C | 1 | a0001c0004t0001g0139 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.946-942A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179967952 | |||||||
| chr5:179968039 | T | C | 1 | a0001c0001t0001g0298 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.946-1029A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179968039 | |||||||
| chr5:179968071 | A | G | 2 | a0001c0001t0001g0253 a0001c0002t0001g0108 |
2 | HG02132.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.946-1061T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179968071 | |||||||
| chr5:179968122 | C | T | 1 | a0001c0002t0001g0012 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.946-1112G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179968122 | |||||||
| chr5:179968156 | A | G | 11 | a0001c0001t0001g0323 a0001c0002t0001g0040 a0001c0002t0001g0096 others(8): Show |
12 | HG01256.hp1 HG01361.hp2 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.946-1146T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179968156 | |||||||
| chr5:179968173 | T | C | 3 | a0001c0001t0001g0252 a0001c0001t0001g0265 a0001c0001t0001g0266 |
3 | NA18955.hp2 NA19005.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.946-1163A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179968173 | |||||||
| chr5:179968175 | C | G | 4 | a0001c0002t0001g0045 a0001c0003t0001g0146 a0001c0003t0001g0147 others(1): Show |
4 | HG01261.hp2 HG01496.hp2 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.946-1165G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179968175 | |||||||
| chr5:179968187 | C | T | 6 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0238 others(3): Show |
6 | HG02145.hp1 HG03041.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.946-1177G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179968187 | |||||||
| chr5:179968293 | A | AAAAC | 20 | a0001c0001t0001g0199 a0001c0001t0001g0260 a0001c0001t0001g0264 others(17): Show |
20 | HG00735.hp2 HG01071.hp2 HG01358.hp1 others(17): Show |
intron_variant | MODIFIER | c.946-1287_946-1284d others(6): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179968293 | |||||||
| chr5:179968293 | AAAACAAA others(1): Show |
A | 4 | a0001c0001t0001g0315 a0001c0003t0001g0001 a0001c0003t0001g0171 others(1): Show |
6 | HG01069.hp1 HG01071.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.946-1291_946-1284d others(10): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179968293 | |||||||
| chr5:179968322 | A | G | 1 | a0001c0002t0001g0034 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.946-1312T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179968322 | |||||||
| chr5:179968323 | A | C | 1 | a0001c0002t0001g0034 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.946-1313T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179968323 | |||||||
| chr5:179968325 | G | A | 166 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(163): Show |
174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.946-1315C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179968325 | |||||||
| chr5:179968326 | C | A | 166 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(163): Show |
174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.946-1316G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179968326 | |||||||
| chr5:179968493 | C | G | 141 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(138): Show |
149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.946-1483G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179968493 | |||||||
| chr5:179968498 | T | G | 1 | a0001c0003t0001g0157 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.946-1488A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179968498 | |||||||
| chr5:179968534 | C | T | 1 | a0001c0003t0001g0157 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.946-1524G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179968534 | |||||||
| chr5:179968667 | T | TA | 33 | a0001c0001t0001g0203 a0001c0001t0001g0207 a0001c0001t0001g0216 others(30): Show |
33 | HG00408.hp1 HG00544.hp2 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.946-1658dupT | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179968667 | |||||||
| chr5:179968667 | TA | T | 12 | a0001c0001t0001g0211 a0001c0001t0001g0261 a0001c0001t0001g0309 others(9): Show |
12 | HG00323.hp1 HG00609.hp1 HG00733.hp2 others(9): Show |
intron_variant | MODIFIER | c.946-1658delT | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179968667 | |||||||
| chr5:179968686 | A | G | 1 | a0001c0002t0001g0010 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.946-1676T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179968686 | |||||||
| chr5:179968687 | A | G | 5 | a0001c0001t0001g0223 a0001c0001t0001g0225 a0001c0001t0001g0226 others(2): Show |
5 | HG02572.hp2 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.946-1677T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179968687 | |||||||
| chr5:179968728 | T | C | 1 | a0001c0002t0001g0009 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.945+1682A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179968728 | |||||||
| chr5:179968736 | G | C | 1 | a0001c0001t0001g0231 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.945+1674C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179968736 | |||||||
| chr5:179968739 | A | G | 2 | a0001c0003t0001g0160 a0001c0003t0001g0161 |
2 | HG03041.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.945+1671T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179968739 | |||||||
| chr5:179968789 | C | T | 3 | a0001c0005t0003g0163 a0001c0005t0003g0191 a0001c0005t0003g0192 |
3 | HG02572.hp1 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.945+1621G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179968789 | |||||||
| chr5:179968992 | C | T | 3 | a0001c0003t0001g0004 a0001c0003t0001g0172 a0001c0003t0001g0185 |
4 | HG01081.hp1 HG01257.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.945+1418G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179968992 | |||||||
| chr5:179968995 | C | G | 1 | a0001c0002t0001g0045 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.945+1415G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179968995 | |||||||
| chr5:179969187 | T | C | 1 | a0001c0002t0001g0107 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.945+1223A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179969187 | |||||||
| chr5:179969235 | G | A | 1 | a0001c0003t0001g0162 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.945+1175C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179969235 | |||||||
| chr5:179969340 | C | T | 5 | a0001c0001t0002g0243 a0001c0002t0002g0132 a0001c0003t0002g0155 others(2): Show |
5 | HG01884.hp2 HG02717.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.945+1070G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179969340 | |||||||
| chr5:179969502 | T | C | 59 | a0001c0001t0001g0005 a0001c0001t0001g0252 a0001c0001t0001g0254 others(56): Show |
64 | HG00673.hp1 HG00733.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.945+908A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179969502 | |||||||
| chr5:179969636 | G | A | 2 | a0001c0001t0001g0304 a0001c0002t0001g0111 |
2 | HG02083.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.945+774C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179969636 | |||||||
| chr5:179969852 | G | C | 1 | a0001c0001t0001g0274 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.945+558C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179969852 | |||||||
| chr5:179969859 | C | T | 2 | a0001c0002t0001g0076 a0001c0002t0001g0109 |
2 | NA18977.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.945+551G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179969859 | |||||||
| chr5:179969866 | C | T | 8 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0225 others(5): Show |
8 | HG02572.hp2 HG02818.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.945+544G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179969866 | |||||||
| chr5:179969950 | C | T | 1 | a0001c0001t0002g0243 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.945+460G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179969950 | |||||||
| chr5:179969977 | G | A | 1 | a0001c0003t0001g0194 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.945+433C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179969977 | |||||||
| chr5:179970087 | C | T | 1 | a0001c0001t0001g0274 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.945+323G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179970087 | |||||||
| chr5:179970183 | C | T | 1 | a0001c0002t0001g0108 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.945+227G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179970183 | |||||||
| chr5:179970407 | T | C | 1 | a0001c0003t0001g0184 | 1 | HG02056.hp1 | splice_region_variant&intron_variant | LOW | c.945+3A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 6/8 | chr5 | 179970407 | |||||||
| chr5:179970595 | T | C | 3 | a0001c0001t0001g0199 a0001c0001t0001g0260 a0001c0002t0001g0110 |
3 | HG01071.hp2 HG02683.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.849-89A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179970595 | |||||||
| chr5:179970604 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.849-98G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179970604 | |||||||
| chr5:179970609 | T | G | 2 | a0001c0001t0001g0199 a0001c0001t0001g0260 |
2 | HG01071.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.849-103A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179970609 | |||||||
| chr5:179970697 | T | A | 13 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0225 others(10): Show |
13 | HG01884.hp2 HG02572.hp2 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.849-191A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179970697 | |||||||
| chr5:179970868 | T | C | 7 | a0001c0001t0001g0237 a0001c0001t0001g0244 a0001c0001t0001g0245 others(4): Show |
7 | HG02055.hp2 HG02896.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.849-362A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179970868 | |||||||
| chr5:179970937 | A | T | 5 | a0001c0003t0001g0157 a0001c0005t0001g0195 a0001c0005t0003g0163 others(2): Show |
5 | HG02280.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.849-431T>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179970937 | |||||||
| chr5:179971027 | TA | T | 3 | a0001c0005t0003g0163 a0001c0005t0003g0191 a0001c0005t0003g0192 |
3 | HG02572.hp1 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.849-522delT | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179971027 | |||||||
| chr5:179971103 | A | ATTTTCT | 4 | a0001c0002t0001g0045 a0001c0003t0001g0146 a0001c0003t0001g0147 others(1): Show |
4 | HG01261.hp2 HG01496.hp2 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.849-603_849-598dup others(6): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179971103 | |||||||
| chr5:179971318 | G | C | 141 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(138): Show |
149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.849-812C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179971318 | |||||||
| chr5:179971365 | G | T | 1 | a0001c0001t0001g0239 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.849-859C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179971365 | |||||||
| chr5:179971400 | T | C | 5 | a0001c0003t0001g0157 a0001c0005t0001g0195 a0001c0005t0003g0163 others(2): Show |
5 | HG02280.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.849-894A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179971400 | |||||||
| chr5:179971536 | A | T | 2 | a0001c0001t0001g0325 a0001c0001t0001g0326 |
2 | HG03195.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.849-1030T>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179971536 | |||||||
| chr5:179971563 | G | A | 5 | a0001c0001t0001g0223 a0001c0001t0001g0225 a0001c0001t0001g0226 others(2): Show |
5 | HG02572.hp2 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.849-1057C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179971563 | |||||||
| chr5:179972082 | C | T | 1 | a0001c0001t0001g0296 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.849-1576G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179972082 | |||||||
| chr5:179972118 | G | A | 1 | a0001c0002t0001g0061 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.849-1612C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179972118 | |||||||
| chr5:179972125 | C | G | 2 | a0001c0001t0001g0316 a0001c0003t0001g0157 |
2 | HG00438.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.849-1619G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179972125 | |||||||
| chr5:179972274 | T | C | 3 | a0001c0005t0003g0163 a0001c0005t0003g0191 a0001c0005t0003g0192 |
3 | HG02572.hp1 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.849-1768A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179972274 | |||||||
| chr5:179972307 | G | A | 5 | a0001c0003t0001g0157 a0001c0005t0001g0195 a0001c0005t0003g0163 others(2): Show |
5 | HG02280.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.849-1801C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179972307 | |||||||
| chr5:179972500 | A | G | 1 | a0001c0005t0001g0195 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.849-1994T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179972500 | |||||||
| chr5:179972568 | G | A | 1 | a0001c0002t0001g0124 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.849-2062C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179972568 | |||||||
| chr5:179972647 | G | A | 3 | a0001c0002t0001g0033 a0001c0002t0001g0034 a0001c0002t0001g0042 |
3 | NA19054.hp2 NA19057.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.849-2141C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179972647 | |||||||
| chr5:179973026 | C | T | 1 | a0001c0005t0001g0195 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.849-2520G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179973026 | |||||||
| chr5:179973353 | T | C | 9 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0225 others(6): Show |
9 | HG02572.hp2 HG02630.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.849-2847A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179973353 | |||||||
| chr5:179973422 | C | A | 1 | a0001c0002t0001g0036 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.849-2916G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179973422 | |||||||
| chr5:179973446 | T | C | 167 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(164): Show |
175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.849-2940A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179973446 | |||||||
| chr5:179973505 | G | A | 5 | a0001c0001t0002g0243 a0001c0002t0002g0132 a0001c0003t0002g0155 others(2): Show |
5 | HG01884.hp2 HG02717.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.849-2999C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179973505 | |||||||
| chr5:179973589 | C | T | 1 | a0001c0002t0001g0038 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.849-3083G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179973589 | |||||||
| chr5:179973625 | C | T | 1 | a0001c0002t0001g0088 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.849-3119G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179973625 | |||||||
| chr5:179973634 | G | A | 6 | a0001c0001t0001g0323 a0001c0001t0002g0243 a0001c0002t0002g0132 others(3): Show |
6 | HG01884.hp2 HG02165.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.849-3128C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179973634 | |||||||
| chr5:179973635 | C | T | 1 | a0001c0002t0001g0094 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.849-3129G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179973635 | |||||||
| chr5:179973650 | T | C | 7 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0225 others(4): Show |
7 | HG02572.hp2 HG02630.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.849-3144A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179973650 | |||||||
| chr5:179973847 | C | A | 150 | a0001c0001t0001g0005 a0001c0001t0001g0202 a0001c0001t0001g0203 others(147): Show |
155 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.849-3341G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179973847 | |||||||
| chr5:179973867 | G | A | 1 | a0001c0002t0001g0042 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.849-3361C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179973867 | |||||||
| chr5:179973870 | C | T | 4 | a0001c0001t0001g0315 a0001c0003t0001g0001 a0001c0003t0001g0171 others(1): Show |
6 | HG01069.hp1 HG01071.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.849-3364G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179973870 | |||||||
| chr5:179973970 | C | T | 1 | a0001c0001t0001g0235 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.849-3464G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179973970 | |||||||
| chr5:179973992 | C | T | 1 | a0001c0003t0002g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.849-3486G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179973992 | |||||||
| chr5:179974087 | G | A | 1 | a0001c0002t0001g0115 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.849-3581C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179974087 | |||||||
| chr5:179974090 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.849-3584C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179974090 | |||||||
| chr5:179974207 | C | T | 5 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 others(2): Show |
5 | HG02055.hp1 HG02109.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.849-3701G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179974207 | |||||||
| chr5:179974244 | G | A | 5 | a0001c0001t0001g0211 a0001c0001t0001g0213 a0001c0001t0001g0217 others(2): Show |
5 | HG01074.hp1 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.849-3738C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179974244 | |||||||
| chr5:179974287 | C | T | 10 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0260 others(7): Show |
10 | HG01361.hp1 HG01934.hp2 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.849-3781G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179974287 | |||||||
| chr5:179974333 | G | A | 23 | a0001c0001t0001g0220 a0001c0001t0001g0251 a0001c0001t0001g0252 others(20): Show |
24 | HG00544.hp2 HG00673.hp1 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.849-3827C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179974333 | |||||||
| chr5:179974490 | C | T | 58 | a0001c0001t0001g0005 a0001c0001t0001g0199 a0001c0001t0001g0250 others(55): Show |
60 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.848+3713G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179974490 | |||||||
| chr5:179974525 | A | C | 8 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0214 others(5): Show |
8 | HG01891.hp2 HG02055.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.848+3678T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179974525 | |||||||
| chr5:179974542 | G | A | 30 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 others(27): Show |
30 | HG01243.hp1 HG01884.hp1 HG01978.hp1 others(27): Show |
intron_variant | MODIFIER | c.848+3661C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179974542 | |||||||
| chr5:179974553 | G | A | 1 | a0001c0011t0001g0145 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.848+3650C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179974553 | |||||||
| chr5:179974608 | G | A | 2 | a0001c0003t0001g0170 a0001c0005t0001g0195 |
2 | HG03704.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.848+3595C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179974608 | |||||||
| chr5:179974618 | A | C | 1 | a0001c0001t0001g0292 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.848+3585T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179974618 | |||||||
| chr5:179974699 | G | A | 34 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 others(31): Show |
34 | HG01243.hp1 HG01884.hp1 HG01978.hp1 others(31): Show |
intron_variant | MODIFIER | c.848+3504C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179974699 | |||||||
| chr5:179974751 | G | A | 1 | a0001c0002t0001g0010 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.848+3452C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179974751 | |||||||
| chr5:179974805 | G | A | 1 | a0001c0002t0001g0121 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.848+3398C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179974805 | |||||||
| chr5:179974874 | G | A | 2 | a0001c0002t0001g0061 a0001c0002t0001g0123 |
2 | HG01192.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.848+3329C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179974874 | |||||||
| chr5:179974890 | G | A | 2 | a0001c0002t0001g0077 a0001c0002t0001g0113 |
2 | NA18977.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.848+3313C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179974890 | |||||||
| chr5:179974939 | C | A | 3 | a0001c0002t0001g0072 a0001c0002t0001g0095 a0001c0002t0001g0098 |
3 | HG03834.hp1 NA18943.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.848+3264G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179974939 | |||||||
| chr5:179974955 | G | A | 1 | a0001c0001t0001g0283 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.848+3248C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179974955 | |||||||
| chr5:179975025 | T | C | 4 | a0001c0001t0001g0325 a0001c0001t0001g0326 a0001c0001t0001g0327 others(1): Show |
4 | HG02258.hp1 HG02809.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.848+3178A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179975025 | |||||||
| chr5:179975034 | G | A | 1 | a0004c0009t0001g0014 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.848+3169C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179975034 | |||||||
| chr5:179975137 | A | G | 1 | a0001c0003t0001g0157 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.848+3066T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179975137 | |||||||
| chr5:179975151 | C | A | 1 | a0001c0001t0001g0323 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.848+3052G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179975151 | |||||||
| chr5:179975190 | G | T | 1 | a0001c0003t0001g0177 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.848+3013C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179975190 | |||||||
| chr5:179975211 | A | C | 51 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(48): Show |
53 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.848+2992T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179975211 | |||||||
| chr5:179975274 | G | A | 3 | a0001c0001t0001g0329 a0001c0001t0001g0330 a0001c0002t0001g0047 |
3 | HG02622.hp1 HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.848+2929C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179975274 | |||||||
| chr5:179975275 | T | G | 186 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(183): Show |
190 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.848+2928A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179975275 | |||||||
| chr5:179975523 | C | T | 2 | a0001c0001t0001g0277 a0001c0001t0001g0280 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.848+2680G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179975523 | |||||||
| chr5:179975624 | G | A | 1 | a0001c0001t0001g0304 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.848+2579C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179975624 | |||||||
| chr5:179975769 | C | T | 59 | a0001c0001t0001g0005 a0001c0001t0001g0250 a0001c0001t0001g0251 others(56): Show |
61 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.848+2434G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179975769 | |||||||
| chr5:179976000 | C | CAG | 212 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(209): Show |
220 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.848+2201_848+2202d others(4): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179976000 | |||||||
| chr5:179976058 | A | G | 1 | a0001c0001t0001g0254 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.848+2145T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179976058 | |||||||
| chr5:179976061 | C | T | 59 | a0001c0001t0001g0005 a0001c0001t0001g0251 a0001c0001t0001g0252 others(56): Show |
61 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.848+2142G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179976061 | |||||||
| chr5:179976124 | G | A | 1 | a0001c0002t0001g0077 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.848+2079C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179976124 | |||||||
| chr5:179976258 | A | C | 171 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(168): Show |
175 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.848+1945T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179976258 | |||||||
| chr5:179976334 | C | T | 4 | a0001c0003t0001g0167 a0001c0003t0001g0170 a0001c0003t0001g0173 others(1): Show |
4 | HG01943.hp1 HG02559.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.848+1869G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179976334 | |||||||
| chr5:179976347 | G | C | 2 | a0001c0002t0001g0019 a0001c0002t0001g0020 |
2 | HG01516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.848+1856C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179976347 | |||||||
| chr5:179976606 | A | G | 60 | a0001c0001t0001g0005 a0001c0001t0001g0250 a0001c0001t0001g0251 others(57): Show |
62 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.848+1597T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179976606 | |||||||
| chr5:179976688 | T | G | 1 | a0001c0002t0001g0112 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.848+1515A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179976688 | |||||||
| chr5:179976691 | A | AT | 28 | a0001c0002t0001g0010 a0001c0002t0001g0049 a0001c0002t0001g0050 others(25): Show |
32 | HG00099.hp1 HG00280.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.848+1511dupA | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179976691 | |||||||
| chr5:179976691 | A | G | 1 | a0001c0003t0002g0155 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.848+1512T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179976691 | |||||||
| chr5:179976691 | AT | A | 23 | a0001c0001t0001g0206 a0001c0001t0001g0224 a0001c0001t0001g0225 others(20): Show |
23 | HG01081.hp2 HG01496.hp2 HG01943.hp2 others(20): Show |
intron_variant | MODIFIER | c.848+1511delA | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179976691 | |||||||
| chr5:179976707 | T | A | 93 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(90): Show |
95 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.848+1496A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179976707 | |||||||
| chr5:179976708 | A | T | 3 | a0001c0001t0001g0292 a0001c0001t0001g0295 a0001c0001t0001g0328 |
3 | HG00738.hp2 HG02486.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.848+1495T>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179976708 | |||||||
| chr5:179976788 | C | T | 1 | a0001c0001t0001g0323 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.848+1415G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179976788 | |||||||
| chr5:179977001 | C | T | 1 | a0001c0001t0001g0306 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.848+1202G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179977001 | |||||||
| chr5:179977008 | A | C | 168 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(165): Show |
172 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.848+1195T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179977008 | |||||||
| chr5:179977039 | G | C | 3 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0323 |
3 | HG00280.hp1 HG00639.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.848+1164C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179977039 | |||||||
| chr5:179977051 | C | T | 1 | a0001c0001t0001g0323 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.848+1152G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179977051 | |||||||
| chr5:179977069 | C | A | 3 | a0001c0003t0001g0157 a0001c0003t0002g0155 a0001c0003t0002g0156 |
3 | HG01884.hp2 HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.848+1134G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179977069 | |||||||
| chr5:179977114 | C | T | 60 | a0001c0001t0001g0005 a0001c0001t0001g0250 a0001c0001t0001g0251 others(57): Show |
62 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.848+1089G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179977114 | |||||||
| chr5:179977227 | C | A | 4 | a0001c0001t0001g0325 a0001c0001t0001g0326 a0001c0001t0001g0327 others(1): Show |
4 | HG02258.hp1 HG02809.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.848+976G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179977227 | |||||||
| chr5:179977330 | T | C | 4 | a0001c0003t0001g0157 a0001c0003t0002g0155 a0001c0003t0002g0156 others(1): Show |
4 | HG01884.hp2 HG02280.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.848+873A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179977330 | |||||||
| chr5:179977375 | G | A | 211 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(208): Show |
219 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.848+828C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179977375 | |||||||
| chr5:179977425 | CAGGAATC others(8): Show |
C | 38 | a0001c0001t0001g0293 a0001c0001t0001g0328 a0001c0002t0001g0096 others(35): Show |
42 | HG00280.hp2 HG00738.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.848+763_848+777del others(15): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179977425 | |||||||
| chr5:179977441 | A | T | 38 | a0001c0001t0001g0293 a0001c0001t0001g0328 a0001c0002t0001g0096 others(35): Show |
42 | HG00280.hp2 HG00738.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.848+762T>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179977441 | |||||||
| chr5:179977510 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.848+693C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179977510 | |||||||
| chr5:179977744 | C | T | 3 | a0001c0003t0001g0158 a0001c0003t0001g0160 a0001c0003t0001g0161 |
3 | HG03041.hp1 HG03139.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.848+459G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179977744 | |||||||
| chr5:179977973 | G | A | 12 | a0001c0001t0001g0204 a0001c0001t0001g0211 a0001c0001t0001g0212 others(9): Show |
12 | HG02451.hp2 HG02717.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.848+230C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179977973 | |||||||
| chr5:179978025 | C | T | 49 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(46): Show |
49 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(46): Show |
intron_variant | MODIFIER | c.848+178G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179978025 | |||||||
| chr5:179978144 | A | G | 51 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(48): Show |
53 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.848+59T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 5/8 | chr5 | 179978144 | |||||||
| chr5:179978379 | T | C | 1 | a0001c0002t0001g0097 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.766-94A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 4/8 | chr5 | 179978379 | |||||||
| chr5:179978399 | C | G | 167 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(164): Show |
171 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.766-114G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 4/8 | chr5 | 179978399 | |||||||
| chr5:179978538 | C | T | 3 | a0001c0001t0001g0266 a0001c0002t0001g0105 a0001c0002t0004g0085 |
3 | HG02074.hp2 NA18953.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.766-253G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 4/8 | chr5 | 179978538 | |||||||
| chr5:179979233 | G | T | 1 | a0001c0001t0001g0323 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.765+896C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 4/8 | chr5 | 179979233 | |||||||
| chr5:179979244 | C | T | 6 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(3): Show |
6 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.765+885G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 4/8 | chr5 | 179979244 | |||||||
| chr5:179979341 | G | A | 1 | a0001c0004t0004g0144 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.765+788C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 4/8 | chr5 | 179979341 | |||||||
| chr5:179979368 | T | C | 1 | a0001c0005t0003g0163 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.765+761A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 4/8 | chr5 | 179979368 | |||||||
| chr5:179979809 | T | C | 1 | a0001c0005t0003g0191 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.765+320A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 4/8 | chr5 | 179979809 | |||||||
| chr5:179980229 | C | T | 248 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(245): Show |
256 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.694-29G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179980229 | |||||||
| chr5:179980378 | T | G | 1 | a0001c0001t0001g0329 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.694-178A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179980378 | |||||||
| chr5:179980416 | A | C | 1 | a0001c0001t0001g0250 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.694-216T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179980416 | |||||||
| chr5:179980428 | G | C | 1 | a0001c0003t0001g0152 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.694-228C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179980428 | |||||||
| chr5:179980708 | C | T | 1 | a0001c0002t0001g0093 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.694-508G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179980708 | |||||||
| chr5:179980885 | T | C | 33 | a0001c0001t0001g0328 a0001c0002t0001g0096 a0001c0003t0001g0001 others(30): Show |
37 | HG00280.hp2 HG00738.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.694-685A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179980885 | |||||||
| chr5:179980965 | G | C | 2 | a0001c0001t0001g0327 a0001c0001t0001g0331 |
2 | HG02258.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.694-765C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179980965 | |||||||
| chr5:179980987 | T | C | 168 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(165): Show |
172 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.694-787A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179980987 | |||||||
| chr5:179981024 | G | C | 3 | a0001c0003t0001g0158 a0001c0003t0001g0160 a0001c0003t0001g0161 |
3 | HG03041.hp1 HG03139.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.694-824C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179981024 | |||||||
| chr5:179981095 | G | A | 1 | a0001c0001t0001g0309 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.694-895C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179981095 | |||||||
| chr5:179981107 | T | C | 2 | a0001c0004t0001g0136 a0001c0004t0001g0138 |
2 | NA18974.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.694-907A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179981107 | |||||||
| chr5:179981174 | G | GT | 69 | a0001c0001t0001g0005 a0001c0001t0001g0221 a0001c0001t0001g0222 others(66): Show |
71 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.694-975dupA | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179981174 | |||||||
| chr5:179981279 | C | T | 5 | a0001c0001t0001g0325 a0001c0001t0001g0326 a0001c0001t0001g0327 others(2): Show |
5 | HG02258.hp1 HG02809.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.694-1079G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179981279 | |||||||
| chr5:179981357 | C | T | 1 | a0001c0001t0001g0323 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.694-1157G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179981357 | |||||||
| chr5:179981358 | G | T | 168 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(165): Show |
172 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.694-1158C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179981358 | |||||||
| chr5:179981366 | C | T | 8 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(5): Show |
8 | HG02572.hp2 HG02809.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.694-1166G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179981366 | |||||||
| chr5:179981535 | C | T | 2 | a0001c0001t0001g0329 a0001c0001t0001g0330 |
2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.694-1335G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179981535 | |||||||
| chr5:179981536 | T | G | 168 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(165): Show |
172 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.694-1336A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179981536 | |||||||
| chr5:179981559 | C | G | 1 | a0001c0003t0001g0175 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.694-1359G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179981559 | |||||||
| chr5:179981631 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.694-1431G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179981631 | |||||||
| chr5:179981728 | C | T | 1 | a0001c0002t0002g0132 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.694-1528G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179981728 | |||||||
| chr5:179981895 | T | C | 5 | a0001c0001t0001g0210 a0001c0003t0001g0157 a0001c0003t0002g0155 others(2): Show |
5 | HG01884.hp2 HG02280.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.694-1695A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179981895 | |||||||
| chr5:179982108 | C | T | 214 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(211): Show |
222 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.694-1908G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179982108 | |||||||
| chr5:179982369 | T | G | 1 | a0001c0001t0001g0284 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.694-2169A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179982369 | |||||||
| chr5:179982405 | G | C | 3 | a0001c0002t0001g0053 a0001c0002t0001g0054 a0001c0002t0001g0055 |
3 | HG01069.hp2 HG01168.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.694-2205C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179982405 | |||||||
| chr5:179982434 | T | C | 2 | a0001c0001t0001g0291 a0001c0001t0001g0297 |
2 | HG01109.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.694-2234A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179982434 | |||||||
| chr5:179982566 | G | GTGTTT | 112 | a0001c0001t0001g0005 a0001c0001t0001g0201 a0001c0001t0001g0202 others(109): Show |
114 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.694-2371_694-2367d others(7): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179982566 | |||||||
| chr5:179982566 | GTGTTT | G | 57 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(54): Show |
59 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.694-2371_694-2367d others(7): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179982566 | |||||||
| chr5:179982613 | C | T | 107 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(104): Show |
109 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.694-2413G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179982613 | |||||||
| chr5:179982772 | C | T | 1 | a0001c0002t0001g0117 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.694-2572G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179982772 | |||||||
| chr5:179983029 | T | C | 1 | a0001c0001t0001g0260 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.694-2829A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179983029 | |||||||
| chr5:179983333 | CT | C | 109 | a0001c0001t0001g0007 a0001c0001t0001g0200 a0001c0001t0001g0201 others(106): Show |
110 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.694-3134delA | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179983333 | |||||||
| chr5:179983546 | T | C | 1 | a0001c0002t0001g0110 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.694-3346A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179983546 | |||||||
| chr5:179983628 | G | C | 1 | a0001c0002t0001g0043 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.694-3428C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179983628 | |||||||
| chr5:179983833 | C | G | 5 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0214 others(2): Show |
5 | HG01891.hp2 HG02145.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.694-3633G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179983833 | |||||||
| chr5:179984243 | C | A | 5 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0287 others(2): Show |
5 | HG00733.hp1 HG01106.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.694-4043G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179984243 | |||||||
| chr5:179984254 | T | C | 1 | a0001c0001t0001g0303 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.694-4054A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179984254 | |||||||
| chr5:179984289 | G | A | 99 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(96): Show |
101 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.694-4089C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179984289 | |||||||
| chr5:179984476 | C | T | 1 | a0001c0001t0001g0323 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.694-4276G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179984476 | |||||||
| chr5:179984477 | G | A | 8 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 others(5): Show |
8 | HG00323.hp1 HG01109.hp2 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.694-4277C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179984477 | |||||||
| chr5:179984482 | A | G | 5 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0287 others(2): Show |
5 | HG00733.hp1 HG01106.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.694-4282T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179984482 | |||||||
| chr5:179984660 | G | T | 205 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(202): Show |
213 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.694-4460C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179984660 | |||||||
| chr5:179985122 | C | T | 1 | a0001c0002t0001g0067 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.694-4922G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179985122 | |||||||
| chr5:179985153 | C | CT | 179 | a0001c0001t0001g0199 a0001c0001t0001g0203 a0001c0001t0001g0204 others(176): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.694-4954dupA | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179985153 | |||||||
| chr5:179985153 | C | CTT | 127 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(124): Show |
131 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.694-4955_694-4954d others(4): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179985153 | |||||||
| chr5:179985153 | C | CTTT | 16 | a0001c0001t0001g0201 a0001c0001t0001g0223 a0001c0001t0001g0224 others(13): Show |
16 | HG00673.hp1 HG02056.hp2 HG02083.hp1 others(13): Show |
intron_variant | MODIFIER | c.694-4956_694-4954d others(5): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179985153 | |||||||
| chr5:179985337 | T | G | 4 | a0001c0003t0001g0157 a0001c0003t0002g0155 a0001c0003t0002g0156 others(1): Show |
4 | HG01884.hp2 HG02280.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.694-5137A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179985337 | |||||||
| chr5:179985370 | T | A | 1 | a0001c0001t0001g0235 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.694-5170A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179985370 | |||||||
| chr5:179985418 | C | T | 1 | a0001c0002t0001g0092 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.694-5218G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179985418 | |||||||
| chr5:179985482 | G | A | 210 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(207): Show |
218 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.694-5282C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179985482 | |||||||
| chr5:179985653 | T | A | 2 | a0001c0003t0001g0193 a0001c0005t0003g0192 |
2 | HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.694-5453A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179985653 | |||||||
| chr5:179985707 | T | G | 210 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(207): Show |
218 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.694-5507A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179985707 | |||||||
| chr5:179985870 | C | T | 35 | a0001c0001t0001g0325 a0001c0001t0001g0326 a0001c0001t0001g0328 others(32): Show |
39 | HG00280.hp2 HG00738.hp2 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.694-5670G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179985870 | |||||||
| chr5:179986168 | G | A | 99 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(96): Show |
101 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.694-5968C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179986168 | |||||||
| chr5:179986190 | T | A | 1 | a0001c0003t0001g0157 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.694-5990A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179986190 | |||||||
| chr5:179986465 | T | C | 6 | a0001c0003t0001g0178 a0001c0003t0001g0179 a0001c0003t0001g0180 others(3): Show |
6 | HG00558.hp2 HG02056.hp1 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.694-6265A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179986465 | |||||||
| chr5:179986643 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.694-6443C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179986643 | |||||||
| chr5:179986779 | A | C | 1 | a0001c0001t0001g0263 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.694-6579T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179986779 | |||||||
| chr5:179986893 | GTATTT | G | 4 | a0001c0003t0001g0157 a0001c0003t0002g0155 a0001c0003t0002g0156 others(1): Show |
4 | HG01884.hp2 HG02280.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.694-6698_694-6694d others(7): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179986893 | |||||||
| chr5:179987050 | A | C | 55 | a0001c0001t0001g0005 a0001c0001t0001g0251 a0001c0001t0001g0252 others(52): Show |
57 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.694-6850T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179987050 | |||||||
| chr5:179987053 | T | A | 1 | a0001c0002t0001g0134 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.694-6853A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179987053 | |||||||
| chr5:179987054 | C | A | 2 | a0001c0004t0001g0137 a0001c0004t0001g0141 |
2 | NA19068.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.694-6854G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179987054 | |||||||
| chr5:179987249 | C | A | 1 | a0001c0003t0002g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.694-7049G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179987249 | |||||||
| chr5:179987621 | G | A | 2 | a0001c0002t0001g0012 a0001c0002t0001g0013 |
2 | HG02165.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.694-7421C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179987621 | |||||||
| chr5:179987645 | T | C | 51 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(48): Show |
53 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.694-7445A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179987645 | |||||||
| chr5:179987695 | C | T | 1 | a0001c0001t0001g0263 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.694-7495G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179987695 | |||||||
| chr5:179987911 | T | C | 6 | a0001c0001t0001g0329 a0001c0001t0001g0330 a0001c0003t0001g0157 others(3): Show |
6 | HG01884.hp2 HG02280.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.694-7711A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179987911 | |||||||
| chr5:179987945 | G | A | 2 | a0001c0002t0001g0019 a0001c0002t0001g0020 |
2 | HG01516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.694-7745C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179987945 | |||||||
| chr5:179988171 | G | A | 1 | a0001c0002t0001g0066 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.694-7971C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179988171 | |||||||
| chr5:179988201 | T | A | 1 | a0001c0002t0001g0009 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.694-8001A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179988201 | |||||||
| chr5:179988259 | G | T | 4 | a0001c0001t0001g0325 a0001c0001t0001g0326 a0001c0001t0001g0327 others(1): Show |
4 | HG02258.hp1 HG02809.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.694-8059C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179988259 | |||||||
| chr5:179988289 | C | G | 2 | a0001c0002t0001g0086 a0001c0002t0001g0107 |
2 | NA18995.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.694-8089G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179988289 | |||||||
| chr5:179988451 | T | A | 2 | a0001c0001t0001g0294 a0001c0001t0001g0296 |
2 | HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.694-8251A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179988451 | |||||||
| chr5:179988561 | C | A | 2 | a0001c0002t0001g0019 a0001c0002t0001g0020 |
2 | HG01516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.694-8361G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179988561 | |||||||
| chr5:179988579 | G | T | 1 | a0001c0002t0001g0048 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.694-8379C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179988579 | |||||||
| chr5:179988609 | CATTT | C | 51 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(48): Show |
53 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.694-8413_694-8410d others(6): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179988609 | |||||||
| chr5:179988654 | A | C | 56 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(53): Show |
56 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(53): Show |
intron_variant | MODIFIER | c.694-8454T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179988654 | |||||||
| chr5:179988891 | C | T | 1 | a0001c0005t0003g0191 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.694-8691G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179988891 | |||||||
| chr5:179988985 | G | A | 55 | a0001c0001t0001g0005 a0001c0001t0001g0251 a0001c0001t0001g0252 others(52): Show |
57 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.694-8785C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179988985 | |||||||
| chr5:179989059 | C | T | 168 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(165): Show |
172 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.694-8859G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179989059 | |||||||
| chr5:179989104 | G | T | 1 | a0001c0003t0002g0156 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.694-8904C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179989104 | |||||||
| chr5:179989210 | C | T | 51 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(48): Show |
53 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.694-9010G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179989210 | |||||||
| chr5:179989221 | T | C | 10 | a0001c0004t0001g0002 a0001c0004t0001g0135 a0001c0004t0001g0136 others(7): Show |
11 | HG02293.hp2 HG03834.hp2 NA18951.hp1 others(8): Show |
intron_variant | MODIFIER | c.694-9021A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179989221 | |||||||
| chr5:179989335 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.694-9135C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179989335 | |||||||
| chr5:179989507 | C | T | 7 | a0001c0001t0001g0237 a0001c0001t0001g0244 a0001c0001t0001g0245 others(4): Show |
7 | HG02055.hp2 HG02257.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.694-9307G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179989507 | |||||||
| chr5:179989699 | C | T | 205 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(202): Show |
213 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.694-9499G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179989699 | |||||||
| chr5:179989868 | G | A | 2 | a0001c0001t0001g0323 a0001c0002t0001g0096 |
2 | HG02165.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.694-9668C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179989868 | |||||||
| chr5:179989930 | T | A | 2 | a0001c0001t0001g0212 a0001c0001t0001g0218 |
2 | HG03098.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.694-9730A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179989930 | |||||||
| chr5:179990034 | G | A | 168 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(165): Show |
172 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.694-9834C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179990034 | |||||||
| chr5:179990078 | C | T | 168 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(165): Show |
172 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.694-9878G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179990078 | |||||||
| chr5:179990170 | C | A | 61 | a0001c0001t0001g0005 a0001c0001t0001g0250 a0001c0001t0001g0251 others(58): Show |
63 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.694-9970G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179990170 | |||||||
| chr5:179990185 | A | G | 205 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(202): Show |
213 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.694-9985T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179990185 | |||||||
| chr5:179990204 | A | G | 3 | a0001c0002t0001g0078 a0001c0002t0001g0083 a0001c0002t0001g0093 |
3 | HG02683.hp2 HG03017.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.694-10004T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179990204 | |||||||
| chr5:179990205 | A | G | 1 | a0001c0001t0002g0243 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.694-10005T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179990205 | |||||||
| chr5:179990271 | T | C | 2 | a0001c0001t0001g0005 a0001c0001t0001g0255 |
3 | HG03209.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.694-10071A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179990271 | |||||||
| chr5:179990335 | C | T | 51 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(48): Show |
53 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.694-10135G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179990335 | |||||||
| chr5:179990449 | C | T | 56 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(53): Show |
56 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(53): Show |
intron_variant | MODIFIER | c.694-10249G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179990449 | |||||||
| chr5:179990564 | G | A | 1 | a0001c0001t0001g0309 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.694-10364C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179990564 | |||||||
| chr5:179990645 | A | G | 248 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(245): Show |
256 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.694-10445T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179990645 | |||||||
| chr5:179990666 | C | T | 1 | a0001c0002t0001g0134 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.694-10466G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179990666 | |||||||
| chr5:179990797 | C | T | 51 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(48): Show |
53 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.694-10597G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179990797 | |||||||
| chr5:179991116 | T | A | 51 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(48): Show |
53 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.694-10916A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179991116 | |||||||
| chr5:179991116 | T | G | 1 | a0001c0002t0001g0113 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.694-10916A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179991116 | |||||||
| chr5:179991134 | T | G | 51 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(48): Show |
53 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.694-10934A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179991134 | |||||||
| chr5:179991172 | T | C | 37 | a0001c0001t0001g0328 a0001c0002t0001g0096 a0001c0003t0001g0001 others(34): Show |
41 | HG00280.hp2 HG00738.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.694-10972A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179991172 | |||||||
| chr5:179991271 | C | A | 6 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(3): Show |
6 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.694-11071G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179991271 | |||||||
| chr5:179991534 | G | T | 16 | a0001c0001t0001g0199 a0001c0002t0001g0077 a0001c0002t0001g0110 others(13): Show |
16 | HG00735.hp2 HG01071.hp2 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.694-11334C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179991534 | |||||||
| chr5:179991635 | C | T | 3 | a0001c0002t0001g0030 a0001c0002t0001g0133 a0002c0010t0001g0031 |
3 | HG01243.hp2 HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.694-11435G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179991635 | |||||||
| chr5:179991800 | C | T | 49 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(46): Show |
49 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(46): Show |
intron_variant | MODIFIER | c.694-11600G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179991800 | |||||||
| chr5:179991964 | G | A | 12 | a0001c0001t0001g0204 a0001c0001t0001g0211 a0001c0001t0001g0212 others(9): Show |
12 | HG02451.hp2 HG02717.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.694-11764C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179991964 | |||||||
| chr5:179991998 | A | T | 2 | a0001c0002t0001g0019 a0001c0002t0001g0020 |
2 | HG01516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.694-11798T>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179991998 | |||||||
| chr5:179992028 | G | A | 1 | a0001c0001t0001g0259 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.694-11828C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179992028 | |||||||
| chr5:179992070 | T | C | 1 | a0001c0003t0001g0157 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.694-11870A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179992070 | |||||||
| chr5:179992158 | T | C | 1 | a0001c0002t0001g0097 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.694-11958A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179992158 | |||||||
| chr5:179992220 | T | C | 168 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(165): Show |
172 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.694-12020A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179992220 | |||||||
| chr5:179992303 | G | A | 1 | a0001c0001t0001g0294 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.694-12103C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179992303 | |||||||
| chr5:179992332 | G | A | 61 | a0001c0001t0001g0005 a0001c0001t0001g0250 a0001c0001t0001g0251 others(58): Show |
63 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.694-12132C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179992332 | |||||||
| chr5:179992544 | G | A | 1 | a0001c0002t0001g0061 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.694-12344C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179992544 | |||||||
| chr5:179992594 | T | G | 12 | a0001c0001t0001g0204 a0001c0001t0001g0211 a0001c0001t0001g0212 others(9): Show |
12 | HG02451.hp2 HG02717.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.694-12394A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179992594 | |||||||
| chr5:179992623 | C | T | 49 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(46): Show |
49 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(46): Show |
intron_variant | MODIFIER | c.694-12423G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179992623 | |||||||
| chr5:179992769 | C | T | 1 | a0001c0002t0001g0046 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.694-12569G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179992769 | |||||||
| chr5:179992779 | G | C | 6 | a0001c0001t0001g0329 a0001c0001t0001g0330 a0001c0003t0001g0157 others(3): Show |
6 | HG01884.hp2 HG02280.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.694-12579C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179992779 | |||||||
| chr5:179992914 | C | G | 1 | a0001c0001t0001g0315 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.694-12714G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179992914 | |||||||
| chr5:179993013 | T | C | 51 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(48): Show |
53 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.694-12813A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179993013 | |||||||
| chr5:179993071 | T | C | 1 | a0001c0002t0001g0134 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.694-12871A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179993071 | |||||||
| chr5:179993113 | C | A | 51 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(48): Show |
53 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.694-12913G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179993113 | |||||||
| chr5:179993187 | G | A | 3 | a0001c0002t0001g0101 a0001c0002t0001g0102 a0001c0002t0001g0103 |
3 | NA18979.hp1 NA19079.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.694-12987C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179993187 | |||||||
| chr5:179993213 | G | A | 1 | a0001c0006t0001g0196 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.694-13013C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179993213 | |||||||
| chr5:179993568 | GTTGT | G | 30 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(27): Show |
32 | HG00438.hp2 HG00544.hp1 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.694-13372_694-1336 others(8): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179993568 | |||||||
| chr5:179993614 | T | A | 56 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(53): Show |
56 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(53): Show |
intron_variant | MODIFIER | c.694-13414A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179993614 | |||||||
| chr5:179993991 | C | T | 61 | a0001c0001t0001g0005 a0001c0001t0001g0250 a0001c0001t0001g0251 others(58): Show |
63 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.694-13791G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179993991 | |||||||
| chr5:179994162 | C | T | 3 | a0001c0002t0001g0044 a0001c0002t0001g0062 a0001c0002t0001g0099 |
3 | HG01106.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.694-13962G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179994162 | |||||||
| chr5:179994191 | C | A | 49 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(46): Show |
49 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(46): Show |
intron_variant | MODIFIER | c.694-13991G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179994191 | |||||||
| chr5:179994482 | G | C | 7 | a0001c0001t0001g0203 a0001c0001t0001g0236 a0001c0001t0001g0238 others(4): Show |
7 | HG02280.hp1 HG02630.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.694-14282C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179994482 | |||||||
| chr5:179994634 | T | C | 49 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(46): Show |
49 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(46): Show |
intron_variant | MODIFIER | c.694-14434A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179994634 | |||||||
| chr5:179994654 | T | C | 1 | a0001c0002t0001g0083 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.694-14454A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179994654 | |||||||
| chr5:179994883 | A | G | 205 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(202): Show |
213 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.694-14683T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179994883 | |||||||
| chr5:179994985 | G | T | 1 | a0001c0001t0001g0323 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.694-14785C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179994985 | |||||||
| chr5:179995047 | G | C | 168 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(165): Show |
172 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.694-14847C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179995047 | |||||||
| chr5:179995195 | G | A | 2 | a0001c0001t0001g0329 a0001c0001t0001g0330 |
2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.694-14995C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179995195 | |||||||
| chr5:179995201 | C | CCT | 37 | a0001c0001t0001g0328 a0001c0002t0001g0096 a0001c0003t0001g0001 others(34): Show |
41 | HG00280.hp2 HG00738.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.694-15003_694-1500 others(6): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179995201 | |||||||
| chr5:179995419 | G | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0306 |
3 | NA18979.hp2 NA19070.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.694-15219C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179995419 | |||||||
| chr5:179995420 | G | C | 2 | a0001c0001t0001g0006 a0001c0001t0001g0306 |
3 | NA18979.hp2 NA19070.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.694-15220C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179995420 | |||||||
| chr5:179995460 | A | G | 2 | a0001c0001t0001g0329 a0001c0001t0001g0330 |
2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.694-15260T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179995460 | |||||||
| chr5:179995573 | T | C | 1 | a0001c0001t0001g0329 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.694-15373A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179995573 | |||||||
| chr5:179995646 | C | T | 4 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0001g0210 others(1): Show |
4 | HG02055.hp1 HG02109.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.694-15446G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179995646 | |||||||
| chr5:179995809 | A | T | 1 | a0001c0001t0001g0282 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.694-15609T>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179995809 | |||||||
| chr5:179995835 | G | A | 37 | a0001c0001t0001g0328 a0001c0002t0001g0096 a0001c0003t0001g0001 others(34): Show |
41 | HG00280.hp2 HG00738.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.694-15635C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179995835 | |||||||
| chr5:179995970 | A | C | 1 | a0001c0002t0001g0115 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.694-15770T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179995970 | |||||||
| chr5:179996379 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.694-16179C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179996379 | |||||||
| chr5:179996519 | C | T | 168 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(165): Show |
172 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.694-16319G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179996519 | |||||||
| chr5:179996536 | T | C | 1 | a0001c0001t0001g0260 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.694-16336A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179996536 | |||||||
| chr5:179996663 | C | T | 1 | a0001c0001t0001g0258 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.693+16398G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179996663 | |||||||
| chr5:179996860 | G | A | 55 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(52): Show |
55 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(52): Show |
intron_variant | MODIFIER | c.693+16201C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179996860 | |||||||
| chr5:179996947 | C | G | 3 | a0001c0002t0001g0053 a0001c0002t0001g0054 a0001c0002t0001g0055 |
3 | HG01069.hp2 HG01168.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.693+16114G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179996947 | |||||||
| chr5:179997001 | G | A | 33 | a0001c0001t0001g0328 a0001c0002t0001g0096 a0001c0003t0001g0001 others(30): Show |
37 | HG00280.hp2 HG00738.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.693+16060C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179997001 | |||||||
| chr5:179997044 | G | A | 1 | a0001c0002t0001g0114 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.693+16017C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179997044 | |||||||
| chr5:179997069 | T | C | 4 | a0001c0001t0001g0271 a0001c0001t0001g0275 a0001c0001t0001g0290 others(1): Show |
4 | NA18998.hp1 NA19007.hp1 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.693+15992A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179997069 | |||||||
| chr5:179997196 | C | T | 3 | a0001c0003t0001g0157 a0001c0003t0002g0155 a0001c0003t0002g0156 |
3 | HG01884.hp2 HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.693+15865G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179997196 | |||||||
| chr5:179997244 | T | C | 14 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(11): Show |
14 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.693+15817A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179997244 | |||||||
| chr5:179997424 | A | C | 328 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(325): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.693+15637T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179997424 | |||||||
| chr5:179997605 | G | A | 1 | a0001c0002t0001g0073 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.693+15456C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179997605 | |||||||
| chr5:179997765 | C | T | 33 | a0001c0001t0001g0328 a0001c0002t0001g0096 a0001c0003t0001g0001 others(30): Show |
37 | HG00280.hp2 HG00738.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.693+15296G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179997765 | |||||||
| chr5:179997821 | T | G | 8 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(5): Show |
8 | HG02572.hp2 HG02809.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.693+15240A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179997821 | |||||||
| chr5:179998109 | G | A | 1 | a0001c0003t0001g0194 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.693+14952C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998109 | |||||||
| chr5:179998119 | G | A | 1 | a0001c0002t0001g0063 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.693+14942C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998119 | |||||||
| chr5:179998128 | T | C | 4 | a0001c0003t0001g0157 a0001c0003t0002g0155 a0001c0003t0002g0156 others(1): Show |
4 | HG01884.hp2 HG02280.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.693+14933A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998128 | |||||||
| chr5:179998132 | C | A | 29 | a0001c0001t0001g0328 a0001c0002t0001g0096 a0001c0003t0001g0001 others(26): Show |
33 | HG00280.hp2 HG00738.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.693+14929G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998132 | |||||||
| chr5:179998496 | C | T | 2 | a0001c0002t0001g0076 a0001c0002t0001g0109 |
2 | NA18977.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.693+14565G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998496 | |||||||
| chr5:179998697 | T | C | 1 | a0001c0001t0001g0296 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.693+14364A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998697 | |||||||
| chr5:179998750 | G | A | 4 | a0001c0001t0001g0325 a0001c0001t0001g0326 a0001c0001t0001g0327 others(1): Show |
4 | HG02258.hp1 HG02809.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.693+14311C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998750 | |||||||
| chr5:179998773 | G | A | 2 | a0001c0001t0001g0329 a0001c0001t0001g0330 |
2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.693+14288C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998773 | |||||||
| chr5:179998780 | C | T | 1 | a0001c0001t0001g0327 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.693+14281G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998780 | |||||||
| chr5:179998854 | ATT | A | 5 | a0001c0001t0001g0204 a0001c0002t0001g0023 a0001c0002t0001g0025 others(2): Show |
5 | HG01934.hp1 NA18959.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.693+14205_693+1420 others(6): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998854 | |||||||
| chr5:179998855 | T | TATATATA others(10): Show |
1 | a0001c0001t0001g0286 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.693+14205_693+1420 others(21): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998855 | |||||||
| chr5:179998857 | T | A | 41 | a0001c0001t0001g0005 a0001c0001t0001g0251 a0001c0001t0001g0255 others(38): Show |
42 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(39): Show |
intron_variant | MODIFIER | c.693+14204A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998857 | |||||||
| chr5:179998857 | T | TATATATA others(24): Show |
1 | a0001c0002t0001g0027 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.693+14203_693+1420 others(35): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998857 | |||||||
| chr5:179998857 | T | TTA | 10 | a0001c0001t0001g0215 a0001c0001t0001g0317 a0001c0002t0001g0028 others(7): Show |
10 | HG00544.hp1 HG02132.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.693+14203_693+1420 others(6): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998857 | |||||||
| chr5:179998857 | T | TTATA | 3 | a0001c0001t0001g0326 a0001c0001t0001g0329 a0001c0002t0001g0056 |
3 | HG02257.hp1 HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.693+14203_693+1420 others(8): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998857 | |||||||
| chr5:179998857 | T | TTATATAT others(1): Show |
4 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0001g0325 others(1): Show |
4 | HG02056.hp1 HG02074.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.693+14203_693+1420 others(12): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998857 | |||||||
| chr5:179998857 | T | TTATATAT others(7): Show |
2 | a0001c0001t0001g0315 a0001c0001t0001g0330 |
2 | HG01358.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.693+14203_693+1420 others(18): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998857 | |||||||
| chr5:179998857 | T | TTATATAT others(9): Show |
2 | a0001c0001t0001g0302 a0001c0005t0001g0195 |
2 | HG00673.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.693+14203_693+1420 others(20): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998857 | |||||||
| chr5:179998857 | T | TTATATAT others(11): Show |
2 | a0001c0001t0001g0320 a0001c0003t0001g0157 |
2 | HG01169.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.693+14203_693+1420 others(22): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998857 | |||||||
| chr5:179998857 | T | TTATATAT others(15): Show |
4 | a0001c0001t0001g0304 a0001c0001t0001g0324 a0001c0002t0001g0048 others(1): Show |
4 | HG00558.hp2 HG00735.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.693+14203_693+1420 others(26): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998857 | |||||||
| chr5:179998857 | T | TTATATAT others(17): Show |
3 | a0001c0001t0001g0318 a0001c0003t0001g0166 a0001c0003t0001g0179 |
3 | HG00642.hp1 NA18612.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.693+14203_693+1420 others(28): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998857 | |||||||
| chr5:179998857 | T | TTATATAT others(19): Show |
1 | a0001c0003t0002g0156 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.693+14203_693+1420 others(30): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998857 | |||||||
| chr5:179998857 | T | TTATATAT others(21): Show |
5 | a0001c0001t0001g0310 a0001c0001t0001g0319 a0001c0002t0001g0127 others(2): Show |
5 | HG01261.hp1 HG02486.hp2 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.693+14203_693+1420 others(32): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998857 | |||||||
| chr5:179998857 | T | TTATATAT others(23): Show |
2 | a0001c0001t0001g0303 a0001c0001t0001g0311 |
2 | HG00140.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.693+14203_693+1420 others(34): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998857 | |||||||
| chr5:179998857 | T | TTATATAT others(25): Show |
2 | a0001c0003t0001g0154 a0001c0003t0001g0180 |
2 | HG00408.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.693+14203_693+1420 others(36): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998857 | |||||||
| chr5:179998857 | T | TTATATAT others(27): Show |
4 | a0001c0001t0001g0309 a0001c0001t0001g0312 a0001c0003t0001g0146 others(1): Show |
4 | HG01261.hp2 NA18943.hp1 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.693+14203_693+1420 others(38): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998857 | |||||||
| chr5:179998857 | T | TTATATAT others(29): Show |
5 | a0001c0001t0001g0007 a0001c0001t0001g0305 a0001c0001t0001g0307 others(2): Show |
6 | HG01123.hp2 HG03492.hp2 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.693+14203_693+1420 others(40): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998857 | |||||||
| chr5:179998857 | T | TTATATAT others(31): Show |
5 | a0001c0001t0001g0298 a0001c0001t0001g0308 a0001c0003t0001g0147 others(2): Show |
5 | HG00733.hp2 HG01175.hp1 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.693+14203_693+1420 others(42): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998857 | |||||||
| chr5:179998857 | T | TTATATAT others(33): Show |
1 | a0001c0003t0001g0165 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.693+14203_693+1420 others(44): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998857 | |||||||
| chr5:179998857 | T | TTATATAT others(41): Show |
1 | a0001c0003t0001g0148 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.693+14203_693+1420 others(52): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998857 | |||||||
| chr5:179998857 | T | TTATATAT others(47): Show |
1 | a0001c0001t0001g0313 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.693+14203_693+1420 others(58): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998857 | |||||||
| chr5:179998857 | TTTTATA | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0306 |
3 | NA18979.hp2 NA19070.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.693+14198_693+1420 others(10): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998857 | |||||||
| chr5:179998857 | TTTTATAT others(3): Show |
T | 7 | a0001c0001t0001g0200 a0001c0001t0001g0301 a0001c0001t0001g0316 others(4): Show |
7 | HG00438.hp2 HG02135.hp1 HG03654.hp2 others(4): Show |
intron_variant | MODIFIER | c.693+14194_693+1420 others(14): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998857 | |||||||
| chr5:179998859 | T | A | 152 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0215 others(149): Show |
159 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.693+14202A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998859 | |||||||
| chr5:179998859 | T | TTA | 12 | a0001c0001t0001g0201 a0001c0001t0001g0214 a0001c0001t0001g0216 others(9): Show |
12 | HG00323.hp2 HG00639.hp2 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.693+14200_693+1420 others(6): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998859 | |||||||
| chr5:179998859 | T | TTATATA | 3 | a0001c0001t0001g0202 a0001c0001t0001g0228 a0001c0001t0001g0331 |
3 | HG01123.hp1 HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.693+14196_693+1420 others(10): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998859 | |||||||
| chr5:179998859 | T | TTATATAT others(27): Show |
1 | a0001c0001t0002g0243 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.693+14201_693+1420 others(38): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998859 | |||||||
| chr5:179998859 | TTA | T | 107 | a0001c0001t0001g0199 a0001c0001t0001g0205 a0001c0001t0001g0206 others(104): Show |
107 | HG00438.hp1 HG00673.hp2 HG00735.hp2 others(104): Show |
intron_variant | MODIFIER | c.693+14200_693+1420 others(6): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998859 | |||||||
| chr5:179998869 | ATATATAT others(12): Show |
A | 1 | a0001c0001t0001g0254 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.693+14173_693+1419 others(23): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998869 | |||||||
| chr5:179998885 | G | A | 58 | a0001c0001t0001g0005 a0001c0001t0001g0250 a0001c0001t0001g0251 others(55): Show |
59 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.693+14176C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998885 | |||||||
| chr5:179998886 | T | TA | 3 | a0001c0001t0001g0277 a0001c0001t0001g0280 a0001c0001t0001g0286 |
3 | HG02109.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.693+14174_693+1417 others(5): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998886 | |||||||
| chr5:179998886 | T | TATATATA others(4): Show |
4 | a0001c0001t0001g0005 a0001c0001t0001g0273 a0001c0001t0001g0279 others(1): Show |
4 | HG00609.hp2 HG01981.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.693+14174_693+1417 others(15): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998886 | |||||||
| chr5:179998886 | T | TATATATA others(6): Show |
5 | a0001c0001t0001g0257 a0001c0001t0001g0263 a0001c0001t0001g0267 others(2): Show |
5 | HG00280.hp1 HG02559.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.693+14174_693+1417 others(17): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998886 | |||||||
| chr5:179998886 | T | TATATATA others(8): Show |
5 | a0001c0001t0001g0261 a0001c0001t0001g0278 a0001c0001t0001g0295 others(2): Show |
5 | HG00323.hp1 HG01433.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.693+14174_693+1417 others(19): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998886 | |||||||
| chr5:179998886 | T | TATATATA others(10): Show |
4 | a0001c0001t0001g0256 a0001c0001t0001g0258 a0001c0001t0001g0259 others(1): Show |
4 | HG00639.hp1 HG01081.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.693+14174_693+1417 others(21): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998886 | |||||||
| chr5:179998886 | T | TATATATA others(12): Show |
5 | a0001c0001t0001g0251 a0001c0001t0001g0262 a0001c0001t0001g0265 others(2): Show |
5 | HG00544.hp2 HG00733.hp1 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.693+14174_693+1417 others(23): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998886 | |||||||
| chr5:179998886 | T | TATATATA others(14): Show |
8 | a0001c0001t0001g0005 a0001c0001t0001g0253 a0001c0001t0001g0255 others(5): Show |
8 | HG01106.hp1 HG02132.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.693+14174_693+1417 others(25): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998886 | |||||||
| chr5:179998886 | T | TATATATA others(16): Show |
5 | a0001c0001t0001g0260 a0001c0001t0001g0269 a0001c0001t0001g0272 others(2): Show |
5 | NA18951.hp1 NA18989.hp1 NA19077.hp1 others(2): Show |
intron_variant | MODIFIER | c.693+14174_693+1417 others(27): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998886 | |||||||
| chr5:179998886 | T | TATATATA others(18): Show |
2 | a0001c0001t0001g0274 a0001c0001t0001g0276 |
2 | HG00408.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.693+14174_693+1417 others(29): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998886 | |||||||
| chr5:179998886 | T | TATATATA others(20): Show |
2 | a0001c0001t0001g0264 a0001c0001t0001g0271 |
2 | HG02155.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.693+14174_693+1417 others(31): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998886 | |||||||
| chr5:179998886 | T | TATATATA others(22): Show |
7 | a0001c0001t0001g0266 a0001c0001t0001g0275 a0001c0004t0001g0136 others(4): Show |
7 | HG02293.hp2 NA18962.hp1 NA18974.hp2 others(4): Show |
intron_variant | MODIFIER | c.693+14174_693+1417 others(33): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998886 | |||||||
| chr5:179998886 | T | TATATATA others(24): Show |
5 | a0001c0001t0001g0252 a0001c0001t0001g0287 a0001c0001t0001g0296 others(2): Show |
5 | HG01358.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.693+14174_693+1417 others(35): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998886 | |||||||
| chr5:179998886 | T | TATATATA others(26): Show |
1 | a0001c0001t0001g0268 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.693+14174_693+1417 others(37): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998886 | |||||||
| chr5:179998886 | T | TATATATA others(28): Show |
1 | a0001c0001t0001g0250 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.693+14174_693+1417 others(39): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998886 | |||||||
| chr5:179998886 | T | TATATATA others(30): Show |
1 | a0001c0004t0001g0135 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.693+14174_693+1417 others(41): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998886 | |||||||
| chr5:179998888 | T | A | 57 | a0001c0001t0001g0005 a0001c0001t0001g0250 a0001c0001t0001g0251 others(54): Show |
58 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.693+14173A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998888 | |||||||
| chr5:179998888 | T | C | 1 | a0001c0001t0001g0256 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.693+14173A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998888 | |||||||
| chr5:179998894 | A | G | 5 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0214 others(2): Show |
5 | HG01891.hp2 HG02145.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.693+14167T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998894 | |||||||
| chr5:179998930 | C | T | 2 | a0001c0002t0001g0116 a0001c0002t0001g0118 |
2 | HG00735.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.693+14131G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998930 | |||||||
| chr5:179998971 | A | G | 1 | a0001c0004t0001g0136 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.693+14090T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998971 | |||||||
| chr5:179998979 | A | T | 1 | a0001c0001t0001g0309 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.693+14082T>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179998979 | |||||||
| chr5:179999107 | C | CTGCCTTG others(5): Show |
61 | a0001c0001t0001g0005 a0001c0001t0001g0250 a0001c0001t0001g0251 others(58): Show |
63 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.693+13942_693+1395 others(16): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179999107 | |||||||
| chr5:179999182 | G | A | 1 | a0001c0002t0001g0061 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.693+13879C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179999182 | |||||||
| chr5:179999460 | G | A | 1 | a0001c0001t0001g0305 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.693+13601C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179999460 | |||||||
| chr5:179999464 | G | C | 1 | a0001c0002t0001g0115 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.693+13597C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179999464 | |||||||
| chr5:179999493 | G | A | 1 | a0001c0001t0001g0328 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.693+13568C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179999493 | |||||||
| chr5:179999619 | AG | A | 2 | a0001c0001t0001g0005 a0001c0001t0001g0255 |
3 | HG03209.hp1 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.693+13441delC | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179999619 | |||||||
| chr5:179999649 | G | A | 7 | a0001c0001t0001g0237 a0001c0001t0001g0244 a0001c0001t0001g0245 others(4): Show |
7 | HG02055.hp2 HG02257.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.693+13412C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179999649 | |||||||
| chr5:179999662 | A | G | 1 | a0001c0003t0001g0184 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.693+13399T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179999662 | |||||||
| chr5:179999670 | T | C | 1 | a0001c0002t0001g0067 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.693+13391A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179999670 | |||||||
| chr5:179999698 | G | C | 112 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(109): Show |
116 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.693+13363C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179999698 | |||||||
| chr5:179999800 | A | G | 5 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0287 others(2): Show |
5 | HG00733.hp1 HG01106.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.693+13261T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179999800 | |||||||
| chr5:179999998 | C | T | 2 | a0001c0001t0001g0256 a0001c0001t0001g0257 |
2 | HG00280.hp1 HG00639.hp1 |
intron_variant | MODIFIER | c.693+13063G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 179999998 | |||||||
| chr5:180000060 | G | C | 4 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0001g0317 others(1): Show |
4 | HG00544.hp1 HG02074.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.693+13001C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180000060 | |||||||
| chr5:180000089 | A | G | 61 | a0001c0001t0001g0005 a0001c0001t0001g0250 a0001c0001t0001g0251 others(58): Show |
63 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.693+12972T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180000089 | |||||||
| chr5:180000246 | T | A | 40 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(37): Show |
40 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.693+12815A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180000246 | |||||||
| chr5:180000268 | C | T | 1 | a0001c0001t0001g0296 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.693+12793G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180000268 | |||||||
| chr5:180000400 | A | G | 162 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(159): Show |
166 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.693+12661T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180000400 | |||||||
| chr5:180000551 | A | T | 1 | a0001c0001t0001g0270 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.693+12510T>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180000551 | |||||||
| chr5:180000584 | CTTAT | C | 5 | a0001c0004t0001g0137 a0001c0004t0001g0138 a0001c0004t0001g0139 others(2): Show |
5 | HG02293.hp2 NA18962.hp1 NA19055.hp1 others(2): Show |
intron_variant | MODIFIER | c.693+12473_693+1247 others(8): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180000584 | |||||||
| chr5:180000592 | T | C | 1 | a0001c0004t0001g0136 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.693+12469A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180000592 | |||||||
| chr5:180000627 | C | A | 1 | a0001c0001t0001g0296 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.693+12434G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180000627 | |||||||
| chr5:180000658 | A | G | 11 | a0001c0002t0001g0009 a0001c0002t0001g0069 a0001c0002t0001g0072 others(8): Show |
11 | HG00673.hp2 HG01993.hp1 HG01993.hp2 others(8): Show |
intron_variant | MODIFIER | c.693+12403T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180000658 | |||||||
| chr5:180000807 | G | A | 1 | a0001c0002t0001g0015 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.693+12254C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180000807 | |||||||
| chr5:180000836 | C | T | 49 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(46): Show |
49 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(46): Show |
intron_variant | MODIFIER | c.693+12225G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180000836 | |||||||
| chr5:180000873 | A | G | 51 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(48): Show |
53 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.693+12188T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180000873 | |||||||
| chr5:180001177 | T | C | 6 | a0001c0001t0001g0329 a0001c0001t0001g0330 a0001c0003t0001g0157 others(3): Show |
6 | HG01884.hp2 HG02280.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.693+11884A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180001177 | |||||||
| chr5:180001285 | G | T | 1 | a0001c0001t0001g0295 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.693+11776C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180001285 | |||||||
| chr5:180001401 | G | C | 1 | a0001c0001t0001g0204 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.693+11660C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180001401 | |||||||
| chr5:180001441 | G | T | 1 | a0001c0001t0001g0305 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.693+11620C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180001441 | |||||||
| chr5:180001735 | T | C | 168 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(165): Show |
172 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.693+11326A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180001735 | |||||||
| chr5:180001867 | G | A | 6 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(3): Show |
6 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.693+11194C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180001867 | |||||||
| chr5:180001887 | G | A | 61 | a0001c0001t0001g0005 a0001c0001t0001g0250 a0001c0001t0001g0251 others(58): Show |
63 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.693+11174C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180001887 | |||||||
| chr5:180002159 | C | T | 3 | a0001c0002t0001g0030 a0001c0002t0001g0133 a0002c0010t0001g0031 |
3 | HG01243.hp2 HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.693+10902G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180002159 | |||||||
| chr5:180002358 | C | T | 1 | a0001c0003t0002g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.693+10703G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180002358 | |||||||
| chr5:180002469 | G | A | 2 | a0001c0003t0001g0188 a0001c0003t0001g0190 |
2 | HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.693+10592C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180002469 | |||||||
| chr5:180002592 | G | C | 1 | a0001c0002t0001g0051 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.693+10469C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180002592 | |||||||
| chr5:180002673 | C | T | 2 | a0001c0002t0001g0121 a0001c0002t0001g0122 |
2 | HG00099.hp2 HG00642.hp2 |
intron_variant | MODIFIER | c.693+10388G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180002673 | |||||||
| chr5:180003005 | A | G | 2 | a0001c0001t0001g0246 a0001c0001t0001g0248 |
2 | HG02055.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.693+10056T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180003005 | |||||||
| chr5:180003046 | T | C | 3 | a0001c0001t0001g0006 a0001c0001t0001g0306 a0001c0001t0001g0309 |
4 | NA18963.hp1 NA18979.hp2 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.693+10015A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180003046 | |||||||
| chr5:180003261 | G | A | 17 | a0001c0002t0001g0010 a0001c0002t0001g0022 a0001c0002t0001g0023 others(14): Show |
17 | HG00099.hp1 HG00738.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.693+9800C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180003261 | |||||||
| chr5:180003266 | T | C | 168 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(165): Show |
172 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.693+9795A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180003266 | |||||||
| chr5:180003267 | G | A | 1 | a0001c0001t0001g0294 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.693+9794C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180003267 | |||||||
| chr5:180003282 | G | A | 1 | a0001c0001t0001g0303 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.693+9779C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180003282 | |||||||
| chr5:180003530 | C | T | 51 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(48): Show |
53 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.693+9531G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180003530 | |||||||
| chr5:180003536 | T | C | 1 | a0001c0001t0001g0302 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.693+9525A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180003536 | |||||||
| chr5:180003607 | C | G | 1 | a0001c0003t0001g0151 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.693+9454G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180003607 | |||||||
| chr5:180003688 | A | AT | 55 | a0001c0001t0001g0005 a0001c0001t0001g0251 a0001c0001t0001g0252 others(52): Show |
57 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.693+9372dupA | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180003688 | |||||||
| chr5:180003689 | T | A | 1 | a0001c0001t0001g0323 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.693+9372A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180003689 | |||||||
| chr5:180003727 | G | T | 113 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(110): Show |
117 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.693+9334C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180003727 | |||||||
| chr5:180003960 | C | A | 33 | a0001c0001t0001g0328 a0001c0002t0001g0096 a0001c0003t0001g0001 others(30): Show |
37 | HG00280.hp2 HG00738.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.693+9101G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180003960 | |||||||
| chr5:180004140 | T | G | 2 | a0001c0002t0001g0015 a0001c0002t0001g0017 |
2 | HG01517.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.693+8921A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180004140 | |||||||
| chr5:180004193 | T | C | 2 | a0001c0001t0001g0329 a0001c0001t0001g0330 |
2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.693+8868A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180004193 | |||||||
| chr5:180004306 | T | C | 61 | a0001c0001t0001g0005 a0001c0001t0001g0250 a0001c0001t0001g0251 others(58): Show |
63 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.693+8755A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180004306 | |||||||
| chr5:180004558 | C | A | 3 | a0001c0002t0001g0030 a0001c0002t0001g0133 a0002c0010t0001g0031 |
3 | HG01243.hp2 HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.693+8503G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180004558 | |||||||
| chr5:180004684 | T | C | 49 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(46): Show |
49 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(46): Show |
intron_variant | MODIFIER | c.693+8377A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180004684 | |||||||
| chr5:180004703 | G | C | 7 | a0001c0001t0001g0203 a0001c0001t0001g0236 a0001c0001t0001g0238 others(4): Show |
7 | HG02280.hp1 HG02630.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.693+8358C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180004703 | |||||||
| chr5:180004933 | T | C | 1 | a0001c0001t0001g0331 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.693+8128A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180004933 | |||||||
| chr5:180004934 | T | G | 2 | a0001c0001t0001g0329 a0001c0001t0001g0330 |
2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.693+8127A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180004934 | |||||||
| chr5:180004990 | G | T | 2 | a0001c0002t0001g0069 a0001c0002t0001g0075 |
2 | HG01993.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.693+8071C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180004990 | |||||||
| chr5:180005085 | C | T | 1 | a0001c0002t0001g0016 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.693+7976G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180005085 | |||||||
| chr5:180005096 | G | A | 51 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(48): Show |
53 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.693+7965C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180005096 | |||||||
| chr5:180005104 | A | G | 3 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 |
3 | HG01891.hp2 HG02886.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.693+7957T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180005104 | |||||||
| chr5:180005135 | A | AC | 3 | a0001c0003t0001g0153 a0001c0003t0001g0164 a0001c0003t0001g0165 |
3 | HG00733.hp2 HG01074.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.693+7925dupG | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180005135 | |||||||
| chr5:180005148 | C | T | 1 | a0001c0002t0002g0132 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.693+7913G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180005148 | |||||||
| chr5:180005164 | G | A | 3 | a0001c0001t0001g0292 a0001c0001t0001g0293 a0001c0001t0001g0295 |
3 | HG02486.hp1 HG02647.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.693+7897C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180005164 | |||||||
| chr5:180005433 | A | AAAC | 60 | a0001c0001t0001g0005 a0001c0001t0001g0250 a0001c0001t0001g0251 others(57): Show |
62 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.693+7625_693+7627d others(5): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180005433 | |||||||
| chr5:180005447 | A | C | 1 | a0001c0003t0002g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.693+7614T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180005447 | |||||||
| chr5:180005577 | C | T | 2 | a0001c0002t0001g0019 a0001c0002t0001g0020 |
2 | HG01516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.693+7484G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180005577 | |||||||
| chr5:180005701 | A | G | 1 | a0001c0001t0001g0253 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.693+7360T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180005701 | |||||||
| chr5:180005894 | T | C | 1 | a0001c0002t0001g0119 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.693+7167A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180005894 | |||||||
| chr5:180005913 | A | C | 1 | a0001c0001t0001g0251 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.693+7148T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180005913 | |||||||
| chr5:180006023 | T | C | 1 | a0001c0001t0001g0261 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.693+7038A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180006023 | |||||||
| chr5:180006295 | GA | G | 51 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(48): Show |
53 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.693+6765delT | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180006295 | |||||||
| chr5:180006524 | T | C | 1 | a0001c0003t0001g0174 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.693+6537A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180006524 | |||||||
| chr5:180007232 | C | T | 10 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0261 others(7): Show |
10 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(7): Show |
intron_variant | MODIFIER | c.693+5829G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180007232 | |||||||
| chr5:180007347 | G | C | 1 | a0001c0003t0001g0173 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.693+5714C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180007347 | |||||||
| chr5:180007613 | G | A | 1 | a0001c0002t0001g0046 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.693+5448C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180007613 | |||||||
| chr5:180007725 | T | C | 48 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(45): Show |
48 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(45): Show |
intron_variant | MODIFIER | c.693+5336A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180007725 | |||||||
| chr5:180007877 | C | T | 1 | a0001c0001t0001g0325 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.693+5184G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180007877 | |||||||
| chr5:180007988 | G | GT | 169 | a0001c0001t0001g0199 a0001c0001t0001g0272 a0001c0001t0001g0277 others(166): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.693+5072dupA | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180007988 | |||||||
| chr5:180007988 | G | GTT | 56 | a0001c0001t0001g0005 a0001c0001t0001g0250 a0001c0001t0001g0251 others(53): Show |
58 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.693+5071_693+5072d others(4): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180007988 | |||||||
| chr5:180007988 | GT | G | 9 | a0001c0001t0001g0237 a0001c0001t0001g0244 a0001c0001t0001g0245 others(6): Show |
9 | HG00558.hp2 HG02055.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.693+5072delA | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180007988 | |||||||
| chr5:180008011 | C | T | 1 | a0001c0001t0001g0284 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.693+5050G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180008011 | |||||||
| chr5:180008118 | T | C | 279 | a0001c0001t0001g0005 a0001c0001t0001g0199 a0001c0001t0001g0201 others(276): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.693+4943A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180008118 | |||||||
| chr5:180008185 | G | A | 1 | a0001c0001t0001g0323 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.693+4876C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180008185 | |||||||
| chr5:180008230 | A | G | 3 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 |
3 | HG01891.hp2 HG02886.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.693+4831T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180008230 | |||||||
| chr5:180008348 | G | A | 61 | a0001c0001t0001g0005 a0001c0001t0001g0250 a0001c0001t0001g0251 others(58): Show |
63 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.693+4713C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180008348 | |||||||
| chr5:180008576 | G | C | 1 | a0001c0003t0001g0184 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.693+4485C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180008576 | |||||||
| chr5:180008621 | A | C | 61 | a0001c0001t0001g0005 a0001c0001t0001g0250 a0001c0001t0001g0251 others(58): Show |
63 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.693+4440T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180008621 | |||||||
| chr5:180008705 | T | C | 49 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(46): Show |
49 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(46): Show |
intron_variant | MODIFIER | c.693+4356A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180008705 | |||||||
| chr5:180008746 | C | T | 1 | a0001c0002t0001g0047 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.693+4315G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180008746 | |||||||
| chr5:180008750 | G | A | 1 | a0001c0003t0001g0182 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.693+4311C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180008750 | |||||||
| chr5:180008898 | A | G | 1 | a0001c0002t0001g0104 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.693+4163T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180008898 | |||||||
| chr5:180008980 | A | G | 3 | a0001c0003t0001g0158 a0001c0003t0001g0160 a0001c0003t0001g0161 |
3 | HG03041.hp1 HG03139.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.693+4081T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180008980 | |||||||
| chr5:180009030 | T | C | 1 | a0001c0001t0001g0304 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.693+4031A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180009030 | |||||||
| chr5:180009278 | T | C | 61 | a0001c0001t0001g0005 a0001c0001t0001g0250 a0001c0001t0001g0251 others(58): Show |
63 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.693+3783A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180009278 | |||||||
| chr5:180009337 | T | C | 1 | a0001c0001t0001g0226 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.693+3724A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180009337 | |||||||
| chr5:180009466 | T | C | 55 | a0001c0001t0001g0005 a0001c0001t0001g0251 a0001c0001t0001g0252 others(52): Show |
57 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.693+3595A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180009466 | |||||||
| chr5:180009499 | A | G | 61 | a0001c0001t0001g0005 a0001c0001t0001g0250 a0001c0001t0001g0251 others(58): Show |
63 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.693+3562T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180009499 | |||||||
| chr5:180009547 | C | T | 1 | a0001c0003t0001g0189 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.693+3514G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180009547 | |||||||
| chr5:180009554 | C | T | 1 | a0001c0002t0001g0111 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.693+3507G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180009554 | |||||||
| chr5:180009670 | C | T | 3 | a0001c0001t0001g0292 a0001c0001t0001g0293 a0001c0001t0001g0295 |
3 | HG02486.hp1 HG02647.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.693+3391G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180009670 | |||||||
| chr5:180009696 | T | G | 279 | a0001c0001t0001g0005 a0001c0001t0001g0199 a0001c0001t0001g0201 others(276): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.693+3365A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180009696 | |||||||
| chr5:180009734 | A | C | 279 | a0001c0001t0001g0005 a0001c0001t0001g0199 a0001c0001t0001g0201 others(276): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.693+3327T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180009734 | |||||||
| chr5:180009960 | T | C | 1 | a0001c0001t0001g0250 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.693+3101A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180009960 | |||||||
| chr5:180010027 | C | G | 1 | a0001c0002t0001g0032 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.693+3034G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180010027 | |||||||
| chr5:180010043 | C | G | 2 | a0001c0001t0001g0282 a0001c0001t0001g0283 |
2 | HG02647.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.693+3018G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180010043 | |||||||
| chr5:180010059 | A | G | 2 | a0001c0001t0001g0304 a0001c0003t0001g0154 |
2 | HG00408.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.693+3002T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180010059 | |||||||
| chr5:180010181 | A | G | 1 | a0001c0001t0001g0323 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.693+2880T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180010181 | |||||||
| chr5:180010244 | C | CA | 42 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(39): Show |
42 | HG01106.hp1 HG01123.hp1 HG01192.hp1 others(39): Show |
intron_variant | MODIFIER | c.693+2816dupT | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180010244 | |||||||
| chr5:180010244 | C | CAA | 11 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0210 others(8): Show |
11 | HG02055.hp1 HG02145.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.693+2815_693+2816d others(4): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180010244 | |||||||
| chr5:180010244 | CA | C | 170 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0199 others(167): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.693+2816delT | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180010244 | |||||||
| chr5:180010425 | T | A | 1 | a0001c0001t0001g0303 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.693+2636A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180010425 | |||||||
| chr5:180010519 | C | T | 49 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(46): Show |
49 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(46): Show |
intron_variant | MODIFIER | c.693+2542G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180010519 | |||||||
| chr5:180010653 | C | T | 2 | a0001c0001t0001g0246 a0001c0001t0001g0248 |
2 | HG02055.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.693+2408G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180010653 | |||||||
| chr5:180010730 | TA | T | 8 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(5): Show |
8 | HG02572.hp2 HG02809.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.693+2330delT | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180010730 | |||||||
| chr5:180010800 | T | C | 218 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0202 others(215): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.693+2261A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180010800 | |||||||
| chr5:180010915 | G | A | 1 | a0001c0002t0002g0132 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.693+2146C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180010915 | |||||||
| chr5:180010934 | T | C | 11 | a0001c0002t0001g0011 a0001c0002t0001g0033 a0001c0002t0001g0034 others(8): Show |
11 | HG02040.hp2 NA18947.hp2 NA18962.hp2 others(8): Show |
intron_variant | MODIFIER | c.693+2127A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180010934 | |||||||
| chr5:180010963 | A | G | 1 | a0001c0001t0001g0323 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.693+2098T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180010963 | |||||||
| chr5:180011023 | T | C | 1 | a0001c0001t0001g0305 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.693+2038A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180011023 | |||||||
| chr5:180011105 | C | T | 4 | a0001c0003t0001g0004 a0001c0003t0001g0168 a0001c0003t0001g0172 others(1): Show |
5 | HG00280.hp2 HG01081.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.693+1956G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180011105 | |||||||
| chr5:180011433 | C | T | 61 | a0001c0001t0001g0005 a0001c0001t0001g0250 a0001c0001t0001g0251 others(58): Show |
63 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.693+1628G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180011433 | |||||||
| chr5:180011626 | T | G | 279 | a0001c0001t0001g0005 a0001c0001t0001g0199 a0001c0001t0001g0201 others(276): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.693+1435A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180011626 | |||||||
| chr5:180011766 | T | TA | 61 | a0001c0001t0001g0005 a0001c0001t0001g0250 a0001c0001t0001g0251 others(58): Show |
63 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.693+1294dupT | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180011766 | |||||||
| chr5:180011891 | T | C | 49 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(46): Show |
49 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(46): Show |
intron_variant | MODIFIER | c.693+1170A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180011891 | |||||||
| chr5:180011920 | T | A | 279 | a0001c0001t0001g0005 a0001c0001t0001g0199 a0001c0001t0001g0201 others(276): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.693+1141A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180011920 | |||||||
| chr5:180011926 | A | G | 1 | a0001c0001t0001g0323 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.693+1135T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180011926 | |||||||
| chr5:180011997 | G | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0255 a0001c0001t0001g0277 others(1): Show |
5 | HG02896.hp2 HG02897.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.693+1064C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180011997 | |||||||
| chr5:180012014 | CCACAGTC others(27): Show |
C | 1 | a0001c0002t0001g0104 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.693+1013_693+1046d others(36): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180012014 | |||||||
| chr5:180012129 | G | A | 1 | a0001c0002t0001g0110 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.693+932C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180012129 | |||||||
| chr5:180012345 | A | G | 279 | a0001c0001t0001g0005 a0001c0001t0001g0199 a0001c0001t0001g0201 others(276): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.693+716T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180012345 | |||||||
| chr5:180012516 | C | T | 279 | a0001c0001t0001g0005 a0001c0001t0001g0199 a0001c0001t0001g0201 others(276): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.693+545G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180012516 | |||||||
| chr5:180013002 | G | A | 7 | a0001c0001t0001g0203 a0001c0001t0001g0236 a0001c0001t0001g0238 others(4): Show |
7 | HG02280.hp1 HG02630.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.693+59C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 3/8 | chr5 | 180013002 | |||||||
| chr5:180013358 | T | C | 48 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(45): Show |
48 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(45): Show |
intron_variant | MODIFIER | c.443-47A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180013358 | |||||||
| chr5:180013576 | A | C | 9 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0324 others(6): Show |
9 | HG00408.hp2 HG00735.hp1 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.443-265T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180013576 | |||||||
| chr5:180013631 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.443-320T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180013631 | |||||||
| chr5:180013838 | C | A | 1 | a0001c0001t0002g0243 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.443-527G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180013838 | |||||||
| chr5:180013908 | T | C | 12 | a0001c0001t0001g0204 a0001c0001t0001g0211 a0001c0001t0001g0212 others(9): Show |
12 | HG02451.hp2 HG02717.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.443-597A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180013908 | |||||||
| chr5:180014151 | G | A | 1 | a0001c0002t0001g0021 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.443-840C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180014151 | |||||||
| chr5:180014173 | A | G | 2 | a0001c0002t0001g0023 a0001c0002t0001g0025 |
2 | NA18974.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.443-862T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180014173 | |||||||
| chr5:180014199 | T | C | 3 | a0001c0001t0001g0200 a0001c0001t0001g0332 a0001c0004t0004g0144 |
3 | NA18953.hp2 NA19074.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.443-888A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180014199 | |||||||
| chr5:180014246 | T | C | 6 | a0001c0001t0001g0324 a0001c0002t0001g0048 a0001c0002t0001g0127 others(3): Show |
6 | HG00735.hp1 HG01261.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.443-935A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180014246 | |||||||
| chr5:180014301 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.443-990G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180014301 | |||||||
| chr5:180014331 | T | A | 218 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0202 others(215): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.443-1020A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180014331 | |||||||
| chr5:180014342 | G | A | 1 | a0001c0001t0001g0323 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.443-1031C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180014342 | |||||||
| chr5:180014648 | C | G | 60 | a0001c0001t0001g0005 a0001c0001t0001g0251 a0001c0001t0001g0252 others(57): Show |
62 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.443-1337G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180014648 | |||||||
| chr5:180014782 | C | T | 1 | a0001c0002t0001g0064 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.443-1471G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180014782 | |||||||
| chr5:180014842 | T | C | 279 | a0001c0001t0001g0005 a0001c0001t0001g0199 a0001c0001t0001g0201 others(276): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.443-1531A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180014842 | |||||||
| chr5:180014952 | C | A | 12 | a0001c0002t0001g0010 a0001c0002t0001g0049 a0001c0002t0001g0050 others(9): Show |
12 | HG00099.hp1 HG00738.hp1 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.443-1641G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180014952 | |||||||
| chr5:180015013 | G | T | 1 | a0001c0002t0001g0012 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.443-1702C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015013 | |||||||
| chr5:180015049 | C | T | 1 | a0001c0001t0001g0303 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.443-1738G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015049 | |||||||
| chr5:180015437 | CAAGCTGG others(5): Show |
C | 1 | a0001c0001t0001g0264 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.443-2138_443-2127d others(14): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015437 | |||||||
| chr5:180015445 | A | AAAAGGAG others(5): Show |
39 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0204 others(36): Show |
39 | HG00639.hp2 HG01123.hp1 HG01891.hp2 others(36): Show |
intron_variant | MODIFIER | c.443-2146_443-2135d others(14): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015445 | |||||||
| chr5:180015445 | AAAAGGAG others(5): Show |
A | 6 | a0001c0001t0001g0329 a0001c0001t0001g0330 a0001c0003t0001g0157 others(3): Show |
6 | HG01884.hp2 HG02280.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.443-2146_443-2135d others(14): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015445 | |||||||
| chr5:180015451 | A | AGTAGGGA others(17): Show |
1 | a0001c0001t0001g0203 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.443-2141_443-2140i others(26): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015451 | |||||||
| chr5:180015479 | GGGAAAGG others(4): Show |
G | 1 | a0001c0001t0001g0200 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.443-2179_443-2169d others(13): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015479 | |||||||
| chr5:180015490 | AGGAAAGG others(5): Show |
A | 3 | a0001c0002t0001g0078 a0001c0002t0001g0083 a0001c0002t0001g0093 |
3 | HG02683.hp2 HG03017.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.443-2191_443-2180d others(14): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015490 | |||||||
| chr5:180015513 | A | AG | 8 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(5): Show |
8 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.443-2203dupC | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015513 | |||||||
| chr5:180015524 | AG | A | 218 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0202 others(215): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.443-2214delC | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015524 | |||||||
| chr5:180015536 | A | AG | 5 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0215 others(2): Show |
5 | HG01891.hp2 HG02145.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.443-2226dupC | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015536 | |||||||
| chr5:180015547 | AG | A | 5 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0215 others(2): Show |
5 | HG01891.hp2 HG02145.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.443-2237delC | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015547 | |||||||
| chr5:180015551 | G | A | 274 | a0001c0001t0001g0005 a0001c0001t0001g0199 a0001c0001t0001g0203 others(271): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(277): Show |
intron_variant | MODIFIER | c.443-2240C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015551 | |||||||
| chr5:180015562 | G | A | 2 | a0001c0002t0001g0061 a0001c0002t0001g0123 |
2 | HG01192.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.443-2251C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015562 | |||||||
| chr5:180015562 | G | GA | 5 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0215 others(2): Show |
5 | HG01891.hp2 HG02145.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.443-2252dupT | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015562 | |||||||
| chr5:180015562 | GAAGGAGT others(5): Show |
G | 8 | a0001c0001t0001g0305 a0001c0002t0001g0048 a0001c0002t0001g0127 others(5): Show |
8 | HG00408.hp2 HG00735.hp1 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.443-2263_443-2252d others(14): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015562 | |||||||
| chr5:180015562 | GAAGGAGT others(17): Show |
G | 2 | a0001c0001t0001g0303 a0001c0001t0001g0304 |
2 | HG00140.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.443-2275_443-2252d others(26): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015562 | |||||||
| chr5:180015571 | G | GGGAAAGG others(108): Show |
2 | a0001c0002t0001g0061 a0001c0002t0001g0123 |
2 | HG01192.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.443-2261_443-2260i others(117): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015571 | |||||||
| chr5:180015583 | G | GGGAAAGG others(40): Show |
12 | a0001c0001t0001g0204 a0001c0001t0001g0211 a0001c0001t0001g0212 others(9): Show |
12 | HG02451.hp2 HG02717.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.443-2319_443-2273d others(49): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015583 | |||||||
| chr5:180015595 | G | GGGAAAGG others(4): Show |
1 | a0001c0003t0001g0151 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.443-2295_443-2285d others(13): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015595 | |||||||
| chr5:180015595 | G | GGGAAAGG others(26): Show |
1 | a0001c0002t0001g0066 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.443-2285_443-2284i others(35): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015595 | |||||||
| chr5:180015607 | G | GGGAAAGG others(27): Show |
1 | a0001c0002t0001g0064 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.443-2297_443-2296i others(36): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015607 | |||||||
| chr5:180015607 | G | GGGAAAGG others(39): Show |
123 | a0001c0001t0001g0199 a0001c0001t0001g0237 a0001c0001t0001g0244 others(120): Show |
123 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.443-2297_443-2296i others(48): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015607 | |||||||
| chr5:180015607 | G | GGGAAAGG others(16): Show |
1 | a0001c0001t0001g0323 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.443-2319_443-2297d others(25): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015607 | |||||||
| chr5:180015607 | G | GGGAAAGG others(51): Show |
29 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(26): Show |
29 | HG00639.hp2 HG01123.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.443-2297_443-2296i others(60): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015607 | |||||||
| chr5:180015619 | G | GGAAAGGA others(26): Show |
1 | a0001c0003t0001g0176 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.443-2309_443-2308i others(35): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015619 | |||||||
| chr5:180015619 | G | GGAAAGGA others(27): Show |
38 | a0001c0001t0001g0328 a0001c0002t0001g0051 a0001c0002t0001g0096 others(35): Show |
42 | HG00280.hp2 HG00738.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.443-2309_443-2308i others(36): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015619 | |||||||
| chr5:180015619 | G | GGAAAGGA others(74): Show |
1 | a0001c0002t0002g0132 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.443-2309_443-2308i others(83): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015619 | |||||||
| chr5:180015619 | G | GGGAAAGG others(4): Show |
1 | a0001c0003t0001g0151 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.443-2319_443-2309d others(13): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015619 | |||||||
| chr5:180015619 | G | GGGAAAGG others(39): Show |
7 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(4): Show |
7 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.443-2309_443-2308i others(48): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015619 | |||||||
| chr5:180015631 | G | GGAAAGGA others(15): Show |
1 | a0001c0001t0001g0296 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.443-2321_443-2320i others(24): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015631 | |||||||
| chr5:180015631 | G | GGAAAGGA others(27): Show |
59 | a0001c0001t0001g0005 a0001c0001t0001g0250 a0001c0001t0001g0251 others(56): Show |
61 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.443-2321_443-2320i others(36): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015631 | |||||||
| chr5:180015643 | G | GGGAAAGG others(62): Show |
1 | a0001c0002t0001g0117 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.443-2333_443-2332i others(71): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015643 | |||||||
| chr5:180015643 | GGGAAAGG others(4): Show |
G | 1 | a0001c0001t0001g0312 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.443-2343_443-2333d others(13): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015643 | |||||||
| chr5:180015654 | A | AG | 61 | a0001c0001t0001g0005 a0001c0001t0001g0250 a0001c0001t0001g0251 others(58): Show |
63 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.443-2344dupC | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015654 | |||||||
| chr5:180015654 | A | AGGAAAGG others(17): Show |
1 | a0001c0001t0001g0252 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.443-2344_443-2343i others(26): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015654 | |||||||
| chr5:180015741 | G | A | 1 | a0001c0003t0001g0186 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.443-2430C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015741 | |||||||
| chr5:180015746 | A | AGGAAAGG others(5): Show |
276 | a0001c0001t0001g0005 a0001c0001t0001g0199 a0001c0001t0001g0201 others(273): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.443-2447_443-2436d others(14): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015746 | |||||||
| chr5:180015776 | G | GGAGTAGG others(5): Show |
1 | a0001c0001t0001g0238 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.443-2466_443-2465i others(14): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015776 | |||||||
| chr5:180015840 | G | C | 1 | a0001c0007t0001g0008 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.443-2529C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015840 | |||||||
| chr5:180015987 | T | G | 1 | a0001c0001t0001g0303 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.443-2676A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180015987 | |||||||
| chr5:180016133 | C | T | 218 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0202 others(215): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.443-2822G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180016133 | |||||||
| chr5:180016156 | A | AAGGACTG others(1385): Show |
1 | a0001c0001t0001g0261 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.443-2846_443-2845i others(1394): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180016156 | |||||||
| chr5:180016190 | G | T | 51 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(48): Show |
53 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.443-2879C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180016190 | |||||||
| chr5:180016342 | T | TAAGGAGG others(6): Show |
1 | a0001c0001t0001g0325 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.443-3032_443-3031i others(15): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180016342 | |||||||
| chr5:180016342 | T | TCAGGAGG others(6): Show |
274 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0199 others(271): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.443-3032_443-3031i others(15): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180016342 | |||||||
| chr5:180016379 | C | T | 3 | a0001c0002t0001g0030 a0001c0002t0001g0133 a0002c0010t0001g0031 |
3 | HG01243.hp2 HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.443-3068G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180016379 | |||||||
| chr5:180016423 | C | T | 51 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(48): Show |
53 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.443-3112G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180016423 | |||||||
| chr5:180016563 | G | A | 48 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(45): Show |
48 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(45): Show |
intron_variant | MODIFIER | c.443-3252C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180016563 | |||||||
| chr5:180016603 | T | C | 1 | a0001c0001t0001g0323 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.443-3292A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180016603 | |||||||
| chr5:180016630 | T | G | 1 | a0001c0002t0001g0114 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.443-3319A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180016630 | |||||||
| chr5:180016664 | T | C | 8 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(5): Show |
8 | HG02572.hp2 HG02809.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.443-3353A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180016664 | |||||||
| chr5:180016888 | G | A | 1 | a0001c0001t0001g0237 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.443-3577C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180016888 | |||||||
| chr5:180016929 | A | G | 1 | a0001c0001t0001g0323 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.443-3618T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180016929 | |||||||
| chr5:180016956 | C | G | 1 | a0001c0002t0001g0100 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.443-3645G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180016956 | |||||||
| chr5:180017079 | T | C | 1 | a0001c0001t0001g0323 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.443-3768A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180017079 | |||||||
| chr5:180017267 | C | T | 269 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0199 others(266): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.443-3956G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180017267 | |||||||
| chr5:180017271 | T | A | 1 | a0001c0002t0001g0127 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.443-3960A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180017271 | |||||||
| chr5:180017395 | T | C | 217 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0202 others(214): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.443-4084A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180017395 | |||||||
| chr5:180017413 | C | T | 1 | a0001c0002t0001g0099 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.443-4102G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180017413 | |||||||
| chr5:180017783 | C | G | 1 | a0001c0001t0001g0330 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.443-4472G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180017783 | |||||||
| chr5:180018029 | T | C | 8 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(5): Show |
8 | HG02572.hp2 HG02809.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.443-4718A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180018029 | |||||||
| chr5:180018248 | C | T | 275 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0199 others(272): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.443-4937G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180018248 | |||||||
| chr5:180018294 | C | T | 1 | a0001c0001t0001g0267 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.443-4983G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180018294 | |||||||
| chr5:180018294 | CA | C | 263 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0199 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.443-4984delT | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180018294 | |||||||
| chr5:180018617 | C | T | 1 | a0001c0002t0001g0010 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.443-5306G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180018617 | |||||||
| chr5:180018711 | C | T | 1 | a0001c0001t0001g0293 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.443-5400G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180018711 | |||||||
| chr5:180018751 | T | C | 4 | a0001c0003t0001g0157 a0001c0003t0002g0155 a0001c0003t0002g0156 others(1): Show |
4 | HG01884.hp2 HG02280.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.443-5440A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180018751 | |||||||
| chr5:180018797 | T | C | 329 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(326): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.443-5486A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180018797 | |||||||
| chr5:180018907 | C | A | 1 | a0001c0002t0001g0101 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.443-5596G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180018907 | |||||||
| chr5:180018908 | A | G | 1 | a0001c0002t0001g0101 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.443-5597T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180018908 | |||||||
| chr5:180018909 | G | A | 1 | a0001c0002t0001g0101 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.443-5598C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180018909 | |||||||
| chr5:180019052 | G | A | 1 | a0001c0003t0001g0152 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.443-5741C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180019052 | |||||||
| chr5:180019189 | CCTGA | C | 218 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0202 others(215): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.443-5882_443-5879d others(6): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180019189 | |||||||
| chr5:180019251 | G | T | 82 | a0001c0002t0001g0009 a0001c0002t0001g0011 a0001c0002t0001g0012 others(79): Show |
82 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.443-5940C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180019251 | |||||||
| chr5:180019277 | G | A | 7 | a0001c0001t0001g0237 a0001c0001t0001g0244 a0001c0001t0001g0245 others(4): Show |
7 | HG02055.hp2 HG02257.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.443-5966C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180019277 | |||||||
| chr5:180019363 | G | A | 6 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0214 others(3): Show |
6 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.443-6052C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180019363 | |||||||
| chr5:180019371 | G | A | 218 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0202 others(215): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.443-6060C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180019371 | |||||||
| chr5:180019383 | C | CA | 49 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(46): Show |
49 | HG00639.hp2 HG01123.hp1 HG01361.hp1 others(46): Show |
intron_variant | MODIFIER | c.443-6073dupT | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180019383 | |||||||
| chr5:180019383 | CA | C | 9 | a0001c0001t0001g0250 a0001c0001t0001g0325 a0001c0001t0001g0326 others(6): Show |
9 | HG02004.hp2 HG02083.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.443-6073delT | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180019383 | |||||||
| chr5:180019468 | A | G | 1 | a0001c0001t0001g0325 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.443-6157T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180019468 | |||||||
| chr5:180019500 | G | A | 49 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(46): Show |
49 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(46): Show |
intron_variant | MODIFIER | c.443-6189C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180019500 | |||||||
| chr5:180019857 | C | G | 1 | a0001c0001t0001g0250 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.443-6546G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180019857 | |||||||
| chr5:180020200 | C | A | 269 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0199 others(266): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.443-6889G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180020200 | |||||||
| chr5:180020221 | C | T | 4 | a0001c0003t0001g0167 a0001c0003t0001g0170 a0001c0003t0001g0173 others(1): Show |
4 | HG01943.hp1 HG02559.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.443-6910G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180020221 | |||||||
| chr5:180020255 | G | A | 3 | a0001c0002t0001g0116 a0001c0002t0001g0117 a0001c0002t0001g0118 |
3 | HG00735.hp2 HG01361.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.443-6944C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180020255 | |||||||
| chr5:180020307 | G | C | 1 | a0001c0002t0001g0101 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.443-6996C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180020307 | |||||||
| chr5:180020310 | A | G | 1 | a0001c0002t0001g0101 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.443-6999T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180020310 | |||||||
| chr5:180020335 | A | C | 2 | a0001c0001t0001g0277 a0001c0001t0001g0280 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.443-7024T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180020335 | |||||||
| chr5:180020456 | C | T | 1 | a0001c0001t0001g0328 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.443-7145G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180020456 | |||||||
| chr5:180020528 | C | T | 6 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(3): Show |
6 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.443-7217G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180020528 | |||||||
| chr5:180020569 | G | T | 1 | a0004c0009t0001g0014 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.443-7258C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180020569 | |||||||
| chr5:180020659 | C | T | 1 | a0001c0002t0001g0046 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.443-7348G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180020659 | |||||||
| chr5:180020661 | A | T | 51 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(48): Show |
53 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.443-7350T>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180020661 | |||||||
| chr5:180020755 | A | C | 218 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0202 others(215): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.443-7444T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180020755 | |||||||
| chr5:180020888 | C | T | 1 | a0001c0003t0002g0155 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.443-7577G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180020888 | |||||||
| chr5:180020965 | T | C | 1 | a0001c0002t0001g0036 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.443-7654A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180020965 | |||||||
| chr5:180021042 | C | CGCAATCT others(9): Show |
269 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0199 others(266): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.443-7732_443-7731i others(18): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180021042 | |||||||
| chr5:180021057 | G | C | 271 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0199 others(268): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.443-7746C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180021057 | |||||||
| chr5:180021103 | T | C | 1 | a0001c0002t0001g0056 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.443-7792A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180021103 | |||||||
| chr5:180021329 | T | C | 1 | a0001c0001t0001g0295 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.443-8018A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180021329 | |||||||
| chr5:180021737 | C | A | 1 | a0001c0002t0001g0134 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.443-8426G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180021737 | |||||||
| chr5:180021742 | G | A | 1 | a0001c0002t0001g0011 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.443-8431C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180021742 | |||||||
| chr5:180021833 | T | A | 1 | a0001c0001t0001g0323 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.443-8522A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180021833 | |||||||
| chr5:180021857 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.443-8546G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180021857 | |||||||
| chr5:180021891 | G | T | 6 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(3): Show |
6 | HG02572.hp2 HG02922.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.443-8580C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180021891 | |||||||
| chr5:180022010 | C | G | 4 | a0001c0003t0001g0157 a0001c0003t0002g0155 a0001c0003t0002g0156 others(1): Show |
4 | HG01884.hp2 HG02280.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.443-8699G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180022010 | |||||||
| chr5:180022105 | T | A | 1 | a0001c0002t0001g0086 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.443-8794A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180022105 | |||||||
| chr5:180022121 | C | A | 13 | a0001c0001t0001g0006 a0001c0001t0001g0200 a0001c0001t0001g0301 others(10): Show |
14 | HG00438.hp2 HG02135.hp1 HG03654.hp2 others(11): Show |
intron_variant | MODIFIER | c.443-8810G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180022121 | |||||||
| chr5:180022370 | C | T | 3 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0001g0317 |
3 | HG00544.hp1 HG02074.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.443-9059G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180022370 | |||||||
| chr5:180022480 | C | T | 1 | a0001c0001t0001g0204 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.443-9169G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180022480 | |||||||
| chr5:180022534 | A | G | 1 | a0001c0002t0001g0102 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.443-9223T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180022534 | |||||||
| chr5:180022902 | G | A | 7 | a0001c0002t0001g0096 a0001c0003t0001g0003 a0001c0003t0001g0174 others(4): Show |
8 | HG01256.hp1 HG01928.hp1 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.443-9591C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180022902 | |||||||
| chr5:180023080 | G | A | 119 | a0001c0001t0001g0199 a0001c0002t0001g0009 a0001c0002t0001g0010 others(116): Show |
119 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.443-9769C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180023080 | |||||||
| chr5:180023252 | G | A | 1 | a0004c0009t0001g0014 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.443-9941C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180023252 | |||||||
| chr5:180023267 | G | A | 1 | a0001c0001t0001g0323 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.443-9956C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180023267 | |||||||
| chr5:180023540 | A | C | 1 | a0001c0002t0001g0101 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.443-10229T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180023540 | |||||||
| chr5:180023544 | C | A | 1 | a0001c0002t0001g0101 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.443-10233G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180023544 | |||||||
| chr5:180023544 | C | T | 1 | a0001c0001t0001g0323 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.443-10233G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180023544 | |||||||
| chr5:180023545 | A | C | 1 | a0001c0002t0001g0101 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.443-10234T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180023545 | |||||||
| chr5:180023814 | T | C | 1 | a0001c0001t0001g0274 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.443-10503A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180023814 | |||||||
| chr5:180023851 | G | A | 269 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0199 others(266): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.443-10540C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180023851 | |||||||
| chr5:180023882 | A | C | 1 | a0001c0001t0001g0205 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.443-10571T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180023882 | |||||||
| chr5:180024222 | G | A | 2 | a0001c0001t0001g0329 a0001c0001t0001g0330 |
2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.443-10911C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180024222 | |||||||
| chr5:180024532 | C | T | 6 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(3): Show |
6 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.443-11221G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180024532 | |||||||
| chr5:180024632 | A | G | 3 | a0001c0003t0001g0174 a0001c0003t0001g0175 a0001c0003t0001g0183 |
3 | HG01256.hp1 HG01928.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.443-11321T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180024632 | |||||||
| chr5:180024750 | T | C | 1 | a0001c0001t0001g0303 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.443-11439A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180024750 | |||||||
| chr5:180024772 | G | A | 1 | a0001c0002t0001g0092 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.443-11461C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180024772 | |||||||
| chr5:180024899 | T | C | 5 | a0001c0002t0001g0022 a0001c0002t0001g0023 a0001c0002t0001g0024 others(2): Show |
5 | NA18948.hp2 NA18970.hp1 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.443-11588A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180024899 | |||||||
| chr5:180024983 | C | G | 1 | a0001c0001t0001g0262 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.443-11672G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180024983 | |||||||
| chr5:180025256 | C | T | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG02145.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.443-11945G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180025256 | |||||||
| chr5:180025260 | G | A | 1 | a0001c0002t0001g0090 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.443-11949C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180025260 | |||||||
| chr5:180025523 | C | T | 12 | a0001c0001t0001g0204 a0001c0001t0001g0211 a0001c0001t0001g0212 others(9): Show |
12 | HG02451.hp2 HG02717.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.443-12212G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180025523 | |||||||
| chr5:180025549 | T | C | 64 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(61): Show |
70 | HG00280.hp2 HG00438.hp2 HG00673.hp1 others(67): Show |
intron_variant | MODIFIER | c.443-12238A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180025549 | |||||||
| chr5:180026077 | A | C | 24 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0001g0303 others(21): Show |
24 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(21): Show |
intron_variant | MODIFIER | c.443-12766T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180026077 | |||||||
| chr5:180026117 | CA | C | 48 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(45): Show |
48 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(45): Show |
intron_variant | MODIFIER | c.443-12807delT | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180026117 | |||||||
| chr5:180026271 | A | T | 1 | a0001c0003t0001g0194 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.443-12960T>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180026271 | |||||||
| chr5:180026403 | G | A | 49 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(46): Show |
49 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(46): Show |
intron_variant | MODIFIER | c.443-13092C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180026403 | |||||||
| chr5:180026680 | T | C | 52 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(49): Show |
54 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.443-13369A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180026680 | |||||||
| chr5:180026733 | C | G | 1 | a0001c0002t0001g0063 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.443-13422G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180026733 | |||||||
| chr5:180026736 | T | C | 1 | a0001c0003t0001g0162 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.443-13425A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180026736 | |||||||
| chr5:180026793 | C | A | 1 | a0001c0004t0005g0142 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.443-13482G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180026793 | |||||||
| chr5:180027428 | G | A | 245 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0199 others(242): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.442+13025C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180027428 | |||||||
| chr5:180027508 | T | C | 64 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(61): Show |
70 | HG00280.hp2 HG00438.hp2 HG00673.hp1 others(67): Show |
intron_variant | MODIFIER | c.442+12945A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180027508 | |||||||
| chr5:180027656 | C | T | 24 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0001g0303 others(21): Show |
24 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(21): Show |
intron_variant | MODIFIER | c.442+12797G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180027656 | |||||||
| chr5:180027670 | G | A | 1 | a0001c0002t0001g0133 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.442+12783C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180027670 | |||||||
| chr5:180027856 | C | T | 4 | a0001c0003t0001g0158 a0001c0003t0001g0160 a0001c0003t0001g0161 others(1): Show |
4 | HG02451.hp1 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.442+12597G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180027856 | |||||||
| chr5:180028067 | G | A | 1 | a0001c0002t0001g0073 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.442+12386C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180028067 | |||||||
| chr5:180028414 | C | T | 1 | a0001c0002t0001g0133 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.442+12039G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180028414 | |||||||
| chr5:180028562 | AGAAC | A | 218 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0202 others(215): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.442+11887_442+1189 others(8): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180028562 | |||||||
| chr5:180028601 | C | T | 2 | a0001c0001t0001g0327 a0001c0001t0001g0331 |
2 | HG02258.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.442+11852G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180028601 | |||||||
| chr5:180028752 | A | G | 1 | a0001c0005t0001g0195 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.442+11701T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180028752 | |||||||
| chr5:180028773 | G | A | 3 | a0001c0002t0001g0101 a0001c0002t0001g0102 a0001c0002t0001g0103 |
3 | NA18979.hp1 NA19079.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.442+11680C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180028773 | |||||||
| chr5:180028852 | A | G | 218 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0202 others(215): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.442+11601T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180028852 | |||||||
| chr5:180028967 | A | G | 1 | a0001c0007t0001g0008 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.442+11486T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180028967 | |||||||
| chr5:180029155 | A | G | 269 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0199 others(266): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.442+11298T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180029155 | |||||||
| chr5:180029289 | C | T | 4 | a0001c0001t0001g0325 a0001c0001t0001g0326 a0001c0001t0001g0327 others(1): Show |
4 | HG02258.hp1 HG02809.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.442+11164G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180029289 | |||||||
| chr5:180029483 | A | G | 1 | a0001c0002t0001g0134 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.442+10970T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180029483 | |||||||
| chr5:180029531 | A | G | 1 | a0001c0001t0001g0323 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.442+10922T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180029531 | |||||||
| chr5:180029852 | C | CT | 138 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(135): Show |
144 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.442+10600dupA | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180029852 | |||||||
| chr5:180029852 | C | CTT | 128 | a0001c0001t0001g0199 a0001c0001t0001g0229 a0001c0001t0001g0237 others(125): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.442+10599_442+1060 others(6): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180029852 | |||||||
| chr5:180030040 | G | GA | 244 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0199 others(241): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.442+10412_442+1041 others(5): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180030040 | |||||||
| chr5:180030108 | G | C | 4 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0265 others(1): Show |
4 | HG02132.hp2 NA18955.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.442+10345C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180030108 | |||||||
| chr5:180030177 | T | C | 6 | a0001c0001t0001g0329 a0001c0001t0001g0330 a0001c0003t0001g0157 others(3): Show |
6 | HG01884.hp2 HG02280.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.442+10276A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180030177 | |||||||
| chr5:180030223 | G | T | 1 | a0001c0002t0001g0030 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.442+10230C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180030223 | |||||||
| chr5:180030505 | C | T | 1 | a0001c0003t0001g0170 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.442+9948G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180030505 | |||||||
| chr5:180030643 | G | T | 6 | a0001c0002t0001g0022 a0001c0002t0001g0023 a0001c0002t0001g0024 others(3): Show |
6 | HG03710.hp1 NA18948.hp2 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.442+9810C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180030643 | |||||||
| chr5:180030818 | C | A | 1 | a0001c0003t0002g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.442+9635G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180030818 | |||||||
| chr5:180030898 | C | T | 203 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0199 others(200): Show |
205 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.442+9555G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180030898 | |||||||
| chr5:180031009 | T | C | 24 | a0001c0001t0001g0299 a0001c0001t0001g0300 a0001c0001t0001g0303 others(21): Show |
24 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(21): Show |
intron_variant | MODIFIER | c.442+9444A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180031009 | |||||||
| chr5:180031026 | A | G | 5 | a0001c0002t0001g0022 a0001c0002t0001g0023 a0001c0002t0001g0024 others(2): Show |
5 | NA18948.hp2 NA18970.hp1 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.442+9427T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180031026 | |||||||
| chr5:180031072 | C | G | 1 | a0001c0001t0001g0296 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.442+9381G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180031072 | |||||||
| chr5:180031147 | C | T | 1 | a0001c0002t0001g0104 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.442+9306G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180031147 | |||||||
| chr5:180031170 | T | C | 1 | a0001c0003t0002g0156 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.442+9283A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180031170 | |||||||
| chr5:180031395 | G | T | 1 | a0001c0001t0001g0208 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.442+9058C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180031395 | |||||||
| chr5:180031527 | C | T | 162 | a0001c0001t0001g0199 a0001c0001t0001g0325 a0001c0001t0001g0326 others(159): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.442+8926G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180031527 | |||||||
| chr5:180031579 | T | C | 4 | a0001c0002t0001g0045 a0001c0002t0001g0120 a0001c0002t0001g0121 others(1): Show |
4 | HG00099.hp2 HG00642.hp2 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.442+8874A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180031579 | |||||||
| chr5:180031665 | C | T | 162 | a0001c0001t0001g0199 a0001c0001t0001g0325 a0001c0001t0001g0326 others(159): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.442+8788G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180031665 | |||||||
| chr5:180031761 | G | C | 56 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(53): Show |
56 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(53): Show |
intron_variant | MODIFIER | c.442+8692C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180031761 | |||||||
| chr5:180031847 | G | A | 162 | a0001c0001t0001g0199 a0001c0001t0001g0325 a0001c0001t0001g0326 others(159): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.442+8606C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180031847 | |||||||
| chr5:180031913 | T | C | 1 | a0001c0002t0002g0132 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.442+8540A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180031913 | |||||||
| chr5:180031940 | T | A | 56 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(53): Show |
56 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(53): Show |
intron_variant | MODIFIER | c.442+8513A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180031940 | |||||||
| chr5:180032027 | T | C | 1 | a0001c0002t0001g0134 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.442+8426A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180032027 | |||||||
| chr5:180032204 | G | C | 2 | a0001c0002t0001g0012 a0001c0002t0001g0013 |
2 | HG02165.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.442+8249C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180032204 | |||||||
| chr5:180032287 | A | G | 51 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(48): Show |
53 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.442+8166T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180032287 | |||||||
| chr5:180032291 | T | C | 1 | a0001c0003t0002g0156 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.442+8162A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180032291 | |||||||
| chr5:180032323 | A | G | 1 | a0001c0001t0001g0304 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.442+8130T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180032323 | |||||||
| chr5:180032735 | G | A | 1 | a0001c0003t0001g0162 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.442+7718C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180032735 | |||||||
| chr5:180032895 | T | A | 4 | a0001c0003t0001g0157 a0001c0003t0002g0155 a0001c0003t0002g0156 others(1): Show |
4 | HG01884.hp2 HG02280.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.442+7558A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180032895 | |||||||
| chr5:180032928 | A | G | 4 | a0001c0003t0001g0158 a0001c0003t0001g0160 a0001c0003t0001g0161 others(1): Show |
4 | HG02451.hp1 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.442+7525T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180032928 | |||||||
| chr5:180032933 | G | A | 5 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0287 others(2): Show |
5 | HG00733.hp1 HG01106.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.442+7520C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180032933 | |||||||
| chr5:180032965 | T | C | 10 | a0001c0004t0001g0002 a0001c0004t0001g0135 a0001c0004t0001g0136 others(7): Show |
11 | HG02293.hp2 HG03834.hp2 NA18951.hp1 others(8): Show |
intron_variant | MODIFIER | c.442+7488A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180032965 | |||||||
| chr5:180033006 | G | A | 4 | a0001c0003t0001g0158 a0001c0003t0001g0160 a0001c0003t0001g0161 others(1): Show |
4 | HG02451.hp1 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.442+7447C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180033006 | |||||||
| chr5:180033020 | C | A | 1 | a0001c0001t0001g0291 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.442+7433G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180033020 | |||||||
| chr5:180033026 | T | C | 1 | a0001c0001t0001g0266 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.442+7427A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180033026 | |||||||
| chr5:180033155 | ATTTTTTT | A | 5 | a0001c0003t0001g0004 a0001c0003t0001g0152 a0001c0003t0001g0168 others(2): Show |
6 | HG00280.hp2 HG01081.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.442+7291_442+7297d others(9): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180033155 | |||||||
| chr5:180033471 | C | T | 1 | a0001c0002t0001g0030 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.442+6982G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180033471 | |||||||
| chr5:180033552 | T | C | 1 | a0001c0001t0001g0219 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.442+6901A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180033552 | |||||||
| chr5:180033563 | G | A | 3 | a0001c0001t0001g0245 a0001c0001t0001g0247 a0001c0001t0001g0249 |
3 | HG02257.hp2 HG02896.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.442+6890C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180033563 | |||||||
| chr5:180033582 | C | T | 1 | a0001c0001t0001g0265 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.442+6871G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180033582 | |||||||
| chr5:180033696 | TA | T | 268 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0199 others(265): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.442+6756delT | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180033696 | |||||||
| chr5:180033773 | CTTGT | C | 125 | a0001c0001t0001g0199 a0001c0001t0001g0325 a0001c0001t0001g0326 others(122): Show |
125 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.442+6676_442+6679d others(6): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180033773 | |||||||
| chr5:180033791 | T | A | 82 | a0001c0002t0001g0009 a0001c0002t0001g0011 a0001c0002t0001g0012 others(79): Show |
82 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.442+6662A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180033791 | |||||||
| chr5:180033936 | A | G | 5 | a0001c0001t0001g0325 a0001c0001t0001g0326 a0001c0001t0001g0327 others(2): Show |
5 | HG02258.hp1 HG02809.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.442+6517T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180033936 | |||||||
| chr5:180033968 | T | A | 51 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(48): Show |
53 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.442+6485A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180033968 | |||||||
| chr5:180034037 | G | A | 2 | a0001c0001t0001g0329 a0001c0001t0001g0330 |
2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.442+6416C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180034037 | |||||||
| chr5:180034093 | C | CT | 119 | a0001c0001t0001g0199 a0001c0002t0001g0009 a0001c0002t0001g0010 others(116): Show |
119 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.442+6359dupA | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180034093 | |||||||
| chr5:180034093 | C | T | 8 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(5): Show |
8 | HG02572.hp2 HG02809.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.442+6360G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180034093 | |||||||
| chr5:180034203 | T | TA | 23 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0204 others(20): Show |
23 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.442+6249dupT | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180034203 | |||||||
| chr5:180034258 | A | G | 1 | a0001c0003t0001g0184 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.442+6195T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180034258 | |||||||
| chr5:180034270 | T | G | 1 | a0001c0005t0001g0195 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.442+6183A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180034270 | |||||||
| chr5:180034313 | G | A | 48 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(45): Show |
48 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(45): Show |
intron_variant | MODIFIER | c.442+6140C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180034313 | |||||||
| chr5:180034591 | G | GTTCAT | 269 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0199 others(266): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.442+5857_442+5861d others(7): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180034591 | |||||||
| chr5:180034662 | C | T | 1 | a0001c0002t0001g0013 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.442+5791G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180034662 | |||||||
| chr5:180034812 | T | C | 1 | a0001c0001t0001g0261 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.442+5641A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180034812 | |||||||
| chr5:180034835 | C | T | 10 | a0001c0001t0001g0203 a0001c0001t0001g0220 a0001c0001t0001g0227 others(7): Show |
10 | HG00639.hp2 HG01123.hp1 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.442+5618G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180034835 | |||||||
| chr5:180034836 | A | G | 1 | a0001c0001t0001g0323 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.442+5617T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180034836 | |||||||
| chr5:180034837 | T | C | 10 | a0001c0002t0001g0096 a0001c0003t0001g0003 a0001c0003t0001g0174 others(7): Show |
11 | HG01256.hp1 HG01361.hp2 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.442+5616A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180034837 | |||||||
| chr5:180034974 | G | C | 4 | a0001c0003t0001g0167 a0001c0003t0001g0170 a0001c0003t0001g0173 others(1): Show |
4 | HG01943.hp1 HG02559.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.442+5479C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180034974 | |||||||
| chr5:180035073 | C | T | 1 | a0001c0001t0001g0251 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.442+5380G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180035073 | |||||||
| chr5:180035233 | C | T | 3 | a0001c0003t0001g0188 a0001c0003t0001g0189 a0001c0003t0001g0190 |
3 | HG01243.hp1 HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.442+5220G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180035233 | |||||||
| chr5:180035635 | T | C | 1 | a0001c0007t0001g0008 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.442+4818A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180035635 | |||||||
| chr5:180035693 | G | C | 1 | a0001c0001t0001g0323 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.442+4760C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180035693 | |||||||
| chr5:180035801 | C | T | 33 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(30): Show |
33 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.442+4652G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180035801 | |||||||
| chr5:180036038 | T | C | 5 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0214 others(2): Show |
5 | HG01891.hp2 HG02145.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.442+4415A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180036038 | |||||||
| chr5:180036057 | A | G | 2 | a0001c0001t0001g0329 a0001c0001t0001g0330 |
2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.442+4396T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180036057 | |||||||
| chr5:180036074 | C | G | 1 | a0001c0001t0001g0309 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.442+4379G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180036074 | |||||||
| chr5:180036153 | T | A | 1 | a0001c0001t0001g0316 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.442+4300A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180036153 | |||||||
| chr5:180036627 | T | A | 1 | a0001c0002t0001g0067 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.442+3826A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180036627 | |||||||
| chr5:180036756 | CA | C | 51 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(48): Show |
53 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.442+3696delT | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180036756 | |||||||
| chr5:180036825 | G | C | 1 | a0001c0002t0001g0067 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.442+3628C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180036825 | |||||||
| chr5:180036836 | C | A | 51 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(48): Show |
53 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.442+3617G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180036836 | |||||||
| chr5:180036845 | TAAGA | T | 269 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0199 others(266): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.442+3604_442+3607d others(6): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180036845 | |||||||
| chr5:180036899 | T | C | 27 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(24): Show |
29 | HG00438.hp2 HG00673.hp1 HG01169.hp2 others(26): Show |
intron_variant | MODIFIER | c.442+3554A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180036899 | |||||||
| chr5:180037076 | G | A | 37 | a0001c0001t0001g0328 a0001c0002t0001g0096 a0001c0003t0001g0001 others(34): Show |
41 | HG00280.hp2 HG00738.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.442+3377C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180037076 | |||||||
| chr5:180037255 | G | A | 1 | a0001c0002t0001g0050 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.442+3198C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180037255 | |||||||
| chr5:180037449 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.442+3004G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180037449 | |||||||
| chr5:180037728 | G | T | 1 | a0001c0002t0001g0108 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.442+2725C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180037728 | |||||||
| chr5:180038247 | GTC | G | 50 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(47): Show |
52 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.442+2204_442+2205d others(4): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180038247 | |||||||
| chr5:180038380 | C | T | 1 | a0001c0003t0002g0155 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.442+2073G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180038380 | |||||||
| chr5:180038385 | AG | A | 10 | a0001c0002t0001g0096 a0001c0003t0001g0003 a0001c0003t0001g0174 others(7): Show |
11 | HG01256.hp1 HG01361.hp2 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.442+2067delC | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180038385 | |||||||
| chr5:180038390 | GAA | G | 51 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(48): Show |
53 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.442+2061_442+2062d others(4): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180038390 | |||||||
| chr5:180038403 | C | G | 1 | a0001c0002t0001g0129 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.442+2050G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180038403 | |||||||
| chr5:180038406 | G | GT | 3 | a0001c0003t0001g0148 a0001c0003t0001g0184 a0001c0003t0001g0194 |
3 | HG01261.hp1 HG01952.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.442+2046dupA | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180038406 | |||||||
| chr5:180038410 | TG | T | 160 | a0001c0001t0001g0199 a0001c0001t0001g0325 a0001c0001t0001g0326 others(157): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.442+2042delC | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180038410 | |||||||
| chr5:180038411 | G | GT | 12 | a0001c0001t0001g0204 a0001c0001t0001g0211 a0001c0001t0001g0212 others(9): Show |
12 | HG02451.hp2 HG02486.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.442+2041dupA | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180038411 | |||||||
| chr5:180038411 | G | T | 53 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(50): Show |
55 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.442+2042C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180038411 | |||||||
| chr5:180038418 | T | A | 1 | a0001c0002t0001g0042 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.442+2035A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180038418 | |||||||
| chr5:180038469 | A | G | 3 | a0001c0002t0001g0030 a0001c0002t0001g0133 a0002c0010t0001g0031 |
3 | HG01243.hp2 HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.442+1984T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180038469 | |||||||
| chr5:180038470 | C | T | 269 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0199 others(266): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.442+1983G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180038470 | |||||||
| chr5:180038486 | C | T | 37 | a0001c0001t0001g0328 a0001c0002t0001g0096 a0001c0003t0001g0001 others(34): Show |
41 | HG00280.hp2 HG00738.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.442+1967G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180038486 | |||||||
| chr5:180038607 | G | A | 1 | a0001c0001t0001g0264 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.442+1846C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180038607 | |||||||
| chr5:180038629 | C | T | 1 | a0001c0002t0001g0104 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.442+1824G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180038629 | |||||||
| chr5:180038678 | G | A | 2 | a0001c0001t0001g0302 a0001c0001t0001g0318 |
2 | HG00673.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.442+1775C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180038678 | |||||||
| chr5:180038776 | T | G | 5 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0214 others(2): Show |
5 | HG01891.hp2 HG02145.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.442+1677A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180038776 | |||||||
| chr5:180038922 | T | G | 1 | a0001c0005t0001g0195 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.442+1531A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180038922 | |||||||
| chr5:180039044 | T | C | 4 | a0001c0003t0001g0157 a0001c0003t0002g0155 a0001c0003t0002g0156 others(1): Show |
4 | HG01884.hp2 HG02280.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.442+1409A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180039044 | |||||||
| chr5:180039263 | G | T | 1 | a0002c0010t0001g0031 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.442+1190C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180039263 | |||||||
| chr5:180039428 | G | C | 1 | a0001c0001t0001g0202 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.442+1025C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180039428 | |||||||
| chr5:180039502 | T | C | 48 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(45): Show |
50 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.442+951A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180039502 | |||||||
| chr5:180039611 | C | A | 3 | a0001c0002t0001g0116 a0001c0002t0001g0117 a0001c0002t0001g0118 |
3 | HG00735.hp2 HG01361.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.442+842G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180039611 | |||||||
| chr5:180039673 | T | A | 3 | a0001c0003t0001g0157 a0001c0003t0002g0155 a0001c0003t0002g0156 |
3 | HG01884.hp2 HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.442+780A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180039673 | |||||||
| chr5:180039790 | A | G | 1 | a0001c0002t0001g0074 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.442+663T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180039790 | |||||||
| chr5:180039936 | G | C | 2 | a0001c0001t0001g0268 a0001c0001t0001g0269 |
2 | NA18950.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.442+517C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180039936 | |||||||
| chr5:180040334 | G | A | 1 | a0001c0002t0001g0097 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.442+119C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 2/8 | chr5 | 180040334 | |||||||
| chr5:180040721 | T | C | 5 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0214 others(2): Show |
5 | HG01891.hp2 HG02145.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.248-74A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180040721 | |||||||
| chr5:180040971 | C | T | 2 | a0001c0001t0001g0329 a0001c0001t0001g0330 |
2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.248-324G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180040971 | |||||||
| chr5:180041039 | C | T | 6 | a0001c0001t0001g0329 a0001c0001t0001g0330 a0001c0003t0001g0157 others(3): Show |
6 | HG01884.hp2 HG02280.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.248-392G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180041039 | |||||||
| chr5:180041234 | T | C | 2 | a0001c0001t0001g0294 a0001c0001t0001g0296 |
2 | HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.248-587A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180041234 | |||||||
| chr5:180041316 | G | A | 1 | a0001c0002t0001g0123 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.248-669C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180041316 | |||||||
| chr5:180041403 | G | A | 1 | a0001c0001t0001g0323 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.248-756C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180041403 | |||||||
| chr5:180041529 | TAAG | T | 48 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(45): Show |
48 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(45): Show |
intron_variant | MODIFIER | c.248-885_248-883del others(3): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180041529 | |||||||
| chr5:180041544 | G | A | 1 | a0001c0002t0001g0023 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.248-897C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180041544 | |||||||
| chr5:180041607 | CAGAAGGG others(3): Show |
C | 1 | a0001c0003t0001g0147 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.248-970_248-961del others(10): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180041607 | |||||||
| chr5:180041653 | C | T | 1 | a0001c0005t0001g0195 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.248-1006G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180041653 | |||||||
| chr5:180041672 | C | T | 5 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0287 others(2): Show |
5 | HG00733.hp1 HG01106.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.248-1025G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180041672 | |||||||
| chr5:180041851 | T | C | 1 | a0001c0001t0001g0323 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.248-1204A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180041851 | |||||||
| chr5:180041855 | T | C | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG02145.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.248-1208A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180041855 | |||||||
| chr5:180042094 | C | T | 1 | a0001c0002t0001g0066 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.248-1447G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180042094 | |||||||
| chr5:180042500 | T | C | 5 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0214 others(2): Show |
5 | HG01891.hp2 HG02145.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.248-1853A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180042500 | |||||||
| chr5:180042532 | T | C | 48 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(45): Show |
50 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.248-1885A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180042532 | |||||||
| chr5:180042600 | G | C | 3 | a0001c0001t0001g0220 a0001c0001t0001g0227 a0001c0001t0001g0228 |
3 | HG00639.hp2 HG01123.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.248-1953C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180042600 | |||||||
| chr5:180042612 | T | A | 2 | a0001c0002t0001g0028 a0001c0002t0001g0029 |
2 | NA18983.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.248-1965A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180042612 | |||||||
| chr5:180042646 | C | T | 2 | a0001c0001t0001g0329 a0001c0001t0001g0330 |
2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.248-1999G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180042646 | |||||||
| chr5:180043141 | A | T | 1 | a0001c0003t0001g0170 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.248-2494T>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180043141 | |||||||
| chr5:180043642 | A | G | 269 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0199 others(266): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.248-2995T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180043642 | |||||||
| chr5:180043682 | A | G | 1 | a0001c0001t0001g0238 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.248-3035T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180043682 | |||||||
| chr5:180043773 | G | C | 269 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0199 others(266): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.248-3126C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180043773 | |||||||
| chr5:180043914 | T | A | 1 | a0001c0001t0001g0242 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.248-3267A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180043914 | |||||||
| chr5:180043930 | A | G | 171 | a0001c0001t0001g0199 a0001c0001t0001g0325 a0001c0001t0001g0326 others(168): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.248-3283T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180043930 | |||||||
| chr5:180043967 | G | A | 1 | a0001c0001t0001g0270 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.248-3320C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180043967 | |||||||
| chr5:180044040 | G | A | 165 | a0001c0001t0001g0199 a0001c0001t0001g0325 a0001c0001t0001g0326 others(162): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.248-3393C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180044040 | |||||||
| chr5:180044145 | G | A | 165 | a0001c0001t0001g0199 a0001c0001t0001g0325 a0001c0001t0001g0326 others(162): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.248-3498C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180044145 | |||||||
| chr5:180044201 | C | T | 49 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(46): Show |
51 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.248-3554G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180044201 | |||||||
| chr5:180044272 | C | A | 1 | a0002c0010t0001g0031 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.248-3625G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180044272 | |||||||
| chr5:180044323 | A | G | 4 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0265 others(1): Show |
4 | HG02132.hp2 NA18955.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.248-3676T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180044323 | |||||||
| chr5:180044337 | C | T | 1 | a0001c0003t0002g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.248-3690G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180044337 | |||||||
| chr5:180044420 | G | A | 2 | a0001c0001t0001g0315 a0001c0001t0001g0320 |
2 | HG01169.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.248-3773C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180044420 | |||||||
| chr5:180044457 | G | A | 1 | a0001c0001t0001g0252 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.248-3810C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180044457 | |||||||
| chr5:180044532 | C | T | 2 | a0001c0001t0001g0329 a0001c0001t0001g0330 |
2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.248-3885G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180044532 | |||||||
| chr5:180044556 | G | A | 48 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(45): Show |
50 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.248-3909C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180044556 | |||||||
| chr5:180044600 | G | T | 1 | a0001c0002t0001g0093 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.248-3953C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180044600 | |||||||
| chr5:180044810 | C | T | 48 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(45): Show |
48 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(45): Show |
intron_variant | MODIFIER | c.248-4163G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180044810 | |||||||
| chr5:180044819 | T | C | 7 | a0001c0001t0001g0237 a0001c0001t0001g0244 a0001c0001t0001g0245 others(4): Show |
7 | HG02055.hp2 HG02257.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.248-4172A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180044819 | |||||||
| chr5:180045009 | G | C | 2 | a0001c0002t0001g0039 a0001c0002t0001g0041 |
2 | NA18989.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.248-4362C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180045009 | |||||||
| chr5:180045011 | G | A | 1 | a0001c0002t0001g0088 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.248-4364C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180045011 | |||||||
| chr5:180045187 | A | G | 269 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0199 others(266): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.248-4540T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180045187 | |||||||
| chr5:180045314 | G | A | 1 | a0001c0002t0001g0089 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.248-4667C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180045314 | |||||||
| chr5:180045316 | G | A | 2 | a0001c0004t0001g0135 a0001c0004t0001g0143 |
2 | NA18951.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.248-4669C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180045316 | |||||||
| chr5:180045324 | A | G | 1 | a0001c0002t0001g0124 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.248-4677T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180045324 | |||||||
| chr5:180045394 | C | T | 220 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0202 others(217): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.248-4747G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180045394 | |||||||
| chr5:180045498 | G | A | 5 | a0001c0001t0001g0292 a0001c0001t0001g0293 a0001c0001t0001g0294 others(2): Show |
5 | HG02486.hp1 HG02647.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.248-4851C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180045498 | |||||||
| chr5:180045586 | A | G | 1 | a0001c0002t0001g0034 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.248-4939T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180045586 | |||||||
| chr5:180045728 | A | G | 269 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0199 others(266): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.248-5081T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180045728 | |||||||
| chr5:180045943 | C | T | 1 | a0001c0002t0001g0095 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.248-5296G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180045943 | |||||||
| chr5:180045985 | C | T | 48 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(45): Show |
50 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.248-5338G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180045985 | |||||||
| chr5:180045992 | C | G | 1 | a0001c0002t0001g0068 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.248-5345G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180045992 | |||||||
| chr5:180046044 | G | A | 48 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(45): Show |
50 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.248-5397C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180046044 | |||||||
| chr5:180046115 | C | T | 1 | a0001c0001t0002g0243 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.248-5468G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180046115 | |||||||
| chr5:180046129 | G | A | 220 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0202 others(217): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.248-5482C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180046129 | |||||||
| chr5:180046161 | G | A | 2 | a0001c0002t0001g0015 a0001c0002t0001g0017 |
2 | HG01517.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.248-5514C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180046161 | |||||||
| chr5:180046207 | G | A | 1 | a0001c0002t0001g0098 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.248-5560C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180046207 | |||||||
| chr5:180046218 | A | T | 171 | a0001c0001t0001g0199 a0001c0001t0001g0325 a0001c0001t0001g0326 others(168): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.248-5571T>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180046218 | |||||||
| chr5:180046328 | G | A | 49 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(46): Show |
51 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.248-5681C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180046328 | |||||||
| chr5:180046346 | G | A | 220 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0202 others(217): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.248-5699C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180046346 | |||||||
| chr5:180046351 | C | T | 4 | a0001c0001t0001g0005 a0001c0001t0001g0255 a0001c0001t0001g0277 others(1): Show |
5 | HG02896.hp2 HG02897.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.248-5704G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180046351 | |||||||
| chr5:180046460 | G | C | 33 | a0001c0001t0001g0328 a0001c0002t0001g0096 a0001c0003t0001g0001 others(30): Show |
37 | HG00280.hp2 HG00738.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.248-5813C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180046460 | |||||||
| chr5:180046574 | T | G | 1 | a0001c0003t0002g0169 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.248-5927A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180046574 | |||||||
| chr5:180046604 | C | T | 1 | a0001c0003t0002g0155 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.248-5957G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180046604 | |||||||
| chr5:180046731 | T | G | 4 | a0001c0001t0001g0005 a0001c0001t0001g0255 a0001c0001t0001g0277 others(1): Show |
5 | HG02896.hp2 HG02897.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.248-6084A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180046731 | |||||||
| chr5:180046900 | G | A | 49 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(46): Show |
51 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.248-6253C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180046900 | |||||||
| chr5:180046915 | A | G | 1 | a0001c0002t0001g0035 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.248-6268T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180046915 | |||||||
| chr5:180047008 | TTC | T | 171 | a0001c0001t0001g0199 a0001c0001t0001g0325 a0001c0001t0001g0326 others(168): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.248-6363_248-6362d others(4): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180047008 | |||||||
| chr5:180047219 | T | C | 33 | a0001c0001t0001g0328 a0001c0002t0001g0096 a0001c0003t0001g0001 others(30): Show |
37 | HG00280.hp2 HG00738.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.248-6572A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180047219 | |||||||
| chr5:180047587 | A | G | 1 | a0001c0001t0002g0243 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.248-6940T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180047587 | |||||||
| chr5:180047637 | G | A | 49 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(46): Show |
51 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.248-6990C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180047637 | |||||||
| chr5:180047705 | C | T | 1 | a0001c0002t0001g0134 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.248-7058G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180047705 | |||||||
| chr5:180047768 | G | A | 1 | a0001c0001t0001g0323 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.248-7121C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180047768 | |||||||
| chr5:180047808 | C | T | 2 | a0001c0002t0001g0019 a0001c0002t0001g0020 |
2 | HG01516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.248-7161G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180047808 | |||||||
| chr5:180047864 | CCA | C | 3 | a0001c0002t0001g0030 a0001c0002t0001g0133 a0002c0010t0001g0031 |
3 | HG01243.hp2 HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.248-7219_248-7218d others(4): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180047864 | |||||||
| chr5:180047925 | C | T | 1 | a0001c0003t0001g0186 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.248-7278G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180047925 | |||||||
| chr5:180047975 | T | C | 269 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0199 others(266): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.248-7328A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180047975 | |||||||
| chr5:180048001 | C | CT | 246 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0199 others(243): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.248-7355dupA | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180048001 | |||||||
| chr5:180048001 | C | CTT | 17 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(14): Show |
17 | HG02055.hp2 HG02257.hp2 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.248-7356_248-7355d others(4): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180048001 | |||||||
| chr5:180048137 | G | T | 1 | a0001c0002t0001g0124 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.248-7490C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180048137 | |||||||
| chr5:180048165 | A | G | 2 | a0001c0001t0001g0307 a0001c0001t0001g0308 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.248-7518T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180048165 | |||||||
| chr5:180048239 | C | T | 220 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0202 others(217): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.248-7592G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180048239 | |||||||
| chr5:180048279 | G | A | 3 | a0001c0002t0001g0049 a0001c0002t0001g0050 a0001c0002t0001g0067 |
3 | HG00099.hp1 HG01109.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.248-7632C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180048279 | |||||||
| chr5:180048336 | G | A | 1 | a0001c0002t0001g0123 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.248-7689C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180048336 | |||||||
| chr5:180048403 | A | T | 8 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(5): Show |
8 | HG02572.hp2 HG02809.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.248-7756T>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180048403 | |||||||
| chr5:180048408 | A | G | 4 | a0001c0003t0001g0158 a0001c0003t0001g0160 a0001c0003t0001g0161 others(1): Show |
4 | HG02451.hp1 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.248-7761T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180048408 | |||||||
| chr5:180048500 | C | T | 1 | a0001c0002t0001g0124 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.248-7853G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180048500 | |||||||
| chr5:180048501 | G | A | 1 | a0001c0002t0001g0050 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.248-7854C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180048501 | |||||||
| chr5:180048527 | C | T | 3 | a0001c0001t0001g0220 a0001c0001t0001g0227 a0001c0001t0001g0228 |
3 | HG00639.hp2 HG01123.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.248-7880G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180048527 | |||||||
| chr5:180048644 | G | A | 1 | a0001c0002t0001g0108 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.248-7997C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180048644 | |||||||
| chr5:180048818 | A | C | 274 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0199 others(271): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.248-8171T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180048818 | |||||||
| chr5:180048818 | A | G | 1 | a0001c0001t0001g0301 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.248-8171T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180048818 | |||||||
| chr5:180049195 | C | A | 47 | a0001c0002t0001g0011 a0001c0002t0001g0016 a0001c0002t0001g0027 others(44): Show |
47 | HG00438.hp1 HG01074.hp2 HG01255.hp2 others(44): Show |
intron_variant | MODIFIER | c.248-8548G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180049195 | |||||||
| chr5:180049336 | T | C | 1 | a0001c0002t0001g0051 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.248-8689A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180049336 | |||||||
| chr5:180049388 | G | C | 4 | a0001c0003t0001g0157 a0001c0003t0002g0155 a0001c0003t0002g0156 others(1): Show |
4 | HG01884.hp2 HG02280.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.248-8741C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180049388 | |||||||
| chr5:180049610 | T | C | 49 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(46): Show |
51 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.248-8963A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180049610 | |||||||
| chr5:180049645 | T | C | 1 | a0001c0002t0001g0066 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.248-8998A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180049645 | |||||||
| chr5:180049713 | G | A | 1 | a0001c0002t0001g0091 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.248-9066C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180049713 | |||||||
| chr5:180049759 | T | C | 1 | a0001c0002t0001g0095 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.248-9112A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180049759 | |||||||
| chr5:180049913 | C | G | 1 | a0001c0002t0001g0039 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.248-9266G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180049913 | |||||||
| chr5:180050020 | A | G | 1 | a0001c0001t0001g0244 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.248-9373T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180050020 | |||||||
| chr5:180050299 | C | T | 1 | a0001c0001t0001g0316 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.248-9652G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180050299 | |||||||
| chr5:180050523 | G | A | 3 | a0001c0002t0001g0030 a0001c0002t0001g0133 a0002c0010t0001g0031 |
3 | HG01243.hp2 HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.248-9876C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180050523 | |||||||
| chr5:180050587 | T | A | 1 | a0001c0007t0001g0008 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.248-9940A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180050587 | |||||||
| chr5:180050627 | C | T | 1 | a0001c0003t0002g0156 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.248-9980G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180050627 | |||||||
| chr5:180050707 | ATCTT | A | 3 | a0001c0001t0001g0325 a0001c0001t0001g0326 a0001c0001t0001g0327 |
3 | HG02809.hp1 HG03195.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.248-10064_248-1006 others(8): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180050707 | |||||||
| chr5:180050787 | G | T | 4 | a0001c0003t0001g0153 a0001c0003t0001g0164 a0001c0003t0001g0165 others(1): Show |
4 | HG00642.hp1 HG00733.hp2 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.248-10140C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180050787 | |||||||
| chr5:180050847 | G | A | 128 | a0001c0001t0001g0199 a0001c0001t0001g0325 a0001c0001t0001g0326 others(125): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.248-10200C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180050847 | |||||||
| chr5:180050919 | T | A | 4 | a0001c0001t0001g0271 a0001c0001t0001g0275 a0001c0001t0001g0290 others(1): Show |
4 | NA18998.hp1 NA19007.hp1 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.248-10272A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180050919 | |||||||
| chr5:180051055 | G | A | 2 | a0001c0001t0001g0329 a0001c0001t0001g0330 |
2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.248-10408C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180051055 | |||||||
| chr5:180051113 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.248-10466G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180051113 | |||||||
| chr5:180051238 | A | ATATT | 45 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(42): Show |
45 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(42): Show |
intron_variant | MODIFIER | c.248-10595_248-1059 others(8): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180051238 | |||||||
| chr5:180051238 | A | ATATTTAT others(1): Show |
10 | a0001c0001t0001g0237 a0001c0001t0001g0244 a0001c0001t0001g0245 others(7): Show |
10 | HG02055.hp2 HG02257.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.248-10599_248-1059 others(12): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180051238 | |||||||
| chr5:180051238 | A | ATATTTAT others(5): Show |
46 | a0001c0001t0001g0200 a0001c0001t0001g0298 a0001c0001t0001g0302 others(43): Show |
47 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.248-10603_248-1059 others(16): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180051238 | |||||||
| chr5:180051238 | A | ATATTTAT others(9): Show |
131 | a0001c0001t0001g0007 a0001c0001t0001g0299 a0001c0001t0001g0300 others(128): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.248-10607_248-1059 others(20): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180051238 | |||||||
| chr5:180051238 | A | ATATTTAT others(13): Show |
30 | a0001c0001t0001g0006 a0001c0001t0001g0199 a0001c0001t0001g0305 others(27): Show |
31 | HG00280.hp2 HG00408.hp2 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.248-10611_248-1059 others(24): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180051238 | |||||||
| chr5:180051238 | A | ATATTTAT others(17): Show |
5 | a0001c0001t0001g0304 a0001c0002t0001g0052 a0001c0002t0001g0109 others(2): Show |
5 | HG02683.hp1 HG03710.hp1 NA18943.hp1 others(2): Show |
intron_variant | MODIFIER | c.248-10615_248-1059 others(28): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180051238 | |||||||
| chr5:180051287 | T | C | 33 | a0001c0001t0001g0328 a0001c0002t0001g0096 a0001c0003t0001g0001 others(30): Show |
37 | HG00280.hp2 HG00738.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.248-10640A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180051287 | |||||||
| chr5:180051319 | G | A | 1 | a0001c0001t0001g0330 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.248-10672C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180051319 | |||||||
| chr5:180051517 | G | A | 1 | a0001c0002t0001g0057 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.248-10870C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180051517 | |||||||
| chr5:180051528 | C | T | 53 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(50): Show |
55 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.248-10881G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180051528 | |||||||
| chr5:180051621 | T | C | 1 | a0001c0001t0001g0323 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.248-10974A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180051621 | |||||||
| chr5:180051891 | C | A | 49 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(46): Show |
51 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.248-11244G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180051891 | |||||||
| chr5:180051929 | T | C | 1 | a0001c0002t0001g0057 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.248-11282A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180051929 | |||||||
| chr5:180052146 | C | T | 49 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(46): Show |
49 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(46): Show |
intron_variant | MODIFIER | c.248-11499G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180052146 | |||||||
| chr5:180052300 | T | C | 7 | a0001c0001t0001g0210 a0001c0001t0001g0329 a0001c0001t0001g0330 others(4): Show |
7 | HG01884.hp2 HG02280.hp2 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.248-11653A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180052300 | |||||||
| chr5:180052589 | C | T | 6 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(3): Show |
6 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.248-11942G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180052589 | |||||||
| chr5:180052621 | G | T | 171 | a0001c0001t0001g0199 a0001c0001t0001g0325 a0001c0001t0001g0326 others(168): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.248-11974C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180052621 | |||||||
| chr5:180053027 | G | A | 183 | a0001c0001t0001g0199 a0001c0001t0001g0276 a0001c0001t0001g0325 others(180): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.248-12380C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180053027 | |||||||
| chr5:180053137 | A | C | 2 | a0001c0003t0001g0146 a0001c0003t0001g0147 |
2 | HG01261.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.248-12490T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180053137 | |||||||
| chr5:180053172 | G | A | 44 | a0001c0001t0001g0328 a0001c0002t0001g0096 a0001c0003t0001g0001 others(41): Show |
48 | HG00280.hp2 HG00558.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.248-12525C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180053172 | |||||||
| chr5:180053418 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.248-12771C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180053418 | |||||||
| chr5:180053578 | T | G | 1 | a0001c0001t0001g0250 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.248-12931A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180053578 | |||||||
| chr5:180053772 | C | T | 1 | a0001c0001t0001g0272 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.248-13125G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180053772 | |||||||
| chr5:180053824 | TC | T | 37 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(34): Show |
39 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.248-13178delG | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180053824 | |||||||
| chr5:180053825 | CT | C | 176 | a0001c0001t0001g0199 a0001c0001t0001g0265 a0001c0001t0001g0323 others(173): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.248-13179delA | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180053825 | |||||||
| chr5:180053826 | T | A | 37 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(34): Show |
39 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.248-13179A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180053826 | |||||||
| chr5:180053968 | T | C | 3 | a0001c0003t0001g0157 a0001c0003t0002g0155 a0001c0003t0002g0156 |
3 | HG01884.hp2 HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.248-13321A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180053968 | |||||||
| chr5:180054042 | C | T | 1 | a0001c0002t0001g0058 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.248-13395G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180054042 | |||||||
| chr5:180054250 | C | T | 1 | a0001c0001t0001g0235 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.248-13603G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180054250 | |||||||
| chr5:180054302 | G | A | 182 | a0001c0001t0001g0199 a0001c0001t0001g0325 a0001c0001t0001g0326 others(179): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.248-13655C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180054302 | |||||||
| chr5:180054711 | C | T | 1 | a0001c0002t0001g0069 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.248-14064G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180054711 | |||||||
| chr5:180054789 | C | T | 269 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0199 others(266): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.248-14142G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180054789 | |||||||
| chr5:180055026 | A | G | 5 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0214 others(2): Show |
5 | HG01891.hp2 HG02145.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.248-14379T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055026 | |||||||
| chr5:180055114 | G | A | 1 | a0001c0002t0001g0126 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.248-14467C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055114 | |||||||
| chr5:180055126 | T | C | 1 | a0001c0002t0001g0093 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.248-14479A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055126 | |||||||
| chr5:180055248 | C | CA | 9 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0272 others(6): Show |
9 | HG00408.hp1 HG00609.hp2 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.248-14602dupT | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055248 | |||||||
| chr5:180055248 | C | CAA | 8 | a0001c0001t0001g0251 a0001c0001t0001g0276 a0001c0001t0001g0278 others(5): Show |
8 | HG00544.hp2 HG01928.hp2 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.248-14603_248-1460 others(6): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055248 | |||||||
| chr5:180055248 | C | CAAAAAAA others(3): Show |
1 | a0001c0004t0005g0142 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.248-14611_248-1460 others(14): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055248 | |||||||
| chr5:180055248 | C | CAAAAAAA others(18): Show |
1 | a0001c0001t0001g0283 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.248-14626_248-1460 others(29): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055248 | |||||||
| chr5:180055248 | CAAAAAAA others(6): Show |
C | 2 | a0001c0001t0001g0277 a0001c0001t0001g0280 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.248-14614_248-1460 others(17): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055248 | |||||||
| chr5:180055248 | CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0001g0291 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.248-14616_248-1460 others(19): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055248 | |||||||
| chr5:180055259 | AAAAAAAA others(15): Show |
A | 3 | a0001c0003t0001g0157 a0001c0003t0002g0156 a0001c0005t0001g0195 |
3 | HG01884.hp2 HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.248-14634_248-1461 others(26): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055259 | |||||||
| chr5:180055260 | AAAAAAAA others(14): Show |
A | 44 | a0001c0001t0001g0328 a0001c0001t0001g0329 a0001c0001t0001g0330 others(41): Show |
46 | HG00280.hp2 HG00558.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.248-14634_248-1461 others(25): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055260 | |||||||
| chr5:180055261 | AAAAAAAA others(13): Show |
A | 122 | a0001c0001t0001g0199 a0001c0001t0001g0325 a0001c0001t0001g0326 others(119): Show |
123 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.248-14634_248-1461 others(24): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055261 | |||||||
| chr5:180055262 | AAAAAAAA others(12): Show |
A | 15 | a0001c0001t0001g0323 a0001c0002t0001g0019 a0001c0002t0001g0020 others(12): Show |
15 | HG00140.hp2 HG00673.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.248-14634_248-1461 others(23): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055262 | |||||||
| chr5:180055267 | AAAAAAAA others(7): Show |
A | 2 | a0001c0001t0001g0231 a0001c0001t0002g0243 |
2 | HG02818.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.248-14634_248-1462 others(18): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055267 | |||||||
| chr5:180055268 | AAAAAAAA others(6): Show |
A | 32 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0211 others(29): Show |
32 | HG00140.hp1 HG00544.hp1 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.248-14634_248-1462 others(17): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055268 | |||||||
| chr5:180055269 | AAAAAAAA others(5): Show |
A | 40 | a0001c0001t0001g0007 a0001c0001t0001g0200 a0001c0001t0001g0201 others(37): Show |
40 | HG00408.hp2 HG00438.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.248-14634_248-1462 others(16): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055269 | |||||||
| chr5:180055270 | AAAAAAAA others(4): Show |
A | 11 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0208 others(8): Show |
11 | HG00639.hp2 HG02055.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.248-14634_248-1462 others(15): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055270 | |||||||
| chr5:180055271 | AAAAAAAA others(3): Show |
A | 5 | a0001c0001t0001g0006 a0001c0001t0001g0244 a0001c0001t0001g0247 others(2): Show |
5 | HG02257.hp2 HG02970.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.248-14634_248-1462 others(14): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055271 | |||||||
| chr5:180055281 | C | A | 3 | a0001c0001t0001g0283 a0001c0004t0001g0002 a0001c0004t0005g0142 |
3 | HG02647.hp2 NA19080.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.248-14634G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055281 | |||||||
| chr5:180055290 | A | C | 37 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(34): Show |
39 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.248-14643T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055290 | |||||||
| chr5:180055440 | T | TCTG | 9 | a0001c0003t0001g0157 a0001c0003t0001g0178 a0001c0003t0001g0179 others(6): Show |
9 | HG00558.hp2 HG01884.hp2 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.248-14794_248-1479 others(7): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055440 | |||||||
| chr5:180055440 | T | TCTGTG | 43 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(40): Show |
45 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.248-14794_248-1479 others(9): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055440 | |||||||
| chr5:180055440 | T | TCTGTGTG | 202 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0202 others(199): Show |
206 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.248-14794_248-1479 others(11): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055440 | |||||||
| chr5:180055440 | T | TCTGTGTG others(2): Show |
10 | a0001c0002t0001g0010 a0001c0002t0001g0052 a0001c0002t0001g0053 others(7): Show |
10 | HG01069.hp2 HG01168.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.248-14794_248-1479 others(13): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055440 | |||||||
| chr5:180055440 | T | TCTGTGTG others(4): Show |
4 | a0001c0002t0001g0049 a0001c0002t0001g0050 a0001c0002t0001g0051 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.248-14794_248-1479 others(15): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055440 | |||||||
| chr5:180055451 | T | C | 4 | a0001c0002t0001g0011 a0001c0002t0001g0035 a0001c0002t0001g0037 others(1): Show |
4 | NA18947.hp2 NA18959.hp2 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.248-14804A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055451 | |||||||
| chr5:180055453 | C | T | 49 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(46): Show |
51 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.248-14806G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055453 | |||||||
| chr5:180055455 | T | C | 44 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(41): Show |
46 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.248-14808A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055455 | |||||||
| chr5:180055457 | T | C | 5 | a0001c0003t0001g0178 a0001c0003t0001g0179 a0001c0003t0001g0180 others(2): Show |
5 | HG00558.hp2 HG02056.hp1 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.248-14810A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055457 | |||||||
| chr5:180055469 | T | C | 7 | a0001c0001t0001g0237 a0001c0001t0001g0244 a0001c0001t0001g0245 others(4): Show |
7 | HG02055.hp2 HG02257.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.248-14822A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055469 | |||||||
| chr5:180055472 | G | A | 182 | a0001c0001t0001g0199 a0001c0001t0001g0325 a0001c0001t0001g0326 others(179): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.248-14825C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055472 | |||||||
| chr5:180055476 | G | A | 1 | a0001c0002t0001g0057 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.248-14829C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055476 | |||||||
| chr5:180055478 | G | A | 3 | a0001c0003t0001g0193 a0001c0005t0003g0191 a0001c0005t0003g0192 |
3 | HG02572.hp1 HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.248-14831C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055478 | |||||||
| chr5:180055603 | A | G | 2 | a0001c0002t0001g0061 a0001c0002t0001g0123 |
2 | HG01192.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.248-14956T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055603 | |||||||
| chr5:180055715 | T | A | 1 | a0001c0002t0001g0095 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.248-15068A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055715 | |||||||
| chr5:180055811 | G | A | 1 | a0001c0004t0001g0143 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.248-15164C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055811 | |||||||
| chr5:180055812 | C | T | 14 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(11): Show |
14 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.248-15165G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055812 | |||||||
| chr5:180055813 | G | A | 1 | a0001c0001t0001g0323 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.248-15166C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055813 | |||||||
| chr5:180055821 | T | C | 269 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0199 others(266): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.248-15174A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180055821 | |||||||
| chr5:180056045 | C | T | 1 | a0001c0001t0001g0324 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.248-15398G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180056045 | |||||||
| chr5:180056059 | G | A | 4 | a0001c0003t0001g0153 a0001c0003t0001g0164 a0001c0003t0001g0165 others(1): Show |
4 | HG00642.hp1 HG00733.hp2 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.247+15397C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180056059 | |||||||
| chr5:180056071 | G | A | 1 | a0001c0002t0001g0124 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.247+15385C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180056071 | |||||||
| chr5:180056253 | GA | G | 174 | a0001c0001t0001g0199 a0001c0001t0001g0325 a0001c0001t0001g0326 others(171): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.247+15202delT | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180056253 | |||||||
| chr5:180056254 | A | G | 1 | a0001c0001t0001g0236 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.247+15202T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180056254 | |||||||
| chr5:180056360 | T | G | 48 | a0001c0001t0001g0328 a0001c0002t0001g0096 a0001c0003t0001g0001 others(45): Show |
52 | HG00280.hp2 HG00558.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.247+15096A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180056360 | |||||||
| chr5:180056405 | C | G | 10 | a0001c0001t0001g0203 a0001c0001t0001g0220 a0001c0001t0001g0227 others(7): Show |
10 | HG00639.hp2 HG01123.hp1 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.247+15051G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180056405 | |||||||
| chr5:180056584 | G | T | 1 | a0001c0002t0001g0108 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.247+14872C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180056584 | |||||||
| chr5:180056622 | G | A | 1 | a0001c0002t0001g0036 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.247+14834C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180056622 | |||||||
| chr5:180056686 | T | A | 38 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(35): Show |
40 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.247+14770A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180056686 | |||||||
| chr5:180056799 | G | A | 1 | a0001c0001t0001g0323 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.247+14657C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180056799 | |||||||
| chr5:180057074 | A | G | 2 | a0001c0001t0001g0321 a0001c0001t0001g0322 |
2 | HG02135.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.247+14382T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180057074 | |||||||
| chr5:180057218 | G | A | 1 | a0001c0002t0002g0132 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.247+14238C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180057218 | |||||||
| chr5:180057265 | C | G | 287 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(284): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.247+14191G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180057265 | |||||||
| chr5:180057307 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.247+14149C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180057307 | |||||||
| chr5:180057310 | A | T | 1 | a0001c0003t0001g0151 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.247+14146T>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180057310 | |||||||
| chr5:180057314 | C | T | 50 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0298 others(47): Show |
52 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(49): Show |
intron_variant | MODIFIER | c.247+14142G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180057314 | |||||||
| chr5:180057320 | G | A | 2 | a0001c0002t0001g0045 a0001c0002t0001g0120 |
2 | HG01943.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.247+14136C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180057320 | |||||||
| chr5:180057323 | A | T | 2 | a0001c0002t0001g0045 a0001c0002t0001g0120 |
2 | HG01943.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.247+14133T>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180057323 | |||||||
| chr5:180057344 | T | G | 1 | a0001c0001t0001g0252 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.247+14112A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180057344 | |||||||
| chr5:180057518 | A | C | 37 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(34): Show |
39 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.247+13938T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180057518 | |||||||
| chr5:180057519 | G | C | 37 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(34): Show |
39 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.247+13937C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180057519 | |||||||
| chr5:180057547 | C | CA | 9 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(6): Show |
9 | HG02572.hp2 HG02809.hp2 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.247+13908dupT | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180057547 | |||||||
| chr5:180057626 | T | C | 1 | a0001c0002t0001g0097 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.247+13830A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180057626 | |||||||
| chr5:180057649 | T | C | 1 | a0001c0001t0001g0235 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.247+13807A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180057649 | |||||||
| chr5:180057838 | C | A | 220 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0199 others(217): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.247+13618G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180057838 | |||||||
| chr5:180057886 | G | A | 1 | a0001c0001t0001g0317 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.247+13570C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180057886 | |||||||
| chr5:180057896 | T | A | 220 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0199 others(217): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.247+13560A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180057896 | |||||||
| chr5:180058000 | T | C | 231 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0202 others(228): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.247+13456A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180058000 | |||||||
| chr5:180058014 | A | G | 1 | a0001c0001t0001g0323 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.247+13442T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180058014 | |||||||
| chr5:180058038 | T | C | 270 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0199 others(267): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.247+13418A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180058038 | |||||||
| chr5:180058070 | A | G | 1 | a0001c0002t0001g0134 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.247+13386T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180058070 | |||||||
| chr5:180058311 | A | G | 2 | a0001c0002t0001g0129 a0005c0008t0001g0128 |
2 | NA18971.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.247+13145T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180058311 | |||||||
| chr5:180058315 | G | A | 270 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0199 others(267): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.247+13141C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180058315 | |||||||
| chr5:180058515 | C | G | 37 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(34): Show |
39 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.247+12941G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180058515 | |||||||
| chr5:180058528 | A | G | 2 | a0001c0002t0001g0059 a0001c0002t0001g0060 |
2 | HG00609.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.247+12928T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180058528 | |||||||
| chr5:180058595 | G | A | 1 | a0001c0001t0001g0331 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.247+12861C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180058595 | |||||||
| chr5:180058624 | C | T | 1 | a0001c0001t0001g0302 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.247+12832G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180058624 | |||||||
| chr5:180058703 | A | C | 2 | a0001c0001t0001g0221 a0001c0001t0001g0222 |
2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.247+12753T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180058703 | |||||||
| chr5:180058957 | G | C | 1 | a0001c0003t0001g0162 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.247+12499C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180058957 | |||||||
| chr5:180059021 | C | T | 39 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(36): Show |
41 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.247+12435G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180059021 | |||||||
| chr5:180059068 | G | T | 1 | a0001c0002t0001g0023 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.247+12388C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180059068 | |||||||
| chr5:180059093 | C | G | 1 | a0001c0003t0001g0167 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.247+12363G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180059093 | |||||||
| chr5:180059400 | T | C | 16 | a0001c0001t0001g0204 a0001c0001t0001g0211 a0001c0001t0001g0212 others(13): Show |
16 | HG01243.hp2 HG02451.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.247+12056A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180059400 | |||||||
| chr5:180059525 | G | A | 27 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0298 others(24): Show |
29 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(26): Show |
intron_variant | MODIFIER | c.247+11931C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180059525 | |||||||
| chr5:180059730 | A | G | 1 | a0001c0003t0001g0186 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.247+11726T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180059730 | |||||||
| chr5:180060030 | C | T | 1 | a0001c0001t0001g0327 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.247+11426G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180060030 | |||||||
| chr5:180060137 | G | C | 2 | a0001c0001t0001g0277 a0001c0001t0001g0280 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.247+11319C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180060137 | |||||||
| chr5:180060258 | A | T | 132 | a0001c0001t0001g0199 a0001c0001t0001g0324 a0001c0001t0001g0325 others(129): Show |
132 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.247+11198T>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180060258 | |||||||
| chr5:180060288 | A | C | 1 | a0001c0002t0001g0134 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.247+11168T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180060288 | |||||||
| chr5:180060323 | T | A | 1 | a0001c0003t0001g0183 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.247+11133A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180060323 | |||||||
| chr5:180060430 | G | A | 32 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(29): Show |
34 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.247+11026C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180060430 | |||||||
| chr5:180060531 | C | T | 3 | a0001c0001t0001g0220 a0001c0001t0001g0227 a0001c0001t0001g0228 |
3 | HG00639.hp2 HG01123.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.247+10925G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180060531 | |||||||
| chr5:180060563 | G | A | 1 | a0001c0005t0003g0163 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.247+10893C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180060563 | |||||||
| chr5:180060648 | C | A | 48 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(45): Show |
48 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(45): Show |
intron_variant | MODIFIER | c.247+10808G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180060648 | |||||||
| chr5:180060691 | C | T | 8 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(5): Show |
8 | HG02572.hp2 HG02809.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.247+10765G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180060691 | |||||||
| chr5:180060721 | T | C | 1 | a0001c0002t0001g0058 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.247+10735A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180060721 | |||||||
| chr5:180060803 | C | T | 1 | a0001c0002t0001g0058 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.247+10653G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180060803 | |||||||
| chr5:180060851 | C | T | 1 | a0001c0001t0001g0204 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.247+10605G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180060851 | |||||||
| chr5:180060880 | T | C | 4 | a0001c0002t0001g0129 a0001c0002t0001g0130 a0001c0002t0001g0131 others(1): Show |
4 | NA18942.hp1 NA18961.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.247+10576A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180060880 | |||||||
| chr5:180060925 | T | C | 1 | a0001c0005t0001g0195 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.247+10531A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180060925 | |||||||
| chr5:180060931 | A | T | 2 | a0001c0002t0001g0098 a0001c0005t0001g0195 |
2 | NA18943.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.247+10525T>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180060931 | |||||||
| chr5:180060935 | A | G | 269 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0199 others(266): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.247+10521T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180060935 | |||||||
| chr5:180060937 | T | C | 1 | a0001c0005t0001g0195 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.247+10519A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180060937 | |||||||
| chr5:180060973 | G | A | 1 | a0001c0001t0001g0323 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.247+10483C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180060973 | |||||||
| chr5:180060981 | A | G | 1 | a0001c0004t0004g0144 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.247+10475T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180060981 | |||||||
| chr5:180060997 | G | T | 2 | a0001c0001t0001g0329 a0001c0001t0001g0330 |
2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.247+10459C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180060997 | |||||||
| chr5:180061068 | C | CA | 168 | a0001c0001t0001g0199 a0001c0001t0001g0203 a0001c0001t0001g0221 others(165): Show |
172 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.247+10387dupT | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180061068 | |||||||
| chr5:180061068 | C | CAA | 42 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0207 others(39): Show |
42 | HG00642.hp2 HG00673.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.247+10386_247+1038 others(6): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180061068 | |||||||
| chr5:180061068 | C | CAAA | 15 | a0001c0001t0001g0204 a0001c0001t0001g0210 a0001c0001t0001g0211 others(12): Show |
15 | HG01243.hp2 HG02055.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.247+10385_247+1038 others(7): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180061068 | |||||||
| chr5:180061068 | C | CAAAA | 9 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0214 others(6): Show |
9 | HG01884.hp2 HG01891.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.247+10384_247+1038 others(8): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180061068 | |||||||
| chr5:180061068 | CA | C | 9 | a0001c0001t0001g0253 a0001c0001t0001g0280 a0001c0001t0001g0298 others(6): Show |
9 | HG00438.hp2 HG00544.hp1 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.247+10387delT | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180061068 | |||||||
| chr5:180061068 | CAA | C | 24 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(21): Show |
26 | HG00140.hp1 HG00408.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.247+10386_247+1038 others(6): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180061068 | |||||||
| chr5:180061278 | C | A | 1 | a0001c0007t0001g0008 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.247+10178G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180061278 | |||||||
| chr5:180061289 | G | A | 1 | a0001c0002t0001g0119 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.247+10167C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180061289 | |||||||
| chr5:180061372 | T | A | 16 | a0001c0001t0001g0199 a0001c0002t0001g0109 a0001c0002t0001g0110 others(13): Show |
16 | HG00735.hp2 HG01071.hp2 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.247+10084A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180061372 | |||||||
| chr5:180061400 | T | A | 1 | a0001c0001t0001g0323 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.247+10056A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180061400 | |||||||
| chr5:180061419 | G | A | 1 | a0001c0002t0001g0041 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.247+10037C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180061419 | |||||||
| chr5:180061451 | A | G | 1 | a0001c0002t0001g0048 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.247+10005T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180061451 | |||||||
| chr5:180061570 | C | T | 23 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0204 others(20): Show |
23 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.247+9886G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180061570 | |||||||
| chr5:180061660 | C | T | 269 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0199 others(266): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.247+9796G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180061660 | |||||||
| chr5:180062055 | CT | C | 11 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 others(8): Show |
12 | HG01256.hp2 HG01257.hp1 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.247+9400delA | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180062055 | |||||||
| chr5:180062199 | C | T | 131 | a0001c0001t0001g0199 a0001c0001t0001g0324 a0001c0001t0001g0325 others(128): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.247+9257G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180062199 | |||||||
| chr5:180062328 | G | A | 32 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(29): Show |
34 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(31): Show |
intron_variant | MODIFIER | c.247+9128C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180062328 | |||||||
| chr5:180062353 | C | T | 1 | a0001c0002t0001g0047 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.247+9103G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180062353 | |||||||
| chr5:180062420 | A | C | 2 | a0001c0001t0001g0201 a0001c0001t0001g0202 |
2 | HG02145.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.247+9036T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180062420 | |||||||
| chr5:180062862 | A | G | 1 | a0001c0003t0001g0162 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.247+8594T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180062862 | |||||||
| chr5:180063127 | C | T | 4 | a0001c0003t0001g0153 a0001c0003t0001g0164 a0001c0003t0001g0165 others(1): Show |
4 | HG00642.hp1 HG00733.hp2 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.247+8329G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180063127 | |||||||
| chr5:180063261 | T | C | 37 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(34): Show |
39 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.247+8195A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180063261 | |||||||
| chr5:180063284 | G | A | 1 | a0001c0001t0002g0243 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.247+8172C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180063284 | |||||||
| chr5:180063360 | G | A | 1 | a0001c0002t0001g0038 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.247+8096C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180063360 | |||||||
| chr5:180063447 | G | C | 36 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(33): Show |
38 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(35): Show |
intron_variant | MODIFIER | c.247+8009C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180063447 | |||||||
| chr5:180063597 | C | T | 50 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(47): Show |
50 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(47): Show |
intron_variant | MODIFIER | c.247+7859G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180063597 | |||||||
| chr5:180063652 | T | C | 4 | a0001c0001t0001g0325 a0001c0001t0001g0326 a0001c0001t0001g0327 others(1): Show |
4 | HG02258.hp1 HG02809.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.247+7804A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180063652 | |||||||
| chr5:180063993 | T | G | 1 | a0001c0003t0002g0156 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.247+7463A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180063993 | |||||||
| chr5:180063995 | C | T | 2 | a0001c0004t0001g0135 a0001c0004t0001g0143 |
2 | NA18951.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.247+7461G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180063995 | |||||||
| chr5:180064461 | T | C | 1 | a0001c0001t0001g0235 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.247+6995A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180064461 | |||||||
| chr5:180064524 | C | G | 1 | a0001c0007t0001g0008 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.247+6932G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180064524 | |||||||
| chr5:180064667 | T | C | 2 | a0001c0002t0001g0121 a0001c0002t0001g0122 |
2 | HG00099.hp2 HG00642.hp2 |
intron_variant | MODIFIER | c.247+6789A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180064667 | |||||||
| chr5:180064927 | TTC | T | 328 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(325): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.247+6527_247+6528d others(4): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180064927 | |||||||
| chr5:180065135 | T | TA | 34 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(31): Show |
36 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.247+6320dupT | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180065135 | |||||||
| chr5:180065135 | TA | T | 44 | a0001c0001t0001g0252 a0001c0002t0001g0044 a0001c0002t0001g0045 others(41): Show |
48 | HG00280.hp2 HG00558.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.247+6320delT | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180065135 | |||||||
| chr5:180065136 | A | T | 1 | a0001c0002t0001g0119 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.247+6320T>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180065136 | |||||||
| chr5:180065396 | A | G | 52 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(49): Show |
52 | HG00639.hp2 HG01123.hp1 HG01243.hp2 others(49): Show |
intron_variant | MODIFIER | c.247+6060T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180065396 | |||||||
| chr5:180065455 | G | T | 1 | a0001c0001t0001g0250 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.247+6001C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180065455 | |||||||
| chr5:180065629 | G | A | 1 | a0001c0001t0001g0296 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.247+5827C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180065629 | |||||||
| chr5:180065725 | A | C | 1 | a0001c0005t0003g0163 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.247+5731T>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180065725 | |||||||
| chr5:180065739 | G | A | 1 | a0001c0003t0001g0157 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.247+5717C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180065739 | |||||||
| chr5:180065753 | CTG | C | 5 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0287 others(2): Show |
5 | HG00733.hp1 HG01106.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.247+5701_247+5702d others(4): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180065753 | |||||||
| chr5:180065759 | C | CA | 12 | a0001c0001t0001g0290 a0001c0002t0001g0030 a0001c0002t0001g0032 others(9): Show |
12 | HG01175.hp1 HG01243.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.247+5696dupT | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180065759 | |||||||
| chr5:180065772 | AC | A | 33 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(30): Show |
35 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.247+5683delG | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180065772 | |||||||
| chr5:180065773 | C | A | 242 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0202 others(239): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.247+5683G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180065773 | |||||||
| chr5:180065811 | AT | A | 136 | a0001c0001t0001g0199 a0001c0001t0001g0324 a0001c0001t0001g0325 others(133): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.247+5644delA | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180065811 | |||||||
| chr5:180065943 | A | G | 1 | a0001c0001t0001g0204 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.247+5513T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180065943 | |||||||
| chr5:180066063 | T | C | 1 | a0001c0002t0001g0021 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.247+5393A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180066063 | |||||||
| chr5:180066225 | A | G | 1 | a0001c0003t0001g0162 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.247+5231T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180066225 | |||||||
| chr5:180066308 | C | A | 3 | a0001c0003t0001g0193 a0001c0005t0003g0191 a0001c0005t0003g0192 |
3 | HG02572.hp1 HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.247+5148G>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180066308 | |||||||
| chr5:180066510 | T | C | 3 | a0001c0003t0001g0188 a0001c0003t0001g0189 a0001c0003t0001g0190 |
3 | HG01243.hp1 HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.247+4946A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180066510 | |||||||
| chr5:180066621 | A | T | 2 | a0001c0001t0001g0236 a0001c0001t0001g0237 |
2 | HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.247+4835T>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180066621 | |||||||
| chr5:180066693 | C | T | 30 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(27): Show |
32 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.247+4763G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180066693 | |||||||
| chr5:180066788 | G | A | 3 | a0001c0003t0001g0193 a0001c0005t0003g0191 a0001c0005t0003g0192 |
3 | HG02572.hp1 HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.247+4668C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180066788 | |||||||
| chr5:180066794 | T | C | 1 | a0001c0002t0001g0042 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.247+4662A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180066794 | |||||||
| chr5:180066833 | T | A | 275 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0199 others(272): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.247+4623A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180066833 | |||||||
| chr5:180066840 | T | C | 1 | a0001c0001t0001g0291 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.247+4616A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180066840 | |||||||
| chr5:180066885 | T | C | 1 | a0001c0001t0001g0323 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.247+4571A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180066885 | |||||||
| chr5:180067123 | T | G | 1 | a0001c0002t0001g0126 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.247+4333A>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180067123 | |||||||
| chr5:180067325 | A | T | 1 | a0001c0001t0001g0292 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.247+4131T>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180067325 | |||||||
| chr5:180067341 | T | C | 1 | a0001c0003t0001g0194 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.247+4115A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180067341 | |||||||
| chr5:180067364 | C | T | 1 | a0001c0001t0001g0251 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.247+4092G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180067364 | |||||||
| chr5:180067469 | G | A | 1 | a0001c0002t0001g0127 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.247+3987C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180067469 | |||||||
| chr5:180067563 | AATC | A | 8 | a0001c0001t0001g0203 a0001c0001t0001g0236 a0001c0001t0001g0237 others(5): Show |
8 | HG02280.hp1 HG02630.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.247+3890_247+3892d others(5): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180067563 | |||||||
| chr5:180067692 | A | G | 1 | a0001c0001t0001g0323 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.247+3764T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180067692 | |||||||
| chr5:180067853 | G | A | 4 | a0001c0002t0001g0129 a0001c0002t0001g0130 a0001c0002t0001g0131 others(1): Show |
4 | NA18942.hp1 NA18961.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.247+3603C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180067853 | |||||||
| chr5:180067902 | A | G | 1 | a0001c0002t0001g0043 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.247+3554T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180067902 | |||||||
| chr5:180067957 | G | A | 5 | a0001c0001t0001g0292 a0001c0001t0001g0293 a0001c0001t0001g0294 others(2): Show |
5 | HG02486.hp1 HG02647.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.247+3499C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180067957 | |||||||
| chr5:180067958 | A | G | 11 | a0001c0002t0001g0011 a0001c0002t0001g0033 a0001c0002t0001g0034 others(8): Show |
11 | HG02040.hp2 NA18947.hp2 NA18962.hp2 others(8): Show |
intron_variant | MODIFIER | c.247+3498T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180067958 | |||||||
| chr5:180068190 | C | G | 1 | a0001c0002t0001g0032 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.247+3266G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180068190 | |||||||
| chr5:180068264 | C | T | 4 | a0001c0003t0001g0158 a0001c0003t0001g0160 a0001c0003t0001g0161 others(1): Show |
4 | HG02451.hp1 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.247+3192G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180068264 | |||||||
| chr5:180068265 | G | A | 49 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0204 others(46): Show |
49 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(46): Show |
intron_variant | MODIFIER | c.247+3191C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180068265 | |||||||
| chr5:180068311 | AGT | A | 47 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 others(44): Show |
47 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(44): Show |
intron_variant | MODIFIER | c.247+3143_247+3144d others(4): Show |
RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180068311 | |||||||
| chr5:180068532 | T | C | 47 | a0001c0001t0001g0328 a0001c0003t0001g0001 a0001c0003t0001g0003 others(44): Show |
51 | HG00280.hp2 HG00558.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.247+2924A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180068532 | |||||||
| chr5:180068607 | T | C | 6 | a0001c0001t0001g0329 a0001c0001t0001g0330 a0001c0003t0001g0157 others(3): Show |
6 | HG01884.hp2 HG02280.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.247+2849A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180068607 | |||||||
| chr5:180068669 | G | C | 1 | a0001c0002t0002g0132 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.247+2787C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180068669 | |||||||
| chr5:180068677 | A | G | 1 | a0001c0001t0001g0250 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.247+2779T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180068677 | |||||||
| chr5:180069232 | T | C | 1 | a0001c0004t0001g0143 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.247+2224A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180069232 | |||||||
| chr5:180069239 | G | A | 188 | a0001c0001t0001g0199 a0001c0001t0001g0324 a0001c0001t0001g0325 others(185): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.247+2217C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180069239 | |||||||
| chr5:180069272 | T | A | 1 | a0001c0001t0002g0243 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.247+2184A>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180069272 | |||||||
| chr5:180069422 | C | T | 31 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0200 others(28): Show |
33 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.247+2034G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180069422 | |||||||
| chr5:180069533 | A | G | 3 | a0001c0002t0001g0030 a0001c0002t0001g0133 a0002c0010t0001g0031 |
3 | HG01243.hp2 HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.247+1923T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180069533 | |||||||
| chr5:180069579 | A | G | 1 | a0001c0001t0001g0244 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.247+1877T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180069579 | |||||||
| chr5:180069787 | C | T | 3 | a0001c0002t0001g0027 a0001c0002t0001g0028 a0001c0002t0001g0029 |
3 | NA18983.hp2 NA18998.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.247+1669G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180069787 | |||||||
| chr5:180070076 | C | T | 1 | a0001c0003t0001g0158 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.247+1380G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180070076 | |||||||
| chr5:180070110 | G | A | 1 | a0001c0001t0001g0297 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.247+1346C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180070110 | |||||||
| chr5:180070152 | G | C | 1 | a0001c0001t0001g0331 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.247+1304C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180070152 | |||||||
| chr5:180070245 | C | T | 5 | a0001c0002t0001g0022 a0001c0002t0001g0023 a0001c0002t0001g0024 others(2): Show |
5 | NA18948.hp2 NA18970.hp1 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.247+1211G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180070245 | |||||||
| chr5:180070249 | C | T | 187 | a0001c0001t0001g0199 a0001c0001t0001g0325 a0001c0001t0001g0326 others(184): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.247+1207G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180070249 | |||||||
| chr5:180070300 | C | T | 3 | a0001c0002t0001g0019 a0001c0002t0001g0020 a0001c0002t0001g0021 |
3 | HG00140.hp2 HG01516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.247+1156G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180070300 | |||||||
| chr5:180070439 | C | G | 3 | a0001c0003t0001g0157 a0001c0003t0002g0155 a0001c0003t0002g0156 |
3 | HG01884.hp2 HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.247+1017G>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180070439 | |||||||
| chr5:180070453 | C | T | 1 | a0001c0002t0001g0010 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.247+1003G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180070453 | |||||||
| chr5:180070476 | G | A | 6 | a0001c0001t0001g0244 a0001c0001t0001g0245 a0001c0001t0001g0246 others(3): Show |
6 | HG02055.hp2 HG02257.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.247+980C>T | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180070476 | |||||||
| chr5:180070641 | C | T | 49 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(46): Show |
49 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(46): Show |
intron_variant | MODIFIER | c.247+815G>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180070641 | |||||||
| chr5:180070748 | T | C | 220 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0199 others(217): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.247+708A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180070748 | |||||||
| chr5:180070870 | T | C | 1 | a0001c0002t0001g0133 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.247+586A>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180070870 | |||||||
| chr5:180070981 | AC | A | 176 | a0001c0001t0001g0199 a0001c0001t0001g0325 a0001c0001t0001g0326 others(173): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.247+474delG | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180070981 | |||||||
| chr5:180071075 | G | C | 3 | a0001c0001t0001g0200 a0001c0001t0001g0332 a0001c0004t0004g0144 |
3 | NA18953.hp2 NA19074.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.247+381C>G | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180071075 | |||||||
| chr5:180071189 | A | G | 130 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0002t0001g0009 others(127): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.247+267T>C | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180071189 | |||||||
| chr5:180071327 | G | T | 1 | a0001c0002t0001g0009 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.247+129C>A | RNF130 | ENSG00000113269.14 | transcript | ENST00000521389.6 | protein_coding | 1/8 | chr5 | 180071327 |